Добірка наукової літератури з теми "Polymer blends and composites"

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Статті в журналах з теми "Polymer blends and composites"

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Shamsuri, Ahmad Adlie, and Siti Nurul Ain Md Jamil. "Application of Quaternary Ammonium Compounds as Compatibilizers for Polymer Blends and Polymer Composites—A Concise Review." Applied Sciences 11, no. 7 (April 2, 2021): 3167. http://dx.doi.org/10.3390/app11073167.

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A wide variety of quaternary ammonium compounds (QACs) have escalated the attraction of researchers to explore the application of QACs. The compounds have frequently been synthesized through alkylation or quaternization of tertiary amines with alkyl halides. Recently, QACs have been applied to compatibilize polymer blends and polymer composites in improving their thermo-mechanical properties. This concise review concentrates on the application of two types of QACs as compatibilizers for polymer blends and polymer composites. The types of QACs that were effectively applied in the blends and composites are quaternary ammonium surfactants (QASs) and quaternary ammonium ionic liquids (QAILs). They have been chosen for the discussion because of their unique chemical structure which can interact with the polymer blend and composite components. The influence of QASs and QAILs on the thermo-mechanical properties of the polymer blends and polymer composites is also described. This review could be helpful for the polymer blend and polymer composite researchers and induce more novel ideas in this research area.
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Mihu, Georgel, Sebastian-Marian Draghici, Vasile Bria, Adrian Circiumaru, and Iulian-Gabriel Birsan. "Mechanical Properties of Some Epoxy-PMMA Blends." Materiale Plastice 58, no. 2 (July 5, 2021): 220–28. http://dx.doi.org/10.37358/mp.21.2.5494.

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The thermoset polymers and the thermoplastic polymers matrix composites require different forming techniques due to the different properties of two classes of polymers. While the forming technique for thermoset polymer matrix composites does not require the use of special equipment, the thermoplastic polymer matrix composites imposes the rigorous control of temperature and pressure values. Each type of polymer transfers to the composite a set of properties that may be required for a certain application. It is difficult to design a composite with commonly brittle thermoset polymer matrix showing properties of a viscoelastic thermoplastic polymer matrix composite. One solution may consist in mixing a thermoset and a thermoplastic polymer getting a polymer blend that can be used as matrix to form a composite. This study is about using PMMA solutions to obtain thermoset-thermoplastic blends and to mechanically characterize the obtained materials. Three well known organic solvents were used to obtain the PMMA solutions, based on a previous study concerning with the effect of solvents presence into the epoxy structure.
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Heino, Markku T., Tommi P. Vainio, and Jukka V. Seppälä. "Blends and Composites Based on Polypropylene and a Thermotropic Liquid Crystalline Polymer." Engineering Plastics 1, no. 6 (January 1993): 147823919300100. http://dx.doi.org/10.1177/147823919300100605.

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Blends of polypropylene (PP) and liquid crystalline polymer (LCP) processed without melting the LCP were compared with conventional melt processed blends. In a first stage, PP was blended with 20 wt.% of LCP in a twin-screw extruder with the take-up speed varied to achieve blends with different LCP fibre dimensions. In the second stage these blends were processed both below and above the T m of the LCP by extrusion and injection moulding. At lower temperatures (180–200°C), where the material was processed without melting the LCP, a real composite structure was formed with solid LCP fibres in the PP matrix. When processed above the T m of the LCP (280°C) all the material was molten during processing and a composite-like blend morphology was created in-situ during cooling of the oriented melt phase. These blends exhibited a skin/core morphology, whereas the composites contained fibres throughout the sample. Due to this difference the impact strength of the composites was significantly higher than that of the blends. The blends exhibited higher modulus than the composites. Moreover, additional drawing can greatly improve the strength and stiffness of the blends. In composites the solid LCP fibres slightly increased the viscosity of PP, while in blends the molten LCP reduced the matrix viscosity and acted as a processing aid.
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Heino, Markku T., Tommi P. Vainio, and Jukka V. Seppälä. "Blends and Composites Based on Polypropylene and a Thermotropic Liquid Crystalline Polymer." Polymers and Polymer Composites 1, no. 6 (January 1993): 439–49. http://dx.doi.org/10.1177/096739119300100605.

