Relevant bibliographies by topics / Polystyrene sulfonated

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers

Academic literature on the topic 'Polystyrene sulfonated'

Author: Grafiati
Published: 4 June 2021
Last updated: 1 February 2022

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Journal articles on the topic "Polystyrene sulfonated"

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Hu, Xiaotian, Lie Chen, Licheng Tan, Ting Ji, Yong Zhang, Lin Zhang, Di Zhang, and Yiwang Chen. "In situ polymerization of ethylenedioxythiophene from sulfonated carbon nanotube templates: toward high efficiency ITO-free solar cells." Journal of Materials Chemistry A 4, no. 17 (2016): 6645–52. http://dx.doi.org/10.1039/c6ta00287k.

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Tan, N. C. Beck, X. Liu, R. M. Briber, and D. G. Peiffer. "Immiscibility in polystyrene/sulfonated polystyrene blends." Polymer 36, no. 10 (May 1995): 1969–73. http://dx.doi.org/10.1016/0032-3861(95)91439-e.

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Hendrana, Sunit, Erwin Erwin, Krisman Krisman, Syakbaniah Syakbaniah, Isna’im Isna’im, Yusmeri Yusmeri, Neti Satria, Tri Susilawati, and Sudirman Sudirman. "APPLICATION OF SULFONATED POLYSTYRENE IN POLYMER ELECTROLYTE FUEL CELL." Jurnal Sains Materi Indonesia 20, no. 1 (October 30, 2018): 44. http://dx.doi.org/10.17146/jsmi.2018.20.1.5406.

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APPLICATION OF SULFONATED POLYSTYRENE IN POLYMER ELECTROLYTE FUEL CELL. Sulfonated polystyrene (SPS) is polyelectrolyte solid that widely used in many aplications. In this works SPS is applied for some parts of polymer electrolyte fuel cell membrane due sulfonate group available in the structure. The investigation involve the application for membrane with addition of small molecules, i.e. benzimidazole and evaluating its microstructure and performance. Application of SPS solution as binding agent in MEA will also be presented. The results show that when using SPS as fuel cell membrane, the additon of small molecules such as benzimidazole would modify its microstrusture as well as improve its ion conductivity. Meanwhile, some improvement still required for application of SPS solution as binding agent for preparation of Membrane Electrode Assembly or MEA.
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Yang, Jung-Eun, Young Taik Hong, and Jae-Suk Lee. "Synthesis and Characterization of Polystyrene-Poly(arylene ether sulfone)-Polystyrene Triblock Copolymer for Proton Exchange Membrane Applications." Journal of Nanoscience and Nanotechnology 6, no. 11 (November 1, 2006): 3594–98. http://dx.doi.org/10.1166/jnn.2006.17989.

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The polystyrene-poly(arylene ether sulfone)-polystyrene (PS-PAES-PS) coil-semirod-coil triblock copolymer was synthesized by the condensation reaction of PS-COCl and H2N-PAES-NH2 telechelic polymers. The reaction was facile characterized by high yields with a perfect control over the block lengths. Following a known reaction protocol it was possible to selectively sulfonate the PS block of the triblock copolymer that led to the sulfonated copolymer sPS-PAES-sPS. Studies on its proton conductivity and methanol permeability were carried out to evaluate its use as the proton exchange membrane in direct methanol fuel cells. Proton conductivity of the membranes was increased depending on the sulfonic acid group content in the sulfonated polymer. The membranes exhibited good dimensional and thermal stability, and low methanol permeability compared to Nafion 117.
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Shi, Chenliang, Ling Lin, Yukun Yang, Wenjia Luo, Maoqing Deng, and Yujie Wu. "Synthesis of aminated polystyrene and its self-assembly with nanoparticles at oil/water interface." e-Polymers 20, no. 1 (June 17, 2020): 317–27. http://dx.doi.org/10.1515/epoly-2020-0038.

