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Sample records for situ polymerization process

  1. Polyolefin nanocomposites in situ polymerization

    International Nuclear Information System (INIS)

    Galland, Griselda Barrera; Fim, Fabiana de C.; Milani, Marceo A.; Silva, Silene P. da; Forest, Tadeu; Radaelli, Gislaine; Basso, Nara R.S.; Quijada, Raul

    2011-01-01

    Polyethylene and polypropylene nanocomposites using grapheme nanosheets and treated chrysotile have been synthesized by in situ polymerization using metallocene catalysts. The fillers have been submitted to acid, thermal and/ou ultrasound treatments before to introduce them into the polymerization reactor. A complete characterization of the fillers has been done. The nanocomposites have been characterized by SEM, TEM, DRX and AFM. The thermal, mechanic -dynamic, mechanical and electrical properties of the nanocomposites are discussed. (author)

  2. Living olefin polymerization processes

    Science.gov (United States)

    Schrock, Richard R.; Baumann, Robert

    2003-08-26

    Processes for the living polymerization of olefin monomers with terminal carbon-carbon double bonds are disclosed. The processes employ initiators that include a metal atom and a ligand having two group 15 atoms and a group 16 atom or three group 15 atoms. The ligand is bonded to the metal atom through two anionic or covalent bonds and a dative bond. The initiators are particularly stable under reaction conditions in the absence of olefin monomer. The processes provide polymers having low polydispersities, especially block copolymers having low polydispersities. It is an additional advantage of these processes that, during block copolymer synthesis, a relatively small amount of homopolymer is formed.

  3. Living olefin polymerization processes

    Science.gov (United States)

    Schrock, Richard R.; Bauman, Robert

    2006-11-14

    Processes for the living polymerization of olefin monomers with terminal carbon-carbon double bonds are disclosed. The processes employ initiators that include a metal atom and a ligand having two group 15 atoms and a group 16 atom or three group 15 atoms. The ligand is bonded to the metal atom through two anionic or covalent bonds and a dative bond. The initiators are particularly stable under reaction conditions in the absence of olefin monomer. The processes provide polymers having low polydispersities, especially block copolymers having low polydispersities. It is an additional advantage of these processes that, during block copolymer synthesis, a relatively small amount of homopolymer is formed.

  4. In-situ polymerized cellulose nanocrystals (CNC)-poly(l-lactide) (PLLA) nanomaterials and applications in nanocomposite processing.

    Science.gov (United States)

    Miao, Chuanwei; Hamad, Wadood Y

    2016-11-20

    CNC-PLLA nanomaterials were synthesized via in-situ ring-opening polymerization of l-lactide in the presence of CNC, resulting in hydrophobic, homogeneous mixture of PLLA-grafted-CNC and free PLLA homopolymer. The free PLLA serves two useful functions: as barrier to further prevent PLLA-g-CNC from forming aggregates, and in creating improved interfacial properties when these nanomaterials are blended with other polymers, hence enhancing their performance. CNC-PLLA nanomaterials can be used for medical or engineering applications as-they-are or by compounding with suitable biopolymers using versatile techniques, such as solution casting, co-extrusion or injection molding, to form hybrid nanocomposites of tunable mechanical properties. When compounded with commercial-grade PLA, the resulting CNC-PLA nanocomposites appear transparent and have tailored (dynamic and static) mechanical and barrier properties, approaching those of poly(ethylene terephthalate), PET. The effect of reaction conditions on the properties of CNC-PLLA nanomaterials have been carefully studied and detailed throughout the paper. Copyright © 2016 Elsevier Ltd. All rights reserved.

  5. Simultaneous AuIII Extraction and In Situ Formation of Polymeric Membrane-Supported Au Nanoparticles: A Sustainable Process with Application in Catalysis.

    Science.gov (United States)

    Mora-Tamez, Lucía; Esquivel-Peña, Vicente; Ocampo, Ana L; Rodríguez de San Miguel, Eduardo; Grande, Daniel; de Gyves, Josefina

    2017-04-10

    A polymeric membrane-supported catalyst with immobilized gold nanoparticles (AuNPs) was prepared through the extraction and in situ reduction of Au III salts in a one-step strategy. Polymeric inclusion membranes (PIMs) and polymeric nanoporous membranes (PNMs) were tested as different membrane-support systems. Transport experiments indicated that PIMs composed of cellulose triacetate, 2-nitrophenyloctyl ether, and an aliphatic tertiary amine (Adogen 364 or Alamine 336) were the most efficient supports for Au III extraction. The simultaneous extraction and reduction processes were proven to be the result of a synergic phenomenon in which all the membrane components were involved. Scanning electron microscopy characterization of cross-sectional samples suggested a distribution of AuNPs throughout the membrane. Transmission electron microscopy characterization of the AuNPs indicated average particle sizes of 36.7 and 2.9 nm for the PIMs and PNMs, respectively. AuNPs supported on PIMs allowed for >95.4 % reduction of a 0.05 mmol L -1 4-nitrophenol aqueous solution with 10 mmol L -1 NaBH 4 solution within 25 min. © 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

  6. Nanoparticles from a controlled polymerization process

    International Nuclear Information System (INIS)

    Tirumala, V.R.; Caneba, G.T.; Dar, Y.; Wang, H.-H.; Mancini, D.C.

    2003-01-01

    Free-radical retrograde precipitation polymerization process in the past has shown excellent control characteristics over reaction rate, molecular weight, and in the entrapment of live radicals for the generation of block copolymers. The same principle has now been extended to study the reaction confinement to a nanoscale region. Nanosized polymer particles have been reported to form from block copolymers, conventional precipitation polymerization methods, or through emulsion polymerization approaches. In this work, we present a new method of generating nanosized polymer particles by polymerizing the monomer in an environment that precipitates the polymer above the lower critical solution temperature. The nanoparticles have been characterized by both tapping-mode atomic force microscopy observations and in situ synchrotron time-resolved small-angle X-ray scattering analysis. The results from both the techniques showed the formation of nanoparticles in the size range of 15-30 nm, directly from the polymerization process.

  7. Polystyrene/magnesium hydroxide nanocomposite particles prepared by surface-initiated in-situ polymerization

    Science.gov (United States)

    Liu, Hui; Yi, Jianhong

    2009-03-01

    In order to avoid their agglomeration and incompatibility with hydrophobic polystyrene substrate, magnesium hydroxide nanoparticles were encapsulated by surface-initiated in-situ polymerization of styrene. The process contained two steps: electrostatic adsorption of initiator and polymerization of monomer on the surface of magnesium hydroxide. It was found that high adsorption ratio in the electrostatic adsorption of initiator could be attained only in acidic region, and the adsorption belonged to typical physical process. Compared to traditional in-situ polymerization, higher grafting ratio was obtained in surface-initiated in-situ polymerization, which can be attributed to weaker steric hindrance. Both Fourier transform infrared spectroscopy (FTIR) and transmission electron microscopy (TEM) indicated that polystyrene/magnesium hydroxide nanocomposite particles had been successfully prepared by surface-initiated in-situ polymerization. The resulting samples were also analyzed and characterized by means of contact angle testing, dispersibility evaluation and thermogravimetric analysis.

  8. Polypropylene/graphite nanocomposites by in situ polymerization

    International Nuclear Information System (INIS)

    Milani, Marceo A.; Galland, Giselda B.; Quijada, Raul

    2011-01-01

    This work presents the synthesis of nanocomposites of polypropylene/graphite by in situ polymerization using metallocene catalyst and graphene nanosheets. Initially was analyzed which of the metallocene catalysts rac-Et(Ind) 2 ZrCl 2 or rac-Me 2 Si(Ind) 2 ZrCl 2 produces polypropylene with mechanical properties more relevant. Then it were performed the in situ polymerization reactions to obtain the nanocomposites. The polymeric materials were characterized by XRD, DSC, GPC and DMTA. (author)

  9. Thermally conductive, electrically insulating and melt-processable polystyrene/boron nitride nanocomposites prepared by in situ reversible addition fragmentation chain transfer polymerization

    International Nuclear Information System (INIS)

    Huang, Xingyi; Wang, Shen; Zhu, Ming; Yang, Ke; Jiang, Pingkai; Bando, Yoshio; Golberg, Dmitri; Zhi, Chunyi

    2015-01-01

    Thermally conductive and electrically insulating polymer/boron nitride (BN) nanocomposites are highly attractive for various applications in many thermal management fields. However, so far most of the preparation methods for polymer/BN nanocomposites have usually caused difficulties in the material post processing. Here, an in situ grafting approach is designed to fabricate thermally conductive, electrically insulating and post-melt processable polystyrene (PS)/BN nanosphere (BNNS) nanocomposites by initiating styrene (St) on the surface functionalized BNNSs via reversible addition fragmentation chain transfer polymerization. The nanocomposites exhibit significantly enhanced thermal conductivity. For example, at a St/BN feeding ratio of 5:1, an enhancement ratio of 1375% is achieved in comparison with pure PS. Moreover, the dielectric properties of the nanocomposites show a desirable weak dependence on frequency, and the dielectric loss tangent of the nanocomposites remains at a very low level. More importantly, the nanocomposites can be subjected to multiple melt processing to form different shapes. Our method can become a universal approach to prepare thermally conductive, electrically insulating and melt-processable polymer nanocomposites with diverse monomers and nanofillers. (paper)

  10. Microencapsulated Comb-Like Polymeric Solid-Solid Phase Change Materials via In-Situ Polymerization

    Directory of Open Access Journals (Sweden)

    Wei Li

    2018-02-01

    Full Text Available To enhance the thermal stability and permeability resistance, a comb-like polymer with crystallizable side chains was fabricated as solid-solid phase change materials (PCMs inside the cores of microcapsules and nanocapsules prepared via in-situ polymerization. In this study, the effects on the surface morphology and microstructure of micro/nanocapsules caused by microencapsulating different types of core materials (i.e., n-hexadecane, ethyl hexadecanoate, hexadecyl acrylate and poly(hexadecyl acrylate were systematically studied via field emission scanning electron microscope (FE-SEM and transmission electron microscope (TEM. The confined crystallization behavior of comb-like polymer PCMs cores was investigated via differential scanning calorimeter (DSC. Comparing with low molecular organic PCMs cores, the thermal stability of PCMs microencapsulated comb-like polymer enhanced significantly, and the permeability resistance improved obviously as well. Based on these resultant analysis, the microencapsulated comb-like polymeric PCMs with excellent thermal stability and permeability resistance showed promising foreground in the field of organic solution spun, melt processing and organic coating.

  11. Conductive cotton prepared by polyaniline in situ polymerization using laccase.

    Science.gov (United States)

    Zhang, Ya; Dong, Aixue; Wang, Qiang; Fan, Xuerong; Cavaco-Paulo, Artur; Zhang, Ying

    2014-09-01

    The high-redox-potential catalyst laccase, isolated from Aspergillus, was first used as a biocatalyst in the oxidative polymerization of water-soluble conductive polyaniline, and then conductive cotton was prepared by in situ polymerization under the same conditions. The polymerization of aniline was performed in a water dispersion of sodium dodecylbenzenesulfonate (SDBS) micellar solution with atmospheric oxygen serving as the oxidizing agent. This method is ecologically clean and permits a greater degree of control over the kinetics of the reaction. The conditions for polyaniline synthesis were optimized. Characterizations of the conducting polyaniline and cotton were carried out using Fourier transform infrared spectroscopy, UV-vis spectroscopy, cyclic voltammetry, the fabric induction electrostatic tester, and the far-field EMC shielding effectiveness test fixture.

  12. In situ self-polymerization of unsaturated metal methacrylate and its dispersion mechanism in rubber-based composites

    International Nuclear Information System (INIS)

    Wen, Shipeng; Zhou, Yao; Yao, Lu; Zhang, Liqun; Chan, Tung W.; Liang, Yongri; Liu, Li

    2013-01-01

    Highlights: • In situ self-polymerization of unsaturated metal methacrylate was investigated mainly by the thermal effect. • UMM with low melting point can self-polymerize to a large extent. • The fine dispersion phase is composed of poly(UMM) nanoparticles formed by in situ self-polymerization in the rubber matrix. • The UMM crystals in the presence of peroxide and rubber undergo the processes of melting, diffusion, polymerization, and phase separation in this order. - Abstract: Unsaturated metal methacrylate (UMM) as one kind of functional filler has played an important role in reinforcing rubber materials. The in situ self-polymerization of UMM in UMM/rubber composite leads to the uniform dispersion of poly(UMM) in the rubber matrix, while the crosslinking of rubber and grafting between UMM and rubber chains occur simultaneously, making it difficult to clarify the effect of the in situ polymerization on the dispersion of poly(UMM) in the rubber matrix. In this work, we investigated the dispersion mechanism of UMM without rubber matrix for the first time using differential scanning calorimetry (DSC) and Fourier transform infrared (FTIR) spectroscopy. Three types of UMMs including zinc methacrylate (Zn(MA) 2 ), sodium methacrylate (Na(MA)) and samarium methacrylate (Sm(MA) 3 ) were chosen to investigate the in situ self-polymerization of UMM. Based on DSC results, we conclude that the crystals with low melting point tend to self-polymerize first and generate a large amount of heat in the presence of peroxide. The high heat of reaction can melt the crystals with high melting point, and more UMM molecules are dissolved in the rubber matrix, thus increasing the extent of the in situ polymerization. Hence, the UMM with low melting point can self-polymerize to a large extent. Our findings provide in-depth understanding of the dispersion mechanism of UMM in rubber

  13. Polyethylene-waste tire dust composites via in situ polymerization

    International Nuclear Information System (INIS)

    Reyes A, Y. K.; Narro C, R. I.; Ramos A, M. E.; Neira V, M. G.; Diaz E, J.; Enriquez M, F.; Valencia L, L. A.; Saade C, H.; Diaz de L, R.

    2014-01-01

    Polyethylene/waste tire dust (WTD) composites were obtained by an in situ polymerization technique. The surface of the WTD was modified with deposition of polyethylene by using plasma polymerization. Ethylene polymerization was carried out using bis(cyclopentadienyl) titanium dichloride (Cp 2 TiCl 2 ) as homogeneous metallocenes catalyst, while diethylaluminum chloride (DEAC), ethyl aluminum sesquichloride (EASC) and methyl alumino xane (Mao) were used as co-catalysts at two different [Al]/[Ti] molar ratio. The main characteristics of the obtained polyethylenes were determined by size exclusion chromatography, thermogravimetric analysis, differential scanning calorimetry and wide-angle X-ray diffraction. The results showed that by using EASC and Mao the highest catalytic activities were presented at a [Al]/[Ti] molar ratio of 9.17 and 18.33 respectively. Even though it was possible to obtain polyethylene using WTD (modified or unmodified) the catalytic activity was lower than in the case in which no WTD was added in ethylene polymerization. Scanning transmission electronic microscopy images evidenced that the original morphology of the polyethylenes was not modified by the presence of WTD. (Author)

  14. Polyethylene-waste tire dust composites via in situ polymerization

    Energy Technology Data Exchange (ETDEWEB)

    Reyes A, Y. K.; Narro C, R. I.; Ramos A, M. E. [Universidad Autonoma de Coahuila, Facultad de Ciencias Quimicas, Blvd. Venustiano Carranza s/n, 25280 Saltillo, Coahuila (Mexico); Neira V, M. G.; Diaz E, J.; Enriquez M, F.; Valencia L, L. A.; Saade C, H.; Diaz de L, R., E-mail: ramon.diazdeleon@ciqa.edu.mx [Centro de Investigacion en Quimica Aplicada, Blvd. Enrique Reyna Hermosillo No. 40, Col. San Jose de los Cerritos, 25293 Saltillo, Coahuila (Mexico)

    2014-10-01

    Polyethylene/waste tire dust (WTD) composites were obtained by an in situ polymerization technique. The surface of the WTD was modified with deposition of polyethylene by using plasma polymerization. Ethylene polymerization was carried out using bis(cyclopentadienyl) titanium dichloride (Cp{sub 2}TiCl{sub 2}) as homogeneous metallocenes catalyst, while diethylaluminum chloride (DEAC), ethyl aluminum sesquichloride (EASC) and methyl alumino xane (Mao) were used as co-catalysts at two different [Al]/[Ti] molar ratio. The main characteristics of the obtained polyethylenes were determined by size exclusion chromatography, thermogravimetric analysis, differential scanning calorimetry and wide-angle X-ray diffraction. The results showed that by using EASC and Mao the highest catalytic activities were presented at a [Al]/[Ti] molar ratio of 9.17 and 18.33 respectively. Even though it was possible to obtain polyethylene using WTD (modified or unmodified) the catalytic activity was lower than in the case in which no WTD was added in ethylene polymerization. Scanning transmission electronic microscopy images evidenced that the original morphology of the polyethylenes was not modified by the presence of WTD. (Author)

  15. In situ polymerization of L-Lactide in the presence of fumed silica

    International Nuclear Information System (INIS)

    Prebe, A.; Alcouffe, P.; Cassagnau, Ph.; Gerard, J.F.

    2010-01-01

    Chemiorheology, i.e. rheological changes during the polymerization, of a biosourced monomer, i.e. L-Lactide, containing fumed silica have been studied. For that purpose, the reaction was proceeded in situ between the plates of a dynamic rheometer. The polymerization kinetics was followed from the variation of the complex shear modulus versus reaction time. Moreover, at temperatures lower than the crystallization temperature, it was possible to follow the crystallization process while the polymerization takes place. Adding fumed silica particles into the monomer leads to the formation of a physical (percolated) network from particle-particle interactions, i.e. silica, in the L-Lactide probably hydrophilic interactions. The gel-like structure was kept while the polymerization as long as the strain remains low indicating that the silica particle network remains weak. Furthermore, the mechanism of the break down of the gel structure under large deformation as well as the recovery was discussed. It seems that the non-linearity effect of the nanocomposites stems in the silica inter-particle interactions. It was found that silica particles do not have any effect on the temperature of crystallization - molar mass relation but could act as nucleating agent. In situ polymerization of L-Lactide in the presence of 5 wt.% of modified fumed silica was carried out in a reactor. It was found that fumed hydrophilic silica leaded to a microcomposite with highly dense agglomerates in the polymer matrix whereas with a less hydrophilic silica it was possible to decrease the size of the agglomerates increasing the dispersion. The finest dispersion state was achieved with the 'initiating' functionalized silica leading to a 'grafting from' polymerization of the L-Lactide. Such functionalized silica leads to a nanoscale dispersion in a one-step bulk polymerization with only a few small agglomerates.

  16. Optimization of Microencapsulation Process for Self-Healing Polymeric Material

    International Nuclear Information System (INIS)

    Then, S.; Neon, G.S.; Noor Hayaty Abu Kasim

    2011-01-01

    A series of poly(urea-formaldehyde) (PUF) microcapsules filled with dicyclopentadiene (DCPD) was successfully prepared by in situ polymerization. The effect of diverse process parameters and ingredients on the morphology of the microcapsules was observed by SEM, optical microscopy (OM) and digital microscopy. Different techniques for the characterization of the chemical structure and the core content were considered such as FT-IR and 1 H-NMR as well as the characterization of thermal properties by DSC. High yields of free flowing powder of spherical microcapsules were produced. The synthesized microcapsules can be incorporated into another polymeric host material. In the event the host material cracks due to excessive stress or strong impact, the microcapsules would rupture to release the DCPD, which could polymerize to repair the crack. (author)

  17. In Situ Thermal Generation of Silver Nanoparticles in 3D Printed Polymeric Structures

    Directory of Open Access Journals (Sweden)

    Erika Fantino

    2016-07-01

    Full Text Available Polymer nanocomposites have always attracted the interest of researchers and industry because of their potential combination of properties from both the nanofillers and the hosting matrix. Gathering nanomaterials and 3D printing could offer clear advantages and numerous new opportunities in several application fields. Embedding nanofillers in a polymeric matrix could improve the final material properties but usually the printing process gets more difficult. Considering this drawback, in this paper we propose a method to obtain polymer nanocomposites by in situ generation of nanoparticles after the printing process. 3D structures were fabricated through a Digital Light Processing (DLP system by disolving metal salts in the starting liquid formulation. The 3D fabrication is followed by a thermal treatment in order to induce in situ generation of metal nanoparticles (NPs in the polymer matrix. Comprehensive studies were systematically performed on the thermo-mechanical characteristics, morphology and electrical properties of the 3D printed nanocomposites.

  18. Polyacrylamide grafting of modified graphene oxides by in situ free radical polymerization

    International Nuclear Information System (INIS)

    Tang, Mingyi; Xu, Xiaoyang; Wu, Tao; Zhang, Sai; Li, Xianxian; Li, Yi

    2014-01-01

    Highlights: • Graphene oxide (GO) was modified by chemical reactions to functionalized GO (FGO). • The FGOs and the GO were then subjected to in situ free radical polymerization. • Hydroxyl groups of GO were the most reactive grafting sites. - Abstract: Graphene oxide (GO) was modified using chemical reactions to obtain three types of functionalized GO sheets (FGO). The FGO sheets and the GO were then subjected to in situ free radical polymerization in order to study the grafting polymerization. The FGO and grafted-.FGO were analyzed with Fourier transform infrared spectroscopy, scanning electronic microscopy, thermo-gravimetric analysis (TGA) and X-ray photoelectron spectroscopy (XPS). The grafting percentages in the materials were calculated using the TGA and XPS results. The FGO sheets with different functional groups exhibited different grafting abilities, and hydroxyl groups were proven to be the most reactive grafting sites for the in situ free radical grafting polymerization of polyacrylamide

  19. Preparation of Polystyrene Nanocomposite by In Situ Atom Transfer Radical Polymerization: Study of Polymerization Kinetics in the Presence of Clay

    Directory of Open Access Journals (Sweden)

    H. Roghani-Mamaqani

    2009-12-01

    Full Text Available Styrene nanocomposites were synthesized by in-situ atom transfer radical polymerization at 110oC. The variations of monomer conversion and the linearity of semilogarithmic kinetic plot, some signs of living polymerizationand constant radical concentration in the reaction medium, were revealed by gas chromatography technique (GC. According to the gel permeation chromatography (GPC results, the number average molecular weight increased linearly against the monomer conversion indicating the living nature of the polymerization. Weight average molecular weight and polydispersity of nanocomposites were also derived from GPC data. In addition, the PDI value was wider for polymers extracted from nanocomposite samples, and still widened as the clay content increased. Moreover, all the samples experienced a fall in PDI value from nearly 2 to almost 1.1 as the reaction progressed. FTIR results are indications of some interactions between clay surface and monomer, which may be attributed to higher rated in polymerization kinetics. XRD displayed no peak in in-situ synthesized nanocomposites indicating an exfoliated structure in the prepared nanocomposites; conversely, a solution blending technique resulted in an intercalated structure. AFM phase images well displayed the dispersion of nanoclay in the polymeric matrix. The delamination of clay platelets in the polymer matrix of in-situ prepared nanocomposite is demonstrated by TEM images; on the other hand, TEM results revealed the intercalated structure of nanocomposites prepared by solution blending technique.

  20. In Situ Polymerization via Environmentally-Borne Initiation Stimuli

    Data.gov (United States)

    National Aeronautics and Space Administration — The goal of my research is to develop novel polymeric materials that solidify upon exposure to an environmentally-borne initiation stimulus. Specifically, I propose...

  1. In situ emulsion cationic polymerization of isoprene onto the surface of graphite oxide sheets

    International Nuclear Information System (INIS)

    Pazat, Alice; Beyou, Emmanuel; Barrès, Claire; Bruno, Florence; Janin, Claude

    2017-01-01

    Highlights: • Graphite oxide sheets were functionalized by polyisoprene in a two steps procedure. • The polyisoprene chains were grafted onto functionalized GO sheets by the grafting through technique. • A polyisoprene weight content of 50% was calculated from TGA measurements. • A decrease of the air permeability coefficient of 27% for the vulcanized PI composites has been reached. - Abstract: Grafting of polymers onto graphite oxide sheets (GO) has been widely studied in recent years due to the numerous applications of GO-based composites. Herein, polyisoprene (PI) chains were anchored on the surface of GO by in situ cationic polymerization using a “grafting through” approach with allyltrimethoxysilane-modified GO (GO-ATMS). First, the functionalization of GO sheets through the hydrolysis-condensation of allyltrimethoxysilane (ATMS) molecules was qualitatively evidenced by infra-red spectroscopy and X-ray photoelectron spectrometry and a weight content of 4% grafted ATMS was calculated from thermogravimetric analysis. Then, isoprene was in situ polymerized through a one-pot cationic mechanism by using a highly water-dispersible Lewis acid surfactant combined catalyst. For comparison, it was shown that the cationic polymerization of isoprene in presence of un-functionalized GO sheets led to a polyisoprene weight content on the solid filler divided by 3 compared to GO-ATMS. Finally, the compounding of the modified GO/PI composites was performed at a processing temperature of 80 °C with 2 phr and 15 phr loadings and it was shown a decrease of the air permeability coefficient of 27% for the vulcanizates with 15 phr loading.

  2. In situ emulsion cationic polymerization of isoprene onto the surface of graphite oxide sheets

    Energy Technology Data Exchange (ETDEWEB)

    Pazat, Alice [Ingénierie des Matériaux Polymères, IMP, CNRS UMR 5223, Université Claude Bernard Lyon 1 and INSA de Lyon, 15 boulevard Latarjet, 69122 Villeurbanne cedex (France); Laboratoire de Recherches et de Contrôle du Caoutchouc et des Plastiques, LRCCP, 60 rue Auber, 94408 Vitry-sur-Seine cedex (France); Beyou, Emmanuel, E-mail: beyou@univ-lyon1.fr [Ingénierie des Matériaux Polymères, IMP, CNRS UMR 5223, Université Claude Bernard Lyon 1 and INSA de Lyon, 15 boulevard Latarjet, 69122 Villeurbanne cedex (France); Barrès, Claire [Ingénierie des Matériaux Polymères, IMP, CNRS UMR 5223, Université Claude Bernard Lyon 1 and INSA de Lyon, 15 boulevard Latarjet, 69122 Villeurbanne cedex (France); Bruno, Florence; Janin, Claude [Laboratoire de Recherches et de Contrôle du Caoutchouc et des Plastiques, LRCCP, 60 rue Auber, 94408 Vitry-sur-Seine cedex (France)

    2017-02-28

    Highlights: • Graphite oxide sheets were functionalized by polyisoprene in a two steps procedure. • The polyisoprene chains were grafted onto functionalized GO sheets by the grafting through technique. • A polyisoprene weight content of 50% was calculated from TGA measurements. • A decrease of the air permeability coefficient of 27% for the vulcanized PI composites has been reached. - Abstract: Grafting of polymers onto graphite oxide sheets (GO) has been widely studied in recent years due to the numerous applications of GO-based composites. Herein, polyisoprene (PI) chains were anchored on the surface of GO by in situ cationic polymerization using a “grafting through” approach with allyltrimethoxysilane-modified GO (GO-ATMS). First, the functionalization of GO sheets through the hydrolysis-condensation of allyltrimethoxysilane (ATMS) molecules was qualitatively evidenced by infra-red spectroscopy and X-ray photoelectron spectrometry and a weight content of 4% grafted ATMS was calculated from thermogravimetric analysis. Then, isoprene was in situ polymerized through a one-pot cationic mechanism by using a highly water-dispersible Lewis acid surfactant combined catalyst. For comparison, it was shown that the cationic polymerization of isoprene in presence of un-functionalized GO sheets led to a polyisoprene weight content on the solid filler divided by 3 compared to GO-ATMS. Finally, the compounding of the modified GO/PI composites was performed at a processing temperature of 80 °C with 2 phr and 15 phr loadings and it was shown a decrease of the air permeability coefficient of 27% for the vulcanizates with 15 phr loading.

  3. Polymeric molecular sieve membranes via in situ cross-linking of non-porous polymer membrane templates

    Science.gov (United States)

    Qiao, Zhen-An; Chai, Song-Hai; Nelson, Kimberly; Bi, Zhonghe; Chen, Jihua; Mahurin, Shannon M.; Zhu, Xiang; Dai, Sheng

    2014-04-01

    High-performance polymeric membranes for gas separation are attractive for molecular-level separations in industrial-scale chemical, energyand environmental processes. Molecular sieving materials are widely regarded as the next-generation membranes to simultaneously achieve high permeability and selectivity. However, most polymeric molecular sieve membranes are based on a few solution-processable polymers such as polymers of intrinsic microporosity. Here we report an in situ cross-linking strategy for the preparation of polymeric molecular sieve membranes with hierarchical and tailorable porosity. These membranes demonstrate exceptional performance as molecular sieves with high gas permeabilities and selectivities for smaller gas molecules, such as carbon dioxide and oxygen, over larger molecules such as nitrogen. Hence, these membranes have potential for large-scale gas separations of commercial and environmental relevance. Moreover, this strategy could provide a possible alternative to ‘classical’ methods for the preparation of porous membranes and, in some cases, the only viable synthetic route towards certain membranes.

  4. Hydrophobic Coatings on Cotton Obtained by in Situ Plasma Polymerization of a Fluorinated Monomer in Ethanol Solutions.

    Science.gov (United States)

    Molina, Ricardo; Teixidó, Josep Maria; Kan, Chi-Wai; Jovančić, Petar

    2017-02-15

    Plasma polymerization using hydrophobic monomers in the gas phase is a well-known technology to generate hydrophobic coatings. However, synthesis of functional hydrophobic coatings using plasma technology in liquids has not yet been accomplished. This work is consequently focused on polymerization of a liquid fluorinated monomer on cotton fabric initiated by atmospheric plasma in a dielectric barrier discharge configuration. Functional hydrophobic coatings on cotton were successfully achieved using in situ atmospheric plasma-initiated polymerization of fluorinated monomer dissolved in ethanol. Gravimetric measurements reveal that the amount of polymer deposited on cotton substrates can be modulated with the concentration of monomer in ethanol solution, and cross-linking reactions occur during plasma polymerization of a fluorinated monomer even without the presence of a cross-linking agent. FTIR and XPS analysis were used to study the chemical composition of hydrophobic coatings and to get insights into the physicochemical processes involved in plasma treatment. SEM analysis reveals that at high monomer concentration, coatings possess a three-dimensional pattern with a characteristic interconnected porous network structure. EDX analysis reveals that plasma polymerization of fluorinated monomers takes place preferentially at the surface of cotton fabric and negligible polymerization takes place inside the cotton fabric. Wetting time measurements confirm the hydrophobicity of cotton coatings obtained although equilibrium moisture content was slightly decreased. Additionally, the abrasion behavior and resistance to washing of plasma-coated cotton has been evaluated.

  5. Development of an in situ polymeric hydrogel implant of ...

    African Journals Online (AJOL)

    Purpose: To prepare and characterize in situ gel-forming implants of methylprednisolone for the treatment of spinal cord injuries. Methods: In situ hydrogels of methylprednisolone were prepared by dispersing polylactide glycolic acid. (PLGA) polymer and methylprednisolone in N-methyl-pyrrolidone solvent, and subsequent ...

  6. Development of an in situ polymeric hydrogel implant of ...

    African Journals Online (AJOL)

    Purpose: To prepare and characterize in situ gel-forming implants of methylprednisolone for the treatment of spinal cord injuries. Methods: In situ hydrogels of methylprednisolone were prepared by dispersing polylactide glycolic acid (PLGA) polymer and methylprednisolone in N-methyl-pyrrolidone solvent, and subsequent ...

  7. Biological in situ characterization of polymeric microbubble contrast agents

    NARCIS (Netherlands)

    Wan, Sha; Egri, Gabriella; Oddo, Letizia; Cerroni, Barbara; Dähne, Lars; Paradossi, Gaio; Salvati, Anna; Lynch, Iseult; Dawson, Kenneth A; Monopoli, Marco P

    Polymeric microbubbles (MBs) are gas filled particles composed of a thin stabilized polymer shell that have been recently developed as valid contrast agents for the combined use of ultrasonography (US), magnetic resonance imaging (MRI) and single photon emission computer tomography (SPECT) imaging.

  8. In-situ polymerized polyaniline films 3. Film formation

    Czech Academy of Sciences Publication Activity Database

    Sapurina, I.; Riede, A.; Stejskal, Jaroslav

    2001-01-01

    Roč. 123, č. 3 (2001), s. 503-507 ISSN 0379-6779 R&D Projects: GA AV ČR IAA4050907; GA AV ČR KSK4050111 Institutional research plan: CEZ:AV0Z4050913 Keywords : polyaniline * oxidative polymerization * thin films Subject RIV: CD - Macromolecular Chemistry Impact factor: 1.158, year: 2001

  9. Polymer-clay nanocomposites prepared via in situ emulsion polymerization

    Czech Academy of Sciences Publication Activity Database

    Sedláková, Zdeňka; Pleštil, Josef; Baldrian, Josef; Šlouf, Miroslav; Holub, P.

    2009-01-01

    Roč. 63, č. 3 (2009), s. 365-384 ISSN 0170-0839 R&D Projects: GA AV ČR KAN100500651; GA MŠk ME09058 Institutional research plan: CEZ:AV0Z40500505 Keywords : organic -inorganic hybrid * organoclay * emulsion polymerization Subject RIV: CD - Macromolecular Chemistry Impact factor: 1.014, year: 2009

  10. Preparation of membranes using solvent-less vapor deposition followed by in-situ polymerization

    Energy Technology Data Exchange (ETDEWEB)

    O' Brien, Kevin C [San Ramon, CA; Letts, Stephan A [San Ramon, CA; Spadaccini, Christopher M [Oakland, CA; Morse, Jeffrey C [Pleasant Hill, CA; Buckley, Steven R [Modesto, CA; Fischer, Larry E [Los Gatos, CA; Wilson, Keith B [San Ramon, CA

    2012-01-24

    A system of fabricating a composite membrane from a membrane substrate using solvent-less vapor deposition followed by in-situ polymerization. A first monomer and a second monomer are directed into a mixing chamber in a deposition chamber. The first monomer and the second monomer are mixed in the mixing chamber providing a mixed first monomer and second monomer. The mixed first monomer and second monomer are solvent-less vapor deposited onto the membrane substrate in the deposition chamber. The membrane substrate and the mixed first monomer and second monomer are heated to produce in-situ polymerization and provide the composite membrane.

  11. Preparation of membranes using solvent-less vapor deposition followed by in-situ polymerization

    Science.gov (United States)

    O'Brien, Kevin C [San Ramon, CA; Letts, Stephan A [San Ramon, CA; Spadaccini, Christopher M [Oakland, CA; Morse, Jeffrey C [Pleasant Hill, CA; Buckley, Steven R [Modesto, CA; Fischer, Larry E [Los Gatos, CA; Wilson, Keith B [San Ramon, CA

    2010-07-13

    A system of fabricating a composite membrane from a membrane substrate using solvent-less vapor deposition followed by in-situ polymerization. A first monomer and a second monomer are directed into a mixing chamber in a deposition chamber. The first monomer and the second monomer are mixed in the mixing chamber providing a mixed first monomer and second monomer. The mixed first monomer and second monomer are solvent-less vapor deposited onto the membrane substrate in the deposition chamber. The membrane substrate and the mixed first monomer and second monomer are heated to produce in-situ polymerization and provide the composite membrane.

  12. Modification of the hydrotalcite with sodium stearate and its influence in the polyurethane nanocomposites obtained by the in situ polymerization

    International Nuclear Information System (INIS)

    Carmo, Danieli M. do; Oliveira, Marcia G. de; Soares, Bluma G.

    2015-01-01

    Nanocomposites of PU with synthetic hydrotalcite and organoclay were obtained by the in situ polymerization. The addition of clay in the reaction has occurred with and without dispersion previous, using equipment ultraturrax and ultrasound bath. The results of XRD and FTIR confirmed the clay organophilization process. The viscosity analysis of the dispersions showed increased nanocarga-monomer interaction with the time counter, especially for samples containing LDH-st. Such interactions with possibility reaction between the phases may have contributed to the unbalance of the stoichiometry required for polymerization, resulting in lower molecular weight polymer formed in situ. As a result there was minor degradation temperature values, modulus and viscosity for samples subjected to the methodologies TBT and T. However, these methods in conjunction with LDH-st were fundamentals to improving dispersion in the matrix, accord to visual analysis. (author)

  13. Synthesis and characterization of PMMA/clay nanocomposites prepared by in situ polymerization assisted by sonication

    International Nuclear Information System (INIS)

    Prado, Bruna R.; Bartoli, Julio R.; Ito, Edson N.

    2015-01-01

    In this work is presented the synthesis of nanocomposites of poly(methyl methacrylate), PMMA, with organically montmorillonite (OMMT) modified clays by in situ polymerization assisted by sonication. A statistically designed experiment was used, central composing design (CCD), to study the effect of synthesis variables on the dispersion of nanoparticles in PMMA matrix. The processing and formulation factors studied were: energy of sonication and Flory-Huggins interaction parameter between PMMA and organoclay. The structural (XRD) and morphological (TEM) characterizations of the PMMA/OMMT nanocomposites are compared with the literature. It was observed significant exfoliation of OMMT modified with hydroxyl groups in the nanocomposites of PMMA, mainly at the low ultrasonic energy level (90 and 105 kJ) studied. (author)

  14. Termite and fungal resistance of in situ polymerized tributyltin acrylate and acetylated Indonesian and USA wood

    Science.gov (United States)

    Rebecca E. Ibach; Yusuf Sudo. Hadi; Dodi. Nandika; Sulaeman. Yusuf; Yuliati. Indrayani

    2000-01-01

    Wood [Indonesian pine (IP), Indonesian Jabon (IJ) and USA southern yellow pine (USP)] was either in situ polymerized with tributyltin acrylate (TBTA) or acetylated and then exposed to termite and fungal degradation both in laboratory tests and field exposure. The TBTA woods had an average weight percent gain (WPG) of 11% for IP, 12% for IJ, and 10% for USP. The...

  15. A Kinetics Study on Electrical Resistivity Transition of In Situ Polymer Aging Sensors Based on Carbon-Black-Filled Epoxy Conductive Polymeric Composites (CPCs)

    Science.gov (United States)

    Liang, Qizhen; Nyugen, Mark T.; Moon, Kyoung-Sik; Watkins, Ken; Morato, Lilian T.; Wong, Ching Ping

    2013-06-01

    Sensors based on carbon-black-filled bisphenol A-type epoxy conductive polymeric composites (CPCs) have been prepared and applied to monitor thermal oxidation aging of polymeric materials. Thermogravimetric analysis (TGA) is applied to characterize weight loss of epoxy resin in the aging process. By using a mathematical model based on the Boltzmann equation, a relationship between the electrical resistivity of the sensors based on epoxy/carbon black composites and aging time is established, making it possible to monitor and estimate the aging status of polymeric components in situ based on a fast and convenient electrical resistance measurement.

  16. Synthesis of polypropylene/graphite nanocomposites by means of in situ polymerization

    International Nuclear Information System (INIS)

    Montagna, Larissa S.; Basso, Nara R.S.

    2009-01-01

    The nanotechnology presents a large field for research and development of new polymeric materials based in nanocomposites. This work is related to the synthesis of nanocomposites of polypropylene with graphite as filler. The sheets of graphite in nanometer dimensions were made by means of the chemical exfoliation and thermal treatment. The synthesis of the nanocomposites was carried through by means of the in situ polymerization using a metallocene catalyst and with different amounts of inorganic load (0,5; 1 and 2%). The synthesized nanocomposites were characterized by scanning electron microscopy (SEM) and X-Ray diffraction (XRD). (author)

  17. Origins and Development of Initiation of Free Radical Polymerization Processes

    Directory of Open Access Journals (Sweden)

    Dietrich Braun

    2009-01-01

    Full Text Available At present worldwide about 45% of the manufactured plastic materials and 40% of synthetic rubber are obtained by free radical polymerization processes. The first free radically synthesized polymers were produced between 1910 and 1930 by initiation with peroxy compounds. In the 1940s the polymerization by redox processes was found independently and simultaneously at IG Farben in Germany and ICI in Great Britain. In the 1950s the systematic investigation of azo compounds as free radical initiators followed. Compounds with labile C–C-bonds were investigated as initiators only in the period from the end of the 1960s until the early 1980s. At about the same time, iniferters with cleavable S–S-bonds were studied in detail. Both these initiator classes can be designated as predecessors for “living” or controlled free radical polymerizations with nitroxyl-mediated polymerizations, reversible addition fragmentation chain transfer processes (RAFT, and atom transfer radical polymerizations (ATRP.

  18. Polyethylene/Clay Nanocomposites Produced by In Situ Polymerization with Zirconocene/MAO Catalyst

    Directory of Open Access Journals (Sweden)

    Pimpatima Panupakorn

    2013-01-01

    Full Text Available Two commercial nanoclays were used here as catalytic fillers for production of polyethylene (PE and linear low-density polyethylene (LLDPE nanocomposites via in situ polymerization with zirconocene/MAO catalyst. It was found that both types of nanoclays designated as clay A and clay B can improve thermal stability to the host polymers as observed from a thermal gravimetric analysis (TGA. The distribution of the clays inside the polymer matrices appeared good due to the in situ polymerization system into which the clays were introduced during the polymer forming reaction. Upon investigating the clays by X-ray diffractometer (XRD and Fourier transform infrared spectroscopy (FTIR, it was observed that the crucial differences between the two clays are the crystallite sizes (A < B and the amounts of amine group (A < B. The higher amount of amine group in clay B was supposed to be a major reason for the lower catalytic activity of the polymerization systems compared to clay A resulting from its deactivating effect on zirconocene catalyst. However, for both clays, increasing their contents in the polymerization systems reduced the catalytic activity due to the higher steric hindrance occurring.

  19. Neutron is a marvelous probe to see the living things as it is alive. Real time and in-situ observation on living polymerization

    International Nuclear Information System (INIS)

    Koizumi, Satoshi

    2011-01-01

    Small-angle neutron scattering was employed in order to perform a real time and in-situ observation on a polymerization-induced self-assembly process in in-vivo or in-vitro systems; precise living anionic polymerization of poly-styrene-b-polyisoprene, pre-irradiation radical polymerization of polystyrene onto a polytetrafluoroethylene film, and microbial or enzymatic polymerization of cellulose. The aim of these studies is to clarify self-organizations of macro-molecular assemblies appeared in open non-equilibrium systems, which are exposed to external energy and mass flows induced by chemical reactions. The open non-equilibrium systems are believed to be important for understanding pattern formations not only in materials processing in industry but also in living things. Small-angle scattering observed for the systems was investigated according to the methods established for condensed matter physics (fractal and computational analyses), bridging with synthetic chemistry and molecular biology. (author)

  20. Preparation and thermal properties of mesoporous silica/phenolic resin nanocomposites via in situ polymerization

    Directory of Open Access Journals (Sweden)

    J. Lv

    2012-10-01

    Full Text Available In order to enhance the adhesion between inorganic particles and polymer matrix, in this paper, the mesoporous silica SBA-15 material was synthesized by the sol-gel method. The surface of SBA-15 was modified using γ-glycidyloxypropyltrimethoxysilane (GOTMS as a coupling agent, and then mesoporous silica/phenolic resin (SBA-15/PF nanocomposites were prepared via in situ polymerization. The structural parameters and physical properties of SBA-15, SBA-15-GOTMS (SBA-15 surface treated using GOTMS as coupling agents and E-SBA-15/PF (SBA-15/PF nanocomposites extracted using ethanol as solvent were characterized by X-ray diffraction (XRD, N2 adsorption-desorption, Fourier transform infrared spectroscopy (FTIR, scanning electron microscopy (SEM, transmission electron microscopy (TEM and thermogravimetric analysis (TGA. The thermal properties of the nanocomposites were studied by differential scanning calorimetry (DSC and thermogravimetric analysis (TGA. The results demonstrated that the GOTMS were successfully grafted onto the surface of SBA-15, and chemical bonds between PF and SBA-15-GOTMS were formed after in situ polymerization. In addition, it is found that the in situ polymerization method has great effects on the textural parameters of SBA-15. The results also showed that the glass transition temperatures and thermal stability of the PF nanocomposites were obviously enhanced as compared with the pure PF at silica contents between 1–3 wt%, due to the uniform dispersion of the modified SBA-15 in the matrix.

  1. Poly(acrylic acid) modifying bentonite with in-situ polymerization for removing lead ions.

    Science.gov (United States)

    He, Y F; Zhang, L; Yan, D Z; Liu, S L; Wang, H; Li, H R; Wang, R M

    2012-01-01

    In this paper, a new kind of poly(acrylic acid) modified clay adsorbent, the poly(acrylic acid)/bentonite composite (PAA/HB) was prepared by in-situ polymerization, and utilized to remove lead(II) ions from solutions. The maximum adsorption of adsorbent is at pH 5 for metal ions, whereas the adsorption starts at pH 2. The effects of contact time (5-60 min), initial concentration of metal ions (200-1,000 mg/L) and adsorbent dosage (0.04-0.12 g/100 mL) have been reported in this article. The experimental data were investigated by means of kinetic and equilibrium adsorption isotherms. The kinetic data were analyzed by the pseudo-first-order and pseudo-second-order equation. The experimental data fitted the pseudo-second-order kinetic model very well. Langmuir and Freundlich isotherms were tried for the system to better understand the adsorption isotherm process. The maximal adsorption capacity of the lead(II) ions on the PAA/HB, as calculated from the Langmuir model, was 769.2 mg/g. The results in this study indicated that PAA/HB was an attractive candidate for removing lead(II) (99%).

  2. Polyurethane/organo clay nano composite materials via in-situ polymerization

    International Nuclear Information System (INIS)

    Rehab, A.; Agag, T; Akelah, A.; Shalaby, N.

    2005-01-01

    Polyurethane/organo clay nano composites have been synthesized via in situ polymerization. The organo clay firstly prepared by intercalation of lyamine or amino lauric acid into montmorillonite-clay (MMT) through ion exchange process. The syntheses of polyurethane/organo clay hybrid films containing different ratio of clay were carried out by swelling the organo clay, into diol and diamine or into different kinds of diols, followed by addition of diisocyanate. The nano composites with dispersed structure of MMT was obtained as evidence by scanning electron microscope and x-ray diffraction. X-ray analysis showed that the d-spacing increased to more than 44A since there is no peaks corresponding to do spacing in organo clay with all the ratios (1, 5, 10, 20%). Also, SEM results confirm the dispersion of nanometer silicate layers in the polyurethane matrix. This indicated that the clay was completely exfoliated and homogeneous dispersion in the polyurethane matrix. Also, it was found that the presence of organo clay leads to improvement the mechanical properties. Since, the tensile strength increased with increasing the organo clay contents to 20% by the ratio 194% in compared to the 1H: with 0% organo clay. Also, the elongation is a decreases with increasing the organo clay contents. The results shown the tensile strength of PU/SMA/ALA-MMT nano composites is high by 6-7 times than the corresponding to PU/Tvr-MMT

  3. Sequence-regulated copolymers via tandem catalysis of living radical polymerization and in situ transesterification.

    Science.gov (United States)

    Nakatani, Kazuhiro; Ogura, Yusuke; Koda, Yuta; Terashima, Takaya; Sawamoto, Mitsuo

    2012-03-07

    Sequence regulation of monomers is undoubtedly a challenging issue as an ultimate goal in polymer science. To efficiently produce sequence-controlled copolymers, we herein developed the versatile tandem catalysis, which concurrently and/or sequentially involved ruthenium-catalyzed living radical polymerization and in situ transesterification of methacrylates (monomers: RMA) with metal alkoxides (catalysts) and alcohols (ROH). Typically, gradient copolymers were directly obtained from the synchronization of the two reactions: the instantaneous monomer composition in feed gradually changed via the transesterification of R(1)MA into R(2)MA in the presence of R(2)OH during living polymerization to give R(1)MA/R(2)MA gradient copolymers. The gradient sequence of monomers along a chain was catalytically controlled by the reaction conditions such as temperature, concentration and/or species of catalysts, alcohols, and monomers. The sequence regulation of multimonomer units was also successfully achieved in one-pot by monomer-selective transesterification in concurrent tandem catalysis and iterative tandem catalysis, providing random-gradient copolymers and gradient-block counterparts, respectively. In contrast, sequential tandem catalysis via the variable initiation of either polymerization or in situ transesterification led to random or block copolymers. Due to the versatile adaptability of common and commercially available reagents (monomers, alcohols, catalysts), this tandem catalysis is one of the most efficient, convenient, and powerful tools to design tailor-made sequence-regulated copolymers. © 2012 American Chemical Society

  4. Cycling performance of lithium polymer cells assembled by in situ polymerization of a non-flammable ionic liquid monomer

    International Nuclear Information System (INIS)

    Lee, Yoon-Sung; Kim, Dong-Won

    2013-01-01

    Highlights: • Gel polymer electrolytes were synthesized by in situ polymerization of ionic liquid in the lithium polymer cells. • Flammability of the electrolyte was significantly reduced by polymerizing electrolyte containing a non-flammable ionic liquid monomer. • The cells assembled with polymeric ionic liquid-based electrolytes exhibited reversible cycling behavior with good capacity retention. -- Abstract: Lithium polymer cells composed of a lithium negative electrode and a LiCoO 2 positive electrode were assembled with a gel polymer electrolyte obtained by in situ polymerization of an electrolyte solution containing an ionic liquid monomer with vinyl groups. The polymerization of the electrolyte solution containing the non-flammable ionic liquid monomer resulted in a significant reduction of the flammability of the gel polymer electrolytes. The lithium polymer cell assembled with the stable gel polymer electrolyte delivered a discharge capacity of 134.3 mAh g −1 at ambient temperature and exhibited good capacity retention

  5. Poly I-lactide-layered double hydroxide nanocomposites via in situ polymerization of I-lactide

    DEFF Research Database (Denmark)

    Katiyar, Vimal; Gerds, N.; Koch, C.B.

    2010-01-01

    The use of clay nanofillers offers a potential route to improved barrier properties in polylactide films. Magnesium–aluminium layered double hydroxides (LDHs) are interesting in this respect and we therefore explored synthesis of PLA-LDH nanocomposites by ring-opening polymerization. This method...... is attractive because it should ensure good dispersion of LDH in the polymer. The effect of adding either LDH carbonate (LDH-CO3) or laurate-modified LDH (LDH-C12) was investigated. X-ray diffraction, scanning electron microscopy, and transmission electron microscopy revealed that exfoliated nanocomposites were...... weight was significantly reduced when in-situ polymerization was conducted in the presence of the LDHs and we suggest that chain termination via LDH surface hydroxyl groups and/or metal-catalyzed degradation could be responsible....

  6. Heterogeneous Initiators for Sustainable Polymerization Processes

    Science.gov (United States)

    Jones, Matthew D.

    One of the main challenges facing the twenty-first century is the need to produce chemicals from renewable resources. The dwindling supplies of fossil fuels coupled with instability in supply mean that technologies that were once deemed too expensive are now becoming more economically viable options. The majority of man-made polymers are derived from crude oil based monomers. However, in recent years a tremendous effort has been channeled into the preparation of polymers from sustainable chemicals. Two classic examples are polylactide (derived from corn starch) and polycarbonates (prepared directly from CO2). This chapter serves as an introduction into these two polymers and reviews the literature associated with heterogeneous catalyst for the polymerizations, concentrating on approaches describing the heterogenization of homogeneous catalysts.

  7. In-situ, time-lapse study of extracellular polymeric substance discharge in Streptococcus mutans biofilm.

    Science.gov (United States)

    Liu, Bernard Haochih; Yu, Li-Chieh

    2017-02-01

    Streptococcus mutans is one of the main pathogens that cause tooth decay. By metabolizing carbohydrates, S. mutans emits extracellular polymeric substance (EPS) that adheres to the tooth surface and forms layers of biofilm. Periodontal disease occurs due to the low pH environment created by S. mutans biofilm, and such an acidic environment gradually erodes tooth enamel. Since the existence of EPS is essential in the formation of biofilm, the in-situ investigation of its generation and distribution in real time is the key to the control and suppression of S. mutans biofilm. Prior studies of the biofilm formation process by fluorescence microscope, scanning electron microscope, or spectroscope have roughly divided the mechanism into three stages: (1) initial attachment; (2) microcolonies; and (3) maturation. However, these analytical methods are incapable to observe real-time changes in different locations of the extracellular matrix, and to analyze mechanical properties for single bacteria in micro and nanoscale. Since atomic force microscopy (AFM) operates by precise control of tip-sample interaction forces in liquid and in air, living microorganisms can be analyzed under near-physiological conditions. Thus, analytical techniques based on AFM constitute powerful tools for the study of biological samples, both qualitatively and quantitatively. In this study, we used AFM to quantitatively track the changes of multiple nanomechanical properties of S. mutans, including dissipation energy, adhesion force, deformation, and elastic modulus at different metabolic stages. The data revealed that the bacterial extracellular matrix has a gradient distribution in stickiness, in which different stickiness indicates the variation of EPS compositions, freshness, and metabolic stages. In-situ, time-lapse AFM images showed the local generation and distribution of EPS at different times, in which the highest adhesion distributed along sides of the S. mutans cells. Through time

  8. The In Situ Polymerization and Characterization of PA6/LiCl Composites

    Directory of Open Access Journals (Sweden)

    Dandan Sun

    2013-01-01

    Full Text Available PA6/LiCl composites were synthesized by in situ anionic polymerization based on the interaction between the inorganic salts and PA6. Sodium hydroxide as initiator and N-acetylcaprolactam as activator were used in the preparation of PA6/LiCl composites with variety of LiCl content. X-ray diffraction (XRD and differential scanning calorimeter (DSC testing results showed that both of degree of crystallinity and melting temperature of the composites were decreased under the influence of LiCl. And the γ crystal phase proportion increased with increasing the LiCl content to appropriate amount.

  9. In-situ polymerized polyaniline films. Preparation in solutions of hydrochloric, sulfuric, or phosphoric acid

    International Nuclear Information System (INIS)

    Sedenkova, Ivana; Trchova, Miroslava; Blinova, Natalia V.; Stejskal, Jaroslav

    2006-01-01

    Polyaniline (PANI) was prepared by the oxidative polymerization of aniline hydrochloride and aniline sulfate with ammonium peroxydisulfate in acidic aqueous medium. Aniline was similarly oxidized in solution of phosphoric acid. Thin PANI films are produced at the interfaces with the reaction mixture. The progress of polymerization and the PANI-film formation were monitored in situ by Fourier transform infrared spectroscopy after depositing a droplet of the reaction mixture on a ZnSe crystal. The influences of chloride, sulfate, and phosphate counter-ions on the initiation and progress of aniline polymerization have been analysed. The spectra of the completed PANI films protonated with various acids have been compared with the spectra of the corresponding PANI bases obtained after deprotonating the films with ammonium hydroxide. The peaks in the region 3400-2800 cm -1 , so-called H-peaks, have been analyzed in detail. The influence of chloride, sulfate, and phosphate counter-ions on the shape and position of some of the peaks has been noted

  10. Nanocapsule of cationic liposomes obtained using "in situ" acrylic acid polymerization: stability, surface charge and biocompatibility.

    Science.gov (United States)

    Scarioti, Giovana Danieli; Lubambo, Adriana; Feitosa, Judith P A; Sierakowski, Maria Rita; Bresolin, Tania M B; de Freitas, Rilton Alves

    2011-10-15

    In this work, didecyldimethylammonium bromide (DDAB) and 1,2-dioleoyl-sn-glycero-3-phosphatidylethanolamine (DOPE) (2.5:1) were used to prepare liposomes coated with polyacrylic acid (PAA) using "in situ" polymerization with 2.5, 5 and 25 mM of acrylic acid (AA). The PAA concentrations were chosen to achieve partially to fully covered capsules, and the polymerization reaction was observed with real-time monitoring using dynamic light scattering (NanoDLS). The DDAB:DOPE liposomes showed stability in the tested temperature range (25-70°C), whereas the results confirmed the success of the polymerization according to superficial charge (zeta potential of +66.7±1.2 mV) results and AFM images. For the liposomes that were fully coated with PAA (zeta potential of +0.3±3.9 mV), cytotoxicity was independent of the concentration of albumin. Cationic liposomes and nanocapsules of the stable liposomes coated with PAA were obtained by controlling the surface charge, which was the most important factor related to cytotoxicity. Thus, a potential, safe drug nanocarrier was successfully developed in this work. Copyright © 2011 Elsevier B.V. All rights reserved.

  11. Advances in radiation processing of polymeric materials

    International Nuclear Information System (INIS)

    Makuuchi, K.; Sasak, T.; Vikis, A.C.; Singh, A.

    1993-12-01

    In this paper we review recent advances in industrial applications of electron-beam irradiation in the field of polymer processing at the Takasaki Radiation Chemistry Research Establishment (TRCRE) of JAERI (Japan Atomic Energy Research Institute), and the Whiteshell Laboratories of AECL Research, Canada. Irradiation of a substrate with ionizing radiation produces free radicals through ionization and excitation events. The subsequent chemistry of these radicals is used in radiation processing as a substitute for conventional processing techniques based on heating and/or the addition of chemicals. The advantages of radiation processing include the formation of novel products with desirable material properties, favourable overall process economics and, often, environmental benefits

  12. Synthesis and Characterization of the in Situ Bulk Polymerization of PMMA Containing Graphene Sheets Using Microwave Irradiation

    Directory of Open Access Journals (Sweden)

    Mohammad A. Aldosari

    2013-03-01

    Full Text Available Polymethylmethacrylate–graphene (PMMA/RGO nanocomposites were prepared via in situ bulk polymerization using two different preparation techniques. In the first approach, a mixture of graphite oxide (GO and methylmethacrylate monomers (MMA were polymerized using a bulk polymerization method with a free radical initiator. After the addition of the reducing agent hydrazine hydrate (HH, the product was reduced via microwave irradiation (MWI to obtain R-(GO-PMMA composites. In the second approach, a mixture of graphite sheets (RGO and MMA monomers were polymerized using a bulk polymerization method with a free radical initiator to obtain RGO-(PMMA composites. The composites were characterized by FTIR, 1H-NMR and Raman spectroscopy and XRD, SEM, TEM, TGA and DSC. The results indicate that the composite obtained using the first approach, which involved MWI, had a better morphology and dispersion with enhanced thermal stability compared with the composites prepared without MWI.

  13. Micro-fluidic partitioning between polymeric sheets for chemical amplification and processing

    Energy Technology Data Exchange (ETDEWEB)

    Anderson, Brian L.

    2017-01-24

    A system for fluid partitioning for chemical amplification or other chemical processing or separations of a sample, comprising a first dispenser of a first polymeric sheet, wherein the first polymeric sheet contains chambers; a second dispenser of a second polymeric sheet wherein the first dispenser and the second dispenser are positioned so that the first polymeric sheet and the second polymeric sheet become parallel; a dispenser of the fluid positioned to dispense the fluid between the first polymeric sheet and the second polymeric sheet; and a seal unit that seals the first polymeric sheet and the second polymeric sheet together thereby sealing the sample between the first polymeric sheet and the second polymeric sheet and partitioning the fluid for chemical amplification or other chemical processing or separations.

  14. Modification of the hydrotalcite with sodium stearate and its influence in the polyurethane nanocomposites obtained by the in situ polymerization; Nanocompositos de poliuretano/hidrotalcita via polimerizacao in situ: efeito da modificacao da argila e dos metodos dispersivos

    Energy Technology Data Exchange (ETDEWEB)

    Carmo, Danieli M. do, E-mail: danielimcarmo@hotmail.com [Universidade Federal Rural do Rio de Janeiro (UFRRJ), Seropedica, RJ (Brazil); Oliveira, Marcia G. de [Instituto Nacional de Tecnologia (INT), Rio de Janeiro, RJ (Brazil); Soares, Bluma G. [Universidade Federal do Rio de Janeiro (IMA/UFRJ), Rio de Janeiro, RJ (Brazil). Instituto de Macromoleculas Profa. Eloisa Mano

    2015-07-01

    Nanocomposites of PU with synthetic hydrotalcite and organoclay were obtained by the in situ polymerization. The addition of clay in the reaction has occurred with and without dispersion previous, using equipment ultraturrax and ultrasound bath. The results of XRD and FTIR confirmed the clay organophilization process. The viscosity analysis of the dispersions showed increased nanocarga-monomer interaction with the time counter, especially for samples containing LDH-st. Such interactions with possibility reaction between the phases may have contributed to the unbalance of the stoichiometry required for polymerization, resulting in lower molecular weight polymer formed in situ. As a result there was minor degradation temperature values, modulus and viscosity for samples subjected to the methodologies TBT and T. However, these methods in conjunction with LDH-st were fundamentals to improving dispersion in the matrix, accord to visual analysis. (author)

  15. The Research on Modeling and Simulation of TFE Polymerization Process

    Directory of Open Access Journals (Sweden)

    Jing Gao Sun

    2014-01-01

    Full Text Available PTFE (polytetrafluoroethylene is the fluorinated straight-chain polymer, made by the polymerization of tetrafluoroethylene monomer; it is used widely because of its excellent performance and can be obtained by the polymerization of body, solutions, suspensions, and emulsions. But only the last two are the main ways. This research paper makes simulation based on Polymer Plus. It uses the emulsion polymerization method at background to carry out a semibatch reactor system. Upon the actual production conditions, simulation process under the steady state conditions is used to analyze the effects of the changes on operating conditions; the corresponding dynamic model is created to analyze the impact of the changes of conditions on the entire system. Moreover, the amount of APS which plays an important part in this reaction is discussed for getting the most suitable amount of initiator. Because of less research work on this job, it is so difficult to find the related data from the literature. Therefore, this research will have a great significance for the process of the tetrafluoroethylene emulsion polymerization in the future.

  16. Synthesis of HNTs@PEDOT composites via in situ chemical oxidative polymerization and their application in electrode materials

    Science.gov (United States)

    Wang, Fang; Zhang, Xianhong; Ma, Yuhong; Yang, Wantai

    2018-01-01

    The hybrid composite of poly(3,4-ethylenedioxythiophene) (PEDOT) and halloysite nanotubes (HNTs) was synthesized by a two-step process. First, poly(sodium styrene sulfonate) (PSSNa) was grafted onto HNTs via surface initiated atom transfer radical polymerization. Then with the HNTs-g-PSS as a template and the grafted PSS chains as the counterion dopant, PEDOT was precipitated onto the template via in situ oxidization polymerization of EDOT to form HNTs@PEDOT hybrid composites. The conductivity of HNTs@PEDOT can reach up to 9.35 S/cm with the content of 40% HNTs-g-PSS, which increased almost 78 times than that of pure PEDOT (about 0.12 S/cm) prepared at the similar condition. Further treated with p-toluenesulfonic acid (TsOH) as external dopant, the conductivity of HNTs@PEDOT increased to 24.3 S/cm. The electrochemical properties of the composites were investigated with cyclic voltammetry, galvanostatic charge-discharge and electrochemical impedance spectroscopy with three-electrode cell configuration. The results showed that the capacitance of HNTs@PEDOT composite increased 55% than that of pure PEDOT.

  17. Synthesis and Characterization of Encapsulated Nanosilica Particles with an Acrylic Copolymer by in Situ Emulsion Polymerization Using Thermoresponsive Nonionic Surfactant

    Directory of Open Access Journals (Sweden)

    Daryoosh Vashaee

    2013-08-01

    Full Text Available Nanocomposites of encapsulated silica nanoparticles were prepared by in situ emulsion polymerization of acrylate monomers. The synthesized material showed good uniformity and dispersion of the inorganic components in the base polymer, which enhances the properties of the nanocomposite material. A nonionic surfactant with lower critical solution temperature (LCST was used to encapsulate the silica nanoparticles in the acrylic copolymer matrix. This in situ method combined the surface modification and the encapsulation in a single pot, which greatly simplified the process compared with other conventional methods requiring separate processing steps. The morphology of the encapsulated nanosilica particles was investigated by dynamic light scattering (DLS and transmission electron microscopy (TEM, which confirmed the uniform distribution of the nanoparticles without any agglomerations. A neat copolymer was also prepared as a control sample. Both the neat copolymer and the prepared nanocomposite were characterized by Fourier transform infrared spectroscopy (FTIR, thermal gravimetric analyses (TGA, dynamic mechanical thermal analysis (DMTA and the flame resistance test. Due to the uniform dispersion of the non-agglomerated nanoparticles in the matrix of the polymer, TGA and flame resistance test results showed remarkably improved thermal stability. Furthermore, DMTA results demonstrated an enhanced storage modulus of the nanocomposite samples compared with that of the neat copolymer, indicating its superior mechanical properties.

  18. Conductive nano composites based on cellulose nano fiber coated poly aniline via in situ polymerization

    International Nuclear Information System (INIS)

    Silva, Michael J. da; Sanches, Alex O.; Malmonge, Luiz F.; Malmonge, Jose A.; Medeiros, Eliton S. de; Rosa, Morsyleide F.

    2011-01-01

    Cellulose nano fiber (CNF) was extracted by acid hydrolysis from cotton microfibril and nano composites of CNF/PANI-DBSA were obtained by in situ polymerization of aniline onto CNF. The ratios between DBSA/aniline and aniline/oxidant were varied and the nano composites were characterized by four probes direct current (dc) electrical conductivity, ultraviolet-visible (UV-Vis-NIR) and FTIR spectroscopy and X-ray diffraction (XRD). Electrical conductive about ∼10 -1 S/cm was research and was independent of DBSA/aniline molar ratio between 2-4 and the aniline/oxidant molar ratio between 1-5. X-ray patterns of the samples show crystalline peaks characteristic of cellulose I. The FTIR spectra confirmed the presence of PANI and CNF in all samples. (author)

  19. Preparation and Characterization of Polymer-Grafted Montmorillonite-Lignocellulose Nanocomposites by In Situ Intercalative Polymerization

    Directory of Open Access Journals (Sweden)

    Tavengwa Bunhu

    2016-01-01

    Full Text Available Lignocellulose-clay nanocomposites were synthesized using an in situ intercalative polymerization method at 60°C and a pressure of 1 atm. The ratio of the montmorillonite clay to the lignocellulose ranged from 1 : 9 to 1 : 1 (MMT clay to lignocelluloses, wt%. The adsorbent materials were characterized by Fourier transform infrared spectroscopy (FTIR, thermogravimetric analysis (TGA, transmission electron microscopy (TEM, and X-ray powder diffraction (XRD. FTIR results showed that the polymers were covalently attached to the nanoclay and the lignocellulose in the nanocomposites. Both TEM and XRD analysis showed that the morphology of the materials ranged from phase-separated to intercalated nanocomposite adsorbents. Improved thermal stability, attributable to the presence of nanoclay, was observed for all the nanocomposites. The nanocomposite materials prepared can potentially be used as adsorbents for the removal of pollutants in water treatment and purification.

  20. Synthesis and characterization of polypropylene/graphite nano composite preparation for in situ polymerization

    International Nuclear Information System (INIS)

    Montagna, L.S.; Fim, F. de C.; Galland, G.B.

    2010-01-01

    This paper presents the synthesis of polypropylene/graphite nanocomposites through in situ polymerization, using the metallocene catalyst C 20 H 16 Cl 2 Zr (dichloro(rac-ethylenebis(indenyl))zircon(IV)). The graphite nanosheets in nano dimensions were added to the polymer matrix in percentages of 0.6;1.0;4.2;4.8 and 6.0% (w/w). The TEM images indicated that the thickness of graphite nanosheets ranged from 4 to 60 nm and by means of XRD analysis it was observed that the physical and chemical treatment did not destroyed the graphite layers. The presence of nanosheets did not decrease the catalytic activity of the nanocomposites. TEM images and XRD analysis of nanocomposites showed a good dispersion of the graphite nanosheets in the polypropylene matrix. (author)

  1. Cost efficient carbon fibre reinforced thermoplastics with in-situ polymerization of polyamide

    Science.gov (United States)

    Köhler, T.; Akdere, M.; Röding, T.; Gries, T.; Seide, G.

    2017-10-01

    Lightweight design has gained more and more relevance over the last decades. Especially in automotive industry it is of paramount importance to reduce weight and save fuel. At the same time the demand for safety and performance increases the components’ weight. To reach a trade-off between driving comfort and efficiency new lightweight materials have to be developed. One possible solution is the usage of carbon fibre reinforced thermoplastics (CFRTP) as a lightweight substitute material. In contrast to conventional carbon fibre reinforced plastics (CFRP), CFRTPs are cheaper and have a higher impact resistance. Furthermore they are characterized by hot forming ability, weldability and recyclability. However, the impregnation of the textile requires high pressure, because of the melted polymer’s high viscosity. A new innovative approach for CFRTP is the usage of in-situ polymerization with ɛ-caprolactam as matrix, which has a much lower viscosity and thus requires much lower pressure for impregnation and consolidation.

  2. Solvent exfoliated graphene for reinforcement of PMMA composites prepared by in situ polymerization

    International Nuclear Information System (INIS)

    Wang, Jialiang; Shi, Zixing; Ge, Yu; Wang, Yan; Fan, Jinchen; Yin, Jie

    2012-01-01

    Graphene (GP)-based polymer nanocomposites have attracted considerable scientific attention due to its pronounced improvement in mechanical, thermal and electrical properties compared with pure polymers. However, the preparation of well-dispersed and high-quality GP reinforced polymer composites remains a challenge. In this paper, a simple and facile approach for preparation of poly(methyl methacrylate) (PMMA) functionalized GP (GPMMA) via in situ free radical polymerization is reported. Fourier transform infrared (FTIR), X-ray photoelectron spectra (XPS), Raman, transmission electron microscope (TEM) and thermogravimetric analysis (TGA) are used to confirm the successful grafting of PMMA chains onto the GP sheets. Composite films are prepared by incorporating different amounts of GPMMA into the PMMA matrix through solution-casting method. Compared with pure PMMA, PMMA/GPMMA composites show simultaneously improved Young's modulus, tensile stress, elongation at break and thermal stability by addition of only 0.5 wt% GPMMA. The excellent reinforcement is attributed to good dispersion of high-quality GPMMA and strong interfacial adhesion between GPMMA and PMMA matrix as evidenced by scanning electron microscope (SEM) images of the fracture surfaces. Consequently, this simple protocol has great potential in the preparation of various high-performance polymer composites. Highlights: ► Functionalization of solvent exfoliated graphene by in situ polymerization. ► A simple and scalable method for preparing high-quality graphene. ► Functionalized graphene can be well-dispersed and have a strong interfacial adhesion with the polymer matrix. ► The nanocomposites exhibit a remarkable improvement of thermal and mechanical properties.

  3. Process for impregnating a concrete or cement body with a polymeric material

    Science.gov (United States)

    Mattus, Alfred J.; Spence, Roger D.

    1989-01-01

    A process for impregnating cementitious solids with polymeric materials by blending polymeric materials in a grout, allowing the grout to cure, and contacting the resulting solidified grout containing the polymeric materials with an organic mixture containing a monomer, a cross-linking agent and a catalyst. The mixture dissolves the polymerized particles and forms a channel for distributing the monomer throughout the network formed by the polymeric particles. The organic components are then cured to form a substantially water-impermeable mass.

  4. N-Vinylcarbazole: As an Additive for Thermal Polymerization at Room Temperature with in situ Formation of Ag(0 Nanoparticules

    Directory of Open Access Journals (Sweden)

    Mohamad-Ali Tehfe

    2015-08-01

    Full Text Available N-vinylcarbazole (NVK is proposed as an additive for acrylates thermal free radical polymerization (FRP and epoxy thermal ring opening polymerization (ROP at room temperature. The new initiating systems are based on a silane/silver salt/N-vinylcarbazole interaction, which ensures good to excellent polymerization. Moreover, the polymerization is much more efficient under air than under argon. The effects of the N-vinylcarbazole, silane, silver salt and monomer structures are investigated. Interestingly, silver nanoparticles Ag(0 are formed in situ. The as-synthesized nanocomposite materials contained spherical nanoparticles homogeneously dispersed in the polymer matrices. Polymers and nanoparticles were characterized by Differential Scanning Calorimetry (DSC, Transmission Electron Microscopy (TEM, Energy-Dispersive X-ray Spectrometry (EDS, Fourier Transform Infrared Spectroscopy (FTIR, and UV-vis spectroscopy. A coherent picture of the involved chemical mechanisms is presented.

  5. Influence of HAp on the polymerization processes of a possible radioactive bone cement

    Energy Technology Data Exchange (ETDEWEB)

    Montaño, Carlos J.; Campos, Tarcísio P.R., E-mail: carlmont@ucm.es, E-mail: tprcampos@yahoo.com.br [Universidade Federal de Minas Gerais (UFMG), Belo Horizonte (Brazil). Dept. de Engenharia Nuclear. Lab. de Radiações Ionizantes; Silva, Adolfo H.M.; Araujo, Maria H., E-mail: adolfohmoraes@ufmg.br, E-mail: mharaujo1993@gmail.com [Universidade Federal de Minas Gerais (RMN/UFMG), Belo Horizonte (Brazil). Dept. de Ressonância Magnética Nuclear

    2017-07-01

    Polymethylmethacrylate PMMA is an acrylic that has been already proposed as a composite to adhere together the fractured bone structures. Subsequently, augmentation bone cements have incorporated Calcium Biophosphonates as vital part of its components to increase the biocompatibility with osseous tissues. Minimally invasive percutaneous techniques such as Vertebroplasty and Kyphoplasty have been developed to reduce surgical impact on patients, but in turn have been reported undesirable effects as extravasation of the cement outside of the planning target volume due to the compression of the internal bone fluids or other tissues. An in situ variable that helps favoring of the PMMA polymerization process is the temperature; however, it may bring deleterious effects. On the methodology, an assay was addressed varying the Hydroxyapatite HAp concentration. Also the cement processing was modified by setting water as a vehicle for particle dispersion. The ratios of HAp/PMMA concentrations were: 0.00000, 0.02167, 0.09062, 0.16619 and 0.50000 mixed in PMMA and liquid catalyst and monomer. The thermal profiles were measured during polymerization and analyzed. Nuclear magnetic resonance NMR analysis was carried out on the polymerization process in an aqueous state to monitor the H-H{sub 2}O proton signal. As results, an increasing in the cement hardness time was found in the proportion of the HAp concentration. The highest τ polymerization time was found for the x{sub 5} concentration and the signal from the water trapped in the HAp amorphous lattice was determined around ∼5 ppm in the {sup 1}H NMR spectra. (author)

  6. Luminescent SiO 2-coated Gd 2O 3:Eu 3+ nanorods/poly(styrene) nanocomposites by in situ polymerization

    Science.gov (United States)

    Macedo, Andreia G.; Martins, Manuel A.; Fernandes, Sílvia E. M.; Barros-Timmons, Ana; Trindade, Tito; Carlos, Luís D.; Rocha, João

    2010-10-01

    Europium doped gadolinium oxide nanorods have been coated with silica via a sol-gel approach. The silica coating increases the Eu 3+ absolute emission quantum yields from 0.51 to 0.86 (255 nm excitation) and decay times from 1.43 to 1.80 ms (394.4 nm excitation). Subsequently the silica coating was modified with 3-(trimethoxysilyl)-propyl-methacrylate. Grafting of silica with the MPS coupling agent was confirmed by FTIR and contact angle measurements. The functionalized nanoparticles were used as core structures in the in situ radical polymerization of styrene via miniemulsion and solution routes. Depending on the polymerization technique used the morphology of the polymer coating consisted in isolated spheres or a homogenous film respectively. Although the optical properties of the ensuing nanocomposites were reduced the synthetic strategy developed to process this type of luminescent nanoparticles proved efficient and can be explored using different vinyl or (meth)acrylate monomers.