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Blends of polypropylene (PP) and liquid crystalline polymer (LCP) processed without melting the LCP were compared with conventional melt processed blends. In a first stage, PP was blended with 20 wt.% of LCP in a twin-screw extruder with the take-up speed varied to achieve blends with different LCP fibre dimensions. In the second stage these blends were processed both below and above the T m of the LCP by extrusion and injection moulding. At lower temperatures (180–200°C), where the material was processed without melting the LCP, a real composite structure was formed with solid LCP fibres in the PP matrix. When processed above the T m of the LCP (280°C) all the material was molten during processing and a composite-like blend morphology was created in-situ during cooling of the oriented melt phase. These blends exhibited a skin/core morphology, whereas the composites contained fibres throughout the sample. Due to this difference the impact strength of the composites was significantly higher than that of the blends. The blends exhibited higher modulus than the composites. Moreover, additional drawing can greatly improve the strength and stiffness of the blends. In composites the solid LCP fibres slightly increased the viscosity of PP, while in blends the molten LCP reduced the matrix viscosity and acted as a processing aid.
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Shamsuri, Ahmad Adlie, Rusli Daik, and Siti Nurul Ain Md. Jamil. "A Succinct Review on the PVDF/Imidazolium-Based Ionic Liquid Blends and Composites: Preparations, Properties, and Applications." Processes 9, no. 5 (April 27, 2021): 761. http://dx.doi.org/10.3390/pr9050761.

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Poly(vinylidene fluoride) (PVDF) is a versatile thermoplastic fluoropolymer with intriguing characteristics, which is receiving considerable attention from researchers in many areas. Recently, PVDF and its copolymer, such as poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP) have been blended with ionic liquids to produce blend and composite materials for target applications. In this succinct review, two types of ionic liquids that are utilized for the preparation of PVDF and PVDF-HFP blends and composites, namely, hydrophilic and hydrophobic imidazolium-based ionic liquids, are reviewed. In addition, the effect of the ionic liquids on the physicochemical properties of the PVDF and PVDF-HFP blends and composites, is described as well. On top of that, a multitude of applications of the blends and composites are also succinctly reviewed. This review may give inspirations to the polymer blend and composite researchers in diversifying the applications of thermoplastic fluoropolymers through the utilization of ionic liquids.
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Gunawardene, Oneesha H. P., Chamila Gunathilake, Sumedha M. Amaraweera, Nimasha M. L. Fernando, Darshana B. Wanninayaka, Asanga Manamperi, Asela K. Kulatunga, et al. "Compatibilization of Starch/Synthetic Biodegradable Polymer Blends for Packaging Applications: A Review." Journal of Composites Science 5, no. 11 (November 16, 2021): 300. http://dx.doi.org/10.3390/jcs5110300.

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The health and environmental concerns of the usage of non-biodegradable plastics have driven efforts to explore replacing them with renewable polymers. Although starch is a vital renewable polymer, poor water resistivity and thermo-mechanical properties have limited its applications. Recently, starch/synthetic biodegradable polymer blends have captured greater attention to replace inert plastic materials; the question of ‘immiscibility’ arises during the blend preparation due to the mixing of hydrophilic starch with hydrophobic polymers. The immiscibility issue between starch and synthetic polymers impacts the water absorption, thermo-mechanical properties, and chemical stability demanded by various engineering applications. Numerous studies have been carried out to eliminate the immiscibility issues of the different components in the polymer blends while enhancing the thermo-mechanical properties. Incorporating compatibilizers into the blend mixtures has significantly reduced the particle sizes of the dispersed phase while improving the interfacial adhesion between the starch and synthetic biodegradable polymer, leading to fine and homogeneous structures. Thus, Significant improvements in thermo-mechanical and barrier properties and water resistance can be observed in the compatibilized blends. This review provides an extensive discussion on the compatibilization processes of starch and petroleum-based polymer blends.
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ZIELINSKI, JANUSZ. "Polymer blends and composites." Polimery 47, no. 05 (May 2002): 303–9. http://dx.doi.org/10.14314/polimery.2002.303.