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AbstractThe influence of density of amino groups, nanoparticles dimension and pH on the interaction between end-functionalized polymers and nanoparticles was extensively investigated in this study. PS–NH2 and H2N–PS–NH2 were prepared using reversible addition–fragmentation chain transfer polymerization and atom transfer radical polymerization. Zero-dimensional carbon dots with sulfonate groups, one-dimensional cellulose nanocrystals with sulfate groups and two-dimensional graphene with sulfonate groups in the aqueous phase were added into the toluene phase containing the aminated PS. The results indicate that aminated PS exhibited the strongest interfacial activity after compounding with sulfonated nanoparticles at a pH of 3. PS ended with two amino groups performed better in reducing the water/toluene interfacial tension than PS ended with only one amino group. The dimension of sulfonated nanoparticles also contributed significantly to the reduction in the water/toluene interfacial tension. The minimal interfacial tension was 4.49 mN/m after compounding PS–NH2 with sulfonated zero-dimensional carbon dots.
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SHIN, J., B. CHANG, J. KIM, S. LEE, and D. SUH. "Sulfonated polystyrene/PTFE composite membranes." Journal of Membrane Science 251, no. 1-2 (April 1, 2005): 247–54. http://dx.doi.org/10.1016/j.memsci.2004.09.050.

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Boris, David C., and Ralph H. Colby. "Rheology of Sulfonated Polystyrene Solutions." Macromolecules 31, no. 17 (August 1998): 5746–55. http://dx.doi.org/10.1021/ma971884i.

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Haryono, Agus, and Sri Budi Harmami. "Sulfonation of Waste High Impact Polystyrene from Food Packaging as a Polymeric Flocculant." Advanced Materials Research 486 (March 2012): 426–31. http://dx.doi.org/10.4028/www.scientific.net/amr.486.426.

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Sulfonation of waste high impact polystyrene from commercial food packaging was studied in this work. The obtained sulfonated polystyrene was characterized by using Fourier Transformed Infrared spectroscopy. Effect of the reaction time and temperature on the degree of sulfonation was observed. Waste high impact polystyrene resin from food packaging showed degree of sulfonation at 72.2% level. This degree of sulfonation was lower than the same reaction on pure polystyrene and pure high impact polystyrene, which showed degree of sulfonation at 97.7% and 85.2% level, respectively. Simulation of flocculation test using kaolin suspension was conducted to evaluate the application of sulfonated polystyrene as a polymeric flocculant.
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Cánovas, M. J., I. Sobrados, J. Sanz, J. L. Acosta, and A. Linares. "Proton mobility in hydrated sulfonated polystyrene." Journal of Membrane Science 280, no. 1-2 (September 2006): 461–69. http://dx.doi.org/10.1016/j.memsci.2006.02.001.

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Nucara, Luca, Vincenzo Piazza, Francesco Greco, Valentina Robbiano, Valentina Cappello, Mauro Gemmi, Franco Cacialli, and Virgilio Mattoli. "Ionic Strength Responsive Sulfonated Polystyrene Opals." ACS Applied Materials & Interfaces 9, no. 5 (January 27, 2017): 4818–27. http://dx.doi.org/10.1021/acsami.6b14455.

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Dissertations / Theses on the topic "Polystyrene sulfonated"

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Huang, Chongwen. "Rheology of Oligomeric Sulfonated Polystyrene Ionomers." University of Akron / OhioLINK, 2016. http://rave.ohiolink.edu/etdc/view?acc_num=akron1471281020.

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Zhang, Huan. "Properties and Structures of Sulfonated Syndiotactic Polystyrene Aerogel and Syndiotactic Polystyrene/Silica Hybrid Aerogel." University of Akron / OhioLINK, 2014. http://rave.ohiolink.edu/etdc/view?acc_num=akron1405298489.

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Buyukyagci, Arzu. "Synthesis And Characterization Of Monoacetylferrocene Added Sulfonated Polystyrene Ionomers." Master's thesis, METU, 2004. http://etd.lib.metu.edu.tr/upload/3/1108026/index.pdf.