  7. Modification of Clays by Sol-Gel Reaction and Their Use in the Ethylene In Situ Polymerization for Obtaining Nanocomposites

    Directory of Open Access Journals (Sweden)

    E. Moncada

    2012-01-01

    Full Text Available The nanocomposites formation by in situ polymerization used a metallocene catalyst (butyl-2-cyclopentadienyl zirconium 2-chlorines and a hectorite synthetic clay type which is discussed. This research was carried out in two phases. The first phase consisted of mixing the components of the metallocenic polymerization reaction (metallocene-methylaluminoxane-ethylene with clay in a reactor. In the second phase, the metallocenic catalytic system was supported by clay particles and then a polymerization reaction was made. In this second phase, the clay particles were modified using a sol-gel reaction with different pH values: pH = 3, pH = 8, and pH = 12. The results were compared in terms of the catalytic activity in the different systems (phase 1 and phase 2 and the nanoparticle morphology of nanocomposites generated in this study.

  8. Preparation of Isotactic Polypropylene/Exfoliated MoS2 Nanocomposites via In Situ Intercalative Polymerization

    Directory of Open Access Journals (Sweden)

    He-Xin Zhang

    2017-10-01

    Full Text Available In this research, a Ziegler–Natta catalyst intercalated MoS2 was synthesized through the intercalation of a Grignard reagent into MoS2 galleries, followed by the anchoring of TiCl4. During propylene polymerization, the intercalated MoS2 exfoliated in situ to form PP/exfoliated MoS2 (EMoS2 nanocomposites. The isotactic index values of the resultant PP/EMoS2 nanocomposites were as high as 99%, varying from 98.1% to 99.0%. It was found that the incorporation of the EMoS2 significantly improved the thermal stability and mechanical properties (tensile strength, modulus, and elongation at break of PP. After introduction of EMoS2, the maximum increases in Td5% and Tdmax were 36.9 and 9.7 °C, respectively, relative to neat PP. After blending with commercial PP, the resultant nanocomposites increase in tensile strength and modulus up to 11.4% and 61.2% after 0.52 wt % EMoS2 loading. Thus, this work provides a new way to produce high-performance PP.

  9. A Facile Route to Synthesize Nanographene Reinforced PBO Composites Fiber via in Situ Polymerization

    Directory of Open Access Journals (Sweden)

    Mingqiang Wang

    2016-07-01

    Full Text Available The polymer matrix with introduced carbon-based nanofiber displays fascinating properties. They have inspired extensive research on the synthesis of polymer composites, which have been applied in catalysis, electronics, and energy storage. In this report, we reported a facile and efficient method to prepare poly(p-phenylene benzobisoxazole (PBO/nanographene (PNG composites fibers via in-situ polymerization, accompanied by the reduction from (nanographene oxide NGO to (nanographene NG. By tuning the ratio of feeding PBO monomer to NGO, various composites fibers with 0.1–1 wt % contents of NG were obtained. The efficient PBO chains grafting made NG uniformly disperse in the PBO matrix, and it also increased the uniformity of the packing orientation of PBO chains. Consequently, the tensile strength, tensile modulus, and thermal stability of the obtained PNG composites fibers had been improved significantly. In addition, the composites fibers with 0.5 wt % NG exhibited a 25% increment in tensile strength, and a 41% enhancement in tensile modulus compared with neat PBO fibers. It reveals an excellent reinforcement to PBO composites fibers with NG.

  10. In Situ Field Testing of Processes

    International Nuclear Information System (INIS)

    Wang, J.

    2001-01-01

    The purpose of this Analysis/Model Report (AMR) is to update and document the data and subsequent analyses from ambient field-testing activities performed in underground drifts of the Yucca Mountain Site Characterization Project (YMP). This revision updates data and analyses presented in the initial issue of this AMR. This AMR was developed in accordance with the ''Technical Work Plan for Unsaturated Zone (UZ) Flow and Transport Process Model Report'' and ''Technical Work Plan for UZ Flow, Transport, and Coupled Processes Process Model Report. These activities were performed to investigate in situ flow and transport processes. The evaluations provide the necessary framework to: (1) refine and confirm the conceptual model of matrix and fracture processes in the unsaturated zone (UZ) and (2) analyze the impact of excavation (including use of construction water and effect of ventilation) on the UZ flow and transport processes. This AMR is intended to support revisions to ''Conceptual and Numerical Models for UZ Flow and Transport'' and ''Unsaturated Zone Flow and Transport Model Process Model Report''. In general, the results discussed in this AMR are from studies conducted using a combination or a subset of the following three approaches: (1) air-injection tests, (2) liquid-release tests, and (3) moisture monitoring using in-drift sensors or in-borehole sensors, to evaluate the impact of excavation, ventilation, and construction-water usage on the surrounding rocks. The liquid-release tests and air-injection tests provide an evaluation of in situ fracture flow and the competing processes of matrix imbibition. Only the findings from testing and data not covered in the ''Seepage Calibration Model and Seepage Testing Data'' are analyzed in detail in the AMR

  11. In Situ Field Testing of Processes

    Energy Technology Data Exchange (ETDEWEB)

    J. Wang

    2001-12-14

    The purpose of this Analysis/Model Report (AMR) is to update and document the data and subsequent analyses from ambient field-testing activities performed in underground drifts of the Yucca Mountain Site Characterization Project (YMP). This revision updates data and analyses presented in the initial issue of this AMR. This AMR was developed in accordance with the ''Technical Work Plan for Unsaturated Zone (UZ) Flow and Transport Process Model Report'' and ''Technical Work Plan for UZ Flow, Transport, and Coupled Processes Process Model Report. These activities were performed to investigate in situ flow and transport processes. The evaluations provide the necessary framework to: (1) refine and confirm the conceptual model of matrix and fracture processes in the unsaturated zone (UZ) and (2) analyze the impact of excavation (including use of construction water and effect of ventilation) on the UZ flow and transport processes. This AMR is intended to support revisions to ''Conceptual and Numerical Models for UZ Flow and Transport'' and ''Unsaturated Zone Flow and Transport Model Process Model Report''. In general, the results discussed in this AMR are from studies conducted using a combination or a subset of the following three approaches: (1) air-injection tests, (2) liquid-release tests, and (3) moisture monitoring using in-drift sensors or in-borehole sensors, to evaluate the impact of excavation, ventilation, and construction-water usage on the surrounding rocks. The liquid-release tests and air-injection tests provide an evaluation of in situ fracture flow and the competing processes of matrix imbibition. Only the findings from testing and data not covered in the ''Seepage Calibration Model and Seepage Testing Data'' are analyzed in detail in the AMR.

  12. Isospecific propylene polymerization with in situ generated bis(phenoxy-amine)zirconium and hafnium single site catalysts.

    Science.gov (United States)

    Makio, Haruyuki; Prasad, Aitha Vishwa; Terao, Hiroshi; Saito, Junji; Fujita, Terunori

    2013-07-07

    Bis(phenoxy-imine) Zr and Hf complexes were activated with (i)Bu3Al or (i)Bu2AlH in conjunction with Ph3CB(C6F5)4 and tested as catalysts for propylene polymerization with emphasis on the enantioselectivity of the isospecific species and the single site polymerization characteristics. The isoselective species was identified as the in situ generated bis(phenoxy-amine) complex whose isoselectivity was sensitive to subtle changes in ligand structure. By employing specific substituents at certain key positions the isotacticity reached an extremely high level comparable to high-end commercial isotactic polypropylenes (Tm > 160 °C). Single site polymerization characteristics depended upon the efficiency and selectivity of the in situ imine reduction which is sensitive to the substituent on the imine nitrogen and the reaction conditions. By using (i)Bu2AlH as a reducing agent, quantitative imine reduction can be achieved with a stoichiometric amount of the reducing agent. This lower alkylaluminum loading is beneficial for the catalyst and significantly enhances the polymerization activity and the molecular weight of the resultant polymer.

  13. A Survey on Synthesis Processes of Structured Materials for Biomedical Applications: Iron-based Magnetic Nanoparticles, Polymeric Materials and Polymerization Processes.

    Science.gov (United States)

    Neto, Weslany Silvério; Jensen, Alan Thyago; Ferreira, Gabriella Ribeiro; Valadares, Leonardo Fonseca; Gambetta, Rossano; Gonçalves, Sílvia Belém; Machado, Fabricio

    2015-01-01

    Magnetic materials based on iron oxides are extensively designed for several biomedical applications. Heterogeneous polymerization processes are powerful tools for the production of tailored micro-sized and nanosized magneto-polymeric particles. Although several polymerization processes have been adopted along the years, suspension, emulsion and miniemulsion systems deserve special attention due to its ability to produce spherical polymer particles containing magnetic nanoparticles homogeneously dispersed into the polymer thermoplastic matrices. The main objective of this paper is to review the main methods of synthesis of iron-based magnetic nanoparticles and to illustrate how typical polymerization processes in different dispersion medium can be successfully used to produce engineered magnetic core-shell structures. It is exemplified the use of suspension, emulsion and miniemulsion polymerization processes in order to support experimental methodologies required for the production of magnetic polymer particles intended for biomedical applications such as intravascular embolization treatments, drug delivery systems and hyperthermia treatment.

  14. Synthesis of Polypropylene/Organoclay Nanocomposites via In Situ Polymerization with Improved Thermal and Dynamic-Mechanical Properties.

    Science.gov (United States)

    Almeida, Lidiane A; Marques, Maria de Fátima V; Dahmouche, Karim

    2015-03-01

    Preparation of polypropylene/clay nanocomposites via in situ polymerization is investigated. MgCl2/organophilic clay bi-supported Ziegler-Natta catalysts were used to prepare these nanocomposites. Three organophilic clays (Cloisite 30B, Cloisite 15A, and Claytone HY) were used as support and reinforcement agents. The nanostructure of the composites was characterized by X-ray diffraction. The results showed that the most active catalyst was that with clay having high inter-layer spacing without functional OH groups. Moreover, the silica layers of the clays (Cloisite 15A and Claytone HY) in these polypropylene/clay nanocomposites were exfoliated and well dispersed in the polypropylene matrix. Differential scanning calorimetric was used to investigate both melting and crystallization temperatures, as well as the crystallinity of the nanocomposite samples. These results showed that Cloisite 15A and Claytone HY acted as nucleating agents in the process of crystallization of polypropylene. Thermogravimetric analysis showed that Cloisite 15A and Claytone HY promoted an increase in resistance to thermal degradation. Dynamic-mechanical analysis showed that nanocomposites presented an increase in the storage modulus. Furthermore, Cloisite 15A and Claytone HY promoted an increase in glass transition temperature. Small-angle X-ray scattering analysis was used to determine how clay and its concentration influence the size of the polymer nanocrystals.

  15. Thermo-stabilized, porous polyimide microspheres prepared from nanosized SiO2 templating via in situ polymerization

    Directory of Open Access Journals (Sweden)

    M. Q. Liu

    2015-01-01

    Full Text Available In this article, we addressed a feasible and versatile method of the fabrication of porous polyimide microspheres presenting excellent heat resistance. The preparation process consisted of two steps. Firstly, a novel polyimide/nano-silica composite microsphere was prepared via the self-assembly structures of poly(amic acid (PAA, precursor of PI/nanosized SiO2 blends after in situ polymerization, following the two-steps imidization. Subsequently, the encapsulated nanoparticles were etched away by hydrofluoric acid treatment, giving rise to the pores. It is found the composite structure of PI/SiO2 is a precondition of the formation of nanoporous structures, furthermore, the morphology of the resultant pore could be relatively tuned by changing the content and initial morphology of silica nano-particles trapped into PI matrix. The thermal properties of the synthesized PI porous spheres were studied, indicating that the introduction of nanopores could not effectively influence the thermal stabilities of PI microspheres. Moreover, the fabrication technique described here may be extended to other porous polymer systems.

  16. Instrumentation for Research on the Microstructure Processing and Mechanical Performance of Polymeric Nanocomposites

    National Research Council Canada - National Science Library

    Boyce, Mary

    2001-01-01

    This report details the acquisition of instrumentation to support fundamental research focused on studying the relationships between microstructure, processing and macroscopic properties of polymeric...

  17. Defense University Research Initiative on Nanotechnology: Microstructure, Processing and Mechanical Performance of Polymeric Nanocomposites

    National Research Council Canada - National Science Library

    Boyce, Mary C; Thomas, Edwin L

    2006-01-01

    This research was directed towards the development of fundamental understanding of the connections amongst the microstructure, processing and macroscopic properties of polymeric based nanocomposites...

  18. Support Routines for In Situ Image Processing

    Science.gov (United States)

    Deen, Robert G.; Pariser, Oleg; Yeates, Matthew C.; Lee, Hyun H.; Lorre, Jean

    2013-01-01

    This software consists of a set of application programs that support ground-based image processing for in situ missions. These programs represent a collection of utility routines that perform miscellaneous functions in the context of the ground data system. Each one fulfills some specific need as determined via operational experience. The most unique aspect to these programs is that they are integrated into the large, in situ image processing system via the PIG (Planetary Image Geometry) library. They work directly with space in situ data, understanding the appropriate image meta-data fields and updating them properly. The programs themselves are completely multimission; all mission dependencies are handled by PIG. This suite of programs consists of: (1)marscahv: Generates a linearized, epi-polar aligned image given a stereo pair of images. These images are optimized for 1-D stereo correlations, (2) marscheckcm: Compares the camera model in an image label with one derived via kinematics modeling on the ground, (3) marschkovl: Checks the overlaps between a list of images in order to determine which might be stereo pairs. This is useful for non-traditional stereo images like long-baseline or those from an articulating arm camera, (4) marscoordtrans: Translates mosaic coordinates from one form into another, (5) marsdispcompare: Checks a Left Right stereo disparity image against a Right Left disparity image to ensure they are consistent with each other, (6) marsdispwarp: Takes one image of a stereo pair and warps it through a disparity map to create a synthetic opposite- eye image. For example, a right eye image could be transformed to look like it was taken from the left eye via this program, (7) marsfidfinder: Finds fiducial markers in an image by projecting their approximate location and then using correlation to locate the markers to subpixel accuracy. These fiducial markets are small targets attached to the spacecraft surface. This helps verify, or improve, the

  19. Synthesis of High cis-Polybutadiene in Styrene Solution with Neodymium-Based Catalysts: Towards the Preparation of HIPS and ABS via In Situ Bulk Polymerization

    Directory of Open Access Journals (Sweden)

    Ramón Díaz de León

    2016-01-01

    Full Text Available In a first step, 1,3-butadiene was selectively polymerized at 60°C in styrene as solvent using NdV3/DIBAH/EASC as the catalyst system. The catalyst system activation process, the addition order of monomers and catalyst components, and the molar ratios [Al]/[Nd] and [Cl]/[Nd] were studied. The catalyst system allowed the selective 1,3-butadiene polymerization, reaching conversions between 57.5 and 88.1% with low polystyrene contents in the order of 6.3 to 15.4%. Molecular weights ranging from 39,000 to 150,000 g/mol were obtained, while cis-1,4 content was found in the interval of 94.4 to 96.4%. On the other hand, the glass transition temperatures of synthesized materials were established in the range of −101.9 to −107.4°C, explained by the presence of polystyrene segments in the polybutadiene chains; in the same sense, the polybutadienes did not show the typical melting endotherm of high cis-polybutadienes. In a second step, the resulting styrene/high cis-1,4 polybutadiene solutions were used to synthesize ABS (adding a fraction of acrylonitrile monomer and HIPS via in situ bulk polymerizations and the results were discussed in terms of morphological development, molecular parameters, dynamical mechanical behavior, and mechanical properties.

  20. Facile synthesis of hollow Sn–Co@PMMA nanospheres as high performance anodes for lithium-ion batteries via galvanic replacement reaction and in situ polymerization

    International Nuclear Information System (INIS)

    Yu, Xiaohui; Jiang, Anni; Yang, Hongyan; Meng, Haowen; Dou, Peng; Ma, Daqian; Xu, Xinhua

    2015-01-01

    Highlights: • Hollow Sn–Co nanospheres were synthesized via a facile galvanic replacement method. • PMMA layers were uniform coated on the surface of Sn–Co composites via in situ emulsion polymerization. • The coating layers are beneficial to suppress the aggregation and stabilize the SEI formation on the surface. • Excellent cycling stability and rate capability were obtained by coating PMMA protective layers on the surface of hollow Sn–Co nanospheres. - Abstract: Polymethyl methacrylate (PMMA)-coated hollow Sn–Co nanospheres (Sn–Co@PMMA) with superior electrochemical performance had been synthesized via a facile galvanic replacement method followed by an in situ emulsion polymerization route. The properties were investigated in detail and results show that the hollow Sn–Co nanospheres were evenly coated with PMMA. Benefiting from the protection of the PMMA layers, the hollow Sn–Co@PMMA nanocomposite is capable of retaining a high capacity of 590 mAh g −1 after 100 cycles with a coulomb efficiency above 98%, revealing better electrochemical properties compared with hollow Sn–Co anodes. The PMMA coating could help accommodate the mechanical strain caused by volume expansion and stabilize the solid electrolyte interphase (SEI) film formed on the electrode. Such a facile process could be further extended to other anode materials for lithium-ion batteries

  1. Facile synthesis of hollow Sn–Co@PMMA nanospheres as high performance anodes for lithium-ion batteries via galvanic replacement reaction and in situ polymerization

    Energy Technology Data Exchange (ETDEWEB)

    Yu, Xiaohui; Jiang, Anni; Yang, Hongyan; Meng, Haowen; Dou, Peng; Ma, Daqian [School of Materials Science and Engineering, Tianjin University, Tianjin 300072 (China); Xu, Xinhua, E-mail: xhxutju@gmail.com [School of Materials Science and Engineering, Tianjin University, Tianjin 300072 (China); Tianjin Key Laboratory of Composite and Functional Materials, Tianjin 300072 (China)

    2015-08-30

    Highlights: • Hollow Sn–Co nanospheres were synthesized via a facile galvanic replacement method. • PMMA layers were uniform coated on the surface of Sn–Co composites via in situ emulsion polymerization. • The coating layers are beneficial to suppress the aggregation and stabilize the SEI formation on the surface. • Excellent cycling stability and rate capability were obtained by coating PMMA protective layers on the surface of hollow Sn–Co nanospheres. - Abstract: Polymethyl methacrylate (PMMA)-coated hollow Sn–Co nanospheres (Sn–Co@PMMA) with superior electrochemical performance had been synthesized via a facile galvanic replacement method followed by an in situ emulsion polymerization route. The properties were investigated in detail and results show that the hollow Sn–Co nanospheres were evenly coated with PMMA. Benefiting from the protection of the PMMA layers, the hollow Sn–Co@PMMA nanocomposite is capable of retaining a high capacity of 590 mAh g{sup −1} after 100 cycles with a coulomb efficiency above 98%, revealing better electrochemical properties compared with hollow Sn–Co anodes. The PMMA coating could help accommodate the mechanical strain caused by volume expansion and stabilize the solid electrolyte interphase (SEI) film formed on the electrode. Such a facile process could be further extended to other anode materials for lithium-ion batteries.

  2. Physical methods for initiation of emulsion polymerization processes (review)

    International Nuclear Information System (INIS)

    Averko-Antonovich, I.Yu.; Liakumovich, A.G.

    1994-01-01

    The known and widely used methods for initiation of emulsion polymerization by the exposure of aqueous and organic media to ionizing radiation, plasmoichemical, mechanochemcial, and magnetic treatments, are briefly reviewed. The advantages of radiation-induced emulsion polymerization of vinyl monomers, as compared to the other methods, are pointed out

  3. One-step synthesis of graphene/polyaniline hybrids by in situ intercalation polymerization and their electromagnetic properties

    Science.gov (United States)

    Chen, Xiangnan; Meng, Fanchen; Zhou, Zuowan; Tian, Xin; Shan, Liming; Zhu, Shibu; Xu, Xiaoling; Jiang, Man; Wang, Li; Hui, David; Wang, Yong; Lu, Jun; Gou, Jihua

    2014-06-01

    A new method is introduced for the preparation of graphene/polyaniline hybrids using a one-step intercalation polymerization of aniline inside the expanded graphite. The structural and morphological characterizations were performed by X-ray diffraction analysis, transmission electron microscopy and field emission scanning electron microscopy. Both the experimental and first-principles simulated results show that the aniline cation formed by aniline and H+ tends to be drawn towards the electron-enriched zone and to intercalate into the interlayer of graphite. Subsequently, an in situ polymerization leads to the separation of graphite into graphene sheet, resulting from the exothermic effect and more vigorous movements of the chain molecules of polyaniline. The interactions between polyaniline and graphene were confirmed by Fourier transform infrared spectroscopy and Raman spectra. In addition, the graphene/polyaniline hybrid exhibited a breakthrough in the improvement of microwave absorption.A new method is introduced for the preparation of graphene/polyaniline hybrids using a one-step intercalation polymerization of aniline inside the expanded graphite. The structural and morphological characterizations were performed by X-ray diffraction analysis, transmission electron microscopy and field emission scanning electron microscopy. Both the experimental and first-principles simulated results show that the aniline cation formed by aniline and H+ tends to be drawn towards the electron-enriched zone and to intercalate into the interlayer of graphite. Subsequently, an in situ polymerization leads to the separation of graphite into graphene sheet, resulting from the exothermic effect and more vigorous movements of the chain molecules of polyaniline. The interactions between polyaniline and graphene were confirmed by Fourier transform infrared spectroscopy and Raman spectra. In addition, the graphene/polyaniline hybrid exhibited a breakthrough in the improvement of

  4. In situ treatment of concrete surfaces by organic impregnation and polymerization

    International Nuclear Information System (INIS)

    Ursella, P.; Moretti, G.; Pellecchia, V.

    1990-01-01

    The impregnation by resins of concrete structures is a process well known at PIC (Polymer Impregnated Concrete). This process improves the physical-chemical features of concrete matrixes in order to extend their durability when severe environmental conditions may occur. The main objective of this research contract has been the verification of a proper impregnation 'in situ' of existing concrete surfaces, of any laying in the space, by means of a prototype machine, expressly designed and implemented, and verification of the increase of mechanical resistance, leach resistance, durability of treated material. In a nuclear facility this goal is very important in relation to the long term integrity of concrete structures during operating lifetime and, in particular, after final shutdown. (author)

  5. Modelling the Load Torques of Electric Drive for Polymerization Process

    Directory of Open Access Journals (Sweden)

    Andrzej Popenda

    2007-01-01

    Full Text Available The problems of mathematical modelling the load torques on shaft of driving motor designed for applications in polymerization reactors are presented in the paper. The real load of polymerization drive is determined as a function of angular velocity. Mentioned function results from friction in roll-formed slide bearing as well as from friction of ethylene molecules with mixer arms in polymerization reactor chamber. Application of mathematical formulas concerning the centrifugal ventilator is proposed to describe the mixer in reactor chamber. The analytical formulas describing the real loads of polymerization drive are applied in mathematical modelling the power unit of polymerization reactor with specially designed induction motor. The numerical analysis of transient states was made on the basis of formulated mathematical model. Examples of transient responses and trajectories resulting from analysis are presented in the paper.

  6. Structural and optical characterization of In2O3/PANI nanocomposite prepared by in-situ polymerization

    International Nuclear Information System (INIS)

    Janeoo, Shashi; Sharma, Mamta; Goswamy, J.; Singh, Gurinder

    2016-01-01

    Polyaniline-indium oxide (In 2 O 3 /PANI) nanocomposite have been prepared by in-situ polymerization of aniline and as-synthesized In 2 O 3 nanoparticles. X-ray diffraction (XRD), Transmission electron microscopy (TEM), Fourier transformation infrared (FTIR) and UV/Vis spectroscopy techniques are used to investigate the structural and optical properties of In 2 O 3 /PANI nanocomposite. TEM analysis shows In 2 O 3 nanoparticles are embedded in PANI nanofibers. FTIR spectra show the good interactions between PANI nanofibers and In 2 O 3 nanoparticles. The band gap and electronic transitions in In 2 O 3 /PANI nanocomposite is determined by using UV/Vis spectra.

  7. Fabrication of mullite-bonded porous SiC ceramics from multilayer-coated SiC particles through sol-gel and in-situ polymerization techniques

    Science.gov (United States)

    Ebrahimpour, Omid

    In this work, mullite-bonded porous silicon carbide (SiC) ceramics were prepared via a reaction bonding technique with the assistance of a sol-gel technique or in-situ polymerization as well as a combination of these techniques. In a typical procedure, SiC particles were first coated by alumina using calcined powder and alumina sol via a sol-gel technique followed by drying and passing through a screen. Subsequently, they were coated with the desired amount of polyethylene via an in-situ polymerization technique in a slurry phase reactor using a Ziegler-Natta catalyst. Afterward, the coated powders were dried again and passed through a screen before being pressed into a rectangular mold to make a green body. During the heating process, the polyethylene was burnt out to form pores at a temperature of about 500°C. Increasing the temperature above 800°C led to the partial oxidation of SiC particles to silica. At higher temperatures (above 1400°C) derived silica reacted with alumina to form mullite, which bonds SiC particles together. The porous SiC specimens were characterized with various techniques. The first part of the project was devoted to investigating the oxidation of SiC particles using a Thermogravimetric analysis (TGA) apparatus. The effects of particle size (micro and nano) and oxidation temperature (910°C--1010°C) as well as the initial mass of SiC particles in TGA on the oxidation behaviour of SiC powders were evaluated. To illustrate the oxidation rate of SiC in the packed bed state, a new kinetic model, which takes into account all of the diffusion steps (bulk, inter and intra particle diffusion) and surface oxidation rate, was proposed. Furthermore, the oxidation of SiC particles was analyzed by the X-ray Diffraction (XRD) technique. The effect of different alumina sources (calcined Al2O 3, alumina sol or a combination of the two) on the mechanical, physical, and crystalline structure of mullite-bonded porous SiC ceramics was studied in the

  8. A simple constrained uniaxial tensile apparatus for in situ investigation of film stretching processing.

    Science.gov (United States)

    Meng, Lingpu; Li, Jing; Cui, Kunpeng; Chen, Xiaowei; Lin, Yuanfei; Xu, Jiali; Li, Liangbin

    2013-11-01

    A simple constrained uniaxial tensile apparatus was designed and constructed to obtain stress-strain curve during stretching and subsequent structural evolution of polymeric films. Stretch is carried out through two motor driven clamps in the machine direction and scissor-like clamps in the transverse direction keeping the sample width constant. The force information during film stretching process is recorded by a tension sensor and structural evolution can be obtained by in situ X-ray scattering technique. All parameters related to film stretching manufacturing, such as temperature, draw ratio, and stretching speed can be set independently, making the apparatus an effective method to explore the relationship between processing parameters and structure.

  9. In situ ring-opening polymerization of hydroxyapatite/poly (ethylene ...

    Indian Academy of Sciences (India)

    2016-08-26

    Aug 26, 2016 ... Hydroxyapatite/poly(ethylene adipate)--poly(ethylene terephthalate) biomaterials (HAp/PEA--PET) have been prepared by ring opening polymerization (ROP) of cyclic oligo(ethylene adipate)--oligo(ethylene terephthalate) (C-OEA--C-OET) in the porous hydroxyapatite (HAp) scaffolds at 250 ...

  10. In situ ring-opening polymerization of hydroxyapatite/poly (ethylene ...

    Indian Academy of Sciences (India)

    Hydroxyapatite/poly(ethylene adipate)--poly(ethylene terephthalate) biomaterials (HAp/PEA--PET) have been prepared by ring opening polymerization (ROP) of cyclic oligo(ethylene adipate)--oligo(ethylene terephthalate) (C-OEA--C-OET) in the porous hydroxyapatite (HAp) scaffolds at 250 °C for 24 h under ...

  11. Facile synthesis of hollow Sn-Co@PMMA nanospheres as high performance anodes for lithium-ion batteries via galvanic replacement reaction and in situ polymerization

    Science.gov (United States)

    Yu, Xiaohui; Jiang, Anni; Yang, Hongyan; Meng, Haowen; Dou, Peng; Ma, Daqian; Xu, Xinhua

    2015-08-01

    Polymethyl methacrylate (PMMA)-coated hollow Sn-Co nanospheres (Sn-Co@PMMA) with superior electrochemical performance had been synthesized via a facile galvanic replacement method followed by an in situ emulsion polymerization route. The properties were investigated in detail and results show that the hollow Sn-Co nanospheres were evenly coated with PMMA. Benefiting from the protection of the PMMA layers, the hollow Sn-Co@PMMA nanocomposite is capable of retaining a high capacity of 590 mAh g-1 after 100 cycles with a coulomb efficiency above 98%, revealing better electrochemical properties compared with hollow Sn-Co anodes. The PMMA coating could help accommodate the mechanical strain caused by volume expansion and stabilize the solid electrolyte interphase (SEI) film formed on the electrode. Such a facile process could be further extended to other anode materials for lithium-ion batteries.

  12. Conductive nano composites based on cellulose nano fiber coated poly aniline via in situ polymerization; Nanocompositos condutores de nanofibras de celulose recobertas com polianilina via polimerizacao in situ

    Energy Technology Data Exchange (ETDEWEB)

    Silva, Michael J. da; Sanches, Alex O.; Malmonge, Luiz F.; Malmonge, Jose A. [Grupo de Polimero, Depto de Fisica e Quimica, Faculdade de Engenharia de Ilha Solteira, Universidade Estadual Paulista, Ilha Solteira, SP (Brazil); Medeiros, Eliton S. de [Depto de Engenharia de Materiais, Universidade Federal da Paraiba, Joao Pessoa, PB (Brazil); Rosa, Morsyleide F. [Embrapa Agroindustria Tropical, Fortaleza, CE (Brazil)

    2011-07-01

    Cellulose nano fiber (CNF) was extracted by acid hydrolysis from cotton microfibril and nano composites of CNF/PANI-DBSA were obtained by in situ polymerization of aniline onto CNF. The ratios between DBSA/aniline and aniline/oxidant were varied and the nano composites were characterized by four probes direct current (dc) electrical conductivity, ultraviolet-visible (UV-Vis-NIR) and FTIR spectroscopy and X-ray diffraction (XRD). Electrical conductive about {approx}10{sup -1}S/cm was research and was independent of DBSA/aniline molar ratio between 2-4 and the aniline/oxidant molar ratio between 1-5. X-ray patterns of the samples show crystalline peaks characteristic of cellulose I. The FTIR spectra confirmed the presence of PANI and CNF in all samples. (author)

  13. Synthesis and characterization of polypropylene/graphite nano composite preparation for in situ polymerization; Sintese e caracterizacao de nanocompositos polipropileno/grafite obtidos pela polimerizacao in situ

    Energy Technology Data Exchange (ETDEWEB)

    Montagna, L.S.; Fim, F. de C.; Galland, G.B. [Universidade Federal do Rio Grande do Sul (UFRGS), Porto Alegre, RS (Brazil). Inst. de Quimica; Basso, N.R.S., E-mail: nrbass@pucrs.b [Pontificia Universidade Catolica do Rio Grande do Sul (PUC-RS), Porto Alegre, RS (Brazil)

    2010-07-01

    This paper presents the synthesis of polypropylene/graphite nanocomposites through in situ polymerization, using the metallocene catalyst C{sub 20}H{sub 16}Cl{sub 2}Zr (dichloro(rac-ethylenebis(indenyl))zircon(IV)). The graphite nanosheets in nano dimensions were added to the polymer matrix in percentages of 0.6;1.0;4.2;4.8 and 6.0% (w/w). The TEM images indicated that the thickness of graphite nanosheets ranged from 4 to 60 nm and by means of XRD analysis it was observed that the physical and chemical treatment did not destroyed the graphite layers. The presence of nanosheets did not decrease the catalytic activity of the nanocomposites. TEM images and XRD analysis of nanocomposites showed a good dispersion of the graphite nanosheets in the polypropylene matrix. (author)

  14. Real-Time In-situ Characterization of Electron-Beam-Induced Bulk Polymerizations

    National Research Council Canada - National Science Library

    Palmese, Giuseppe R

    2005-01-01

    ..., our research team focused on two major tasks: (1) Performing real-time in-situ characterization of EB cure kinetics for representative cationic and free radical cured systems and the development of appropriate mechanistically based cure models...

  15. Effect of homopolymer in polymerization-induced microphase separation process

    Energy Technology Data Exchange (ETDEWEB)

    Park, Jongmin; Saba, Stacey A.; Hillmyer, Marc A.; Kang, Dong-Chang; Seo, Myungeun (IBS-Korea); (KAIST); (UMMN)

    2017-09-01

    We report on the phase separation behaviors of polymerization mixtures containing a polylactide macro-chain transfer agent (PLA-CTA), styrene, divinylbenzene, hydroxyl-terminated PLA (PLA-OH), and a molecular chain transfer agent which enable the ability to tune the pore size of a cross-linked polymer monolith in a facile manner. Cross-linked monoliths were produced from the mixtures via reversible addition-fragmentation chain transfer (RAFT) polymerization and converted into cross-linked porous polymers by selective removal of PLA while retaining the parent morphology. We demonstrate that pore sizes are tunable over a wide range of length scales from the meso- to macroporous regimes by adjusting the ratio of PLA-CTA to PLA-OH in the reaction mixture which causes the phase separation mechanism to change from polymerization-induced microphase separation to polymerization-induced phase separation. The possibility of increasing porosity and inducing simultaneous micro- and macrophase separation was also realized by adjustments in the molar mass of PLA which enabled the synthesis of hierarchically meso- and macroporous polymers.

  16. IN SITU FIELD TESTING OF PROCESSES

    Energy Technology Data Exchange (ETDEWEB)

    J.S.Y. YANG

    2004-11-08

    The purpose of this scientific analysis report is to update and document the data and subsequent analyses from ambient field-testing activities performed in underground drifts and surface-based boreholes through unsaturated zone (UZ) tuff rock units. In situ testing, monitoring, and associated laboratory studies are conducted to directly assess and evaluate the waste emplacement environment and the natural barriers to radionuclide transport at Yucca Mountain. This scientific analysis report supports and provides data to UZ flow and transport model reports, which in turn contribute to the Total System Performance Assessment (TSPA) of Yucca Mountain, an important document for the license application (LA). The objectives of ambient field-testing activities are described in Section 1.1. This report is the third revision (REV 03), which supercedes REV 02. The scientific analysis of data for inputs to model calibration and validation as documented in REV 02 were developed in accordance with the Technical Work Plan (TWP) ''Technical Work Plan for: Performance Assessment Unsaturated Zone'' (BSC 2004 [DIRS 167969]). This revision was developed in accordance with the ''Technical Work Plan for: Unsaturated Zone Flow Analysis and Model Report Integration'' (BSC 2004 [DIRS 169654], Section 1.2.4) for better integrated, consistent, transparent, traceable, and more complete documentation in this scientific analysis report and associated UZ flow and transport model reports. No additional testing or analyses were performed as part of this revision. The list of relevant acceptance criteria is provided by ''Technical Work Plan for: Unsaturated Zone Flow Analysis and Model Report Integration'' (BSC 2004 [DIRS 169654]), Table 3-1. Additional deviations from the TWP regarding the features, events, and processes (FEPs) list are discussed in Section 1.3. Documentation in this report includes descriptions of how, and under what

  17. IN SITU FIELD TESTING OF PROCESSES

    International Nuclear Information System (INIS)

    YANG, J.S.Y.

    2004-01-01

    The purpose of this scientific analysis report is to update and document the data and subsequent analyses from ambient field-testing activities performed in underground drifts and surface-based boreholes through unsaturated zone (UZ) tuff rock units. In situ testing, monitoring, and associated laboratory studies are conducted to directly assess and evaluate the waste emplacement environment and the natural barriers to radionuclide transport at Yucca Mountain. This scientific analysis report supports and provides data to UZ flow and transport model reports, which in turn contribute to the Total System Performance Assessment (TSPA) of Yucca Mountain, an important document for the license application (LA). The objectives of ambient field-testing activities are described in Section 1.1. This report is the third revision (REV 03), which supercedes2. The scientific analysis of data for inputs to model calibration and validation as documented in2 were developed in accordance with the Technical Work Plan (TWP) ''Technical Work Plan for: Performance Assessment Unsaturated Zone'' (BSC 2004 [DIRS 167969]). This revision was developed in accordance with the ''Technical Work Plan for: Unsaturated Zone Flow Analysis and Model Report Integration'' (BSC 2004 [DIRS 169654], Section 1.2.4) for better integrated, consistent, transparent, traceable, and more complete documentation in this scientific analysis report and associated UZ flow and transport model reports. No additional testing or analyses were performed as part of this revision. The list of relevant acceptance criteria is provided by ''Technical Work Plan for: Unsaturated Zone Flow Analysis and Model Report Integration'' (BSC 2004 [DIRS 169654]), Table 3-1. Additional deviations from the TWP regarding the features, events, and processes (FEPs) list are discussed in Section 1.3. Documentation in this report includes descriptions of how, and under what conditions, the tests were conducted. The descriptions and analyses

  18. Acrylamide inverse miniemulsion polymerization: in situ, real-time monitoring using nir spectroscopy

    Directory of Open Access Journals (Sweden)

    M. M. E. Colmán

    2014-12-01

    Full Text Available In this work, the ability of on-line NIR spectroscopy for the prediction of the evolution of monomer concentration, conversion and average particle diameter in acrylamide inverse miniemulsion polymerization was evaluated. The spectral ranges were chosen as those representing the decrease in concentration of monomer. An increase in the baseline shift indicated that the NIR spectra were affected by particle size. Multivariate partial least squares calibration models were developed to relate NIR spectra collected by the immersion probe with off-line conversion and polymer particle size data. The results showed good agreement between off-line data and values predicted by the NIR calibration models and these latter were also able to detect different types of operational disturbances. These results indicate that it is possible to monitor variables of interest during acrylamide inverse miniemulsion polymerizations.

  19. Studies in reactive extrusion processing of biodegradable polymeric materials

    Science.gov (United States)

    Balakrishnan, Sunder

    Various reaction chemistries such as Polymerization, Polymer cross-linking and Reactive grafting were investigated in twin-screw extruders. Poly (1,4-dioxan-2-one) (PPDX) was manufactured in melt by the continuous polymerization of 1,4-dioxan-2-one (PDX) monomer in a twin-screw extruder using Aluminum tri-sec butoxide (ATSB) initiator. Good and accurate control over molecular weight was obtained by controlling the ratio of monomer to initiator. A screw configuration consisting of only conveying elements was used for the polymerization. The polymerization reaction was characterized by a monomer-polymer dynamic equilibrium, above the melting temperature of the polymer, limiting the equilibrium conversion to 78-percent. Near complete (˜100-percent) conversion was obtained on co-polymerizing PDX monomer with a few mol-percent (around 8-percent) Caprolactone (CL) monomer in a twin-screw extruder using ATSB initiator. The co-polymers exhibited improved thermal stability with reduction in glass transition temperature. The extruder was modeled as an Axial Dispersed Plug Flow Reactor for the polymerization of CL monomer using Residence Time Distribution (RTD) Analysis. The model provided a good fit to the experimental RTD and conversion data. Aliphatic and aliphatic-aromatic co-polyesters, namely Polycaprolactone (PCL) and Poly butylenes (adipate-co-terephthalate) (Ecoflex) were cross-linked in a twin-screw extruder using radical initiator to form micro-gel reinforced biodegradable polyesters. Cross-linked Ecoflex was further extrusion blended with talc to form blends suitable to be blown into films. A screw configuration consisting of conveying and kneading elements was found to be effective in dispersion of the talc particles (5--10 microns) in the polyester matrix. While the rates of crystallization increased for the talc filled polyester blends, overall crystallinity reduced. Mechanical, tear and puncture properties of films made using the talc filled polyester blends

  20. Ferroferric oxide/polystyrene (Fe3O4/PS superparamagnetic nanocomposite via facile in situ bulk radical polymerization

    Directory of Open Access Journals (Sweden)

    2010-03-01

    Full Text Available Organo-modified ferroferric oxide superparamagnetic nanoparticles, synthesized by the coprecipitation of superparamagnetic nanoparticles in presence of oleic acid (OA, were incorporated in polystyrene (PS by the facile in situ bulk radical polymerization by using 2,2-azobisisobutyronitrile (AIBN as initiator. The transmission electron microscopy (TEM analysis of the resultant uniform ferroferric oxide/polystyrene superparamagnetic nanocomposite (Fe3O4/PS showed that the superparamagnetic nanoparticles had been dispersed homogeneously in the polymer matrix due to the surface grafted polystyrene, confirmed by Fourier transform infrared (FT-IR spectroscopy and thermogravimetric analysis (TGA. The superparamagnetic property of the Fe3O4/PS nanocomposite was testified by the vibrating sample magnetometer (VSM analysis. The strategy developed is expected to be applied for the large-scale industrial manufacturing of the superparamagnetic polymer nanocomposite.

  1. In situ polymerization synthesis of Z-scheme tungsten trioxide/polyimide photocatalyst with enhanced visible-light photocatalytic activity

    Science.gov (United States)

    Meng, Pengcheng; Heng, Huimin; Sun, Yanhong; Liu, Xia

    2018-01-01

    A novel direct Z-scheme P-containing tungsten trioxide/polyimide (PWO/PI) photocatalyst was synthesized by an in-situ solid-state polymerization strategy to enhance the visible-light photocatalytic oxidation capacity of PI. The effects of polymerization temperature and PWO content on the physicochemical properties of PWO/PI composites and photocatalytic degradation efficiency of imidacloprid were investigated. The photocatalysts were characterized by X-ray powder diffraction, Fourier transformed infrared spectra, X-ray photoelectron spectroscopy, scanning electron microscopy, transmission electron microscopy, UV-vis diffused reflection spectra and N2 adsorption-desorption isothermals. The results showed that the photocatalysts with visible-light photocatalytic activity can already be prepared at 300 °C. The PWO/PI composites exhibited a lamellar structure and PWO was wrapped by PI. After PWO was introduced, there was a significant interaction between PWO and PI, and the visible light response of photocatalysts was also improved. The visible-light photocatalytic degradation efficiency of imidacloprid on 3% PWO/PI-300 composite was about 3.2 times of commercial P25, and the corresponding pseudo-first-order rate constant was about 2.9 times of pristine PI. The Z-scheme photocatalytic system of PWO/PI composites was confirmed by the electron spin resonance technology, terephthalic acid photoluminescence probing technique, reactive species trapping experiments, X-ray photoelectron spectroscopy and photoluminescence of PWO/PI composites and pristine photocatalysts.

  2. Nanocomposites Derived From a Low-Color Aromatic Polyimide (CP2) and Amine-Functionalized Vapor-Grown Carbon Nanofibers: In Situ Polymerization and Characterization (Preprint)

    National Research Council Canada - National Science Library

    Wang, David H; Arlen, Michael J; Back, Jong-Beom; Vaia, Richard A; Tan, Loon-Seng

    2007-01-01

    ...%) was also used in the in situ polymerization of 6FDA and ABP. These two series of CP2/VGCNF nanocomposite films were cast from the respective polyamic acid/VGCNF DMAC solutions, followed by thermal imidization at curing temperatures up to 250 ?C...

  3. Combining On-Line Characterization Tools with Modern Software Environments for Optimal Operation of Polymerization Processes

    Directory of Open Access Journals (Sweden)

    Navid Ghadipasha

    2016-02-01

    Full Text Available This paper discusses the initial steps towards the formulation and implementation of a generic and flexible model centric framework for integrated simulation, estimation, optimization and feedback control of polymerization processes. For the first time it combines the powerful capabilities of the automatic continuous on-line monitoring of polymerization system (ACOMP, with a modern simulation, estimation and optimization software environment towards an integrated scheme for the optimal operation of polymeric processes. An initial validation of the framework was performed for modelling and optimization using literature data, illustrating the flexibility of the method to apply under different systems and conditions. Subsequently, off-line capabilities of the system were fully tested experimentally for model validations, parameter estimation and process optimization using ACOMP data. Experimental results are provided for free radical solution polymerization of methyl methacrylate.

  4. In-situ Polymerization of Polyaniline/Polypyrrole Copolymer using Different Techniques

    Science.gov (United States)

    Hammad, A. S.; Noby, H.; Elkady, M. F.; El-Shazly, A. H.

    2018-01-01

    The morphology and surface area of the poly(aniline-co-pyrrole) copolymer (PANPY) are important properties which improve the efficiency of the copolymer in various applications. In this investigation, different techniques were employed to produce PANPY in different morphologies. Aniline and pyrrole were used as monomers, and ammonium peroxydisulfate (APS) was used as an oxidizer with uniform molar ratio. Rapid mixing, drop-wise mixing, and supercritical carbon dioxide (ScCO2) polymerization techniques were appointed. The chemical structure, crystallinity, porosity, and morphology of the composite were distinguished by Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), Brunauer, Emmett and Teller (BET) analysis, and transmission electron microscopy (TEM) respectively. The characterization tests indicated that the polyaniline/polypyrrole copolymer was successfully prepared with different morphologies. Based on the obtained TEM, hollow nanospheres were formed using rapid mixing technique with acetic acid that have a diameter of 75 nm and thickness 26 nm approximately. Also, according to the XRD, the produced structures have a semi- crystalline structure. The synthesized copolymer with ScCO2-assisted polymerization technique showed improved surface area (38.1 m2/g) with HCl as dopant.

  5. Advancement in conductive cotton fabrics through in situ polymerization of polypyrrole-nanocellulose composites.

    Science.gov (United States)

    Hebeish, A; Farag, S; Sharaf, S; Shaheen, Th I

    2016-10-20

    Current research was undertaking with a view to innovate a new approach for development of conductive - coated textile materials through coating cotton fabrics with nanocellulose/polypyrrole composites. The study was designed in order to have a clear understanding of the role of nanocellulose as well as modified composite thereof under investigation. It is anticipated that incorporation of nanocellulose in the pyrrole/cotton fabrics/FeCl3/H2O system would form an integral part of the composites with mechanical, electrical or both properties. Three different nanocellulosic substrates are involved in the oxidation polymerization reaction of polypyrrole (Ppy) in presence of cotton fabrics. Polymerization was subsequently carried out by admixing at various ratios of FeCl3 and pyrrole viz. Ppy1, Ppy2 and pp3. The conductive, mechanical and thermal properties of cotton fabrics coated independently with different nanocellulose/polypyrrole were investigated. FTIR, TGA, XRD, SEM and EDX were also used for further characterization. Results signify that, the conductivity of cotton fabrics increases exponentially with increasing the dose of pyrrole and oxidant irrespective of nanocellulose substrate used. While, the mechanical properties of cotton fabrics are not significantly affected by the oxidant treatment. Copyright © 2016 Elsevier Ltd. All rights reserved.

  6. Reflectometric monitoring of the dissolution process of thin polymeric films.

    Science.gov (United States)

    Laitinen, Riikka; Räty, Jukka; Korhonen, Kristiina; Ketolainen, Jarkko; Peiponen, Kai-Erik

    2017-05-15

    Pharmaceutical thin films are versatile drug-delivery platforms i.e. allowing transdermal, oral, sublingual and buccal administration. However, dissolution testing of thin films is challenging since the commonly used dissolution tests for conventional dosage forms correspond rather poorly to the physiological conditions at the site of administration. Here we introduce a traditional optical reflection method for monitoring the dissolution behavior of thin polymeric films. The substances, e.g. drug molecules, released from the film generate an increase in the refractive index in the liquid medium which can be detected by reflectance monitoring. Thin EUDRAGIT ® RL PO poly(ethyl acrylate-co-methyl methacrylate-co trimethylammonioethyl methacrylate chloride) (RLPO) films containing the model drug perphenazine (PPZ) were prepared by spraying on a glass substrate. The glass substrates were placed inside the flow cell in the reflectometer which was then filled with phosphate buffer solution. Dissolution was monitored by measuring the reflectance of the buffer liquid. The method was able to detect the distinctive dissolution characteristics of different film formulations and measured relatively small drug concentrations. In conclusion, it was demonstrated that a traditional optical reflection method can provide valuable information about the dissolution characteristics of thin polymeric films in low liquid volume surroundings. Copyright © 2017 Elsevier B.V. All rights reserved.

  7. Integrating In-Situ and Ex-Situ Data Management Processes for Biodiversity Conservation

    Directory of Open Access Journals (Sweden)

    Karin R. Schwartz

    2017-10-01

    Full Text Available There is an increasing need for a “one plan approach” for conservation strategies that integrate in-situ and ex-situ management processes. Zoological institutions contribute directly to threatened species conservation through paradigms, such as reintroduction, head-starting, supplementation, or rescue/rehabilitation/release. This in-situ/ex-situ integration necessitates collaboration at all levels of conservation action including planning, implementation, monitoring and assessment to drive adaptive management processes. Each component is dependent on the availability and accuracy of data for evidence to facilitate evaluation and adaptive management processes. The Zoological Information Management System (ZIMS, managed by Species360, is a centralized web-based information system used in zoological institutions worldwide to pool life history, behavior and health data and facilitate animal husbandry, health, and breeding management processes. Currently used for few integrated conservation programs, ZIMS is an innovative tool that offers a new opportunity to link data management processes for animals that spend a part of their lives under human care and part in their natural environment and has great potential for use in managed wild populations.

  8. Master of Puppets: Cooperative Multitasking for In Situ Processing

    Energy Technology Data Exchange (ETDEWEB)

    Morozov, Dmitriy [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States); Lukic, Zarija [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States)

    2016-01-01

    Modern scientific and engineering simulations track the time evolution of billions of elements. For such large runs, storing most time steps for later analysis is not a viable strategy. It is far more efficient to analyze the simulation data while it is still in memory. Here, we present a novel design for running multiple codes in situ: using coroutines and position-independent executables we enable cooperative multitasking between simulation and analysis, allowing the same executables to post-process simulation output, as well as to process it on the fly, both in situ and in transit. We present Henson, an implementation of our design, and illustrate its versatility by tackling analysis tasks with different computational requirements. This design differs significantly from the existing frameworks and offers an efficient and robust approach to integrating multiple codes on modern supercomputers. The techniques we present can also be integrated into other in situ frameworks.

  9. Effect of telechelic ionic groups on the dispersion of organically modified clays in bisphenol A polycarbonate nanocomposites by in-situ polymerization using activated carbonates

    Directory of Open Access Journals (Sweden)

    M. Colonna

    2017-05-01

    Full Text Available Nanocomposites of bisphenol A polycarbonate with organically modified clays have been prepared for the first time by in-situ polymerization using bis(methyl salicyl carbonate as activated carbonate. The use of the activated carbonate permits to conduct the polymerization reaction at lower temperature and with shorter polymerization time with respect to those necessary for traditional melt methods that uses diphenyl carbonate, affording a nanocomposite with improved color. Moreover, an imidazolium salt with two long alkyl chains has been used to modify the montmorillonite, providing an organically modified clay with high thermal stability and wide d-spacing. The addition of ionic groups at the end of the polymer chain increases the interaction between the clay surface and the polymer producing a better dispersion of the clay. The presence of the clay increases the thermal stability of the polymer.

  10. Polypropylene Nano composites Obtained by In Situ Polymerization Using Metallocenes Catalyst: Influence of the Nanoparticles on the Final Polymer Morphology

    International Nuclear Information System (INIS)

    Zapata, P.; Quijada, R.

    2012-01-01

    Polypropylene nano composites containing silica nanospheres based on the sol-gel methods were produced via in situ polymerization using a rac-Et(Ind) 2 ZrCl 2 /methylaluminoxane (MAO) system. Two different routes were used depending on the interaction between the silica nanoparticles with the catalytic system. In route 1 the nanoparticles were added together with the catalytic system (rac-Et(Ind) 2 ZrCl 2 )/(MAO) directly into the reactor, and in route 2 the metallocenes rac-Et(Ind) 2 ZrCl 2 was supported on silica nanospheres pretreated with (MAO). SEM images show that when the nanospheres were added by both routes, they were replicated in the final polymer particle morphology; this phenomenon was more pronounced for PP obtained by route 2. The polypropylene (PP) nano composites obtained by both routes had a slightly higher percent crystallinity and crystallinity temperatures than pure PP. Transmission electron microscopy (TEM) images show that the nanospheres were well dispersed into the polypropylene matrix, particularly in the nano composites obtained by the support system (route 2).

  11. Cation Exchange Efficiency Of Modified Bentonite Using In-Situ GAMMA Radiation Polymerization Of Acrylic Acid Or Acrylamide

    International Nuclear Information System (INIS)

    ISMAIL, S.A.; FALAZI, B.

    2009-01-01

    Modified bentonites as cation exchangers were prepared by treating raw bentonite with 3N NaOH at 95 0 C followed by in-situ polymerization using gamma irradiation as well as hydrogen peroxide initiation of acrylic acid or acrylamide in the matrix.Water swelling and acid capacity were determined and cation exchange capacity for Cu 2+ , Ni 2+ and Co 2+ was evaluated. It has been found that catiexchange capacity of treated bentonite was increased as result of formed polyacrylic acid and polyacrylamide in the matrix. In case of acrylic acid, the maximum cation exchange capacities of 3.5, 3.1 and 2.5 mg equivalent/g were determined for Cu 2+ , Ni 2+ and Co 2+ , respectively, and for acrylamide, the corresponding capacities were 2.9, 2.8 and 2.6 mg equivalent/g, respectively. Water swelling was found to be associated with holding large amounts of water, for instance, 49 g of water was sorbed per one gram of the sodium salt form of polyacrylic acid in bentonite matrix, in other words the degree of swelling in water achieved 4500%.

  12. Improved properties of chemically modified graphene/poly(methyl methacrylate nanocomposites via a facile in-situ bulk polymerization

    Directory of Open Access Journals (Sweden)

    X. Y. Yuan

    2012-10-01

    Full Text Available The nanosheet of graphene was chemically modified by long alkyl chain for enhanced compatibility with polymer matrix and graphene/poly(methyl methacrylate (PMMA nanocomposites with homogeneous dispersion of the nanosheets and enhanced nanofiller-matrix interfacial interaction were fabricated via a facile in-situ bulk polymerization. The nanocomposites were characterized by X-ray diffraction, Fourier transform infrared spectroscopy, Scanning electron microscopy and thermogravimetry. The results showed that the graphene nanosheets were fully exfoliated in PMMA matrix and the thermal and mechanical properties of the nanocomposites were significantly improved at low graphene loadings. Large shifts of 15°C in the glass transition temperature and 27°C improvement of onset thermal degradation temperature were achieved with graphene loading as low as 0.07 wt%. A 67% increase in tensile strength was also observed by the addition of only 0.5 wt% graphene. The method used in this study provided a novel route to other graphene-based polymers.

  13. Characterization of electro-conductive fabrics prepared by in situ chemical and electrochemical polymerization of pyrrole onto polyester fabric

    International Nuclear Information System (INIS)

    Maiti, Syamal; Das, Dipayan; Sen, Kushal

    2014-01-01

    Highlights: • Surface resistivity of the fabrics decreased rapidly with an increase in add-on. • Add-on and resistivity were not correlated below a resistivity value of about 200 Ω. • Higher add-on but lower surface roughness resulted in lower surface resistivity. • The voltage–current and voltage–temperature behaviours were found to be non-linear. • Electro-conductive fabric exhibited 98% electromagnetic shielding efficiency. - Abstract: This paper reports a study on electro-conductive fabrics prepared by a combined in situ chemical and electrochemical polymerization of pyrrole. Specific observations are made to establish the roles of add-on and surface roughness on the surface resistivity of the electro-conductive fabrics. The performance characteristics of the fabrics are reported in terms of electrical conductivity, voltage–current and voltage–temperature characteristics and electromagnetic interference (EMI) shielding capability. The surface resistivity of the fabric was found to be as low as 11.79 Ω. The voltage–current profile of the fabric is observed to be non-ohmic as well as the voltage–temperature curve is found to be exponential. The EMI shielding efficiency of the fabric was found to be about 98%

  14. Layered double hydroxides as fillers in poly(l-lactide nanocomposites, obtained by in situ bulk polymerization

    Directory of Open Access Journals (Sweden)

    Telma Nogueira

    Full Text Available Abstract In this study in situ bulk polymerization of L-lactide filled with layered double hydroxides (LDH was investigated. Four different LDHs intercalated with two different organic anions (salicylate and sebacate were synthesized and characterized. After characterization, these synthetic layered compounds were used as fillers in poly(L-lactide (PLLA nanocomposites with two different fillers’s loadings (1 wt% and 2 wt%. PLLA and PLLA nanocomposites were evaluated by X-ray diffraction (XRD, Fourier transform infrared spectroscopy (FTIR, ultraviolet and visible spectroscopy, thermogravimetric analysis (TGA, dynamical mechanical analysis (DMA, flexural testing and differential scanning calorimetry (DSC. The results demonstrated that, compared to PLLA, the nanocomposite containing 1 wt% of Zn/Al salicylate transmitted less UVA and UVB light, while keeping a similar transparency in the visible region. Thermogravimetric analysis revealed that the nanocomposite with 1 wt% of Zn/Al salicylate exhibited the highest thermal stability. In general the flexural and dynamical mechanical properties were reduced in compassion to neat PLLA. DSC results, demonstrated that, compared to PLLA, all the nanocomposites exhibited lower glass transition temperature and melting temperature values.

  15. Synthesis of CdS nanocrystals in polymeric films studied by in-situ GID and GISAXS

    KAUST Repository

    Di Luccio, Tiziana

    2015-07-07

    In this work, we describe the synthesis of CdS nanocrystals in thin polymeric films by in-situ Grazing Incidence Diffraction (GID) and Grazing Incidence Small Angle Scattering (GISAXS). The 2D GISAXS patterns indicate how the precursor structure is altered as the temperature is varied from 25°C to 300°C. At 150°C, the CdS nanocrystals start to arrange themselves in a hexagonal lattice with a lattice parameter of 27 A. The diffraction intensity from the hexagonal lattice reaches a maximum at 170"C and decreases steadily upon further heating above 220°C indicating loss of symmetry. Correspondingly, the GID scans at 170°C show strong crystalline peaks from cubic CdS nanocrystals that are about 2 nm size. The results indicate that a temperature of 170°C is sufficient to synthesize CdS nanocrystals without degradation of the polymer matrix (Topas) in thin films (about 30nm). © 2015 Materials Research Society.

  16. Surface modification of magnesium aluminum hydroxide nanoparticles with poly(methyl methacrylate) via one-pot in situ polymerization

    Energy Technology Data Exchange (ETDEWEB)

    Guo Xiaojun, E-mail: guoxj6906@163.com [College of Chemistry and Chemical Engineering, Northwest Normal University, 967 Anning East Road, Lanzhou 730070 (China); Zhao Leihua; Zhang Li; Li Jing [College of Chemistry and Chemical Engineering, Northwest Normal University, 967 Anning East Road, Lanzhou 730070 (China)

    2012-01-15

    Hydrophobic magnesium aluminum hydroxide composite particles (PMMA-MAH) were obtained by means of grafting poly(methyl methacrylate) (PMMA) onto the surface of magnesium aluminum hydroxide(MAH) nanoparticles after a novel type of phosphate coupling agent (DN-27) modification. The introduction of functional double bonds was firstly conducted on the surface of nanoparticles by DN-27 modification, followed by one-pot in situ polymerization on the particles surface using methyl methacrylate (MMA) as monomer, azoisobutyronitrile (AIBN) as initiator and sodium dodecyl sulfate (SDS) as stabilizer to graft PMMA on the surface of DN-27-modified MAH particles. The obtained composite particles were characterized by field-emission scanning electron microscope (FESEM), Fourier transform infrared spectroscopy (FT-IR), thermogravimetric analysis (TGA), X-ray powder diffraction (XRD). The results show that the organic macromolecule PMMA could be successfully grafted on the surface of DN-27-modified MAH nanoparticles and the thermal stability of the PMMA-MAH composite particles had been improved. Compared with unmodified blank MAH sample, the product obtained with this method possesses better hydrophobic properties such as a higher water contact angle of 108 Degree-Sign and a well dispersion.

  17. Polypropylene Nanocomposites Obtained by In Situ Polymerization Using Metallocene Catalyst: Influence of the Nanoparticles on the Final Polymer Morphology

    Directory of Open Access Journals (Sweden)

    Paula Zapata

    2012-01-01

    Full Text Available Polypropylene nanocomposites containing silica nanospheres based on the sol-gel methods were produced via in situ polymerization using a rac-Et(Ind2ZrCl2/methylaluminoxane (MAO system. Two different routes were used depending on the interaction between the silica nanoparticles with the catalytic system. In route 1 the nanoparticles were added together with the catalytic system (rac-Et(Ind2ZrCl2/(MAO directly into the reactor, and in route 2 the metallocene rac-Et(Ind2ZrCl2 was supported on silica nanospheres pretreated with (MAO. SEM images show that when the nanospheres were added by both routes, they were replicated in the final polymer particle morphology; this phenomenon was more pronounced for PP obtained by route 2. The polypropylene (PP nanocomposites obtained by both routes had a slightly higher percent crystallinities and crystallinity temperatures than pure PP. Transmission electron microscopy (TEM images show that the nanospheres were well dispersed into the polypropylene matrix, particularly in the nanocomposites obtained by the support system (route 2.

  18. Process for introducing electrical conductivity into high-temperature polymeric materials

    Science.gov (United States)

    Liepins, R.; Jorgensen, B.S.; Liepins, L.Z.

    1987-08-27

    High-temperature electrically conducting polymers. The in situ reactions: AgNO/sub 3/ + RCHO ..-->.. Ag/sup 0/ + RCOOH and R/sub 3/M ..-->.. M/sup 0/ + 3R, where M = Au or Pt have been found to introduce either substantial bulk or surface conductivity in high- temperature polymers. The reactions involving the R/sub 3/M were caused to proceed thermally suggesting the possibility of using laser means for initiating such reactions in selected areas or volumes of the polymeric materials. The polymers successfully investigated to date are polyphenylquinoxaline, polytolylquinoxaline, polyquinoline, polythiazole, and pyrrone. 3 tabs.

  19. In-situ biogas upgrading process: modeling and simulations aspects

    DEFF Research Database (Denmark)

    Lovato, Giovanna; Alvarado-Morales, Merlin; Kovalovszki, Adam

    2017-01-01

    Biogas upgrading processes by in-situ hydrogen (H2) injection are still challenging and could benefit from a mathematical model to predict system performance. Therefore, a previous model on anaerobic digestion was updated and expanded to include the effect of H2 injection into the liquid phase of...

  20. Investigation of glycerol polymerization in the clinker grinding process

    NARCIS (Netherlands)

    Parvulescu, A.N.; Rossi, M.; Della Pina, C.; Ciriminna, R.; Pagliaro, M.

    2011-01-01

    Concrete production is a large scale process that involves high energy consumption. In order to increase the sustainability of this process, the reduction of energy input is necessary. Bio-glycerol was demonstrated to be a highly efficient renewable-based additive in the grinding process for

  1. Effect of light intensity and irradiation time on the polymerization process of a dental composite resin

    Directory of Open Access Journals (Sweden)

    Discacciati José Augusto César

    2004-01-01

    Full Text Available Polymerization shrinkage is a critical factor affecting the longevity and acceptability of dental composite resins. The aim of this work was to evaluate the effect of light intensity and irradiation time on the polymerization process of a photo cured dental composite resin by measuring the Vickers hardness number (VHN and the volumetric polymerization shrinkage. Samples were prepared using a dental manual light-curing unit. The samples were submitted to irradiation times of 5, 10, 20 and 40 s, using 200 and 400 mW.cm-2 light intensities. Vickers hardness number was obtained at four different moments after photoactivation (immediate, 1 h, 24 h and 168 h. After this, volumetric polymerization shrinkage values were obtained through a specific density method. The values were analyzed by ANOVA and Duncan's (p = 0.05. Results showed increase in hardness values from the immediate reading to 1 h and 24 h readings. After 24 h no changes were observed regardless the light intensities or activation times. The hardness values were always smaller for the 200 mW.cm-2 light intensity, except for the 40 s irradiation time. No significant differences were detected in volumetric polymerization shrinkage considering the light intensity (p = 0.539 and the activation time (p = 0.637 factors. In conclusion the polymerization of the material does not terminate immediately after photoactivation and the increase of irradiation time can compensate a lower light intensity. Different combinations between light intensity and irradiation time, i.e., different amounts of energy given to the system, have not affected the polymerization shrinkage.

  2. Ion assisted deposition processes: in situ control; Ionengestuetzte Beschichtungsprozesse in situ kontrollieren

    Energy Technology Data Exchange (ETDEWEB)

    Ehlers, H.; Gross, T.; Lappschies, M.; Ristau, D. [Laser Zentrum Hannover e.V. (Germany). Abteilung Laserkomponeneten, Gruppe Prozessentwicklung

    2004-12-01

    Ion assisted deposition processes for optical precision components exhibit a high potential, in particular in the near and mid infrared spectral region. The presented results demonstrate the important criterion of a minimized water adsorption in the thin film structures by measurements of the optical losses in the wavelength range around 3 {mu}m as well as by the determination of the spectral stability of the optics. Furthermore, the employment of an in situ monitor, which allows wide-band transmission measurements directly at the product, provides an extensive database for the process analysis and development. Thus, additional information about the growth behavior, the vacuum-to-air-shift, and about layer inhomogeneities is available. The combination of the in situ monitor with the coating plant control results in an automated process system, which allows a precise determination of the layer thickness and represents a basis for the rapid prototyping of complex layer systems. In contrast to standard monitor strategies, test coatings and calibration factors are not necessary. With the presented combination of the stable ion assisted deposition process and the in situ monitor, the production of demanding NIR/MIR multilayer systems with high reproducibility could be automated. (orig.)

  3. A combined interfacial and in-situ polymerization strategy to construct well-defined core-shell epoxy-containing SiO2-based microcapsules with high encapsulation loading, super thermal stability and nonpolar solvent tolerance

    Directory of Open Access Journals (Sweden)

    Yin Jia

    2016-10-01

    Full Text Available SiO2-based microcapsules containing hydrophobic molecules exhibited potential applications such as extrinsic self-healing, drug delivery, due to outstanding thermal and chemical stability of SiO2. However, to construct SiO2-based microcapsules with both high encapsulation loading and long-term structural stability is still a troublesome issue, limiting their further utilization. We herein design a single-batch route, a combined interfacial and in-situ polymerization strategy, to fabricate epoxy-containing SiO2-based microcapsules with both high encapsulation loading and long-term structural stability. The final SiO2-based microcapsules preserve high encapsulation loading of 85.7 wt% by controlling exclusively hydrolysis and condensed polymerization at oil/water interface in the initial interfacial polymerization step. In the subsequent in-situ polymerization step, the initial SiO2-based microcapsules as seeds could efficiently harvest SiO2 precursors and primary SiO2 particles to finely tune the SiO2 wall thickness, thereby enhancing long-term structural stability of the final SiO2-based microcapsules including high thermal stability with almost no any weight loss until 250°C, and strong tolerance against nonpolar solvents such as CCl4 with almost unchanged core-shell structure and unchanged core weight after immersing into strong solvents for up to 5 days. These SiO2-based microcapsules are extremely suited for processing them into anticorrosive coating in the presence of nonpolar solvents for self-healing application.

  4. Conductivity enhancement of surface-polymerized polyaniline films via control of processing conditions

    Science.gov (United States)

    Park, Chung Hyoi; Jang, Sung Kyu; Kim, Felix Sunjoo

    2018-01-01

    We investigate a fast and facile approach for the simultaneous synthesis and coating of conducting polyaniline (PANI) onto a substrate and the effects of processing conditions on the electrical properties of the fabricated films. Simultaneous polymerizing and depositing on the substrate forms a thin film with the average thickness of 300 nm and sheet resistance of 304 Ω/sq. Deposition conditions such as polymerization time (3-240 min), temperature (-10 to 40 °C), concentrations of monomer and oxidant (0.1-0.9 M), and type of washing solvents (acetone, water, and/or HCl solution) affect the film thickness, doping state, absorption characteristics, and solid-state nanoscale morphology, therefore affecting the electrical conductivity. Among the conditions, the surface-polymerized PANI film deposited at room temperature with acetone washing showed the highest conductivity of 22.2 S/cm.

  5. Properties of Nitrile Rubber/Clay Nanocomposites Prepared by In-Situ Emulsifier-free Emulsion Polymerization

    Directory of Open Access Journals (Sweden)

    Alireza Bagherian Mahmoodabadi

    2015-07-01

    Full Text Available Nitrile rubber/clay nanocomposites were prepared via in-situ emulsifier-free emulsion polymerization technique in the presence of 2-acrylamido-2-methylpropane sulfonic acid (AMPS and pristine sodium montmorillonite (Na-MMT. The morphology of the nanocomposites was studied using X-ray diffraction (XRD patterns and transmission electron microscopy (TEM. The XRD results showed exfoliated morphology for the nanocomposites containing up to 3 wt% nanoclay and exfoliated-intercalated morphology for the nanocomposite containing 5 wt% nanoclay. The basal spacing of the nanocomposite, containing 5 wt% nanoclay, was increased to 1.8 nm, which was 0.61 nm wider than that obtained using pristine Na-MMT. Compared to neat rubber, the thermogravimetric analysis (TGA revealed improvements in the thermal stability of all nanocomposite samples, in which the thermal degradation temperature was increased by increasing the clay content. The maximum increase in the thermal stability of the nanocomposites was obtained for the nanocomposite containing 5 wt% nanoclay with exfoliated-intercalated morphology. The tensile testing results showed remarkable improvements in the mechanical strength of the nanocomposites. In comparison with the neat nitrile rubber, the exfoliated nanocomposite, containing 3 wt% nanoclay, showed 302% and 219% increases in tensile modulus and tensile strength, respectively. The reason for improvementin mechanical properties of a nanocomposite, containing 3 wt% of nanoclay with respect to the nanocomposite containing 5 wt% of nanoclay, was related to the better dispersion of nanoclay platelets in the matrix and formation of exfoliated morphology. In addition, elongation-at-break and hardness were increased in the  nanocomposites, when compared with the neat nitrile rubber.

  6. Terminology of Polymers and Polymerization Processes in Dispersed Systems (IUPAC Recommendations 2011

    Directory of Open Access Journals (Sweden)

    Rogošić, M.

    2012-07-01

    Full Text Available A large group of industrially important polymerization processes is carried out in dispersed systems. These processes differ with respect to their physical nature, mechanism of particle formation, particle morphology, size, charge, types of interparticle interactions, and many other aspects. Polymer dispersions, and polymers derived from polymerization in dispersed systems,are used in diverse areas such as paints, adhesives, microelectronics, medicine, cosmetics, biotechnology, and others. Frequently, the same names are used for different processes and products or different names are used for the same processes and products. The document contains a list of recommended terms and definitions necessary for the unambiguous description of processes, products, parameters, and characteristic features relevant to polymers in dispersed systems.

  7. Platinum nanoparticles from size adjusted functional colloidal particles generated by a seeded emulsion polymerization process

    Directory of Open Access Journals (Sweden)

    Nicolas Vogel

    2011-08-01

    Full Text Available The benefits of miniemulsion and emulsion polymerization are combined in a seeded emulsion polymerization process with functional seed particles synthesized by miniemulsion polymerization. A systematic study on the influence of different reaction parameters on the reaction pathway is conducted, including variations of the amount of monomer fed, the ratio of initiator to monomer and the choice of surfactant and composition of the continuous phase. Critical parameters affecting the control of the reaction are determined. If carefully controlled, the seeded emulsion polymerization with functional seed particles yields monodisperse particles with adjustable size and functionalities. Size-adjusted platinum-acetylacetonate containing latex particles with identical seed particles and varied shell thicknesses are used to produce arrays of highly ordered platinum nanoparticles with different interparticle distances but identical particle sizes. For that, a self-assembled monolayer of functional colloids is prepared on a solid substrate and subsequently treated by oxygen plasma processing in order to remove the organic constituents. This step, however, leads to a saturated state of a residual mix of materials. In order to determine parameters influencing this saturation state, the type of surfactant, the amount of precursor loading and the size of the colloids are varied. By short annealing at high temperatures platinum nanoparticles are generated from the saturated state particles. Typically, the present fabrication method delivers a maximum interparticle distance of about 260 nm for well-defined crystalline platinum nanoparticles limited by deformation processes due to softening of the organic material during the plasma applications.

  8. CoCl 2 reinforced polymeric nanocomposites of conjugated polymer

    Indian Academy of Sciences (India)

    Polyaniline (PANI) was synthesized by chemical oxidative polymerization of aniline using ammonium persulphate as an oxidant in acidic aqueous medium. Cobalt chloride hexahydrate (CoCl2⋅6H2O)-doped PANI composite was synthesized by in-situ oxidative polymerization process by using various concentrations of ...