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Quitadamo, Alessia, Valerie Massardier, and Marco Valente. "Eco-Friendly Approach and Potential Biodegradable Polymer Matrix for WPC Composite Materials in Outdoor Application." International Journal of Polymer Science 2019 (January 27, 2019): 1–9. http://dx.doi.org/10.1155/2019/3894370.

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Blends based on high-density polyethylene (HDPE) and poly(lactic) acid (PLA) with different ratios of both polymers were produced: a blend with equal amounts of HDPE and PLA, hence 50 wt.% each, proved to be a useful compromise, allowing a high amount of bioderived charge without this being too detrimental for mechanical properties and considering its possibility to biodegradation behaviour in outdoor application. In this way, an optimal blend suitable for producing a composite with cellulosic fillers is proposed. In the selected polymer blend, wood flour (WF) was added as a natural filler in the proportion of 20, 30, and 40 wt.%, considering as 100 the weight of the polymer blend matrix. There are two compatibilizers to modify both HDPE-PLA blend and wood-flour/polymer interfaces, i.e., polyethylene-grafted maleic anhydride and a random copolymer of ethylene and glycidyl methacrylate. The most suitable percentage of compatibilizer for HDPE-PLA blends appears to be 3 wt.%, which was selected also for use with wood flour. In order to evaluate properties of blends and composites tensile tests, scanning electron microscopy, differential scanning calorimetry, thermogravimetric analyses, and infrared spectroscopy have been performed. Wood flour seems to affect heavy blend behaviour in process production of material suggesting that future studies are needed to reduce defectiveness.
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Alo, Oluwaseun Ayotunde, and Iyiola Olatunji Otunniyi. "Highly Conductive Polymer Composite Based on Graphite-Filled Immiscible Polyolefin/Epoxy Blends." Key Engineering Materials 917 (April 13, 2022): 10–21. http://dx.doi.org/10.4028/p-ytr30y.

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Conductive polymer composites (CPCs) based on polypropylene (PP)/epoxy (EP) and high-density polyethylene (HDPE)/EP blends filled with synthetic graphite (SG) were produced and characterized to explore their potential for high electrical conductivity applications. The polymer blends were chosen as matrices due to their immiscibility and potential to enable co-continuous morphology formation and preferential distribution of filler, which allows formation of maximized conducting networks. In-plane and through-plane resistivities of PP/EP/SG composites decreased from 0.083 Ω.cm to 0.015 Ω.cm and 10.16 Ω.cm to 0.31 Ω.cm, respectively, while for HDPE/EP/SG composites, in-plane and through-plane resistivities decreased from 0.086 Ω.cm to 0.014 Ω.cm and 5.02 Ω.cm to 0.24 Ω.cm, respectively, when SG content was increased from 30 to 80 wt%. The immiscible blend-based composites produced in this study have the potential to achieve significantly higher conductivity than filled single polymers due to concentration of filler in one of the polymer phases and the co-continuous structure of the blends. Also, resistivity anisotropy of the PP/EP/SG and HDPE/EP/SG composites generally decreased with increase in SG content, with HDPE/EP/SG composites showing lower resistivity anisotropy than PP/EP/SG composites at the same SG content.
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Xu, Huagen, Muchao Qu, Qiancheng Yang, and Dirk W. Schubert. "Investigating the electrical percolation threshold of ternary composite films with different compatibility between polymer blends." Journal of Polymer Engineering 41, no. 6 (April 22, 2021): 450–57. http://dx.doi.org/10.1515/polyeng-2021-0018.