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Incorporation of monoacetylferrocene to the sulfonated polystyrene ionomers imparted some changes in the properties of sulfonated polystyrene. Sulfonation was carried out by acetic anhydride and concentrated sulphuric acid. The sulfonation reaction and the degree of sulfonation were determined by analytical titration and adiabatic bomb calorimeter . For this purpose, sulfonated polystyrene (SPS) samples with varying percentages of sulfonation were prepared between 0.85% and 6.51%. Monoacetyl ferrocene was used in equivalent amount of sulfonation through addition procedure. FTIR Spectroscopy was one of the major techniques used to support the successful addition of AcFe to the SPS samples. Altering the sulfonation degree did not change the characteristic peak positions, but increased the peak intensities with increasing the degrees of sulfonation. Mechanical properties of resultant polymers were investigated. As a result, elastic modulus of polymers decreased by the amount of monoacetylferrocene. Thermal characteristic were found by Differential Scanning Calorimeter (DSC). Thermal analysis revealed that sulfonated polystyrene samples after addition of monoacetylferrocene displayed lower values of Tg. Microscopic analysis were made by Scanning Electron Microscopy (SEM) and single phase for each sample was observed. Besides, energy dispersed micro analysis showed an increase in the intensity of the iron (II) peaks that is related to the amount of monoacetylferrocene added to the SPS samples. Flame retardancy for each polymer was also examined and found that addition of monoacetylferrocene to sulfonated polystyrene does not change the Limiting Oxygen Index value (LOI)(17). However, LOI value for polystyrene is 18.
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LI, XINDI. "MODIFICATION OF SULFONATED SYNDIOTACTIC POLYSTYRENE AEROGELS THROUGH IONIC INTERACTIONS." University of Akron / OhioLINK, 2018. http://rave.ohiolink.edu/etdc/view?acc_num=akron1525801145416997.

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Cui, Xiaoyu. "POLYCATION REINFORCED SULFONATED SYDIOTACTIC POLYSTYRENE GELS& SELF-HEALING LATEX CONTAINING POLYELECTROLYTE MULTILAYERS." University of Akron / OhioLINK, 2017. http://rave.ohiolink.edu/etdc/view?acc_num=akron1495204173832965.

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Benson, Sonya Denese. "The Effect of Nanoscale Particles and Ionomer Architecture on the Crystallization Behavior of Sulfonated Syndiotactic Polystyrene." Diss., Virginia Tech, 2011. http://hdl.handle.net/10919/26137.

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Semicrystalline ionomers are an important class of polymers that are utilized in a wide range of applications. The particular end-use applications of these materials are determined by their chemical, physical, and thermomechanical properties which are directly related to their crystallization behavior. It is therefore critical to identify structure-property relationships for these materials. Sulfonated syndiotactic polystyrene (SsPS) is used as a model semicrystalline ionomer and two approaches are utilized to control the rate of crystallization of the SsPS ionomer in the presence of ionic aggregates. The first approach investigates the effect of the incorporation of nanoscale particles, montmorillonite clay, on the crystallization behavior of SsPS. The morphology of the ionomer clay hybrids were studies via TEM and WAXD while the crystallization behavior of SsPS in the presence of the clay was evaluated using DSC. It was found that the SsPS matrix containing 5 wt.% organically-modified clay crystallized more rapidly than the sPS homopolymer containing the same clay content. This behavior is attributed to the presence of homogenously dispersed nanoscale clay platelets that act as nucleation sites distributed throughout the ionomer matrix. The second approach that employed involved the manipulation of SsPS ionomer architecture via a controlled placement of the ionic sulfonate groups along the polymer backbone. A post-polymerization sulfonation technique was developed to place the sulfonate groups along the homopolymer backbone in a non-random fashion leading to a pseudo-block ionomer architecture. The crystallization behavior of the non-randomly sulfonated SsPS ionomer is compared to randomly sulfonated SsPS using differential scanning calorimetry. The morphologies of the two ionomers were studied using SALLS and SAXS. We have found that the non-randomly sulfonated SsPS ionomer crystallizes much more rapidly than the randomly sulfonated ionomer. The more rapid crystallization behavior of the non-random ionomer to the presence of longer sequences of unsulfonated homopolymer that are able to readily organize into crystalline structures than the random SsPS ionomer containing the same ionic content. â
Ph. D.
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Fahs, Gregory Bain. "The Effect of Ionomer Architecture on the Morphology in Gel State Functionalized Sulfonated Syndiotactic Polystyrene." Diss., Virginia Tech, 2020. http://hdl.handle.net/10919/97193.