  9. CoCl2 reinforced polymeric nanocomposites of conjugated polymer ...

    Indian Academy of Sciences (India)

    Polyaniline (PANI) was synthesized by chemical oxidative polymerization of aniline using ammonium persulphate as an oxidant in acidic aqueous medium. Cobalt chloride hexahydrate (CoCl2⋅6H2O)-doped PANI composite was synthesized by in-situ oxidative polymerization process by using various concentrations of ...

  10. Process for the in-situ leaching of uranium

    International Nuclear Information System (INIS)

    Habib, E.T.; Vogt, T.C.

    1982-01-01

    Process for the in-situ leaching of uranium employing an alkaline lixiviant and an alkali metal or alkaline earth metal hypochlorite as an oxidizing agent. The use of the hypochlorite oxidant results in significantly higher uranium recoveries and leaching rates than those attained by the use of conventional oxidants. The invention is particularly suitable for use in subterranean deposits in which the uranium mineral is associated with carbonaceous material which retards access to the uranium by the lixiviant

  11. Assessment of the impact strength of the denture base resin polymerized by various processing techniques

    Directory of Open Access Journals (Sweden)

    Rajashree Jadhav

    2013-01-01

    Full Text Available Aim : To measure the impact strength of denture base resins polymerized using short and long curing cycles by water bath, pressure cooker and microwave techniques. Materials and Methods: For impact strength testing, 60 samples were made. The sample dimensions were 60 mm × 12 mm × 3 mm, as standardized by the American Standards for Testing and Materials (ASTM. A digital caliper was used to locate the midpoint of sample. The impact strength was measured in IZOD type of impact tester using CEAST Impact tester. The pendulum struck the sample and it broke. The energy required to break the sample was measured in Joules. Data were analyzed using Student′s " t" test. Results: There was statistically significant difference in the impact strength of denture base resins polymerized by long curing cycle and short curing cycle in each technique, with the long curing processing being the best. Conclusion: The polymerization technique plays an important role in the influence of impact strength in the denture base resin. This research demonstrates that the denture base resin polymerized by microwave processing technique possessed the highest impact strength.

  12. A necessary and sufficient condition for gelation of a reversible Markov process of polymerization

    CERN Document Server

    Han, D

    2003-01-01

    A reversible Markov process as a chemical polymerization model which permits the coagulation and fragmentation reactions is considered. We present a necessary and sufficient condition for the occurrence of a gelation in the process. We show that a gelation transition may or may not occur, depending on the value of the fragmentation strength, and, in the case that gelation takes place, a critical value for the occurrence of the gelation and the mass of the gel can be determined by close forms.

  13. Nonlinearities in Drug Release Process from Polymeric Microparticles: Long-Time-Scale Behaviour

    Directory of Open Access Journals (Sweden)

    Elena Simona Bacaita

    2012-01-01

    Full Text Available A theoretical model of the drug release process from polymeric microparticles (a particular type of polymer matrix, through dispersive fractal approximation of motion, is built. As a result, the drug release process takes place through cnoidal oscillations modes of a normalized concentration field. This indicates that, in the case of long-time-scale evolutions, the drug particles assemble in a lattice of nonlinear oscillators occur macroscopically, through variations of drug concentration. The model is validated by experimental results.

  14. Organophilization process of Brazilian bentonite for preparation of polymeric nanocomposites

    International Nuclear Information System (INIS)

    Oliveira, Carlos I.R. de; Rocha, Marisa C.G.; Ferreira, Joao L.A.N.G.

    2015-01-01

    Bentonite clay from the municipality of Cubati, PB, was used for the preparation of an organophilic clay. First, the clay was treated with sodium chloride to obtain the homo-ionic sodium clay. The organoclay was, then, obtained from the reaction of homo-ionic clay with the quaternary ammonium salt, cetyltrimethyl ammonium chloride. The natural clay and the modified clays were characterized by X-ray fluorescence (XRF), X-ray diffraction (XRD) and Fourier transform infrared spectroscopy (FTIR). The chemical analysis showed a decrease in the concentration of the majority of the metallic oxides when the bentonite was organophilizated. This result is characteristic of the metal cation exchange process by organic salt molecules. The X-ray diffraction confirmed the intercalation among the layers of the clay. The results obtained by FTIR showed the presence of the characteristic groups of the salt in the clay, thus confirming the obtaining of organophilic bentonite. (author)

  15. Microgravity Processing and Photonic Applications of Organic and Polymeric Materials

    Science.gov (United States)

    Frazier, Donald 0; Penn, Benjamin G.; Smith, David; Witherow, William K.; Paley, M. S.; Abdeldayem, Hossin A.

    1998-01-01

    In recent years, a great deal of interest has been directed toward the use of organic materials in the development of high-efficiency optoelectronic and photonic devices. There is a myriad of possibilities among organic which allow flexibility in the design of unique structures with a variety of functional groups. The use of nonlinear optical (NLO) organic materials such as thin-film waveguides allows full exploitation of their desirable qualities by permitting long interaction lengths and large susceptibilities allowing modest power input. There are several methods in use to prepare thin films, such as Langmuir-Blodgett (LB) and self-assembly techniques, vapor deposition, growth from sheared solution or melt, and melt growth between glass plates. Organics have many features that make Abstract: them desirable for use in optical devices such as high second- and third-order nonlinearities, flexibility of molecular design, and damage resistance to optical radiation. However, their use in devices has been hindered by processing difficulties for crystals and thin films. In this chapter, we discuss photonic and optoelectronic applications of a few organic materials and the potential role of microgravity on processing these materials. It is of interest to note how materials with second- and third-order nonlinear optical behavior may be improved in a diffusion-limited environment and ways in which convection may be detrimental to these materials. We focus our discussion on third-order materials for all-optical switching, and second-order materials for all-optical switching, and second-order materials for frequency conversion and electrooptics.

  16. Chattanooga shale: uranium recovery by in situ processing

    International Nuclear Information System (INIS)

    Jackson, D.D.

    1977-01-01

    The increasing demand for uranium as reactor fuel requires the addition of sizable new domestic reserves. One of the largest potential sources of low-grade uranium ore is the Chattanooga shale--a formation in Tennessee and neighboring states that has not been mined conventionally because it is expensive and environmentally disadvantageous to do so. An in situ process, on the other hand, might be used to extract uranium from this formation without the attendant problems of conventional mining. We have suggested developing such a process, in which fracturing, retorting, and pressure leaching might be used to extract the uranium. The potential advantages of such a process are that capital investment would be reduced, handling and disposing of the ore would be avoided, and leaching reagents would be self-generated from air and water. If successful, the cost reductions from these factors could make the uranium produced competitive with that from other sources, and substantially increase domestic reserves. A technical program to evaluate the processing problems has been outlined and a conceptual model of the extraction process has been developed. Preliminary cost estimates have been made, although it is recognized that their validity depends on how successfully the various processing steps are carried out. In view of the preliminary nature of this survey (and our growing need for uranium), we have urged a more detailed study on the feasibility of in situ methods for extracting uranium from the Chattanooga shale

  17. Lipase catalyzed HEMA initiated ring-opening polymerization: in situ formation of mixed polyester methacrylates by transesterification.

    Science.gov (United States)

    Takwa, Mohamad; Xiao, Yan; Simpson, Neil; Malmström, Eva; Hult, Karl; Koning, Cor E; Heise, Andreas; Martinelle, Mats

    2008-02-01

    2-Hydroxyethyl methacrylate (HEMA) was used as initiator for the enzymatic ring-opening polymerization (ROP) of omega-pentadecalactone (PDL) and epsilon-caprolactone (CL). The lipase B from Candida antarctica was found to catalyze the cleavage of the ester bond in the HEMA end group of the formed polyesters, resulting in two major transesterification processes, methacrylate transfer and polyester transfer. This resulted in a number of different polyester methacrylate structures, such as polymers without, with one, and with two methacrylate end groups. Furthermore, the 1,2-ethanediol moiety (from HEMA) was found in the polyester products as an integral part of HEMA, as an end group (with one hydroxyl group) and incorporated within the polyester (polyester chains acylated on both hydroxyl groups). After 72 h, as a result of the methacrylate transfer, 79% (48%) of the initial amount of the methacrylate moiety (from HEMA) was situated (acylated) on the end hydroxyl group of the PPDL (PCL) polyester. In order to prepare materials for polymer networks, fully dimethacrylated polymers were synthesized in a one-pot procedure by combining HEMA-initiated ROP with end-capping using vinyl methacrylate. The novel PPDL dimethacrylate (>95% incorporated methacrylate end groups) is currently in use for polymer network formation. Our results show that initiators with cleavable ester groups are of limited use to obtain well-defined monomethacrylated macromonomers due to the enzyme-based transesterification processes. On the other hand, when combined with end-capping, well-defined dimethacrylated polymers (PPDL, PCL) were prepared.

  18. Polymerization of aniline in an organic peroxide system by the inverted emulsion process

    OpenAIRE

    Rao, Palle Swapna; Sathyanarayana, DN; Palaniappan, S

    2002-01-01

    An inverted emulsion process for the synthesis of the emeraldine salt of polyaniline using a novel oxidizing agent, namely benzoyl peroxide, is described. The polymerization is carried out in a nonpolar solvent in the presence of a functionalized protonic acid (sulfosalicylic acid) as the dopant and an emulsifier (sodium lauryl sulfate). The influence of synthesis conditions such as the duration of the reaction, temperature, concentration of the reactants, etc., on the properties of polyanili...

  19. Flow Characteristics of a Thermoset Fiber Composite Photopolymer Resin in a Vat Polymerization Additive Manufacturing Process

    DEFF Research Database (Denmark)

    Hofstätter, Thomas; Spangenberg, Jon; Pedersen, David B.

    understood. Research indicates an orientation within the manufacturing layer and efforts have been made to achieve a more uniform orientation within the part. A vat polymerization machine consisting of a resin vat and a moving build plate has been simulated using the fluid flow module of Comsol Multiphysics...... photopolymer resin. The prediction can be used to identify potential clusters or misalignment of fibers and in the future allow for optimization of the machine design and manufacturing process....

  20. Revisiting the Brønsted acid catalysed hydrolysis kinetics of polymeric carbohydrates in ionic liquids by in situ ATR-FTIR spectroscopy

    DEFF Research Database (Denmark)

    Kunov-Kruse, Andreas Jonas; Riisager, Anders; Shunmugavel, Saravanamurugan

    2013-01-01

    A new versatile method to measure rates and determine activation energies for the Brønsted acid catalysed hydrolysis of cellulose and cellobiose (and other polymeric carbohydrates) in ionic liquids is demonstrated by following the C–O stretching band of the glycoside bond with in situ ATR......-FTIR. An activation energy in excellent agreement with the literature was determined for cellulose hydrolysis, whereas a distinctly lower activation energy was determined for cellobiose hydrolysis. The methodology also allowed to independently determine activation energies for the formation of 5-hydroxymethylfurfural...

  1. Processing and storage effects on monomeric anthocyanins, percent polymeric color, and antioxidant capacity of processed blackberry products.

    Science.gov (United States)

    Hager, Tiffany J; Howard, Luke R; Prior, Ronald L

    2008-02-13

    Blackberries are a rich source of polyphenolics, particularly anthocyanins, that may contribute to the reduced risk of chronic disease; however, as with most berries, the fresh fruit are only seasonally available. With most of the blackberries consumed as frozen or in thermally processed forms after long-term storage, the purpose of this study was to evaluate the effects of processing and 6 months of storage on the anthocyanins and antioxidant capacity of blackberries that were individually quick-frozen (IQF), canned-in-syrup, canned-in-water, pureed, and juiced (clarified and nonclarified). Monomeric anthocyanins, percent polymeric color, and antioxidant capacity by oxygen radical absorbance capacity (ORAC FL) and photochemiluminescence (PCL) were determined postprocessing (1 day) and after 1, 3, and 6 months of storage. Processing resulted in increases in polymeric color values (up to 7%) and losses in monomeric anthocyanins (up to 65%). For most products, processing also resulted in losses in antioxidant capacity (by ORAC FL and PCL). Storage at 25 degrees C of all processed products resulted in dramatic losses in monomeric anthocyanins with as much as 75% losses of anthocyanins throughout storage, which coincided with marked increases of percent polymeric color values of these products over 6 months of storage. There were no changes in ORAC FL or PCL for processed products throughout long-term storage. No significant changes in antioxidant capacity or anthocyanin content were observed in IQF fruit during long-term storage at -20 degrees C.

  2. Mechanism of in situ surface polymerization of gallic acid in an environmental-inspired preparation of carboxylated core-shell magnetite nanoparticles.

    Science.gov (United States)

    Tóth, Ildikó Y; Szekeres, Márta; Turcu, Rodica; Sáringer, Szilárd; Illés, Erzsébet; Nesztor, Dániel; Tombácz, Etelka

    2014-12-30

    Magnetite nanoparticles (MNPs) with biocompatible coatings are good candidates for MRI (magnetic resonance imaging) contrasting, magnetic hyperthermia treatments, and drug delivery systems. The spontaneous surface induced polymerization of dissolved organic matter on environmental mineral particles inspired us to prepare carboxylated core-shell MNPs by using a ubiquitous polyphenolic precursor. Through the adsorption and in situ surface polymerization of gallic acid (GA), a polygallate (PGA) coating is formed on the nanoparticles (PGA@MNP) with possible antioxidant capacity. The present work explores the mechanism of polymerization with the help of potentiometric acid-base titration, dynamic light scattering (for particle size and zeta potential determination), UV-vis (UV-visible light spectroscopy), FTIR-ATR (Fourier-transformed infrared spectroscopy by attenuated total reflection), and XPS (X-ray photoelectron spectroscopy) techniques. We observed the formation of ester and ether linkages between gallate monomers both in solution and in the adsorbed state. Higher polymers were formed in the course of several weeks both on the surface of nanoparticles and in the dispersion medium. The ratio of the absorbances of PGA supernatants at 400 and 600 nm (i.e., the E4/E6 ratio commonly used to characterize the degree of polymerization of humic materials) was determined to be 4.3, similar to that of humic acids. Combined XPS, dynamic light scattering, and FTIR-ATR results revealed that, prior to polymerization, the GA monomers became oxidized to poly(carboxylic acid)s due to ring opening while Fe(3+) ions reduced to Fe(2+). Our published results on the colloidal and chemical stability of PGA@MNPs are referenced thoroughly in the present work. Detailed studies on biocompatibility, antioxidant property, and biomedical applicability of the particles will be published.

  3. Potentiometric in Situ Monitoring of Anions in the Synthesis of Copper and Silver Nanoparticles Using the Polyol Process.

    Science.gov (United States)

    Carey, Jesse L; Whitcomb, David R; Chen, Suyue; Penn, R Lee; Bühlmann, Philippe

    2015-12-22

    Potentiometric sensors, such as polymeric membrane, ion-selective electrodes (ISEs), have been used in the past to monitor a variety of chemical processes. However, the use of these sensors has traditionally been limited to aqueous solutions and moderate temperatures. Here we present an ISE with a high-capacity ion-exchange sensing membrane for measurements of nitrate and nitrite in the organic solvent propylene glycol at 150 °C. It is capable of continuously measuring under these conditions for over 180 h. We demonstrate the usefulness of this sensor by in situ monitoring of anion concentrations during the synthesis of copper and silver nanoparticles in propylene glycol using the polyol method. Ion chromatography and a colorimetric method were used to independently confirm anion concentrations measured in situ. In doing so, it was shown that in this reaction the co-ion nitrate is reduced to nitrite.

  4. Monitoring dynamic electrochemical processes with in situ ptychography

    Science.gov (United States)

    Kourousias, George; Bozzini, Benedetto; Jones, Michael W. M.; Van Riessen, Grant A.; Dal Zilio, Simone; Billè, Fulvio; Kiskinova, Maya; Gianoncelli, Alessandra

    2018-03-01

    The present work reports novel soft X-ray Fresnel CDI ptychography results, demonstrating the potential of this method for dynamic in situ studies. Specifically, in situ ptychography experiments explored the electrochemical fabrication of Co-doped Mn-oxide/polypyrrole nanocomposites for sustainable and cost-effective fuel-cell air-electrodes. Oxygen-reduction catalysts based on Mn-oxides exhibit relatively high activity, but poor durability: doping with Co has been shown to improve both reduction rate and stability. In this study, we examine the chemical state distribution of the catalytically crucial Co dopant to elucidate details of the Co dopant incorporation into the Mn/polymer matrix. The measurements were performed using a custom-made three-electrode thin-layer microcell, developed at the TwinMic beamline of Elettra Synchrotron during a series of experiments that were continued at the SXRI beamline of the Australian Synchrotron. Our time-resolved ptychography-based investigation was carried out in situ after two representative growth steps, controlled by electrochemical bias. In addition to the observation of morphological changes, we retrieved the spectroscopic information, provided by multiple ptychographic energy scans across Co L3-edge, shedding light on the doping mechanism and demonstrating a general approach for the molecular-level investigation complex multimaterial electrodeposition processes.

  5. Preparation of nanocomposites based on poly(Butylene Succinate) and montmorillonite organoclay via in situ polymerization; Preparo de nanocompositos de poli(succinato de butileno) (PDS) e argila motmorilonita organofilica via polimerizaco in situ

    Energy Technology Data Exchange (ETDEWEB)

    Ferreira, Leticia P.; Moreira, Andrei N.; Souza Junior, Fernando G. de, E-mail: fgsj@ufrj.br [Universidade Federal do Rio de Janeiro (UFRJ), Rio de Janeiro, RJ (Brazil). Inst. de Macromoleculas; Pinto, Jose Carlos Costa da Silva [Coordenacao dos Cursos de Pos-Graduacao em Engenharia (COPPE/UFRJ), Rio de Janeiro, RJ (Brazil). Programa de Engenharia Quimica

    2014-09-15

    Nanocomposites based on poly(butylene succinate) (PBS) and organophilic montmorillonite were synthesized via in situ polymerization using three different clay compositions (4, 6 and 8 wt%). The products were characterized by several different techniques. X-ray diffraction was useful to confirm the increase of the interlayer spacing of the clay due to the presence of the polymer chains among layers. Thermal analysis indicated that the polymerization method chosen led to materials with lower thermal stability compared to the pure PBS, due to the difficulty of chain growth in the presence of the clay. Low-field NMR technique was used to assess clay dispersion in the polymer, with exfoliated structures predominating in the nanocomposites. (author)

  6. Advanced Polymeric and Organic–Inorganic Membranes for Pressure-Driven Processes

    KAUST Repository

    Le, Ngoc Lieu

    2017-02-13

    The state-of-the-art of membranes for reverse osmosis, nanofiltration, and gas separation is shortly reviewed, taking in account the most representative examples currently in application. Emphasis is also done on recent developments of advanced polymeric and organic–inorganic materials for pressure-driven processes. Many of the more recent membranes are not only polymeric but also contain an inorganic phase. Tailoring innovative materials with organic and inorganic phases coexisting in a nanoscale with multifunctionalization is an appealing approach to control at the same time diffusivity and gas solubility. Other advanced materials that are now being considered for membrane development are organic or organic–inorganic self-assemblies, metal-organic frameworks, and different forms of carbon fillers.

  7. Effect of Graphene Oxide on the Reaction Kinetics of Methyl Methacrylate In Situ Radical Polymerization via the Bulk or Solution Technique

    Directory of Open Access Journals (Sweden)

    Ioannis S. Tsagkalias

    2017-09-01

    Full Text Available The synthesis of nanocomposite materials based on poly(methyl methacrylate and graphene oxide (GO is presented using the in situ polymerization technique, starting from methyl methacrylate, graphite oxide, and an initiator, and carried out either with (solution or without (bulk in the presence of a suitable solvent. Reaction kinetics was followed gravimetrically and the appropriate characterization of the products took place using several experimental techniques. X-ray diffraction (XRD data showed that graphite oxide had been transformed to graphene oxide during polymerization, whereas FTIR spectra revealed no significant interactions between the polymer matrix and GO. It appears that during polymerization, the initiator efficiency was reduced by the presence of GO, resulting in a reduction of the reaction rate and a slight increase in the average molecular weight of the polymer formed, measured by gel permeation chromatography (GPC, along with an increase in the glass transition temperature obtained from differential scanning calorimetry (DSC. The presence of the solvent results in the suppression of the gel-effect in the reaction rate curves, the synthesis of polymers with lower average molecular weights and polydispersities of the Molecular Weight Distribution, and lower glass transition temperatures. Finally, from thermogravimetric analysis (TG, it was verified that the presence of GO slightly enhances the thermal stability of the nano-hybrids formed.

  8. Cotton fabric coated with nano TiO2-acrylate copolymer for photocatalytic self-cleaning by in-situ suspension polymerization

    International Nuclear Information System (INIS)

    Jiang Xue; Tian Xiuzhi; Gu Jian; Huang Dan; Yang Yiqi

    2011-01-01

    Two kinds of nano TiO 2 -polyacrylate hybrid dispersions, TBM-w and TBM-e were synthesized by in-situ suspension polymerization and solution polymerization respectively, in order to fix the nano TiO 2 on fabrics. The photocatalytic self-cleaning fabrics have received much attention in recent years for its water-saving and environment-protection advantages. However, the fixation of the photocatalyst on fabrics is still a key problem that inhibits industrialization of these eco-friendly fabrics. The cotton fabric was treated by the two hybrid dispersions. The photocatalytic self-cleaning property was characterized. Infrared spectroscopy, burning loss test and thermogravimetry showed that some copolymer chains entangled with the nano TiO 2 . Transmission electron microscope illustrated that there was a polymeric layer on the surface of nano TiO 2 . The average diameter of TBM-w was smaller than that of TBM-e based on size analysis. The photocatalytic decoloration of the grape syrup indicated that the fabric with TiO 2 -polymer hybrid had excellent self-cleaning property.

  9. Fault Diagnosis Method on Polyvinyl Chloride Polymerization Process Based on Dynamic Kernel Principal Component and Fisher Discriminant Analysis Method

    Directory of Open Access Journals (Sweden)

    Shu-zhi Gao

    2016-01-01

    Full Text Available In view of the fact that the production process of Polyvinyl chloride (PVC polymerization has more fault types and its type is complex, a fault diagnosis algorithm based on the hybrid Dynamic Kernel Principal Component Analysis-Fisher Discriminant Analysis (DKPCA-FDA method is proposed in this paper. Kernel principal component analysis and Dynamic Kernel Principal Component Analysis are used for fault diagnosis of Polyvinyl chloride (PVC polymerization process, while Fisher Discriminant Analysis (FDA method was adopted to make failure data for further separation. The simulation results show that the Dynamic Kernel Principal Component Analyses to fault diagnosis of Polyvinyl chloride (PVC polymerization process have better diagnostic accuracy, the Fisher Discriminant Analysis (FDA can further realize the fault isolation, and the actual fault in the process of Polyvinyl chloride (PVC polymerization production can be monitored by Dynamic Kernel Principal Component Analysis.

  10. Influence of selective dispersion of MWCNT on electrical percolation of in-situ polymerized high-impact polystyrene/MWCNT nanocomposites

    Directory of Open Access Journals (Sweden)

    B. B. Khatua

    2014-01-01

    Full Text Available This work demonstrates a simple method to develop highly conducting high impact polystyrene (HIPS/multiwall carbon nanotube (MWCNT nanocomposites through selective dispersion of MWCNT in HIPS matrix. The method involves in-situ polymerization of polybutadiene containing styrene monomer in the presence of HIPS beads and MWCNT. A significantly lower percolation threshold value than ever reported for HIPS/MWCNT systems was obtained using unmodified unaligned MWCNTs. With the increase in HIPS bead content (at a particular MWCNT loading in the HIPS/MWCNT nanocomposites, the conductivity value was increased, suggesting that the presence of HIPS beads acted as excluded volume that decreased the percolation threshold. An increase in electrical conductivity from 1.91•10–7 to 1.15•10–5 S/cm was evident, when the HIPS bead content was increased from 30 to 60 wt% at a constant loading of MWCNT (i.e. 0.6 wt%. The morphological investigation of the HIPS/MWCNT nanocomposites revealed that, the MWCNTs were selectively dispersed in the in-situ polymerized HIPS region, outside the HIPS beads, which resulted in the lowering of the percolation threshold to a lower value of 0.54 wt%. The morphology and electrical properties of the nanocomposites have been discussed in detail in the manuscript.

  11. Processing and storage effects on monomeric anthocyanins, percent polymeric color, and antioxidant capacity of processed black raspberry products.

    Science.gov (United States)

    Hager, A; Howard, L R; Prior, R L; Brownmiller, C

    2008-08-01

    This study evaluated the effects of processing and 6 mo of storage on total monomeric anthocyanins, percent polymeric color, and antioxidant capacity of black raspberries that were individually quick-frozen (IQF), canned-in-syrup, canned-in-water, pureed, and juiced (clarified and nonclarified). Total monomeric anthocyanins, percent polymeric color, and ORAC(FL) were determined 1 d postprocessing and after 1, 3, and 6 mo of storage. Thermal processing resulted in marked losses in total anthocyanins ranging from 37% in puree to 69% to 73% in nonclarified and clarified juices, respectively, but only the juices showed substantial losses (38% to 41%) in ORAC(FL). Storage at 25 degrees C of all thermally processed products resulted in dramatic losses in total anthocyanins ranging from 49% in canned-in-syrup to 75% in clarified juices. This coincided with marked increases in percent polymeric color values of these products over the 6-mo storage. ORAC(FL) values showed little change during storage, indicating that the formation of polymers compensated for the loss of antioxidant capacity due to anthocyanin degradation. Total anthocyanins and ORACFL of IQF berries were well retained during long-term storage at -20 degrees C.

  12. Effect of Mn doped-titania on the activity of metallocene catalyst by in situ ethylene polymerization

    KAUST Repository

    Abdul Kaleel, S. H.

    2012-09-01

    Ethylene polymerization was carried out using highly active metallocene catalysts (Cp 2ZrCl 2 and Cp 2TiCl 2) in combination with methylalumoxane. Titanium(IV) oxide containing 1% Mn as dopant was used as nanofillers. The influence of filler concentration, reaction temperature and pressure on the catalytic activity and polymer properties was investigated. There was a fourfold increase in the activity of zirconocene catalyst by addition of doped-titania. The morphology indicates that the doped-titania nanoparticles have a nucleus effect on the polymerization and caused a homogeneous PE shell around them. The optimum condition for polymerization was found to be 30°C. © 2012 The Korean Society of Industrial and Engineering Chemistry.

  13. Chemical Reactor Automation as a way to Optimize a Laboratory Scale Polymerization Process

    Science.gov (United States)

    Cruz-Campa, Jose L.; Saenz de Buruaga, Isabel; Lopez, Raymundo

    2004-10-01

    The automation of the registration and control of variables involved in a chemical reactor improves the reaction process by making it faster, optimized and without the influence of human error. The objective of this work is to register and control the involved variables (temperatures, reactive fluxes, weights, etc) in an emulsion polymerization reaction. The programs and control algorithms were developed in the language G in LabVIEW®. The designed software is able to send and receive RS232 codified data from the devices (pumps, temperature sensors, mixer, balances, and so on) to and from a personal Computer. The transduction from digital information to movement or measurement actions of the devices is done by electronic components included in the devices. Once the programs were done and proved, chemical reactions of emulsion polymerization were made to validate the system. Moreover, some advanced heat-estimation algorithms were implemented in order to know the heat caused by the reaction and the estimation and control of chemical variables in-line. All the information gotten from the reaction is stored in the PC. The information is then available and ready to use in any commercial data processor software. This work is now being used in a Research Center in order to make emulsion polymerizations under efficient and controlled conditions with reproducible results. The experiences obtained from this project may be used in the implementation of chemical estimation algorithms at pilot plant or industrial scale.

  14. Process for in-situ leaching of uranium

    International Nuclear Information System (INIS)

    Habib, E.T. Jr.

    1979-01-01

    Process for the in-situ leaching of uranium from a subterranean ore deposit employing a lixiviant containing a carbonate leaching agent and an oxidizing agent. The lixiviant is heated to a temperature of at least 110 degrees Fahrenheit prior to injection into the subterranean ore deposit. The use of a heated lixiviant provides for a substantially greater ultimate uranium recovery than that attained through the use of a lixiviant injected at ambient temperature conditions. The process may be carried out in several stages. In the first stage, a relatively low temperature lixiviant is injected. This is followed by a second stage in which the lixiviant is heated to an elevated temperature and then injected into the deposit. The invention is particularly applicable for use in subterranean deposits which contain uranium associated with carbonaceous material

  15. Process for in-situ leaching of uranium

    International Nuclear Information System (INIS)

    Habib, E.T.

    1981-01-01

    A process is described for the in-situ leaching of uranium from a subterranean ore deposit employing a lixiviant containing a carbonate leaching agent and an oxidizing agent. The lixiviant is heated to a temperature of at least 110* F. Prior to injection into the subterranean ore deposit. The use of a heated lixiviant provides for a substantially greater ultimate uranium recovery than that attained through the use of a lixiviant injected at ambient temperature conditions. The process may be carried out in several stages. In the first stage, a relatively low temperature lixiviant is injected. This is followed by a second stage in which the lixiviant is heated to an elevated temperature and then injected into the deposit. The invention is particularly applicable for use in subterranean deposits which contain uranium associated with carbonaceous material

  16. Using artificial neural networks to model extrusion processes for the manufacturing of polymeric micro-tubes

    International Nuclear Information System (INIS)

    Mekras, N; Artemakis, I

    2012-01-01

    In this paper a methodology and an application example are presented aiming to show how Artificial Neural Networks (ANNs) can be used to model manufacturing processes when mathematical models are missing or are not applicable e.g. due to the micro- and nano-scaling, due to non-conventional processes, etc. Besides the ANNs methodology, the results of a Software System developed will be presented, which was used to create ANNs models for micro and nano manufacturing processes. More specifically results of a specific application example will be presented, concerning the modeling of extrusion processes for polymeric micro-tubes. ANNs models are capable for modeling manufacturing processes as far as adequate experimental and/or historical data of processes' inputs and outputs are available for their training. The POLYTUBES ANNs models have been trained and tested with experimental data records of process' inputs and outputs concerning a micro-extrusion process of polymeric micro-tubes for several materials such as: COC, PC, PET, PETG, PP and PVDF. The main ANN model of the extrusion application example has 3 inputs and 9 outputs. The inputs are: tube's inner and outer diameters, and the material density. The model outputs are 9 process parameters, which correspond to the specific inputs e.g. process temperature, die inner and outer diameters, extrusion pressure, draw speed etc. The training of the ANN model was completed, when the errors for the model's outputs, which expressed the difference between the training target values and the ANNs outputs, were minimized to acceptable levels. After the training, the micro-extrusion ANN is capable to simulate the process and can be used to calculate model's outputs, which are the process parameters for any new set of inputs. By this way a satisfactory functional approximation of the whole process is achieved. This research work has been supported by the EU FP7 NMP project POLYTUBES.

  17. A new application of passive samplers as indicators of in-situ biodegradation processes.

    Science.gov (United States)

    Belles, Angel; Alary, Claire; Criquet, Justine; Billon, Gabriel

    2016-12-01

    In this paper, a method for evaluating the in-situ degradation of nitro polycyclic aromatic hydrocarbons (nitro-PAH) in sediments is presented. The methodology is adapted from the passive sampler technique, which commonly uses the dissipation rate of labeled compounds loaded in passive sampler devices to sense the environmental conditions of exposure. In the present study, polymeric passive samplers (made of polyethylene strips) loaded with a set of labeled polycyclic aromatic hydrocarbons (PAH) and nitro-PAH were immersed in sediments (in field and laboratory conditions) to track the degradation processes. This approach is theoretically based on the fact that a degradation process induces a steeper concentration gradient of the labeled compounds in the surrounding sediment, thereby increasing their compound dissipation rates compared with their dissipation in abiotic conditions. Postulating that the degradation magnitude is the same for the labeled compounds loaded in polyethylene strips and for their native homologs that are potentially present in the sediment, the field degradation of 3 nitro-PAH (2-nitro-fluorene, 1-nitro-pyrene, 6-nitro-chrysene) was semi-quantitatively analyzed using the developed method. Copyright © 2016 Elsevier Ltd. All rights reserved.

  18. Processing of novel bioactive polymeric matrixes for tissue engineering using supercritical fluid technology

    Energy Technology Data Exchange (ETDEWEB)

    Duarte, Ana Rita C., E-mail: aduarte@dep.uminho.pt [3B' s Research Group, Biomaterials, Biodegradables and Biomimetics, University of Minho, Headquarters of the European Institute of Excellence on Tissue Engineering and Regenerative Medicine, AvePark, 4806-909 Taipas, Guimaraes (Portugal); IBB, Institute for Biotechnology and Bioengineering, PT Government Associated Laboratory, Guimaraes (Portugal); Caridade, Sofia G.; Mano, Joao F.; Reis, Rui L. [3B' s Research Group, Biomaterials, Biodegradables and Biomimetics, University of Minho, Headquarters of the European Institute of Excellence on Tissue Engineering and Regenerative Medicine, AvePark, 4806-909 Taipas, Guimaraes (Portugal); IBB, Institute for Biotechnology and Bioengineering, PT Government Associated Laboratory, Guimaraes (Portugal)

    2009-08-31

    The aim of this study was to develop a new process for the production of bioactive 3D scaffolds using a clean and environmentally friendly technology. The possibility of preparing composite scaffolds of Bioglass and a polymeric blend of starch and poly(L-lactic acid) (SPLA50) was evaluated. Supercritical phase-inversion technique was used to prepare inorganic particles loaded starch-based porous composite matrixes in a one-step process for bone tissue engineering purposes. Due to their osteoconductive properties some glasses and ceramics are interesting materials to be used for bone tissue engineering purposes; however their poor mechanical properties create the need of a polymeric support where the inorganic fraction can be dispersed. Samples impregnated with different concentrations of Bioglass (10 and 15% wt/wt polymer) were prepared at 200 bar and 55 deg. C. The presence of Bioglass did not affect the porosity or interconnectivity of the polymeric matrixes. Dynamic mechanical analysis has proven that the modulus of the SPLA50 scaffolds increases when glass particles are impregnated within the matrix. In vitro bioactivity studies were carried out using simulated body fluid and the results show that a calcium-phosphate layer started to be formed after only 1 day of immersion. Chemical analysis of the apatite layer formed on the surface of the scaffold was performed by different techniques, namely EDS and FTIR spectroscopy and X-ray diffraction (XRD). The ion concentration in the simulated body fluid was also carried out by ICP analysis. Results suggest that a bone-like apatite layer was formed. This study reports the feasibility of using supercritical fluid technology to process, in one step, a porous matrix loaded with a bioactive material for tissue engineering purposes.

  19. Polymeric Nanocomposite Membranes for Next Generation Pervaporation Process: Strategies, Challenges and Future Prospects

    Directory of Open Access Journals (Sweden)

    Sagar Roy

    2017-09-01

    Full Text Available Pervaporation (PV has been considered as one of the most active and promising areas in membrane technologies in separating close boiling or azeotropic liquid mixtures, heat sensitive biomaterials, water or organics from its mixtures that are indispensable constituents for various important chemical and bio-separations. In the PV process, the membrane plays the most pivotal role and is of paramount importance in governing the overall efficiency. This article evaluates and collaborates the current research towards the development of next generation nanomaterials (NMs and embedded polymeric membranes with regard to its synthesis, fabrication and application strategies, challenges and future prospects.

  20. Optimization of polymerization process conditions during development of micro- and nanocapsules of hydrophobic agents based on Pickering emulsions

    Directory of Open Access Journals (Sweden)

    Saule Aidarova

    2015-09-01

    Full Text Available The polymerization process is one of the most important processes to obtain stable emulsions. This is especially important when the emulsion evaporates. In the work, the protocol of optimum polymerization conditions was developed, which comprises carrying out the polymerization at a temperature of 80°C using potassium persulfate as an initiator at a concentration 0.4 mM. It was found that the formed monodisperse particles with an average size of 200 nm have a distinct morphology capsules, which according cryo-SEM pictures have spherical shape, similar to the morphology of raspberry. These results are also consistent with the data of TEM images, whereby submicrocapsules were densely coated by silica particles. It was proved by zeta-potential measurements according to which, after polymerization the disperse systems become more colloidally stable and less prone to aggregation and sedimentation.

  1. Rapid production of large-area polymeric cold mirror via a simultaneous layer formation process

    Science.gov (United States)

    Wheatley, John A.; Lewis, Ray A.; Schrenk, Walter J.; Lutz, W.; Motter, Gregg A.

    1994-09-01

    Recent technology advances in the processing of polymeric multilayers has made possible the production of an all polymeric cold mirror reflector via coextrusion processing. The simultaneous formation of up to 5200 alternating layers of optically dissimilar polymers allows the continuous extrusion of a self supporting cold mirror at high linear speeds and widths of over 0.6 m (2 ft). The material can be post formed into shallow 3-dimensional reflector shapes, given proper attention to the initial film optical properties, the final part geometry, and forming considerations. The self supporting nature of the film allows it to be wound on rolls and stored for later part fabrication. Reflectance of 95-99% over the visible wavelengths has been achieved with commercially available polymers. The polymers used have high transmission in the near infrared region of 700-2000 nm, and sharp cut- on and cut-offs have been achieved. Uniformity of optical properties across the surface of the film will be discussed, as will thickness, angle of incidence, and temperature effects. The large area capability of this material may make possible applications for heat/light separation not previously viable due to deposition chamber size limitations or the high cost per area of conventional deposition technologies. Scale up of the process to much larger widths is feasible and will be discussed. Prototyped parts and potential applications of this new material will also be covered.

  2. Modelling and optimization of process variables for the solution polymerization of styrene using response surface methodology

    Directory of Open Access Journals (Sweden)

    Rasheed Uthman Owolabi

    2018-01-01

    Full Text Available A satisfactory model for predicting monomer conversion in free radical polymerization has been a challenge due to the complexity and rigors associated with classical kinetic models. This renders the usage of such model an exciting endeavour in the academia but not exactly so in industrial practice. In this study, the individual and interactive effects of three processing conditions (reaction temperature, reaction time and initiator concentration on monomer conversion in the solution polymerization of styrene using acetone as solvent was investigated in a batch reactor through the central composite design (CCD model of response surface methodology (RSM for experimental design, modelling and process optimization. The modelled optimization conditions are: reaction time of 30 min, reaction temperature of 120 °C, and initiator concentration of 0.1135 mol/l, with the corresponding monomer conversion of 76.82% as compared to the observed conversion of 70.86%. A robust model for predicting monomer conversion that is very suitable for routine industrial usage is thus obtained.

  3. Effect of leaching residual methyl methacrylate concentrations on in vitro cytotoxicity of heat polymerized denture base acrylic resin processed with different polymerization cycles.

    Science.gov (United States)

    Bural, Canan; Aktaş, Esin; Deniz, Günnur; Ünlüçerçi, Yeşim; Bayraktar, Gülsen

    2011-08-01

    Residual methyl methacrylate (MMA) may leach from the acrylic resin denture bases and have adverse effects on the oral mucosa. This in vitro study evaluated and correlated the effect of the leaching residual MMA concentrations ([MMA]r) on in vitro cytotoxicity of L-929 fibroblasts. A total of 144 heat-polymerized acrylic resin specimens were fabricated using 4 different polymerization cycles: (1) at 74ºC for 9 h, (2) at 74ºC for 9 h and terminal boiling (at 100ºC) for 30 min, (3) at 74ºC for 9 h and terminal boiling for 3 h, (4) at 74ºC for 30 min and terminal boiling for 30 min. Specimens were eluted in a complete cell culture medium at 37ºC for 1, 2, 5 and 7 days. [MMA]r in eluates was measured using high-performance liquid chromatography. In vitro cytotoxicity of eluates on L-929 fibroblasts was evaluated by means of cell proliferation using a tetrazolium salt XTT (sodium 3´-[1-phenyl-aminocarbonyl)-3,4-tetrazolium]bis(4-methoxy-6-nitro)benzenesulphonic acid) assay. Differences in [MMA]r of eluates and cell proliferation values between polymerization cycles were statistically analyzed by Kruskal-Wallis, Friedman and Dunn's multiple comparison tests. The correlation between [MMA]r of eluates and cell proliferation was analyzed by Pearson's correlation test (p<0.05). [MMA]r was significantly (p<0.001) higher in eluates of specimens polymerized with cycle without terminal boiling after elution of 1 and 2 days. Cell proliferation values for all cycles were significantly (p<0.01) lower in eluates of 1 day than those of 2 days. The correlation between [MMA]r and cell proliferation values was negative after all elution periods, showing significance (p<0.05) for elution of 1 and 2 days. MMA continued to leach from acrylic resin throughout 7 days and leaching concentrations markedly reduced after elution of 1 and 2 days. Due to reduction of leaching residual MMA concentrations, use of terminal boiling in the polymerization process for at least 30 min and water

  4. Effect of leaching residual methyl methacrylate concentrations on in vitro cytotoxicity of heat polymerized denture base acrylic resin processed with different polymerization cycles

    Directory of Open Access Journals (Sweden)

    Canan Bural

    2011-08-01

    the polymerization process for at least 30 min and water storage of the heat-polymerized denture bases for at least 1 to 2 days before denture delivery is clinically recommended for minimizing the residual MMA and possible cytotoxic effects.

  5. Preparation of polyaniline-TiO2 composite film with in situ polymerization approach and its gas-sensitivity at room temperature

    International Nuclear Information System (INIS)

    Ma Xingfa; Wang Mang; Li Guang; Chen Hongzheng; Bai Ru

    2006-01-01

    Polyaniline composite was prepared with chemical oxide method by adding a small amount of TiO 2 sol-gel. This film on the interdigital electrodes of carbon paste was formed via spin-coating or immersion method with in situ polymerization approach. And its gas-sensitivity to trimethylamine was examined at room temperature. The results indicated that, the heat stability of polyaniline film was improved obviously by adding 10 wt% TiO 2. Meanwhile, this film still showed excellent gas-sensitivity to trimethylamine of 5.14 x 10 -7 mol mL -1 , its value of gas-sensitivity was up to three to five orders of magnitude within 3 min, and had good selectivity to analogy gases. The film also exhibited good reproducibility and stability, and easily recovered with high-purity N 2 at room temperature

  6. Preparation of polyaniline-TiO{sub 2} composite film with in situ polymerization approach and its gas-sensitivity at room temperature

    Energy Technology Data Exchange (ETDEWEB)

    Ma Xingfa [Department of Polymer Science and Engineering, State Key Laboratory of Silicon Materials, Zhejiang University, Hangzhou 310027 (China) and Shandong Research Institute of Non-metallic Materials, Jinan 250031 (China)]. E-mail: xingfazju@163.com; Wang Mang [Department of Polymer Science and Engineering, State Key Laboratory of Silicon Materials, Zhejiang University, Hangzhou 310027 (China); Li Guang [Key Laboratory of Biomedical Engineering of the Ministry of Education and State Key Lab of Biosensor, Department of Biomedical Engineering, Zhejiang University, Hangzhou 310027 (China); Chen Hongzheng [Department of Polymer Science and Engineering, State Key Laboratory of Silicon Materials, Zhejiang University, Hangzhou 310027 (China); Bai Ru [Department of Polymer Science and Engineering, State Key Laboratory of Silicon Materials, Zhejiang University, Hangzhou 310027 (China)

    2006-08-01

    Polyaniline composite was prepared with chemical oxide method by adding a small amount of TiO{sub 2} sol-gel. This film on the interdigital electrodes of carbon paste was formed via spin-coating or immersion method with in situ polymerization approach. And its gas-sensitivity to trimethylamine was examined at room temperature. The results indicated that, the heat stability of polyaniline film was improved obviously by adding 10 wt% TiO{sub 2.} Meanwhile, this film still showed excellent gas-sensitivity to trimethylamine of 5.14 x 10{sup -7} mol mL{sup -1}, its value of gas-sensitivity was up to three to five orders of magnitude within 3 min, and had good selectivity to analogy gases. The film also exhibited good reproducibility and stability, and easily recovered with high-purity N{sub 2} at room temperature.

  7. Log-pile photonic crystal of CdS-polymer nanocomposites fabricated by combination of two-photon polymerization and in situ synthesis

    International Nuclear Information System (INIS)

    Sun, Z.-B.; Dong, X.-Z.; Chen, W.-Q.; Duan, X.-M.; Nakanishi, S.; Kawata, S.

    2007-01-01

    A log-pile photonic crystal of CdS nanoparticles-polymer nanocomposites was successfully fabricated by a novel method combining the two-photon polymerization technique and in situ synthesis of CdS nanoparticles in a polymer matrix. The photonic band gap of the three-dimensional (3D) log-pile photonic crystal is confirmed and becomes more effective for CdS nanoparticles-polymer nanocomposites than polymer doped with Cd 2+ ions, because the nanocomposites possess a higher refractive index than the polymer. The proposed concept in the new fabrication method for a 3D microstructure of polymer nanocomposites should be of critical importance in providing a general methodology for functionalization of materials via functional nanocomposites used in the field of laser microstructure fabrication. (orig.)

  8. Structural and optical characterization of In{sub 2}O{sub 3}/PANI nanocomposite prepared by in-situ polymerization

    Energy Technology Data Exchange (ETDEWEB)

    Janeoo, Shashi; Sharma, Mamta, E-mail: mamta.phy85@gmail.com; Goswamy, J. [Department of Applied Sciences (Physics), UIET, Panjab University, Chandigarh-160 014 (India); Singh, Gurinder [Department of Applied Sciences (Physics), UIET, PUSSGSRC, Hoshiarpur (Punjab) (India)

    2016-05-23

    Polyaniline-indium oxide (In{sub 2}O{sub 3}/PANI) nanocomposite have been prepared by in-situ polymerization of aniline and as-synthesized In{sub 2}O{sub 3} nanoparticles. X-ray diffraction (XRD), Transmission electron microscopy (TEM), Fourier transformation infrared (FTIR) and UV/Vis spectroscopy techniques are used to investigate the structural and optical properties of In{sub 2}O{sub 3}/PANI nanocomposite. TEM analysis shows In{sub 2}O{sub 3} nanoparticles are embedded in PANI nanofibers. FTIR spectra show the good interactions between PANI nanofibers and In{sub 2}O{sub 3} nanoparticles. The band gap and electronic transitions in In{sub 2}O{sub 3}/PANI nanocomposite is determined by using UV/Vis spectra.

  9. New functional nanocomposites based on poly(trimethylene 2,5-furanoate and few layer graphene prepared by in situ polymerization

    Directory of Open Access Journals (Sweden)

    S. Paszkiewicz

    2018-06-01

    Full Text Available Poly(trimethylene 2,5-furanoate (PTF nanocomposites reinforced with few layer graphene (FLG were prepared through in situ polymerization. The method in question allows obtaining well-dispersed nanoplatelets in the whole volume of PTF matrix. The mechanical properties of the PTF/FLG nanocomposites slightly increased with as quantity of FLG as small as 0.1 wt%, which was best seen in the improvement of elongation at break by about two times. The presence of FLG did not affect the crystallization and chain mobility of PTF matrix. However, the incorporation of a small quantity of FLG slightly improved the thermal stability of the nanocomposites. Additionally, the cold and hot water absorption and oxygen permittivity measurements confirmed that FLG affected the tortuosity of the diffusive path for the penetrant molecule. Moreover, along with a successive addition of FLG a linear increase in thermal conductivity was visible.

  10. High Dielectric Constant Study of TiO2-Polypyrrole Composites with Low Contents of Filler Prepared by In Situ Polymerization

    Directory of Open Access Journals (Sweden)

    Khalil Ahmed

    2016-01-01

    Full Text Available TiO2/polypyrrole composites with high dielectric constant have been synthesized by in situ polymerization of pyrrole in an aqueous dispersion of low concentration of TiO2, in the presence of small amount of HCl. Structural, optical, surface morphological, and thermal properties of the composites were investigated by X-ray diffractometer, Fourier transform infrared spectroscopy, field-emission scanning electron microscopy, and thermogravimetric analysis, respectively. The data obtained from diffractometer and thermal gravimetric analysis confirmed the crystalline nature and thermal stability of the prepared composites. The dielectric constant of 5 wt% TiO2 increased with filler content up to 4.3 × 103 at 1 kHz and then decreased to 1.25 × 103 at 10 kHz.

  11. Primary processes of the radiation-induced cationic polymerization of aromatic olefins studied by pulse radiolysis

    International Nuclear Information System (INIS)

    Brede, O.; Boes, J.; Helmstreit, W.; Mehnert, R.

    1982-01-01

    By pulse radiolysis of solutions of aromatic olefins (styrene, 1-methylstyrene, 1,1-diphenylethylene) in non-polar solvents (cyclohexane, carbon tetrachloride, n-butylchloride) the mechanism and kinetics of primary processes of radiation-induced cationic polymerization were investigated. In cyclohexane, radical cations of the olefins are generated by charge transfer from solvent cations. These cations dimerize in a diffusion-controlled reaction. The next step of chain-growth is slower by 3 to 4 orders of magnitude. In carbon tetrachloride and in n-butyl chloride growing olefin cations are produced by a reaction of radical cations with solvent as well as by addition of solvent carbonium ions to the monomer. In strongly acidic aqueous solution of olefins radical cations produced indirectly from hydroxycyclohexadienyl radicals dimerize and react in a subsequent step by deprotonation forming non-saturated dimer radicals. The reaction mechanism established shows that in the case of radiation-induced cationic polymerization it is not possible to define a uniform first step of the chain reaction. (author)

  12. Primary processes of the radiation-induced cationic polymerization of aromatic olefins studied by pulse radiolysis

    International Nuclear Information System (INIS)

    Brede, O.; Boes, J.; Helmstreit, W.; Mehnert, R.

    1981-01-01

    By pulse radiolysis of solutions of aromatic olefins (styrene, 1-methylstyrene, 1,1-diphenylethylene) in nonpolar solvents (cyclohexane, carbon tetrachloride, n-butyl chloride) the mechanism and kinetics of primary processes of radiation-induced cationic polymerization were investigated. In cyclohexane, radical cations of the olefins are generated by charge transfer from solvent cations (k about 10 11 l mol -1 s -1 ). These cations dimerize in a diffusion-controlled reaction (k approximately 10 10 l mol -1 s -1 ). The next step of chain-growth is slower by 3 to 4 orders of magnitude. Furthermore, in carbon tetrachloride and in n-butyl chloride growing olefin cations are produced by a reaction of the radical cations with the solvent as well as by addition of solvent carbonium ions to the monomer. In strongly acidic aqueous solution of olefins radical cations produced indirectly from hydroxycyclohexadienyl radicals dimerize and react in a subsequent step by deprotonation forming non-saturated dimer radicals. The established reaction mechanism shows that in the case of radiation-induced cationic polymerization it is not possible to define a uniform first step of the chain reaction. (author)

  13. UV-Vis/FT-NIR in situ monitoring of visible-light induced polymerization of PEGDA hydrogels initiated by eosin/triethanolamine/O2

    Science.gov (United States)

    Kaastrup, Kaja; Aguirre-Soto, Alan; Wang, Chen; Bowman, Christopher N.; Stansbury, Jeffery; Sikes, Hadley D.

    2016-01-01

    In conjunction with a tertiary amine coinitiator, eosin, a photoreducible dye, has been shown to successfully circumvent oxygen inhibition in radical photopolymerization reactions. However, the role of O2 in the initiation and polymerization processes remains inconclusive. Here, we employ a UV-Vis/FT-NIR analytical tool for real-time, simultaneous monitoring of chromophore and monomer reactive group concentrations to investigate the eosin-activated photopolymerization of PEGDA-based hydrogels under ambient conditions. First, we address the challenges associated with spectroscopic monitoring of the polymerization of hydrogels using UV-Vis and FT-NIR, proposing metrics for quantifying the extent of signal loss from reflection and scattering, and showing their relation to microgelation and network formation. Second, having established a method for extracting kinetic information by eliminating the effects of changing refractive index and scattering, the coupled UV-Vis/FT-NIR system is applied to the study of eosin-activated photopolymerization of PEGDA in the presence of O2. Analysis of the inhibition time, rate of polymerization, and rate of eosin consumption under ambient and purged conditions indicates that regeneration of eosin in the presence of oxygen and consumption of oxygen occur via a nonchain process. This suggests that the uniquely high O2 resilience is due to alternative processes such as energy transfer from photo-activated eosin to oxygen. Uncovering the intricacies of the role of O2 in eosin-mediated initiation aids the design of O2 resistant free radical polymerization systems relevant to photonics, optoelectronics, biomaterials, and biosensing. PMID:26755925

  14. Study of stability and temperature effects on tetrafluoroethylene irradiated for the safe process of monomer polymerization induced by gamma radiation

    International Nuclear Information System (INIS)

    Moura, E.A.B.; Lugao, A.B.; Silva, L.B.A.

    1997-01-01

    The superior objective of this work the determination of the procedures for the safe process of TFE polymerization induced by radiation. It was studied the effects of the initial temperature on tetrafluoroethylene (TFE) irradiation. It was also studied the efficiency of terpenes (dipentene, terpinolene, α-pinene) on TFE stabilization. Both studies used gamma radiation to induce the polymerization and disproportionation reactions. For the temperature effect study, 40 g of liquid TFE was introduced in a explosion proof vessel and initially irradiated in the range of -78 0 C and 20 0 C to 24 0 C. The inhibition efficiency of terpenes on the TFE polymerization was studied by irradiating TFE with terpenes and without them, using a similar vessel also explosion proof. Surprisingly, the results on the irradiation temperature showed that the reactions in the range 20 0 C to 24 0 C were more controllable than the one in-78 0 C to -64 0 C. The results on TFE stability showed that the TFE polymerization was completely inhibited by the addition of 0.1% of all tested terpenes or 1:1:1 mixture of them. As a final conclusion it was shown that the use of the irradiation induced polymerization of TFE was a safe, satisfactory and more controllable method for the study of TFE stabilization and polymerization in the range of 20 0 C to 24 0 C. (author). 8 refs., 5 figs., 2 tabs

  15. Antibacterial polymeric nanocomposites synthesized by in-situ photoreduction of silver ions without additives inside biocompatible hydrogel matrices based on N-isopropylacrylamide and derivatives

    Directory of Open Access Journals (Sweden)

    M. Monerris

    2017-12-01

    Full Text Available Synthesis of antibacterial nanocomposite obtained by in-situ photoreduction of Ag+ ions impregnated inside a biocompatible hydrogel matrix is described. Hydrogel matrixes based on N-isopropylacrylamide (PNIPAM and copolymers are synthesized by free radical polymerization in aqueous medium. The hydrogels are loaded with Ag+ ions and then silver nanoparticles (Ag-NPs are obtained in-situ by application of UV light without using additives. Ag-NPs formation inside hydrogels is confirmed by UV–visible spectroscopy, scanning electronic microscopy (SEM and transmission electronic microscopy (TEM. An extensive characterization of nanocomposites is performed by determining the partition coefficient of Ag+ ions before photoreduction, the Ag-NPs mass loaded per gram of hydrogel as a function of irradiation time, swelling capacity and volume phase transition temperature. Fourier Transform Infrared (FTIR spectra indicate the loss of some functional groups of the polymer backbone during reduction of Ag+ ions whereas 13C NMR spectra do not show any change in the main carbon chain. Nanocomposites show antibacterial activity against Pseudomonas aeruginosas by release of Ag+ ions while Ag-NPs remain inside matrix. Reducing/stabilizing character of hydrogel and antibacterial activity of nanocomposite depend on the chemical composition of the matrix.

  16. Process Chain for the Manufacture of Polymeric Tubular Micro-Components and “POLYTUBES Micro-Factory” Concept

    DEFF Research Database (Denmark)

    Qin, Yi; Perzon, Erik; Chronakis, Ioannis S.

    The paper presents a process chain for the shaping of poly-meric tubular micro-components for the volume production as well as presents a concept for the integration of the developed processes and modular machines onto a platform to form a "POLYTUBES Micro-Factory", being resulting from the Europ...

  17. Polyamide from lactams by reactive rotational molding via anionic ring-opening polymerization: Optimization of processing parameters

    Directory of Open Access Journals (Sweden)

    N. Barhoumi

    2013-01-01

    Full Text Available A reactive rotational molding (RRM process was developed to obtain a PA6 by activated anionic ring-opening polymerization of epsilon-caprolactam (APA6. Sodium caprolactamate (C10 and caprolactam magnesium bromide (C1 were employed as catalysts, and difunctional hexamethylene-1,6-dicarbamoylcaprolactam (C20 was used as an activator. The kinetics of the anionic polymerization of !-caprolactam into polyamide 6 was monitored through dynamic rheology and differential scanning calorimetry measurements. The effect of the processing parameters, such as the polymerization temperature, different catalyst/activator combinations and concentrations, on the kinetics of polymerization is discussed. A temperature of 150°C was demonstrated to be the most appropriate. It was also found that crystallization may occur during PA6 polymerization and that the combination C1/C20 was well suited as it permitted a suitable induction time. Isoviscosity curves were drawn in order to determine the available processing window for RRM. The properties of the obtained APA6 were compared with those of a conventionally rotomolded PA6. Results pointed at lower cycle times and increased tensile properties at weak deformation.

  18. New green polymeric composites based on hemp and natural rubber processed by electron beam irradiation.

    Science.gov (United States)

    Stelescu, Maria-Daniela; Manaila, Elena; Craciun, Gabriela; Dumitrascu, Maria

    2014-01-01

    A new polymeric composite based on natural rubber reinforced with hemp has been processed by electron beam irradiation and characterized by several methods. The mechanical characteristics: gel fraction, crosslink density, water uptake, swelling parameters, and FTIR of natural rubber/hemp fiber composites have been investigated as a function of the hemp content and absorbed dose. Physical and mechanical properties present a significant improvement as a result of adding hemp fibres in blends. Our experiments showed that the hemp fibers have a reinforcing effect on natural rubber similar to mineral fillers (chalk, carbon black, silica). The crosslinking rates of samples, measured using the Flory-Rehner equation, increase as a result of the amount of hemp in blends and the electron beam irradiation dose increasing. The swelling parameters of samples significantly depend on the amount of hemp in blends, because the latter have hydrophilic characteristics.

  19. Process, Design and Materials for Unidirectionally Tilted Polymeric Micro/Nanohairs and Their Adhesion Characteristics

    Directory of Open Access Journals (Sweden)

    Hyeon Seong Im

    2016-09-01

    Full Text Available Recent research in the field of gecko-inspired dry adhesive has focused on modifying the material and structural properties of polymer-based nanohairs. Polymers such as polystyrene (PS, high-density polyethylene (HDPE, ultraviolet curable epoxy (SU-8, polyurethane acrylate (PUA, polycarbonate (PC, and polydimethyl siloxane (PDMS can fulfill many mechanical property requirements, are easily tunable, and can be produced via large-scale fabrication. However, the fabrication process for tilted structure remains challenging. The tilted structure is a crucial factor in high-degree conformal contact, which facilitates high adhesion, low effective modulus, and directional adhesion properties. Recent studies have attempted to create a tilted structure by applying beam irradiation, mechanical and thermal stress, and magnetic fields. This review provides a comprehensive investigation into advanced strategies for producing tilted polymeric nanostructures and their potential applications in the near future.

  20. In situ synthesis of silver nanoparticles on the cotton fabrics modified by plasma induced vapor phase graft polymerization of acrylic acid for durable multifunction

    Energy Technology Data Exchange (ETDEWEB)

    Wang, C.X., E-mail: cxwang@mail.dhu.edu.cn [College of Textiles and Clothing, Yancheng Institute of Technology, Jiangsu, 224003 (China); Collaborative Innovation Center for Ecological Building, Materials and Environmental Protection Equipments, Jiangsu, 224051 (China); Laboratory for Advanced Technology in Environmental Protection, Jiangsu, 224051 (China); School of Textile and Clothing, Nantong University, Jiangsu, 226019 (China); Ren, Y. [School of Textile and Clothing, Nantong University, Jiangsu, 226019 (China); Lv, J.C.; Zhou, Q.Q.; Ma, Z.P.; Qi, Z.M.; Chen, J.Y.; Liu, G.L.; Gao, D.W. [College of Textiles and Clothing, Yancheng Institute of Technology, Jiangsu, 224003 (China); Lu, Z.Q. [College of Textiles and Clothing, Yancheng Institute of Technology, Jiangsu, 224003 (China); Collaborative Innovation Center for Ecological Building, Materials and Environmental Protection Equipments, Jiangsu, 224051 (China); Laboratory for Advanced Technology in Environmental Protection, Jiangsu, 224051 (China); Zhang, W. [College of Textiles and Clothing, Yancheng Institute of Technology, Jiangsu, 224003 (China); Jin, L.M. [Shanghai Institute of Applied Physics, Chinese Academy of Sciences, Shanghai, 201204 (China)

    2017-02-28

    Highlights: • A new means for multifunctional cotton fabrics by PIVPGP of AA and AgNPs synthesis. • Surface modification by PIVPGP of AA had a positive effect on AgNPs loading. • Antibacterial, self-cleaning and thermal stability were greatly improved. • AgNP loaded cotton fabric exhibited excellent laundering durability. • Mechanism of AgNPs in situ synthesis on cotton fabrics by PIVPGP of AA was proposed. - Abstract: A practical and ecological method for preparing the multifunctional cotton fabrics with excellent laundering durability was explored. Cotton fabrics were modified by plasma induced vapor phase graft polymerization (PIVPGP) of acrylic acid (AA) and subsequently silver nanoparticles (AgNPs) were in situ synthesized on the treated cotton fabrics. The AgNP loaded cotton fabrics were characterized by scanning electron microscope (SEM), energy dispersive X-ray (EDX), X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD), antibacterial activity, self-cleaning activity, thermal stability and laundering durability, respectively. SEM observation and EDX, XPS and XRD analysis demonstrated the much more AgNPs deposition on the cotton fabrics modified by PIVPGP of AA. The AgNP loaded cotton fabrics also exhibited better antibacterial activity, self-cleaning activity, thermal stability and laundering durability. It was concluded that the surface modification of the cotton fabrics by PIVPGP of AA could increase the loading efficiency and binding fastness of AgNPs on the treated cotton fabrics, which could fabricate the cotton fabrics with durable multifunction. In addition, the mechanism of in situ synthesis of AgNPs on the cotton fabrics modified by PIVPGP of AA was proposed.

  1. A review on the processing accuracy of two-photon polymerization

    International Nuclear Information System (INIS)

    Zhou, Xiaoqin; Hou, Yihong; Lin, Jieqiong

    2015-01-01

    Two-photon polymerization (TPP) is a powerful and potential technology to fabricate true three-dimensional (3D) micro/nanostructures of various materials with subdiffraction-limit resolution. And it has been applied to microoptics, electronics, communications, biomedicine, microfluidic devices, MEMS and metamaterials. These applications, such as microoptics and photon crystals, put forward rigorous requirements on the processing accuracy of TPP, including the dimensional accuracy, shape accuracy and surface roughness and the processing accuracy influences their performance, even invalidate them. In order to fabricate precise 3D micro/nanostructures, the factors influencing the processing accuracy need to be considered comprehensively and systematically. In this paper, we review the basis of TPP micro/nanofabrication, including mechanism of TPP, experimental set-up for TPP and scaling laws of resolution of TPP. Then, we discuss the factors influencing the processing accuracy. Finally, we summarize the methods reported lately to improve the processing accuracy from improving the resolution and changing spatial arrangement of voxels

  2. A review on the processing accuracy of two-photon polymerization

    Energy Technology Data Exchange (ETDEWEB)

    Zhou, Xiaoqin; Hou, Yihong [School of Mechanical Science and Engineering, Jilin University, Changchun, 130022 (China); Lin, Jieqiong, E-mail: linjieqiong@mail.ccut.edu.cn [School of Electromechanical Engineering, Changchun University of Technology, Changchun, 130012 (China)

    2015-03-15

    Two-photon polymerization (TPP) is a powerful and potential technology to fabricate true three-dimensional (3D) micro/nanostructures of various materials with subdiffraction-limit resolution. And it has been applied to microoptics, electronics, communications, biomedicine, microfluidic devices, MEMS and metamaterials. These applications, such as microoptics and photon crystals, put forward rigorous requirements on the processing accuracy of TPP, including the dimensional accuracy, shape accuracy and surface roughness and the processing accuracy influences their performance, even invalidate them. In order to fabricate precise 3D micro/nanostructures, the factors influencing the processing accuracy need to be considered comprehensively and systematically. In this paper, we review the basis of TPP micro/nanofabrication, including mechanism of TPP, experimental set-up for TPP and scaling laws of resolution of TPP. Then, we discuss the factors influencing the processing accuracy. Finally, we summarize the methods reported lately to improve the processing accuracy from improving the resolution and changing spatial arrangement of voxels.

  3. Poly(vinyl acetate-Based Block Copolymer/Clay Nanocomposites Prepared by In Situ Atom Transfer Radical Polymerization

    Directory of Open Access Journals (Sweden)

    M.A. Semsarzadeh

    2009-12-01

    Full Text Available Atom transfer radical polymerization of styrene (St and methyl methacrylate (MMA was performed at 90oC in the absence and presence of nanoclay (Cloisite 30B. Trichloromethyl-terminated poly(vinyl acetate telomerand CuCl/ PMDETA were used as a macroinitiator and catalyst system, respectively. The experimental results showed that the atom transfer radical polymerization of St and MMA in the absence or presence of nanoclay proceeds via a controlled/living mode. It was observed that nanoclay significantly enhances the homopolymerization rate of MMA, which was attributed to the activated conjugated C=C bond of MMA monomer via interaction between the carbonyl group of MMA monomer and the hydroxyl moiety (Al-O-H of nanoclay as well as the effect of nanoclay on the dynamic equilibrium between the active (macro radicals and dormant species.Homopolymerization rate of St (a non-coordinative monomer with nanoclay decreased slightly in the presence of nanoclay. This could be explained by insertion of a portion of macroinitiator into the clay galleries, where no sufficient St monomer exists due to the low compatibility or interaction of St monomer with nanoclay to react with the macroinitiator. The results obtained from XRD, TEM and TGA analyses were fully in agreement with the kinetic data. Structure of the poly(vinyl acetate-bpolystyrene nanocomposite was found to be a combination of stacking layers and exfoliated structures while poly(vinyl acetate-b-poly(methyl methacryale nanocomposite had an exfoliated structure. This difference in the structure of nanocomposites was attributed to the different capability of the monomers (styrene and methyl methacrylate to react with the hydroxyl moiety (Al-O-H of nanoclay.

  4. Mimicking the Nanostructure of Bone: Comparison of Polymeric Process-Directing Agents

    Directory of Open Access Journals (Sweden)

    Laurie B. Gower

    2010-12-01

    Full Text Available The nanostructure of bone has been replicated using a polymer-induced liquid-precursor (PILP mineralization process. This polymer-mediated crystallization process yields intrafibrillar mineralization of collagen with uniaxially-oriented hydroxyapatite crystals. The process-directing agent, an anionic polymer which we propose mimics the acidic non-collagenous proteins associated with bone formation, sequesters calcium and phosphate ions to form amorphous precursor droplets that can infiltrate the interstices of collagen fibrils. In search of a polymeric agent that produces the highest mineral content in the shortest time, we have studied the influence of various acidic polymers on the in vitro mineralization of collagen scaffolds via the PILP process. Among the polymers investigated were poly-L-aspartic acid (PASP, poly-L-glutamic acid (PGLU, polyvinylphosphonic acid (PVPA, and polyacrylic acid (PAA. Our data indicate that PASP and the combination of PGLU/PASP formed stable mineralization solutions, and yielded nano-structured composites with the highest mineral content. Such studies contribute to our goal of preparing biomimetic bone graft substitutes with composition and structure that mimic bone.

  5. Effect of anionic dopants on thickness, morphology and electrical properties of polypyrrole ultra-thin films prepared by in situ chemical polymerization

    International Nuclear Information System (INIS)

    Mahmoodian, Mehrnoosh; Pourabbas, Behzad; Mohajerzadeh, Shams

    2015-01-01

    The effect of different dopant anions on deposition and characteristics of polypyrrole (PPy) thin film has been studied in this work. Ultra-thin films of conducting PPy were deposited on insulating surfaces of glass and oxidized silicon wafer by in situ chemical polymerization in the presence of different anionic dopants including sodium dodecylbenzenesulfonate, sodium dodecyl sulfate, α-naphthalene sulfonic acid, anthraquinone-2-sulfonic acid sodium salt monohydrate/5-sulfosalicylic acid dehydrate, and camphor sulfonic acid. Hydrophilic/hydrophobic properties and morphology of the self-assembled monolayer of N-(3-trimethoxysilylpropyl)pyrrole, the surface modifying agent in this work, and PPy thin films were characterized before and after deposition by contact angle measurements, field emission scanning electron microscopy, and atomic force microscopy. Chemical structure, thickness, and conductivity of the thin films were also studied by attenuated total reflectance Fourier transform infrared spectrometer, ellipsometry, and four-point probe measurements. The results showed deposition of thin films of conducting PPy with comparable thickness in the range of 6-31 nm and different morphologies, uniformity, and smoothness with average roughness in the range of 0.3-6 nm and relatively high range of conductivity on the modified surfaces. - Highlights: • Conducting thin films of polypyrrole were deposited on glass and SiO 2 substrates. • Surface modification using pyrrole-silane was employed prior to polymerization. • Films as thin as ≈ 7 nm were deposited using different surfactant/counter ions. • Chemistry of the counter ion affects thickness, conductivity and morphology. • Lower thickness/higher conductivity were obtained by structurally flexible dopants

  6. Effect of molecular chain length on the mechanical and thermal properties of amine-functionalized graphene oxide/polyimide composite films prepared by in situ polymerization.

    Science.gov (United States)

    Liao, Wei-Hao; Yang, Shin-Yi; Wang, Jen-Yu; Tien, Hsi-Wen; Hsiao, Sheng-Tsung; Wang, Yu-Sheng; Li, Shin-Ming; Ma, Chen-Chi M; Wu, Yi-Fang

    2013-02-01

    This study fabricates amine (NH(2))-functionalized graphene oxide (GO)/polyimide(PI) composite films with high performance using in situ polymerization. Linear poly(oxyalkylene)amines with two different molecular weights 400 and 2000 (D400 and D2000) have been grafted onto the GO surfaces, forming two types of NH(2)-functionalized GO (D400-GO/D2000-GO). NH(2)-functionalized GO, especially D400-GO, demonstrated better reinforcing efficiency in mechanical and thermal properties. The observed property enhancement are due to large aspect ratio of GO sheets, the uniform dispersion of the GO within the PI matrix, and strong interfacial adhesion due to the chemical bonding between GO and the polymeric matrix. The Young's modulus of the composite films with 0.3 wt % D400-GO loading is 7.4 times greater than that of neat PI, and tensile strength is 240% higher than that of neat PI. Compared to neat PI, 0.3 wt % D400-GO/PI film exhibits approximately 23.96 °C increase in glass transition temperature (T(g)). The coefficient of thermal expansion below T(g) is significantly decreased from 102.6 μm/°C (neat PI) to 53.81 μm/°C (decreasing 48%) for the D400-GO/PI composites with low D400-GO content (0.1 wt %). This work not only provides a method to develop the GO-based polyimide composites with superior performances but also conceptually provides a chance to modulate the interfacial interaction between GO and the polymer through designing the chain length of grafting molecules on NH(2)-functionalized GO.

  7. Effect of anionic dopants on thickness, morphology and electrical properties of polypyrrole ultra-thin films prepared by in situ chemical polymerization

    Energy Technology Data Exchange (ETDEWEB)

    Mahmoodian, Mehrnoosh [Dep. of Polymer Engineering, Nanostructured Materials Research Center, Sahand University of Technology, Tabriz 51335-1996 (Iran, Islamic Republic of); Pourabbas, Behzad, E-mail: pourabas@sut.ac.ir [Dep. of Polymer Engineering, Nanostructured Materials Research Center, Sahand University of Technology, Tabriz 51335-1996 (Iran, Islamic Republic of); Mohajerzadeh, Shams [Nano-Electronics and Thin Film Lab, School of Electrical and Computer Engineering, University of Tehran, P.O. Box 14395/515, Tehran (Iran, Islamic Republic of)

    2015-05-29

    The effect of different dopant anions on deposition and characteristics of polypyrrole (PPy) thin film has been studied in this work. Ultra-thin films of conducting PPy were deposited on insulating surfaces of glass and oxidized silicon wafer by in situ chemical polymerization in the presence of different anionic dopants including sodium dodecylbenzenesulfonate, sodium dodecyl sulfate, α-naphthalene sulfonic acid, anthraquinone-2-sulfonic acid sodium salt monohydrate/5-sulfosalicylic acid dehydrate, and camphor sulfonic acid. Hydrophilic/hydrophobic properties and morphology of the self-assembled monolayer of N-(3-trimethoxysilylpropyl)pyrrole, the surface modifying agent in this work, and PPy thin films were characterized before and after deposition by contact angle measurements, field emission scanning electron microscopy, and atomic force microscopy. Chemical structure, thickness, and conductivity of the thin films were also studied by attenuated total reflectance Fourier transform infrared spectrometer, ellipsometry, and four-point probe measurements. The results showed deposition of thin films of conducting PPy with comparable thickness in the range of 6-31 nm and different morphologies, uniformity, and smoothness with average roughness in the range of 0.3-6 nm and relatively high range of conductivity on the modified surfaces. - Highlights: • Conducting thin films of polypyrrole were deposited on glass and SiO{sub 2} substrates. • Surface modification using pyrrole-silane was employed prior to polymerization. • Films as thin as ≈ 7 nm were deposited using different surfactant/counter ions. • Chemistry of the counter ion affects thickness, conductivity and morphology. • Lower thickness/higher conductivity were obtained by structurally flexible dopants.