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Abstract Electrical conductive of polystyrene (PS)/poly(butyl methacrylate) (PBMA)/carbon black (CB) and PS/poly (cyclohexyl methacrylate) (PChMA)/CB ternary composite films with different polymer blend ratios are prepared through solution casting. The percolation thresholds (ϕ c ) of all the composite films before and after thermal annealing have been determined through the McLachlan GEM equation. Moreover, the PS/poly (methyl methacrylate) (PMMA)/CB and PS/poly (ethyl methacrylate) (PEMA)/CB films obtained from the same method while only considering conductivity after thermal annealing as well in this work for comparison. Though the CB particles are revealed to be located at only one polymer phase of all four different polymer blends, with compatibility between polymer blends increasing, the ternary composite films show different ϕ c behaviors by changing polymer blend ratios. In PS/PChMA/CB case, the phase separation between PChMA and PS cannot be observed under scanning electron microscope (SEM). After thermal annealing, all the ϕ c of PS/PChMA/CB films with different PS/PChMA ratios almost show a linear behavior instead of the double percolation behavior with PChMA content increasing. Suppose both ϕ c of binary systems (polymer A/filler and polymer B/filler) is determined. In that case, a linear behavior relationship between the ϕ c of the ternary composites (A + B + fillers) with the ratio of two polymers can be revealed when polymer A and B are miscible.
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Дисертації з теми "Polymer blends and composites"

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Guo, Molin. "PROCESSING-STRUCTURE-PROPERTY RELATIONSHIPS INCO-CONTINUOUS POLYMER BLENDS AND COMPOSITES." Case Western Reserve University School of Graduate Studies / OhioLINK, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=case1593786851492932.

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Holloway, Matthew James. "Electrically conducting composites formed from polymer blends." Thesis, Brunel University, 1992. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.316533.

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Johnson, Jack Royce III. "POLYMER BLENDS, COMPOSITES AND AEROGEL MODIFICATION BY INNOVATIVE APPROACHES." Case Western Reserve University School of Graduate Studies / OhioLINK, 2011. http://rave.ohiolink.edu/etdc/view?acc_num=case1317409667.

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Villechevrolle, Viviane Louise. "Polymer blends for multi-extruded wood-thermoplastic composites." Pullman, Wash. : Washington State University, 2008. http://www.dissertations.wsu.edu/Thesis/Fall2008/v_villechevrolle_121008.pdf.

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Thesis (M.S. in civil engineering)--Washington State University, December 2008.
Title from PDF title page (viewed on Mar. 2, 2009). "Department of Civil and Environmental Engineering." Includes bibliographical references.
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Cankaya, Burhan Fuat. "Foamed Eva-bitumen Blends And Composites." Master's thesis, METU, 2009. http://etd.lib.metu.edu.tr/upload/3/12610215/index.pdf.

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The thermal conductivities of foamed polymer based materials are much lower thermal conductivity values than unfoamed polymeric materials. Especially, thermal conductivity values of foamed polymers with closed-cell structure decreases to 0.03 W/m.K. The reinforcement of foamed polymeric materials by mixing with bitumen lowers the raw material cost. The main objective of this study is to make a new thermal insulation material with low thermal conductance. In this study, the effects of concentration of calcium carbonate as inorganic filler and the effects of cross-linking on the properties foamed and unfoamed ethylene-vinyl acetate (EVA) copolymer based bituminous blends and composites were investigated. Applications such as thermal, mechanical characteristics of foamed and unfoamed EVA based bituminous composites were investigated. Foamed EVA based bituminous composites were prepared by using Brabender Plastic Coder, PLV 151. Mixing was made at 120 º
C at 60 rpm for 15 minutes. The prepared blends were molded by a technique called Hand Lay-up Self-expanding Batch Molding (HLUSEBM) which was firstly applied by our group. The molding temperature was 170 º
C at which chemical blowing agent and cross-linking agent decomposes. According to test results, at moderate chemical blowing agent and EVA content, the best closed-cell structure with high porosity and low thermal conductivity values were obtained. The compressive properties of foamed polymer based bituminous composites (FPBBCs) increase with increasing CBA and EVA content. With increasing calcium carbonate and EVA concentration, the porosity of FPBBCs increases but thermal conductivity of them decreases. On the other hand, with increasing filler content but with decreasing EVA concentration elastic modulus of FPBBCs increases but elastic recovery decreases.
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Iyer, Subramanian. "Structure Property Relationships in Polymer Blends and Composites. Part I - Polymer/POSS Composites Part II - Poly(ethylene terepthalate) ionomer/Polyamide 6 Blends Part III - Elastomer/Boron Nitride Composites." online version, 2006. http://rave.ohiolink.edu/etdc/view?acc%5Fnum=case1152121344.