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This dissertation presents a discussion of blocky and randomly functionalized sulfonated syndiotactic polystyrene copolymers. These copolymers have been prepared over a range of functionalization (from 2% to 10%) in order to assess the effect of the incorporation of these polar side groups on both the thermal behavior and morphology of these polymer systems. The two different architectures are achieved by conducting the reaction in both the heterogeneous gel-state to obtain blocky copolymers and in the homogeneous solution state to obtain randomly functionalized copolymers. In order to compare both the thermal properties and morphology of these two systems several sets of samples were prepared at comparable levels of sulfonation. Thermal analysis of these two systems proved that the blocky functionalized copolymers provided superior properties with regard to the speed and total amount of the crystalline component of sulfonated syndiotactic polystyrene. Above 3% functionalizion the randomly functionalized copolymer was no longer able to crystallize, whereas, the blocky functionalized copolymer is able to crystallize even at a functionalization level of 10.5% sulfonate groups. When considering the morphology of these systems even at low percentages of sulfonation it is clear that the distribution of these groups is different based on the amplitude of the signal measured by small angle x-ray scattering. Additionally, methods were developed to describe both the distribution of ionic multiplets, which varies between blocky and randomly functionalized systems, but also the distribution of crystals. At a larger scale ultra-small angle x-ray scattering was employed to attempt to understand the clustering of ionic multiplets in these systems. Randomly functionalized polymers should a peak that is attributed to ion clusters, whereas blocky polymers show no such peak. Additional studies have also been done to look at the analysis of crystallite sizes in these systems when there are multiplet polymorphs present, it was observed the polymorphic composition is drastically different. All of these studies support that these systems bear vastly different thermal behavior and possess significantly different morphologies. This supports the hypothesis that this gel-state heterogeneous functionalization procedure produces a much different chain architecture compared to homogeneous functionalization in the solution-state.
Doctor of Philosophy
Polymers are a class of chemicals that are defined by having a very large set of molecules that are chemically linked together where each unit (monomer) is repeated within the chemical structure. In particular, this dissertation focuses on the construction what are termed as "blocky" copolymers, which are defined by having two chemically different monomers that are incorporated in the polymer chain. The "blocky" characteristic of these polymers means that these two different monomers are physically segregated from each other on the polymer chain, where long portions of the chain that are of one type, followed by another section of the polymer that has the other type of monomer. The goal of creating this type of structure is to try to take advantage of the properties of both types of monomers, which can create materials with superior synergistic properties. In this case a hydrophobic (water hating) monomer is combined with a hydrophilic (water loving) chain. This hydrophobic component in the polymer is able to crystallize, which provides mechanical and thermal stability in the material by acting as a physical tether to hold neighboring chains together. With the other set of hydrophilic monomers, which in this case have an ionic component incorporated, we can now take advantage of this chemical components ability to aide in the transportation of ions. Transportation of ions is useful in a variety of commercially relevant applications, two of the most important applications of these ionic materials is in membranes that can be used to purify water or membrane materials in fuel cell technologies, specifically for proton exchange membranes. The focus of this research in particular was to create a simple synthesis technique that can create these blocky polymer chain architectures, which is done by performing the reaction while the polymer is made into a gel. The key to this is that the crystals within the gel act as a barrier to chemical reactions, creating conditions where we have substantial portions of the material that are able to be functionalized and the crystals within the material that are protected from being functionalized. By looking at the thermal characteristics, such as melting temperatures and amount of crystals within these systems we have seen that functionalizing these polymers in the heterogeneous gel state gives substantially better properties than functionalizing these materials randomly. Much like oil and water, incompatible polymer chains will phase separate from each other. In this case the hydrophobic and ionic components will phase separate from each other. The shape and distribution of these phase separated structure will dictate many of the material properties, which can be described by modeling the data collected from x-ray scattering experiments. All of this information will tell us based on the initial conditions that these polymers were created in, what properties should be expected based on the morphology and thermal behavior. This gives a better understanding of how to fine tune these properties based on the structure of the gel and chemical reaction conditions.
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Cai, Liang. "GRAFT COPOLYMER AEROGELS FROM SULFONATED SYNDIOTACTIC POLYSTYRENE FUNCTIONALIZED WITH A QUATERNARY PHOSPHONIUM-CONTAINING RAFT AGENT." University of Akron / OhioLINK, 2016. http://rave.ohiolink.edu/etdc/view?acc_num=akron1468851884.