  8. Modeling and monitoring of a high pressure polymerization process using multivariate statistical techniques

    Science.gov (United States)

    Sharmin, Rumana

    This thesis explores the use of multivariate statistical techniques in developing tools for property modeling and monitoring of a high pressure ethylene polymerization process. In polymer industry, many researchers have shown, mainly in simulation studies, the potential of multivariate statistical methods in identification and control of polymerization process. However, very few, if any, of these strategies have been implemented. This work was done using data collected from a commercial high pressure LDPE/EVA reactor located at AT Plastics, Edmonton. The models or methods developed in the course of this research have been validated with real data and in most cases, implemented in real time. One main objective of this PhD project was to develop and implement a data based inferential sensor to estimate the melt flow index of LDPE and EVA resins using regularly measured process variables. Steady state PLS method was used to develop the soft sensor model. A detailed description of the data preprocessing steps are given that should be followed in the analysis of industrial data. Models developed for two of the most frequently produced polymer grades at AT Plastics have been implemented. The models were tested for many sets of data and showed acceptable performance when applied with an online bias updating scheme. One observation from many validation exercises was that the model prediction becomes poorer with time as operators use new process conditions in the plant to produce the same resin with the same specification. During the implementation of the soft sensors, we suggested a simple bias update scheme as a remedy to this problem. An alternative and more rigorous approach is to recursively update the model with new data, which is also more suitable to handle grade transition. Two existing recursive PLS methods, one based on NIPALS algorithm and the other based on kernel algorithm were reviewed. In addition, we proposed a novel RPLS algorithm which is based on the

  9. Preparation of poly(vinyl alcohol)-grafted graphene oxide/poly(vinyl alcohol) nanocomposites via in-situ low-temperature emulsion polymerization and their thermal and mechanical characterization

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Shengchang; Liu, Pengqing, E-mail: liupq@scu.edu.cn; Zhao, Xiangsen; Xu, Jianjun, E-mail: xujj@scu.edu.cn

    2017-02-28

    Highlights: • In-situ emulsion polymerization and alcoholysis reaction is a good method to prepare GO/PVA nanocomposites. • Surface chemical grafting modification of GO with PVA chains was also carried out during the in-situ emulsion polymerization and alcoholysis reaction. • The surface chemical grafting modification of GO by in-situ polymerization and alcoholysis reaction could not only improve the dispersion of fillers in matrix, but also the interfacial interactions between fillers and matrix. • The thermal and mechanical properties of PVA-g-GO/PVA nanocompistes were also studied. - Abstract: An in-situ polymerization combined with chemical grafting modification method for preparing Poly(vinyl alcohol)-grafted graphene oxide/Poly(vinyl alcohol) (PVA-g-GO/PVA) nanocomposites was reported. Firstly, Poly(vinyl acetate)-grafted graphene oxide/Poly(vinyl acetate) nanocomposites were prepared, and then the PVA-g-GO/PVA nanocomposites could be obtained through alcoholysis reaction. X-ray photoelectron spectrometer and fourier-transform infrared spectrometer confirmed that the PVAc or PVA chains were successfully grafted to GO sheets during in-situ polymerization and alcoholysis. And the results from transmission electron microscopy, scanning electron microscopy and X-ray diffraction showed that the well compatibility and homogenous dispersion of PVA-g-GO in PVA matrix could be achieved. Differential scanning calorimetric, thermogravimetry analysis and tensile test were employed to study the thermal and mechanical properties of the PVA-g-GO/PVA nanocomposites. The results indicated that a 53% improvement of tensile strength and a 36% improvement of Young’s modulus were achieved by addition of 0.5 wt% of GO sheets. And the glass transition temperature of PVA-g-GO/PVA nanocomposites was increased, and their thermal stability and crystallization degree were both decreased. Due to well dispersion of fillers and strong interfacial interactions at the filler

  10. Preparation of poly(vinyl alcohol)-grafted graphene oxide/poly(vinyl alcohol) nanocomposites via in-situ low-temperature emulsion polymerization and their thermal and mechanical characterization

    International Nuclear Information System (INIS)

    Zhang, Shengchang; Liu, Pengqing; Zhao, Xiangsen; Xu, Jianjun

    2017-01-01

    Highlights: • In-situ emulsion polymerization and alcoholysis reaction is a good method to prepare GO/PVA nanocomposites. • Surface chemical grafting modification of GO with PVA chains was also carried out during the in-situ emulsion polymerization and alcoholysis reaction. • The surface chemical grafting modification of GO by in-situ polymerization and alcoholysis reaction could not only improve the dispersion of fillers in matrix, but also the interfacial interactions between fillers and matrix. • The thermal and mechanical properties of PVA-g-GO/PVA nanocompistes were also studied. - Abstract: An in-situ polymerization combined with chemical grafting modification method for preparing Poly(vinyl alcohol)-grafted graphene oxide/Poly(vinyl alcohol) (PVA-g-GO/PVA) nanocomposites was reported. Firstly, Poly(vinyl acetate)-grafted graphene oxide/Poly(vinyl acetate) nanocomposites were prepared, and then the PVA-g-GO/PVA nanocomposites could be obtained through alcoholysis reaction. X-ray photoelectron spectrometer and fourier-transform infrared spectrometer confirmed that the PVAc or PVA chains were successfully grafted to GO sheets during in-situ polymerization and alcoholysis. And the results from transmission electron microscopy, scanning electron microscopy and X-ray diffraction showed that the well compatibility and homogenous dispersion of PVA-g-GO in PVA matrix could be achieved. Differential scanning calorimetric, thermogravimetry analysis and tensile test were employed to study the thermal and mechanical properties of the PVA-g-GO/PVA nanocomposites. The results indicated that a 53% improvement of tensile strength and a 36% improvement of Young’s modulus were achieved by addition of 0.5 wt% of GO sheets. And the glass transition temperature of PVA-g-GO/PVA nanocomposites was increased, and their thermal stability and crystallization degree were both decreased. Due to well dispersion of fillers and strong interfacial interactions at the filler

  11. Condensation Polymerization

    Indian Academy of Sciences (India)

    building blocks, is essentially the process of polycondensation or step-growth polymerization. Before we leave this LEGO-style discussion, I would leave you with two alternate scenarios; one is to use building blocks bearing two sockets and two balls, as de- picted in the figure, and the other is to use blocks that contain two.

  12. Condensation Polymerization

    Indian Academy of Sciences (India)

    At first, let us begin by treating molecules as LEGO-type building blocks with certain strict rules for linking them; a ball can readily fit with a socket, ... is essentially the process of polycondensation or step-growth polymerization. Before we leave this LEGO-style discussion, I would leave you with two alternate scenarios; one is.

  13. Scale-up of the Reversible Addition-Fragmentation Chain Transfer (RAFT Polymerization Using Continuous Flow Processing

    Directory of Open Access Journals (Sweden)

    Nenad Micic

    2014-01-01

    Full Text Available A controlled radical polymerization process using the Reversible Addition-Fragmentation Chain Transfer (RAFT approach was scaled up by a factor of 100 from a small laboratory scale of 5 mL to a preparative scale of 500 mL, using batch and continuous flow processing. The batch polymerizations were carried out in a series of different glass vessels, using either magnetic or overhead stirring, and different modes of heating: Microwave irradiation or conductive heating in an oil bath. The continuous process was conducted in a prototype tubular flow reactor, consisting of 6 mm ID stainless steel tubing, fitted with static mixers. Both reactor types were tested for polymerizations of the acid functional monomers acrylic acid and 2-acrylamido-2-methylpropane-1-sulfonic acid in water at 80 °C with reaction times of 30 to 40 min. By monitoring the temperature during the exothermic polymerization process, it was observed that the type and size of reactor had a significant influence on the temperature profile of the reaction.

  14. Supramolecular 1-D polymerization of DNA origami through a dynamic process at the 2-dimensionally confined air-water interface.

    Science.gov (United States)

    Yonamine, Yusuke; Cervantes-Salguero, Keitel; Minami, Kosuke; Kawamata, Ibuki; Nakanishi, Waka; Hill, Jonathan P; Murata, Satoshi; Ariga, Katsuhiko

    2016-05-14

    In this study, a Langmuir-Blodgett (LB) system has been utilized for the regulation of polymerization of a DNA origami structure at the air-water interface as a two-dimensionally confined medium, which enables dynamic condensation of DNA origami units through variation of the film area at the macroscopic level (ca. 10-100 cm(2)). DNA origami sheets were conjugated with a cationic lipid (dioctadecyldimethylammonium bromide, 2C18N(+)) by electrostatic interaction and the corresponding LB-film was prepared. By applying dynamic pressure variation through compression-expansion processes, the lipid-modified DNA origami sheets underwent anisotropic polymerization forming a one-dimensionally assembled belt-shaped structure of a high aspect ratio although the thickness of the polymerized DNA origami was maintained at the unimolecular level. This approach opens up a new field of mechanical induction of the self-assembly of DNA origami structures.

  15. Preparation and application of conducting polymer/Ag/clay composite nanoparticles formed by in situ UV-induced dispersion polymerization

    Science.gov (United States)

    Zang, Limin; Qiu, Jianhui; Yang, Chao; Sakai, Eiichi

    2016-02-01

    In this work, composite nanoparticles containing polypyrrole, silver and attapulgite (PPy/Ag/ATP) were prepared via UV-induced dispersion polymerization of pyrrole using ATP clay as a templet and silver nitrate as photoinitiator. The effects of ATP concentration on morphology, structure and electrical conductivity were studied. The obtained composite nanoparticles with an interesting beads-on-a-string morphology can be obtained in a short time (10 min), which indicates the preparation method is facile and feasible. To explore the potential applications of the prepared PPy/Ag/ATP composite nanoparticles, they were served as multifunctional filler and blended with poly(butylene succinate) (PBS) matrix to prepare biodegradable composite material. The distribution of fillers in polymer matrix and the interfacial interaction between fillers and PBS were confirmed by scanning electron microscope, elemental mapping and dynamic mechanical analysis. The well dispersed fillers in PBS matrix impart outstanding antibacterial property to the biodegradable composite material as well as enhanced storage modulus due to Ag nanoparticles and ATP clay. The biodegradable composite material also possesses modest surface resistivity (106 ~ 109 Ω/◻).

  16. Preparation and application of conducting polymer/Ag/clay composite nanoparticles formed by in situ UV-induced dispersion polymerization.

    Science.gov (United States)

    Zang, Limin; Qiu, Jianhui; Yang, Chao; Sakai, Eiichi

    2016-02-03

    In this work, composite nanoparticles containing polypyrrole, silver and attapulgite (PPy/Ag/ATP) were prepared via UV-induced dispersion polymerization of pyrrole using ATP clay as a templet and silver nitrate as photoinitiator. The effects of ATP concentration on morphology, structure and electrical conductivity were studied. The obtained composite nanoparticles with an interesting beads-on-a-string morphology can be obtained in a short time (10 min), which indicates the preparation method is facile and feasible. To explore the potential applications of the prepared PPy/Ag/ATP composite nanoparticles, they were served as multifunctional filler and blended with poly(butylene succinate) (PBS) matrix to prepare biodegradable composite material. The distribution of fillers in polymer matrix and the interfacial interaction between fillers and PBS were confirmed by scanning electron microscope, elemental mapping and dynamic mechanical analysis. The well dispersed fillers in PBS matrix impart outstanding antibacterial property to the biodegradable composite material as well as enhanced storage modulus due to Ag nanoparticles and ATP clay. The biodegradable composite material also possesses modest surface resistivity (10(6)~ 10(9) Ω/◻).

  17. Process for in-situ leaching of uranium

    International Nuclear Information System (INIS)

    Espenscheid, W.F.; Yan, F.Y.

    1983-01-01

    The present invention relates to the recovery of uranium from subterranean ore deposits, and more particularly to an in-situ leaching operation employing an aqueous solution of sulfuric acid and carbon dioxide as the lixiviant. Uranium is solubilized in the lixiviant as it traverses the subterranean uranium deposit. The lixiviant is subsequently recovered and treated to remove the uranium

  18. Synthesis and characterization of a novel nitric oxide fluorescent probe CdS-PMMA nanocomposite via in-situ bulk polymerization

    International Nuclear Information System (INIS)

    Ding, Liyun; Li, Tao; Zhong, Yunming; Fan, Chao; Huang, Jun

    2014-01-01

    A novel nitric oxide (NO) fluorescent probe CdS-poly(methyl methacrylate) (PMMA) nanocomposites with different molar ratios of CdS quantum dots (QDs) to PMMA are developed successfully via in-situ bulk polymerization method. The optical properties of CdS/PMMA nanocomposites are studied by UV–Vis absorption spectra and fluorescence (FL) spectra in detail. It is demonstrated that the optical properties from such nanocomposite solution are tuned and stabilized by simply varying the concentration of CdS in the final product. X-ray diffraction (XRD) patterns of CdS-PMMA nanocomposite with higher loading of CdS show broad pattern for cubic CdS, which has narrow particle size distribution with less than 5 nm in PMMA observed by transmission electron microscopy (TEM). The surface morphological characterization of the CdS-PMMA nanocomposite has been done through atomic force microscopy (AFM). The thermo-gravimetric analyses (TGA) and differential scanning calorimetry (DSC) confirm the enhanced thermal stability of CdS-PMMA nanocomposites than PMMA. NO can coordinate with Cd 2+ as a ligand for transition metal complexes, which will cause a quenching effect on the fluorescence of CdS QDs. Therefore, a significant quenching effect on the fluorescence of the CdS-PMMA nanocomposite is observed in the presence of NO. The fluorescence responses are concentration-dependent and can be well described by the typical Stern–Volmer equation, and a linear calibration I 0 /I = 1.0021 + 0.1944[NO] (R 2 = 0.96052) is obtained in the range from 1.4 × 10 −5 to 9.3 × 10 −3 mol/L NO with a detection limit of 1.0 × 10 −6 mol/L (S/N = 3). - Highlights: • CdS-PMMA nanocomposite was developed by in-situ bulk polymerization for NO detection. • The fluorescence quenching mechanism relies on the interaction between NO and Cd 2+ . • The fluorescence response shows a good linear reproducibility with NO concentrations. • A linear calibration is obtained in the range from 1.4 × 10

  19. Synthesis and characterization of a novel nitric oxide fluorescent probe CdS-PMMA nanocomposite via in-situ bulk polymerization

    Energy Technology Data Exchange (ETDEWEB)

    Ding, Liyun, E-mail: dlyw@whut.edu.cn; Li, Tao; Zhong, Yunming; Fan, Chao; Huang, Jun

    2014-02-01

    A novel nitric oxide (NO) fluorescent probe CdS-poly(methyl methacrylate) (PMMA) nanocomposites with different molar ratios of CdS quantum dots (QDs) to PMMA are developed successfully via in-situ bulk polymerization method. The optical properties of CdS/PMMA nanocomposites are studied by UV–Vis absorption spectra and fluorescence (FL) spectra in detail. It is demonstrated that the optical properties from such nanocomposite solution are tuned and stabilized by simply varying the concentration of CdS in the final product. X-ray diffraction (XRD) patterns of CdS-PMMA nanocomposite with higher loading of CdS show broad pattern for cubic CdS, which has narrow particle size distribution with less than 5 nm in PMMA observed by transmission electron microscopy (TEM). The surface morphological characterization of the CdS-PMMA nanocomposite has been done through atomic force microscopy (AFM). The thermo-gravimetric analyses (TGA) and differential scanning calorimetry (DSC) confirm the enhanced thermal stability of CdS-PMMA nanocomposites than PMMA. NO can coordinate with Cd{sup 2+} as a ligand for transition metal complexes, which will cause a quenching effect on the fluorescence of CdS QDs. Therefore, a significant quenching effect on the fluorescence of the CdS-PMMA nanocomposite is observed in the presence of NO. The fluorescence responses are concentration-dependent and can be well described by the typical Stern–Volmer equation, and a linear calibration I{sub 0}/I = 1.0021 + 0.1944[NO] (R{sup 2} = 0.96052) is obtained in the range from 1.4 × 10{sup −5} to 9.3 × 10{sup −3} mol/L NO with a detection limit of 1.0 × 10{sup −6} mol/L (S/N = 3). - Highlights: • CdS-PMMA nanocomposite was developed by in-situ bulk polymerization for NO detection. • The fluorescence quenching mechanism relies on the interaction between NO and Cd{sup 2+}. • The fluorescence response shows a good linear reproducibility with NO concentrations. • A linear calibration is

  20. Effect of different oxidants on polyaniline/single walled carbon nanotubes composites synthesized via ultrasonically initiated in-situ chemical polymerization

    Energy Technology Data Exchange (ETDEWEB)

    Gull, Nafisa, E-mail: gullchemist@gmail.com [Department of Polymer Engineering and Technology, University of the Punjab, Lahore, 54590 (Pakistan); Khan, Shahzad Maqsood, E-mail: shahzadkhan81@hotmail.com [Department of Polymer Engineering and Technology, University of the Punjab, Lahore, 54590 (Pakistan); Islam, Atif; Zia, Saba; Shafiq, Muhammad; Sabir, Aneela; Munawar, Muhammad Azeem [Department of Polymer Engineering and Technology, University of the Punjab, Lahore, 54590 (Pakistan); Butt, Muhammad Taqi Zahid [College of Engineering and Emerging Technologies, University of the Punjab, Lahore, 54590 (Pakistan); Jamil, Tahir [Department of Polymer Engineering and Technology, University of the Punjab, Lahore, 54590 (Pakistan)

    2016-04-01

    This study is aimed at investigating the effect of different oxidants on properties of polyaniline/single walled carbon nanotubes (PANI/SWCNT) composites and scrutinizing a suitable oxidant to improve the properties of composites. PANI/SWCNT composites were fabricated via ultrasonically initiated in-situ chemical polymerization technique using four different oxidants; hydrogen peroxide (H{sub 2}O{sub 2}), ammonium peroxidisulphate ((NH{sub 4}){sub 2}S{sub 2}O{sub 8}), potassium dichromate (K{sub 2}Cr{sub 2}O{sub 7}) and potassium iodate (KIO{sub 3}). Percent yield (97%), molecular weight (45532 g mol{sup −1}) and electrical conductivity (0.835 S cm{sup −1}) were found maximum for composite prepared in the presence of H{sub 2}O{sub 2}. Structural confirmation of PANI and charge transfer complex formation between PANI and SWCNT were confirmed by fourier transform infrared spectroscopy, UV–visible spectroscopy and X-ray diffraction spectroscopy. Thermogravimetric analysis verified that the PANI/SWCNT composite synthesized using H{sub 2}O{sub 2} had maximum thermal stability with least thermal degradation (∼28%). Minimal thermal transitions of the composite were also observed for same composite by differential scanning calorimetry. Scanning electron microscopic images of PANI/SWCNT composites revealed that SWCNT were properly dispersed in PANI matrix when H{sub 2}O{sub 2} was used. Above results provide the valuable suggestion that; H{sub 2}O{sub 2} is a promising oxidant to enhance structural, thermal, electrical and microscopic properties of composites. - Highlights: • Ultrasonically initiated in-situ chemical polymerization protocol was devised for synthesis of PANI/SWCNT composites. • SEM micrographs of PANI/SWCNT-1 showed uniform dispersed structure. • Better thermal stability and conductivity was evidenced for H{sub 2}O{sub 2} based PANI/SWCNT composite. • π–π interaction between PANI and SWCNT is confirmed by FTIR and UV

  1. Roles of extracellular polymeric substances in enhanced biological phosphorus removal process.

    Science.gov (United States)

    Li, Wen-Wei; Zhang, Hai-Ling; Sheng, Guo-Ping; Yu, Han-Qing

    2015-12-01

    Enhanced biological phosphorus removal (EBPR) process is known to mainly rely on the ability of phosphorus-accumulating organisms to take up, transform and store excess amount of phosphorus (P) inside the cells. However, recent studies have revealed considerable accumulation of P also in the extracellular polymeric substances (EPS) of sludge, implying a non-negligible role of EPS in P removal by EBPR sludge. However, the contribution of EPS to P uptake and the forms of accumulated extracellular P vary substantially in different studies, and the underlying mechanism of P transformation and transportation in EPS remains poorly understood. This review provides a new recognition into the P removal process in EBPR system by incorporating the role of EPS. It overviews on the characteristics of P accumulation in EPS, explores the mechanism of P transformation and transportation in EBPR sludge and EPS, summarizes the main influential factors for the P-accumulation properties of EPS, and discusses the remaining knowledge gaps and needed future efforts that may lead to better understanding and use of such an EPS role for maximizing P recovery from wastewater. Copyright © 2015 Elsevier Ltd. All rights reserved.

  2. Controlling the Plasma-Polymerization Process of N-Vinyl-2-pyrrolidone

    DEFF Research Database (Denmark)

    Norrman, Kion; Winther-Jensen, Bjørn

    2005-01-01

    N-vinyl-2-pyrrolidone was plasma-polymerized on glass substrates using a pulsed AC plasma. Pulsed AC plasma produces a chemical surface structure different from that produced by conventional RF plasma; this is ascribed to the different power regimes used. A high degree of control over the structure...... of the chemical surface was obtained using pulsed AC plasma, as shown by ToF-SIMS. It is demonstrated how the experimental conditions to some extent control the chemical structure of the plasma-polymerized film, e.g., film thickness, density of post-plasma-polymerized oligomeric chains, and the density of intact...

  3. Utilization of poly(methyl methacrylate – carbon nanotube and polystyrene – carbon nanotube in situ polymerized composites as masterbatches for melt mixing

    Directory of Open Access Journals (Sweden)

    M. Lahelin

    2012-10-01

    Full Text Available Carbon nanotubes (CNTs were melt mixed directly or by using an in situ polymerized masterbatch into a matrix polymer, polystyrene (PS or poly(methyl methacrylate (PMMA. The mechanical properties of the composites were mostly determined by the amount of CNTs, and not by the use of directly melt mixed CNTs or the use of the masterbatch. In contrast, the electrical resistivity of the composites was dependent on the manner in which the CNTs were added to the matrix polymer. When there was increased interfacial adhesion between the components, as for PS and the CNTs, the use of directly melt mixed CNTs gave better resistivity results. Without strong interactions between the CNTs and the matrix, as with PMMA and CNTs, the use of a tailored masterbatch had a significant effect on properties of the final composites. The molecular weight and viscosity of masterbatches can be varied and when the PMMA-masterbatch had optimized viscosity with respect to the PMMA matrix, electrical resistivity of the final composites decreased noticeably.

  4. In situ electrochemical polymerization of a nanorod-PANI-Graphene composite in a reverse micelle electrolyte and its application in a supercapacitor.

    Science.gov (United States)

    Hu, Liwen; Tu, Jiguo; Jiao, Shuqiang; Hou, Jungang; Zhu, Hongmin; Fray, Derek J

    2012-12-05

    Highly porous nanorod-PANI-Graphene composite films were prepared by in situ electrochemical polymerization onto an ITO substrate in a reverse micelle electrolyte. The morphology and microstructure of the composite films were analyzed by using a field emission scanning electron microscope. It was observed that the films were highly porous and the nanorod PANI films were inserted by graphene nanosheets. This indicated that a good conductive network between PANI nanorods and graphene sheets was formed. Further electrochemical tests involved cyclic voltammetry (CV), galvanostatic charge-discharge (GCD) and electrochemical impedance spectroscopy (EIS) in 1 mol L(-1) HClO(4) solution. The results showed that the composite film had a favorable capacitance with a high electron transfer rate and low resistance. The highest specific capacitance that could be achieved was as high as 878.57 F g(-1) with the charge loading of 500 mC at a current density of 1 A g(-1). The GCD at different charge loadings showed good cycle stability with a low fading rate of specific capacitance after 1000 cycles. The results demonstrated that the nanorod-PANI-Graphene composite was proved to be of great potential as an electrode material for supercapacitors.

  5. Preparation of open tubular capillary columns by in situ ring-opening polymerization and their applications in cLC-MS/MS analysis of tryptic digest.

    Science.gov (United States)

    Wang, Hongwei; Yao, Yating; Li, Ya; Ma, Shujuan; Peng, Xiaojun; Ou, Junjie; Ye, Mingliang

    2017-08-01

    An open tubular (OT) column (25 μm i.d.) was prepared by in situ ring-opening polymerization of octaglycidyldimethylsilyl polyhedral oligomeric silsesquioxanes (POSS-epoxy) with 4-aminophenyl disulfide (APDS) in a binary porogenic system of ethanol/H 2 O. It was found that porogenic composition played an important role in the formation of OT stationary phases. The ratio of ethanol/H 2 O at 6/1 (v/v) would lead to the fabrication of hybrid monoliths, while the ratio of ethanol/H 2 O at 13/1 (v/v) would result in the synthesis of OT phases. In addition, the effects of precursor content and reaction duration on the thickness of OT stationary phases were investigated. Either lower precursor content or shorter reaction duration would produce thinner layer of OT column. The repeatability of OT columns was evaluated through relative standard deviation (RSD%) with benzene as the analyte. The run-to-run, column-to-column and batch-to-batch repeatabilities were 1.7%, 4.8% and 5.6%, respectively, exhibiting satisfactory repeatability of the OT column. Then tryptic digest of mouse liver proteins was used to evaluate the performance of the resulting OT columns (25 μm i.d. × 2.5 m in length) by cLC-MS/MS analysis, demonstrating their potential in proteome analysis. Copyright © 2017 Elsevier B.V. All rights reserved.

  6. Thermal stability and kinetic study of poly(ethyl methacrylate-co-acrylonitrile) nanocomposites prepared by in situ polymerization in presence of an Algerian bentonite

    Energy Technology Data Exchange (ETDEWEB)

    Kadi, Souad [Université des Sciences et de la Technologie Houari Boumediene, Laboratoire des Matériaux Polymères, Faculté de Chimie, BP 32 El-Alia, Bab-Ezzouar, 16111 Algiers (Algeria); Djadoun, Saïd, E-mail: matpolylab@yahoo.fr [Université des Sciences et de la Technologie Houari Boumediene, Laboratoire des Matériaux Polymères, Faculté de Chimie, BP 32 El-Alia, Bab-Ezzouar, 16111 Algiers (Algeria); Sbirrazzuoli, Nicolas [Univ. Nice Sophia Antipolis, CNRS, LPMC, UMR 7336, 06100 Nice (France)

    2013-10-10

    Graphical abstract: - Highlights: • poly(ethyl methacrylate-co-acrylonitrile) nanocomposites were successfully prepared. • These nanocomposites were of higher T{sub g} and improved thermal stability. • Their (E{sub α}) of thermal decomposition were higher than those of the virgin copolymer. • Increase of (E{sub α}), confirmed change in the degradation mechanism with clay loading. - Abstract: Poly(ethyl methacrylate-co-acrylonitrile) (PEAMN20) nanocomposites were successfully prepared via free radical in situ polymerization using a bentonite from Algeria modified by Hexadecyltrimethylammonium chloride (HDTMA). X-ray diffraction (XRD) and transmission electronic microscopy (TEM) investigations revealed that depending on the OMMT loading, intercalated or partially exfoliated nanocomposites were obtained. These nanocomposites exhibited an overall improved thermal stability and an increase in their glass transition temperature compared to the pure copolymer (PEMAN20) as evidenced by Thermogravimetric (TGA) and Differential Scanning Calorimetry (DSC) analysis. Apparent activation energies (E{sub α}) of thermal decomposition of the elaborated nanocomposites, determined by Tang method, were higher than those of the virgin copolymer. The significant increase of (E{sub α}), observed with PEMAN20/OMMT (1 wt%) confirmed the change in the degradation mechanism with OMMT loading and the ratio of intercalated/exfoliated structures.

  7. Construction of Au@Pt core—satellite nanoparticles based on in-situ reduction of polymeric ionic liquid protected gold nanoparticles

    Science.gov (United States)

    Wu, Wenlan; Li, Junbo; Zou, Sheng; Guo, Jinwu; Zhou, Huiyun

    2017-03-01

    A method of in-situ reduction to prepare Au@Pt core-satellite nanoparticles (NPs) is described by using Au NPs coating poly[1-methyl 3-(2-methacryloyloxy propylimidazolium bromine)] (PMMPImB-@-Au NPs) as the template. After electrostatic complex chloroplatinic acid with PMMPImB shell, the composite NP was directly reduced with N2H4 to produce Au@Pt core-satellite NPs. The characterization of composite and core-satellite NPs under different amounts of chloroplatinic acid were studied by DLS, UV-vis absorption spectrum and TEM. The satellite Pt NPs with a small size ( 2 nm) dotted around Au core, and the resulting Au@Pt core-satellite NPs showed a red-shift surface plasmon resonance (SPR) and a good dispersion due to effectively electrostatic repulsion providing by the polymeric ionic liquid (PIL) shell. Finally, Au@Pt core-satellite NPs exhibit an enhanced catalytic activity and cycled catalytic capability for the reduction of p-nitrophenol with NaBH4.

  8. Defense University Research Initiative on Nanotechnology: Microstructure, Processing and Mechanical Performance of Polymeric Nanocomposites

    National Research Council Canada - National Science Library

    Boyce, Mary C; Thomas, Edwin L

    2006-01-01

    .... Blending of 0-, 1-, and 2- dimensional inorganic fillers such as POSS, carbon nanotubes, and nano-clay platelets into polymeric matrices enabled exploration of various filler/matrix combinations...

  9. Silicoaluminates as “Support Activator” Systems in Olefin Polymerization Processes

    Science.gov (United States)

    Tabernero, Vanessa; Camejo, Claudimar; Terreros, Pilar; Alba, María Dolores; Cuenca, Tomás

    2010-01-01

    In this work we report the polymerization behaviour of natural clays (montmorillonites, MMT) as activating supports. These materials have been modified by treatment with different aluminium compounds in order to obtain enriched aluminium clays and to modify the global Brönsted/Lewis acidity. As a consequence, the intrinsic structural properties of the starting materials have been changed. These changes were studied and these new materials used for ethylene polymerization using a zirconocene complex as catalyst. All the systems were shown to be active in ethylene polymerization. The catalyst activity and the dependence on acid strength and textural properties have been also studied. The behaviour of an artificial silica (SBA 15) modified with an aluminium compound to obtain a silicoaluminate has been studied, but no ethylene polymerization activity has been found yet.

  10. Formation of extracellular polymeric substances from acidogenic sludge in H2-producing process.

    Science.gov (United States)

    Sheng, Guo-Ping; Yu, Han-Qing

    2007-02-01

    In this study, the formation of extracellular polymeric substances (EPS) and surface characteristics of an acidogenic sludge in anaerobic H(2)-producing process was investigated. Results show that carbohydrates, proteins, and humic substances were the dominant components in bound EPS (BEPS), while in soluble EPS (SEPS), carbohydrates were the main component. The total content of BEPS initially increased but then kept almost unchanged during fermentation from 25 to 35 h; after that, it slightly decreased. The total content of SEPS increased to 172.5 +/- 0.05 mg C g(-1) volatile suspended solid with the time that increased to 23.5 h, and then rapidly decreased until 43 h; thereafter, it kept almost unchanged. The SEPS had good correlations with the specific H(2) production rate, substrate degradation rate, and specific aqueous products formation rate, but the BEPS seemed to have no such correlations with these specific rates. Results also confirm that part of EPS could be utilized by the H(2)-producing sludge. As the substrate was in short supply, the EPS would be hydrolyzed to sever as carbon and energy source.

  11. Development of silver nanoparticle loaded antibacterial polymer mesh using plasma polymerization process.

    Science.gov (United States)

    Kumar, Virendra; Jolivalt, Claude; Pulpytel, Jerome; Jafari, Reza; Arefi-Khonsari, Farzaneh

    2013-04-01

    Plasma polymerized polyacrylic acid (PPAA) was deposited on a polymer substrate, namely polyethylene terephthalate (PET) mesh, for entrapment of silver nanoparticle (Ag-NP) in order to achieve antibacterial property to the material. Carboxylic groups of PPAA act as anchor as well as capping and stabilizing agents for Ag-NPs synthesized by chemical reduction method using NaBH(4) as a reducing agent. Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy (XPS), and water contact angle analysis were used to characterize the PPAA coatings. The Ag-NPs loaded polymer samples were characterized by UV-visible spectroscopy, field emission scanning electron microscopy, energy dispersive X-ray, and XPS techniques. XPS analysis showed ~1.0 at.% loading of Ag-NPs on to the PPAA-PET-mesh, which was composed of 79% zero-valent (Ag°) and 21% oxidized nano-Ag (Ag(+) ). The plasma processed PET meshes samples were tested for antibacterial activity against two bacterial strains, namely Staphylococcus aureus (Gram positive) and Escherichia coli (Gram negative). Qualitative and quantitative tests showed that silver containing PPAA-PET meshes exhibit excellent antibacterial property against the tested bacteria with percent reduction of bacterial concentration >99%, compared to the untreated PET mesh. Copyright © 2012 Wiley Periodicals, Inc.

  12. Influence of substituents in vinyl groups on reactivity of parylene during polymerization process

    International Nuclear Information System (INIS)

    Freza, Sylwia; Skurski, Piotr; Bobrowski, Maciej

    2010-01-01

    The MCSCF calculations indicate that both triplet and singlet state of biradical di-para-xylylene can exist during polymerization of parylene in gas phase and both can potentially react with vinyl molecules. The singlet-state open-shell dimer turned out to exhibit multiconfigurational character. In the case of triplet state of the dimer two mechanisms of the reactions with various species containing vinyl groups have been examined at the B3LYP/6-31G level. The kinetic and thermodynamical barriers have been estimated for the reaction path involving the π-bond cleavage as well as for the route describing the hydrogen atom transfer. It was found that the overall reactions are thermodynamically favorable, whereas appropriate kinetic barriers for certain derivatives are very small (close to 0 kcal/mol) which in turn makes allowances for easy reactivity under accessible conditions. The calculated mechanisms indicate the influence of substituents in vinyl groups for reactivity of parylene during LPCVD process.

  13. On dual nature of effect of adsorbed polymeric hydroxide films on rate of different electrode processes

    International Nuclear Information System (INIS)

    Zakharkina, P.S.; Korshunov, V.N.

    1985-01-01

    The effect of cation Er 3+ hydrolysis products on the electrochemical behaviour of Zn and Na amalgams is studied. The i, t-curves are presented which are moasUred from a film Hg-electrode in 1M LiCl- and 1MNaCl solUtions both with and without the 10 -3 MErCl 3 addition, along with the I, t-dependences obtained from a rotation disk Zn-electrode at E=-1.45 B against the background of 0.1 MLi 2 SO 4 with the 1.5x10 -3 M Er 2 (SO 4 ) 3 addition. Polymeric films of REE oxohydroxo compounds exhibit a distinct dualism in the effect on the rate of different electrode reactions; provided a proton donor is the depolarizator, the films being considered confirm their name of catalytically active matrices accelerating hydrogen evolution by a modified bridge mechanism variant. In case of metal charge-ionization process these films become inhibitors and the more effective, the more hydrated is the corresponding REE ion

  14. Preparation of poly(vinyl alcohol)-grafted graphene oxide/poly(vinyl alcohol) nanocomposites via in-situ low-temperature emulsion polymerization and their thermal and mechanical characterization

    Science.gov (United States)

    Zhang, Shengchang; Liu, Pengqing; Zhao, Xiangsen; Xu, Jianjun

    2017-02-01

    An in-situ polymerization combined with chemical grafting modification method for preparing Poly(vinyl alcohol)-grafted graphene oxide/Poly(vinyl alcohol) (PVA-g-GO/PVA) nanocomposites was reported. Firstly, Poly(vinyl acetate)-grafted graphene oxide/Poly(vinyl acetate) nanocomposites were prepared, and then the PVA-g-GO/PVA nanocomposites could be obtained through alcoholysis reaction. X-ray photoelectron spectrometer and fourier-transform infrared spectrometer confirmed that the PVAc or PVA chains were successfully grafted to GO sheets during in-situ polymerization and alcoholysis. And the results from transmission electron microscopy, scanning electron microscopy and X-ray diffraction showed that the well compatibility and homogenous dispersion of PVA-g-GO in PVA matrix could be achieved. Differential scanning calorimetric, thermogravimetry analysis and tensile test were employed to study the thermal and mechanical properties of the PVA-g-GO/PVA nanocomposites. The results indicated that a 53% improvement of tensile strength and a 36% improvement of Young's modulus were achieved by addition of 0.5 wt% of GO sheets. And the glass transition temperature of PVA-g-GO/PVA nanocomposites was increased, and their thermal stability and crystallization degree were both decreased. Due to well dispersion of fillers and strong interfacial interactions at the filler-matrix interface, in-situ polymerization combined with chemical grafting modification was a good choice to prepare graphene/PVA nanocomposite with excellent mechanical properties.

  15. Evaluation of integrated biotreatment processes for in situ application

    International Nuclear Information System (INIS)

    Maher, A.; Lamptey, J.C.; Kennel, N.D.

    1994-01-01

    Petroleum hydrocarbon contamination of soils and groundwater associated with Underground Storage Tanks (UST) and aboveground fuel spills has become the focus of many bioremediation efforts. Two case studies in the application of in situ bioremediation to degrade petroleum hydrocarbons are presented. Site A has a history of fuel-handling practices associated with bulk petroleum storage and railroad yard activities. The majority of the hydrocarbon contamination appeared to be the result of past surface spills. Pre-treatment investigation indicated the presence of both volatile and semi- or non-volatile hydrocarbons in the soil. About 3,000 cubic yards of highly contaminated soils was excavated and is being treated in 2, lined, closed loop treatment cells. Groundwater is treated in situ with addition of nutritional cofactors and oxygen introduced through 3 infiltration galleries that are placed 6 feet deep and are each 100 feet in length. Groundwater is also recovered from 3 extraction wells placed 80 to 100 feet from each other, and subsequently treated in a bioreactor. Site B has a history of leaking underground gasoline storage tanks and spills from aboveground diesel fuel associated with county maintenance shed activities. One hundred cubic yards of soil contaminated with diesel components were excavated and treated aboveground in a lined cell. Gasoline contaminated groundwater and soil is being treated in situ by the addition of nutritional cofactors and oxygen through an infiltration gallery 4 feet below surface. The groundwater is recovered from an extraction gallery 92.5 feet down gradient of the infiltration gallery. Nutritional cofactors are introduced on a daily basis with on-site controls. Hydrocarbon reduction, up to 76%, was observed within 3 months of treatment startup in monitoring wells

  16. Evaluating Acoustic Emission Signals as an in situ process monitoring technique for Selective Laser Melting (SLM)

    Energy Technology Data Exchange (ETDEWEB)

    Fisher, Karl A. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Candy, Jim V. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Guss, Gabe [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Mathews, M. J. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States)

    2016-10-14

    In situ real-time monitoring of the Selective Laser Melting (SLM) process has significant implications for the AM community. The ability to adjust the SLM process parameters during a build (in real-time) can save time, money and eliminate expensive material waste. Having a feedback loop in the process would allow the system to potentially ‘fix’ problem regions before a next powder layer is added. In this study we have investigated acoustic emission (AE) phenomena generated during the SLM process, and evaluated the results in terms of a single process parameter, of an in situ process monitoring technique.

  17. Evaluation and selection of in-situ leaching mining method using analytic hierarchy process

    International Nuclear Information System (INIS)

    Zhao Heyong; Tan Kaixuan; Liu Huizhen

    2007-01-01

    According to the complicated conditions and main influence factors of in-situ leaching min- ing, a model and processes of analytic hierarchy are established for evaluation and selection of in-situ leaching mining methods based on analytic hierarchy process. Taking a uranium mine in Xinjiang of China for example, the application of this model is presented. The results of analyses and calculation indicate that the acid leaching is the optimum project. (authors)

  18. An evaluation of in-situ bioremediation processes

    International Nuclear Information System (INIS)

    Cole, L.L.; Rashidi, M.

    1996-08-01

    Remediation of petroleum hydrocarbons in groundwater was the primary focus in the initial application of in-situ bioremediation which, from its development in the 1970s, has grown to become one of the most promising technologies for the degradation of a wide variety of organic contaminants. The degradation of contaminants in subsurface soils is the current new focus of the technology. While the need for improvements in the technology does exist, the indisputable fact remains that this technology is by far the least expensive and that it has the capability to provide long term reduced levels of contaminants or long term complete remediation of contaminated sites. The aim of this paper is to disclose pertinent information related to current conditions and current feelings in the area of new research, novel applications, new government regulations, and an overview of new topics on the horizon that relate to the overall technology

  19. An evaluation of in-situ bioremediation processes

    Energy Technology Data Exchange (ETDEWEB)

    Cole, L.L. [Prairie View A and M Univ., TX (United States); Rashidi, M. [Lawrence Livermore National Lab., CA (United States). Environmental Programs Directorate

    1996-08-01

    Remediation of petroleum hydrocarbons in groundwater was the primary focus in the initial application of in-situ bioremediation which, from its development in the 1970s, has grown to become one of the most promising technologies for the degradation of a wide variety of organic contaminants. The degradation of contaminants in subsurface soils is the current new focus of the technology. While the need for improvements in the technology does exist, the indisputable fact remains that this technology is by far the least expensive and that it has the capability to provide long term reduced levels of contaminants or long term complete remediation of contaminated sites. The aim of this paper is to disclose pertinent information related to current conditions and current feelings in the area of new research, novel applications, new government regulations, and an overview of new topics on the horizon that relate to the overall technology.

  20. In situ preparation and fluorescence quenching properties of polythiophene/ZnO nanocrystals hybrids through atom-transfer radical polymerization and hydrolysis

    International Nuclear Information System (INIS)

    Peng Xiaoming; Zhang Lin; Chen Yiwang; Li Fan; Zhou Weihua

    2010-01-01

    In this paper, a new approach for in situ preparing nanocomposites of conjugated polymers (CPs) and semiconductor nanocrystals was developed. Polythiophene grafted poly(zinc methacrylate) (PTh-g-PZMA) copolymer was synthesized by atom-transfer radical polymerization (ATRP) of zinc methacrylate (ZMA) initiated from the macroinitiator poly(2,5-(3-(bromoisopropyl-carbonyl-oxymethylene) thiophene)) (PTh-Br) with pendant initiator groups. Subsequently, the polythiophene grafted poly(methacrylate)/ZnO (PTh-g-PMA/ZnO) hybrid heterojunction nanocomposites were successfully prepared by in situ hydrolysis of PTh-g-PZMA casting films in alkaline aqueous solution. The structures of PTh-Br, PTh-g-PZMA and PTh-g-PMA/ZnO were confirmed by the proton nuclear magnetic resonance ( 1 H NMR) spectra, Fourier transform infrared (FTIR) spectra and X-ray photoelectron spectroscopy (XPS). The morphologies of PTh-g-PMA/ZnO films prepared for different hydrolysis time were observed in the cross-sections by scanning electron microscope (SEM). The SEM images revealed that ZnO nanocrystals were uniformly dispersed in polymers without any aggregation and the appearances of ZnO nanocrystals changed from nanoparticles to nanorods with the hydrolysis treatment time increasing. The optical properties of these nanocomposites were studied by ultraviolet-visible (UV-vis) absorption and fluorescence spectroscopy. UV-vis absorption spectroscopy showed that the adsorption band of PTh-g-PMA/ZnO hybrids was broader than that of PTh-Br, implying that the existence of ZnO nanocrystals increased the optical absorption region of hybrids. The photoluminescence (PL) spectra of the hybrids showed that fluorescence quenching occurred in PTh-g-PMA/ZnO blends and a maximum of 85% of the fluorescence intensity quenched in the PTh-g-PMA/ZnO obtained from treatment in NaOH aqueous solution for 2 h, which revealed the existence of photo-induced charge transfer between the polythiophene chains and ZnO. These results

  1. Influence of the chain-transfer reactions on the emulsion post-polymerization process

    International Nuclear Information System (INIS)

    Lukhovitskij, V.I.; Polikarpov, V.V.; Pozdeeva, R.M.

    1975-01-01

    A probability of free radical exit from latex particle in the course of chain transfer reaction is defined by properties of the radical itself. In the case of emulsive post-polymerization of styrene in the presence of H-dodecylmercantane the value α for CCL 3 is about 3x10 -2 , for radical C 12 H 25 it is close to zero and for the radical generated under transfer to the monomer it is approximately 10 -2 . The effect of transfer to the monomer on the emulsive post-polymerization is discussed: it is responsible for the high degree of monomer conversion

  2. Synthesis and characterization of a novel nitric oxide fluorescent probe CdS-PMMA nanocomposite via in-situ bulk polymerization.

    Science.gov (United States)

    Ding, Liyun; Li, Tao; Zhong, Yunming; Fan, Chao; Huang, Jun

    2014-02-01

    A novel nitric oxide (NO) fluorescent probe CdS-poly(methyl methacrylate) (PMMA) nanocomposites with different molar ratios of CdS quantum dots (QDs) to PMMA are developed successfully via in-situ bulk polymerization method. The optical properties of CdS/PMMA nanocomposites are studied by UV-Vis absorption spectra and fluorescence (FL) spectra in detail. It is demonstrated that the optical properties from such nanocomposite solution are tuned and stabilized by simply varying the concentration of CdS in the final product. X-ray diffraction (XRD) patterns of CdS-PMMA nanocomposite with higher loading of CdS show broad pattern for cubic CdS, which has narrow particle size distribution with less than 5 nm in PMMA observed by transmission electron microscopy (TEM). The surface morphological characterization of the CdS-PMMA nanocomposite has been done through atomic force microscopy (AFM). The thermo-gravimetric analyses (TGA) and differential scanning calorimetry (DSC) confirm the enhanced thermal stability of CdS-PMMA nanocomposites than PMMA. NO can coordinate with Cd(2+) as a ligand for transition metal complexes, which will cause a quenching effect on the fluorescence of CdS QDs. Therefore, a significant quenching effect on the fluorescence of the CdS-PMMA nanocomposite is observed in the presence of NO. The fluorescence responses are concentration-dependent and can be well described by the typical Stern-Volmer equation, and a linear calibration I0/I=1.0021+0.1944[NO] (R(2)=0.96052) is obtained in the range from 1.4×10(-5) to 9.3×10(-3) mol/L NO with a detection limit of 1.0×10(-6) mol/L (S/N=3). © 2013.

  3. Synthesis and properties of epoxy-polyurethane/silica nanocomposites by a novel sol method and in-situ solution polymerization route

    Science.gov (United States)

    Lin, Jing; Wu, Xu; Zheng, Cheng; Zhang, Peipei; Huang, Bowei; Guo, Ninghai; Jin, LiYazi

    2014-06-01

    In this work, a novel nonaqueous sol method for preparing 3-methacryloxypropyltrimethoxysilane modified nano-SiO2 (MPS-SiO2) in N,N-dimethylformamide (DMF) substituting alcoholic solvents was developed, and epoxy acrylate resins (EA) based on novolac epoxy resin (EP) were prepared. Epoxy acrylate copolymers (EPAc/SiO2) with core/shell structure were prepared by one-step in-situ solution polymerization of EA, acrylic monomers and a certain amount of modified silica sol as core. Epoxy acrylate based polyurethane composites/SiO2 (EPUAs/SiO2) were finally obtained by curing action among as-prepared EPAc/SiO2, isocyanate and anhydride curing agent. The obtained EA and MPS-SiO2 were also characterized using Fourier transform infrared spectroscopy (FTIR), 1H nuclear magnetic resonance spectra (1H NMR), thermogravimetric analysis (TGA), X-ray photoelectron spectroscopy(XPS), and surface contact angle analysis(CA). Microstructures of MPS-SiO2 and EPAc/SiO2 in DMF were observed by transmission electron microscope (TEM). Furthermore, the influence of MPS-SiO2 on the properties of EPUAs/SiO2 including fracture surface morphology, thermal stability, glass transition temperature (Tg), tensile strength, elongation at break, cross-linking density, shore hardness, water absorption, etc. were also investigated. The results demonstrate that colloidal MPS-SiO2 with DMF as solvent can be directly added into polyurethane system and has industrial application value, EPAc/SiO2 with core-shell morphologies have good individual dispersion in DMF, and incorporating MPS-SiO2 into EPUAs/SiO2 greatly enhances physico-chemical properties of EPUAs/SiO2 composites.

  4. Enhancement of thermal and mechanical properties of poly(MMA-co-BA)/Cloisite 30B nanocomposites by ultrasound-assisted in-situ emulsion polymerization.

    Science.gov (United States)

    Sharma, Sachin; Kumar Poddar, Maneesh; Moholkar, Vijayanand S

    2017-05-01

    This study reports synthesis and characterization of poly(MMA-co-BA)/Cloisite 30B (organo-modified montmorillonite clay) nanocomposites by ultrasound-assisted in-situ emulsion polymerization. Copolymers have been synthesized with MMA:BA monomer ratio of 4:1, and varying clay loading (1-5wt% monomer). The poly(MMA-co-BA)/Cloisite 30B nanocomposites have been characterized for their thermal and mechanical properties. Ultrasonically synthesized nanocomposites have been revealed to possess higher thermal degradation resistance and mechanical strength than the nanocomposites synthesized using conventional techniques. These properties, however, show an optimum (or maxima) with clay loading. The maximum values of thermal and mechanical properties of the nanocomposites with optimum clay loading are as follows. Thermal degradation temperatures: T 10% =320°C (4wt%), T 50 =373°C (4wt%), maximum degradation temperature=384°C (4wt%); glass transition temperature=64.8°C (4wt%); tensile strength=20MPa (2wt%), Young's modulus=1.31GPa (2wt%), Percentage elongation=17.5% (1wt%). Enhanced properties of poly(MMA-co-BA)/Cloisite 30B nanocomposites are attributed to effective exfoliation and dispersion of clay nanoparticles in copolymer matrix due to intense micro-convection induced by ultrasound and cavitation. Clay platelets help in effective heat absorption with maximum surface interaction/adhesion that results in increased thermal resistivity of nanocomposites. Hindered motion of the copolymer chains due to clay platelets results in enhancement of tensile strength and Young's modulus of nanocomposite. Rheological (liquid) study of the nanocomposites reveals that nanocomposites have higher yield stress and infinite shear viscosity than neat copolymer. Nonetheless, nanocomposites still display shear thinning behavior - which is typical of the neat copolymer. Copyright © 2016 Elsevier B.V. All rights reserved.

  5. Pt- and TCO-Free Flexible Cathode for DSSC from Highly Conducting and Flexible PEDOT Paper Prepared via in Situ Interfacial Polymerization.

    Science.gov (United States)

    Anothumakkool, Bihag; Agrawal, Ishita; Bhange, Siddheshwar N; Soni, Roby; Game, Onkar; Ogale, Satishchandra B; Kurungot, Sreekumar

    2016-01-13

    Here, we report the preparation of a flexible, free-standing, Pt- and TCO-free counter electrode in dye-sensitized solar cell (DSSC)-derived from polyethylenedioxythiophene (PEDOT)-impregnated cellulose paper. The synthetic strategy of making the thin flexible PEDOT paper is simple and scalable, which can be achieved via in situ polymerization all through a roll coating technique. The very low sheet resistance (4 Ω/□) obtained from a film of 40 μm thick PEDOT paper (PEDOT-p-5) is found to be superior to the conventional fluorine-doped tin oxide (FTO) substrate. The high conductivity (357 S/cm) displayed by PEDOT-p-5 is observed to be stable under ambient conditions as well as flexible and bending conditions. With all of these features in place, we could develop an efficient Pt- and TCO-free flexible counter electrode from PEDOT-p-5 for DSSC applications. The catalytic activity toward the tri-iodide reduction of the flexible electrode is analyzed by adopting various electrochemical methodologies. PEDOT-p-5 is found to display higher exchange current density (7.12 mA/cm(2)) and low charge transfer resistance (4.6 Ω) compared to the benchmark Pt-coated FTO glass (2.40 mA/cm(2) and 9.4 Ω, respectively). Further, a DSSC fabricated using PEDOT-p-5 as the counter electrode displays a comparable efficiency of 6.1% relative to 6.9% delivered by a system based on Pt/FTO as the counter electrode.

  6. IN-SITU TEST OF PRESSURE PIPELINE VIBRATION BASED ON DATA ACQUISITION AND SIGNAL PROCESSING

    OpenAIRE

    Hou, Huimin; Xu, Cundong; Liu, Hui; Wang, Rongrong; Jie, Junkun; Ding, Lianying

    2015-01-01

    Pipeline vibration of high frequency and large amplitude is an important factor that impacts the safe operation of pumping station and the efficiency of the pumps. Through conducting the vibration in-situ test of pipeline system in the pumping station, we can objectively analyze the mechanism of pipeline vibration and evaluate the stability of pipeline operation. By using DASP (data acquisition & signal processing) in the in-situ test on the 2# pipeline of the third pumping station in the gen...

  7. Preparation of interconnected highly porous polymeric structures by a replication and freeze-drying process

    NARCIS (Netherlands)

    Hou, Q.; Grijpma, Dirk W.; Feijen, Jan

    2003-01-01

    Three-dimensional degradable porous polymeric structures with high porosities (93-98%) and well-interconnected pore networks have been prepared by freeze-drying polymer solutions in the presence of a leachable template followed by leaching of the template. Templates of the pore network were prepared

  8. Finite element analysis of in-situ alignment of nanoparticles in polymeric nanofibers using magnetic field assisted electrospinning

    International Nuclear Information System (INIS)

    Jayaseelan, D; Biji, P

    2015-01-01

    In this study, a three-dimensional magnetic field assisted electrospinning (MFAES) system has been modeled to understand the correlation between the applied magnetic field and electric field distributions during nanoparticle alignment. The results reveal that the electric field distribution has been altered by positioning the magnets at the needle end. The analysis explored the possibility to create a stable liquid jet under a magnetic field, which allows the formation of organized nanostructures in nanofibers. The polarity of the magnet has been used to manipulate the electric field distribution in the electrospinning system. Based on the configuration of magnetic flux lines, the distribution of the electric field has been found to be altered. An axial magnetic field has been provided by the repulsive mode configuration, which could be the reason for alignment of nanoparticles during electrospinning. Simulation proved that the bending instability of the charged liquid jet can be efficiently controlled by placing the magnets on both sides of the fiber formation path in the electrospinning system. The impact of an axial magnetic field on nanofiber formation and nanoparticle alignment during the MFAES process was further experimentally validated. (paper)

  9. Wireless sensor technology for in-situ plasma process monitoring

    Science.gov (United States)

    Gahan, David

    2015-09-01

    There is an increasing demand for plasma measurement and control solutions to cope with the growing complexity of integrated circuit manufacture in the semiconductor industry. Standard plasma diagnostic instruments used in research, such as the Langmuir probe, are not suitable for use in the production environment for myriad reasons - contamination of the process being one of the main concerns. Silicon wafer based wireless sensors, which measure temperature during the process, have gained the most traction with tool manufacturers and chip makers - albeit during process development or the PM cycle rather than live production. In this presentation we will discuss two novel wireless technologies that have the potential for use in process tools. The first is an ion detector embedded in a silicon wafer. The sensor measures the average ion flux and the maximum ion energy during the process. This information is stored and is downloaded later for analysis. The second technology consists of a wireless sensor that sits inside the process and communicates data in real time to a detector installed on the rf power line. This platform is similar to RFID technology and can be combined with various sensor types to transmit data to the user during the process.

  10. An investigation of the structure–property relationships in ionic polymer polymer composites (IP2Cs) manufactured by polymerization in situ of PEDOT/PSS on Nafion®117

    International Nuclear Information System (INIS)

    Di Pasquale, G; Messina, F G; Pollicino, A; Puglisi, R; Graziani, S; Umana, E

    2014-01-01

    Ionic polymer polymer composites (IP 2 Cs) are all-organic electroactive polymers (EAPs) that show sensing and actuation capabilities when a deformation or a voltage is applied, respectively. They are fabricated starting from an ionic polymer coated on both sides with a conducting polymer as electrode element. In this work, poly(3,4-ethylendioxytiophene)–poly-(styrenesulfonate) (PEDOT/PSS) has been polymerized directly on Nafion ® 117 membrane and devices have been manufactured varying the polymerization time. Water and ethylene glycol (EG) have been used as solvents. The obtained IP 2 Cs have been characterized using thermal and mechanical analyses and electromechanically tested. The results have shown that in IP 2 Cs manufactured by polymerization in situ the PEDOT/PSS layer adheres very strongly on the Nafion ® 117 film, improving the possibility of rehydrating the devices after use. Moreover, taking into account that the different polymerization times influence the uniformity of the surface of the organic electrode and, consequently, both device stiffness and electrode conductivity, the structure–property relationships of the obtained devices have been investigated. The influence of the different solvents inside the devices has also been studied when IP 2 Cs have been used as actuators or sensors. Reported results show that it is possible to modulate the performances of IP 2 Cs by varying some manufacture parameters and the solvent. (paper)

  11. Process defects and in situ monitoring methods in metal powder bed fusion: a review

    Science.gov (United States)

    Grasso, Marco; Colosimo, Bianca Maria

    2017-04-01

    Despite continuous technological enhancements of metal Additive Manufacturing (AM) systems, the lack of process repeatability and stability still represents a barrier for the industrial breakthrough. The most relevant metal AM applications currently involve industrial sectors (e.g. aerospace and bio-medical) where defects avoidance is fundamental. Because of this, there is the need to develop novel in situ monitoring tools able to keep under control the stability of the process on a layer-by-layer basis, and to detect the onset of defects as soon as possible. On the one hand, AM systems must be equipped with in situ sensing devices able to measure relevant quantities during the process, a.k.a. process signatures. On the other hand, in-process data analytics and statistical monitoring techniques are required to detect and localize the defects in an automated way. This paper reviews the literature and the commercial tools for in situ monitoring of powder bed fusion (PBF) processes. It explores the different categories of defects and their main causes, the most relevant process signatures and the in situ sensing approaches proposed so far. Particular attention is devoted to the development of automated defect detection rules and the study of process control strategies, which represent two critical fields for the development of future smart PBF systems.

  12. In situ polymerized polyaniline films

    Czech Academy of Sciences Publication Activity Database

    Riede, A.; Helmdstedt, M.; Sapurina, I.; Stejskal, Jaroslav

    2002-01-01

    Roč. 248, č. 2 (2002), s. 413-418 ISSN 0021-9797 R&D Projects: GA AV ČR KSK4050111 Institutional research plan: CEZ:AV0Z4050913 Keywords : polyaniline * conducting polymer * thin films Subject RIV: CD - Macromolecular Chemistry Impact factor: 1.466, year: 2002

  13. Polymeric Membrane Reactors

    OpenAIRE

    José M. Sousa; Luís M. Madeira; João C. Santos; Adélio Mendes

    2008-01-01

    The aim of this chapter is the study of membrane reactors with polymeric membranes, particularly catalytic polymeric membranes. After an introduction where the main advantages and disadvantages of the use of polymeric membranes are summarised, a review of the main areas where they have been applied, integrated in chemical reactors, is presented. This excludes the field of bio-membranes processes, which is analysed in a specific chapter of this book. Particular attention is then given to model...

  14. Modeling segregated in- situ combustion processes through a vertical displacement model applied to a Colombian field

    International Nuclear Information System (INIS)

    Guerra Aristizabal, Jose Julian; Grosso Vargas, Jorge Luis

    2005-01-01

    Recently it has been proposed the incorporation of horizontal well technologies in thermal EOR processes like the in situ combustion process (ISC). This has taken to the conception of new recovery mechanisms named here as segregated in-situ combustion processes, which are conventional in-situ combustion process with a segregated flow component. Top/Down combustion, Combustion Override Split-production Horizontal-well and Toe-to-Heel Air Injection are three of these processes, which incorporate horizontal producers and gravity drainage phenomena. When applied to thick reservoirs a process of this nature could be reasonably modeled under concepts of conventional in-situ combustion and Crestal Gas injection, especially for heavy oils mobile at reservoir conditions. A process of this nature has been studied through an analytic model conceived for the particular conditions of the Castilla field, a homogeneous thick anticline structure containing high mobility heavy oil, which seems to be an excellent candidate for the application of these technologies

  15. An integrated numerical and physical modeling system for an enhanced in situ bioremediation process

    International Nuclear Information System (INIS)

    Huang, Y.F.; Huang, G.H.; Wang, G.Q.; Lin, Q.G.; Chakma, A.

    2006-01-01

    Groundwater contamination due to releases of petroleum products is a major environmental concern in many urban districts and industrial zones. Over the past years, a few studies were undertaken to address in situ bioremediation processes coupled with contaminant transport in two- or three-dimensional domains. However, they were concentrated on natural attenuation processes for petroleum contaminants or enhanced in situ bioremediation processes in laboratory columns. In this study, an integrated numerical and physical modeling system is developed for simulating an enhanced in situ biodegradation (EISB) process coupled with three-dimensional multiphase multicomponent flow and transport simulation in a multi-dimensional pilot-scale physical model. The designed pilot-scale physical model is effective in tackling natural attenuation and EISB processes for site remediation. The simulation results demonstrate that the developed system is effective in modeling the EISB process, and can thus be used for investigating the effects of various uncertainties. - An integrated modeling system was developed to enhance in situ bioremediation processes

  16. Carbono polimérico: processamento e aplicação Polymeric carbon: processing and applications

    Directory of Open Access Journals (Sweden)

    Paulo Eduardo Ferrari

    1998-12-01

    Full Text Available RESUMO: Carbonos poliméricos são materiais constituídos basicamente do elemento carbono, arranjado em orbitais sp², formando camadas de planos de hexágonos com diferentes graus de ordenação. Em função de suas características mecânicas, elétricas e de inércia química o processamento desses materiais é considerado como tecnologia de ponta e os produtos obtidos têm encontrado aplicação em diferentes áreas. Os pontos sensíveis desta tecnologia são o processamento dos precursores poliméricos orgânicos utilizados como matérias-primas, e os parâmetros de tratamento térmico adotados. Em função da aplicação final deste tipo de material o seu processamento é ajustado, de modo a permitir a obtenção de produtos com diferentes características finais, podendo-se citar o carbono vítreo monolítico com um volume de poros fechados inferior a 1% e as espumas de carbono com aproximadamente 98% de poros de transporte. Este artigo tem como objetivo divulgar esta classe de material, abordando os conceitos básicos de sua estrutura, tópicos de seu processamento e o seu potencial de utilização.ABSTRACT: Polymeric carbons are materials whose molecular structure is made basically up of carbon element. Their atoms are bonded through the sp² orbitals forming hexagonal units, which are arranged in stacks of planar layers with different degrees of ordering. The chemical, mechanical and electric characteristics resulting from this structure is known as polymeric carbon, uniquely useful for high-tech applications. The main aspects of the polymeric carbon technology are related to the organic polymer precursor processing, used as raw materials, and to the heat treatment for the carbonization/graphitization steps. Changes in either one can lead to polymeric carbon materials with very different characteristics. Thus, monolithic vitreous carbon structures can be obtained, with less than 1% of closed pores as well as carbon foam structures

  17. Fluorescent-magnetic Janus particles prepared via seed emulsion polymerization.

    Science.gov (United States)

    Kaewsaneha, Chariya; Bitar, Ahmad; Tangboriboonrat, Pramuan; Polpanich, Duangporn; Elaissari, Abdelhamid

    2014-06-15

    Anisotropic polymeric colloidal or Janus particles possessing simultaneous magnetic and fluorescent properties were successfully prepared via the swelling-diffusion or the in situ emulsion polymerization method. In the swelling-diffusion process, magnetic emulsions (an organic ferrofluid dispersed in aqueous medium) were synthesized and used for seeds of submicron magnetic Janus particles. After swelling the anisotropic particles obtained by 1-pyrene-carboxaldehyde fluorescent dye dissolved in tetrahydrofuran, well-defined fluorescent-magnetic Janus particles were produced. In the in situ emulsion polymerization, styrene monomer mixed with fluorescent dye monomers, i.e., 1-pyrenylmethyl methacrylate (PyMMA) or fluorescein dimethacrylate (FDMA), and an oil-soluble initiator (2,2'-azobis(2-isobutyronitrile)) were emulsified in the presence of magnetic seed emulsions. The confocal microscopic images showed the fluorescent-magnetic Janus particles with high fluorescent intensity when a fluorescent crosslinker monomer FDMA was employed. Copyright © 2014 Elsevier Inc. All rights reserved.

  18. Phosphazene-promoted anionic polymerization

    KAUST Repository

    Zhao, Junpeng

    2014-01-01

    In the recent surge of metal-free polymerization techniques, phosphazene bases have shown their remarkable potential as organic promoters/catalysts for the anionic polymerization of various types of monomers. By complexation with the counterion (e.g. proton or lithium cation), phosphazene base significantly improve the nucleophilicity of the initiator/chain-end resulting in rapid and usually controlled anionic/quasi-anionic polymerization. In this review, we will introduce the general mechanism, i.e. in situ activation (of initiating sites) and polymerization, and summarize the applications of such a mechanism on macromolecular engineering toward functionalized polymers, block copolymers and complex macromolecular architectures.

  19. A DFT Study of R-X Bond Dissociation Enthalpies of Relevance to the Initiation Process of Atom Transfer Radical Polymerization

    DEFF Research Database (Denmark)

    Gillies, Malcolm Bjørn; Matyjaszewski, Krzysztof; Norrby, Per-Ola

    2003-01-01

    DFT calculations at the B3P86/6-31G** level have been carried out to derive the bond dissociation energies (BDE) and free energies for a number of R-X systems (X ) Cl, Br, I, N3, and S2-CNMe2) that have been or can potentially be used as initiators for atom transfer radical polymerization (ATRP...... with the equilibrium constants that have been determined from ATRP polymerization rates and from model studies of activation-deactivation-termination processes in the absence of monomer. These comparisons reveal the effectiveness of the DFT-computed BDEs for predicting polymerization rates for new monomers in ATRP...

  20. Electrosleeve process for in-situ nuclear steam generator repair

    Energy Technology Data Exchange (ETDEWEB)

    Barton, R.A. [Ontario Hydro Technologies, Toronto, ON (Canada); Moran, T.E. [Framatome Technologies Inc., Lynchburg, VA (United States); Renaud, E. [Babcock and Wilcox Industries Ltd., Cambridge, ON (Canada)

    1997-07-01

    Degradation of steam generator (SG) tubing by localized corrosion is a widespread problem in the nuclear industry that can lead to costly forced out-ages, unit de-rating, SG replacement or even the permanent shutdown of a reactor. In response to the onset of SG tubing degradation at Ontario Hydro's Pickering Nuclear Generating Station (PNGS) Unit 5, and the determined unsuitability of conventional repair methods (mechanically expanded or welded sleeves) for Alloy 400, an alternative repair technology was developed. Electrosleeve is a non-intrusive, low-temperature process that involves the electrodeposition of a nanocrystalline nickel microalloy forming a continuously bonded, structural layer over the internal diameter of the degraded region. This technology is designed to provide a long-term pressure boundary repair, fully restoring the structural integrity of the damaged region to its original state. This paper describes the Electrosleeve process for SG tubing repair and the unique properties of the advanced sleeve material. The successful installation of Electrosleeves that have been in service for more than three years in Alloy 400 SG tubing at the Pickering-5 CANDU unit, the more recent extension of the technology to Alloy 600 and its demonstration in a U.S. pressurized water reactor (PWR), is presented. A number of PWR operators have requested plant operating technical specification changes to permit Electrosleeve SG tube repair. Licensing of the Electrosleeve by the U.S. Nuclear Regulatory Commission (NRC) is expected imminently. (author)

  1. IPCS: An integrated process control system for enhanced in-situ bioremediation

    International Nuclear Information System (INIS)

    Huang, Y.F.; Wang, G.Q.; Huang, G.H.; Xiao, H.N.; Chakma, A.

    2008-01-01

    To date, there has been little or no research related to process control of subsurface remediation systems. In this study, a framework to develop an integrated process control system for improving remediation efficiencies and reducing operating costs was proposed based on physical and numerical models, stepwise cluster analysis, non-linear optimization and artificial neural networks. Process control for enhanced in-situ bioremediation was accomplished through incorporating the developed forecasters and optimizers with methods of genetic algorithm and neural networks modeling. Application of the proposed approach to a bioremediation process in a pilot-scale system indicated that it was effective in dynamic optimization and real-time process control of the sophisticated bioremediation systems. - A framework of process control system was developed to improve in-situ bioremediation efficiencies and reducing operating costs

  2. Experimental Investigation and High Resolution Simulation of In-Situ Combustion Processes

    Energy Technology Data Exchange (ETDEWEB)

    Margot Gerritsen; Tony Kovscek

    2008-04-30

    This final technical report describes work performed for the project 'Experimental Investigation and High Resolution Numerical Simulator of In-Situ Combustion Processes', DE-FC26-03NT15405. In summary, this work improved our understanding of in-situ combustion (ISC) process physics and oil recovery. This understanding was translated into improved conceptual models and a suite of software algorithms that extended predictive capabilities. We pursued experimental, theoretical, and numerical tasks during the performance period. The specific project objectives were (i) identification, experimentally, of chemical additives/injectants that improve combustion performance and delineation of the physics of improved performance, (ii) establishment of a benchmark one-dimensional, experimental data set for verification of in-situ combustion dynamics computed by simulators, (iii) develop improved numerical methods that can be used to describe in-situ combustion more accurately, and (iv) to lay the underpinnings of a highly efficient, 3D, in-situ combustion simulator using adaptive mesh refinement techniques and parallelization. We believe that project goals were met and exceeded as discussed.

  3. Preparation of Ultrahigh Molecular Weight Polyethylene/Graphene Nanocomposite In situ Polymerization via Spherical and Sandwich Structure Graphene/Sio2 Support

    Science.gov (United States)

    Su, Enqi; Gao, Wensheng; Hu, Xinjun; Zhang, Caicai; Zhu, Bochao; Jia, Junji; Huang, Anping; Bai, Yongxiao

    2018-04-01

    Reduced graphene oxide/SiO2 (RGO/SiO2) serving as a novel spherical support for Ziegler-Natta (Z-N) catalyst is reported. The surface and interior of the support has a porous architecture formed by RGO/SiO2 sandwich structure. The sandwich structure is like a brick wall coated with a graphene layer of concreted as skeleton which could withstand external pressures and endow the structure with higher support stabilities. After loading the Z-N catalyst, the active components anchor on the surface and internal pores of the supports. When the ethylene molecules meet the active centers, the molecular chains grow from the surface and internal catalytic sites in a regular and well-organized way. And the process of the nascent molecular chains filled in the sandwich structure polymerization could ensure the graphene disperse uniformly in the polymer matrix. Compared with traditional methods, the porous spherical graphene support of this strategy has far more advantages and could maintain an intrinsic graphene performance in the nanocomposites.

  4. Physical chemistry research for engineering and applied sciences, v.2 polymeric materials and processing

    CERN Document Server

    Pearce, Eli M; Pethrick, Richard A

    2015-01-01

    PrefaceInvestigation on the Influence of a Strong Electric Field on the Electrical, Transport and Diffusion Properties of Carbon Nanostructures; S. A. Sudorgin and N. G. LebedevA Study Thermal Stability of Polyurethane Elastomers; I. A. Novakov, M. A. Vaniev, D. V. Medvedev, N. V. Sidorenko, G. V. Medvedev, and D. O. GusevTrends in Aromatic Polyesters; Z. S. Khasbulatova and G. E. ZaikovMicroheterogeneous Titanium Ziegler-Natta Catalysts: 1,3-Diene Polymerization Under Ultrasound Irradiations; V. P. Zakharov, V. Z. Mingaleev, I. D. Zakirov

  5. Investigating the Use of Polymeric Binders in Twin Screw Melt Granulation Process for Improving Compactibility of Drugs.

    Science.gov (United States)

    Batra, Amol; Desai, Dipen; Serajuddin, Abu T M

    2017-01-01

    Traditionally, the melt granulation for pharmaceutical products was performed at low temperature (granulators using low-melting waxy binders, and tablets produced using such granules were not amenable to large-scale manufacturing. The situation has changed in recent years by the use of twin screw extruder where the processing temperature could be increased to as high as 180°C and polymers with high T g could be used as binders. In this study, different polymeric binders were screened for their suitability in improving compactibility of 2 drugs, metformin hydrochloride and acetaminophen, by twin screw melt granulation. Processing temperatures for the 2 drugs were set at 180°C and 130°C, respectively. Screw configuration, screw speed, and feed rate were optimized such that all polymeric binders used produced granules. Several hydroxypropyl cellulose, hydroxypropyl methylcellulose, polyvinylpyrrolidone, and methacrylate-based polymers, including Klucel ® EXF, Eudragit ® EPO, and Soluplus ® , demonstrated good tablet tensile strength (>2 MPa) when granules were produced using only 10% wt/wt polymer concentration. Certain polymers provided acceptable compactibility even at 5% wt/wt. Thus, twin screw melt granulation process may be used with different polymers at a wide range of temperature. Due to low excipient concentration, this granulation method is especially suitable for high-dose tablets. Copyright © 2016 American Pharmacists Association®. Published by Elsevier Inc. All rights reserved.

  6. Process, engineering and design aspects of contaminated soil bioremediation. Pt. 1 In situ treatments

    International Nuclear Information System (INIS)

    De Fraja Frangipane, E.; Andreottola, G.; Tatano, F.

    1995-01-01

    The present paper is an up-to-date overview of contaminated soil bioremediation techniques, which are analyzed in detail with regard to main process, engineering and design aspects. General biochemical/kinetic aspects of bioremediation of contaminated soil, and in situ treatments, are discussed in this part one

  7. EPA SITE DEMONSTRATION OF THE TERRA VAC IN SITU VACUUM EXTRACTION PROCESS IN GROVELAND, MASSACHUSETTS

    Science.gov (United States)

    This paper presents an EPA evaluation of the patented Terra Vac, Inc.'s in situ vacuum extraction process that was field-demonstrated on a trichloroethylene (TCE) contaminated soil in Groveland, MA, under the EPA Superfund Innovative Technology Evaluation (SITE) program. he Terra...

  8. Step-Growth Polymerization.

    Science.gov (United States)

    Stille, J. K.