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O'Donnell, Hugh J. "In situ composites of compatibilized polypropylene/liquid crystalline polymer blends." Diss., This resource online, 1993. http://scholar.lib.vt.edu/theses/available/etd-02052007-081243/.

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Cheerarot, Onanong. "The effects of nanoparticles on structure development in immiscible polymer blends." Thesis, University of Manchester, 2012. https://www.research.manchester.ac.uk/portal/en/theses/the-effects-of-nanoparticles-on-structure-development-in-immiscible-polymer-blends(cca9d075-dfcd-46c5-b865-290c414b4315).html.

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Composites based on binary polymer blends of polystyrene (PS)/poly(ethylene-co-vinyl alcohol) (EVOH) (70/30 wt%) containing natural Montmorillonite, Na-MMTs (Nanomer PGW or Cloisite Na+) and organically modified Montmorillonite clays, OMMTs (Nanomer I.30T, Cloisite 30B or Cloisite 10A) were prepared via melt compounding. The interactions between the polymers and clays were studied using flow micro-calorimetry (FMC). Data obtained from FMC indicated that the probe molecule mimicking EVOH (butan-2-ol) interacted with the MMTs and OMMTs much more strongly than PS. Scanning electron microscopy (SEM) revealed that composites based on binary blends had dispersed/continuous morphologies, in which EVOH was dispersed in a PS matrix. The size of the EVOH droplets in the PS matrix increased with increasing clay loading. Transmission electron microscopy (TEM) and wide angle X-ray diffraction (WAXD) were used to determine the extent of dispersion and location of clay in the PS/EVOH/clay composites. These techniques confirmed the formation of intercalated clay structures. As predicted by FMC, the clay platelets were selectively located in the EVOH phase, independent of the blending sequence and the type of organic modifier in the OMMT. Composites containing OMMTs showed better dispersion of platelets within the EVOH phase than those containing Na-MMTs. Differential scanning calorimetry (DSC); showed the crystallisation behaviour of EVOH to depend on the clay loading and the nature of the organic modifier in the OMMT. Nanomer PGW, Cloisite Na+ and Cloisite 30B acted as weak nucleating agents. In contrast, Nanomer I.30T and Cloisite 10A significantly hindered the crystallisation of EVOH in the blends due to the restriction of chain segment mobility. Dynamic mechanical thermal analysis (DMTA) confirmed that the presence of clay increases the storage modulus of the composites compared to an unfilled blend. In addition, the improvement in storage modulus reflected the dispersion state of the different clays and their interaction with the polymers of the blend. Ternary-blend based composites were formed by adding poly(styrene-co-acrylonitrile) (SAN) to the composites based on binary PS/EVOH blends. This resulted in a finer dispersion of the EVOH phase and the development of a core-shell morphology, in which SAN encapsulated and formed shells around EVOH droplets. In contrast to binary blend composites, the clay platelets were found at the interface between SAN and EVOH in the ternary blends.
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Sharma, Suraj. "Fabrication and characterization of polymer blends and composites derived from biopolymers." Connect to this title online, 2008. http://etd.lib.clemson.edu/documents/1239894269/.

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Lim, Kate. "Supramolecular polymer blends for composite matrices." Thesis, University of Reading, 2016. http://centaur.reading.ac.uk/66400/.