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Merche, Delphine. "Synthèse et caractérisation de couches de polystyrène et de polystyrène sulfoné obtenues par polymérisation-plasma à pression (sub)-atmosphérique." Doctoral thesis, Universite Libre de Bruxelles, 2011. http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/209871.

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Lors de ce travail, de fins films de polystyrène ont été déposés dans la post-décharge d’une torche plasma atmosphérique commerciale, mais aussi dans la décharge d’une DBD (Décharge à Barrière Diélectrique), conçue et développée par nos soins au laboratoire. Une DBD est un procédé permettant d’obtenir des plasmas froids à pression atmosphérique.

Nos résultats ont montré que la DBD permettait d’obtenir des films de polystyrène de meilleure qualité (degré d’oxydation moindre…) qu’avec la torche commerciale en raison de l’atmosphère contrôlée de l’enceinte DBD. Les films sont déposés en présence d’un gaz porteur (Ar ou He dans la DBD). Nous avons pu mettre en évidence l’influence de la nature de ce gaz porteur sur la structure des films (degré de branchement, et de réticulation des films et de préservation des cycles aromatiques de la molécule de départ).

Les dépôts de polystyrène sulfoné ont été synthétisés dans la DBD en une seule étape, par « copolymérisation » de deux précurseurs (styrène et acide trifluorométhane sulfonique) injectés simultanément dans la décharge. Ces membranes pourraient servir d’électrolyte dans les piles à combustibles miniaturisées de type PEMFC (« Polymer Electrolyte Membrane Fuel Cell »), utilisant de l’hydrogène ou du méthanol et ce pour des applications portables.

L’acide trifluorométhane sulfonique permet le greffage de groupements sulfoniques échangeurs d’ions (nécessaires pour la conductivité de la membrane) sur le squelette de polystyrène.

La complémentarité des différentes techniques spectroscopiques utilisées -Spectroscopie des Photoélectrons X (XPS), Infra-Rouge à Transformée de Fourier (FTIR), Spectroscopie des Ions Secondaires (SIMS) statique et dynamique- ont montré que les groupements acides sulfoniques (bien préservés dans la décharge à pression sub-atmosphérique) étaient bien greffés dans la matrice de polystyrène, et ce sur toute l’épaisseur de la membrane. L’influence des paramètres (température de l’acide, tension appliquée entre les électrodes, nature du gaz porteur…) sur la quantité de groupements ionisables greffés, sur la vitesse de dépôt et aussi sur la morphologie des films a été étudiée respectivement par XPS et par microscopie.

En plus des dépôts sur substrats usuels (Si, acier…) utilisés pour les caractérisations chimiques, nous avons synthétisé les films directement sur des électrodes de carbone enrichies en platine.