    1981-01-01

    Following a comparison of chain-growth and step-growth polymerization, focuses on the latter process by describing requirements for high molecular weight, step-growth polymerization kinetics, synthesis and molecular weight distribution of some linear step-growth polymers, and three-dimensional network step-growth polymers. (JN)

  9. Comparison of temperature change among different adhesive resin cement during polymerization process

    Directory of Open Access Journals (Sweden)

    Murat Alkurt

    2017-01-01

    Full Text Available Purpose: The aim of this study was to assess the intra-pulpal temperature changes in adhesive resin cements during polymerization. Materials and Methods: Dentin surface was prepared with extracted human mandibular third molars. Adhesive resin cements (Panavia F 2.0, Panavia SA, and RelyX U200 were applied to the dentin surface and polymerized under IPS e.max Press restoration. K-type thermocouple wire was positioned in the pulpal chamber to measure temperature change (n = 7. The temperature data were recorded (0.0001 sensible and stored on a computer every 0.1 second for sixteen minutes. Differences between the baseline temperature and temperatures of various time points (2, 4, 6, 8, 10, 12, 14, and 16 minute were determined and mean temperature changes were calculated. At various time intervals, the differences in temperature values among the adhesive resin cements were analyzed by two-way ANOVA and post-hoc Tukey honestly test (α = 0.05. Results: Significant differences were found among the time points and resin cements (P < 0.05. Temperature values of the Pan SA group were significantly higher than Pan F and RelyX (P < 0.05. Conclusion: Result of the study on self-adhesive and self-etch adhesive resin cements exhibited a safety intra-pulpal temperature change.

  10. Polymeric microspheres

    Science.gov (United States)

    Walt, David R.; Mandal, Tarun K.; Fleming, Michael S.

    2004-04-13

    The invention features core-shell microsphere compositions, hollow polymeric microspheres, and methods for making the microspheres. The microspheres are characterized as having a polymeric shell with consistent shell thickness.

  11. Compositional Simulation of In-Situ Combustion EOR: A Study of Process Characteristics

    DEFF Research Database (Denmark)

    Jain, Priyanka; Stenby, Erling Halfdan; von Solms, Nicolas

    2010-01-01

    In order to facilitate the study of the influence of reservoir process characteristics in In-Situ combustion modeling and advance the work of Kristensen et al. in this domain; a fully compositional In-situ combustion (ISC) model of Virtual Kinetic Cell (VKC; single-cell model) for laboratory scale...... of the combustion front and thus decrease oil recovery, while increase in oxygen feed assists combustion and contributes towards improved oil recovery. The critical properties of the pseudo components are not determined experimentally, thus extending significance to fluid characterization. The composition plays...

  12. Impact of process temperature on GaSb metal-oxide-semiconductor interface properties fabricated by ex-situ process

    Science.gov (United States)

    Yokoyama, Masafumi; Asakura, Yuji; Yokoyama, Haruki; Takenaka, Mitsuru; Takagi, Shinichi

    2014-06-01

    We have studied the impact of process temperature on interface properties of GaSb metal-oxide-semiconductor (MOS) structures fabricated by an ex-situ atomic-layer-deposition (ALD) process. We have found that the ALD temperature strongly affects the Al2O3/GaSb MOS interface properties. The Al2O3/GaSb MOS interfaces fabricated at the low ALD temperature of 150 °C have the minimum interface-trap density (Dit) of ˜4.5 × 1013 cm-2 eV-1. We have also found that the post-metalization annealing at temperature higher than 200 °C degrades the Al2O3/GaSb MOS interface properties. The low-temperature process is preferable in fabricating GaSb MOS interfaces in the ex-situ ALD process to avoid the high-temperature-induced degradations.

  13. Process Design and Economics for the Conversion of Lignocellulosic Biomass to Hydrocarbon Fuels: Thermochemical Research Pathways with In Situ and Ex Situ Upgrading of Fast Pyrolysis Vapors

    Energy Technology Data Exchange (ETDEWEB)

    Dutta, Abhijit [National Renewable Energy Lab. (NREL), Golden, CO (United States); Sahir, A. H. [National Renewable Energy Lab. (NREL), Golden, CO (United States); Tan, Eric [National Renewable Energy Lab. (NREL), Golden, CO (United States); Humbird, David [DWH Process Consulting, Denver, CO (United States); Snowden-Swan, Lesley J. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Meyer, Pimphan A. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Ross, Jeff [Harris Group, Inc., Seattle, WA (United States); Sexton, Danielle [Harris Group, Inc., Seattle, WA (United States); Yap, Raymond [Harris Group, Inc., Seattle, WA (United States); Lukas, John [Harris Group, Inc., Seattle, WA (United States)

    2015-03-01

    This report was developed as part of the U.S. Department of Energy’s Bioenergy Technologies Office’s efforts to enable the development of technologies for the production of infrastructure-compatible, cost-competitive liquid hydrocarbon fuels from biomass. Specifically, this report details two conceptual designs based on projected product yields and quality improvements via catalyst development and process integration. It is expected that these research improvements will be made within the 2022 timeframe. The two conversion pathways detailed are (1) in situ and (2) ex situ upgrading of vapors produced from the fast pyrolysis of biomass. While the base case conceptual designs and underlying assumptions outline performance metrics for feasibility, it should be noted that these are only two of many other possibilities in this area of research. Other promising process design options emerging from the research will be considered for future techno-economic analysis. Both the in situ and ex situ conceptual designs, using the underlying assumptions, project MFSPs of approximately $3.5/gallon gasoline equivalent (GGE). The performance assumptions for the ex situ process were more aggressive with higher distillate (diesel-range) products. This was based on an assumption that more favorable reaction chemistry (such as coupling) can be made possible in a separate reactor where, unlike in an in situ upgrading reactor, one does not have to deal with catalyst mixing with biomass char and ash, which pose challenges to catalyst performance and maintenance. Natural gas was used for hydrogen production, but only when off gases from the process was not sufficient to meet the needs; natural gas consumption is insignificant in both the in situ and ex situ base cases. Heat produced from the burning of char, coke, and off-gases allows for the production of surplus electricity which is sold to the grid allowing a reduction of approximately 5¢/GGE in the MFSP.

  14. Tunable hole injection of solution-processed polymeric carbon nitride towards efficient organic light-emitting diode

    Science.gov (United States)

    Zhang, Xiaowen; Zheng, Qinghong; Tang, Zhenyu; Li, Wanshu; Zhang, Yan; Xu, Kai; Xue, Xiaogang; Xu, Jiwen; Wang, Hua; Wei, Bin

    2018-02-01

    Polymeric carbon nitride (CNxHy) has been facilely synthesized from dicyandiamide and functions as a solution-processed hole injection layer in organic light-emitting diodes (OLEDs). The measurements using X-ray diffraction, atomic force microscopy, X-ray photoelectron spectroscopy, ultraviolet photoelectron spectroscopy, and impedance spectroscopy elucidate that CNxHy exhibits superior film morphology and extra electric properties such as tailored work function and tunable hole injection. The luminous efficiency of CNxHy-based OLED is found to improve by 76.6% in comparison to the counterpart using favorite solution-processed poly(ethylene dioxythiophene):poly(styrene sulfonate) as the hole injection layer. Our results also pave a way for broadening carbon nitride applications in organic electronics using the solution process.

  15. Downstream processing from melt granulation towards tablets: In-depth analysis of a continuous twin-screw melt granulation process using polymeric binders.

    Science.gov (United States)

    Grymonpré, W; Verstraete, G; Vanhoorne, V; Remon, J P; De Beer, T; Vervaet, C

    2018-03-01

    The concept of twin-screw melt granulation (TSMG) has steadily (re)-gained interest in pharmaceutical formulation development as an intermediate step during tablet manufacturing. However, to be considered as a viable processing option for solid oral dosage forms there is a need to understand all critical sources of variability which could affect this granulation technique. The purpose of this study was to provide an in-depth analysis of the continuous TSMG process in order to expose the critical process parameters (CPP) and elucidate the impact of process and formulation parameters on the critical quality attributes (CQA) of granules and tablets during continuous TSMG. A first part of the study dealt with the screening of various amorphous polymers as binder for producing high-dosed melt granules of two model drug (i.e. acetaminophen and hydrochlorothiazide). The second part of this study described a quality-by-design (QbD) approach for melt granulation of hydrochlorothiazide in order to thoroughly evaluate TSMG, milling and tableting stage of the continuous TSMG line. Using amorphous polymeric binders resulted in melt granules with high milling efficiency due to their brittle behaviour without producing excessive amounts of fines, providing high granule yields with low friability. Therefore, it makes them extremely suitable for further downstream processing. One of the most important CPP during TSMG with polymeric binders was the granulation-torque, which - in case of polymers with high T g - increased during longer granulation runs to critical levels endangering the continuous process flow. However, by optimizing both screw speed and throughput or changing to polymeric binders with lower T g it was possible to significantly reduce this risk. This research paper highlighted that TSMG must be considered as a viable option during formulation development of solid oral dosage forms based on the robustness of the CQA of both melt granules and tablets. Copyright © 2017

  16. Design of Hybrid Steam-In Situ Combustion Bitumen Recovery Processes

    International Nuclear Information System (INIS)

    Yang Xiaomeng; Gates, Ian D.

    2009-01-01

    Given enormous capital costs, operating expenses, flue gas emissions, water treatment and handling costs of thermal in situ bitumen recovery processes, improving the overall efficiency by lowering energy requirements, environmental impact, and costs of these production techniques is a priority. Steam-assisted gravity drainage (SAGD) is the most widely used in situ recovery technique in Athabasca reservoirs. Steam generation is done on surface and consequently, because of heat losses, the energy efficiency of SAGD can never be ideal with respect to the energy delivered to the sandface. An alternative to surface steam generation is in situ combustion (ISC) where heat is generated within the formation through injection of oxygen at a sufficiently high pressure to initiate combustion of bitumen. In this manner, the heat from the combustion reactions can be used directly to mobilize the bitumen. As an alternative, the heat can be used to generate steam within the formation which then is the agent to move heat in the reservoir. In this research, alternative hybrid techniques with simultaneous and sequential steam-oxygen injection processes are examined to maximize the thermal efficiency of the recovery process. These hybrid processes have the advantage that during ISC, steam is generated within the reservoir from injected and formation water and as a product of oxidation. This implies that ex situ steam generation requirements are reduced and if there is in situ storage of combustion gases, that overall gas emissions are reduced. In this research, detailed reservoir simulations are done to examine the dynamics of hybrid processes to enable design of these processes. The results reveal that hybrid processes can lower emitted carbon dioxide-to-oil ratio by about 46%, decrease the consumed natural gas-to-oil ratio by about 73%, reduce the cumulative energy-to-oil ratio by between 40% and 70% compared to conventional SAGD, and drop water consumption per unit oil produced

  17. Deformation processes in functional materials studied by in situ neutron diffraction and ultrasonic techniques

    International Nuclear Information System (INIS)

    Sittner, P.; Novak, V.; Landa, M.; Lukas, P.

    2007-01-01

    The unique thermomechanical functions of shape memory alloys (hysteretic stress-strain-temperature responses) not their structural properties (as strength, fatigue, corrosion resistance, etc.) are primarily utilized in engineering applications. In order to better understand and predict the functional behavior, we have recently employed two dedicated non-invasive in situ experimental methods capable to follow the deformation/transformation processes in thermomechanically loaded polycrystalline samples. The in situ neutron diffraction method takes advantage of the ability of thermal neutrons to penetrate bulk samples. As a diffraction technique sensitive to interplanar spacings in crystalline solids, it provides in situ information on the changes in crystal structure, phase composition, phase stress and texture in the transforming samples. The combined in situ ultrasonic and electric resistance method follows variations of the electric resistance as well as speed and attenuation of acoustic waves propagating through the transforming sample. The acoustic waves are mainly sensitive to changes of elastic properties accompanying the deformation/transformation processes. The latter method thus follows the changes in interatomic bonds rather than changes in the interplanar lattice spacings focused in the neutron diffraction method. The methods are thus complementary. They are briefly described and selected experimental results obtained recently on NiTi alloys are presented and discussed

  18. Study on underground-water restoration of acid in-situ leaching process with electrodialytic desalination

    International Nuclear Information System (INIS)

    Huang Chongyuan; Meng Jin; Li Weicai

    2003-01-01

    The study focus undergrounder water restoration of acid in-situ leaching process with electrodialysis desalination in Yining Uranium Mine. It is shown in field test that electrodialysis desalination is an effective method for underground water restoration of acid in-situ leaching process. When TDS of underground-water at the decommissioning scope is 10-12 g/L, and TDS will be less than 1 g/L after the desalination process, the desalination rate is more than 90%, freshwater recovery 60%-70%, power consumption for freshwater recovery 5 kW·h/m 3 , the distance of the desalination flow 12-13 m, current efficiency 80%, and the throughput of the twin membrane 0.22-0.24 m 3 /(m 2 ·d)

  19. Effect of process parameters on flow length and flash formation in injection moulding of high aspect ratio polymeric micro features

    DEFF Research Database (Denmark)

    Eladl, Abdelkhalik; Mostafa, Rania; Islam, Aminul

    2018-01-01

    part with four micro fingers with different aspect ratios (from 21 up to 150) and was carried out according to the Design of Experiments (DOE) statistical technique. The results show that holding pressure and injection velocity are the most influential parameters on part mass with a direct effect......This paper reports an investigation of the effects of process parameters on the quality characteristics of polymeric parts produced by micro injection moulding (µIM) with two different materials. Four injection moulding process parameters (injection velocity, holding pressure, melt temperature...... for both materials. Both parameters have a similar effect on flow length for both PP and ABS at all aspect ratios and have higher effects as the feature thickness decreased below 300 µm. The study shows that for the investigated materials the injection speed and packing pressure were the most influential...

  20. On-line in-situ control of the resin transfer molding process

    Science.gov (United States)

    Kranbuehl, D.; Eichinger, D.; Williamson, A.; Levy, D.; Reyzer, M.

    1990-01-01

    Resin transfer molding of three-dimensionally stitched fabrics promises to be a cost effective process for obtaining composite parts of exceptional strength. The technique eliminates many problems involving prepreg preparation, storage and layup. It replaces, on the other hand, the single step cure process with a two-stage impregnation and cure process. Of particular importance therefore is selecting and controlling the viscosity during impregnation and cure. The use of in-situ frequency-dependent electromagnetic sensors and the Loos-Springer model for selecting and controllng the processing properties of the resin transfer molding resin during impregnation and cure are discussed.

  1. Comparison of the Emulsion Mixing and In Situ Polymerization Techniques for Synthesis of Water- Borne Reduced Graphene Oxide/Polymer Composites: Advantages and Drawbacks

    Czech Academy of Sciences Publication Activity Database

    Arzac, A.; Leal, G.L.; Fajgar, Radek; Tomovska, R.

    2014-01-01

    Roč. 31, č. 1 (2014), s. 143-151 ISSN 0934-0866 Grant - others:BG(ES) NanoIker 2012–2013; NATO(US) SfP 984399 Institutional support: RVO:67985858 Keywords : polymerization * composite films * latex blends Subject RIV: CA - Inorganic Chemistry Impact factor: 3.081, year: 2014

  2. In situ characterization of the nitridation of dysprosium during mechanochemical processing

    Energy Technology Data Exchange (ETDEWEB)

    Jaques, Brian J.; Osterberg, Daniel D.; Alanko, Gordon A.; Tamrakar, Sumit; Smith, Cole R.; Hurley, Michael F.; Butt, Darryl P., E-mail: DarrylButt@BoiseState.edu

    2015-01-15

    Highlights: • A nitridation reaction in a high energy planetary ball mill was monitored in situ. • Dysprosium mononitride was synthesized from Dy at low temperatures in short times. • Ideal gas law and in situ temperature and pressure used to assess reaction extent. • It is proposed that reaction rate is proportional to the creation of new surface. - Abstract: Processing of advanced nitride ceramics traditionally requires long durations at high temperatures and, in some cases, in hazardous atmospheres. In this study, dysprosium mononitride (DyN) was rapidly formed from elemental dysprosium in a closed system at ambient temperatures. An experimental procedure was developed to quantify the progress of the nitridation reaction during mechanochemical processing in a high energy planetary ball mill (HEBM) as a function of milling time and intensity using in situ temperature and pressure measurements, SEM, XRD, and particle size analysis. No intermediate phases were formed. It was found that the creation of fresh dysprosium surfaces dictates the rate of the nitridation reaction, which is a function of milling intensity and the number of milling media. These results show clearly that high purity nitrides can be synthesized with short processing times at low temperatures in a closed system requiring a relatively small processing footprint.

  3. Synthesis of gold and silver nanoparticle S-ovalbumin protein conjugates by in situ conjugation process

    Science.gov (United States)

    Joshi, Deepti; Soni, R. K.

    2015-05-01

    Pure gold and silver nanoparticle (NP) generation and their conjugation with protein S-ovalbumin using in situ conjugation process have been reported. The in situ conjugation involves nanosecond pulse laser ablation of pure metal target in the protein S-ovalbumin solution. Transmission electron microscopy (TEM) and UV-Visible absorption results show decrease in mean NP size along with narrow particle size distribution on ablation in S-ovalbumin solution as compared to ablation in water for both Au and Ag NPs. Also, the NP size reduction was found to be dependent on the concentration of S-ovalbumin. For AuNPs, spherical NPs of mean size 4 nm with particle size distribution 2-6 nm were obtained at 300 nM S-ovalbumin concentration. Further, it has been observed that the resultant in situ-conjugated colloid gold and silver NP solutions were quite stable even in the presence of NaCl at physiological salt concentration (0.15 M). On post-laser irradiation (532 nm, 15 mJ) for 20 min, 9 nm red shift in surface plasmon resonance peak (SPR), along with increased broadening towards longer wavelength, was observed in the AuNPs-S-ovalbumin sample. Further increase in the time of irradiation showed shift in AuNPs-S-ovalbumin SPR towards lower wavelength. On laser irradiation (532 nm, 15 mJ) for 20 min, no significant change was observed in the line shape of the plasmon absorption band of the AgNPs-S-ovalbumin conjugate. FTIR spectra revealed that S-ovalbumin peptide backbone and secondary structure remain unchanged on laser irradiation during in situ conjugation process. Thus, integrity of S-ovalbumin does not get affected, and no degradation of S-ovalbumin takes place on laser-induced in situ conjugation. Raman results confirm that both Au and Ag NPs interact with S-ovalbumin via thiol-bearing cysteine residues of the disulfide bond.

  4. Solubility of drugs in aqueous polymeric solution: effect of ovalbumin on microencapsulation process.

    Science.gov (United States)

    Aziz, Hesham Abdul; Tan, Yvonne Tze Fung; Peh, Kok Khiang

    2012-03-01

    Microencapsulation of water-soluble drugs using coacervation-phase separation method is very challenging, as these drugs partitioned into the aqueous polymeric solution, resulting in poor drug entrapment. For evaluating the effect of ovalbumin on the microencapsulation of drugs with different solubility, pseudoephedrine HCl, verapamil HCl, propranolol HCl, paracetamol, and curcuminoid were used. In addition, drug mixtures comprising of paracetamol and pseudoephedrine HCl were also studied. The morphology, encapsulation efficiency, particle size, and in vitro release profile were investigated. The results showed that the solubility of the drug determined the ratio of ovalbumin to be used for successful microencapsulation. The optimum ratios of drug, ovalbumin, and gelatin for water-soluble (pseudoephedrine HCl, verapamil HCl, and propranolol HCl), sparingly water-soluble (paracetamol), and water-insoluble (curcuminoid) drugs were found to be 1:1:2, 2:3:5, and 1:3:4. As for the drug mixture, the optimum ratio of drug, ovalbumin, and gelatin was 2:3:5. Encapsulated particles prepared at the optimum ratios showed high yield, drug loading, entrapment efficiency, and sustained release profiles. The solubility of drug affected the particle size of the encapsulated particle. Highly soluble drugs resulted in smaller particle size. In conclusion, addition of ovalbumin circumvented the partitioning effect, leading to the successful microencapsulation of water-soluble drugs.

  5. A new miniature instrument for in situ measuring, processing, recording and display of oceanographic properties

    OpenAIRE

    Gytre, Trygve

    1987-01-01

    The paper describes the design philosophy and functions of a new general purpose oceanographic instrument which is presently being tested as a prototype. The instrument combines established oceanic sensors with modern microprocessor and display technology. The basic idea behind the design is to make a compact and modular "workhorse" instrument that interacts with both humans and computers in a natural way. The instrument is presently able to measure and to in situ process...

  6. In-situ electrical analysis in view of monitoring the processing of thermoplastics

    Science.gov (United States)

    Gonnet, J. M.; Guillet, J.; Ainser, A.; Boiteux, G.; Fulchiron, R.; Seytre, Gerard

    1999-12-01

    In the last recent years, electrical techniques like microdielectrometry have presented an attracting and increasing interest for continuous monitoring, in a nondestructive way, of the advancement of the reaction of thermoset resins under cure. We think that the use of electrical analysis for in situ monitoring of chemical reactions can be extended to get information on thermoplastic and the physical phenomena such sa crystallization or study of residence time distribution in processing machines such as extruders.

  7. Total internal reflection fluorescence anisotropy imaging microscopy: setup, calibration, and data processing for protein polymerization measurements in living cells

    Science.gov (United States)

    Ströhl, Florian; Wong, Hovy H. W.; Holt, Christine E.; Kaminski, Clemens F.

    2018-01-01

    Fluorescence anisotropy imaging microscopy (FAIM) measures the depolarization properties of fluorophores to deduce molecular changes in their environment. For successful FAIM, several design principles have to be considered and a thorough system-specific calibration protocol is paramount. One important calibration parameter is the G factor, which describes the system-induced errors for different polarization states of light. The determination and calibration of the G factor is discussed in detail in this article. We present a novel measurement strategy, which is particularly suitable for FAIM with high numerical aperture objectives operating in TIRF illumination mode. The method makes use of evanescent fields that excite the sample with a polarization direction perpendicular to the image plane. Furthermore, we have developed an ImageJ/Fiji plugin, AniCalc, for FAIM data processing. We demonstrate the capabilities of our TIRF-FAIM system by measuring β -actin polymerization in human embryonic kidney cells and in retinal neurons.

  8. The asymptotic behavior in a reversible random coagulation-fragmentation polymerization process with sub-exponential decay

    Science.gov (United States)

    Dong, Siqun; Zhao, Dianli

    2018-01-01

    This paper studies the subcritical, near-critical and supercritical asymptotic behavior of a reversible random coagulation-fragmentation polymerization process as N → ∞, with the number of distinct ways to form a k-clusters from k units satisfying f(k) =(1 + o (1)) cr-ke-kαk-β, where 0 0. When the cluster size is small, its distribution is proved to converge to the Gaussian distribution. For the medium clusters, its distribution will converge to Poisson distribution in supercritical stage, and no large clusters exist in this stage. Furthermore, the largest length of polymers of size N is of order ln N in the subcritical stage under α ⩽ 1 / 2.

  9. Geophysical Characterization of in situ Serpentinization Processes at the Coast Range Ophiolite Microbial Observatory (CROMO)

    Science.gov (United States)

    Ortiz, E.; Tominaga, M.; Cardace, D.; Schrenk, M. O.; Hoehler, T. M.; Kubo, M. D.

    2016-12-01

    Electrical and magnetic remote sensing both on land and at sea have emerged as a powerful approach to characterize in situ serpentinization and carbonation processes in time and space. We conducted 2D Electrical Resistivity Tomography (ERT) surveys to investigate in situ geological and hydrogeological architecture within the rock formation of the Jurassic age tectonic mélange portion of the Coast Range Ophiolite Microbiological Observatory (CROMO) where serpentinization processes are thought to facilitate an active deep biosphere. We acquired ERT imagery during both wet and dry seasons, along 9 survey tracks traversing two previously drilled wells, CSW1.1 and QV1.1, at different lateral and horizontal resolutions, yielding imagery with depth of 6.9 - 41m. Integrating ERT inversion models with wire-line and core data, we successfully documented temporal changes in the in situ hydrological properties at CROMO, i.e. the lateral and vertical water table boundaries (unconfined aquifer), non-permeable zones (confining bed), and possible confined aquifers that are juxtaposed within three dominant lithological units of serpentinite top soil, serpentinite gravel with clay, and serpentinite basement formation. We conducted rock magnetic experiments on core samples from drilled sites, including Magnetic Property Measurement System (MPMS) measurements, to better understand the connection between these hydrogeological properties and in situ serpentinization processes. Based on the observed downhole distribution of magnetite in correlation with ERT results and lithostratigraphy, we proposed that, at CROMO: (i) zones enriched in ferromagnetic minerals, correspond to in situ serpentinite formation with both high and low resistivity, suggesting that resistivity zones represent in situ architecture of consolidated serpentinite confining beds and possible fractured serpentinite aquifers, respectively; and (ii) zones (e.g. 14 - 31m at CSW site) enriched in superparamagnetic size

  10. Description and capabilities of the large-scale in situ vitrification process

    Energy Technology Data Exchange (ETDEWEB)

    Buelt, J.L.; Carter, J.G.

    1986-01-01

    An emerging thermal treatment process known as in situ vitrification is being developed to immobilize selected portions of radioactively contaminated soils. The process is a permanent remedial action that destroys solid and liquid organic contaminants and incorporates radionuclides and heavy metals into a glass and crystalline form. The process's flexibility in design and broad capabilities make it potentially adaptable to mixed and chemical wastes, as well. The process consists of an electrical power system for vitrifying contaminated soil, a hood to contain gaseous effluents, an off-gas treatment system, an off-gas cooling system, and a process control station. The process is mounted in three transportable trailers that can be easily moved from site to site. The process is capable of treating contaminated soils at least 13 m deep. The system components are designed to accommodate waste inclusions in the soil such as metals, combustibles, and large voids. Selectively applied to the more troublesome radioactively contaminated soils, in situ vitrification provides a potentially useful and permanent tool for remedial action.

  11. A DFT Study of R-X Bond Dissociation Enthalpies of Relevance to the Initiation Process of Atom Transfer Radical Polymerization

    DEFF Research Database (Denmark)

    Gillies, Malcolm Bjørn; Matyjaszewski, Krzysztof; Norrby, Per-Ola

    2003-01-01

    DFT calculations at the B3P86/6-31G** level have been carried out to derive the bond dissociation energies (BDE) and free energies for a number of R-X systems (X ) Cl, Br, I, N3, and S2-CNMe2) that have been or can potentially be used as initiators for atom transfer radical polymerization (ATRP...... energies are in good agreement with the experimentally available BDEs and reveal a small weakening effect caused by the substitution of an R-H atom with a CH3 group. The free energies are used to derive the relative equilibrium constant for the ATRP activation/deactivation process. These are compared...... with the equilibrium constants that have been determined from ATRP polymerization rates and from model studies of activation-deactivation-termination processes in the absence of monomer. These comparisons reveal the effectiveness of the DFT-computed BDEs for predicting polymerization rates for new monomers in ATRP...

  12. Seismic monitoring of in situ combustion process in a heavy oil field

    International Nuclear Information System (INIS)

    Zadeh, Hossein Mehdi; Srivastava, Ravi P; Vedanti, Nimisha; Landrø, Martin

    2010-01-01

    Three time-lapse 3D seismic surveys are analysed to monitor the effect of in situ combustion, a thermal-enhanced oil recovery process in the Balol heavy oil reservoir in India. The baseline data were acquired prior to the start of the in situ combustion process in four injection wells, while the two monitor surveys were acquired 1 and 2 years after injection start, respectively. We present the results of baseline and second monitor surveys. Fluid substitution studies based on acoustic well logs predict a seismic amplitude decrease at the top reservoir and an increase at the base reservoir. Both the amplitude dimming at the top reservoir and the brightening at the base reservoir are observed in the field data. The extent of the most pronounced 4D anomaly is estimated from the seismic amplitude and time shift analysis. The interesting result of seismic analysis is that the anomalies are laterally shifted towards the northwest, rather than the expected east, from the injector location suggesting a northwest movement of the in situ combustion front. No clear evidence of air leakage into other sand layers, neither above nor below the reservoir sand, is observed. This does not necessarily mean that all the injected air is following the reservoir sand, especially if the thief sand layers are thin. These layers might be difficult to observe on seismic data

  13. In situ moisture determination of a cytotoxic compound during process optimization.

    Science.gov (United States)

    Hicks, Michael B; Zhou, George X; Lieberman, David R; Antonucci, Vincent; Ge, Zhihong; Shi, Yao-Jun; Cameron, Mark; Lynch, Joseph E

    2003-03-01

    A simple and safe prototype apparatus was designed and adapted for the in situ determination of the moisture content of a cytotoxic compound (9-fluorenylmethyl-protected doxorubicin-peptide conjugate, or Fm-DPC) by near-infrared absorbance spectroscopy during optimization of the chemical isolation procedure. The cytotoxic nature of the compound restricts one's ability to safely sample such drying processes for more traditional means of moisture determination for fear of hazardous solids dusting, hence in situ sampling approaches are of great importance. These concerns also exist for the process development laboratory, where despite the smaller scale of operations, the volume of experiments (hence cytotoxic samples) required to define a chemical process is often more significant. In this application, partial least squares regression was used with Karl Fischer volumetric titration analysis to generate a calibration model. Although pronounced differences in cake density were observed as a function of the buffer selected for the isolation process, the model still achieved a standard error of calibration of 0.63% w/w and a standard error of prediction of 0.99% (w/w). These results demonstrated the versatility of the prototype apparatus/data processing approach to model Fm-DPC drying under extremely variable conditions, as inherently expected during the investigational laboratory development of a chemical process. Copyright 2003 Wiley-Liss Inc. and the American Pharmaeceutical Association

  14. In situ monitoring of biomolecular processes in living systems using surface-enhanced Raman scattering

    Science.gov (United States)

    Altunbek, Mine; Kelestemur, Seda; Culha, Mustafa

    2015-12-01

    Surface-enhanced Raman scattering (SERS) continues to strive to gather molecular level information from dynamic biological systems. It is our ongoing effort to utilize the technique for understanding of the biomolecular processes in living systems such as eukaryotic and prokaryotic cells. In this study, the technique is investigated to identify cell death mechanisms in 2D and 3D in vitro cell culture models, which is a very important process in tissue engineering and pharmaceutical applications. Second, in situ biofilm formation monitoring is investigated to understand how microorganisms respond to the environmental stimuli, which inferred information can be used to interfere with biofilm formation and fight against their pathogenic activity.

  15. Organometallic Polymeric Conductors

    Science.gov (United States)

    Youngs, Wiley J.

    1997-01-01

    For aerospace applications, the use of polymers can result in tremendous weight savings over metals. Suitable polymeric materials for some applications like EMI shielding, spacecraft grounding, and charge dissipation must combine high electrical conductivity with long-term environmental stability, good processability, and good mechanical properties. Recently, other investigators have reported hybrid films made from an electrically conductive polymer combined with insulating polymers. In all of these instances, the films were prepared by infiltrating an insulating polymer with a precursor for a conductive polymer (either polypyrrole or polythiophene), and oxidatively polymerizing the precursor in situ. The resulting composite films have good electrical conductivity, while overcoming the brittleness inherent in most conductive polymers. Many aerospace applications require a combination of properties. Thus, hybrid films made from polyimides or other engineering resins are of primary interest, but only if conductivities on the same order as those obtained with a polystyrene base could be obtained. Hence, a series of experiments was performed to optimize the conductivity of polyimide-based composite films. The polyimide base chosen for this study was Kapton. 3-MethylThiophene (3MT) was used for the conductive phase. Three processing variables were identified for producing these composite films, namely time, temperature, and oxidant concentration for the in situ oxidation. Statistically designed experiments were used to examine the effects of these variables and synergistic/interactive effects among variables on the electrical conductivity and mechanical strength of the films. Multiple linear regression analysis of the tensile data revealed that temperature and time have the greatest effect on maximum stress. The response surface of maximum stress vs. temperature and time (for oxidant concentration at 1.2 M) is shown. Conductivity of the composite films was measured for

  16. Effect of Process Parameters on Flow Length and Flash Formation in Injection Moulding of High Aspect Ratio Polymeric Micro Features

    Directory of Open Access Journals (Sweden)

    Abdelkhalik Eladl

    2018-01-01

    Full Text Available This paper reports an investigation of the effects of process parameters on the quality characteristics of polymeric parts produced by micro injection moulding (μIM with two different materials. Four injection moulding process parameters (injection velocity, holding pressure, melt temperature and mould temperature were investigated using Polypropylene (PP and Acrylonitrile Butadiene Styrene (ABS. Three key characteristics of the mouldings were evaluated with respect to process settings and the material employed: part mass, flow length and flash formation. The experimentation employs a test part with four micro fingers with different aspect ratios (from 21 up to 150 and was carried out according to the Design of Experiments (DOE statistical technique. The results show that holding pressure and injection velocity are the most influential parameters on part mass with a direct effect for both materials. Both parameters have a similar effect on flow length for both PP and ABS at all aspect ratios and have higher effects as the feature thickness decreased below 300 μm. The study shows that for the investigated materials the injection speed and packing pressure were the most influential parameters for increasing the amount of flash formation, with relative effects consistent for both materials. Higher melt and mould temperatures settings were less influential parameters for increasing the flash amount when moulding with both materials. Of the two investigated materials, PP was the one exhibiting more flash formation as compared with ABS, when corresponding injection moulding parameters settings for both materials were considered.

  17. Polymeric microspheres with N-methyl-D-glucamine ligands for boron removal from water solution by adsorption-membrane filtration process.

    Science.gov (United States)

    Wolska, Joanna; Bryjak, Marek; Kabay, Nalan

    2010-08-01

    Polymeric microspheres with N-methyl-D-glucamine (NMDG) ligands have been tested in the adsorption-membrane filtration process for boron removal from aqueous solutions. The chelating resins were synthesized by reacting NMDG with the vinylbenzyl chloride-styrene-1,4-divinylbenzene (VBC/S/DVB) copolymer at the reflux temperature and in the microwave reactor. VBC/S/DVB spheres with a gel structure that contained 6 wt% DVB were obtained by membrane emulsification followed by suspension polymerization. By selecting the optimal emulsification and polymerization parameters, it was possible to obtain 25-microm-diameter particles with a narrow size distribution. Resins obtained by microwave modification showed the higher boron adsorption capacity.

  18. Robotic-Controlled, Autonomous Friction Stir Welding Processes for In-Situ Fabrication, Maintenance, and Repair

    Science.gov (United States)

    Zhou, W.

    NASA s new vision of human and robotic missions to the Moon Mars and beyond will demand large and permanent infrastructures on the Moon and other planets including power plants communication towers human and biomass habitats launch and landing facilities fabrication and repair workshops and research facilities so that material utilization and product development can be carried out and subsisted in-situ The conventional approach of transporting pre-constructed fabricated structures from earth to the Moon planets will no longer be feasible due to limited lifting capacity and extremely high transportation costs associated with long duration space travel To minimize transport of pre-made large structures between earth and the Moon planets minimize crew time for the fabrication and assembly of infrastructures on the Moon planets and to assure crew safety and maintain quality during the operation there is a strong need for robotic capabilities for in-situ fabrication maintenance and repair Clearly development of innovative autonomous in-situ fabrication maintenance and repair technologies is crucial to the success of both NASA s unmanned preparation missions and manned exploration missions In-space material joining is not new to NASA Many lessons were learned from NASA s International Space Welding Experiment which employed the Electron Beam Welding process for space welding experiments Significant safety concerns related to high-energy beams arcing spatter elecromagnetic fields and molten particles were

  19. Impact of process temperature on GaSb metal-oxide-semiconductor interface properties fabricated by ex-situ process

    Energy Technology Data Exchange (ETDEWEB)

    Yokoyama, Masafumi, E-mail: yokoyama@mosfet.t.u-tokyo.ac.jp; Takenaka, Mitsuru; Takagi, Shinichi [Department of Electrical Engineering and Information Systems, The University of Tokyo, Yayoi 2-11-16, Bunkyo, Tokyo 113-0032 (Japan); JST-CREST, Yayoi 2-11-16, Bunkyo, Tokyo 113-0032 (Japan); Asakura, Yuji [Department of Electrical Engineering and Information Systems, The University of Tokyo, Yayoi 2-11-16, Bunkyo, Tokyo 113-0032 (Japan); Yokoyama, Haruki [NTT Photonics Laboratories, NTT Corporation, Atsugi 243-0198 (Japan)

    2014-06-30

    We have studied the impact of process temperature on interface properties of GaSb metal-oxide-semiconductor (MOS) structures fabricated by an ex-situ atomic-layer-deposition (ALD) process. We have found that the ALD temperature strongly affects the Al{sub 2}O{sub 3}/GaSb MOS interface properties. The Al{sub 2}O{sub 3}/GaSb MOS interfaces fabricated at the low ALD temperature of 150 °C have the minimum interface-trap density (D{sub it}) of ∼4.5 × 10{sup 13 }cm{sup −2} eV{sup −1}. We have also found that the post-metalization annealing at temperature higher than 200 °C degrades the Al{sub 2}O{sub 3}/GaSb MOS interface properties. The low-temperature process is preferable in fabricating GaSb MOS interfaces in the ex-situ ALD process to avoid the high-temperature-induced degradations.

  20. In situ Resource Utilization for Processing of Metal Alloys on Lunar and Mars Bases

    Science.gov (United States)

    Stefanescu, D. M.; Grugel, R. N.; Curreri, P. A.

    1998-01-01

    Current plans for practical missions leading to a sustained human presence on our Moon and Mars rely on utilizing their in situ resources. Initially, resource availability must be assessed followed by the development of economically acceptable and technically feasible extractive processes. In regard to metals processing and fabrication, the lower gravity level on the Moon (0.125 g) and Mars (0.369 g) will dramatically change the presently accepted hierarchy of materials in terms of specific properties, a factor which must be understood and exploited. Furthermore, significant changes are expected in the behavior of liquid metals during processing. In metal casting, for example, mold filling and associated solidification processes have to be reevaluated. Finally, microstructural development and therefore material properties, presently being documented through ongoing research in microgravity science and applications, needs to be understood and scaled to the reduced gravity environments. These and other issues are addressed in this paper.

  1. Synthesis of gold and silver nanoparticle S-ovalbumin protein conjugates by in situ conjugation process

    Energy Technology Data Exchange (ETDEWEB)

    Joshi, Deepti, E-mail: deeptimishrajoshi@gmail.com; Soni, R. K. [Indian Institute of Technology Delhi, Physics Department (India)

    2015-05-15

    Pure gold and silver nanoparticle (NP) generation and their conjugation with protein S-ovalbumin using in situ conjugation process have been reported. The in situ conjugation involves nanosecond pulse laser ablation of pure metal target in the protein S-ovalbumin solution. Transmission electron microscopy (TEM) and UV–Visible absorption results show decrease in mean NP size along with narrow particle size distribution on ablation in S-ovalbumin solution as compared to ablation in water for both Au and Ag NPs. Also, the NP size reduction was found to be dependent on the concentration of S-ovalbumin. For AuNPs, spherical NPs of mean size 4 nm with particle size distribution 2–6 nm were obtained at 300 nM S-ovalbumin concentration. Further, it has been observed that the resultant in situ-conjugated colloid gold and silver NP solutions were quite stable even in the presence of NaCl at physiological salt concentration (0.15 M). On post-laser irradiation (532 nm, 15 mJ) for 20 min, 9 nm red shift in surface plasmon resonance peak (SPR), along with increased broadening towards longer wavelength, was observed in the AuNPs–S-ovalbumin sample. Further increase in the time of irradiation showed shift in AuNPs–S-ovalbumin SPR towards lower wavelength. On laser irradiation (532 nm, 15 mJ) for 20 min, no significant change was observed in the line shape of the plasmon absorption band of the AgNPs–S-ovalbumin conjugate. FTIR spectra revealed that S-ovalbumin peptide backbone and secondary structure remain unchanged on laser irradiation during in situ conjugation process. Thus, integrity of S-ovalbumin does not get affected, and no degradation of S-ovalbumin takes place on laser-induced in situ conjugation. Raman results confirm that both Au and Ag NPs interact with S-ovalbumin via thiol-bearing cysteine residues of the disulfide bond.

  2. 3D printing processes for photocurable polymeric materials: technologies, materials, and future trends.

    Science.gov (United States)

    Taormina, Gabriele; Sciancalepore, Corrado; Messori, Massimo; Bondioli, Federica

    2018-04-01

    The aim of this review is a faithful report of the panorama of solutions adopted to fabricate a component using vat photopolymerization (VP) processes. A general overview on additive manufacturing and on the different technologies available for polymers is given. A comparison between stereolithography and digital light processing is also presented, with attention to different aspects and to the advantages and limitations of both technologies. Afterward, a quick overview of the process parameters is given, with an emphasis on the necessities and the issues associated with the VP process. The materials are then explored, starting from base matrix materials to composites and nanocomposites, with attention to examples of applications and explanations of the main factors involved.

  3. Methods of producing alkylated hydrocarbons from an in situ heat treatment process liquid

    Science.gov (United States)

    Roes, Augustinus Wilhelmus Maria [Houston, TX; Mo, Weijian [Sugar Land, TX; Muylle, Michel Serge Marie [Houston, TX; Mandema, Remco Hugo [Houston, TX; Nair, Vijay [Katy, TX

    2009-09-01

    A method for producing alkylated hydrocarbons is disclosed. Formation fluid is produced from a subsurface in situ heat treatment process. The formation fluid is separated to produce a liquid stream and a first gas stream. The first gas stream includes olefins. The liquid stream is fractionated to produce at least a second gas stream including hydrocarbons having a carbon number of at least 3. The first gas stream and the second gas stream are introduced into an alkylation unit to produce alkylated hydrocarbons. At least a portion of the olefins in the first gas stream enhance alkylation.

  4. AVARIS - AREVA Valve Repair in-Situ. Innovative technology and processes

    International Nuclear Information System (INIS)

    Schultz, Ch.

    2012-01-01

    Concept of in-situ welding and turning machine is explained. The AVARIS processes are: Disassembly Evaluation Turning Welding Finish turning Penetration test Grinding Reassembly Result - The seats are within the dimensional and hardness tolerances. The repaired valves with AVARIS as in the case of Isar 2 in 2010 did not show any indications after one year in operation Advantages: Development based on an approved and safe technology; Capability for improving and/or modification of the hardfacing material according to specific system conditions; Minimization of dose exposure (ALARA)

  5. Atmospheric pressure plasma processing of polymeric materials utilizing close proximity indirect exposure

    Science.gov (United States)

    Paulauskas, Felix L.; Bonds, Truman

    2016-09-20

    A plasma treatment method that includes providing treatment chamber including an intermediate heating volume and an interior treatment volume. The interior treatment volume contains an electrode assembly for generating a plasma and the intermediate heating volume heats the interior treatment volume. A work piece is traversed through the treatment chamber. A process gas is introduced to the interior treatment volume of the treatment chamber. A plasma is formed with the electrode assembly from the process gas, wherein a reactive species of the plasma is accelerated towards the fiber tow by flow vortices produced in the interior treatment volume by the electrode assembly.

  6. In-situ Non-destructive Studies on Biofouling Processes in Reverse Osmosis Membrane Systems

    KAUST Repository

    Farhat, Nadia

    2016-12-01

    Reverse osmosis (RO) and nanofiltration (NF) membrane systems are high-pressure membrane filtration processes that can produce high quality drinking water. Biofouling, biofilm formation that exceeds a certain threshold, is a major problem in spiral wound RO and NF membrane systems resulting in a decline in membrane performance, produced water quality, and quantity. In practice, detection of biofouling is typically done indirectly through measurements of performance decline. Existing direct biofouling detection methods are mainly destructive, such as membrane autopsies, where biofilm samples can be contaminated, damaged and resulting in biofilm structural changes. The objective of this study was to test whether transparent luminescent planar oxygen sensing optodes, in combination with a simple imaging system, can be used for in-situ, non-destructive biofouling characterization. Aspects of the study were early detection of biofouling, biofilm spatial patterning in spacer filled channels, and the effect of feed cross-flow velocity, and feed flow temperature. Oxygen sensing optode imaging was found suitable for studying biofilm processes and gave detailed spatial and quantitative biofilm development information enabling better understanding of the biofouling development process. The outcome of this study attests the importance of in-situ, non-destructive imaging in acquiring detailed knowledge on biofilm development in membrane systems contributing to the development of effective biofouling control strategies.

  7. Focused beam reflectance measurement as a tool for in situ monitoring of the lactose crystallization process.

    Science.gov (United States)

    Pandalaneni, K; Amamcharla, J K

    2016-07-01

    Lactose accounts for about 75 and 85% of the solids in whey and deproteinized whey, respectively. Production of lactose is usually carried out by a process called crystallization. Several factors including rate of cooling, presence of impurities, and mixing speed influence the crystal size characteristics. To optimize the lactose crystallization process parameters to maximize the lactose yield, it is important to monitor the crystallization process. However, efficient in situ tools to implement at concentrations relevant to the dairy industry are lacking. The objective of the present work was to use a focused beam reflectance measurement (FBRM) system for in situ monitoring of lactose crystallization at supersaturated concentrations (wt/wt) 50, 55, and 60% at 20 and 30°C. The FBRM data were compared with Brix readings collected using a refractometer during isothermal crystallization. Chord length distributions obtained from FBRM in the ranges of lactose crystallization at various concentrations and temperatures was successfully assessed in the study. Copyright © 2016 American Dairy Science Association. Published by Elsevier Inc. All rights reserved.

  8. Optimization of continuous triboelectrification process for polymeric materials in dry contact

    Science.gov (United States)

    Prawatya, Y. E.; Neagoe, M. B.; Zeghloul, T.; Dascalescu, L.

    2017-02-01

    Triboelectrification (i.e., generation of electric charge by friction between two materials) is a complex process. Besides the nature and condition of the surfaces in contact, several factors can have an influence on charge generation: pressure load and relative velocity between the two bodies, number of friction cycles, ambient temperature and humidity, condition and type of material surface. This paper aims at demonstrating that associating the experimental response surface methodology and genetic algorithms is an effective technique for the optimisation of triboelectrification process. The quadratic model derived from the experiments is used in a genetic algorithm program to find the optimal combination of factor values (10 sliding cycles; normal force: 10 N; sliding speed: 55 mm/s) that maximize the average potential at the surface of the tribocharged materials: -1633 V. A final experiment confirmed the prediction of the genetic algorithm. The conclusions of this experimental study can be applied to the optimisation of industrial triboelectrification processes, and contribute to the reduction of the related maintenance, energy and raw-material costs.

  9. Immobilization and continuous culture of cells with radiation polymerized supports for the uses of biomass conversion processes

    International Nuclear Information System (INIS)

    Kaetsu, I.; Kumakura, M.; Fujimura, T.; Tamada, M.; Kasai, N.

    1988-01-01

    A novel technique for immobilization and biofunctional components such as enzyme, antibody, protein, drug, hormone and organella by means of radiation polymerization was studied and developed. (E.G.) [pt

  10. In-situ observation of particles deposition process on a ferromagnetic filter during high-gradient magnetic separation process

    Energy Technology Data Exchange (ETDEWEB)

    Hirota, Noriyuki, E-mail: hirota.noriyuki@nims.go.jp [Fine Particle Engineering Group, National Institute for Materials Science, 3-13 Sakura, Tsukuba (Japan); Ando, Tsutomu; Takano, Tadamitsu [Department of Mechanical Engineering, Nihon University, 1-2-1 Izumicho, Narashino 275-8575 (Japan); Okada, Hidehiko [Fine Particle Engineering Group, National Institute for Materials Science, 3-13 Sakura, Tsukuba (Japan)

    2017-04-01

    Abstracts: In-situ observations of particles deposition process on a ferromagnetic filter in high gradient magnetic separation were carried out under high magnetic fields to obtain information for the optimization of separation condition. The spike-like deposition structure was observed on the upper stream of the magnetic filter, different from the conventional deposition image obtained for paramagnetic particles. The length of the spike structure tends to be long with lower flow velocity and lower applied magnetic field. It was also observed that the chain structure or the bundle of such chaines were formed on the way to the filter under the condition of the low applied magnetic field and low flow rates. Results obtained here indicate that the effect of deposited particles on the spatial distribution of the magnetic field and the hydrodynamics, they are often ignored in the simulation so far, should be considered appropriately. - Highlights: • In-situ observation of particles deposition process on a ferromagnetic filter in HGMS. • The spike-like deposition structure was observed on the upper stream. • Longer spike structure formed under lower magnetic fields and lower flow rates. • Effect of the magnetization of deposited particles should be considered appropriately.

  11. Discrete magic angle turning system, apparatus, and process for in situ magnetic resonance spectroscopy and imaging

    Science.gov (United States)

    Hu, Jian Zhi [Richland, WA; Sears, Jr., Jesse A.; Hoyt, David W [Richland, WA; Wind, Robert A [Kennewick, WA

    2009-05-19

    Described are a "Discrete Magic Angle Turning" (DMAT) system, devices, and processes that combine advantages of both magic angle turning (MAT) and magic angle hopping (MAH) suitable, e.g., for in situ magnetic resonance spectroscopy and/or imaging. In an exemplary system, device, and process, samples are rotated in a clockwise direction followed by an anticlockwise direction of exactly the same amount. Rotation proceeds through an angle that is typically greater than about 240 degrees but less than or equal to about 360 degrees at constant speed for a time applicable to the evolution dimension. Back and forth rotation can be synchronized and repeated with a special radio frequency (RF) pulse sequence to produce an isotropic-anisotropic shift 2D correlation spectrum. The design permits tubes to be inserted into the sample container without introducing plumbing interferences, further allowing control over such conditions as temperature, pressure, flow conditions, and feed compositions, thus permitting true in-situ investigations to be carried out.

  12. In situ diffraction studies of scale formation under Bayer processing conditions

    International Nuclear Information System (INIS)

    Webster, N.; Madsen, I.; Loan, J.

    2009-01-01

    Full text: The Bayer process is used to extract alumina (A I 203) from bauxite ore. The efficiency of the proc severely compromised by the build-up of insoluble species (scale) on the surfaces of mild process equipment, which impedes the material flow through, and heat transfer to, the pr streams [1]. In precipitation areas operating at 60-8 C gibbsite, AI(OHh, scales predominate the spent liquor heaters which typically operate at 150-250 0 C, sodalite and cancrinite-type s aluminosilicate scales are formed (1). An improved understanding of the scale formation mechanism may lead to the development of a practical and economic method for scale prevention. Characterisation of the structure, composition and crystallographic orientation of phases present early stages of formation is crucial for this understanding, making x-ray and neutron diffraction important analytical techniques. In situ synchrotron x-ray diffraction experiments were performed Australian Synchrotron during AI(OHh deposition on mild steel substrates using a purpose built stainless steel flow cell (3). The high resolution data enabled identification of three polymors AI(OH)3 (gibbsite, bayerite and nordtsrandite) in the deposited material, each displaying ori growth along (001). Additional in situ synchrotron XRD experiments, where AI(OH)3 precipitatiol 'seeded' with various iron oxides and oxyhydroxides, have also been performed and some ' results will be discussed. Similar neutron diffraction experiments on Wombat are planned investigations of seeded aluminosilicate precipitation at 150-250 0 C using an Inconel hydrothermal cell.

  13. Why in situ, real-time characterization of thin film growth processes?

    International Nuclear Information System (INIS)

    Auciello, O.; Krauss, A.R.

    1995-01-01

    Since thin-film growth occurs at the surface, the analytical methods should be highly surface-specific. although subsurface diffusion and chemical processes also affect film properties. Sampling depth and ambient-gas is compatibility are key factors which must be considered when choosing in situ probes of thin-film growth phenomena. In most cases, the sampling depth depends on the mean range of the exit species (ion, photon, or electron) in the sample. The techniques that are discussed in this issue of the MRS Bulletin (1) have been chosen because they may be used for in situ, real-time analysis of film-growth phenomena in vacuum and in the presence of ambient gases resulting either from the deposition process or as a requirement for the production of the desired chemical phase. A second criterion for inclusion is that the instrumentation be sufficiently compact and inexpensive to permit use as a dedicated tool in a thin-film deposition system

  14. Poly-thiosemicarbazide/gold nanoparticles catalytic membrane: In-situ growth of well-dispersed, uniform and stable gold nanoparticles in a polymeric membrane

    KAUST Repository

    Villalobos, Luis Francisco

    2014-11-01

    This work presents a method that achieves the highest loading, published so far, of non-agglomerated and well-distributed gold nanoparticles (AuNPs) inside a polymeric membrane. The method uses poly-thiosemicarbazide (PTSC) as the starting material for fabricating the membranes. This polymer contains one chelate site per monomeric unit, resulting in a high content of adsorption sites. This helps to achieve such high loading without agglomeration, along with the strong interaction of the chelate sites with the metal ions and the fact that they are distributed homogeneously along the membrane structure. The simple and scalable three-step procedure developed in this work resulted in a PTSC membrane containing 33.5 wt.% Au/PTSC in the form of 2.9 nm AuNPs. The membrane demonstrated catalytic activity for the reduction of 4-Nitrophenol (4-NP) to 4-Aminophenol (4-AP). © 2013 Elsevier B.V.

  15. Comparison of residual monomer loss from cold-cure orthodontic acrylic resins processed by different polymerization techniques.

    Science.gov (United States)

    Nik, Tahereh Hosseinzadeh; Shahroudi, Atefe Saffar; Eraghihzadeh, Zeinab; Aghajani, Farzaneh

    2014-03-01

    This investigation aimed to assess and compare the amount of residual monomer (RM) released from removable orthodontic appliances constructed by sprinkle-on and dough techniques. One hundred and twenty acrylic samples were prepared from orthodontic autopolymerized acrylic resins and divided into three groups, according to the processing method: sprinkle-on with polyclave, sprinkle-on without polyclave and dough technique. After polymerization, the specimens of each group were immersed in distilled water for 24 h, 48 h, 72 h and 1 week. High-performances liquid chromatography (HPLC) was utilized to measure residual monomer content. Maximum observed RM was 1284·91±129·07 ppm measured for sprinkle-on technique without polyclave after 24 h of water immersion. At this time, the level of RM was significantly different among the three applied techniques (Psprinkle-on technique with polyclave released the least amount of RM. Within each group, the maximum monomer releasing was observed after the first 24 h and decreases were observed in subsequent time groups. The reduction over the time was not significant in the polyclave groups (P>0·05). The sprinkle-on technique with polyclave and longer water immersion reduced residual monomer released from acrylic orthodontic appliances.

  16. Process Design and Economics for the Conversion of Lignocellulosic Biomass to Hydrocarbon Fuels. Thermochemical Research Pathways with In Situ and Ex Situ Upgrading of Fast Pyrolysis Vapors

    Energy Technology Data Exchange (ETDEWEB)

    Dutta, A.; Sahir, A.; Tan, E.; Humbird, D.; Snowden-Swan, L. J.; Meyer, P.; Ross, J.; Sexton, D.; Yap, R.; Lukas, J.

    2015-03-01

    This report was developed as part of the U.S. Department of Energy’s Bioenergy Technologies Office’s efforts to enable the development of technologies for the production of infrastructurecompatible, cost-competitive liquid hydrocarbon fuels from biomass. Specifically, this report details two conceptual designs based on projected product yields and quality improvements via catalyst development and process integration. It is expected that these research improvements will be made within the 2022 timeframe. The two conversion pathways detailed are (1) in situ and (2) ex situ upgrading of vapors produced from the fast pyrolysis of biomass. While the base case conceptual designs and underlying assumptions outline performance metrics for feasibility, it should be noted that these are only two of many other possibilities in this area of research. Other promising process design options emerging from the research will be considered for future techno-economic analysis.

  17. Up-scaling the production of modified a-C:H coatings in the framework of plasma polymerization processes

    Science.gov (United States)

    Corbella, C.; Bialuch, I.; Kleinschmidt, M.; Bewilogua, K.

    2009-10-01

    Hydrogenated amorphous carbon (a-C:H) films with silicon and oxygen additions, which exhibit mechanical, tribological and wetting properties adequate for protective coating performance, have been synthesized at room temperature in a small- (0.1 m 3) and a large-scale (1 m 3) coaters by low-pressure Plasma-Activated Chemical Vapour Deposition (PACVD). Hence, a-C:H:Si and a-C:H:Si:O coatings were produced in atmospheres of tetramethylsilane (TMS) and hexamethyldisiloxane (HMDSO), respectively, excited either by radiofrequency (RF - small scale) or by pulsed-DC power (large scale). Argon was employed as a carrier gas to stabilize the glow discharge. Several series of 2-5 μm thick coatings have been prepared at different mass deposition rates, Rm, by varying total gas flow, F, and input power, W. Arrhenius-type plots of Rm/ F vs. ( W/ F) -1 show linear behaviours for both plasma reactors, as expected for plasma polymerization processes at moderated energies. The calculation of apparent activation energy, Ea, in each series permitted us to define the regimes of energy-deficient and monomer-deficient PACVD processes as a function of the key parameter W/ F. Moreover, surface properties of the modified a-C:H coatings, such as contact angle, abrasive wear rate and hardness, appear also correlated to this parameter. This work shows an efficient methodology to scale up PACVD processes from small, lab-scale plasma machines to industrial plants by the unique evaluation of macroscopic parameters of deposition.

  18. A numerical approach to drying process of hygroscopic polymeric granulates with different drying configurations and parameter comparison

    Science.gov (United States)

    Mahbub, A. M. Ishtiaque; Mawa, Zannatul

    2017-06-01

    Some polymers tend to possess affinity with water and eventually, absorb significant moisture content from the surrounding air, causing difficulties during their industrial processing. Drying of these hygroscopic polymers, therefore, plays a vital role in their usability in industrial applications. In this work, the drying kinetics of the polymeric granulates is numerically formulated and the influence of different parameters pertaining to the drying procedure has been investigated. Backward Euler or implicit algorithm has been considered for solving the second order partial differential heat and mass transfer equations for simulating the drying kinetics of Polyamide 6 (PA-6). At first, the conduction of heat from the granulate surface towards the core was formulated using one dimensional transient heat conduction law and corresponding diffusion coefficients were determined using Arrhenius diffusion model. Afterwards, the migration of moisture from the granulate core towards the surface has been calculated using Fick's second law of diffusion. The data obtained from the single polymer granulate was then used to calculate the amount of moisture removed and the drying rate. The numerical results showed similitude with the experimental data obtained from the literature, although deviated quantitatively. To investigate the influence of different parameters on the drying process, different cases with varying drying air temperature, granulate radius and initial moisture content were compared. The numerical analysis qualitatively predicted all the dependencies to be expected. With higher drying air temperature, drying rate was observed to be faster and with higher granulate radius, drying rate was slower. With better approximations of the applied parameters and algorithms, the accuracy of the developed numerical model could be improved and used as a prediction tool for the drying process of polymer samples with reasonable tolerance.

  19. Sustained-release microsphere formulation containing an agrochemical by polyurethane polymerization during an agitation granulation process.

    Science.gov (United States)

    Terada, Takatoshi; Tagami, Manabu; Ohtsubo, Toshiro; Iwao, Yasunori; Noguchi, Shuji; Itai, Shigeru

    2016-07-25

    In this report, a new solventless microencapsulation method by synthesizing polyurethane (PU) from polyol and isocyanate during an agglomeration process in a high-speed mixing apparatus was developed. Clothianidin (CTD), which is a neonicotinoid insecticide and highly effective against a wide variety of insect pests, was used as the model compound. The microencapsulated samples covered with PU (CTD microspheres) had a median diameter of <75μm and sustained-release properties. The CTD microspheres were analyzed by synchrotron X-ray computed tomography measurements. Multiple cores of CTD and other solid excipient were dispersed in PU. Although voids appeared in the CTD microspheres after CTD release, the spherical shape of the microspheres remained stable and no change in its framework was observed. The experimental release data were highly consistent with the Baker-Lonsdale model derived from drug release of spherical monolithic dispersions and consistent with the computed tomography measurements. Copyright © 2016 Elsevier B.V. All rights reserved.

  20. In-situ OMVPE process sensing of GaAs and AlGaAs by photoreflectance

    Science.gov (United States)

    Capuder, K.; Norris, P. E.; Shen, H.; Hang, Z.; Pollak, F. H.

    1990-04-01

    The contactless electromodulation method of photoreflectance has been successfully applied as an in-situ sensor of the OMVPE process. The direct band gap, E 0, of GaAs and AIGaAs has been measured, in-situ, under OMVPE growth conditions. To the best of our knowledge, this is the first report of an in-situ photoreflectance measurement of III-V materials properties in an OMVPE system. This is significant in that it illustrates the potential for the application of photoreflectance as an in-situ process monitor, analogous to the use of RHEED measurements in MBE. The GaAs substrate temperature of 650°, as measured by an optical pyrometer, corresponds to the temperature derived using the Varshni equation and published Varshni coefficients to within the error of the published data.

  1. Morphology Development in Solution-Processed Functional Organic Blend Films: An In Situ Viewpoint

    KAUST Repository

    Richter, Lee J.

    2017-04-17

    Solution-processed organic films are a facile route to high-speed, low cost, large-area deposition of electrically functional components (transistors, solar cells, emitters, etc.) that can enable a diversity of emerging technologies, from Industry 4.0, to the Internet of things, to point-of-use heath care and elder care. The extreme sensitivity of the functional performance of organic films to structure and the general nonequilibrium nature of solution drying result in extreme processing-performance correlations. In this Review, we highlight insights into the fundamentals of solution-based film deposition afforded by recent state-of-the-art in situ measurements of functional film drying. Emphasis is placed on multimodal studies that combine surface-sensitive X-ray scattering (GIWAXS or GISAXS) with optical characterization to clearly define the evolution of solute structure (aggregation, crystallinity, and morphology) with film thickness.

  2. Identification of chemical processes influencing constituent mobility during in-situ uranium leaching

    International Nuclear Information System (INIS)

    Sherwood, D.R.; Hostetler, C.J.; Deutsch, W.J.

    1984-07-01

    In-situ leaching of uranium has become a widely accepted method for production of uranium concentrate from ore zones that are too small, too deep, and/or too low in grade to be mined by conventional techniques. One major environmental concern that exists with in-situ leaching of uranium is the possible adverse effects mining might have on regional ground water quality. The leaching solution (lixiviant), which extracts uranium from the ore zone, might also mobilize other potential contaminants (As, Se, Mo, and SO 4 ) associated with uranium ore. Column experiments were performed to investigate the geochemical interactions between a lixiviant and a uranium ore during in-situ leaching and to identify chemical processes that might influence contaminant mobility. The analytical composition data for selected column effluents were used with the MINTEQ code to develop a computerized geochemical model of the system. MINTEQ was used to calculate saturation indices for solid phases based on the composition of the solution. A potential constraint on uranium leaching efficiency appears to be the solubility control of schoepite. Gypsum and powellite solubilities may limit the mobilities of sulfate and molybdenum, respectively. In contrast, the mobilities of arsenic and selenium were not limited by solubility constraints, but were influenced by other chemical interaction between the solution and sediment, perhaps adsorption. Bulk chemical and mineralogical analyses were performed on both the original and leached ores. Using these analyses together with the column effluent data, mass balance calculations were performed on five constituents based on solution chemical analysis and bulk chemical and γ-spectroscopy analysis for the sediment. 6 references, 10 figures, 10 tables

  3. In situ biosynthesis of bacterial nanocellulose-CaCO3 hybrid bionanocomposite: One-step process

    International Nuclear Information System (INIS)

    Mohammadkazemi, Faranak; Faria, Marisa; Cordeiro, Nereida

    2016-01-01

    In this work, a simple and green route to the synthesis of the bacterial nanocellulose-calcium carbonate (BNC/CaCO 3 ) hybrid bionanocomposites using one-step in situ biosynthesis was studied. The CaCO 3 was incorporated in the bacterial nanocellulose structure during the cellulose biosynthesis by Gluconacetobacter xylinus PTCC 1734 bacteria. Hestrin-Schramm (HS) and Zhou (Z) culture media were used to the hybrid bionanocomposites production and the effect of ethanol addition was investigated. Attenuated total reflection Fourier transform infrared spectroscopy, field emission scanning electron microscopy, X-ray diffraction, energy-dispersive X-ray spectroscopy, inverse gas chromatography and thermogravimetric analysis were used to characterize the samples. The experimental results demonstrated that the ethanol and culture medium play an important role in the BNC/CaCO 3 hybrid bionanocomposites production, structure and properties. The BNC/CaCO 3 biosynthesized in Z culture medium revealed higher O/C ratio and amphoteric surface character, which justify the highest CaCO 3 content incorporation. The CaCO 3 was incorporated into the cellulosic matrix decreasing the bacterial nanocellulose crystallinity. This work reveals the high potential of in situ biosynthesis of BNC/CaCO 3 hybrid bionanocomposites and opens a new way to the high value-added applications of bacterial nanocellulose. - Graphical Abstract: Display Omitted - Highlights: • BNC/CaCO 3 hybrid bionanocomposites were produced using in situ biosynthesis process. • Ethanol and culture medium play an important role in the production and properties. • Z-BNC/CaCO 3 bionanocomposites revealed higher O/C ratio and amphoteric surface character. • CaCO 3 incorporated into the BNC decreased crystallinity.

  4. Properties and electronic structures of titanium aluminides-alumina composites from in-situ SHS process

    Energy Technology Data Exchange (ETDEWEB)

    Shen, Y.F., E-mail: dinahyfsh@hotmail.com [School of Chemistry and Chemical Engineering, Guangxi University, Nanning, Guangxi 530000 (China); Key Laboratory of New Processing Technology for Nonferrous Metals and Materials, Ministry of Education, Guilin University of Technology, Guilin, Guangxi 541004 (China); Zou, Z.G., E-mail: zouzg@glite.edu.cn [Key Laboratory of New Processing Technology for Nonferrous Metals and Materials, Ministry of Education, Guilin University of Technology, Guilin, Guangxi 541004 (China); Xiao, Z.G.; Liu, K.; Long, F.; Wu, Y. [Key Laboratory of New Processing Technology for Nonferrous Metals and Materials, Ministry of Education, Guilin University of Technology, Guilin, Guangxi 541004 (China)

    2011-02-25

    Research highlights: {yields} In-situ SHS processing method plus vacuum hot-pressing process were applied. {yields} Mechanical and electronic properties and microscopic structures were studied. {yields} First principle pseudopotential plane-wave-based DFT calculations were performed. - Abstract: Titanium aluminides-alumina composite was synthesized by in-situ self-propagating high-temperature synthesis (SHS) method, followed by hot-pressing process. To understand the fundamental differences between the composite and A1{sub 2}O{sub 3} ceramic, a comparative study was carried out using first-principles plane-wave pseudopotential method based on density functional theory (DFT). XRD analysis of final products confirmed the formation of TiAl, A1{sub 2}O{sub 3} and a small amount of Ti{sub 3}Al phases in the composites and the reaction mechanisms of the process were proposed. SEM observation revealed that a two-phase ({gamma} + {alpha}{sub 2}) TiAl-Ti{sub 3}Al lamellar structure was formed, and the composites exhibited a homogeneous microstructure. Moreover, density of states (DOS), band structure, charge density difference and Mulliken population analysis showed that metallic, covalent and ionic bonding were produced at the interfaces of the composite. O-Al interface bonds showed more covalent character with respect to pure Al{sub 2}O{sub 3}. Therefore, interface combination of the composite was improved, making the composite tougher (a toughness as high as 7.9 MPa m{sup 1/2}) than monophase Al{sub 2}O{sub 3} ceramic.

  5. Microstructures of Metallic NiCrBSi Coatings Manufactured via Hybrid Plasma Spray and In Situ Laser Remelting Process

    OpenAIRE

    Serres, Nicolas; Hlawka, Françoise; Costil, Sophie; Langlade, Cécile; Machi, Frédérique

    2011-01-01

    International audience; This paper deals with coating alternatives to hard chromium plating. Thermal spraying is already used in industry, but results are not always satisfactory for reasons of porosity and microstructures. In this study, atmospheric plasma spraying (APS) and in situ laser irradiation by diode laser processes were combined to modify the structural characteristics of thick NiCrBSi alloy layers. The microstructure evolution was studied, and results show that in situ laser remel...

  6. Development and Modeling of a Novel Self-Assembly Process for Polymer and Polymeric Composite Nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Sumpter, Bobby G. [ORNL; Carrillo, Jan-Michael Y. [ORNL; Ahn, Suk-Kyun [ORNL; Barnes, Mike D. [University of Massachusetts, Amherst; Shelton, William A. [Pacific Northwest National Laboratory (PNNL); Harrison, Robert J. [Stony Brook University (SUNY); W. Noid, Donald [Retired

    2017-10-01

    Extensive computational simulations and experiments have been used to investigate the structure, dynamics and resulting photophysical properties of a number para-phenylenevinylene (PPV) based polymers and oligomers. These studies have shown how the morphology and structure are controlled to a large extent by the nature of the solute-solvent interactions in the initial solution phase preparation. A good solvent such as dichloromethane generates non-compact structures with more of a defect-extended chain like morphology while a bad solvent such as toluene leads to compact organized and folded structures with rod-like morphologies. Secondary structural organization is induced by using the solution phase structures to generate solvent-free single molecule nanoparticles. These nanoparticles are very compact and rod shaped, consisting of near-cofacial ordering of the conjugated PPV chain backbones between folds located at tetrahedral defects (sp3 C-C bonds). The resulting photophysical properties exhibit a significant enhancement in the photoluminescence quantum yield, lifetime, and stability. In addition, the single molecule nanoparticles have Gaussian-like emission spectra with discrete center frequencies that are correlated to a conjugation length, allowing the design of nanoparticles which luminesces at a particular frequency. We followed a similar approach and applied a comparable methodology in our recent work on polythiophenes in order to study the effect of polymer architecture on nanoscale assembly. Unlike linear chains of comparable size, we observed aggregation of the bottlebrush architecture of poly(norbornene)-g-poly(3-hexylthiophene) (PNB-g-P3HT) after the freeze-drying and dissolution processes. The behavior can be attributed to a significant enhancement in the number of π-π interactions between grafted P3HT side chains.

  7. STANFORD IN-SITU HIGH RATE YBCO PROCESS: TRANSFER TO METAL TAPES AND PROCESS SCALE UP

    Energy Technology Data Exchange (ETDEWEB)

    Malcolm R. Beasley; Robert H.Hammond

    2009-04-14

    Executive Summary The materials science understanding of high rate low cost processes for Coated Conductor will benefit the application to power utilities for low loss energy transportation and power generation as well for DOD applications. The research in this program investigated several materials processing approaches that are new and original, and are not being investigated elsewhere. This work added to the understanding of the material science of high rate PVD growth of HTSC YBCO assisted by a liquid phase. A new process discovered uses amorphous glassy precursors which can be made at high rate under flexible conditions of temperature and oxygen, and later brought to conditions of oxygen partial pressure and temperature for rapid conversion to YBCO superconductor. Good critical current densities were found, but further effort is needed to optimize the vortex pinning using known artificial inclusions. A new discovery of the physics and materials science of vortex pinning in the HTSC system using Sm in place of Y came at growth at unusually low oxygen pressure resulting in clusters of a low or non superconducting phase within the nominal high temperature phase. The driving force for this during growth is new physics, perhaps due to the low oxygen. This has the potential for high current in large magnetic fields at low cost, applicable to motors, generators and transformers. The technical demands of this project were the motivation for the development of instrumentation that could be essential to eventual process scale up. These include atomic absorption based on tunable diode lasers for remote monitoring and control of evaporation sources (developed under DARPA support), and the utility of Fourier Transform Infrared Reflectivity (FTIR) for aid in the synthesis of complex thin film materials (purchased by a DURIP-AFOSR grant).

  8. Understanding aquatic microbial processes using EEM's and in-situ fluorescence sensors

    Science.gov (United States)

    Fox, Bethany; Attridge, John; Rushworth, Cathy; Cox, Tim; Anesio, Alexandre; Reynolds, Darren

    2015-04-01

    The diverse origin of dissolved organic matter (DOM) in aquatic systems is well documented within the literature. Previous literature indicates that coloured dissolved organic matter (CDOM) is, in part, transformed by aquatic microbial processes, and that dissolved organic material derived from a microbial origin exhibits tryptophan-like fluorescence. However, this phenomenon is not fully understood and very little data is available within the current literature. The overall aim of our work is to reveal the microbial-CDOM interactions that give rise to the observed tryptophan-like fluorescence. The work reported here investigates the microbial processes that occur within freshwater aquatic samples, as defined by the biochemical oxygen demand (BOD) test, as a function of the T1 peak (λex/em 280/330-370 nm). A series of standard water samples were prepared using glucose, glutamic acid, BOD dilution water and a bacterial seed (Cole-Parmer BOD microbe capsules). Samples were spiked with CDOM (derived from an environmental water body) and subjected to time resolved BOD analysis and as excitation-emission fluorescence spectroscopy. All EEM spectral data was interrogated using parallel factor analysis (PARAFAC) in an attempt to determine the presence and dominance (relative intensities) of the CDOM-related and T1-related fluorophores within the samples. In-situ fluorescence sensors (Chelsea Technologies Group Ltd.) were also used to monitor the T1 fluorescence peak (UviLux Tryptophan) and the CDOM fluorescence peak (UviLux CDOM) during experiments. Tryptophan-like fluorescence was observed (albeit transient) in both spiked and un-spiked standard water samples. By furthering our understanding of aquatic organic matter fluorescence, its origin, transformation, fate and interaction with aquatic microbiological processes, we aim to inform the design of a new generation in-situ fluorescence sensor for the monitoring of aquatic ecosystem health.

  9. A Micro-Comb Test System for In Situ Investigation of Infiltration and Crystallization Processes

    Directory of Open Access Journals (Sweden)

    Dominik Gruber

    2017-10-01

    Full Text Available The investigation of mineralization and demineralization processes is important for the understanding of many phenomena in daily life. Many crystalline materials are exposed to decay processes, resulting in lesions, cracks, and cavities. Historical artifacts, for example, often composed of calcium carbonate (CaCO3, are damaged by exposure to acid rain or temperature cycles. Another example for lesions in a crystalline material is dental caries, which lead to the loss of dental hard tissue, mainly composed of hydroxyapatite (HAp. The filling of such cavities and lesions, to avoid further mineral loss and enable or support the remineralization, is a major effort in both areas. Nevertheless, the investigation of the filling process of these materials into the cavities is difficult due to the non-transparency and crystallinity of the concerned materials. In order to address this problem, we present a transparent, inexpensive, and reusable test system for the investigation of infiltration and crystallization processes in situ, being able to deliver datasets that could potentially be used for quantitative evaluation of the infiltration process. This was achieved using a UV-lithography-based micro-comb test system (MCTS, combined with self-assembled monolayers (SAMs to mimic the surface tension/wettability of different materials, like marble, sandstone, or human enamel. Moreover, the potential of this test system is illustrated by infiltration of a CaCO3 crystallization solution and a hydroxyapatite precursor (HApP into the MCTS.