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This research project reports a new approach to thermoplastic composite matrix design, in which a low-MW polymer additive acts as a plasticiser and flow-promoter at high temperatures, but as a non-covalent cross-linking agent at lower temperatures. Thus, poly(aryl ether ketone)s (PAEKs) are functionalised with π-electron rich terminal groups and blended with π-electron deficient polyimides. A non-covalent charge-transfer stacking interaction between the two polymers forms a self-assembled supramolecular network. Carbon fibre composites with matrices composed of these supramolecular polymer blends were produced, and the thermomechanical performance of these materials are reported. In designing functionalised PAEKs, novel benzoyl-pyrene and -perylene derived compounds were synthesised. The synthesis of these compounds and their subsequent use as functional end-groups in polycondensations are also discussed. During the course of polymer synthesis, the effect of varying polymerisation conditions involving different alkali metal carbonates was systematically investigated. It was found that monomer sequence distribution in PAEKs can be controlled by changing the alkali metal cation used in the nucleophilic synthesis. The mechanism of modifying monomer sequence distribution is presented herein. Investigating the interaction of polycyclic aromatic molecules pyrene and perylene with binary co-polyimides containing both strongly-binding and weakly-binding diimide sequences results in the emergence of fractal-like patterns in the 1H NMR spectra of the polyimide. The polyimide spectrum at high intercalator loadings shows self-similarity over a range of different length scales.
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Книги з теми "Polymer blends and composites"

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Efremovich, Zaikov Gennadiĭ, Bouchachenko A. L, and Ivanov V. B, eds. Aging of polymers, polymer blends and polymer composites. New York: Nova Science Publishers, 2002.

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Efremovich, Zaikov Gennadiĭ, Bouchachenko A. L, and Ivanov V. B, eds. Aging of polymers, polymer blends, and polymer composites. New York: Nova Science Publishers, 2002.

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Subramanian, Muralisrinivasan Natamai. Polymer Blends and Composites. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2017. http://dx.doi.org/10.1002/9781119383581.

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Functional polymer blends: Synthesis, properties, and performances. Boca Raton: CRC Press, 2012.

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Nanostructured polymer blends and composites in textiles. Toronto: Apple Academic Press, 2015.

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Holloway, Matthew James. Electrically conducting composites formed from polymer blends. Uxbridge: Brunel University, 1992.

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International Workshop on Polymer Blends and Polymer Composites (1997 Sydney, Australia). Polymer blends and polymer composites: Proceedings of the International Workshop on Polymer Blends and Polymer Composites, 8th-11th July 1997, Sydney, Australia. Edited by Ye L and Mai Y. W. 1946-. Switzerland: Trans Tech, 1998.

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Biodegradable polymer blends and composites from renewable resources. Hoboken, N.J: Wiley, 2009.

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Karger-Kocsis, József, and Stoyko Fakirov. Nano- and Micromechanics of Polymer Blends and Composites. München: Carl Hanser Verlag GmbH & Co. KG, 2009. http://dx.doi.org/10.3139/9783446430129.

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Visakh, P. M., and Yoshihiko Arao, eds. Thermal Degradation of Polymer Blends, Composites and Nanocomposites. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-03464-5.

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Частини книг з теми "Polymer blends and composites"

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Khan, Ibrahim, Muhammad Mansha, and Mohammad Abu Jafar Mazumder. "Polymer Blends." In Polymers and Polymeric Composites: A Reference Series, 513–49. Cham: Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-319-95987-0_16.

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Khan, Ibrahim, Muhammad Mansha, and Mohammad Abu Jafar Mazumder. "Polymer Blends." In Polymers and Polymeric Composites: A Reference Series, 1–38. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-92067-2_16-1.

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Logothetidis, Stergios. "Polymer Blends and Composites." In Ellipsometry of Functional Organic Surfaces and Films, 173–95. Berlin, Heidelberg: Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-642-40128-2_9.

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Logothetidis, Stergios. "Polymer Blends and Composites." In Ellipsometry of Functional Organic Surfaces and Films, 271–94. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-75895-4_12.