Nous avons déposé le catalyseur à partir d’une solution colloïdale de platine nébulisée dans la post-décharge d’une torche plasma atmosphérique sur des couches de carbones poreuse et sur du carbone vitreux (utilisé comme modèle pour le profilage par SIMS dynamique) dans différentes configurations et ce pour différents paramètres afin de constituer des électrodes servant de substrat pour l’adhésion de la membrane-plasma pour des perspectives d’assemblage membrane-électrodes pour PAC. /

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Doctorat en Sciences
info:eu-repo/semantics/nonPublished

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Proença, Marcela Pinheiro. "Desenvolvimento de membranas íon-seletivas com poliestireno sulfonado e polianilina dopada para a aplicação em eletrodiálise." reponame:Biblioteca Digital de Teses e Dissertações da UFRGS, 2009. http://hdl.handle.net/10183/18585.

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Atualmente, a preocupação com a redução da poluição industrial tem motivado os pesquisadores na busca de novas tecnologias para o tratamento de resíduos industriais. Tecnologias limpas, como a eletrodiálise, são capazes de tratar alguns destes resíduos, como por exemplo o efluente da indústria de galvanoplastia, minimizando os impactos que ocorreriam caso eles fossem descartados diretamente no meio ambiente. O componente principal desta técnica é a membrana na qual ocorre a etapa de retirada dos íons da solução. Atualmente estas membranas são importadas e caras, o que justifica o desenvolvimento de membranas eficientes e acessíveis. Neste sentido, no presente trabalho membranas de poliestireno sulfonado/ poliestireno de alto impacto (SPS/HIPS), polianilina dopada com ácido canforsulfônico/ poliestireno sulfonado/ poliestireno de alto impacto (PAniCSA/SPS/HIPS), polianilina sulfonada/ poliestireno sulfonado/ poliestireno de alto impacto (SPAN/SPS/HIPS), e polianilina dopada com ácido p-tolueno sulfônico/ poliestireno sulfonado/ poliestireno de alto impacto (PAniTSA/SPS/HIPS) foram desenvolvidas usando o método de mistura química. As membranas foram caracterizadas utilizando as técnicas Análise termogravimétrica (TGA), Análise dinâmico Mecânica (DMA), e Microscopia Eletrônica de Varredura (MEV). Membranas foram submetidas a curvas corrente-potencial e ensaios de eletrodiálise em soluções de NaCl e KCl, a fim de determinar o transporte iônico através das mesmas. Os resultados foram comparados com uma membrana comercial Selemion CMT. A extração percentual média para íons de Na+ obtidos pelas membranas desenvolvidas foi superior a 20%.
Nowadays the concern with the reduction of industrial pollution has motivated researchers to found out new technologies for treatment of industrial waste. The clean technologies, as electrodialysis, are capable of treating some these residues, as for example the galvanoplasty’s waste, minimizing the impacts that would happen to them if they were discarded directly on the environment. The main component of this technique is the membrane on which occurs the ions removal stage of the solution. The membranes are imported and expensive what justifies the development of efficient and accessible membranes. In this sense, in the present work membranes of sulfonated polystyrene / high impact polystyrene (SPS/HIPS), polyaniline doped with camphorsulfonic acid / sulfonated polystyrene / high impact polystyrene (PAniCSA/SPS/HIPS), sulfonated polyaniline/ sulfonated polystyrene / high impact polystyrene (SPAN/SPS/HIPS), and polyaniline doped with p-toluenesulfonic acid / sulfonated polystyrene / high impact polystyrene (PAniTSA/SPS/HIPS) were developed using chemical mixture method. Membranes were characterized by Infrared Spectroscopy (FTIR), Thermogravimetric Analysis (TGA), Dynamic Mechanical Analysis (DMA) and Scanning Electronic Microscopy (SEM). Membranes were submitted to current-voltage curves and electrodialysis experiments with NaCl and KCl solutions, in order to determine ionic transport through them. Results were compared with a commercial membrane, Selemion CMT. The average percent extraction for Na+ ions obtained by membranes developed were beyond 20%.
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Books on the topic "Polystyrene sulfonated"

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Belanger, Denis R. Effect of sodium polystyrene sulfonate on lithium bioavailability. [Ottawa: Ottawa General Hospital, 1989.