  10. Novel in situ resistance measurement for the investigation of CIGS growth in a selenization process

    International Nuclear Information System (INIS)

    Liu Wei; He Qing; Li Fengyan; Li Changjian; Sun Yun; Tian Jianguo; Li Zubin

    2009-01-01

    During the selenization process of CIGS thin films, the relation between the element loss rate and the precursor depositions are analyzed. The growth of the CIGS thin films during the selenization process is investigated by the novel in situ resistance measurement, by which the formation of compound semiconductors can be observed directly and simultaneously. Their structures, phase evolutions and element losses are analyzed by XRD and XRF. Based on the experimental results, it can be concluded that the phase transforms have nothing to do with the deposition sequences of precursors, while the element loss rates are related to the deposition sequences in this process. In addition, element loss mechanisms of CIGS thin films prepared by the selenization process are analyzed by the phase evolutions and chemical combined path in the In, Ga–Se reaction processes. Moreover it is verified that the element losses are depressed by increasing the ramping-up rate finally. The results provide effective methods to fabricate high-quality CIGS thin films with low element losses

  11. Modeling and Analysis of the Reverse Water Gas Shift Process for In-Situ Propellant Production

    Science.gov (United States)

    Whitlow, Jonathan E.

    2000-01-01

    This report focuses on the development of mathematical models and simulation tools developed for the Reverse Water Gas Shift (RWGS) process. This process is a candidate technology for oxygen production on Mars under the In-Situ Propellant Production (ISPP) project. An analysis of the RWGS process was performed using a material balance for the system. The material balance is very complex due to the downstream separations and subsequent recycle inherent with the process. A numerical simulation was developed for the RWGS process to provide a tool for analysis and optimization of experimental hardware, which will be constructed later this year at Kennedy Space Center (KSC). Attempts to solve the material balance for the system, which can be defined by 27 nonlinear equations, initially failed. A convergence scheme was developed which led to successful solution of the material balance, however the simplified equations used for the gas separation membrane were found insufficient. Additional more rigorous models were successfully developed and solved for the membrane separation. Sample results from these models are included in this report, with recommendations for experimental work needed for model validation.

  12. Enhanced thermal and mechanical properties of PLA/MoS2 nanocomposites synthesized via the in-situ ring-opening polymerization

    Science.gov (United States)

    Chen, Pengpeng; Liang, Xiao; Xu, Ying; Zhou, Yifeng; Nie, Wangyan

    2018-05-01

    In this work, MoS2 nanosheets were employed to reinforce PLA. In order to promote the homogeneous dispersion of MoS2 in PLA and form a strong interface between MoS2 and PLA, the MoS2 nanosheets were firstly modified by mercapto-ethylamine, and then functionalized with PLA chains through ring-opening polymerization of poly(L-lactide). The XRD, XPS, TGA and 1H NMR characterizations confirmed the successful amino and PLA functionalization of MoS2 nanosheets. The obtained MoS2-g-PLA nanosheets were then introduced to reinforce PLA. SEM images displayed that the MoS2-g-PLA nanosheets were dispersed in PLA matrix uniformly. TGA results showed that initial decomposition temperature was improved from 275.6 °C to 334.8 °C with 0.5 wt% of MoS2-g-PLA nanosheets. The storage modulus of PLA/MoS2-g-PLA-0.5 wt% in the glass state and rubber state were both greatly enhanced compared with neat PLA.

  13. Hydrous pyrolysis/oxidation process for in situ destruction of chlorinated hydrocarbon and fuel hydrocarbon contaminants in water and soil

    Science.gov (United States)

    Knauss, Kevin G.; Copenhaver, Sally C.; Aines, Roger D.

    2000-01-01

    In situ hydrous pyrolysis/oxidation process is useful for in situ degradation of hydrocarbon water and soil contaminants. Fuel hydrocarbons, chlorinated hydrocarbons, polycyclic aromatic hydrocarbons, petroleum distillates and other organic contaminants present in the soil and water are degraded by the process involving hydrous pyrolysis/oxidation into non-toxic products of the degradation. The process uses heat which is distributed through soils and water, optionally combined with oxygen and/or hydrocarbon degradation catalysts, and is particularly useful for remediation of solvent, fuel or other industrially contaminated sites.

  14. Comparison of the flexural strength of polymethyl methacrylate resin reinforced with multiwalled carbon nanotubes and processed by conventional water bath technique and microwave polymerization.

    Science.gov (United States)

    Somkuwar, Surabhi; Mishra, Sunil Kumar; Agrawal, Benaiffer; Choure, Rupali

    2017-01-01

    This in vitro study was done to compare the flexural strength of polymethyl methacrylate resin reinforced with multiwalled carbon nanotubes (MWCNTs) and processed by conventional water bath technique and using microwave energy. A total of 180 acrylic resin specimens measuring 65 mm × 10 mm × 2.5 mm were fabricated, with conventional water bath groups and microwave group having ninety specimens each. Ninety specimens were divided into thirty specimens as control and subgroups containing 0.025% MWCNTs and 0.050% MWCNTs with thirty specimens each. The specimens were tested for flexural strength by three-point bending test on universal testing machine. The statistical analysis was done using Student's t -test and one-way analysis of variance, and the intercomparison between each group was done using Tukey's post hoc analysis. The mean flexural strength of specimens cured by water bath technique was 95.563 MPa and microwave technique was 118.416 MPa. Control Group B possesses highly significant increase in flexural strength than Control Group A with P < 0.01. Unpaired Student's t -test showed that Subgroup B1 and Subgroup B2 possess highly significant increase in flexural strength than Subgroup A1and Subgroup A2. Heat polymerized denture base resin with and without reinforcement of MWCNTs and polymerized by microwave technique possess higher flexural strength than heat polymerized fiber reinforced denture resin polymerized by water bath technique. MWCNTs could be used as an effective reinforcement material for denture base resin polymerized by either water bath technique or microwave energy.

  15. Sintering process optimization for multi-layer CGO membranes by in situ techniques

    DEFF Research Database (Denmark)

    Kaiser, Andreas; Prasad, A.S.; Foghmoes, Søren Preben Vagn

    2013-01-01

    changing in a narrow temperature range of less than 100 degrees C. Below 1030 degrees C, a higher densification rate in the dense membrane layer than in the porous support leads to concave shape, whereas the densification rate of the support is dominant above 1030 degrees C, leading to convex shape. A fiat...... bi-layer could be prepared at 1030 degrees C, when shrinkage rates were similar. In situ van der Pauw measurements on tape cast layers during sintering allowed following the conductivity during sintering. A strong increase in conductivity and in activation energy E-a for conduction was observed...... between 900 and 1030 degrees C indicating an activation of the reactive sintering process and phase transformation of cobalt oxide. (C) 2012 Elsevier Ltd. All rights reserved....

  16. In situ observation of magnetic orientation process of feeble magnetic materials under high magnetic fields

    Directory of Open Access Journals (Sweden)

    Noriyuki Hirota et al

    2008-01-01

    Full Text Available An in situ microscopic observation of the magnetic orientation process of feeble magnetic fibers was carried out under high magnetic fields of up to 10 T using a scanning laser microscope. In the experiment, carbon fibers and needle-like titania fibers with a length of 1 to 20 μm were used. The fibers were observed to gradually orient their axes parallel to the direction of the magnetic field. The orientation behavior of the sample fibers was evaluated on the basis of the measured duration required for a certain angular variation. As predicted from the theoretical consideration, it was confirmed that the duration required for a certain angular variation normalized by the viscosity of the fluid is described as a function of the fiber length. The results obtained here appear useful for the consideration of the magnetic orientation of materials suspended in a static fluid.

  17. In Situ Spectroscopic Analysis of the Carbothermal Reduction Process of Iron Oxides during Microwave Irradiation

    Directory of Open Access Journals (Sweden)

    Jun Fukushima

    2018-01-01

    Full Text Available The effects of microwave plasma induction and reduction on the promotion of the carbothermal reduction of iron oxides (α-Fe2O3, γ-Fe2O3, and Fe3O4 are investigated using in situ emission spectroscopy measurements during 2.45 GHz microwave processing, and the plasma discharge (such as CN and N2 is measured during microwave E-field irradiation. It is shown that CN gas or excited CN molecules contribute to the iron oxide reduction reactions, as well as to the thermal reduction. On the other hand, no plasma is generated during microwave H-field irradiation, resulting in thermal reduction. Magnetite strongly interacts with the microwave H-field, and the reduction reaction is clearly promoted by microwave H-field irradiation, as well as thermal reduction reaction.

  18. Influence of thickness increase of intraoral autopolymerizing hard denture base liners on the temperature rise during the polymerization process.

    Science.gov (United States)

    Dimiou, Anna Maria; Michalakis, Konstantinos; Pissiotis, Argirios

    2014-06-01

    Increasing the thickness of intraoral autopolymerizing hard denture base liners may result in a temperature rise and a burning sensation for patients. The purpose of the study was to determine whether increasing the thickness of hard autopolymerizing reline resin increases the temperature of the basal seat area of a denture during the polymerization process. Four polyethyl methacrylate and 1 polymethyl methacrylate autopolymerizing reline resin products of 3 different thicknesses were tested. A cobalt-chromium edentulous maxillary cast was used to obtain 150 stone casts, 50 for each thickness of 1, 2, and 3 mm (n=10). Polystyrene record bases were filled with the autopolymerizing reline resin mixture and placed on the cobalt-chromium cast, which was mounted on a reline index, to serve as denture substitutes. Two thermal probes were used to monitor the temperature rise, which was recorded at 30-second intervals until no further increase was noted. Collected data were subjected to a 2-way ANOVA and the Tukey honestly significant difference test (α=.05). The mean temperature increase for the chairside denture reline procedure ranged from 39.45°C for the 1-mm thickness to 46.10°C for the 3-mm thickness. The 2-way ANOVA found significant differences (Pbase liner produced a significantly higher (P<.001) exothermic reaction than the other materials included in this study. One of the polyethyl methacrylate resins presented a higher exothermic reaction than the polymethyl methacrylate product at a 3-mm thickness, but the difference was not statistically significant. The polymethyl methacrylate resin presented the highest mean time to reach the maximum temperature for all 3 thicknesses. Copyright © 2014 Editorial Council for the Journal of Prosthetic Dentistry. Published by Elsevier Inc. All rights reserved.

  19. On the Way to Improve the Environmental Benignity of Chemical Processes: Novel Catalysts for a Polymerization Process

    Directory of Open Access Journals (Sweden)

    Silvana F. Rach

    2009-03-01

    Full Text Available An example for a process that can, in principle, be improved by the application of a catalyst is the synthesis of poly(2-methyl-propenes (“polyisobutenes”, which are important for numerous industrial applications. Each year several 100,000 t are produced. The production of low-molecular weight polyisobutenes by means of cationic initiation by an excess of Lewis acids is well established. Typically, these initiators require the usage of solvents like chloroform, dichloromethane and ethylene and temperatures far below 0 °C (–100 °C in the case of ethylene as solvent. Solvent stabilized transition metal complexes with weakly coordinating counter anions overcome these drawbacks and thus are not only more efficient, but also more environmentally benign: they can be applied at ambient temperature and in non chlorinated solvents at low concentrations.

  20. PETMA-g-PETMA-b-PS 'palm tree' graft copolymer: A new polymeric architecture obtained via RAFT and ROP process

    International Nuclear Information System (INIS)

    Soares, Paula P.; Silva, Eduardo de O. da; Petzhold, Cesar L.

    2009-01-01

    Block copolymer with pendant thiirane moiety PETMA-b-PS is the base for a new class of 'palm tree' graft copolymers, which can show interesting properties. ETMA can be polymerized through ring opening polymerization with Lewis bases as initiator, e.g., Br- and tertiary amines. We used this reaction as a way to graft a copolymer PETMA-b-PS possessing 5% of ETMA unities, with chains having poly(propylene sulfide), obtained by graft from method. Produced materials were characterized through H1 NMR, SEC and DSC. (author)

  1. In-situ real-time x-ray scattering for probing the processing-structure-performance relation

    KAUST Repository

    Smilgies, Detlef-M.

    2014-01-01

    © 2014 Materials Research Society. In-situ X-ray scattering methodology is discussed, in order to analyze the microstructure development of soft functional materials during coating, annealing, and drying processes in real-time. The relevance of a fundamental understanding of coating processes for future industrial production is pointed out.

  2. Loose nanofiltration membrane for dye/salt separation through interfacial polymerization with in-situ generated TiO{sub 2} nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Qi; Fan, Lin; Yang, Zhen; Zhang, Runnan; Liu, Ya-nan; He, Mingrui [Key Laboratory for Green Chemical Technology, School of Chemical Engineering and Technology, Tianjin University, Tianjin 300072 (China); Collaborative Innovation Center of Chemical Science and Engineering (Tianjin), Tianjin University, Tianjin 300072 (China); Su, Yanlei, E-mail: suyanlei@tju.edu.cn [Key Laboratory for Green Chemical Technology, School of Chemical Engineering and Technology, Tianjin University, Tianjin 300072 (China); Collaborative Innovation Center of Chemical Science and Engineering (Tianjin), Tianjin University, Tianjin 300072 (China); Jiang, Zhongyi [Key Laboratory for Green Chemical Technology, School of Chemical Engineering and Technology, Tianjin University, Tianjin 300072 (China); Collaborative Innovation Center of Chemical Science and Engineering (Tianjin), Tianjin University, Tianjin 300072 (China)

    2017-07-15

    Highlights: • A in-situ generated TiO{sub 2} approach was used to fabricate loose nanofiltration membrane. • The membrane contained small channels owing to the interaction between TiO{sub 2} and the polyamide. • The membranes exhibited high water fluxes and separation performance for dye/salt solutions. - Abstract: In this study, a high flux nanofiltration (NF) membrane with hybrid polymer-nanoparticle active layer was fabricated by chemical crosslinking of piperazine (PIP) and 1, 3, 5-benzene tricarbonyl trichloride (TMC). An in-situ generated method was applied to deposit titanium dioxide (TiO{sub 2}) nanoparticles uniformly on the membrane surface, leading to the enhancement of the surface hydrophilicity, roughness and relative surface area of the polyamide (PA) layer. The morphology of the modified membrane was investigated by scanning electron microscopy (SEM) and Atomic force microscopy (AFM), also energy dispersive X-ray microanalysis (EDX) was used to analyze the distribution of Ti element. Chemical structure was observed by Fourier transmission infrared attenuated total reflectance (FTIR-ATR) spectroscopy. Remarkably, the optimal water flux of the loose NF membrane was 65.0 Lm{sup −2} h{sup −1} bar{sup −1} nearly 5 times as much as the pure PA membrane flux. The rejections of the loose NF membranes for dyes were almost all greater than 95.0%, while the rejection for sodium sulfate (Na{sub 2}SO{sub 4}) was only about 17.0%, which indicated that the modified membrane had an impressive potential application for dye desalination and purification.

  3. Infiltration of Z-direction Injection RTM Process Based on Ex-situ Toughening Technology

    Directory of Open Access Journals (Sweden)

    DONG Shu-hua

    2017-09-01

    Full Text Available Aimed at ex-situ toughening technology and Z-direction RTM process,Darcy's law was modified by introducing the saturation parameter. The partial differential equation describing the unsteady flow of the resin in the fiber preform was established. The effect of process parameters such as volume flow rate, resin viscosity and fiber preform's permeability during the constant flow process on the injection pressure was investigated. The resin flow between intra-tow and inter-tow of the preform with untoughened layers and toughened layers was simulated. The results show that the numerical simulation results are reliable. The inner pressure in the fiber performs increases with the increase of injection time. The injection pressure increases linearly with the increase of volume flow rate and resin viscosity, while decreases with the increase of fiber preform's permeability, which accords with Darcy's law. The infiltration visualization of resin flow through meso-scale and micro-scale fiber preform is realized, which provides an important supplement for prediction of the macro-flow in fiber preforms and provides guidance for actual process.

  4. In situ treatment of mixed contaminants in groundwater: Review of candidate processes

    International Nuclear Information System (INIS)

    Korte, N.E.; Siegrist, R.L.; Ally, M.

    1994-10-01

    This document describes the screening and preliminary evaluation of candidate treatment for use in treating mixed contaminants volatile organic compounds (VOCs) and radionuclides in groundwater. Treating mixed contaminants presents unusual difficulties. Typically, VOCs are the most abundant contaminants, but the presence of radionuclides results in additional health concerns that must be addressed, usually by a treatment approach different from that used for VOCs. Furthermore, the presence of radionuclides may yield mixed solid wastes if the VOCs are treated by conventional means. These issues were specifically addressed in the evaluation of candidate treatment processes for testing in this program. Moreover, because no research or early development of a particular process would be performed, the technology review also focused on technologies that could be readily adapted and integrated for use with mixed contaminants. The objective is to couple emerging or available processes into treatment modules for use in situ. The three year project, to be completed in September 1996, includes a full-scale field demonstration. The findings reported in this document encompass all activities through the treatment process evaluations

  5. In situ treatment of mixed contaminants in groundwater: Review of candidate processes

    Energy Technology Data Exchange (ETDEWEB)

    Korte, N.E. [ed.] [Oak Ridge National Lab., Grand Junction, CO (United States); Siegrist, R.L. [ed.] [Oak Ridge National Lab., TN (United States); Ally, M. [and others

    1994-10-01

    This document describes the screening and preliminary evaluation of candidate treatment for use in treating mixed contaminants volatile organic compounds (VOCs) and radionuclides in groundwater. Treating mixed contaminants presents unusual difficulties. Typically, VOCs are the most abundant contaminants, but the presence of radionuclides results in additional health concerns that must be addressed, usually by a treatment approach different from that used for VOCs. Furthermore, the presence of radionuclides may yield mixed solid wastes if the VOCs are treated by conventional means. These issues were specifically addressed in the evaluation of candidate treatment processes for testing in this program. Moreover, because no research or early development of a particular process would be performed, the technology review also focused on technologies that could be readily adapted and integrated for use with mixed contaminants. The objective is to couple emerging or available processes into treatment modules for use in situ. The three year project, to be completed in September 1996, includes a full-scale field demonstration. The findings reported in this document encompass all activities through the treatment process evaluations.

  6. In Situ Acoustic Monitoring of Thermal Spray Process Using High-Frequency Impulse Measurements

    Science.gov (United States)

    Tillmann, Wolfgang; Walther, Frank; Luo, Weifeng; Haack, Matthias; Nellesen, Jens; Knyazeva, Marina

    2018-01-01

    In order to guarantee their protective function, thermal spray coatings must be free from cracks, which expose the substrate surface to, e.g., corrosive media. Cracks in thermal spray coatings are usually formed because of tensile residual stresses. Most commonly, the crack occurrence is determined after the thermal spraying process by examination of metallographic cross sections of the coating. Recent efforts focus on in situ monitoring of crack formation by means of acoustic emission analysis. However, the acoustic signals related to crack propagation can be absorbed by the noise of the thermal spraying process. In this work, a high-frequency impulse measurement technique was applied to separate different acoustic sources by visualizing the characteristic signal of crack formation via quasi-real-time Fourier analysis. The investigations were carried out on a twin wire arc spraying process, utilizing FeCrBSi as a coating material. The impact of the process parameters on the acoustic emission spectrum was studied. Acoustic emission analysis enables to obtain global and integral information on the formed cracks. The coating morphology and coating defects were inspected using light microscopy on metallographic cross sections. Additionally, the resulting crack patterns were imaged in 3D by means of x-ray microtomography.

  7. Mistura PAni.DBSA/SBS Obtida por Polimerização "In Situ": Propriedades Elétrica, Dielétrica e Dinâmico-Mecânica PAni.DBSA/SBS blends prepared from "in situ" polymerization: electric, dielectric and dynamic-mechanical properties

    Directory of Open Access Journals (Sweden)

    María E. Leyva

    2002-01-01

    Full Text Available Misturas elastoméricas condutoras de eletricidade envolvendo copolímero tribloco poli(estireno-b-butadieno-b-estireno (SBS e polianilina dopada com ácido dodecilbenzenosulfônico (Pani.DBSA foram obtidas por polimerização "in situ". Os filmes obtidos por moldagem por compressão mostraram baixo limiar de percolação, apresentando valores de condutividade semelhantes aos encontrados para o polímero condutor puro com cerca de 20 % em massa de Pani.DBSA. A caracterização das misturas por análise termodinâmico-mecânica (DMTA evidenciou uma ligeira interação da Pani.DBSA com ambas fases do copolímero SBS. Na região borrachosa, o módulo da mistura aumenta com o aumento do conteúdo de Pani. No entanto, existe uma progressiva queda no fator de amortecimento ("damping" com o aumento da concentração de Pani. A energia de ativação, Ea, do processo de transição vítreo-borrachoso de ambas fases do SBS foi calculada, utilizando a equação de Arrhenius com os dados obtidos tanto por DMTA como por análise termodielétrica (DETA. A caracterização dielétrica não proporcionou informações a respeito da localização da Pani.DBSA na matriz de SBS. No entanto, observou-se o fenômeno de polarização interfacial entre a Pani e o SBS. Uma morfologia do tipo microtubos foi observada para Pani.DBSA na mistura SBS/Pani.DBSA, utilizando-se a técnica de microscopia eletrônica de varredura.Conducting rubbery blends of styrene-butadiene-styrene (SBS triblock copolymer and polyaniline doped with dodecylbenzenesulfonic acid (Pani.DBSA were produced by "in situ" polymerization. The films obtained by compression-molding display low percolation threshold with conductivity values similar to that found for pure Pani.DBSA with only 20 wt% of Pani.DBSA in the SBS/Pani.DBSA blend. The dynamic-mechanical characterization demonstrated that PAni.DBSA presents a slight interaction with both phases of the SBS copolymer. In the rubbery region, the modulus

  8. Study of the Radical Chain Mechanism of Hydrocarbon Oxidation for In Situ Combustion Process

    Directory of Open Access Journals (Sweden)

    Alexandra Ushakova

    2017-01-01

    Full Text Available Despite the abundance of in situ combustion models of oil oxidation, many of the effects are still beyond consideration. For example, until now, initial stages of oxidation were not considered from a position of radical chain process. This is a serious difficulty for the simulation of oil recovery process that involves air injection. To investigate the initial stages of oxidation, the paper considers the sequence of chemical reactions, including intermediate short-living compounds and radicals. We have attempted to correlate the main stages of the reaction with areas of heat release observed in the experiments. The system of differential equations based on the equations of oxidation reactions was solved. Time dependence of peroxides formation and start of heat release is analytically derived for the initial stages. We have considered the inhibition of initial oxidation stages by aromatic oil compounds and have studied the induction time in dependence on temperature. Chain ignition criteria for paraffins and crude oil in presence of core samples were obtained. The calculation results are compared with the stages of oxidation that arise by high-pressure differential scanning calorimetry. According to experimental observations we have determined which reactions are important for the process and which can be omitted or combined into one as insignificant.

  9. Comparative studies on the corrosion protection effect of DBSA-doped polyaniline prepared from in situ emulsion polymerization in the presence of hydrophilic Na+-MMT and organophilic organo-MMT clay platelets

    International Nuclear Information System (INIS)

    Chang, K.-C.; Lai, M.-C.; Peng, C.-W.; Chen, Y.-T.; Yeh, J.-M.; Lin, C.-L.; Yang, J.-C.

    2006-01-01

    A series of polyaniline (PANI)/Na + -montmorillonite (MMT) clay and PANI/organo-MMT nanocomposite materials have been successfully prepared by in situ emulsion polymerization in the presence of inorganic nanolayers of hydrophilic Na + -MMT clay or organophilic organo-MMT clay with DBSA and KPS as surfactant and initiator, respectively. The as-synthesized Na + -PCN and organo-PCN materials were characterized and compared by Fourier transformation infrared (FTIR) spectroscopy, wide-angle powder X-ray diffraction (XRD) and transmission electron microscopy (TEM). Na + -PCN materials in the form of coatings with low loading of Na + -MMT clay (e.g., 3 wt.%, CLAN3) on cold-rolled steel (CRS) were found much superior in corrosion protection over those of organo-PCN materials with same clay loading based on a series of electrochemical measurements of corrosion potential, polarization resistance, corrosion current and impedance spectroscopy in 5 wt.% aqueous NaCl electrolyte. The molecular weights of PANI extracted from PCN materials and neat PANI were determined by gel permeation chromatography (GPC) with NMP as eluant. Effects of material composition on the gas permeability, optical properties and electrical conductivity of neat PANI and a series of PCN materials, in the form of free-standing film, solution and powder-pressed pellet, were also studied by gas permeability analyzer (GPA), ultraviolet-vis spectra and four-point probe technique, respectively

  10. Enhanced thermal and mechanical properties of poly(trimethylene terephthalate-block-poly(tetramethylene oxide segmented copolymer based hybrid nanocomposites prepared by in situ polymerization via synergy effect between SWCNTs and graphene nanoplatelets

    Directory of Open Access Journals (Sweden)

    S. Paszkiewicz

    2015-06-01

    Full Text Available Graphene nanoplatelets/single walled carbon nanotubes/poly(trimethylene terephthalate-block-poly(tetramethylene oxide segmented copolymer (GNP/SWCNT/PTT-PTMO hybrid nanocomposites were synthesized via in situ polymerization. A remarkable synergistic effect between GNPs and SWCNTs on improving thermal and mechanical properties of nanocomposites based on segmented block copolymers was observed. Heterogeneous structure of the PTT-PTMO allowed for a better and more uniform distribution of both types of nanoparticles and stabilized the structure in question. This enabled us to observe a so-called ‘synergistic effect’, caused by the use of mixture of carbon nanotubes and graphene nanopletelets, on the enhancement of thermal and mechanical properties of the obtained polymer. In order to ascertain the influence of mentioned carbon nanostructures on the nano-phase-separated structure of the synthesized PTT-PTMO block copolymers, differential scanning calorimetric (DSC and dynamic mechanical thermoanalysis (DMTA measurements were performed. Scanning electron microscopic (SEM and transmission electron microscopic (TEM images of the PTTPTMO nanocomposites displayed that hybrid nanofillers exhibited better distribution and compatibility than SWCNTs and GNPs did individually. The tensile modulus of 0.5SWCNT/0.1GNP/PTT-PTMO composites was 68% higher than that of the PTT-PTMO alone, compared to only a 10 and 28% increase in tensile modulus for 0.3GNP/PTT-PTMO and 0.3SWCNT/PTT-PTMO composites respectively (the highest concentration when single nanofiller was added.

  11. Influence of CdSe/ZnS quantum dots in the polymerization process and in the grating recording in acrylate materials.

    Science.gov (United States)

    Barichard, Anne; Galstian, Tigran; Israëli, Yaël

    2010-11-25

    The initiation step of the polymerization of acrylate materials is first studied in detail by UV-visible spectroscopy, showing the involvement of each species of the three-component photosensitizer. Then, the implementation of a combined holographic and physicochemical investigation approach is used to determine the influence of photoluminescent CdSe/ZnS quantum dots (QDs) in the photopolymerization and grating recording process in composites containing those QD nanoparticles. The fluorescence microscopy evidences the dynamic distribution profile of QDs due to their diffusion from the irradiated zones to the interface between the bright and the dark zones and, finally, their accumulation in nonirradiated zones. At the same time, the infrared spectroscopy shows that the presence of QDs provides a noticeable decrease of the polymerization rate, which favors the diffusion of the monomer and QDs. These two phenomena contribute to the enhancement of the refractive index modulation depth.

  12. Loose nanofiltration membrane for dye/salt separation through interfacial polymerization with in-situ generated TiO2 nanoparticles

    Science.gov (United States)

    Zhang, Qi; Fan, Lin; Yang, Zhen; Zhang, Runnan; Liu, Ya-nan; He, Mingrui; Su, Yanlei; Jiang, Zhongyi

    2017-07-01

    In this study, a high flux nanofiltration (NF) membrane with hybrid polymer-nanoparticle active layer was fabricated by chemical crosslinking of piperazine (PIP) and 1, 3, 5-benzene tricarbonyl trichloride (TMC). An in-situ generated method was applied to deposit titanium dioxide (TiO2) nanoparticles uniformly on the membrane surface, leading to the enhancement of the surface hydrophilicity, roughness and relative surface area of the polyamide (PA) layer. The morphology of the modified membrane was investigated by scanning electron microscopy (SEM) and Atomic force microscopy (AFM), also energy dispersive X-ray microanalysis (EDX) was used to analyze the distribution of Ti element. Chemical structure was observed by Fourier transmission infrared attenuated total reflectance (FTIR-ATR) spectroscopy. Remarkably, the optimal water flux of the loose NF membrane was 65.0 Lm-2 h-1 bar-1 nearly 5 times as much as the pure PA membrane flux. The rejections of the loose NF membranes for dyes were almost all greater than 95.0%, while the rejection for sodium sulfate (Na2SO4) was only about 17.0%, which indicated that the modified membrane had an impressive potential application for dye desalination and purification.

  13. Solution-Processing of Organic Solar Cells: From In Situ Investigation to Scalable Manufacturing

    KAUST Repository

    Abdelsamie, Maged

    2016-12-05

    implementation of organic solar cells with high efficiency and manufacturability. In this dissertation, we investigate the mechanism of the BHJ layer formation during solution processing from common lab-based processes, such as spin-coating, with the aim of understanding the roles of materials, formulations and processing conditions and subsequently using this insight to enable the scalable manufacturing of high efficiency organic solar cells by such methods as wire-bar coating and blade-coating. To do so, we have developed state-of-the-art in situ diagnostics techniques to provide us with insight into the thin film formation process. As a first step, we have developed a modified spin-coater which allows us to perform in situ UV-visible absorption measurements during spin coating and provides key insight into the formation and evolution of polymer aggregates in solution and during the transformation to the solid state. Using this method, we have investigated the formation of organic BHJs made of a blend of poly (3-hexylthiophene) (P3HT) and fullerene, reference materials in the organic solar cell field. We show that process kinetics directly influence the microstructure and morphology of the bulk heterojunction, highlighting the value of in situ measurements. We have investigated the influence of crystallization dynamics of a wide-range of small-molecule donors and their solidification pathways on the processing routes needed for attaining high-performance solar cells. The study revealed the reason behind the need of empirically-adopted processing strategies such as solvent additives or alternatively thermal or solvent vapor annealing for achieving optimal performance. The study has provided a new perspective to materials design linking the need for solvent additives or annealing to the ease of crystallization of small-molecule donors and the presence or absence of transient phases before crystallization. From there, we have extended our investigation to small-molecule (p

  14. Deformation processing of the Nb-10 a/o Si in-situ composite

    International Nuclear Information System (INIS)

    Srinivasan, R.; Thirukkonda, M.; Weiss, I.

    1994-01-01

    Isothermal constant strain rate compressive deformation of the Nb 10 a/o Si in-situ composite was studied in order to establish the conditions under which the alloy deformed uniformly. The microstructure of the alloy was modified by hot extrusion. The different microstructures obtained were: as-cast (AC-I Generation), once-extruded (E1-II Generation), and twice-extruded (E2-III Generation). In the as-cast condition, the alloy undergoes uniform deformation only at very high temperatures (∼1,800 C) or at very slow strain rates (var-epsilon ≤ 10 -4 s -1 ). Through microstructural modification it was possible to change the conditions for uniform deformation to lower temperatures and faster strain rates. The thermomechanical processing of Nb-10 a/o Si alloy resulted in the recrystallization and the morphological alignment of the Nb 3 Si and Nb phases in the extrusion direction. A consequence of these microstructural modifications was an improvement in the mechanical properties of the alloy. Room temperature fracture toughness of the alloy increased from about 11 MPa√ bar m in the AC condition to 21 MPa√ bar m in the E1 condition, and to 26 MPa√ bar m in the E2 condition. Thermomechanical processing also resulted in considerable increases in both the room temperature and the elevated temperature strength of the alloy

  15. In situ studies on controlling an atomically-accurate formation process of gold nanoclusters.

    Science.gov (United States)

    Yang, Lina; Cheng, Hao; Jiang, Yong; Huang, Ting; Bao, Jie; Sun, Zhihu; Jiang, Zheng; Ma, Jingyuan; Sun, Fanfei; Liu, Qinghua; Yao, Tao; Deng, Huijuan; Wang, Shuxin; Zhu, Manzhou; Wei, Shiqiang

    2015-09-14

    Knowledge of the molecular formation mechanism of metal nanoclusters is essential for developing chemistry for accurate control over their synthesis. Herein, the "top-down" synthetic process of monodisperse Au13 nanoclusters via HCl etching of polydisperse Aun clusters (15 ≤ n ≤ 65) is traced by a combination of in situ X-ray/UV-vis absorption spectroscopy and time-dependent mass spectrometry. It is revealed experimentally that the HCl-induced synthesis of Au13 is achieved by accurately controlling the etching process with two distinctive steps, in sharp contrast to the traditional thiol-etching mechanism through release of the Au(i) complex. The first step involves the direct fragmentation of the initial larger Aun clusters into metastable intermediate Au8-Au13 smaller clusters. This is a critical step, which allows for the secondary size-growth step of the intermediates toward the atomically monodisperse Au13 clusters via incorporating the reactive Au(i)-Cl species in the solution. Such a secondary-growth pathway is further confirmed by the successful growth of Au13 through reaction of isolated Au11 clusters with AuClPPh3 in the HCl environment. This work addresses the importance of reaction intermediates in guiding the way towards controllable synthesis of metal nanoclusters.

  16. Experimental optimization of catalytic process in-situ for heavy oil and bitumen upgrading

    Energy Technology Data Exchange (ETDEWEB)

    Shah, A.; Fishwick, R.P.; Leeke, G.A.; Wood, J. [Birmingham Univ., Birmingham (United Kingdom); Rigby, S.P.; Greaves, M. [Bath Univ., Bath (United Kingdom)

    2010-07-01

    Peak crude oil production is expected to occur in the second decade of this century, followed by a phase of permanent decline in conventional crude oil production. However, very large resources of heavy oil and bitumen exist throughout the world, most notably in Canada and Venezuela. The high viscosity and density of these non-conventional crude oils require more energy intensive operations for production and upgrading, and also for transportation. As such, they are more costly to extract. This paper described some of the technological innovations that are being considered to extract heavier oil supplies with reduced environmental impact. The toe-to-heel air injection (THAI) process and its catalytic added-on (CAPRI) process combine in-situ combustion with catalytic upgrading using an annular catalyst packed around a horizontal producer well. Results of an experimental study concerning optimization of catalyst type and operating conditions showed that CAPRI can effect further upgrading of partially upgraded THAI oil, with upgrading levels of viscosity and API gravity dependent upon temperature and flow rate. 20 refs., 8 tabs., 10 figs.

  17. Aquifer restoration at in-situ leach uranium mines: evidence for natural restoration processes

    International Nuclear Information System (INIS)

    Deutsch, W.J.; Serne, R.J.; Bell, N.E.; Martin, W.J.

    1983-04-01

    Pacific Northwest Laboratory conducted experiments with aquifer sediments and leaching solution (lixiviant) from an in-situ leach uranium mine. The data from these laboratory experiments and information on the normal distribution of elements associated with roll-front uranium deposits provide evidence that natural processes can enhance restoration of aquifers affected by leach mining. Our experiments show that the concentration of uranium (U) in solution can decrease at least an order of magnitude (from 50 to less than 5 ppM U) due to reactions between the lixiviant and sediment, and that a uranium solid, possibly amorphous uranium dioxide, (UO 2 ), can limit the concentration of uranium in a solution in contact with reduced sediment. The concentrations of As, Se, and Mo in an oxidizing lixiviant should also decrease as a result of redox and precipitation reactions between the solution and sediment. The lixiviant concentrations of major anions (chloride and sulfate) other than carbonate were not affected by short-term (less than one week) contact with the aquifer sediments. This is also true of the total dissolved solids level of the solution. Consequently, we recommend that these solution parameters be used as indicators of an excursion of leaching solution from the leach field. Our experiments have shown that natural aquifer processes can affect the solution concentration of certain constituents. This effect should be considered when guidelines for aquifer restoration are established

  18. Cyanobacteria to Link Closed Ecological Systems and In-Situ Resources Utilization Processes

    Science.gov (United States)

    Brown, Igor

    Introduction: A major goal for the Vision of Space Exploration is to extend human presence across the solar sys-tem. With current technology, however, all required consumables for these missions (propellant, air, food, water) as well as habitable volume and shielding to support human explorers will need to be brought from Earth. In-situ pro-duction of consumables (In-Situ Resource Utilization-ISRU) will significantly facilitate current plans for human ex-ploration and colonization of the solar system, especially by reducing the logistical overhead such as recurring launch mass. The production of oxygen from lunar materials is generally recognized as the highest priority process for lunar ISRU, for both human metabolic and fuel oxidation needs. The most challenging technology developments for future lunar settlements may lie in the extraction of elements (O, Fe, Mn, Ti, Si, etc) from local rocks and soils for life support, industrial feedstock and the production of propellants. With few exceptions (e.g., Johannson, 1992), nearly all technology development to date has employed an ap-proach based on inorganic chemistry (e.g. Allen et al., 1996). None of these technologies include concepts for inte-grating the ISRU system with a bioregenerative life support system and a food production systems. Bioregenerative life support efforts have recently been added to the Constellation ISRU development program (Sanders et al, 2007). Methods and Concerns: The European Micro-Ecological Life Support System Alternative (MELiSSA) is an ad-vanced concept for organizing a bioregenerative system for long term space flights and extraterrestrial settlements (Hendrickx, De Wever et al., 2005). However the MELiSSA system is a net consumer of ISRU products without a net return to in-situ technologies, e.g.. to extract elements as a result of complete closure of MELiSSA. On the other hand, the physical-chemical processes for ISRU are typically massive (relative to the rate of oxygen

  19. A Novel Polyamide 12 Polymerization System and its Use for a LCM-process to Produce CFRP

    OpenAIRE

    2005-01-01

    Abstract The aim of this study was to investigate the scope of the recently developed polymerization molding system for polyamide 12 (PA12), especially with respect to the formation of carbon fiber-reinforced PA12 composites. Initial screening of PA12 composite formation was performed by means of an internal mixer in order to identify the suitable type of surface-treated carbon fiber (CF). The content of re...

  20. Remediation of PCB-contaminated soils. Risk analysis of biological in situ processes

    Energy Technology Data Exchange (ETDEWEB)

    Rein, Arno

    2006-12-08

    effects on other soil organisms. Potential field release applications of in situ bioremediation using GMOs require performance control in the source zone (to ensure the functionality of the degradation process) and compliance monitoring, addressing contaminants, metabolites and GMOs. Detailed guidelines were compiled for respective tasks. (orig.)

  1. Identification of bacteria used for microbial enhanced oil recovery process by fluorescence in situ hybridization technique

    Energy Technology Data Exchange (ETDEWEB)

    Fujiwara, K.; Tanaka, S.; Otsuka, M. [Kansai Research Institute, Kyoto (Japan). Lifescience Lab.; Yonebayashi, H. [Japan National Oil Corp., Chiba (Japan). Tech. Research Center; Enomoto, H. [Tohoku University, Sendai (Japan). Dept. of Geoscience and Tech.

    2000-01-01

    A fluorescence in situ hybridization (FISH) technique using 16S rRNA-targeted oligonucleotide probes was developed for rapid detection of microorganisms for use in the microbial enhancement of oil recovery (MEOR) process. Two microorganisms, Enterobacter cloacae TRC-322 and Bacillus licheniformis TRC-18-2-a, were selected from a collection of Enterobacter sp. and Bacillus sp. which were screened in previous studies as candidate microorganisms for injection, and were used for this experiment. Oligonucleotide probes, design based on specific sequences in the 16S rRNA gene were labeled with either fluorescein isothiocyanate (FITC), or 6-car-boxy-X-rhodamine (ROX), and were allowed to hybridize with fixed cells of the two microorganisms noted above. The fluorescence signal emitted from each microorganism cells could clearly be detected by an epifluorescence microscope. Moreover, E. cloacae TRC-322 and B, licheniformis TRC-18-2-a, suspended in actual reservoir brine, including inorganic salts, oil and aboriginal cells of the reservoir brine, could be detected directly by this hybridization method, without the need for cultivation and isolation. (author)

  2. Magic angle spinning nuclear magnetic resonance apparatus and process for high-resolution in situ investigations

    Science.gov (United States)

    Hu, Jian Zhi; Sears, Jr., Jesse A.; Hoyt, David W.; Mehta, Hardeep S.; Peden, Charles H. F.

    2015-11-24

    A continuous-flow (CF) magic angle sample spinning (CF-MAS) NMR rotor and probe are described for investigating reaction dynamics, stable intermediates/transition states, and mechanisms of catalytic reactions in situ. The rotor includes a sample chamber of a flow-through design with a large sample volume that delivers a flow of reactants through a catalyst bed contained within the sample cell allowing in-situ investigations of reactants and products. Flow through the sample chamber improves diffusion of reactants and products through the catalyst. The large volume of the sample chamber enhances sensitivity permitting in situ .sup.13C CF-MAS studies at natural abundance.

  3. In Situ Mass Spectrometric Monitoring of the Dynamic Electrochemical Process at the Electrode–Electrolyte Interface: a SIMS Approach

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Zhaoying; Zhang, Yanyan; Liu, Bingwen; Wu, Kui; Thevuthasan, Suntharampillai; Baer, Donald R.; Zhu, Zihua; Yu, Xiao-Ying; Wang, Fuyi

    2017-01-03

    The in situ molecular characterization of reaction intermediates and products at electrode-electrolyte interfaces is central to mechanistic studies of complex electrochemical processes, yet a great challenge. The coupling of electrochemistry (EC) and mass spectrometry (MS) has seen rapid development and found broad applicability in tackling challenges in analytical and bioanalytical chemistry. However, few truly in situ and real-time EC-MS studies have been reported at electrode-electrolyte interfaces. An innovative EC-MS coupling method named in situ liquid secondary ion mass spectrometry (SIMS) was recently developed by combining SIMS with a vacuum compatible microfluidic electrochemical device. Using this novel capability we report the first in situ elucidation of the electro-oxidation mechanism of a biologically significant organic compound, ascorbic acid (AA), at the electrode-electrolyte interface. The short-lived radical intermediate was successfully captured, which had not been detected directly before. Moreover, we demonstrated the power of this new technique in real-time monitoring of the formation and dynamic evolution of electrical double layers at the electrode-electrolyte interface. This work suggests further promising applications of in situ liquid SIMS in studying more complex chemical and biological events at the electrode-electrolyte interface.

  4. Processing and characterization of in-situ aluminum bronze titanium carbide composites

    Science.gov (United States)

    Pillai, Balathandan S.

    The present study was carried out to develop a process for manufacturing in-situ aluminum bronze titanium carbide (TiC) friction drums using the centrifugal casting method and to characterize the material under optimum performance. The in-situ method of manufacturing is based on the reactive gas injection technique (RGI). The gas used in this study is high purity methane (CH 4). It was found that the methane gas injection time into the molten bath of aluminum bronze alloyed with titanium promotes the formation of titanium carbide (TiC) in the bronze matrix. The maximum amount of TiC incorporated in the matrix was 3.1 wt.%. This lead to 11.5 wt.% incorporation of TiC in the inner diameter of centrifugal castings as carbide particles drifted towards this region due to the centrifugal forces and their relatively low density. The hardness and strength of these composites when compared with the as cast condition was improved by heat treatment. However, the alloy ductility was decreased at the expense of the strength. It was found that the wear resistance properties of the composites were superior to those of pure cast and heat treated aluminum bronze currently in use. Optical and Scanning Electron Microscopy indicated that the composite surfaces did not scratch deeply when wearing against a hardened 4340 steel. The wear resistance of the as cast aluminum bronze was inferior to that of heat treated one. Moreover, the heat treated aluminum bronze showed a lack of high abrasion resistance. The frictional coefficient was relatively low for the as cast aluminum bronze as a result of adhesive wear behavior for the load and speed chosen in this present investigation. The corrosion studies showed that these composites do not lead to improved corrosion resistance in marine water environments. Apparently, there is a galvanic corrosion of TiC to bronze. In addition, pitting was observed on the corroded surfaces and increased with the volume fraction of TiC. Model validation was

  5. A flow cell for in situ synchrotron x-ray diffraction studies of scale formation under Bayer processing conditions

    Science.gov (United States)

    Webster, Nathan A. S.; Madsen, Ian C.; Loan, Melissa J.; Scarlett, Nicola V. Y.; Wallwork, Kia S.

    2009-08-01

    The design, construction, and commissioning of a stainless steel flow cell for in situ synchrotron x-ray diffraction studies of scale formation under Bayer processing conditions is described. The use of the cell is demonstrated by a study of Al(OH)3 scale formation on a mild steel substrate from synthetic Bayer liquor at 70 °C. The cell design allows for interchangeable parts and substrates and would be suitable for the study of scale formation in other industrial processes.

  6. Electrochemically Modulated Gas/Liquid Separation Technology for In Situ Resource Utilization Process Streams, Phase I

    Data.gov (United States)

    National Aeronautics and Space Administration — In this phase I program MicroCell Technologies, LLC (MCT) proposes to demonstrate the feasibility of an electrochemically modulated phase separator for in situ...

  7. Immunoglobulin heavy-chain fluorescence in situ hybridization-chromogenic in situ hybridization DNA probe split signal in the clonality assessment of lymphoproliferative processes on cytological samples.

    Science.gov (United States)

    Zeppa, Pio; Sosa Fernandez, Laura Virginia; Cozzolino, Immacolata; Ronga, Valentina; Genesio, Rita; Salatiello, Maria; Picardi, Marco; Malapelle, Umberto; Troncone, Giancarlo; Vigliar, Elena

    2012-12-25

    The human immunoglobulin heavy-chain (IGH) locus at chromosome 14q32 is frequently involved in different translocations of non-Hodgkin lymphoma (NHL), and the detection of any breakage involving the IGH locus should identify a B-cell NHL. The split-signal IGH fluorescence in situ hybridization-chromogenic in situ hybridization (FISH-CISH) DNA probe is a mixture of 2 fluorochrome-labeled DNAs: a green one that binds the telomeric segment and a red one that binds the centromeric segment, both on the IGH breakpoint. In the current study, the authors tested the capability of the IGH FISH-CISH DNA probe to detect IGH translocations and diagnose B-cell lymphoproliferative processes on cytological samples. Fifty cytological specimens from cases of lymphoproliferative processes were tested using the split-signal IGH FISH-CISH DNA probe and the results were compared with light-chain assessment by flow cytometry (FC), IGH status was tested by polymerase chain reaction (PCR), and clinicohistological data. The signal score produced comparable results on FISH and CISH analysis and detected 29 positive, 15 negative, and 6 inadequate cases; there were 29 true-positive cases (66%), 9 true-negative cases (20%), 6 false-negative cases (14%), and no false-positive cases (0%). Comparing the sensitivity of the IGH FISH-CISH DNA split probe with FC and PCR, the highest sensitivity was obtained by FC, followed by FISH-CISH and PCR. The split-signal IGH FISH-CISH DNA probe is effective in detecting any translocation involving the IGH locus. This probe can be used on different samples from different B-cell lymphoproliferative processes, although it is not useful for classifying specific entities. Cancer (Cancer Cytopathol) 2012;. © 2012 American Cancer Society. Copyright © 2012 American Cancer Society.

  8. Electrochemical Processes for In-Situ Treatment of Contaminated Soils - Final Report - 09/15/1996 - 01/31/2001

    Energy Technology Data Exchange (ETDEWEB)

    Huang, Chin-Pao

    2001-05-31

    This project will study electrochemical processes for the in situ treatment of soils contaminated by mixed wastes, i.e., organic and inorganic. Soil samples collected form selected DOE waste sites will be characterized for specific organic and metal contaminants and hydraulic permeability. The soil samples are then subject to desorption experiments under various physical-chemical conditions such as pH and the presence of surfactants. Batch electro-osmosis experiments will be conducted to study the transport of contaminants in the soil-water systems. Organic contaminants that are released from the soil substrate will be treated by an advanced oxidation process, i.e., electron-Fantan. Finally, laboratory reactor integrating the elector-osmosis and elector-Fantan processes will be used to study the treatment of contaminated soil in situ.

  9. Constraining processes of landscape change with combined in situ cosmogenic 14C-10Be analysis

    Science.gov (United States)

    Hippe, Kristina

    2017-10-01

    Reconstructing Quaternary landscape evolution today frequently builds upon cosmogenic-nuclide surface exposure dating. However, the study of complex surface exposure chronologies on the 102-104 years' timescale remains challenging with the commonly used long-lived radionuclides (10Be, 26Al, 36Cl). In glacial settings, key points are the inheritance of nuclides accumulated in a rock surface during a previous exposure episode and (partial) shielding of a rock surface after the main deglaciation event, e.g. during phases of glacier readvance. Combining the short-lived in situ cosmogenic 14C isotope with 10Be dating provides a valuable approach to resolve and quantify complex exposure histories and burial episodes within Lateglacial and Holocene timescales. The first studies applying the in situ14C-10Be pair have demonstrated the great benefit from in situ14C analysis for unravelling complex glacier chronologies in various glacial environments worldwide. Moreover, emerging research on in situ14C in sedimentary systems highlights the capacity of combined in situ14C-10Be analysis to quantify sediment transfer times in fluvial catchments or to constrain changes in surface erosion rates. Nevertheless, further methodological advances are needed to obtain truly routine and widely available in situ14C analysis. Future development in analytical techniques has to focus on improving the analytical reproducibility, reducing the background level and determining more accurate muonic production rates. These improvements should allow extending the field of applications for combined in situ14C-10Be analysis in Earth surface sciences and open up a number of promising applications for dating young sedimentary deposits and the quantification of recent changes in surface erosion dynamics.

  10. Surface Initiated Polymerizations via e-ATRP in Pure Water

    Directory of Open Access Journals (Sweden)

    Seyed Schwan Hosseiny

    2013-10-01

    Full Text Available Here we describe the combined process of surface modification with electrochemical atom transfer radical polymerization (e-ATRP initiated from the surface of a modified gold-electrode in a pure aqueous solution without any additional supporting electrolyte. This approach allows for a very controlled growth of the polymer chains leading towards a steady increase in film thickness. Electrochemical quartz crystal microbalance displayed a highly regular increase in surface confined mass only after the addition of the pre-copper catalyst which is reduced in situ and transformed into the catalyst. Even after isolation and washing of the modified electrode surface, reinitiation was achieved with retention of the controlled electrochemical ATRP reaction. This reinitiation after isolation proves the livingness of the polymerization. This approach has interesting potential for smart thin film materials and offers also the possibility of post-modification via additional electrochemical induced reactions.

  11. Effects of aqueous effluents from in situ fossil fuel processing technologies on aquatic systems. Annual progress report

    Energy Technology Data Exchange (ETDEWEB)

    Bergman, H.L.; Anderson, A.D.

    1977-12-01

    This is the first annual report issued under a project to evaluate the effects of aqueous effluents from in-situ fossil fuel processing technologies on aquatic biota. Briefly, the goals of the project are to: evaluate the toxicity of process water effluents on aquatic biota; recommend maximum exposure concentrations for process water constituents; and assist DOE in using project data and recommendations to design control technologies and to assess environmental impacts. The project objectives for Year 1 were pursued through the following five tasks: a literature review on process water constituents; toxicity studies on the effect of process waters and six process water constituents on aquatic biota; degradation rate studies on four to six process water constituents; bioaccumulation studies on four to six process water constituents; and recommendations on maximum exposure concentrations for process water constituents based on data from the project and from the literature. Progress toward completion of these goals is presented.

  12. In-situ solvothermal processing of polycaprolactone/hydroxyapatite nanocomposites with enhanced mechanical and biological performance for bone tissue engineering

    Directory of Open Access Journals (Sweden)

    Saeed Moeini

    2017-09-01

    Full Text Available The interest in biodegradable polymer-matrix nanocomposites with bone regeneration potential has been increasing in recent years. In the present work, a solvothermal process is introduced to prepare hydroxyapatite (HA nanorod-reinforced polycaprolactone in-situ. A non-aqueous polymer solution containing calcium and phosphorous precursors is prepared and processed in a closed autoclave at different temperatures in the range of 60–150 °C. Hydroxyapatite nanorods with varying aspect ratios are formed depending on the processing temperature. X-ray diffraction analysis and field-emission scanning electron microscopy indicate that the HA nanorods are semi-crystalline. Energy-dispersive X-ray spectroscopy and Fourier transform infrared spectrometry determine that the ratio of calcium to phosphorous increases as the processing temperature increases. To evaluate the effect of in-situ processing on the mechanical properties of the nanocomposites, highly porous scaffolds (>90% containing HA nanorods are prepared by employing freeze drying and salt leaching techniques. It is shown that the elastic modulus and strength of the nanocomposites prepared by the in-situ method is superior (∼15% to those of the ex-situ samples (blended HA nanorods with the polymer solution. The enhanced bone regeneration potential of the nanocomposites is shown via an in vitro bioactivity assay in a saturated simulated body fluid. An improved cell viability and proliferation is also shown by employing (3-(4,5- dimethylthiazol-2-yl-2, 5-diphenyl tetrazolium bromide (MTT assay in human osteosarcoma cell lines. The prepared scaffolds with in vitro regeneration capacity could be potentially useful for orthopaedic applications and maxillofacial surgery.

  13. Dormant Polymers and Their Role in Living and Controlled Polymerizations; Influence on Polymer Chemistry, Particularly on the Ring Opening Polymerization

    Directory of Open Access Journals (Sweden)

    Stanislaw Penczek

    2017-11-01

    Full Text Available Living polymerization discovered by Professor Szwarc is known well to all chemists. Some of the living polymerizations involve dormancy, a process in which there is an equilibrium (or at least exchange between two types of living polymers, namely active at the given moment and dormant at this moment and becoming active in the process of activation. These processes are at least equally important although less known. This mini review is devoted to these particular living polymerizations, mostly polymerizations by the Ring-Opening Polymerization mechanisms (ROP compared with some selected close to living vinyl polymerizations (the most spectacular is Atom Transfer Radical Polymerization (ATRP involving dormancy. Cationic polymerization of tetrahydrofuran was the first one, based on equilibrium between oxonium ions (active and covalent (esters dormant species, i.e., temporarily inactive, and is described in detail. The other systems discussed are polymerization of oxazolines and cyclic esters as well as controlled radical and cationic polymerizations of vinyl monomers.

  14. In Situ 3D Monitoring of Geometric Signatures in the Powder-Bed-Fusion Additive Manufacturing Process via Vision Sensing Methods.

    Science.gov (United States)

    Li, Zhongwei; Liu, Xingjian; Wen, Shifeng; He, Piyao; Zhong, Kai; Wei, Qingsong; Shi, Yusheng; Liu, Sheng

    2018-04-12

    Lack of monitoring of the in situ process signatures is one of the challenges that has been restricting the improvement of Powder-Bed-Fusion Additive Manufacturing (PBF AM). Among various process signatures.

  15. In Situ Study of Catalytic Processes: Neutron Diffraction of a Methanol Synthesis Catalyst at Industrially Relevant Pressure

    OpenAIRE

    Kandemir, T.; Girgsdies, F.; Hansen, T.; Liss, K.; Kasatkin, I.; Kunkes, E.; Wowsnick, G.; Jacobsen, N.; Schlögl, R.; Behrens, M.

    2013-01-01

    Studying the workplace: An industrial methanol synthesis catalyst operating at high pressure was studied by in situ neutron diffraction. The peculiar microstructure of Cu/ZnO/Al2O3 nanocatalysts was found to be stable under reaction conditions. Stacking fault annealing and brass formation was only observed at temperatures higher than used in the methanol synthesis process, providing support for active role of defects in this catalyst system.

  16. High temperature structural, polymeric foams from high internal emulsion polymerization

    Energy Technology Data Exchange (ETDEWEB)

    Hoisington, M.A.; Duke, J.R.; Apen, P.G.

    1996-02-01

    In 1982, a high internal phase emulsion (HIPE) polymerization process to manufacture microcellular, polymeric foam systems was patented by Unilever. This patent discloses a polymerization process that occurs in a water-in-oil emulsion in which the water represents at least 76% of the emulsion by volume. The oil phase consists of vinyl monomers such as styrene and acrylates that are crosslinked by divinyl monomers during polymerization. After polymerization and drying to remove the water phase, the result is a crosslinked polymer foam with an open cell microstructure that is homogeneous throughout in terms of morphology, density, and mechanical properties. Since 1982, numerous patents have examined various HIPE polymerized foam processing techniques and applications that include absorbents for body fluids, cleaning materials, and ion exchange systems. All the published HIPE polymerized foams have concentrated on materials for low temperature applications. Copolymerization of styrene with maleic anhydride and N-substituted maleimides to produce heat resistant thermoplastics has been studied extensively. These investigations have shown that styrene will free radically copolymerize with N-substituted maleimides to create an alternating thermoplastic copolymer with a Tg of approximately 200{degrees}C. However, there are many difficulties in attempting the maleimide styrene copolymerization in a HIPE such as lower polymerization temperatures, maleimide solubility difficulties in both styrene and water, and difficulty obtaining a stable HIPE with a styrene/maleimide oil phase. This work describes the preparation of copolymer foams from N-ethylmaleimide and Bis(3-ethyl-5-methyl-4-maleimide-phenyl)methane with styrene based monomers and crosslinking agents.

  17. Photo-processing P3HT conjugated polymers, in solution: A new route towards ordered polymeric structures.

    Science.gov (United States)

    Barbosa Neto, Newton; Dutra, Marcia; Araujo, Paulo; Sampaio, Renato

    Solution aggregated thin films of conjugated polymers have demonstrated to be promising materials for many applications, e.g., solar cells and field-effect transistors. There are many standard methods to generate aggregates in polymeric solution, which includes poor solvent addiction and solution temperature manipulation. Here, we demonstrate a new approach to induce aggregate formation on solution of P3HT polymer. Under light excitation with 355 nm or 532 nm pulsed laser the polymer exhibit significant changes on its UV-Vis spectrum which are most known in the literature as the formation of H-J aggregates and additional new bands associated with polaron formation. Such changes in the amorphous phase of the polymers are seen in specific conditions of solvent combinations. We show also the dependency on the excitation laser power which can be identified as a threshold to ignite the formation of the new structure. We are grateful to CNPq and CAPES for financial support.

  18. Modeling biogeochemical processes and isotope fractionation of enhanced in situ biodenitrification in a fractured aquifer

    NARCIS (Netherlands)

    Rodríguez-Escales, Paula; Folch, Albert; Vidal-Gavilan, Georgina; van Breukelen, B.M.

    2016-01-01

    Enhanced in situ biodenitrification (EIB) is a feasible technology to clean nitrate-polluted groundwater and reach
    drinking water standards. Aimed at enabling a better monitoring and management of the technology at the field
    scale, we developed a two-dimensional reactive transport model

  19. In-Situ Anaerobic Biosurfactant Production Process For Remediation Of DNAPL Contamination In Subsurface Aquifers

    Science.gov (United States)

    Albino, J. D.; Nambi, I. M.

    2009-12-01

    Microbial Enhanced Oil Recovery (MEOR) and remediation of aquifers contaminated with hydrophobic contaminants require insitu production of biosurfactants for mobilization of entrapped hydrophobic liquids. Most of the biosurfactant producing microorganisms produce them under aerobic condition and hence surfactant production is limited in subsurface condition due to lack of oxygen. Currently bioremediation involves expensive air sparging or excavation followed by exsitu biodegradation. Use of microorganisms which can produce biosurfactants under anaerobic conditions can cost effectively expedite the process of insitu bioremediation or mobilization. In this work, the feasibility of anaerobic biosurfactant production in three mixed anaerobic cultures prepared from groundwater and soil contaminated with chlorinated compounds and municipal sewage sludge was investigated. The cultures were previously enriched under complete anaerobic conditions in the presence of Tetrachloroethylene (PCE) for more than a year before they were studied for biosurfactant production. Biosurfactant production under anaerobic conditions was simulated using two methods: i) induction of starvation in the microbial cultures and ii) addition of complex fermentable substrates. Positive result for biosurfactant production was not observed when the cultures were induced with starvation by adding PCE as blobs which served as the only terminal electron acceptor. However, slight reduction in interfacial tension was noticed which was caused by the adherence of microbes to water-PCE interface. Biosurfactant production was observed in all the three cultures when they were fed with complex fermentable substrates and surface tension of the liquid medium was lowered below 35 mN/m. Among the fermentable substrates tested, vegetable oil yielded highest amount of biosurfactant in all the cultures. Complete biodegradation of PCE to ethylene at a faster rate was also observed when vegetable oil was amended to the

  20. Closed-looped in situ nano processing on a culturing cell using an inverted electron beam lithography system

    International Nuclear Information System (INIS)

    Hoshino, Takayuki; Mabuchi, Kunihiko

    2013-01-01

    Highlights: ► An electron beam lithography (EBL) was used as an in situ nano processing for a living cell. ► A synchronized optics was containing an inverted EBL and an optical microscope. ► This system visualized real-time images of the EB-induced nano processing. ► We demonstrated the nano processing for a culturing cell with 200–300 nm resolution. ► Our system would be able to provide high resolution display of virtual environments. -- Abstract: The beam profile of an electron beam (EB) can be focused onto less than a nanometer spot and scanned over a wide field with extremely high speed sweeping. Thus, EB is employed for nano scale lithography in applied physics research studies and in fabrication of semiconductors. We applied a scanning EB as a control system for a living cell membrane which is representative of large scale complex systems containing nanometer size components. First, we designed the opposed co-axial dual optics containing inverted electron beam lithography (I-EBL) system and a fluorescent optical microscope. This system could provide in situ nano processing for a culturing living cell on a 100-nm-thick SiN nanomembrane, which was placed between the I-EBL and the fluorescent optical microscope. Then we demonstrated the EB-induced chemical direct nano processing for a culturing cell with hundreds of nanometer resolution and visualized real-time images of the scanning spot of the EB-induced luminescent emission and chemical processing using a high sensitive camera mounted on the optical microscope. We concluded that our closed-loop in situ nano processing would be able to provide a nanometer resolution display of virtual molecule environments to study functional changes of bio-molecule systems

  1. Characterization behavior of some polymeric composite ion exchangers

    International Nuclear Information System (INIS)

    El-Zahhar, A.A; Ahdel-Aziz, H.M.; Siyam, T.

    2005-01-01

    Polymeric composite resins were prepared by template polymerization process in aqueous solution. Thermogravimetric analysis (TGA), differential thermal analysis (DTA) and The X-ray diffraction patterns (XRD) were performed to evaluate the physico chemical properties of the different polymeric composite resins. The TGA and DTA clarify high thermal stability of prepared polymeric composite resins. XRD of prepared polymeric composite shows that there is crystalline structure of some resins while other are amorphous one

  2. Photocatalytic polymerization induced by a transparent anatase titania aqueous sol and fabrication of polymer composites

    Directory of Open Access Journals (Sweden)

    2010-06-01

    Full Text Available The surface modification of the anatase titania nanoparticles prepared via a controlled nonhydrolytic sol-gel process is achieved by the formation of the bidentate coordination between titania and methacrylic acid (MAA molecules. The in situ photocatalytic polymerization of methyl methacrylate (MMA monomer is initiated by surface modified anatase titania nanoparticles under Xe lamp irradiation. A variety of techniques including differential scanning calorimetry (DSC, thermo-gravimetric analysis (TGA and scanning electron microscopy (SEM are employed to characterize the resulting materials. The glass transition temperatures and the thermal stabilities of polymethyl methacrylate (PMMA composite materials prepared via photocatalytic polymerization are enhanced compared with pure polymer. The partial aggregation of titania nanoparticles in PMMA composite films is derived from the surface polymerization of MMA, which makes the inorganic particles hydrophobic and drives them to the water/oil interfaces.

  3. A modular reactor design for in situ synchrotron x-ray investigation of atomic layer deposition processes

    Science.gov (United States)

    Klug, Jeffrey A.; Weimer, Matthew S.; Emery, Jonathan D.; Yanguas-Gil, Angel; Seifert, Sönke; Schlepütz, Christian M.; Martinson, Alex B. F.; Elam, Jeffrey W.; Hock, Adam S.; Proslier, Thomas

    2015-11-01

    Synchrotron characterization techniques provide some of the most powerful tools for the study of film structure and chemistry. The brilliance and tunability of the Advanced Photon Source allow access to scattering and spectroscopic techniques unavailable with in-house laboratory setups and provide the opportunity to probe various atomic layer deposition (ALD) processes in situ starting at the very first deposition cycle. Here, we present the design and implementation of a portable ALD instrument which possesses a modular reactor scheme that enables simple experimental switchover between various beamlines and characterization techniques. As first examples, we present in situ results for (1) X-ray surface scattering and reflectivity measurements of epitaxial ZnO ALD on sapphire, (2) grazing-incidence small angle scattering of MnO nucleation on silicon, and (3) grazing-incidence X-ray absorption spectroscopy of nucleation-regime Er2O3 ALD on amorphous ALD alumina and single crystalline sapphire.

  4. Direct in situ observations of single Fe atom catalytic processes and anomalous diffusion at graphene edges

    Science.gov (United States)

    Zhao, Jiong; Deng, Qingming; Avdoshenko, Stanislav M.; Fu, Lei; Eckert, Jürgen; Rümmeli, Mark H.

    2014-01-01

    Single-atom catalysts are of great interest because of their high efficiency. In the case of chemically deposited sp2 carbon, the implementation of a single transition metal atom for growth can provide crucial insight into the formation mechanisms of graphene and carbon nanotubes. This knowledge is particularly important if we are to overcome fabrication difficulties in these materials and fully take advantage of their distinct band structures and physical properties. In this work, we present atomically resolved transmission EM in situ investigations of single Fe atoms at graphene edges. Our in situ observations show individual iron atoms diffusing along an edge either removing or adding carbon atoms (viz., catalytic action). The experimental observations of the catalytic behavior of a single Fe atom are in excellent agreement with supporting theoretical studies. In addition, the kinetics of Fe atoms at graphene edges are shown to exhibit anomalous diffusion, which again, is in agreement with our theoretical investigations. PMID:25331874

  5. In situ flash x-ray high-speed computed tomography for the quantitative analysis of highly dynamic processes

    Science.gov (United States)

    Moser, Stefan; Nau, Siegfried; Salk, Manfred; Thoma, Klaus

    2014-02-01

    The in situ investigation of dynamic events, ranging from car crash to ballistics, often is key to the understanding of dynamic material behavior. In many cases the important processes and interactions happen on the scale of milli- to microseconds at speeds of 1000 m s-1 or more. Often, 3D information is necessary to fully capture and analyze all relevant effects. High-speed 3D-visualization techniques are thus required for the in situ analysis. 3D-capable optical high-speed methods often are impaired by luminous effects and dust, while flash x-ray based methods usually deliver only 2D data. In this paper, a novel 3D-capable flash x-ray based method, in situ flash x-ray high-speed computed tomography is presented. The method is capable of producing 3D reconstructions of high-speed processes based on an undersampled dataset consisting of only a few (typically 3 to 6) x-ray projections. The major challenges are identified, discussed and the chosen solution outlined. The application is illustrated with an exemplary application of a 1000 m s-1 high-speed impact event on the scale of microseconds. A quantitative analysis of the in situ measurement of the material fragments with a 3D reconstruction with 1 mm voxel size is presented and the results are discussed. The results show that the HSCT method allows gaining valuable visual and quantitative mechanical information for the understanding and interpretation of high-speed events.

  6. Deformation processes in functional materials studied by in-situ neutron diffraction and ultrasonic techniques

    Czech Academy of Sciences Publication Activity Database

    Šittner, Petr; Novák, Václav; Landa, Michal; Lukáš, Petr

    2007-01-01

    Roč. 462, - (2007), s. 12-22 ISSN 0921-5093 R&D Projects: GA AV ČR IAA1048107; GA ČR GA106/03/1073 Institutional research plan: CEZ:AV0Z10100520; CEZ:AV0Z10480505; CEZ:AV0Z20760514 Keywords : in situ neutron diffraction * ultrasonics * SMA * NiTi * phase transformations Subject RIV: BM - Solid Matter Physics ; Magnetism Impact factor: 1.457, year: 2007

  7. In-situ investigation of the calcination process of mixed oxide xerogels with Raman spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Panitz, J.C. [Paul Scherrer Inst. (PSI), Villigen (Switzerland)

    1997-06-01

    The controlled calcination of materials derived by sol-gel reactions is important for the evolution of the final structure. Raman spectroscopy is an ideal tool for the identification of surface species under in-situ conditions, as demonstrated in the following for the example of a molybdenum oxide-silica xerogel. Raman spectra of this particular sample were recorded at temperatures as high as 1173 K, and compared with those of a reference material.(author) 3 figs., 4 refs.

  8. One step process of decomposition and polymerization to fabricate SiO{sub 2} hollow spheres/polyimide composite for foldable OLEDs

    Energy Technology Data Exchange (ETDEWEB)

    Kim, Min Kyu [SKKU Advanced Institute of Nanotechnology (SAINT) and Center for Human Interface Nano Technology (HINT), Sungkyunkwan University, Suwon 440-746 (Korea, Republic of); Kim, Dong Won; Moon, Soo Hyun [School of Advanced Materials Science & Engineering, Sungkyunkwan University, Suwon 440-746 (Korea, Republic of); Shin, Dong-Wook [SKKU Advanced Institute of Nanotechnology (SAINT) and Center for Human Interface Nano Technology (HINT), Sungkyunkwan University, Suwon 440-746 (Korea, Republic of); College of Engineering, Mathematics and Physical Sciences, University of Exeter, Stocker Road, Exeter EX4 4QL (United Kingdom); Oh, Tae Sik [School of Mechanical and ICT Convergence Engineering, Sunmoon University, Asan 336-708 (Korea, Republic of); Yoo, Ji Beom, E-mail: jbyoo@skku.edu [SKKU Advanced Institute of Nanotechnology (SAINT) and Center for Human Interface Nano Technology (HINT), Sungkyunkwan University, Suwon 440-746 (Korea, Republic of); School of Advanced Materials Science & Engineering, Sungkyunkwan University, Suwon 440-746 (Korea, Republic of)

    2017-03-15

    Graphical abstract: The SiO{sub 2} hollow spheres and polyimide hybrid synthesized using one step process, simultaneous occurrence of decomposition and polymerization (SODP) is useful with a ultra-low dielectric constant and high thermal stability for flexible OLED. - Highlights: • We fabricated hybrid films of SHS/PI by using a one step process with SODP. • The film has ultralow dielectric constant (50 vol% at k = 1.67). • There is no collapse of SiO{sub 2} hollow spheres in the PI matrix after bending test for 50,000 cycles. - Abstract: The fabrication of interlayer dielectrics (ILDs) in flexible organic light-emitting diodes (OLEDs) requires flexible materials with a low dielectric constant as well as materials with excellent electrical, thermal, and mechanical properties for optimal device performance. Hybrid films of SiO{sub 2} hollow spheres (SHS)/polyimide (PI) were prepared using a one-step process, with simultaneous occurrence of decomposition (polystyrene, PS) and polymerization (PI) (SODP). No collapse of SiO{sub 2} hollow spheres in PI was observed from 10 vol% to 60 vol% SHS in hybrid films. The dielectric constant of hybrid films was reduced from 3.45 to 1.67 and was saturated at above 50 vol% of SHS due to the maximum fill factor of SHS in the PI matrix. The thermal stability was excellent up to 500 °C due to the inherent thermal property of PI. After a bending test for 50,000 cycles at a bending radius of 1 mm, the SHS/PI hybrid films retained their dielectric constant and current density. These results indicate the hybrid film to be the most promising candidate for flexible ILDs with a low dielectric constant and high thermal stability for foldable OLEDs.

  9. In situ Remediation Technologies

    NARCIS (Netherlands)

    Grotenhuis, J.T.C.; Rijnaarts, H.H.M.

    2011-01-01

    A summary of two decades of developments of In Situ remediation is presented in this chapter. The basic principles of In Situ technology application are addressed, such as equilibrium relations between contaminant phases, factors controlling biological and geochemical processes, contaminant

  10. Copper-mediated controlled radical polymerization under biological conditions: SET-LRP in blood serum.

    Science.gov (United States)

    Zhang, Qiang; Li, Zaidong; Wilson, Paul; Haddleton, David M

    2013-07-28

    The polymerization of hydrophilic monomers is reported utilizing Cu(0)-mediated living radical polymerization, SET-LRP. Highly active Cu(0) is formed in situ as a result of rapid disproportionation of [Cu(I)(Me6-Tren)Br] in serum. Disproportionation and homogenous controlled radical polymerization (PDI 1.09-1.25) are performed for the first time in blood (sheep) serum.

  11. Síntese e caracterização de Nanocompósitos Esfoliados de Poliestireno: Hidróxido Duplo Lamelar via polimerização in situ Synthesis and characterization of Exfoliated Polystyrene: Layered Double Hydroxide Nanocomposites via in situ polymerization

    Directory of Open Access Journals (Sweden)

    Rodrigo Botan

    2011-01-01

    Full Text Available Nanocompósitos Esfoliados de Poliestireno (PS e Hidróxido Duplo Lamelar (HDL composto por zinco, alumínio e dodecil sulfato de sódio, como ânion interlamelar, foram sintetizados via polimerização in situ. O efeito de diferentes composições de HDL (0,5, 1, 3 e 5% em massa foi avaliado. Os nanocompósitos obtidos foram caracterizados através de ensaios de Difração de Raios X (DRX, Espectroscopia no Infravermelho por Transformada de Fourier (FTIR, Microscopia Eletrônica de Transmissão (MET e Análise Termogravimétrica (TGA. Os resultados obtidos através das análises de DRX e MET mostraram que todos os nanocompósitos produzidos apresentaram morfologia esfoliada. Os resultados das TGA, quando se utilizam 50% de perda de peso como ponto para comparação, apresentaram ganhos significativos de estabilidade térmica para todas as composições dos nanocompósitos em comparação ao poliestireno puro. Este comportamento possibilita uma vasta gama de aplicação destes novos materiais em diversos campos da indústria e pesquisa.Exfoliated nanocomposites of polystyrene (PS and layered double hydroxide (LDH compound of zinc, aluminium and sodium dodecyl sulfate, as interlayer anion, have been synthesized via in situ polymerization. The effect from the LDH compositions (0.5, 1, 3, 5% weight was studied. The nanocomposites were characterized by X-ray Diffraction (XRD, Fourier Transform Infrared Spectroscopy (FTIR, Transmission Electron Microscopy (TEM and Thermogravimetric Analysis (TGA. The XRD and TEM results showed an exfoliated morphology for the nanocomposites in all compositions. With the 50% weight loss taken as a reference, the TGA results indicated significant improvement in thermal stability for all compositions of the nanocomposites, in comparison to pure polystyrene. This is promising for the application of these new materials in many fields of industry and research.