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Asano, Atsushi. "Polymer Blends and Composites." In Modern Magnetic Resonance, 1–15. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-28275-6_57-1.

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Asano, Atsushi. "Polymer Blends and Composites." In Modern Magnetic Resonance, 793–807. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-28388-3_57.

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McNeill, Christopher R. "Conjugated Polymer Blends: Toward All-Polymer Solar Cells." In Semiconducting Polymer Composites, 399–425. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2013. http://dx.doi.org/10.1002/9783527648689.ch14.

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Loos, Joachim. "Nanoscale Morphological Characterization for Semiconductive Polymer Blends." In Semiconducting Polymer Composites, 39–64. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2013. http://dx.doi.org/10.1002/9783527648689.ch2.

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Sarifuddin, Norshahida, and Hanafi Ismail. "Applications of Kenaf-Lignocellulosic Fiber in Polymer Blends." In Lignocellulosic Polymer Composites, 499–521. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2014. http://dx.doi.org/10.1002/9781118773949.ch22.

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Chen, Guo-Qiang, and Rong-Cong Luo. "Polyhydroxyalkanoate Blends and Composites." In Biodegradable Polymer Blends and Composites from Renewable Resources, 191–207. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2009. http://dx.doi.org/10.1002/9780470391501.ch8.

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Тези доповідей конференцій з теми "Polymer blends and composites"

1

Sartore, Luciana, and Luca Di Landro. "Polymer blends with biodegradable components and reinforcements." In TIMES OF POLYMERS (TOP) AND COMPOSITES 2014: Proceedings of the 7th International Conference on Times of Polymers (TOP) and Composites. AIP Publishing LLC, 2014. http://dx.doi.org/10.1063/1.4876894.

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Antonioli, Diego, Michele Laus, and Alina Sionkowska. "Natural polymer blends: Thermal and mechanical behavior." In 9TH INTERNATIONAL CONFERENCE ON “TIMES OF POLYMERS AND COMPOSITES”: From Aerospace to Nanotechnology. Author(s), 2018. http://dx.doi.org/10.1063/1.5045973.

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Pereira, R. C. T., S. M. M. Franchetti, J. A. M. Agnelli, L. H. C. Mattoso, Alberto D’Amore, Domenico Acierno, and Luigi Grassia. "EFFECTS OF THE BIODEGRADATION ON BIODEGRADABLE POLYMER BLENDS AND POLYPROPYLENE." In IV INTERNATIONAL CONFERENCE TIMES OF POLYMERS (TOP) AND COMPOSITES. AIP, 2008. http://dx.doi.org/10.1063/1.2989055.

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4

de Luna, Martina Salzano, Andrea Causa, Domenico Acierno, and Giovanni Filippone. "Melt state dynamics of plate-like nanoparticles in immiscible polymer blends." In TIMES OF POLYMERS (TOP) AND COMPOSITES 2014: Proceedings of the 7th International Conference on Times of Polymers (TOP) and Composites. AIP Publishing LLC, 2014. http://dx.doi.org/10.1063/1.4876833.

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5

Rapp, Géraldine, Pierre-Olivier Bussière, and Sandrine Therias. "Multiscale analysis of the degradation of polymer blends and composites." In 9TH INTERNATIONAL CONFERENCE ON “TIMES OF POLYMERS AND COMPOSITES”: From Aerospace to Nanotechnology. Author(s), 2018. http://dx.doi.org/10.1063/1.5045915.

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Akhilesan, S., Susy Varughese, and C. Lakshmana Rao. "Electromechanical Behavior of Conductive Polyaniline/Poly (Vinyl Alcohol) Blend Films Under Uniaxial Loading." In ASME 2012 Conference on Smart Materials, Adaptive Structures and Intelligent Systems. American Society of Mechanical Engineers, 2012. http://dx.doi.org/10.1115/smasis2012-7937.