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Chambers, Cynthia Anne. The antigenicity of polystyrene sulfonate. 1986.

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Book chapters on the topic "Polystyrene sulfonated"

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Fitzgerald, J. J., and R. A. Weiss. "Cation-Anion and Cation-Cation Interactions in Sulfonated Polystyrene Ionomers." In ACS Symposium Series, 35–53. Washington, DC: American Chemical Society, 1986. http://dx.doi.org/10.1021/bk-1986-0302.ch003.

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Zhang, Zhicheng, Elena Chalkova, Mark Fedkin, Chunmei Wang, Serguei N. Lvov, Sridhar Komarneni, and T. C. Chung. "Synthesis and Characterization of Poly(vinylidene fluoride)-g-Sulfonated Polystyrene Graft Copolymers for Proton Exchange Membrane." In ACS Symposium Series, 31–48. Washington, DC: American Chemical Society, 2010. http://dx.doi.org/10.1021/bk-2010-1040.ch003.

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Bährle-Rapp, Marina. "Sodium Polystyrene Sulfonate." In Springer Lexikon Kosmetik und Körperpflege, 516. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_9693.

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Storey, F., and Scott E. George. "Synthesis and Characterization of Star-Branched Ionomers Composed of Sulfonated Polystyrene Outer Blocks and Elastomeric Inner Blocks." In ACS Symposium Series, 330–52. Washington, DC: American Chemical Society, 1989. http://dx.doi.org/10.1021/bk-1989-0395.ch013.

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Stockton, Jon D., Joseph F. Lomax, Charles A. Edmondson, John J. Fontanella, and Mary C. Wintersgill. "Studies in Mesoporous Silicates: Impedance Measurements on SBA-15 Loaded with Sulfonated-Polystyrene and Nafion with SBA-15 Filler." In Advances in Science and Technology, 2033–38. Stafa: Trans Tech Publications Ltd., 2006. http://dx.doi.org/10.4028/3-908158-01-x.2033.

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Möller, Martin, Jürgen Omeis, and Elke Mühleisen. "Association and Gelation of Polystyrenes via Terminal Sulfonate Groups." In Reversible Polymeric Gels and Related Systems, 87–106. Washington, DC: American Chemical Society, 1987. http://dx.doi.org/10.1021/bk-1987-0350.ch007.

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Tomita, Hidemi, and Richard A. Register. "Blends of lightly sulfonated polystyrene ionomers with poly (xylenyl ether)." In Advanced Materials '93, 207–10. Elsevier, 1994. http://dx.doi.org/10.1016/b978-1-4832-8380-7.50054-7.

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"Polystyrene sulfonates." In Meyler's Side Effects of Drugs, 868–71. Elsevier, 2016. http://dx.doi.org/10.1016/b978-0-444-53717-1.01317-2.

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"Polystyrene sulfonates." In Meyler's Side Effects of Drugs: The International Encyclopedia of Adverse Drug Reactions and Interactions, 2894–98. Elsevier, 2006. http://dx.doi.org/10.1016/b0-44-451005-2/01462-5.

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"X-ray evanescent wave-induced fluorescence study of adsorption of a sulfonated polystyrene ionomer from dimethyl sulfoxide to the solution/vapor interface." In Fundamentals of Adhesion and Interfaces, 109–24. De Gruyter, 1995. http://dx.doi.org/10.1515/9783112318515-009.

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Conference papers on the topic "Polystyrene sulfonated"

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Yanhou Geng, Xianhong Wang, Lixiang Wang, Xiabin Jing, and Fosong Wang. "Macromolecular complex of polyaniline/sulfonated polystyrene." In International Conference on Science and Technology of Synthetic Metals. IEEE, 1994. http://dx.doi.org/10.1109/stsm.1994.835258.