  12. Morphological, thermal and dynamic mechanical properties of Cathay poplar/organoclay composites prepared by in situ process

    International Nuclear Information System (INIS)

    Wang, Wang; Zhu, Yuan; Cao, Jinzhen

    2014-01-01

    Highlights: • We produced poplar wood/organoclay composites by an in situ process. • OMMT uniformly dispersed in cell lumen and cell wall of reinforced wood composites. • Thermal properties of composites were improved by using OMMT without intermediate. - Abstract: In order to improve the thermal stability and dynamic mechanical properties of Cathay poplar (Populus cathayana Rehd.) wood, a kind of organoclay, that is, organo-montmorillonite (OMMT), was introduced into its structure via an in situ process by sequentially impregnating poplar wood with sodium-montmorillonite (Na-MMT, in concentrations of 1.0%, 2.0%, and 4.0%) and didecyldimethylammonium chloride (DDAC, in a concentration of 2.0%). Consequently, the wood/organoclay composites were prepared. The X-ray diffraction (XRD), scanning electron microscopy coupled with energy dispersed X-ray analysis (SEM-EDXA) and Fourier transform infrared spectroscopy (FTIR) were used to characterize the morphological and chemical alterations of the composites. Also the effects of clay type and concentrations on the thermal stability and dynamic mechanical properties of the composites were studied. The results showed that didecyldimethylammonium ions were intercalated into the galleries of Na-MMT through cation exchange, partially separating the silicate layers. Thereafter, the inorganic Na-MMT transformed to OMMT during the in situ synthesis process, and the latter was successfully intercalated into the wood cell wall. The thermal degradation was alleviated in the wood/clay composites, among which the wood/OMMT composites exhibited the best thermal stability. According to dynamic mechanical analysis (DMA) results, the wood/OMMT composites showed an enhancement in energy storage and a diminution in energy dissipation compared to other groups. The improvements in the thermal stability and dynamic mechanical properties of the composites became more significant with the increasing clay content

  13. Laser processing of in situ TiN/Ti composite coating on titanium.

    Science.gov (United States)

    Sahasrabudhe, Himanshu; Soderlind, Julie; Bandyopadhyay, Amit

    2016-01-01

    Laser remelting of commercially pure titanium (CP-Ti) surface was done in a nitrogen rich inert atmosphere to form in situ TiN/Ti composite coating. Laser surface remelting was performed at two different laser powers of 425 W and 475 W. At each power, samples were fabricated with one or two laser scans. The resultant material was a nitride rich in situ coating that was created on the surface. The cross sections revealed a graded microstructure. There was presence of nitride rich dendrites dispersed in α-Ti matrix at the uppermost region. The structure gradually changed with lesser dendrites and more heat affected α-Ti phase maintaining a smooth interface. With increasing laser power, the dendrites appeared to be larger in size. Samples with two laser scans showed discontinuous dendrites and more α-Ti phase as compared to the samples with one laser scan. The resultant composite of TiN along with Ti2N in α-Ti showed substantially higher hardness and wear resistance than the untreated CP-Ti substrate. Coefficient of friction was also found to reduce due to surface nitridation. Leaching of Ti(4+) ions during wear test in DI water medium was found to reduce due to laser surface nitriding. Copyright © 2015 Elsevier Ltd. All rights reserved.

  14. In situ biosynthesis of bacterial nanocellulose-CaCO3 hybrid bionanocomposite: One-step process.

    Science.gov (United States)

    Mohammadkazemi, Faranak; Faria, Marisa; Cordeiro, Nereida

    2016-08-01

    In this work, a simple and green route to the synthesis of the bacterial nanocellulose-calcium carbonate (BNC/CaCO3) hybrid bionanocomposites using one-step in situ biosynthesis was studied. The CaCO3 was incorporated in the bacterial nanocellulose structure during the cellulose biosynthesis by Gluconacetobacter xylinus PTCC 1734 bacteria. Hestrin-Schramm (HS) and Zhou (Z) culture media were used to the hybrid bionanocomposites production and the effect of ethanol addition was investigated. Attenuated total reflection Fourier transform infrared spectroscopy, field emission scanning electron microscopy, X-ray diffraction, energy-dispersive X-ray spectroscopy, inverse gas chromatography and thermogravimetric analysis were used to characterize the samples. The experimental results demonstrated that the ethanol and culture medium play an important role in the BNC/CaCO3 hybrid bionanocomposites production, structure and properties. The BNC/CaCO3 biosynthesized in Z culture medium revealed higher O/C ratio and amphoteric surface character, which justify the highest CaCO3 content incorporation. The CaCO3 was incorporated into the cellulosic matrix decreasing the bacterial nanocellulose crystallinity. This work reveals the high potential of in situ biosynthesis of BNC/CaCO3 hybrid bionanocomposites and opens a new way to the high value-added applications of bacterial nanocellulose. Copyright © 2016 Elsevier B.V. All rights reserved.

  15. Fatigue processes in commercial LiCoO2 batteries: in situ neutron diffraction and electrochemical study

    OpenAIRE

    Dolotko, O.; Senyshyn, A.; Mühlbauer, M. J.; Nikolowski, K.; Ehrenberg, H.

    2012-01-01

    In situ high-resolution neutron powder diffraction along with electrochemical analysis was used to study fatigue processes in commercial LiCoO2 (18650-type) batteries. The electrochemical and structural behavior of cathode and anode materials in fully charged and discharged states has been studied for cells exhibiting different cycling at 25°C and 50°C. High-resolution neutron powder diffraction leads us to observe simultaneous changes in LiCoO2 cathode and graphitic anode, which are relat...

  16. Polymerization Initiated at the Sidewalls of Carbon Nanotubes

    Science.gov (United States)

    Tour, James M.; Hudson, Jared L.

    2011-01-01

    A process has been developed for growing polymer chains via anionic, cationic, or radical polymerization from the side walls of functionalized carbon nanotubes, which will facilitate greater dispersion in polymer matrices, and will greatly enhance reinforcement ability in polymeric material.

  17. Thermal conductivity of pressure polymerized C60

    International Nuclear Information System (INIS)

    Soldatov, A.; Andersson, O.

    1997-01-01

    We have studied the kinetics of C 60 polymerization in the temperature interval 450-500 K at pressures below 1 GPa by measurements of the time dependence of the thermal conductivity. It has been found at 450 K that the polymerization process at 0.8 GPa is slower than the reverse transformation from ''polymeric'' to ''monomeric'' phase at 0.08 GPa. The thermal conductivity λ of polymerized C 60 was measured in the temperature range 100-430 K and found to increase with increasing temperature, which reflects strong phonon scattering. Both the presence of non-bonded C 60 molecules and a high degree of structural disorder in the crystalline lattice of the polymeric phase might be responsible for the behaviour of λ(T). The results for λ(T) are qualitatively similar to those reported previously for C 60 polymerized at higher p, T but an order of magnitude smaller. (orig.)

  18. In situ reflectance and virtual interface analysis for compound semiconductor process control

    Energy Technology Data Exchange (ETDEWEB)

    Breiland, W.G.; Hou, H.Q.; Hammons, B.E.; Klem, J.F.

    1998-05-01

    The authors review the use of in-situ normal incidence reflectance, combined with a virtual interface model, to monitor and control the growth of complex compound semiconductor devices. The technique is being used routinely on both commercial and research metal-organic chemical vapor deposition (MOCVD) reactors and in molecular beam epitaxy (MBE) to measure growth rates and high temperature optical constants of compound semiconductor alloys. The virtual interface approach allows one to extract the calibration information in an automated way without having to estimate the thickness or optical constants of the alloy, and without having to model underlying thin film layers. The method has been used in a variety of data analysis applications collectively referred to as ADVISOR (Analysis of Deposition using Virtual Interfaces and Spectroscopic Optical Reflectance). This very simple and robust monitor and ADVISOR method provides one with the equivalent of a real-time reflection high energy electron reflectance (RHEED) tool for both MBE and MOCVD applications.

  19. In situ observations of solidification processes in γ-TiAl alloys by synchrotron radiation

    International Nuclear Information System (INIS)

    Shuleshova, Olga; Holland-Moritz, Dirk; Loeser, Wolfgang; Voss, Andrea; Hartmann, Helena; Hecht, Ulrike; Witusiewicz, Victor T.; Herlach, Dieter M.; Buechner, Bernd

    2010-01-01

    In situ observations of phase transformations involving melts are performed using energy-dispersive diffraction of synchrotron X-rays on electromagnetically levitated γ-TiAl alloys containing Nb. The determined primary solidification modes, confirmed by microstructure analysis, delivered new reliable data about the boundary of the α(Ti) solidification domain, which differs in the various Ti-Al-Nb phase diagram descriptions. These data have been used for a reassessment of the thermodynamic database of the ternary Ti-Al-Nb system. The new description realistically reflects the experimental findings. Liquidus and solidus temperatures determined by the pyrometric method agree fairly well with the calculated values. Direct experimental information on the nature of the reactions along the univariant lines is provided.

  20. Highly efficient and selective pressure-assisted photon-induced polymerization of styrene

    Energy Technology Data Exchange (ETDEWEB)

    Guan, Jiwen [Department of Physics and Astronomy, University of Western Ontario, London, Ontario N6A 3K7 (Canada); Song, Yang, E-mail: yang.song@uwo.ca [Department of Physics and Astronomy, University of Western Ontario, London, Ontario N6A 3K7 (Canada); Department of Chemistry, University of Western Ontario, London, Ontario N6A 5B7 (Canada)

    2016-06-07

    The polymerization process of condensed styrene to produce polystyrene as an industrially important polymeric material was investigated using a novel approach by combining external compression with ultraviolet radiation. The reaction evolution was monitored as a function of time and the reaction products were characterized by in situ Fourier transform infrared spectroscopy. By optimizing the loading pressures, we observed highly efficient and selective production of polystyrene of different tacticities. Specifically, at relatively low loading pressures, infrared spectra suggest that styrene monomers transform to amorphous atactic polystyrene (APS) with minor crystalline isotactic polystyrene. In contrast, APS was found to be the sole product when polymerization occurs at relatively higher loading pressures. The time-dependent reaction profiles allow the examination of the polymerization kinetics by analyzing the rate constant and activation volume as a function of pressure. As a result, an optimized pressure condition, which allows a barrierless reaction to proceed, was identified and attributed to the very desirable reaction yield and kinetics. Finally, the photoinitiated reaction mechanism and the growth geometry of the polymer chains were investigated from the energy diagram of styrene and by the topology analysis of the crystal styrene. This study shows strong promise to produce functional polymeric materials in a highly efficient and controlled manner.

  1. Vapor phase reactions in polymerization plasma for divinylsiloxane-bis-benzocyclobutene film deposition

    International Nuclear Information System (INIS)

    Kinoshita, Keizo; Nakano, Akinori; Kawahara, Jun; Kunimi, Nobutaka; Hayashi, Yoshihiro; Kiso, Osamu; Saito, Naoaki; Nakamura, Keiji; Kikkawa, Takamaro

    2006-01-01

    Vapor phase reactions in plasma polymerization of divinylsiloxane-bis-benzocyclobutene (DVS-BCB) low-k film depositions on 300 mm wafers were studied using mass spectrometry, in situ Fourier transform infrared, and a surface wave probe. Polymerization via Diels-Alder cycloaddition reaction was identified by the detection of the benzocyclohexene group. Hydrogen addition and methyl group desorption were also detected in DVS-BCB monomer and related large molecules. The dielectric constant k of plasma polymerized DVS-BCB with a plasma source power range up to 250 W was close to ∼2.7 of thermally polymerized DVS-BCB, and increased gradually over 250 W. The electron density at 250 W was about 1.5x10 10 cm -3 . The increase of the k value at higher power was explained by the decrease of both large molecular species via multistep dissociation and incorporation of silica components into the polymer. It was found that the reduction of electron density as well as precursor residence time is important for the plasma polymerization process to prevent the excess dissociation of the precursor

  2. Continuous Preparation of Hollow Polymeric Nanocapsules Using Self-Assembly and a Photo-Crosslinking Process of an Amphiphilic Block Copolymer

    Directory of Open Access Journals (Sweden)

    Xuan Don Nguyen

    2017-11-01

    Full Text Available This paper presents a fabrication method of hollow polymeric nanocapsules (HPNCs. The HPNCs were examined to reduce light trapping in an organic light emitting diodes (OLED device by increasing the refractive index contrast. They were continuously fabricated by the sequential process of self-assembly and photo-crosslinking of an amphiphilic block copolymer of SBR-b-PEGMA, poly(styrene-r-butadiene-b-poly(poly(ethylene glycol methyl ether methacrylate in a flow-focusing microfluidic device. After the photo-crosslinking process, the produced HPNCs have a higher resistance to water and organic solvents, which is applicable to the fabrication process of optical devices. The morphology and hollow structure of the produced nanocapsules were determined by transmission electron microscopy (TEM, scanning electron microscopy (SEM, and atomic force microscopy (AFM. Also, their size control was examined by varying the ratio of inlet flow rates and the morphological difference was studied by changing the polymer concentration. The size was measured by dynamic light scattering (DLS. The refractive index of the layer with and without the HPNCs was measured, and a lower refractive index was obtained in the HPNCs-dispersed layer. In future work, the light extraction efficiency of the HPNCs-dispersed OLED will be examined.

  3. Enhancement of Biodiesel Production from Marine Alga, Scenedesmus sp. through In Situ Transesterification Process Associated with Acidic Catalyst

    Directory of Open Access Journals (Sweden)

    Ga Vin Kim

    2014-01-01

    Full Text Available The aim of this study was to increase the yield of biodiesel produced by Scenedesmus sp. through in situ transesterification by optimizing various process parameters. Based on the orthogonal matrix analysis for the acidic catalyst, the effects of the factors decreased in the order of reaction temperature (47.5% > solvent quantity (26.7% > reaction time (17.5% > catalyst amount (8.3%. Based on a Taguchi analysis, the effects of the factors decreased in the order of solvent ratio (34.36% > catalyst (28.62% > time (19.72% > temperature (17.32%. The overall biodiesel production appeared to be better using NaOH as an alkaline catalyst rather than using H2SO4 in an acidic process, at 55.07 ± 2.18% (based on lipid weight versus 48.41 ± 0.21%. However, in considering the purified biodiesel, it was found that the acidic catalyst was approximately 2.5 times more efficient than the alkaline catalyst under the following optimal conditions: temperature of 70°C (level 2, reaction time of 10 hrs (level 2, catalyst amount of 5% (level 3, and biomass to solvent ratio of 1 : 15 (level 2, respectively. These results clearly demonstrated that the acidic solvent, which combined oil extraction with in situ transesterification, was an effective catalyst for the production of high-quantity, high-quality biodiesel from a Scenedesmus sp.

  4. Enhancement of Biodiesel Production from Marine Alga, Scenedesmus sp. through In Situ Transesterification Process Associated with Acidic Catalyst

    Science.gov (United States)

    Kim, Ga Vin; Choi, WoonYong; Kang, DoHyung; Lee, ShinYoung; Lee, HyeonYong

    2014-01-01

    The aim of this study was to increase the yield of biodiesel produced by Scenedesmus sp. through in situ transesterification by optimizing various process parameters. Based on the orthogonal matrix analysis for the acidic catalyst, the effects of the factors decreased in the order of reaction temperature (47.5%) > solvent quantity (26.7%) > reaction time (17.5%) > catalyst amount (8.3%). Based on a Taguchi analysis, the effects of the factors decreased in the order of solvent ratio (34.36%) > catalyst (28.62%) > time (19.72%) > temperature (17.32%). The overall biodiesel production appeared to be better using NaOH as an alkaline catalyst rather than using H2SO4 in an acidic process, at 55.07 ± 2.18% (based on lipid weight) versus 48.41 ± 0.21%. However, in considering the purified biodiesel, it was found that the acidic catalyst was approximately 2.5 times more efficient than the alkaline catalyst under the following optimal conditions: temperature of 70°C (level 2), reaction time of 10 hrs (level 2), catalyst amount of 5% (level 3), and biomass to solvent ratio of 1 : 15 (level 2), respectively. These results clearly demonstrated that the acidic solvent, which combined oil extraction with in situ transesterification, was an effective catalyst for the production of high-quantity, high-quality biodiesel from a Scenedesmus sp. PMID:24689039

  5. In situ Raman characterization of minerals and degradation processes in a variety of cultural and geological heritage sites.

    Science.gov (United States)

    Gázquez, F; Rull, F; Sanz-Arranz, A; Medina, J; Calaforra, J M; de Las Heras, C; Lasheras, J A

    2017-02-05

    We test the capabilities of in situ Raman spectroscopy for non-destructive analysis of degradation processes in invaluable masterpieces, as well as for the characterization of minerals and prehistoric rock-art in caves. To this end, we have studied the mechanism of decay suffered by the 15th-century limestone sculptures that decorate the retro-choir of Burgos Cathedral (N Spain). In situ Raman probe detected hydrated sulfate and nitrate minerals on the sculptures, which are responsible for the decay of the original limestone. In addition, in situ Raman analyses were performed on unique speleothems in El Soplao Cave (Cantabria, N Spain) and in the Gruta de las Maravillas (Aracena, SW Spain). Unusual cave minerals were detected in El Soplao Cave, such as hydromagnesite (Mg 5 (CO 3 ) 4 (OH) 2 ·4H 2 O), as well as ferromanganese oxides in the black biogenic speleothems recently discovered in this cavern. In the Gruta de las Maravillas, gypsum (CaSO 4 ·2H 2 O) was identified for the first time, as part of the oldest cave materials, so providing additional evidence of hypogenic mechanisms that occurred in this cave during earlier stages of its formation. Finally, we present preliminary analyses of several cave paintings in the renowned "Polychrome Hall" of Altamira Cave (Cantabria, N. Spain). Hematite (Fe 2 O 3 ) is the most abundant mineral phase, which provides the characteristic ochre-reddish color to the Altamira bison and deer paintings. Thus, portable Raman spectroscopy is demonstrated to be an analytical technique compatible with preserving our cultural and natural heritage, since the analysis does not require physical contact between the Raman head and the analyzed items. Copyright © 2016 Elsevier B.V. All rights reserved.

  6. In situ biosynthesis of bacterial nanocellulose-CaCO{sub 3} hybrid bionanocomposite: One-step process

    Energy Technology Data Exchange (ETDEWEB)

    Mohammadkazemi, Faranak, E-mail: f_mkazemi@sbu.ac.ir [Department of Cellulose and Paper Technology, Faculty of New Technologies Engineering, Shahid Beheshti University, Science and Research Campus, Zirab, Savadkooh, Mazandaran (Iran, Islamic Republic of); Faria, Marisa; Cordeiro, Nereida [Faculty of Exact Science and Engineering, University of Madeira, Funchal (Portugal)

    2016-08-01

    In this work, a simple and green route to the synthesis of the bacterial nanocellulose-calcium carbonate (BNC/CaCO{sub 3}) hybrid bionanocomposites using one-step in situ biosynthesis was studied. The CaCO{sub 3} was incorporated in the bacterial nanocellulose structure during the cellulose biosynthesis by Gluconacetobacter xylinus PTCC 1734 bacteria. Hestrin-Schramm (HS) and Zhou (Z) culture media were used to the hybrid bionanocomposites production and the effect of ethanol addition was investigated. Attenuated total reflection Fourier transform infrared spectroscopy, field emission scanning electron microscopy, X-ray diffraction, energy-dispersive X-ray spectroscopy, inverse gas chromatography and thermogravimetric analysis were used to characterize the samples. The experimental results demonstrated that the ethanol and culture medium play an important role in the BNC/CaCO{sub 3} hybrid bionanocomposites production, structure and properties. The BNC/CaCO{sub 3} biosynthesized in Z culture medium revealed higher O/C ratio and amphoteric surface character, which justify the highest CaCO{sub 3} content incorporation. The CaCO{sub 3} was incorporated into the cellulosic matrix decreasing the bacterial nanocellulose crystallinity. This work reveals the high potential of in situ biosynthesis of BNC/CaCO{sub 3} hybrid bionanocomposites and opens a new way to the high value-added applications of bacterial nanocellulose. - Graphical Abstract: Display Omitted - Highlights: • BNC/CaCO{sub 3} hybrid bionanocomposites were produced using in situ biosynthesis process. • Ethanol and culture medium play an important role in the production and properties. • Z-BNC/CaCO{sub 3} bionanocomposites revealed higher O/C ratio and amphoteric surface character. • CaCO{sub 3} incorporated into the BNC decreased crystallinity.

  7. Polymerization with freezing

    International Nuclear Information System (INIS)

    Ben-Naim, E; Krapivsky, P L

    2005-01-01

    Irreversible aggregation processes involving reactive and frozen clusters are investigated using the rate equation approach. In aggregation events, two clusters join irreversibly to form a larger cluster; additionally, reactive clusters may spontaneously freeze. Frozen clusters do not participate in merger events. Generally, freezing controls the nature of the aggregation process, as demonstrated by the final distribution of frozen clusters. The cluster mass distribution has a power-law tail, F k ∼k -γ , when the freezing process is sufficiently slow. Different exponents, γ = 1 and 3, are found for the constant and the product aggregation rates, respectively. For the latter case, the standard polymerization model, either no gels, or a single gel, or even multiple gels, may be produced

  8. Hydro-physical processes at the plunge point: an analysis using satellite and in situ data

    Directory of Open Access Journals (Sweden)

    A. T. Assireu

    2011-12-01

    Full Text Available The plunge point is the main mixing point between river and epilimnetic reservoir water. Plunge point monitoring is essential for understanding the behavior of density currents and their implications for reservoir. The use of satellite imagery products from different sensors (Landsat TM band 6 thermal signatures and visible channels for the characterization of the river-reservoir transition zone is presented in this study. It is demonstrated the feasibility of using Landsat TM band imagery to discern the subsurface river plumes and the plunge point. The spatial variability of the plunge point evident in the hydrologic data illustrates the advantages of synoptic satellite measurements over in situ point measurements alone to detect the river-reservoir transition zone. During the dry season, when the river-reservoir water temperature differences vanish and the river circulation is characterized by interflow-overflow, the river water inserts into the upper layers of the reservoir, affecting water quality. The results indicate a good agreement between hydrologic and satellite data and that the joint use of thermal and visible channel data for the operational monitoring of a plunge point is feasible. The deduced information about the density current from this study could potentially be assimilated into numerical models and hence be of significant interest for environmental and climatological research.

  9. Stability investigations of zinc and cobalt precipitates immobilized by in situ bioprecipitation (ISBP) process

    KAUST Repository

    Satyawali, Yamini

    2010-09-01

    In situ bioprecipitation (ISBP), which involves immobilizing the metals as precipitates (mainly sulphides) in the solid phase, is an effective method of metal removal from contaminated groundwater. This study investigated the stability of metal precipitates formed after ISBP in two different solid-liquid matrices (artificial and natural). The artificial matrix consisted of sand, Zn (200mgL-1), artificial groundwater and a carbon source (electron donor). Here the stability of the Zn precipitates was evaluated by manipulation of redox and pH. The natural system matrices included aquifer material and groundwater samples collected from three different metal (Zn and Co) contaminated sites and different carbon sources were provided as electron donors. In the natural matrices, metal precipitates stability was assessed by changing aquifer redox conditions, sequential extraction, and BIOMET® assay. The results indicated that, in the artificial matrix, redox manipulation did not impact the Zn precipitates. However the sequential pH change proved detrimental, releasing 58% of the precipitated Zn back into liquid phase. In natural matrices, the applied carbon source largely affected the stability of metal precipitates. Elemental analysis performed on the precipitates formed in natural matrix showed that the main elements of the precipitates were sulphur with Zn and Co. © 2010 Elsevier B.V.

  10. In situ resistance measurements of bronze process Nb-Sn-Cu-Ta multifilamentary composite conductors during reactive diffusion

    International Nuclear Information System (INIS)

    Tan, K S; Hopkins, S C; Glowacki, B A; Majoros, M; Astill, D

    2004-01-01

    The conditions under which the Nb 3 Sn intermetallic layer is formed by solid-state reactive diffusion processes in bronze process multifilamentary conductors greatly influence the performance of the conductors. By convention, isothermal heat treatment is used and often causes non-uniformity of A15 layers formed across the wire. Therefore, characterization and optimization of the conductor during the reactive diffusion processes is crucial in order to improve the overall conductor's performance. In this paper, a different characterization approach and perhaps an optimization technique is presented, namely in situ resistance measurement by an alternating current (AC) method. By treating the components of such multifilamentary wires as a set of parallel resistors, the resistances of the components may be combined using the usual rules for resistors in parallel. The results show that the resistivity of the entire wire changes significantly during the reactive diffusion processes. The development of the Nb 3 Sn layer in bronze process Nb-Sn-Cu-Ta multifilamentary wires at different stages of the reactive diffusion processes has been monitored using measured resistivity changes, and correlated with results from DTA, ACS, SEM and EDS

  11. Antibacterial and hemolysis activity of polypyrrole nanotubes decorated with silver nanoparticles by an in-situ reduction process.

    Science.gov (United States)

    Upadhyay, J; Kumar, A; Gogoi, B; Buragohain, A K

    2015-09-01

    Polypyrrole nanotube-silver nanoparticle nanocomposites (PPy-NTs:Ag-NPs) have been synthesized by in-situ reduction of silver nitrate (AgNO3) to suppress the agglomeration of Ag-NPs. The morphology and chemical structure of the nanocomposites have been studied by HRTEM, SEM, XRD, FTIR and UV-vis spectroscopy. The average diameter of the polypyrrole nanotubes (PPy-NTs) is measured to be 130.59±5.5 nm with their length in the micrometer range, while the silver nanoparticles (Ag-NPs) exhibit spherical shape with an average diameter of 23.12±3.23 nm. In-vitro blood compatibility of the nanocomposites has been carried out via hemolysis assay. Antimicrobial activity of the nanocomposites has been investigated with Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus) bacteria. The results depict that the hemolysis and antimicrobial activities of the nanocomposites increase with increasing Ag-NP concentration that can be controlled by the AgNO3 precursor concentration in the in-situ process. Copyright © 2015 Elsevier B.V. All rights reserved.

  12. Preparation of a Strong Gelatin-Short Linear Glucan Nanocomposite Hydrogel by an in Situ Self-Assembly Process.

    Science.gov (United States)

    Ge, Shengju; Li, Man; Ji, Na; Liu, Jing; Mul, Hongyan; Xiong, Liu; Sun, Qingjie

    2018-01-10

    Gelatin hydrogels exhibit excellent biocompatibility, nonimmunogenicity, and biodegradability, but they have limited applications in the food and medical industries because of their poor mechanical properties. Herein, we first developed an in situ self-assembly process for the preparation of gelatin-short linear glucan (SLG) nanocomposite hydrogels with enhanced mechanical strength. The microstructure, dynamic viscoelasticity, compression behavior, and thermal characteristics of the gelatin-SLG nanocomposite hydrogels were determined using scanning electron microscopy (SEM), dynamic rheological experiments, compression tests, and texture profile analysis tests. The SEM images revealed that nanoparticles were formed by the in situ self-assembly of SLG in the gelatin matrix and that the size of these nanoparticles ranged between 200 and 600 nm. The pores of the nanocomposite hydrogels were smaller than those of the pure gelatin hydrogels. Transmission electron microscopy images and X-ray diffraction further confirmed the presence of SLG nanoparticles with spherical shapes and B-type structures. Compared with pure gelatin hydrogels, the nanocomposite hydrogels exhibited improved mechanical behavior. Notably, the hardness and maximum values of the compressive stress of gelatin-SLG nanocomposites containing 5% SLG increased by about 2-fold and 3-fold, respectively, compared to the corresponding values of pure gelatin hydrogels.

  13. Enhanced Cyclability of Lithium-Oxygen Batteries with Electrodes Protected by Surface Films Induced via In-Situ Electrochemical Process

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Bin; Xu, Wu; Tao, Jinhui; Yan, Pengfei; Zheng, Jianming; Engelhard, Mark H.; Lu, Dongping; Wang, Chongmin; Zhang, Jiguang

    2018-04-16

    Although the rechargeable lithium-oxygen (Li-O2) batteries have extremely high theoretical specific energy, the practical application of these batteries is still limited by the instability of their carbon-based air-electrode, Li metal anode, and electrolytes towards reduced oxygen species. Here we demonstrate a simple one-step in-situ electrochemical pre-charging strategy to generate thin protective films on both carbon nanotubes (CNTs) air-electrode and Li metal anode simultaneously under an inert atmosphere. Li-O2 cells after such pre-treatment demonstrate significantly extended cycle life of 110 and 180 cycles under the capacity-limited protocol of 1000 mAh g-1 and 500 mAh g-1, respectively, which is far more than those without pre-treatment. The thin-films formed from decomposition of electrolyte during in-situ electrochemical pre-charging process in an inert environment can protect both CNTs air-electrode and Li metal anode prior to conventional Li-O2 discharge/charge cycling where reactive reduced oxygen species are formed. This work provides a new approach for protections of carbon-based air-electrode and Li metal anode in practical Li-O2 batteries, and may also be applied to other battery systems.

  14. Geochemical processes in the Febex bentonite after a heating and hydration in situ test in the Grimsel URL

    International Nuclear Information System (INIS)

    Fernandez, A.M.; Rivas, P.; Muurinen, A.; Montarges-Pelletier, E.; Jockwer, N.

    2010-01-01

    Document available in extended abstract form only. Unsaturated compacted bentonite is foreseen by several countries as a backfill and sealing material in high-level radioactive waste repositories. The FEBEX project provides the opportunity to understand and quantify the geochemical processes taking place in the near-field and to evaluate the long-term behaviour of the FEBEX bentonite. FEBEX is a demonstration and research project, which includes a large-scale in situ experiment performed in a gallery excavated in granite at the Grimsel underground laboratory research (URL) in Switzerland. Two main operational phases have been executed: a) the First Operational Phase (1996-2002), which corresponds to the FEBEX-I and FEBEX-II projects, and b) the Second Operational Phase (2002-2007), which was carried out within the frame of the NF-PRO project. In the first Operation Phase, the in situ test consisted of: 1) the heating system formed by two heaters separated horizontally by 1 m, which simulate full-sized canisters and maintain a temperature of 100 deg. C; 2) the bentonite barrier, made of blocks of highly compacted bentonite (w.c.: 14.4%;ρ d : 1.70 g/cm 3 ); 3) the drift excavated in the granite. This rock is saturated and hydrates the clay with a water flow of 7-12 L/ day; and 4) the instrumentation, monitoring and control systems. The in situ test began on February 27 1997. Heater 1 was switched-off in February 2002. The dismantling of section 1 of the in situ test provided the opportunity to analyse the thermo-hydro-geochemical (THG) processes taking place in the bentonite barrier. In the second Operational Phase, after removing the buffer and all the components, a dummy steel cylinder with a length of 1 m was inserted in the void left by Heater 1 in the centre of the buffer. A new concrete plug with a total length of 3 m was constructed by shotcreting. Heater 2 maintained its temperature of 100 deg. C at contact with the bentonite throughout the entire

  15. Hydrochemical processes in lowland rivers: insights from in situ, high-resolution monitoring

    Directory of Open Access Journals (Sweden)

    A. J. Wade

    2012-11-01

    Full Text Available This paper introduces new insights into the hydrochemical functioning of lowland river systems using field-based spectrophotometric and electrode technologies. The streamwater concentrations of nitrogen species and phosphorus fractions were measured at hourly intervals on a continuous basis at two contrasting sites on tributaries of the River Thames – one draining a rural catchment, the River Enborne, and one draining a more urban system, The Cut. The measurements complement those from an existing network of multi-parameter water quality sondes maintained across the Thames catchment and weekly monitoring based on grab samples. The results of the sub-daily monitoring show that streamwater phosphorus concentrations display highly complex dynamics under storm conditions dependent on the antecedent catchment wetness, and that diurnal phosphorus and nitrogen cycles occur under low flow conditions. The diurnal patterns highlight the dominance of sewage inputs in controlling the streamwater phosphorus and nitrogen concentrations at low flows, even at a distance of 7 km from the nearest sewage treatment works in the rural River Enborne. The time of sample collection is important when judging water quality against ecological thresholds or standards. An exhaustion of the supply of phosphorus from diffuse and multiple septic tank sources during storm events was evident and load estimation was not improved by sub-daily monitoring beyond that achieved by daily sampling because of the eventual reduction in the phosphorus mass entering the stream during events. The results highlight the utility of sub-daily water quality measurements and the discussion considers the practicalities and challenges of in situ, sub-daily monitoring.

  16. Coupling purification and in situ immobilization process of monoclonal antibodies to clenbuterol for immunosensor application.

    Science.gov (United States)

    Cao, Hui; Yuan, Min; Wang, Lili; Yu, Jingsong; Xu, Fei

    2015-05-01

    Clenbuterol (CL), which promotes the growth of muscular tissue and the reduction of body fat in pigs and cattle, has been confirmed to be a potential hazard to human health. In this study, a monoclonal antibody to clenbuterol (CL mAb) from a hybridoma culture supernatant was purified by an aqueous two-phase system (ATPS) at different polyethylene glycol (PEG) concentrations, PEG molecular weights, pH values, and NaCl concentrations. Then the CL mAb was immobilized in situ by directly adding polystyrene microspheres (PSMSs) into a PEG phase containing CL mAb. Using the immobilized antibody, an immunosensor was constructed to detect the CL residues in pork samples. The results showed that using an ATPS composed of 15% (w/w) PEG6000, 15% (w/w) phosphate, and 15% (w/w) NaCl at pH 8.0, the partition coefficient was 7.24, the activity recovery was 87.86%, and the purification fold was 2.88. The PEG-CL mAb-PSMS retained approximately 98% of its initial activity after 30-ml phosphate buffer (PBS) washings. After 30days of storage, the CL mAb-PSMS lost nearly 75% of its activity, whereas the PEG-CL mAb-PSMS retained as much as 95% of its initial activity. Furthermore, the constructed immunosensor obtained recoveries of 90.5 to 102.6% when applied to pork samples spiked with CL. Copyright © 2015 Elsevier Inc. All rights reserved.

  17. Investigation of the influence of polymerization temperature on the agglomeration process of the CNT in the composite matrix

    Science.gov (United States)

    Goshev, A. A.; Eseev, M. K.

    2017-11-01

    The goal of this work is experimental study of electrophysical properties of polymer nanocomposites reinforced with multiwalled carbon nanotubes (MWCNTs) in alternating electric field in low frequency band of 0.01 Hz – 10 MHz. In this paper we present investigation concentration properties, different conduction mechanism, agglomeration effects and activation carrier process in composites based on epoxy resin with CNTs as addition of temperature region from 150÷300 K.

  18. Consciousness as a process of queries and answers in architectures based on in situ representations

    NARCIS (Netherlands)

    van der Velde, F.; van der Velde, Frank

    2013-01-01

    Functional or access consciousness can be described as an ongoing dynamic process of queries and answers. Whenever we have an awareness of an object or its surroundings, it consists of the dynamic process that answers (implicit) queries like "What is the color or shape of the object?" or "What

  19. Carboxyl-Functionalized Polymeric Microspheres Prepared by One-Stage Photoinitiated RAFT Dispersion Polymerization

    Directory of Open Access Journals (Sweden)

    Jianbo Tan

    2017-12-01

    Full Text Available Herein, we report a photoinitiated reversible addition-fragmentation chain transfer (RAFT dispersion copolymerization of methyl methacrylate (MMA and methyl methacrylic (MAA for the preparation of highly monodisperse carboxyl-functionalized polymeric microspheres. High rates of polymerization were observed, with more than 90% particle yields being achieved within 3 h of UV irradiation. Effects of reaction parameters (e.g., MAA concentration, RAFT agent concentration, photoinitiator concentration, and solvent composition were studied in detail, and highly monodisperse polymeric microspheres were obtained in most cases. Finally, silver (Ag composite microspheres were prepared by in situ reduction of AgNO3 using the carboxyl-functionalized polymeric microspheres as the template. The obtained Ag composite microspheres were able to catalyze the reduction of methylene blue (MB with NaBH4 as a reductant.

  20. Post polymerization cure shape memory polymers

    Science.gov (United States)

    Wilson, Thomas S; Hearon, Michael Keith; Bearinger, Jane P

    2014-11-11

    This invention relates to chemical polymer compositions, methods of synthesis, and fabrication methods for devices regarding polymers capable of displaying shape memory behavior (SMPs) and which can first be polymerized to a linear or branched polymeric structure, having thermoplastic properties, subsequently processed into a device through processes typical of polymer melts, solutions, and dispersions and then crossed linked to a shape memory thermoset polymer retaining the processed shape.

  1. Post polymerization cure shape memory polymers

    Energy Technology Data Exchange (ETDEWEB)

    Wilson, Thomas S.; Hearon, II, Michael Keith; Bearinger, Jane P.

    2017-01-10

    This invention relates to chemical polymer compositions, methods of synthesis, and fabrication methods for devices regarding polymers capable of displaying shape memory behavior (SMPs) and which can first be polymerized to a linear or branched polymeric structure, having thermoplastic properties, subsequently processed into a device through processes typical of polymer melts, solutions, and dispersions and then crossed linked to a shape memory thermoset polymer retaining the processed shape.

  2. Ultrasonic monitoring of recrystallization: An example of in-situ process control with NDE

    Science.gov (United States)

    Liu, Guizhong

    Technology development in materials science, electrical engineering, NDE, mechanical engineering, and computer science, makes it possible to produce advanced materials of designed microstructure and properties. A control model for materials processing with NDE technology was proposed and a prototype of the high temperature EMAT measurement system was built. The example studied is the ultrasonic monitoring of recrystallization in 5XXX aluminum alloys. There are two distinguished textures in aluminum alloys, i.e., recrystallization texture and rolling texture. These two textures change in opposite directions during the hot rolling process: the rolling process will produce rolling texture, while the annealing process produces recrystallization texture. The control goal of the hot rolling process is to produce predefined texture and microstructure. Texture information is inferred from ultrasonic velocity measurements and the microstructure information is inferred from ultrasonic attenuation measurements. Several models in interdisciplinary fields are proposed and preliminary verification experimental results were presented. A pattern recognition technique was introduced to process OIM raw data, which results in a new algorithm to extract texture information. A new model was proposed to model the texture evolution during annealing. Several pieces of computer software were developed to process experimental data and to implement the models proposed.

  3. Polymerization of epoxy resins studied by positron annihilation

    International Nuclear Information System (INIS)

    Suzuki, T.; Hayashi, T.; Ito, Y.

    1999-01-01

    The polymerization process of epoxy resins (bisphenol-A dicyanate) was studied using positron-annihilation spectroscopy. The polymerization from monomer to polymer through a polymerization reaction was followed by positron-annihilation lifetime spectroscopy measurements. Resins kept at curing temperatures (120, 150 and 200 o C) changed form from of powder to a solid through a liquid. The size of the intermolecular spaces of the solid samples increased along with the progress of polymerization. (author)

  4. Formulation and process considerations for the design of sildenafil-loaded polymeric microparticles by vibrational spray-drying

    DEFF Research Database (Denmark)

    Beck-Broichsitter, Moritz; Bohr, Adam; Aragão-Santiago, Leticia

    2017-01-01

    CONTEXT AND OBJECTIVE: The current study reports the preparation and characterization of sildenafil-loaded poly(lactide-co-glycolide) (PLGA)-based microparticles (MPs) by means of vibrational spray-drying. Emphasis was placed on relevant formulation and process parameters with influence on the pr......CONTEXT AND OBJECTIVE: The current study reports the preparation and characterization of sildenafil-loaded poly(lactide-co-glycolide) (PLGA)-based microparticles (MPs) by means of vibrational spray-drying. Emphasis was placed on relevant formulation and process parameters with influence......), respectively. Furthermore, interactions between sildenafil and the PLGA matrix were observed for the spray-dried MPs. Optimization of spray-drying conditions allowed for a fabrication of defined MPs (size range of ∼4-8 μm) displaying a high sildenafil encapsulation efficiency (>90%) and sustained sildenafil...... properties of the prepared powders. CONCLUSION: Identification of relevant formulation and spray-drying parameters enabled the fabrication of tailored sildenafil-loaded PLGA-based MPs, which meet the needs of the individual application (e.g. controlled drug delivery to the lungs)....

  5. Instrumentation and process control development for in situ coal gasification. Fourth quarterly report, September--November 1975

    Energy Technology Data Exchange (ETDEWEB)

    Northrop, D.A. (ed.)

    1976-01-01

    The instrumentation effort for Phases 2 and 3 of the Second Hanna In Situ Coal Gasification Experiment was fielded and background data obtained prior to the initiation of Phase 2 on November 25, 1975. A total of over 600 channels of instrumentation in 15 instrumentation wells and two surface arrays was fielded for the instrumentation techniques under evaluation. The feasibility of the passive acoustic technique to locate the source of process-related noises has been demonstrated; its utility is presently hampered by the inexact definition of signal arrivals and the lack of automated signal monitoring and analysis systems. A revised mathematical model for the electrical techniques has been developed which demonstrates the potential for remote monitoring. (auth)

  6. Processing and Mechanical Properties of NiAl-Based In-Situ Composites. Ph.D. Thesis Final Report

    Science.gov (United States)

    Johnson, David Ray

    1994-01-01

    In-situ composites based on the NiAl-Cr eutectic system were successfully produced by containerless processing and evaluated. The NiAl-Cr alloys had a fibrous microstructure while the NiAl-(Cr,Mo) alloys containing 1 at. percent or more molybdenum exhibited a lamellar structure. The NiAl-28Cr-6Mo eutectic displays promising high temperature strength while still maintaining a reasonable room temperature fracture toughness when compared to other NiAl-based materials. The Laves phase NiAlTa was used to strengthen NiAl and very promising creep strengths were found for the directionally solidified NiAl-NiAlTa eutectic. The eutectic composition was found to be near NiAl-15.5Ta (at. percent) and well aligned microstructures were produced at this composition. An off-eutectic composition of NiAl-14.5Ta was also processed, consisting of NiAl dendrites surrounded by aligned eutectic regions. The room temperature toughness of these two phase alloys was similar to that of polycrystalline NiAl even with the presence of the brittle Laves phase NiAlTa. Polyphase in-situ composites were generated by directional solidification of ternary eutectics. The systems investigated were the Ni-Al-Ta-X (X=Cr, Mo, or V) alloys. Ternary eutectics were found in each of these systems and both the eutectic composition and temperature were determined. Of these ternary eutectics, the one in the NiAl-Ta-Cr system was found to be the most promising. The fracture toughness of the NiAl-(Cr,Al)NiTa-Cr eutectic was intermediate between those of the NiAl-NiAlTa eutectic and the NiAl-Cr eutectic. The creep strength of this ternary eutectic was similar to or greater than that of the NiAl-Cr eutectic.

  7. Propagation of kink—antikink pair along microtubules as a control mechanism for polymerization and depolymerization processes

    International Nuclear Information System (INIS)

    Kavitha, L.; Muniyappan, A.; Dhamayanthi, S.; Zdravković, S.; Satarić, M. V.; Marlewski, A.; Gopi, D.

    2014-01-01

    Among many types of proteinaceous filaments, microtubules (MTs) constitute the most rigid components of the cellular cytoskeleton. Microtubule dynamics is essential for many vital cellular processes such as intracellular transport, metabolism, and cell division. We investigate the nonlinear dynamics of inhomogeneous microtubulin systems and the MT dynamics is found to be governed by a perturbed sine-Gordon equation. In the presence of various competing nonlinear inhomogeneities, it is shown that this nonlinear model can lead to the existence of kink and antikink solitons moving along MTs. We demonstrate kink—antikink pair collision in the framework of Hirota's bilinearization method. We conjecture that the collisions of the quanta of energy propagating in the form of kinks and antikinks may offer a new view of the mechanism of the retrograde and anterograde transport direction regulation of motor proteins in microtubulin systems. (interdisciplinary physics and related areas of science and technology)

  8. In situ investigation of wet chemical processes for chalcopyrite solar cells by L-edge XAS under ambient conditions

    Energy Technology Data Exchange (ETDEWEB)

    Greil, Stefanie M. [Helmholtz-Zentrum Berlin fuer Materialien und Energie, Albert-Einstein-Strasse 15, 12489 Berlin (Germany); Lauermann, Iver, E-mail: Iver.lauermann@helmholtz-berlin.d [Helmholtz-Zentrum Berlin fuer Materialien und Energie, Albert-Einstein-Strasse 15, 12489 Berlin (Germany); Ennaoui, Ahmed; Kropp, Timo; Lange, Kathrin M.; Weber, Matthieu [Helmholtz-Zentrum Berlin fuer Materialien und Energie, Albert-Einstein-Strasse 15, 12489 Berlin (Germany); Aziz, Emad F., E-mail: Emad.Aziz@helmholtz-berlin.d [Helmholtz-Zentrum Berlin fuer Materialien und Energie, Albert-Einstein-Strasse 15, 12489 Berlin (Germany)

    2010-02-15

    Two instrumental setups for in situ soft X-ray absorption spectroscopy in liquid systems are demonstrated in this work. One for investigating chemical reactions in solutions and a new one for the solid component of a liquid / (as in both / absorber) solid interface. We used these setups for investigating two production processes for chalcopyrite solar cells under ambient conditions, probing the L-edge of Zn and Cu. The first one is a flow cell with a silicon nitride membrane to study the chemical bath deposition process for Cd-free buffer layers. Examining the electronic structure of involved Zn complexes allows to determine the exact reaction mechanism taking place during this process. The second setup is a rotating disk for investigating the bath/absorber interface upon the etching process of superficial binary copper compounds of the absorber as a function of time. The time resolution of the chemical reaction demonstrated in this study ranges from the second to minute time scale.

  9. In situ investigation of wet chemical processes for chalcopyrite solar cells by L-edge XAS under ambient conditions

    International Nuclear Information System (INIS)

    Greil, Stefanie M.; Lauermann, Iver; Ennaoui, Ahmed; Kropp, Timo; Lange, Kathrin M.; Weber, Matthieu; Aziz, Emad F.

    2010-01-01

    Two instrumental setups for in situ soft X-ray absorption spectroscopy in liquid systems are demonstrated in this work. One for investigating chemical reactions in solutions and a new one for the solid component of a liquid / (as in both / absorber) solid interface. We used these setups for investigating two production processes for chalcopyrite solar cells under ambient conditions, probing the L-edge of Zn and Cu. The first one is a flow cell with a silicon nitride membrane to study the chemical bath deposition process for Cd-free buffer layers. Examining the electronic structure of involved Zn complexes allows to determine the exact reaction mechanism taking place during this process. The second setup is a rotating disk for investigating the bath/absorber interface upon the etching process of superficial binary copper compounds of the absorber as a function of time. The time resolution of the chemical reaction demonstrated in this study ranges from the second to minute time scale.

  10. In situ investigation of wet chemical processes for chalcopyrite solar cells by L-edge XAS under ambient conditions

    Science.gov (United States)

    Greil, Stefanie M.; Lauermann, Iver; Ennaoui, Ahmed; Kropp, Timo; Lange, Kathrin M.; Weber, Matthieu; Aziz, Emad F.

    2010-02-01

    Two instrumental setups for in situ soft X-ray absorption spectroscopy in liquid systems are demonstrated in this work. One for investigating chemical reactions in solutions and a new one for the solid component of a liquid / (as in both / absorber) solid interface. We used these setups for investigating two production processes for chalcopyrite solar cells under ambient conditions, probing the L-edge of Zn and Cu. The first one is a flow cell with a silicon nitride membrane to study the chemical bath deposition process for Cd-free buffer layers. Examining the electronic structure of involved Zn complexes allows to determine the exact reaction mechanism taking place during this process. The second setup is a rotating disk for investigating the bath/absorber interface upon the etching process of superficial binary copper compounds of the absorber as a function of time. The time resolution of the chemical reaction demonstrated in this study ranges from the second to minute time scale.

  11. In-situ monitoring of Saccharomyces cerevisiae ITV01 bioethanol process using near-infrared spectroscopy NIRS and chemometrics.

    Science.gov (United States)

    Corro-Herrera, Víctor Abel; Gómez-Rodríguez, Javier; Hayward-Jones, Patricia Margaret; Barradas-Dermitz, Dulce María; Aguilar-Uscanga, María Guadalupe; Gschaedler-Mathis, Anne Christine

    2016-03-01

    The application feasibility of in-situ or in-line monitoring of S. cerevisiae ITV01 alcoholic fermentation process, employing Near-Infrared Spectroscopy (NIRS) and Chemometrics, was investigated. During the process in a bioreactor, in the complex analytical matrix, biomass, glucose, ethanol and glycerol determinations were performed by a transflection fiber optic probe immersed in the culture broth and connected to a Near-Infrared (NIR) process analyzer. The NIR spectra recorded between 800 and 2,200 nm were pretreated using Savitzky-Golay smoothing and second derivative in order to perform a partial least squares regression (PLSR) and generate the calibration models. These calibration models were tested by external validation and then used to predict concentrations in batch alcoholic fermentations. The standard errors of calibration (SEC) for biomass, ethanol, glucose and glycerol were 0.212, 0.287, 0.532, and 0.296 g/L and standard errors of prediction (SEP) were 0.323, 0.369, 0.794, and 0.507 g/L, respectively. Calibration and validation criteria were defined and evaluated in order to generate robust and reliable models for an alcoholic fermentation process matrix. © 2016 American Institute of Chemical Engineers Biotechnol. Prog., 32:510-517, 2016. © 2016 American Institute of Chemical Engineers.

  12. In-Situ Real Time Monitoring and Control of Mold Making and Filling Processes: Final Report

    Energy Technology Data Exchange (ETDEWEB)

    Mohamed Abdelrahman; Kenneth Currie

    2010-12-22

    This project presents a model for addressing several objectives envisioned by the metal casting industries through the integration of research and educational components. It provides an innovative approach to introduce technologies for real time characterization of sand molds, lost foam patterns and monitoring of the mold filling process. The technology developed will enable better control over the casting process. It is expected to reduce scrap and variance in the casting quality. A strong educational component is integrated into the research plan to utilize increased awareness of the industry professional, the potential benefits of the developed technology, and the potential benefits of cross cutting technologies.

  13. In situ observation of plutonium transfer processes in the marine environment

    International Nuclear Information System (INIS)

    Guary, J.-C.; Fraizier, Andre

    1975-09-01

    A preliminary observation of plutonium transfer processes in the marine environment was carried out and showed that concentration of the radionuclide was lower when marine organisms stood at a higher trophic level. This observation supplemented by an investigation on contamination pathways showed that plutonium was not concentrated along the food chain and its uptake occured preferentially by direct contact of species with seawater, a process chiefly affecting producers and primary consumers. It appeared that the marine sediment was not a significant vector of plutonium transfer in burrowing species [fr

  14. One-Pot Synthesis of Waterborne Polymeric Dispersions Stabilized with Alkali-Soluble Resins

    Directory of Open Access Journals (Sweden)

    Massimo Bandiera

    2018-01-01

    Full Text Available Alkali-soluble resins (ASRs are a type of electrosteric emulsifiers of high interest because they can profitably improve the features of waterborne dispersions. In this work, they have been synthesized in-situ through a one-pot approach and they have been used as polymeric surfactants for a second emulsion polymerization step in the same reactor. This strategy provides some advantages compared to other polymerization techniques, like the intensification of the process and the absence of organic solvents. Their use can also further reduce the environmental impact of formulations for film-forming applications, since grafting reactions with the particles have been observed and quantified in relation with the synthetic parameters. These chemical linkages with the particles may reduce the leaching and the release of surfactants from polymeric films, for example in water-based coatings or adhesives. The systems have been also studied from the kinetics point of view, finding relevant differences with other electrosterically stabilized processes from the literature, as well as concerns the nucleation mechanism.

  15. In-Situ Real Time Monitoring and Control of Mold Making and Filling Processes

    Energy Technology Data Exchange (ETDEWEB)

    None

    2004-11-01

    This factsheet describes a research effort to develop an innovative approach to introduce technologies for real-time characterization of sand molds, lost foam patterns, and monitoring of the mold filling process. This will reduce scrap, improve product quality, and save energy.

  16. In-situ observations and modeling of spring snowmelt processes in an Altay Mountains river basin

    Science.gov (United States)

    Wu, Xuejiao; Wang, Ninglian; Shen, Yongping; He, Jianqiao; Zhang, Wei

    2014-01-01

    Snowmelt is a principal source for ground-water recharge and stream flows in mountainous regions of northwestern China. Knowledge of the timing, magnitude, and processes of snowmelt under changing climate conditions is required for appropriate water resource management. The Utah energy balance (UEB) model was used to simulate the development and melting of spring (March 2012) snow cover at an observation site in the Kayiertesi River Basin in the Altay Mountains in Xinjiang. The modeled results were validated by field measurements and remotely sensed data. Results show that the simulation of the snowmelt process lasted for 24 days and the modeled snow water equivalent (SWE) closely matched the observed SWE, with a mean relative error of 7.2%. During the snowmelt process, net radiation was the major energy source of the snow layer. The variation of the snowmelt outflow was closely related to the snowmelt amounts and air temperature. The initial results of this modeling process show that our calibrated parameters were reasonable and the UEB model can be used for simulating and forecasting peak snowmelt outflows in this region.

  17. Reaction and Transport Processes Controlling In Situ Chemical Oxidation of DNAPLs

    National Research Council Canada - National Science Library

    Siegrist, Robert L; Crimi, Michelle; Munakata-Marr, Junko; Illangasekare, Tissa; Dugan, Pamela; Heiderscheidt, Jeff; Jackson, Shannon; Petri, Ben; Sahl, Jason; Seitz, Sarah

    2006-01-01

    ..., and/or toxicity of contamination. The objective of this project was to quantify the pore/interfacial scale DNAPL reactions and porous media transport processes that govern the delivery of oxidant to a DNAPL-water interface and degradation of the DNAPL...

  18. Polymerization catalyst, production and use

    International Nuclear Information System (INIS)

    Best, S.A.

    1987-01-01

    A process is described for polymerization of ethylene and alpha-olefins having from 1 to 20 carbon atoms or mixtures of ethylene, alpha-olefins and diolefins. The process comprises polymerizing one or more olefins in the presence of the catalyst system comprising (a) an organoaluminum cocatalyst, and (b) a vanadium containing a catalyst component obtained by treating an inert solid support material in an inert solvent with (i) an organoaluminum compound represented by the formula R/sub m/AIX/sub 3-m/, wherein R represents an alkyl group, cycloalkyl group or aryl group having from 1 to 18 carbon atoms, X represents halogen atoms, and 1≤m≤3, (ii) an acyl halide, and (iii) a vanadium compound. Another process is identified wherein the inert solid support material is an inorganic oxide or mixtures of inorganic oxides. Also a process wherein the inorganic oxide is silica is described

  19. How in-situ combustion process works in a fractured system : two-dimensional, core and block scale simulation

    Energy Technology Data Exchange (ETDEWEB)

    Fadaei, H.; Renard, G. [Inst. Francais du Petrole, Lyon (France); Quintard, M.; Debenest, G. [L' Inst. de Mecanique des Fluides de Toulouse, Toulouse (France); Kamp, A.M. [Centre Huile Lourde Ouvert et Experimental CHLOE, Pau (France)

    2008-10-15

    Core and matrix block scale simulations of in situ combustion (ISC) processes in a fractured reservoir were conducted. ISC propagation conditions and oil recovery mechanisms were studied at core scale, while the 2-D behaviour of ISC was also studied at block-scale in order to determine dominant processes for combustion propagation and the characteristics of different steam fronts. The study examined 2-phase combustion in a porous medium containing a solid fuel as well as 2-D conventional dry combustion methods. The aim of the study was to predict ISC extinction and propagation conditions as well as to understand the mechanisms of oil recovery using ISC processes. The simulations were also used to develop up-scaling guidelines for fractured systems. Computations were performed using different oxygen diffusion and matrix permeability values. The effect of each production mechanism was studied separately. The multi-phase simulations showed that ISC in fractured reservoirs is feasible. The study showed that ISC propagation is dependent on the oxygen diffusion coefficient, while matrix permeability plays an important role in oil production. Oil production was governed by gravity drainage and thermal effects. Heat transfer due to the movement of combustion front velocity in the study was minor when compared to heat transfer by conduction and convection. It was concluded that upscaling methods must also consider the different zones distinguished for oil saturation and temperatures. 15 refs., 2 tabs., 15 figs.

  20. In-situ observation and modelling of solidification and fluid flow on GTAW process

    Science.gov (United States)

    Chiocca, A.; Soulié, F.; Deschaux-Beaume, F.; Bordreuil, C.

    2015-06-01

    An experimental setup is presented in order to obtain experimental data during solidification of a static weld pool after arc extinction with a GTAW process. Several devices have been set up to extract three kinds of measurements: (i) solidification front velocity (ii) fluid flow velocity at the vicinity of the front (iii) temperature field in the solid part. A high-speed camera is used to film the interface during welding at microscopic level and an infra-red in order to take the temperature field around the weld pool in the solid part. After processing and calibration of the videos, the experimental results are compared to theoritical results founded on an adapted model from the KGT [1] and from the one of Gandin et al. [2]. All the tests are done thin plate of Cu-30wt.%Ni.

  1. Characterization of boron carbide particulate reinforced in situ copper surface composites synthesized using friction stir processing

    Energy Technology Data Exchange (ETDEWEB)

    Sathiskumar, R., E-mail: sathiscit2011@gmail.com [Department of Mechanical Engineering, Coimbatore Institute of Technology, Coimbatore, 641 014 Tamil Nadu (India); Murugan, N., E-mail: murugan@cit.edu.in [Department of Mechanical Engineering, Coimbatore Institute of Technology, Coimbatore, 641 014 Tamil Nadu (India); Dinaharan, I., E-mail: dinaweld2009@gmail.com [Department of Mechanical Engineering, V V College of Engineering, Tisaiyanvilai, 627 657 Tamil Nadu (India); Vijay, S.J., E-mail: vijayjoseph@karunya.edu [Centre for Research in Metallurgy (CRM), School of Mechanical Sciences, Karunya University, Coimbatore, 641 114 Tamil Nadu (India)

    2013-10-15

    Friction stir processing has evolved as a novel solid state technique to fabricate surface composites. The objective of this work is to apply the friction stir processing technique to fabricate boron carbide particulate reinforced copper surface composites and investigate the effect of B{sub 4}C particles and its volume fraction on microstructure and sliding wear behavior of the same. A groove was prepared on 6 mm thick copper plates and packed with B{sub 4}C particles. The dimensions of the groove was varied to result in five different volume fractions of B{sub 4}C particles (0, 6, 12, 18 and 24 vol.%). A single pass friction stir processing was done using a tool rotational speed of 1000 rpm, travel speed of 40 mm/min and an axial force of 10 kN. Metallurgical characterization of the Cu/B{sub 4}C surface composites was carried out using optical microscope and scanning electron microscope. The sliding wear behavior was evaluated using a pin-on-disk apparatus. Results indicated that the B{sub 4}C particles significantly influenced the area, dispersion, grain size, microhardness and sliding wear behavior of the Cu/B{sub 4}C surface composites. When the volume fraction of B{sub 4}C was increased, the wear mode changed from microcutting to abrasive wear and wear debris was found to be finer. Highlights: • Fabrication of Cu/B{sub 4}C surface composite by friction stir processing • Analyzing the effect of B{sub 4}C particles on the properties of Cu/B4C surface composite • Increased volume fraction of B{sub 4}C particles reduced the area of surface composite. • Increased volume fraction of B{sub 4}C particles enhanced the microhardness and wear rate. • B{sub 4}C particles altered the wear mode from microcutting to abrasive.

  2. Enhancement of In Situ Bioremediation of Energetic Compounds by Coupled Abiotic/Biotic Processes

    Science.gov (United States)

    2007-08-01

    few sites have groundwater contamination of all three energetics in xx x x the same location. RDX and HMX are common groundwater contaminants due...contaminant with limited TNT subsurface migration because of aerobic and anaerobic degradation in soils and significantly greater sorption. TNT groundwater ...experiments with live, killed, and bioaugmented microbial communities (Task 3) • Upscale the process by aqueous flow experiments of energetic compounds

  3. In-situ Monitoring of Dynamic Phenomena during Solidification and Phase Transformation Processing

    Energy Technology Data Exchange (ETDEWEB)

    Clarke, Amy J. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Cooley, Jason C. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Morris, Christopher [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Merrill, Frank E. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Hollander, Brian J [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Mariam, Fesseha G [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Patterson, Brian M. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Imhoff, Seth D. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Lee, Wah Keat [Brookhaven National Lab. (BNL), Upton, NY (United States); Fezzaa, Kamel [Argonne National Lab. (ANL), Argonne, IL (United States); Deriy, Alex [Argonne National Lab. (ANL), Argonne, IL (United States); Tucker, Tim J. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Clarke, Kester D. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Field, Robert D. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Thoma, Dan J. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Teter, David F. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Beard, Timothy V. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Hudson, Richard W. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Freibert, Franz J. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Korzekwa, Deniece R. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Farrow, Adam M. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Cross, Carl E. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Mihaila, Bogdan [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Lookman, Turab [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Hunter, Abigail [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Choudhury, Samrat [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Karma, Alain [Northeastern Univ., Boston, MA (United States); Ott, Jr., Thomas J. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Barker, Martha R. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); O' Neill, Finian [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Hill, Joshua [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Emigh, Megan G. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States)

    2012-07-30

    The purpose of this project is to: (1) Directly observe phase transformations and microstructure evolution using proton (and synchrotron x-ray) radiography and tomography; (2) Constrain phase-field models for microstructure evolution; (3) Experimentally control microstructure evolution during processing to enable co-design; and (4) Advance toward the MaRIE vision. Understand microstructure evolution and chemical segregation during solidification {yields} solid-state transformations in Pu-Ga.

  4. Analysis of In-Situ Vibration Monitoring for End-Point Detection of CMP Planarization Processes

    International Nuclear Information System (INIS)

    Hetherington, Dale L.; Lauffer, James P.; Shingledecker, David M.; Stein, David J.; Wyckoff, Edward E.

    1999-01-01

    This paper details the analysis of vibration monitoring for end-point control in oxide CMP processes. Two piezoelectric accelerometers were integrated onto the backside of a stainless steel polishing head of an IPEC 472 polisher. One sensor was placed perpendicular to the carrier plate (vertical) and the other parallel to the plate (horizontal). Wafers patterned with metal and coated with oxide material were polished at different speeds and pressures. Our results show that it is possible to sense a change in the vibration signal over time during planarization of oxide material on patterned wafers. The horizontal accelerometer showed more sensitivity to change in vibration amplitude compared to the vertical accelerometer for a given polish condition. At low carrier and platen rotation rates, the change in vibration signal over time at fixed frequencies decreased approximately ampersand frac12; - 1 order of magnitude (over the 2 to 10 psi polish pressure ranges). At high rotation speeds, the vibration signal remained essentially constant indicating that other factors dominated the vibration signaL These results show that while it is possible to sense changes in acceleration during polishing, more robust hardware and signal processing algorithms are required to ensure its use over a wide range of process conditions

  5. In situ study of the epoxy cure process using a fibre-optic sensor

    Czech Academy of Sciences Publication Activity Database

    Chailleux, E.; Salvia, M.; Jaffrezic-Renault, N.; Matějec, Vlastimil; Kašík, Ivan

    2001-01-01

    Roč. 10, č. 2 (2001), s. 194-202 ISSN 0964-1726. [SPIE Annual International Symposium on Smart Structures and Materials /8./. Newport Beach, 04.03.2001-08.03.2001] R&D Projects: GA ČR GA102/99/0548; GA AV ČR KSK2067107 Projekt 07/01:4074 Institutional research plan: CEZ:AV0Z2067918 Keywords : fibre optic sensors * process monitoring Subject RIV: JA - Electronics ; Optoelectronics, Electrical Engineering Impact factor: 1.199, year: 2001

  6. Polymerization catalyst, production and use

    International Nuclear Information System (INIS)

    Best, S.A.

    1987-01-01

    A process is described for the polymerization of ethylene and alpha-olefins having from 1 to 2 carbon atoms of mixtures of ethylene, alpha-olefins or diolefins. The process comprises polymerizing one or more olefins in the presence of the catalyst system comprising (A) an organo aluminum cocatalyst, and (B) a vanadium-containing catalyst component obtained by sequentially treating an inert solid support material in an inert solvent with (i) a dihydrocarbyl magnesium compound, (ii) optionally an oxygen-containing compound which is an alcohol, ketone or aldehyde, (iii) a vanadium compound, and (iv) a Group IIIa metal halide. The process as above is described wherein the inert solid support material is an inorganic oxide or mixtures of inorganic oxides

  7. In situ diagnostics of the crystal-growth process through neutron imaging

    DEFF Research Database (Denmark)

    Tremsin, Anton S.; Makowska, Malgorzata Grazyna; Perrodin, Didier

    2016-01-01

    Neutrons are known to be unique probes in situations where other types of radiation fail to penetrate samples and their surrounding structures. In this paper it is demonstrated how thermal and cold neutron radiography can provide time-resolved imaging of materials while they are being processed (e...... in concentration of one of the elements with a sufficient neutron attenuation cross section. Tomographic imaging of the BaBrCl:0.1% Eu sample reveals a strong correlation between crystal fractures and Eu-deficient clusters. The results of these experiments demonstrate the unique capabilities of neutron imaging......, as limited by the resolution of the present experiments). It is also demonstrated that the dopant concentration can be quantified even for very low concentration levels (∼ 0.1%) in 10 mm thick samples. The interface between the solid and liquid phases can also be imaged, provided there is a sufficient change...

  8. Numerical analysis of a one-dimensional multicomponent model of the in-situ combustion process

    DEFF Research Database (Denmark)

    Nesterov, Igor; Shapiro, Alexander; Stenby, Erling Halfdan

    2013-01-01

    parameter, the critical ignition saturation, is introduced, in order to describe the easiness of oil ignition. Its dependence on the different parameters of the oil mixture and injection gas is studied. The conclusions on the processes governing the ignition of oil in the presence of water are made......, the model is based on SARA representation of a petroleum mixture (saturates–aromatics–resins–asphaltenes), which may react differently with oxygen and produce other components (for example, light oils and coke). In total, the model contains 14 components, which may undergo 15 chemical reactions. The set...... of reactions in the original model of M.R. Kristensen has been modified in order to account for secondary combustion of the light oil fraction. The results of the model implementation are applied to the four heavy oil systems and qualitatively compared to the results of previous experimental studies. A new...

  9. Polymerization Using Phosphazene Bases

    KAUST Repository

    Zhao, Junpeng

    2015-09-01

    In the recent rise of metal-free polymerization techniques, organic phosphazene superbases have shown their remarkable strength as promoter/catalyst for the anionic polymerization of various types of monomers. Generally, the complexation of phosphazene base with the counterion (proton or lithium cation) significantly improves the nucleophilicity of the initiator/chain end resulting in highly enhanced polymerization rates, as compared with conventional metalbased initiating systems. In this chapter, the general features of phosphazenepromoted/catalyzed polymerizations and the applications in macromolecular engineering (synthesis of functionalized polymers, block copolymers, and macromolecular architectures) are discussed with challenges and perspectives being pointed out.

  10. Composition-thermal expandability relations and oxidation processes in tourmaline studied by in situ Raman spectroscopy

    Science.gov (United States)

    Watenphul, Anke; Malcherek, Thomas; Wilke, Franziska D. H.; Schlüter, Jochen; Mihailova, Boriana

    2017-11-01

    The crystal chemistry of tourmaline, XY3Z6(T6O18)(BO3)3V3W, has a strong influence on the structure and physical properties. Since tourmalines occur in a wide range of geological settings and have large temperature and pressure stability fields, the understanding of the relation between the tourmaline chemistry and thermal expansion allows for better thermodynamic modeling of geological processes. Here, we report dynamic and static thermal expansions as well as mode Grüneisen parameters studied by Raman spectroscopy and single-crystal X-ray diffraction data on several tourmaline species. In addition, oxidation processes in fluor-schorl and Fe2+-bearing elbaite were followed by Raman spectroscopy. Our results emphasize the role of Y-/Z-site occupancy disorder to reduce the local strains and demonstrate that small-size octahedrally coordinated cations perturb the topology of the SiO4 rings, which in turn seems to enhance the anisotropic thermal-expansion response. In addition, it is shown that the temperature-dependent behavior of the VOH modes primarily depends on the occupancy of the Y site, whereas that of the WOH modes depends on the occupancy of the X site. High-temperature Raman experiments in air allowed to follow the oxidation of Fe2+ to Fe3+ in fluor-schorl by analyzing both the framework and OH-stretching phonon modes. It is further demonstrated that under the same conditions, no oxidation of iron is observed for Fe2+-bearing elbaite, which implies that at high oxygen fugacity, iron is only oxidized in tourmaline species with prevalent divalent cations at the Y site.

  11. Processing of Bi-2212 and Nb$_3$Sn studied in situ by high energy synchrotron diffraction and micro-tomography

    CERN Document Server

    Kadar, Julian

    Next generation superconducting wires have been studied to obtain more information on the evolution of phase growth, crystallite size and strain state during wire processing. The high energy scattering beam line ID15 at the European Synchrotron Radiation Facility provides a very high flux of high energy photons for very fast in situ X-ray diffraction and micro-tomography studies of Bi-2212/Ag and Nb$_3$S/Cu wire samples. The typical wire processing conditions could be imitated in the X-ray transparent furnace at ID15 for diffraction and tomography studies. Efficient data analysis is mandatory in order to handle the very fast data acquisition rate. For this purpose an Excel-VBA based program was developed that allows a semi-automated fitting and tracking of peaks with pre-set constraints. With this method, more than one thousand diffraction patterns have been analysed to extract d-spacing, peak intensity and peak width values. X ray absorption micro tomograms were recorded simultaneously with the X-ray diffrac...

  12. Microwave Processing of Polymeric Materials

    Science.gov (United States)

    1992-04-01

    1355 (1983). 112. R. P. Kambour, J. Polym. Sci.: Macromol. Rev., 7, 1 (1973). 113. R. N. Haward , The Physics of Glassy Polymers, John Wiley and Sons...Polymer Science and Engneering, Ed. J. I. Kroschwitz, John Wiley and Sons, Vol. 5, pp. 1-23, 1986. 66. S. Matsuoka, in Encyclopedia of Polymer Science...and Engineering, Ed. J. I. Kroschwitz, John Wiley and Sons, Vol. 5, pp. 23-36, 1986. 67. N. G. McCrum, B. E. Read and G. Williams, Anelastic and

  13. Glycine Polymerization on Oxide Minerals

    Science.gov (United States)

    Kitadai, Norio; Oonishi, Hiroyuki; Umemoto, Koichiro; Usui, Tomohiro; Fukushi, Keisuke; Nakashima, Satoru

    2017-06-01

    It has long been suggested that mineral surfaces played an important role in peptide bond formation on the primitive Earth. However, it remains unclear which mineral species was key to the prebiotic processes. This is because great discrepancies exist among the reported catalytic efficiencies of minerals for amino acid polymerizations, owing to mutually different experimental conditions. This study examined polymerization of glycine (Gly) on nine oxide minerals (amorphous silica, quartz, α-alumina and γ-alumina, anatase, rutile, hematite, magnetite, and forsterite) using identical preparation, heating, and analytical procedures. Results showed that a rutile surface is the most effective site for Gly polymerization in terms of both amounts and lengths of Gly polymers synthesized. The catalytic efficiency decreased as rutile > anatase > γ-alumina > forsterite > α- alumina > magnetite > hematite > quartz > amorphous silica. Based on reported molecular-level information for adsorption of Gly on these minerals, polymerization activation was inferred to have arisen from deprotonation of the NH3 + group of adsorbed Gly to the nucleophilic NH2 group, and from withdrawal of electron density from the carboxyl carbon to the surface metal ions. The orientation of adsorbed Gly on minerals is also a factor influencing the Gly reactivity. The examination of Gly-mineral interactions under identical experimental conditions has enabled the direct comparison of various minerals' catalytic efficiencies and has made discussion of polymerization mechanisms and their relative influences possible Further systematic investigations using the approach reported herein (which are expected to be fruitful) combined with future microscopic surface analyses will elucidate the role of minerals in the process of abiotic peptide bond formation.

  14. Actin Polymerization and ATP Hydrolysis

    Science.gov (United States)

    Korn, Edward D.; Carlier, Marie-France; Pantaloni, Dominique

    1987-10-01

    F-actin is the major component of muscle thin filaments and, more generally, of the microfilaments of the dynamic, multifunctional cytoskeletal systems of nonmuscle eukaryotic cells. Polymeric F-actin is formed by reversible noncovalent self-association of monomeric G-actin. To understand the dynamics of microfilament systems in cells, the dynamics of polymerization of pure actin must be understood. The following model has emerged from recent work. During the polymerization process, adenosine 5'-triphosphate (ATP) that is bound to G-actin is hydrolyzed to adenosine 5'-diphosphate (ADP) that is bound to F-actin. The hydrolysis reaction occurs on the F-actin subsequent to the polymerization reaction in two steps: cleavage of ATP followed by the slower release of inorganic phosphate (Pi). As a result, at high rates of filament growth a transient cap of ATP-actin subunits exists at the ends of elongating filaments, and at steady state a stabilizing cap of ADP \\cdot Pi-actin subunits exists at the barbed ends of filaments. Cleavage of ATP results in a highly stable filament with bound ADP \\cdot Pi, and release of Pi destabilizes the filament. Thus these two steps of the hydrolytic reaction provide potential mechanisms for regulating the monomer-polymer transition.

  15. Ultrahigh surface area carbon from carbonated beverages: Combining self-templating process and in situ activation

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Pengfei; Zhang, Zhiyong; Chen, Jihua; Dai, Sheng

    2015-11-01

    Ultrahigh surface area carbons (USACs, e.g., >2000 m2/g) are attracting tremendous attention due to their outstanding performance in energy-related applications. The state-of-art approaches to USACs involve templating or activation methods and all these techniques show certain drawbacks. In this work, a series of USACs with specific surface areas up to 3633 m2/g were prepared in two steps: hydrothermal carbonization (200 °C) of carbonated beverages (CBs) and further thermal treatment in nitrogen (600–1000 °C). The rich inner porosity is formed by a self-templated process during which acids and polyelectrolyte sodium salts in the beverage formulas make some contribution. This strategy covers various CBs such as Coca Cola®, Pepsi Cola®, Dr. Pepper®, and Fanta® and it enables an acceptable product yield (based on sugars), for example: 21 wt% for carbon (2940 m2/g) from Coca Cola®. Being potential electrode materials for supercapacitors, those carbon materials possessed a good specific capacitance (57.2–185.7 F g-1) even at a scan rate of 1000 mV s-1. Thus, a simple and efficient strategy to USACs has been presented.

  16. In-situ Characterization of Molecular Processes in Liquids by Ultrafast X-ray Absorption Spectroscopy

    Science.gov (United States)

    Chergui, Majed

    The need to visualize molecular and electronic structure in the course of a chemical reaction, a phase transformation a biological function has been the dream of scientists for decades. The development of time-resolved X-ray and electron based methods is making this true. X-ray absorption spectroscopy is ideal for the study of structural dynamics in liquids, because it can be implemented in amorphous media and it is chemically selective. Using X-ray absorption near edge structure (XANES) and extended X-ray absorption fine structure (EXAFS) in laser pump/X-ray probe experiments allows the retrieval of the local geometric structure of the system under study, but also the underlying photoinduced electronic structure changes that drive the structural dynamics. We review the recent development in picosecond and femtosecond X-ray absorption spectroscopy applied to molecular systems in solution: examples on ultrafast photoinduced processes such as intramolecular electron transfer, high-to-low spin change, bond formation and water dynamics are presented.

  17. Survey and research on precision polymerization polymeric materials; Seimitsu jugo kobunshi zairyo ni kansuru chosa kenkyu

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1996-03-01

    Survey and research on the precision control of primary structure of polymeric materials and the precision evaluation technology have been conducted to develop advanced polymeric materials. It is proposed that the three basic processes of polymer synthesis, i.e., addition, condensation, and biomimesis, in forming the precision polymerization skeleton are to be covered through a centralized joint research effort with participation of industry, academia, and the government institute and under the leadership of researchers from academic institutions as the team leaders. For the study of technology trends, international conferences held in UK, Germany, and Hawaii are introduced, and domestic meetings, i.e., Annual Polymer Congress and Polymer Conference, are summarized. In addition, Precision Polymerization Forum and International Workshop on Precision Polymerization were held. The basic studies include a quantum-chemical elucidation of the elementary process in polymerization reaction, time-resolved analysis of polymerization process and polymer properties, synthesis of polymers with controlled microstructures by coordination polymerization using metal complexes, synthesis of polymer with controlled microstructures by precision polycondensation, molecular recognition in catalyst-reaction site, and synthesis of imprinting polymers. 246 refs., 117 figs., 14 tabs.

  18. Synthesis and characterization of cellulose whiskers/polymer nanocomposite dispersion by mini-emulsion polymerization.

    Science.gov (United States)

    Ben Mabrouk, Ayman; Rei Vilar, Manuel; Magnin, Albert; Belgacem, Mohamed Naceur; Boufi, Sami

    2011-11-01

    Stable film-forming nanocomposite particles with diameters ranging from 120 to 300 nm, based on polybutylmethacrylate (PBMA) and cellulose whiskers in water dispersions, were successfully synthesized in one step through mini-emulsion polymerization. The nanocomposite dispersion with a solid content of 25 wt.% and up to 5 wt.% of nanofiller loading was prepared by in situ polymerization, in the presence of the whiskers using dodecylpyridinium chloride (DPC), as a cationic surfactant, and 2,2-azobis(isobutyronitrile) (AIBN), as initiator. The electrostatic interaction between the positively charged droplets and negatively charged whiskers ensured the anchoring of the nanofiller around the polymer particles. The ensuing dispersions were characterized by Dynamic Light Scattering (DLS), ζ-Potential Measurements, and Field-Emission Scanning Electron Microscopy (FE-SEM). After the film formation process, the nanocomposite film exhibits a high transparency, denoting the good dispersion of the whiskers throughout the matrix. Copyright © 2011 Elsevier Inc. All rights reserved.

  19. Radiation polymerization of tetrafluoroethylene in gas-phase

    International Nuclear Information System (INIS)

    Enslin, S.E.; Schnautz, N.G.; Van der Ende, E.

    1986-01-01

    The radiation polymerization of tetrafluoroethylene in gas-phase was studied over a temperature range of -80 to 200 degrees Celsius and an irradiation dose-rate of 0,30 to 10,8 kGy h sup(-1). The rate of polymerization was observed during the course of the polymerization process, to be a zero-order function of monomer pressure. However, the rate of polymerization was profoundly influenced by the initial monomer pressure, in this case exhibiting a 4,6-order dependence. The rate of polymerization was also observed to exhibit a 0,36-order dependence on radiation intensity. Both the rate of polymerization and the molecular mass of the product, polytetrafluoroethylene, reached maximum values over the temperature range of 90 to 150 degrees Celsius. The activation energy for the polymerization process was determined to be 8,7 kJ mol sup(-1) over the temperature range of -80 to 90 degrees Celsius

  20. Environmentally degradable bio-based polymeric blends and composites.

    Science.gov (United States)

    Chiellini, Emo; Cinelli, Patrizia; Chiellini, Federica; Imam, Syed H

    2004-03-15

    Blends and composites based on environmentally degradable-ecocompatible synthetic and natural polymeric materials and fillers of natural origin have been prepared and processed under different conditions. Poly(vinyl alcohol) (PVA) was used as the synthetic polymer of choice by virtue of its capability to be processed from water solution or suspension as well as from the melt by blow extrusion and injection molding. Starch and gelatin were taken as the polymeric materials from renewable resources. The fillers were all of natural origin, as waste from food and agro-industry consisted of sugar cane bagasse (SCB), wheat flour (WF), orange peels (OR), apple peels (AP), corn fibres (CF), saw dust (SD) and wheat straw (WS). All the natural or hybrid formulations were intended to be utilized for the production of: a) Environmentally degradable mulching films (hydro-biomulching) displaying, in some cases, self-fertilizing characteristics by in situ spraying of water solutions or suspensions; b) Laminates and containers to be used in agriculture and food packaging by compression and injection molding followed by baking. Some typical prototype items have been prepared and characterized in relation to their morphological and mechanical properties and tested with different methodology for their propensity to environmental degradation and biodegradation as ultimate stage of their service life. A relationship between chemical composition and mechanical properties and propensity to biodegradation has been discussed in a few representative cases.

  1. New insight in the template decomposition process of large zeolite ZSM-5 crystals: an in situ UV-Vis/fluorescence micro-spectroscopy study

    NARCIS (Netherlands)

    Karwacki, L.; Weckhuysen, B.M.

    2011-01-01

    A combination of in situ UV-Vis and confocal fluorescence micro-spectroscopy was used to study the template decomposition process in large zeolite ZSM-5 crystals. Correlation of polarized light dependent UV-Vis absorption spectra with confocal fluorescence emission spectra in the 400–750 nm region

  2. A Pd-Catalyzed in situ domino process for mild and quantitative production of 2,5-dimethylfuran directly from carbohydrates

    DEFF Research Database (Denmark)

    Li, Hu; Zhao, Wenfeng; Riisager, Anders

    2017-01-01

    and hydrophobic Pd/C as a H-donor and a bifunctional catalyst, respectively. Among the cascade reactions, the hydrosilylation process was confirmed by deuterium-labeling and kinetic studies to be favorable for sugar dehydration and exclusively acts on deoxygenation of in situ formed intermediates including...

  3. Nanoporous Polymeric Grating-Based Optical Biosensors (Preprint)

    National Research Council Canada - National Science Library

    Hsiao, Vincent K; Waldeisen, John R; Lloyd, Pamela F; Bunning, Timothy J; Huang, Tony J

    2007-01-01

    .... The fabrication process of the nanoporous polymeric grating involves holographic interference patterning and a functionalized pre-polymer syrup that facilitates the immobilization of biomolecules...

  4. Comparison of biodiesel production from sewage sludge obtained from the A²/O and MBR processes by in situ transesterification.

    Science.gov (United States)

    Qi, Juanjuan; Zhu, Fenfen; Wei, Xiang; Zhao, Luyao; Xiong, Yiqun; Wu, Xuemin; Yan, Fawei

    2016-03-01

    The potential of two types of sludge obtained from the anaerobic-anoxic-oxic (A(2)/O) and membrane bioreactor (MBR) processes as lipid feedstock for biodiesel production via in situ transesterification was investigated. Experiments were conducted to determine the optimum conditions for biodiesel yield using three-factor and four-level orthogonal and single-factor tests. Several factors, namely, methanol-to-sludge mass ratio, acid concentration, and temperature, were examined. The optimum yield of biodiesel (16.6% with a fatty acid methyl ester purity of 96.7%) from A(2)/O sludge was obtained at a methanol-to-sludge mass ratio of 10:1, a temperature of 60°C, and a H2SO4 concentration of 5% (v/v). Meanwhile, the optimum yield of biodiesel (4.2% with a fatty acid methyl ester purity of 92.7%) from MBR sludge was obtained at a methanol-to-sludge mass ratio of 8:1, a temperature of 50°C, and a H2SO4 concentration of 5% (v/v). In this research, A(2)/O technology with a primary sedimentation tank is more favorable for obtaining energy from wastewater than MBR technology. Copyright © 2016 Elsevier Ltd. All rights reserved.

  5. In situ synchrotron x-ray characterization of microstructure formation in solidification processing of Al-based metallic alloys

    International Nuclear Information System (INIS)

    Billia, Bernard; Nguyen-Thi, Henri; Mangelinck-Noel, Nathalie

    2010-01-01

    The microstructure formed during the solidification step has a major influence on the properties of materials processed by major techniques (casting, welding ...). In situ and real-time characterization by synchrotron X-ray imaging is the method of choice to unveil the dynamical formation of the solidification microstructure in metallic alloys, and thus provide precise data for the critical validation of the theoretical predictions that is needed for sound advancement of modeling and numerical simulation. After a description of the experimental procedure used at the European Synchrotron Radiation Facility (ESRF), dynamical phenomena in the formation of the grain structure and dendritic or equiaxed solidification microstructure in Al-based alloys are presented. Beyond fluid flow interaction, earth gravity induces stresses, deformation and fragmentation in the dendritic mush. Settling of dendrite arms and equiaxed grains thus occurs, in particular in the columnar to equiaxed transition. Other types of stresses and strains are caused by the mere formation of the solidification microstructure itself. In white-beam X-ray topography, stresses and strains are manifested by specific contrasts and breaking of the Laue images into several pieces. Finally, quantitative analysis of the grey level in radiographs enables the analysis of solute segregation, which noticeably results in solutal poisoning of growth when equiaxed grains are interacting. (author)

  6. Enzymatic in-situ generation of H2O2 for decolorization of Acid Blue 113 by fenton process

    Directory of Open Access Journals (Sweden)

    Karimi Afzal

    2012-01-01

    Full Text Available Decolorization of Acid Blue 113 in an aqueous medium by bio-Fenton process has been investigated in this research. Enzymatic oxidation of glucose was performed to in-situ generation of H2O2 which was employed to react with Fe2+ for producing hydroxyl radicals. The effect of various parameters include concentrations of 113, glucose, and FeSO4, activity of glucose oxidase (GOx and the effect of pH were assessed. The highest decolorization of AB 113 were achieved at Fe2+ concentration of 0.2 mmol/L, pH =4.0, glucose concentration of 0.018 mol/L, and glucose oxidase activity of 2500 U/L in the constant temperature (23 ±0.1ºC and constant shaking rate (160 r/min, while the concentration of 113 was 40 mg/L. In these conditions, 113 decolorization efficiency after 60 min was obtained about 95%.

  7. In Situ Synthesis of Al-Si-Cu Alloy During Brazing Process and Mechanical Property of Brazing Joint

    Directory of Open Access Journals (Sweden)

    LONG Wei-min

    2016-06-01

    Full Text Available The Al-Si-Cu alloy system is considered to be a promising choice of filler metal for aluminium alloys brazing due to its high strength and low melting point. The greatest obstacle is its lack of plastic forming ability and being difficult to be processed by conventional methods. This disadvantage is ascribed to the considerable amount of brittle CuAl2 intermetallic compound which forms when alloy composition is around the ternary eutectic point. In order to overcome this deficiency, authors of this article proposed to synthesize Al-Si-Cu filler metal by using in situ synthesis method, and the structure and properties of brazing joints were studied. The results show that AlSi alloy is used as the wrap layer, and CuAl alloy is used as the powder core in the composite brazing wire, the two alloys have similar melting points. The machinability of the composite brazing wire is much superior to the traditional Al-Si-Cu filler metal. During the induction brazing of 3A21 alloy, when using AlSi-CuAl composite filler wire, AlSi and CuAl alloys melt almost simultaneously, then after short time holding, Al-Si-Cu braze filler is obtained, the brazing seam has uniform composition and good bonding interface, also, the shearing strength of the brazing joints is higher than the joint brazed by conventional Al-Si-Cu filler metal.

  8. In situ X-ray diffraction study of crystallization process of GeSbTe thin films during heat treatment

    International Nuclear Information System (INIS)

    Kato, Naohiko; Konomi, Ichiro; Seno, Yoshiki; Motohiro, Tomoyoshi

    2005-01-01

    The crystallization processes of the Ge 2 Sb 2 Te 5 thin film used for PD and DVD-RAM were studied in its realistic optical disk film configurations for the first time by X-ray diffraction using an intense X-ray beam of a synchrotron orbital radiation facility (SPring-8) and in situ quick detection with a Position-Sensitive-Proportional-Counter. The dependence of the amorphous-to-fcc phase-change temperature T 1 on the rate of temperature elevation R et gave an activation energy E a : 0.93 eV much less than previously reported 2.2 eV obtained from a model sample 25-45 times thicker than in the real optical disks. The similar measurement on the Ge 4 Sb 1 Te 5 film whose large reflectance change attains the readability by CD-ROM drives gave E a : 1.13 eV with larger T 1 than Ge 2 Sb 2 Te 5 thin films at any R et implying a lower sensitivity in erasing as well as a better data stability of the phase-change disk

  9. Applied bioactive polymeric materials

    CERN Document Server

    Carraher, Charles; Foster, Van

    1988-01-01

    The biological and biomedical applications of polymeric materials have increased greatly in the past few years. This book will detail some, but not all, of these recent developments. There would not be enough space in this book to cover, even lightly, all of the major advances that have occurred. Some earlier books and summaries are available by two of this book's Editors (Gebelein & Carraher) and these should be consul ted for additional information. The books are: "Bioactive Polymeric Systems" (Plenum, 1985); "Polymeric Materials In Medication" (Plenum, 1985); "Biological Acti vi ties of Polymers" (American Chemical Society, 1982). Of these three, "Bioacti ve Polymeric Systems" should be the most useful to a person who is new to this field because it only contains review articles written at an introductory level. The present book primarily consists of recent research results and applications, with only a few review or summary articles. Bioactive polymeric materials have existed from the creation of life...

  10. Surface Analytics in Support of the Development of Static AutoClean - an In-Situ Cleaning Process for Ion Implanters

    International Nuclear Information System (INIS)

    Stawasz, Michele; Yedave, Sharad; Hiscock, Laura; Sweeney, Joseph; Kaim, Robert

    2008-01-01

    Static AutoClean is a new in-situ cleaning strategy in development at ATMI registered that enables increased process efficiency and safety in the ion implantation process. Like the Dynamic in-situ AutoClean technology previously introduced and released by ATMI, Static AutoClean utilizes XeF 2 chemistry for in-situ cleaning of hazardous contaminants and deposits. Static AutoClean, however, is targeted towards cleaning areas of the beam-line (like electrode insulators or source bushings) where cleaning efforts using Dynamic AutoClean may not be sufficient. An explanation of this cleaning strategy and results showing its effectiveness will be presented in a separate paper at this conference (S. Yedave et al.). This paper presents the surface analytical data and methods used to understand and evaluate the effectiveness of Static AutoClean in removing contaminants from surfaces within the source vacuum chamber. Energy Dispersive Spectroscopy (EDS) was used to track the magnitude and spatial distribution of contaminants present on the surfaces within various regions in the source chamber space of an implanter following ion source operation with a commonly used dopant gas. After in-situ cleaning, these same components and surfaces were re-evaluated by EDS to quantitatively determine the reduction in surface contaminants present within the chamber. Learnings regarding the distribution of implant process contamination within the source chamber as well as Static AutoClean's effectiveness in removing it will be presented.

  11. Quantitative in-situ EPR spectroelectrochemical studies of doping processes in poly(3,4-alkylenedioxythiophene)s

    International Nuclear Information System (INIS)

    Domagala, Wojciech; Pilawa, Barbara; Lapkowski, Mieczyslaw

    2008-01-01

    Quantitative in-situ EPR spectroelectrochemical studies of poly(3,4-ethylenedioxythiophene) (PEDOT) have been carried out with an aim to gain new insights into the doping processes taking place in this polymer. Corroborating the findings made during previous studies of this polymer, absolute measurements conducted in this study provided new detailed information regarding some of the basic parameters characterising the doping process of this conjugated polymer. It was found that concentrations of paramagnetic centres in PEDOT vary from 0.02 spin per mer in the dedoped state up to a maximum of 0.12 spin per mer at 0.15 [e - /mer] doping level, corresponding to 1 spin per ca. 8.5 meric units. Such notable concentration values indicate that polarons represent a numerous charge carrier group in PEDOT, contrary to observations made for other members of polythiophene family. Furthermore polarons do not disappear at high doping levels of PEDOT but rather decrease their numbers gradually down to 0.08 spins per mer at a maximum doping level of 0.55 [e - /mer] attained in this study. Based on information about concentrations of spins and polymer doping charges, concentrations of bipolarons have been evaluated as a function of doping level. Results indicate that bipolaron formation starts at ca. 0.06 [e - /mer] doping level when spin generation efficiency begins to deviate from 1 and interspin interactions emerge as evidenced by doping level dependency of EPR signal linewidth (ΔB pp ). Decomposition of complex EPR spectra of PEDOT in its doped state corroborated the presence of two groups of paramagnetic centres in this polymer. Based upon doping level dependencies of their spectroscopic parameters (concentration, ΔB pp linewidth and g-factor), the identity of these centres has been redefined compared to our previous reports, linking their properties with the type of polymer phase (crystalline or amorphous) they reside in

  12. Bleeding evaluation of the stationary phase from a few novel macroporous silica-substrate polymeric materials used for radionuclide partitioning from HLLW in MAREC process

    International Nuclear Information System (INIS)

    Zhang, A.; Wei, Y.; Kumagai, M.

    2005-01-01

    To separate minor actinides from HLLW by extraction chromatography, a few novel silica-based di(2-ethylhexyl)phosphoric acid (HDEHP), 4,4',(5')-di(tert-butylcyclohexano)-18-crown-6 (DtBuCH18C6), octyl(phenyl)-N,N-diisobutylcarbamoylmethylphosphine oxide (CMPO), and N,N,N',N'-tetraoctyl-3-oxapentane-1,5-diamide (TODGA) polymeric adsorption materials (HDEHP/SiO 2 -P, DtBuCH18C6/SiO 2 -P, CMPO/SiO 2 -P, and TODGA/SiO 2 -P) were synthesized by impregnating HDEHP, DtBuCH18C6, CMPO, and TODGA into the pores of porous SiO 2 -P particles, which were the new kind of inorganic/organic composites consisted of macroporous SiO 2 and copolymer. The bleeding behavior of these composites was investigated by examining the effect of contact time and HNO 3 concentration. It was found that in the tested HNO 3 concentration range, a noticeable quantity of DtBuCH18C6, at least 600 ppm, leaked out from DtBuCH18C6/SiO 2 -P because of the protonation of DtBuCH18C6 with hydrogen ion, while the others were lower and basically equivalent to the solubility of HDEHP, CMPO, or TODGA in corresponding acidities solutions. Based on the batch experiment, the bleeding of CMPO/SiO 2 -P and TODGA/SiO 2 -P, the main adsorbents used in MAREC process for HLLW partitioning, was evaluated by column operation in 0.01M HNO 3 and 3M HNO 3 . The quantity of CMPO leaked was ∼48 ppm in 0.01M HNO 3 and ∼37 ppm in 3.0M HNO 3 . The bleeding of TODGA decreased from 23.2 ppm to 7.27 ppm at the initial stage and then basically kept constant. An actual bleeding of TODGA was evaluated by the separation of Sr(II) from a 2.0M HNO 3 solution containing 5.0 x 10 -3 M of 6 typically simulated elements. (author)

  13. Self-Strengthening Hybrid Dental Adhesive via Visible-light Irradiation Triple Polymerization

    OpenAIRE

    Song, Linyong; Ye, Qiang.; Ge, Xueping; Misra, Anil; Tamerler, Candan; Spencer, Paulette

    2016-01-01

    A self-strengthening methacrylate-based dental adhesive system was developed by introducing an epoxy cyclohexyl trimethoxysilane (TS) which contains both epoxy and methoxysilyl functional groups. The experimental formulation, HEMA/BisGMA/TS (22.5/27.5/50, wt%), was polymerized by visible-light. Real-time Fourier transform infrared spectroscopy (FTIR) was used to investigate in situ the free radical polymerization of methacrylate, ring-opening cationic polymerization of epoxy, and photoacid-in...

  14. Kinetics of silica polymerization

    Energy Technology Data Exchange (ETDEWEB)

    Weres, O.; Yee, A.; Tsao, L.

    1980-05-01

    The polymerization of silicic acid in geothermal brine-like aqueous solutions to produce amorphous silica in colloidal form has been studied experimentally and theoretically. A large amount of high quality experimental data has been generated over the temperature rang 23 to 100{sup 0}C. Wide ranges of dissolved silica concentration, pH, and sodium chloride concentration were covered. The catalytic effects of fluoride and the reaction inhibiting effects of aluminum and boron were studied also. Two basic processes have been separately studied: the formation of new colloidal particles by the homogeneous nucleation process and the deposition of dissolved silica on pre-existing colloidal particles. A rigorous theory of the formation of colloidal particles of amorphous silica by homogeneous nucleation was developed. This theory employs the Lothe-Pound formalism, and is embodied in the computer code SILNUC which quantitatively models the homogeneous nucleation and growth of colloidal silica particles in more than enough detail for practical application. The theory and code were extensively used in planning the experimental work and analyzing the data produced. The code is now complete and running in its final form. It is capable of reproducing most of the experimental results to within experimental error. It is also capable of extrapolation to experimentally inaccessible conditions, i.e., high temperatures, rapidly varying temperature and pH, etc.

  15. Charge Splitting In Situ Recorder (CSIR) for Real-Time Examination of Plasma Charging Effect in FinFET BEOL Processes

    Science.gov (United States)

    Tsai, Yi-Pei; Hsieh, Ting-Huan; Lin, Chrong Jung; King, Ya-Chin

    2017-09-01

    A novel device for monitoring plasma-induced damage in the back-end-of-line (BEOL) process with charge splitting capability is first-time proposed and demonstrated. This novel charge splitting in situ recorder (CSIR) can independently trace the amount and polarity of plasma charging effects during the manufacturing process of advanced fin field-effect transistor (FinFET) circuits. Not only does it reveal the real-time and in situ plasma charging levels on the antennas, but it also separates positive and negative charging effect and provides two independent readings. As CMOS technologies push for finer metal lines in the future, the new charge separation scheme provides a powerful tool for BEOL process optimization and further device reliability improvements.

  16. Charge Splitting In Situ Recorder (CSIR) for Real-Time Examination of Plasma Charging Effect in FinFET BEOL Processes.

    Science.gov (United States)

    Tsai, Yi-Pei; Hsieh, Ting-Huan; Lin, Chrong Jung; King, Ya-Chin

    2017-09-18

    A novel device for monitoring plasma-induced damage in the back-end-of-line (BEOL) process with charge splitting capability is first-time proposed and demonstrated. This novel charge splitting in situ recorder (CSIR) can independently trace the amount and polarity of plasma charging effects during the manufacturing process of advanced fin field-effect transistor (FinFET) circuits. Not only does it reveal the real-time and in situ plasma charging levels on the antennas, but it also separates positive and negative charging effect and provides two independent readings. As CMOS technologies push for finer metal lines in the future, the new charge separation scheme provides a powerful tool for BEOL process optimization and further device reliability improvements.

  17. TRANSITION METAL CATALYSIS IN CONTROLLED RADICAL POLYMERIZATION: ATOM TRANSFER RADICAL POLYMERIZATION. (R826735)

    Science.gov (United States)

    Novel and diversified macromolecular structures, which include polymers with designed topologies (top), compostions (middle), and functionalities (bottom), can be prepared by atom transfer radical polymerization processes. These polymers can be synthesized from a large variety of...

  18. Ring opening metathesis polymerization catalysts

    Energy Technology Data Exchange (ETDEWEB)

    Grubbs, R.H.; Johnson, L.K.; Novak, B.M.; Hillmyer, M.; Benedicto, A.; France, M.; Nguyen, S.T. [California Institute of Technology, Pasadena, CA (United States)

    1993-12-31

    Over the past eight years, a number of new catalysts for the ring opening metathesis polymerization of cyclic olefins have been developed. These catalysts are simple organometallic complexes containing metal carbon multiple bonds that in most cases polymerize olefins by a living process. These catalysts have been used to prepare a family of near monodispersed and structurally homogeneous polymers, a series of telechelic polymers with controlled molecular weight and functionality and triblock polymers with segments with potentially interesting electronic properties. A series of new group VIII catalysts are being developed that allow a wide range of functionality to be incorporated into the polymer side chains. The same catalysts can also be used in the synthesis of fine chemicals.

  19. In situ

    Science.gov (United States)

    Tremsin, Anton S; Makowska, Małgorzata G; Perrodin, Didier; Shalapska, Tetiana; Khodyuk, Ivan V; Trtik, Pavel; Boillat, Pierre; Vogel, Sven C; Losko, Adrian S; Strobl, Markus; Kuhn, L Theil; Bizarri, Gregory A; Bourret-Courchesne, Edith D

    2016-06-01

    Neutrons are known to be unique probes in situations where other types of radiation fail to penetrate samples and their surrounding structures. In this paper it is demonstrated how thermal and cold neutron radiography can provide time-resolved imaging of materials while they are being processed ( e.g. while growing single crystals). The processing equipment, in this case furnaces, and the scintillator materials are opaque to conventional X-ray interrogation techniques. The distribution of the europium activator within a BaBrCl:Eu scintillator (0.1 and 0.5% nominal doping concentrations per mole) is studied in situ during the melting and solidification processes with a temporal resolution of 5-7 s. The strong tendency of the Eu dopant to segregate during the solidification process is observed in repeated cycles, with Eu forming clusters on multiple length scales (only for clusters larger than ∼50 µm, as limited by the resolution of the present experiments). It is also demonstrated that the dopant concentration can be quantified even for very low concentration levels (∼0.1%) in 10 mm thick samples. The interface between the solid and liquid phases can also be imaged, provided there is a sufficient change in concentration of one of the elements with a sufficient neutron attenuation cross section. Tomographic imaging of the BaBrCl:0.1%Eu sample reveals a strong correlation between crystal fractures and Eu-deficient clusters. The results of these experiments demonstrate the unique capabilities of neutron imaging for in situ diagnostics and the optimization of crystal-growth procedures.

  20. Lessons learned from the Febex in situ test: geochemical processes associated to the microbial degradation and gas generation

    International Nuclear Information System (INIS)

    Fernandez, A. M.; Sanchez, D.M.; Melon, A.; Mingarro, M.; Wieczorek, K.

    2012-01-01

    existence of gaps between the bentonite blocks, which favour the development and growth of inactive and dormant cells or spores belonging to the original bentonite. In this work, the observed geochemical and corrosion processes influenced both by organic matter degradation and micro-organisms in the 1:1 scale FEBEX in situ test (Grimsel, Switzerland) are described. This test consists of two heaters, simulating radioactive waste containers, emplaced in a horizontal gallery and surrounded by a highly compacted bentonite barrier. Samples from pore water, gases and bentonite (SHSDI-01: clay in contact with AISI 316L metal; S29 and BSBI-26: clay in contact with carbon steel) have been analysed. The samples were obtained during the test and the dismantling of the heater 1 after six years of experiment. The solid samples were analysed by XRD, SEM, XPS, FTIR, ATD-TG and chemical analysis; the water samples by IC and ICP-OES, and the gases by gas chromatography. Different geochemical processes have been detected as a function of the temperature and water content of the samples. When the water content is high, there are aerobic respiration and fermentation processes, anaerobic respiration with SO 4 2- as electron acceptor, and anaerobic production of methane with CO 2 as electron acceptor. In a first phase, both oxygen consumption and an increase of CH 4 and CO 2 is observed. Afterwards, there is a reduction of sulfates by SRB bacteria, which provokes corrosion processes. As a consequence, a precipitation of sulphurs, iron oxy-hydroxides and carbonates occurs, as well as H 2 generation. There is an increase of the iron content in the smectite and the neo-formation of zeolites. However this alteration is punctual and localized. The redox potential of the bentonite pore water was of -284 mV. When the temperature is high and water content is low, other processes take place

  1. The tempered polymerization of human neuroserpin.

    Directory of Open Access Journals (Sweden)

    Rosina Noto

    Full Text Available Neuroserpin, a member of the serpin protein superfamily, is an inhibitor of proteolytic activity that is involved in pathologies such as ischemia, Alzheimer's disease, and Familial Encephalopathy with Neuroserpin Inclusion Bodies (FENIB. The latter belongs to a class of conformational diseases, known as serpinopathies, which are related to the aberrant polymerization of serpin mutants. Neuroserpin is known to polymerize, even in its wild type form, under thermal stress. Here, we study the mechanism of neuroserpin polymerization over a wide range of temperatures by different techniques. Our experiments show how the onset of polymerization is dependent on the formation of an intermediate monomeric conformer, which then associates with a native monomer to yield a dimeric species. After the formation of small polymers, the aggregation proceeds via monomer addition as well as polymer-polymer association. No further secondary mechanism takes place up to very high temperatures, thus resulting in the formation of neuroserpin linear polymeric chains. Most interesting, the overall aggregation is tuned by the co-occurrence of monomer inactivation (i.e. the formation of latent neuroserpin and by a mechanism of fragmentation. The polymerization kinetics exhibit a unique modulation of the average mass and size of polymers, which might suggest synchronization among the different processes involved. Thus, fragmentation would control and temper the aggregation process, instead of enhancing it, as typically observed (e.g. for amyloid fibrillation.

  2. Novel hybrid polymeric materials for barrier coatings

    Science.gov (United States)

    Pavlacky, Erin Christine

    Polymer-clay nanocomposites, described as the inclusion of nanometer-sized layered silicates into polymeric materials, have been widely researched due to significant enhancements in material properties with the incorporation of small levels of filler (1--5 wt.%) compared to conventional micro- and macro-composites (20--30 wt.%). One of the most promising applications for polymer-clay nanocomposites is in the field of barrier coatings. The development of UV-curable polymer-clay nanocomposite barrier coatings was explored by employing a novel in situ preparation technique. Unsaturated polyesters were synthesized in the presence of organomodified clays by in situ intercalative polymerization to create highly dispersed clays in a precursor resin. The resulting clay-containing polyesters were crosslinked via UV-irradiation using donor-acceptor chemistry to create polymer-clay nanocomposites which exhibited significantly enhanced barrier properties compared to alternative clay dispersion techniques. The impact of the quaternary alkylammonium organic modifiers, used to increase compatibility between the inorganic clay and organic polymer, was studied to explore influence of the organic modifier structure on the nanocomposite material properties. By incorporating just the organic modifiers, no layered silicates, into the polyester resins, reductions in film mechanical and thermal properties were observed, a strong indicator of film plasticization. An alternative in situ preparation method was explored to further increase the dispersion of organomodified clay within the precursor polyester resins. In stark contrast to traditional in situ polymerization methods, a novel "reverse" in situ preparation method was developed, where unmodified montmorillonite clay was added during polyesterification to a reaction mixture containing the alkylammonium organic modifier. The resulting nanocomposite films exhibited reduced water vapor permeability and increased mechanical properties

  3. Chelating polymeric membranes

    KAUST Repository

    Peinemann, Klaus-Viktor

    2015-01-22

    The present application offers a solution to the current problems associated with recovery and recycling of precious metals from scrap material, discard articles, and other items comprising one or more precious metals. The solution is premised on a microporous chelating polymeric membrane. Embodiments include, but are not limited to, microporous chelating polymeric membranes, device comprising the membranes, and methods of using and making the same.

  4. Polymeric coordination compounds

    Indian Academy of Sciences (India)

    Administrator

    Ce(dipic)3Sr(dipicH2)(OH2)3·5H2O (4) (dipicH2 – dipicolinic acid) exhibits 1-D polymeric chain structure, built up of alternating nine coordinate Ce and eight coordinate. Sr polyhedra. The analogous Ce–Ba compound (5) exhibits a polymeric chain built up of nine coordinate Ba units only, arranged in a hexagonal lattice.

  5. Rapid mixing chemical oxidative polymerization: an easy route to ...

    Indian Academy of Sciences (India)

    Administrator

    bon nanomaterial suspensions (Gedela et al 2012); here, the problems of poor solvability and/or dispersion of the constituent materials in the solvents used in synthesis protocols can be overcome. In this study, an easy method. (in situ chemical oxidative polymerization) to synthesize small diameter carbon nanotubes ...

  6. Effects of aqueous effluents from in situ fossil fuel processing technologies on aquatic systems. Annual progress report, January 1-December 31, 1979

    Energy Technology Data Exchange (ETDEWEB)

    Bergman, H.L.

    1980-01-04

    This is the third annual progress report for a continuing EPA-DOE jointly funded project to evaluate the effects of aqueous effluents from in situ fossil-fuel processing technologies on aquatic biota. The project is organized into four project tasks: (1) literature review; (2) process water screening; (3) methods development; and (4) recommendations. Our Bibliography of aquatic ecosystem effects, analytical methods and treatment technologies for organic compounds in advanced fossil-fuel processing effluents was submitted to the EPA for publication. The bibliography contains 1314 citations indexed by chemicals, keywords, taxa and authors. We estimate that the second bibliography volume will contain approximately 1500 citations and be completed in February. We compiled results from several laboratories of inorganic characterizations of 19 process waters: 55 simulated in situ oil-shale retort waters; and Hanna-3, Hanna-4B 01W and Lawrence Livermore Hoe Creek underground coal gasification condenser waters. These process waters were then compared to a published summary of the analyses from 18 simulated in situ oil-shale retort waters. We completed this year 96-h flow-through toxicity bioassays with fathead minnows and rainbow trout and 48-h flow-through bioassays with Daphnia pulicaria exposed to 5 oil-shale process waters, 1 tar-sand process water, 2 underground coal gasification condenser waters, 1 post-gasification backflood condenser water, as well as 2 bioassays with fossil-fuel process water constituents. The LC/sub 50/ toxicity values for these respective species when exposed to these waters are given in detail. (LTN)

  7. Effect of residual chips on the material removal process of the bulk metallic glass studied by in situ scratch testing inside the scanning electron microscope

    Directory of Open Access Journals (Sweden)

    Hu Huang

    2012-12-01

    Full Text Available Research on material removal mechanism is meaningful for precision and ultra-precision manufacturing. In this paper, a novel scratch device was proposed by integrating the parasitic motion principle linear actuator. The device has a compact structure and it can be installed on the stage of the scanning electron microscope (SEM to carry out in situ scratch testing. Effect of residual chips on the material removal process of the bulk metallic glass (BMG was studied by in situ scratch testing inside the SEM. The whole removal process of the BMG during the scratch was captured in real time. Formation and growth of lamellar chips on the rake face of the Cube-Corner indenter were observed dynamically. Experimental results indicate that when lots of chips are accumulated on the rake face of the indenter and obstruct forward flow of materials, materials will flow laterally and downward to find new location and direction for formation of new chips. Due to similar material removal processes, in situ scratch testing is potential to be a powerful research tool for studying material removal mechanism of single point diamond turning, single grit grinding, mechanical polishing and grating fabrication.

  8. In situ TEM observation of stress-induced martensitictransformations and twinning processes in CuAlNi single crystals

    Czech Academy of Sciences Publication Activity Database

    Zárubová, Niva; Gemperlová, Juliana; Gemperle, Antonín; Dlabáček, Zdeněk; Šittner, Petr; Novák, Václav

    2010-01-01

    Roč. 58, č. 15 (2010), s. 5109-5119 ISSN 1359-6454 R&D Projects: GA AV ČR(CZ) IAA200100627 Institutional research plan: CEZ:AV0Z10100520 Keywords : CuAlNi shape memory alloy * martensitic transformation * in situ TEM straining Subject RIV: BM - Solid Matter Physics ; Magnetism Impact factor: 3.781, year: 2010

  9. Environmental survey - tar sands in situ processing research program (Vernal, Uintah County, Utah). [Reverse-forward combustion; steam injection

    Energy Technology Data Exchange (ETDEWEB)

    Skinner, Q.

    1980-03-01

    Research will be done on the reverse-forward combustion and steam injection for the in-situ recovery of oil from tar sands. This environmental survey will serve as a guideline for the consideration of environmental consequences of such research. It covers the construction phase, operational phase, description of the environment, potential impacts and mitigations, coordination, and alternatives. (DLC)

  10. Dynamical observation of lithium insertion/extraction reaction during charge-discharge processes in Li-ion batteries by in situ spatially resolved electron energy-loss spectroscopy.

    Science.gov (United States)

    Shimoyamada, Atsushi; Yamamoto, Kazuo; Yoshida, Ryuji; Kato, Takehisa; Iriyama, Yasutoshi; Hirayama, Tsukasa

    2015-12-01

    All-solid-state Li-ion batteries (LIBs) with solid electrolytes are expected to be the next generation devices to overcome serious issues facing conventional LIBs with liquid electrolytes. However, the large Li-ion transfer resistance at the electrode/solid-electrolyte interfaces causes low power density and prevents practical use. In-situ-formed negative electrodes prepared by decomposing the solid electrolyte Li(1+x+3z)Alx(Ti,Ge)(2-x)Si(3z)P(3-z)O12 (LASGTP) with an excess Li-ion insertion reaction are effective electrodes providing low Li-ion transfer resistance at the interfaces. Prior to our work, however, it had still been unclear how the negative electrodes were formed in the parent solid electrolytes. Here, we succeeded in dynamically visualizing the formation by in situ spatially resolved electron energy-loss spectroscopy in a transmission electron microscope mode (SR-TEM-EELS). The Li-ions were gradually inserted into the solid electrolyte region around 400 nm from the negative current-collector/solid-electrolyte interface in the charge process. Some of the ions were then extracted in the discharge process, and the rest were diffused such that the distribution was almost flat, resulting in the negative electrodes. The redox reaction of Ti(4+)/Ti(3+) in the solid electrolyte was also observed in situ during the Li insertion/extraction processes. The in situ SR-TEM-EELS revealed the mechanism of the electrochemical reaction in solid-state batteries. © The Author 2015. Published by Oxford University Press on behalf of The Japanese Society of Microscopy. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

  11. Atomic layer deposition of ZrO2 for graphene-based multilayer structures: In situ and ex situ characterization of growth process

    International Nuclear Information System (INIS)

    Tamm, Aile; Kozlova, Jekaterina; Aarik, Lauri; Aidla, Aleks; Kiisler, Alma-Asta; Kasikov, Aarne; Ritslaid, Peeter; Maendar, Hugo; Aarik, Jaan; Lu, Jun; Hultman, Lars; Sammelselg, Vaeino; Kukli, Kaupo

    2014-01-01

    Real time monitoring of atomic layer deposition by quartz crystal microbalance (QCM) was used to follow the growth of ZrO 2 thin films on graphene. The films were grown from ZrCl 4 and H 2 O on graphene prepared by chemical vapor deposition method on 100-nm thick nickel film or on Cu-foil and transferred onto QCM sensor. The deposition was performed at a substrate temperature of 190 C. The growth of the dielectric film on graphene was significantly retarded compared to the process carried out on QCM without graphene. After the deposition of dielectric films, the basic structure of graphene was retained. (copyright 2014 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  12. Chain-growth click polymerization of AB2 monomers for the formation of hyperbranched polymers with low polydispersities in a one-pot process.

    Science.gov (United States)

    Shi, Yi; Graff, Robert W; Cao, Xiaosong; Wang, Xiaofeng; Gao, Haifeng

    2015-06-22

    Hyperbranched polymers are important soft nanomaterials but robust synthetic methods with which the polymer structures can be easily controlled have rarely been reported. For the first time, we present a one-pot one-batch synthesis of polytriazole-based hyperbranched polymers with both low polydispersity and a high degree of branching (DB) using a copper-catalyzed azide-alkyne cycloaddition (CuAAC) polymerization. The use of a trifunctional AB2 monomer that contains one alkyne and two azide groups ensures that all Cu catalysts are bound to polytriazole polymers at low monomer conversion. Subsequent CuAAC polymerization displayed the features of a "living" chain-growth mechanism with a linear increase in molecular weight with conversion and clean chain extension for repeated monomer additions. Furthermore, the triazole group in a linear (L) monomer unit complexed Cu(I) , which catalyzed a faster reaction of the second azide group to quickly convert the L unit into a dendritic unit, producing hyperbranched polymers with DB=0.83. © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  13. Influence of diblock copolymer PCL-mPEG and of various iodinated oils on the formulation by the emulsion-solvent diffusion process of radiopaque polymeric nanoparticles.

    Science.gov (United States)

    Hallouard, François; Briançon, Stéphanie; Anton, Nicolas; Li, Xiang; Vandamme, Thierry; Fessi, Hatem

    2013-11-01

    This pioneer study in the domain of blood pool contrast media formulation presents the influence of poly-ɛ-caprolactone-monomethoxy poly(ethylene glycol) (PCL-mPEG) and oils on the formulation of polymeric nanoparticles by emulsion-solvent diffusion. The nature of the oil used had no influence on the encapsulation rate, even if particles were formulated with a mix of PCL/PCL-mPEG. It did, however, influence the particle size and polydispersity, with macroglycerides appearing to be the lipid structure best suited to obtain the smallest monodisperse particles. When we used PCL-mPEG to form a PEG-hydrated layer to surround the nanoparticles, its tension active property had a favorable effect on particle size and polydispersity. We also showed the strong deleterious effect on particle size and polydispersity when the polymer proportion was increased to over 1% (w/v) in the pre-emulsion organic phase. Conversely, increasing the oil proportion in this organic phase simply resulted in a slight to insignificant deleterious effect on size and polydispersity, enabling the oil proportion to be enhanced up to 3% (w/v). Finally, we showed the favorable combined effect of oil iodination and the presence of PCL-mPEG on particles formulated by emulsion-solvent diffusion leading to the preparation of smaller polymeric iodine-containing particles. © 2013 Wiley Periodicals, Inc. and the American Pharmacists Association.

  14. Nitroxide radicals formed in situ as polymer chain growth regulators

    Energy Technology Data Exchange (ETDEWEB)

    Kolyakina, Elena V; Grishin, Dmitry F [Research Insitute of Chemistry, N.I. Lobachevskii Nizhnii Novgorod State University, Nizhnii Novgorod (Russian Federation)

    2009-06-30

    Published data on controlled synthesis of macromolecules using nitroxide radicals, formed in situ during polymerization, as polymer chain growth regulators are systematized and generalized. The attention is focused on the mechanism of polymer chain growth control during reversibly inhibited radical homopolymerization and the effect of structure of precursors and regulating additives on the polymerization kinetics of monomers of different nature and the molecular-mass characteristics of the polymers thus formed. The key methods for generation of nitroxide radicals directly during polymerization are considered. The prospects for development and practical use of these approaches for the synthesis of new polymeric materials are evaluated.

  15. In situ investigation of titanium nitride surface dynamics: The role of surface and bulk mass transport processes

    Science.gov (United States)

    Bareno, Javier

    NaCl-structure TiN and related transition-metal (TM) nitrides are widely used as hard wear-resistant coatings on cutting tools, diffusion-barriers in microelectronic devices, corrosion-resistant layers on mechanical components, and abrasion-resistant thin films on optics and architectural glass. Since the elastic and physical properties of TiN are highly anisotropic, controlling the microstructural and surface morphological evolution of polycrystalline TM nitride films is important for all of the above applications. In this thesis, I used in-situ high-temperature low-energy electron microscopy (LEEM) to gain insight into film growth and microstructure development dynamics by studying mass-transport processes occurring during annealing of three dimensional (3D) structures on TiN surfaces. Additionally, in order to extend the current understanding of nanostructure development in binary nitride films to more complex ternary TM-nitride-based nanocomposites, I employed in-situ scanning tunneling microscopy (STM) and low-energy electron diffraction (LEED), as well as ab-initio modeling, to investigate the atomic structure of the SiNx/TiN heterointerfaces which control the properties of SiNx-TiN nanocomposites. The LEEM studies of mass transport on TiN(111) focus on two specific surface morphologies which are observed to be present during growth of TiN single-crystals. (1) I investigated the temperature-dependent coarsening/decay kinetics of three-dimensional TiN island mounds on large (>1000 A) atomically-flat terraces; showing that TiN(111) steps are highly permeable and exhibit strong repulsive temperature-dependent step-step interactions that vary from 0.03 eV-A at 1559 K to 0.76 eV-A at 1651 K. (2) I studied the nucleation and growth of spiral steps originating at surface-terminated screw dislocations; I developed a model of spiral growth relating the emission rate of point defects from the bulk to the temperature-dependent spiral rotation frequency o(T); and I

  16. Effect of directional solidification rate on the microstructure and properties of deformation-processed Cu–7Cr–0.1Ag in situ composites

    International Nuclear Information System (INIS)

    Liu, Keming; Jiang, Zhengyi; Zhao, Jingwei; Zou, Jin; Chen, Zhibao; Lu, Deping

    2014-01-01

    Highlights: • Effect of directional solidification (DS) rate on a Cu–Cr–Ag in situ composite. • The microstructure and properties of the DS in situ composite were investigated. • The second-phase Cr grains were parallel to drawing direction, and were finer. • The tensile strength was higher and the combination of properties was better. - Abstract: The influence of directional solidification rate on the microstructure, mechanical properties and conductivity of deformation-processed Cu–7Cr–0.1Ag in situ composites produced by thermo-mechanical processing was systematically investigated. The microstructure was analyzed by optical microscopy and scanning electronic microscopy. The mechanical properties and conductivity were evaluated by tensile-testing machine and micro-ohmmeter, respectively. The results indicate that the size, shape and distribution of second-phase Cr grains are significantly different in the Cu–7Cr–0.1Ag alloys with different growth rates. At a growth rate of 200 μm s −1 , the Cr grains transform into fine Cr fiber-like grains parallel to the pulling direction from the Cr dendrites. The tensile strength of the Cu–7Cr–0.1Ag in situ composites from the directional solidification (DS) alloys is significantly higher than that from the as-cast alloy, while the conductivity of the in situ composites from the DS alloys is slightly lower than that from the as-cast alloy. The following combinations of tensile strength, elongation to fracture and conductivity of the Cu–7Cr–0.1Ag in situ composites from the DS alloy with a growth rate of 200 μm s −1 and a cumulative cold deformation strain of 8 after isochronic aging treatment for 1 h can be obtained respectively as: (i) 1067 MPa, 2.9% and 74.9% IACS; or (ii) 1018 MPa, 3.0%, and 76.0% IACS or (iii) 906 MPa, 3.3% and 77.6% IACS

  17. Effect of directional solidification rate on the microstructure and properties of deformation-processed Cu–7Cr–0.1Ag in situ composites

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Keming [Jiangxi Key Laboratory for Advanced Copper and Tungsten Materials, Jiangxi Academy of Sciences, Nanchang 330029 (China); School of Mechanical, Materials and Mechatronic Engineering, University of Wollongong, NSW 2522 (Australia); Jiang, Zhengyi; Zhao, Jingwei [School of Mechanical, Materials and Mechatronic Engineering, University of Wollongong, NSW 2522 (Australia); Zou, Jin; Chen, Zhibao [Jiangxi Key Laboratory for Advanced Copper and Tungsten Materials, Jiangxi Academy of Sciences, Nanchang 330029 (China); Lu, Deping, E-mail: llludp@163.com [Jiangxi Key Laboratory for Advanced Copper and Tungsten Materials, Jiangxi Academy of Sciences, Nanchang 330029 (China)

    2014-11-05

    Highlights: • Effect of directional solidification (DS) rate on a Cu–Cr–Ag in situ composite. • The microstructure and properties of the DS in situ composite were investigated. • The second-phase Cr grains were parallel to drawing direction, and were finer. • The tensile strength was higher and the combination of properties was better. - Abstract: The influence of directional solidification rate on the microstructure, mechanical properties and conductivity of deformation-processed Cu–7Cr–0.1Ag in situ composites produced by thermo-mechanical processing was systematically investigated. The microstructure was analyzed by optical microscopy and scanning electronic microscopy. The mechanical properties and conductivity were evaluated by tensile-testing machine and micro-ohmmeter, respectively. The results indicate that the size, shape and distribution of second-phase Cr grains are significantly different in the Cu–7Cr–0.1Ag alloys with different growth rates. At a growth rate of 200 μm s{sup −1}, the Cr grains transform into fine Cr fiber-like grains parallel to the pulling direction from the Cr dendrites. The tensile strength of the Cu–7Cr–0.1Ag in situ composites from the directional solidification (DS) alloys is significantly higher than that from the as-cast alloy, while the conductivity of the in situ composites from the DS alloys is slightly lower than that from the as-cast alloy. The following combinations of tensile strength, elongation to fracture and conductivity of the Cu–7Cr–0.1Ag in situ composites from the DS alloy with a growth rate of 200 μm s{sup −1} and a cumulative cold deformation strain of 8 after isochronic aging treatment for 1 h can be obtained respectively as: (i) 1067 MPa, 2.9% and 74.9% IACS; or (ii) 1018 MPa, 3.0%, and 76.0% IACS or (iii) 906 MPa, 3.3% and 77.6% IACS.

  18. Revealing Chemical Processes Involved in Electrochemical (De)Lithiation of Al with in Situ Neutron Depth Profiling and X-ray Diffraction.

    Science.gov (United States)

    Liu, Danny X; Co, Anne C

    2016-01-13

    Herein we report a direct measurement of Li transport in real-time during charge and discharge process within an Al matrix using neutron depth profiling (NDP). In situ NDP was used to reveal and quantify parasitic losses during the first 25 mAhr/g of lithiation, followed by the formation of LiAl protrusions from the surface of pristine Al. Evidence of Li entrapment is also reported during delithiation. Subsequent lithiation and delithiation showed electrochemical charge passed to be equivalent to the amount of lithium incorporated into the Al matrix with negligible difference, suggesting that the parasitic losses including the formation of the solid electrolyte layer may be confined to the first lithiation. Parallel in situ XRD measurements also confirm the transformation of β-LiAl from a solid solution of α-LiAl, revealing solid solution-mediated crystallization of β-LiAl.

  19. Microstructure Evolution and Mechanical Properties of Al-TiB2/TiC In Situ Aluminum-Based Composites during Accumulative Roll Bonding (ARB) Process

    Science.gov (United States)

    Nie, Jinfeng; Wang, Fang; Li, Yusheng; Cao, Yang; Liu, Xiangfa; Zhao, Yonghao; Zhu, Yuntian

    2017-01-01

    In this study, a kind of Al-TiB2/TiC in situ composite was successfully prepared using the melt reaction method and the accumulative roll-bonding (ARB) technique. The microstructure evolution of the composites with different deformation treatments was characterized using field emission scanning electron microscopy (FESEM) and a transmission electron microscope (TEM). The mechanical properties of the Al-TiB2/TiC in situ composite were also studied with tensile and microhardness tests. It was found that the distribution of reinforcement particles becomes more homogenous with an increasing ARB cycle. Meanwhile, the mechanical properties showed great improvement during the ARB process. The ultimate tensile strength (UTS) and microhardness of the composites were increased to 173.1 MPa and 63.3 Hv after two ARB cycles, respectively. Furthermore, the strengthening mechanism of the composite was analyzed based on its fracture morphologies. PMID:28772467

  20. Synthesis of Glycopolymer Architectures by Reversible-Deactivation Radical Polymerization

    Directory of Open Access Journals (Sweden)

    Ali Ghadban

    2013-05-01

    Full Text Available This review summarizes the state of the art in the synthesis of well-defined glycopolymers by Reversible-Deactivation Radical Polymerization (RDRP from its inception in 1998 until August 2012. Glycopolymers architectures have been successfully synthesized with four major RDRP techniques: Nitroxide-mediated radical polymerization (NMP, cyanoxyl-mediated radical polymerization (CMRP, atom transfer radical polymerization (ATRP and reversible addition-fragmentation chain transfer (RAFT polymerization. Over 140 publications were analyzed and their results summarized according to the technique used and the type of monomer(s and carbohydrates involved. Particular emphasis was placed on the experimental conditions used, the structure obtained (comonomer distribution, topology, the degree of control achieved and the (potential applications sought. A list of representative examples for each polymerization process can be found in tables placed at the beginning of each section covering a particular RDRP technique.

  1. Analysis of surface leaching processes in vitrified high-level nuclear wastes using in-situ raman imaging and atomistic modeling. 1998 annual progress report

    International Nuclear Information System (INIS)

    Clark, D.E.; Simmons, J.H.

    1998-01-01

    'The research objective was to test and develop optical methods for real-time, remote and in-situ testing of corrosion processes on the surface of vitrified nuclear wastes. This report summarizes the research conducted in the first 1.5 years of a 3 year grant. At this point, the authors have identified the conditions for optimal tests and demonstrated that both IR reflection and Raman spectroscopies can be used to determine the dealkalization process in the surface of simple glasses in real time.'

  2. MODERN TECHNOLOGY OF ANIONIC POLYMERIZATION MONOMERS

    Directory of Open Access Journals (Sweden)

    A. V. Tkachev

    2013-01-01

    Full Text Available The preconditions of use in the manufacture of automobile tyres of vulcanizates-based mortar butadienestyrene rubber with a high content of 1.2 links butadiene and statistical distribution of styrene are formulated. Set out scientific researches in the field of anionic co-polymerization of diene and vinyl aromatic monomers. Formulation of catalytic systems applied in processes of anionic copolymerization of monomers are given. The reasons of formation of gel in the process of anionic polymerization of monomers and terms of their elimination are considered.

  3. Remedial Process Optimization and Green In-Situ Ozone Sparging for Treatment of Groundwater Impacted with Petroleum Hydrocarbons

    Science.gov (United States)

    Leu, J.

    2012-12-01

    A former natural gas processing station is impacted with TPH and BTEX in groundwater. Air sparging and soil vapor extraction (AS/AVE) remediation systems had previously been operated at the site. Currently, a groundwater extraction and treatment system is operated to remove the chemicals of concern (COC) and contain the groundwater plume from migrating offsite. A remedial process optimization (RPO) was conducted to evaluate the effectiveness of historic and current remedial activities and recommend an approach to optimize the remedial activities. The RPO concluded that both the AS/SVE system and the groundwater extraction system have reached the practical limits of COC mass removal and COC concentration reduction. The RPO recommended an in-situ chemical oxidation (ISCO) study to evaluate the best ISCO oxidant and approach. An ISCO bench test was conducted to evaluate COC removal efficiency and secondary impacts to recommend an application dosage. Ozone was selected among four oxidants based on implementability, effectiveness, safety, and media impacts. The bench test concluded that ozone demand was 8 to 12 mg ozone/mg TPH and secondary groundwater by-products of ISCO include hexavalent chromium and bromate. The pH also increased moderately during ozone sparging and the TDS increased by approximately 20% after 48 hours of ozone treatment. Prior to the ISCO pilot study, a capture zone analysis (CZA) was conducted to ensure containment of the injected oxidant within the existing groundwater extraction system. The CZA was conducted through a groundwater flow modeling using MODFLOW. The model indicated that 85%, 90%, and 95% of an injected oxidant could be captured when a well pair is injecting and extracting at 2, 5, and 10 gallons per minute, respectively. An ISCO pilot test using ozone was conducted to evaluate operation parameters for ozone delivery. The ozone sparging system consisted of an ozone generator capable of delivering 6 lbs/day ozone through two ozone

  4. Online observation of emulsion polymerization by fluorescence technique

    CERN Document Server

    Rudschuck, S; Fuhrmann, J

    1999-01-01

    An online observation of local polarity via fluorescence spectroscopy was used to study the formation and growth of polymer particles during an emulsifier-free heterogeneous polymerization. The reaction mixture consisted of styrene dispersed in water and the polymerization was initiated by a macro-initiator (hydrolyzed propene-maleic acid copolymer with t-butyl perester groups). Pyrenyl probes were attached to the backbone of the initiator to analyze the heterogeneous reaction. The experimental results allow a clear distinction of different time regions during the heterogeneous polymerization. Information about the heating period, the latex formation, the particle growth and the final stage of the polymerization process (gel point) were obtained. (11 refs).

  5. Combining nanocalorimetry and dynamic transmission electron microscopy for in situ characterization of materials processes under rapid heating and cooling

    Energy Technology Data Exchange (ETDEWEB)

    Grapes, Michael D., E-mail: mgrapes1@jhu.edu [Department of Materials Science and Engineering, Johns Hopkins University, Baltimore, Maryland 21218 (United States); Materials Measurement Science Division, Material Measurement Laboratory, National Institute of Standards and Technology, Gaithersburg, Maryland 20899 (United States); LaGrange, Thomas; Reed, Bryan W.; Campbell, Geoffrey H. [Condensed Matter and Materials Division, Lawrence Livermore National Laboratory, Livermore, California 94550 (United States); Friedman, Lawrence H.; LaVan, David A., E-mail: david.lavan@nist.gov [Materials Measurement Science Division, Material Measurement Laboratory, National Institute of Standards and Technology, Gaithersburg, Maryland 20899 (United States); Weihs, Timothy P., E-mail: weihs@jhu.edu [Department of Materials Science and Engineering, Johns Hopkins University, Baltimore, Maryland 21218 (United States)

    2014-08-15

    Nanocalorimetry is a chip-based thermal analysis technique capable of analyzing endothermic and exothermic reactions at very high heating and cooling rates. Here, we couple a nanocalorimeter with an extremely fast in situ microstructural characterization tool to identify the physical origin of rapid enthalpic signals. More specifically, we describe the development of a system to enable in situ nanocalorimetry experiments in the dynamic transmission electron microscope (DTEM), a time-resolved TEM capable of generating images and electron diffraction patterns with exposure times of 30 ns–500 ns. The full experimental system consists of a modified nanocalorimeter sensor, a custom-built in situ nanocalorimetry holder, a data acquisition system, and the DTEM itself, and is capable of thermodynamic and microstructural characterization of reactions over a range of heating rates (10{sup 2} K/s–10{sup 5} K/s) accessible by conventional (DC) nanocalorimetry. To establish its ability to capture synchronized calorimetric and microstructural data during rapid transformations, this work describes measurements on the melting of an aluminum thin film. We were able to identify the phase transformation in both the nanocalorimetry traces and in electron diffraction patterns taken by the DTEM. Potential applications for the newly developed system are described and future system improvements are discussed.

  6. Plasma polymerization by Softplasma

    DEFF Research Database (Denmark)

    Jiang, J.; Wu, Zhenning; Benter, Maike

    2008-01-01

    In the late 19th century, the first depositions - known today as plasma polymers, were reported. In the last century, more and more research has been put into plasma polymers. Many different deposition systems have been developed. [1, 2] Shi F. F. broadly classified them into internal electrode......, external electrode, and electrodeless microwave or high frequency reactors. [3] Softplasma™ is an internal electrode plasma setup powered by low frequenc~ gower supply. It was developed in late 90s for surface treatment of silicone rubber. [ ]- 5] It is a low pressure, low electron density, 3D homogenous...... plasma. In this study, we are presenting the surface modification"pf polymers by plasma polymerization using Softplasma™. Softplasma™ can be used for two major types of polymerization: polymerization of vinyl monomers, where plasma acts as initiator; chemical vapour deposition, where plasma acts...

  7. Effect of simulated microwave disinfection on the linear dimensional change, hardness and impact strength of acrylic resins processed by different polymerization cycles.

    Science.gov (United States)

    Xediek Consani, R L; Chorwat, V; Ferraz Mesquita, M; Fernandes Santos, M B; Bortolazzo Correr, A; Consani, S

    2014-05-01

    This study investigated the effect of simulated microwave disinfection (SMD) on the linear dimensional changes, hardness and impact strength of acrylic resins under different polymerization cycles. Metal dies with referential points were embedded in flasks with dental stone. Samples of Classico and Vipi acrylic resins were made following the manufacturers' recommendations. The assessed polymerization cycles were: A) water bath at 74 ºC for 9 h; B) water bath at 74 ºC for 8 h and temperature increased to 100 ºC for 1 h; C) water bath at 74 ºC for 2 h and temperature increased to 100 ºC for 1 h; and D) water bath at 120 ºC and pressure of 60 pounds. Linear dimensional distances in length and width were measured after SMD and water storage at 37 ºC for 7 and 30 days using an optical microscope. SMD was carried out with the samples immersed in 150 mL of water in an oven (650 W for 3 min). A load of 25 gf for 10 s was used in the hardness test. Charpy impact test was performed with 40 kpcm. Data were submitted to ANOVA and Tukey's test (5%). The Classico resin was dimensionally steady in length in the A and D cycles for all periods, while the Vipi resin was steady in the A, B and C cycles for all periods. The Classico resin was dimensionally steady in width in the C and D cycles for all periods, and the Vipi resin was steady in all cycles and periods. The hardness values for Classico resin were steady in all cycles and periods, while the Vipi resin was steady only in the C cycle for all periods. Impact strength values for Classico resin were steady in the A, C and D cycles for all periods, while Vipi resin was steady in all cycles and periods. SMD promoted different effects on the linear dimensional changes, hardness and impact strength of acrylic resins submitted to different polymerization cycles when after SMD and water storage were considered.

  8. Effect of simulated microwave disinfection on the linear dimensional change, hardness and impact strength of acrylic resins processed by different polymerizing cycles.

    Science.gov (United States)

    Xediek Consani, R L; Chorwat, V; Ferraz Mesquita, M; Fernandes Santos, M B; Bortolazzo Correr, A; Consani, S

    2014-06-20

    This study investigated the effect of simulated microwave disinfection (SMD) on the linear dimensional changes, hardness and impact strength of acrylic resins under different polymerization cycles. Metal dies with referential points were embedded in flasks with dental stone. Samples of Classico and Vipi acrylic resins were made following the manufacturers' recommendations. The assessed polymerization cycles were: A-- water bath at 74ºC for 9 h; B-- water bath at 74ºC for 8 h and temperature increased to 100ºC for 1 h; C-- water bath at 74ºC for 2 h and temperature increased to 100ºC for 1 h;; and D-- water bath at 120ºC and pressure of 60 pounds. Linear dimensional distances in length and width were measured after SMD and water storage at 37ºC for 7 and 30 days using an optical microscope. SMD was carried out with the samples immersed in 150 mL of water in an oven (650 W for 3 min). A load of 25 gf for 10 sec was used in the hardness test. Charpy impact test was performed with 40 kpcm. Data were submitted to ANOVA and Tukey's test (5%). The Classico resin was dimensionally steady in length in the A and D cycles for all periods, while the Vipi resin was steady in the A, B and C cycles for all periods. The Classico resin was dimensionally steady in width in the C and D cycles for all periods, and the Vipi resin was steady in all cycles and periods. The hardness values for Classico resin were steady in all cycles and periods, while the Vipi resin was steady only in the C cycle for all periods. Impact strength values for Classico resin were steady in the A, C and D cycles for all periods, while Vipi resin was steady in all cycles and periods. SMD promoted different effects on the linear dimensional changes, hardness and impact strength of acrylic resins submitted to different polymerization cycles when after SMD and water storage were considered.

  9. Controllable surface morphology and properties via mist polymerization on a plasma-treated polymethyl methacrylate surface.

    Science.gov (United States)

    Wan, S J; Wang, L; Xu, X J; Zhao, C H; Liu, X D

    2014-02-14

    Surface modification by grafting polymers on solid materials is an important strategy used to improve surface properties. This article reports that under appropriate conditions, very thin layers with desired morphologies may be constructed on a plasma-treated substrate by feeding a small quantity of a monomer with a mist stream carrying droplets produced from monomer solutions. We investigate the effects of process parameters that affect layer morphology, including exposure time to the mist stream, concentration of the monomer solution, and solvent selectivity. For a methyl methacrylate solution in ethanol, nanoparticles are uniformly grown with increasing monomer concentration or exposure time and finally form a porous layer at 3.65 mol L(-1) for 30 min. Decreasing solvent polarity not only affects surface morphology, but also increases hydrophobicity of the resulting surface. With 2,2,3,4,4,4-hexafluorobutyl methacrylate as the monomer, SEM and AFM micrographs indicated that mist polymerization results in numerous microspheres on the activated surface. These experimental results were interpreted by a mechanism in terms of an in situ polymerization accompanied by a phase transformation of the resulting polymer. Specifically, plasma treatment provides highly active cations and radicals to initiate very rapid polymerization, and the resulting polymers are consequently deposited from the liquid onto the surface under phase transition mechanisms.

  10. Redox-Controlled Olefin (Co)Polymerization Catalyzed by Ferrocene-Bridged Phosphine-Sulfonate Palladium Complexes.

    Science.gov (United States)

    Chen, Min; Yang, Bangpei; Chen, Changle

    2015-12-14

    The facile and reversible interconversion between neutral and oxidized forms of palladium complexes containing ferrocene-bridged phosphine sulfonate ligands was demonstrated. The activity of these palladium complexes could be controlled using redox reagents during ethylene homopolymerization, ethylene/methyl acrylate copolymerization, and norbornene oligomerization. Specifically in norbornene oligomerization, the neutral complexes were not active at all whereas the oxidized counterparts showed appreciable activity. In situ switching between the neutral and oxidized forms resulted in an interesting "off" and "on" behavior in norbornene oligomerization. This work provides a new strategy to control the olefin polymerization process. © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  11. Power ultrasound effects for in situ compatibilization of polymer-clay nanocomposites

    International Nuclear Information System (INIS)

    Ryu, Joung Gul; Park, Sang Wan; Kim, Hyungsu; Lee, Jae Wook

    2004-01-01

    Polymer-clay nanocomposites of various concentrations were prepared by ultrasonically assisted polymerization and melt mixing processes. The sonication process using power ultrasonic wave was employed to enhance nano-scale dispersion during melt mixing of monomer, polymer and organically modified clay. According to the unique mode of power ultrasound wave, we expected enhanced breakup of layered silicate bundle and further reduction in the size of dispersed phase with better homogeneity compared to the in situ polymerization. The optimum conditions to perform stable exfoliated nanocomposites were studied by various compositions and conditions. Dispersion characteristics and morphology of the nanocomposites were verified by X-ray diffraction (XRD) and transmission electron microscopy (TEM). Rheological behaviors were measured under dynamic frequency sweep mode using Rheometric science ARES

  12. Controlled free radical polymerization of vinyl acetate with cobalt ...

    Indian Academy of Sciences (India)

    able processes but also to the hydrolysis of environmen- tally friendly polyvinyl alcohol in the film formations, separation and bioprocesses, or coatings (figure 4). 4. Conclusion. The cobalt-mediated controlled radical polymerization of vinyl acetate was studied in bulk. It indicated a faster rate than solution polymerization.

  13. Inflation of a Polymeric Menbrane

    DEFF Research Database (Denmark)

    Kristensen, Susanne B.; Larsen, Johannes R.; Hassager, Ole

    1998-01-01

    We consider an axisymmetric polymeric membrane inflated by a uniform pressure difference acting across the membrane.......We consider an axisymmetric polymeric membrane inflated by a uniform pressure difference acting across the membrane....

  14. Preparation of Superhydrophobic Polymeric Film on Aluminum Plates by Electrochemical Polymerization

    Directory of Open Access Journals (Sweden)

    Juan Xu

    2009-11-01

    Full Text Available 6-(N-Allyl-1,1,2,2-tetrahydroperfluorododecylamino-1,3,5-triazine-2,4-dithiol monosodium (ATP was used to prepare polymeric thin films on pure aluminum plates to achieve a superhydrophobic surface. The electrochemical polymerization process of ATP on aluminum plates in NaNO2 aqueous solution and the formation of poly(6-(N-allyl-1,1,2,2-tetrahydroperfluorododecylamino-1,3,5-triazine-2,4-dithiol (PATP thin film were studied by means of optical ellipsometry and film weight. The chemical structure of the polymeric film is investigated using FT-IR spectra and X-ray photoelectron spectroscopy (XPS. Contact angle goniometry was applied to measure the contact angles with distilled water drops at ambient temperature. The experimental results indicate that the polymeric film formed on pure aluminum plates exhibits superhydrophobic properties with a distilled water contact angle of 153°. The electrochemical polymerization process is time-saving, inexpensive, environmentally friendly and fairly convenient to carry out. It is expected that this technique will advance the production of superhydrophobic materials with new applications on a large scale. Moreover, this kind of polymeric thin film can be used as a dielectric material due to its insulating features.

  15. Aplicação de análise multivariada aos dados de espectroscopia no infravermelho obtidos na polimerização in situ de adesivo à base de cianoacrilato Multivariate analyses on FT-IR data of polymerization in situ of cyanoacrylate adhesive

    Directory of Open Access Journals (Sweden)

    Francisco A. A. Miranda

    1998-06-01

    Full Text Available A polimerização de adesivo à base de cianoacrilato foi acompanhada por FT-IR durante 30 minutos. A aplicação das técnicas de estatística multivariada (análise de agrupamento hierárquico e a análise dos componentes principais aos espectros de infravermelho, permitiram uma melhor identificação das diferenças espectrais entre monômero e polímero e possibilitou, também, inferir que a quantidade de monômero e do mero no polímero se eqüivalem com seis minutos de polimerização. A técnica de infravermelho mostrou-se uma ferramenta adequada para o acompanhamento da cinética de reação de adesivo à base de cianoacrilato, que torna-se ainda mais eficiente quando associada às técnicas de estatística multivariada.The polymerization of a cyanoacrylate adhesive was accompanied by FT-IR during 30 minutes. The application of multivariate statistics techniques (Hierarchical Clusters Analyses and Principal Components on infrared spectra allowed a better identification of spectral differences between monomer and polymer and also permitted to infer that the quantity of monomer and of mer of the polymer are equal in six minutes polymerization (half-life. The infrared technique appeared as an apropriate tool for observing the kinetics of cyanoacrylate adhesive reaction, which becomes even more efficient when associated to multivariate statistics techniques.

  16. In-situ gelling polymers for biomedical applications

    CERN Document Server

    2015-01-01

    This book presents the research involving in situ gelling polymers and can be used as a guidebook for academics, industrialists and postgraduates interested in this area. This work summaries the academic contributions from the top authorities in the field and explore the fundamental principles of in situ gelling polymeric networks, along with examples of their major applications. This book aims to provide an up-to-date resource of in situ gelling polymer research.

  17. Polymeric coordination compounds

    Indian Academy of Sciences (India)

    Administrator

    Metal coordination polymers with one- and two-dimensional structures are of current interest due to their possible relevance to material science 1. In continuation of our previous studies 2,3, several new polymeric compounds are reported here. Among the complexes of silver with aminomethyl pyridine (amp) ...

  18. Polymerized and functionalized triglycerides

    Science.gov (United States)

    Plant oils are useful sustainable raw materials for the development of new chemical products. As part of our research emphasis in sustainability and green polymer chemistry, we have explored a new method for polymerizing epoxidized triglycerides with the use of fluorosulfonic acid. Depending on the ...

  19. Evaluation of solid polymeric organic materials for use in bioreactive sediment capping to stimulate the degradation of chlorinated aliphatic hydrocarbons

    NARCIS (Netherlands)

    Atashgahi, S.; Maphosa, F.; Vrieze, de J.; Haest, P.J.; Boon, N.; Smidt, H.; Springael, D.; Dejonghe, W.

    2014-01-01

    In situ bioreactive capping is a promising technology for mitigation of surface water contamination by discharging polluted groundwater. Organohalide respiration (OHR) of chlorinated ethenes in bioreactive caps can be stimulated through incorporation of solid polymeric organic materials (SPOMs) that

  20. The control of H2S in biogas using iron ores as in situ desulfurizers during anaerobic digestion process.

    Science.gov (United States)

    Zhou, Qiying; Jiang, Xia; Li, Xi; Jiang, Wenju

    2016-09-01

    In this study, five kinds of iron ores, limonite, hematite, manganese ore, magnetite and lava rock, were used as the in situ desulfurizers in the anaerobic digestion reactors to investigate their effects on controlling H2S in biogas. The results show that the addition of the five iron ores could significantly control the content of H2S in biogas, with the best performance for limonite. As limonite dosages increase (10-60 g/L), the contents of H2S in biogas were evidently decreased in the digesters with different initial sulfate concentrations (0-1000 mg/L). After the anaerobic digestion, the removed sulfur was mostly deposited on the surface of limonite. A possible mechanism of H2S control in biogas by limonite was proposed preliminarily, including adsorption, FeS precipitation, and Fe (III) oxidation. The results demonstrated that limonite was a promising in situ desulfurizer for controlling H2S in biogas with low cost and high efficiency.