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Dai, Ying, Haiping Hong, and Jeffry S. Welsh. "Reinforced membrane based on crosslink reaction between water soluble sulfonated carbon nanotubes and sulfonated polystyrene." In NanoScience + Engineering, edited by Geoffrey B. Smith and Akhlesh Lakhtakia. SPIE, 2008. http://dx.doi.org/10.1117/12.792933.

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Sousa, W. S., A. C. Maciel, A. J. F. Carvalho, and R. M. Faria. "Thermally stimulated depolarization current studies in thin films of sulfonated polystyrene ionomers." In 2011 IEEE 14th International Symposium on Electrets ISE 14. IEEE, 2011. http://dx.doi.org/10.1109/ise.2011.6085003.

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Zubir, N. A., A. F. Ismail, M. M. Nasef, and H. I. Maarof. "Thermal stability and structural investigations of sulfonated polystyrene pore-filled poly(vinylidene fluoride) membranes." In 2010 International Conference on Science and Social Research (CSSR). IEEE, 2010. http://dx.doi.org/10.1109/cssr.2010.5773783.

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Büchi, F. N., B. Gupta, M. Rouilly, P. C. Hauser, A. Chapiró, and G. G. Scherer. "Radiation Grafted and Sulfonated (FEP-g-Polystyrene) - An Alternative to Perfluorinated Membranes for PEM Fuel Cells?" In 27th Intersociety Energy Conversion Engineering Conference (1992). 400 Commonwealth Drive, Warrendale, PA, United States: SAE International, 1992. http://dx.doi.org/10.4271/929293.

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Lee, Haisung, Yoongon Park, Myungwhun Chang, Gangpil Kim, Sangsu Hong, Hyungsik Won, Jongmyeon Lee, and Yongsoo Oh. "The enhancement of light efficiency using modified phosphor which is coated sub-micro size sulfonated polystyrene beads." In SPIE Optics + Photonics, edited by Zeno Gaburro and Stefano Cabrini. SPIE, 2006. http://dx.doi.org/10.1117/12.678629.

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Pulungan, Ahmad Nasir, Basuki Wirjosentono, Eddiyanto, and Sunit Hendrana. "X-Ray Diffraction and Morphology Studies of Sulfonated Polystyrene and Maleated Natural Rubber Blend with PE-g-MA as Compatibilished." In International Conference on Chemical Science and Technology Innovation. SCITEPRESS - Science and Technology Publications, 2019. http://dx.doi.org/10.5220/0008935003240328.

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Khanum, Khadija Kanwal, Pritom J. Bora, K. J. Vinoy, and Praveen C. Ramamurthy. "Evaluation of electromagnetic interference shielding using Poly(3,4-ethylenedioxythiophene) Polystyrene sulfonate blend." In 2016 3rd International Conference on Emerging Electronics (ICEE). IEEE, 2016. http://dx.doi.org/10.1109/icemelec.2016.8074607.

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Pathak, Gaurav, and Dusko Cakara. "Variable Angle Spectroscopic Ellipsometry Study of Poly(3,4-ethylenedioxythiophene):Polystyrene Sulfonate Thin Films in Contact with Air." In 2020 43rd International Convention on Information, Communication and Electronic Technology (MIPRO). IEEE, 2020. http://dx.doi.org/10.23919/mipro48935.2020.9245443.

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SHADRYNA, V. I., T. G. SHUTAVA, and V. E. AGABEKOV. "INVESTIGATION OF HORSERADISH PEROXIDASE ADSORPTION ON GOLD AND POLYSTYRENE SULFONATE MODIFIED SURFACES BY QUARTZ CRYSTAL MICROBALANCE TECHNIQUE." In Proceedings of the International Conference on Nanomeeting 2009. WORLD SCIENTIFIC, 2009. http://dx.doi.org/10.1142/9789814280365_0085.

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