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Анотація:
Polyaniline (PANI) an electronically conducting polymer, and its charge transfer complexes are interesting engineering materials due to their unique electronic conductivity, electrochemical behavior, low raw material cost, ease of synthesis and environmental stability in comparison with other conjugated polymers. The main disadvantage of PANI is its limited processability. Blending of conducting polymers with insulating polymers is a good choice to overcome the processability problem. In this study a solution-blend method is adopted to prepare conductive polyaniline/polyvinyl alcohol (PANI/PVA) blend films at various blend ratios. Interest in applications for polyaniline (PANI) has motivated investigators to study its electro mechanical properties, and its use in polymer composites or blends with common polymers. The work described here looks at the uniaxial deformation behavior of the conducting polymer films and the anisotropic dependency of electrical conductivity of the blend films exposed to static and dynamic loading conditions. The relation between mechanical strain, electrical conductivity and film microstructure is investigated on PANI/PVA blend films.
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Altobelli, Rosaria, Martina Salzano de Luna, Andrea Causa, Domenico Acierno, and Giovanni Filippone. "Morphology stabilization of co-continuous polymer blends through clay nanoparticles." In VIII INTERNATIONAL CONFERENCE ON “TIMES OF POLYMERS AND COMPOSITES”: From Aerospace to Nanotechnology. Author(s), 2016. http://dx.doi.org/10.1063/1.4949632.

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Filippone, G., D. Acierno, A. D’Amore, Domenico Acierno, and Luigi Grassia. "Impact of Nanoparticles on the Microstructure and Properties of Immiscible Polymer Blends: Preliminary Investigations." In V INTERNATIONAL CONFERENCE ON TIMES OF POLYMERS (TOP) AND COMPOSITES. AIP, 2010. http://dx.doi.org/10.1063/1.3455574.

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Hwang, Ho-Sang, Bum-Kyoung Seo, and Kune-Woo Lee. "Strippable Core-Shell Polymer Emulsion for Decontamination of Radioactive Surface Contamination." In ASME 2010 13th International Conference on Environmental Remediation and Radioactive Waste Management. ASMEDC, 2010. http://dx.doi.org/10.1115/icem2010-40193.

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Анотація:
In this study, the core-shell composite polymer for decontamination from the surface contamination was synthesized by the method of emulsion polymerization and blends of polymers. The strippable polymer emulsion is composed of the poly(styrene-ethyl acrylate) [poly(St-EA)] composite polymer, poly(vinyl alcohol) (PVA) and polyvinylpyrrolidone (PVP). The morphology of the poly(St-EA) composite emulsion particle was core-shell structure, with polystyrene (PS) as the core and poly(ethyl acrylate) (PEA) as the shell. Core-shell polymers of styrene (St)/ethyl acrylate (EA) pair were prepared by sequential emulsion polymerization in the presence of sodium dodecyl sulfate (SDS) as an emulsifier using ammonium persulfate (APS) as an initiator. Related tests and analysis confirmed the success in synthesis of composite polymer. The products are characterized by FT-IR spectroscopy, TGA that were used, respectively, to show the structure, the thermal stability of the prepared polymer. Two-phase particles with a core-shell structure were obtained in experiments where the estimated glass transition temperature and the morphologies of emulsion particles. Decontamination factors of the strippable polymeric emulsion were evaluated with the polymer blend contents.
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Patel, R. H., P. H. Kachhia, S. N. Patel, S. T. Rathod, and J. K. Valand. "Studies on fabrication of glass fiber reinforced composites using polymer blends." In 2ND INTERNATIONAL CONFERENCE ON CONDENSED MATTER AND APPLIED PHYSICS (ICC 2017). Author(s), 2018. http://dx.doi.org/10.1063/1.5032874.

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Звіти організацій з теми "Polymer blends and composites"

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Kelley, S. S. Composites and blends from biobased materials. Office of Scientific and Technical Information (OSTI), May 1995. http://dx.doi.org/10.2172/105128.

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Mulkern, Thomas J., Donovan Harris, and Alan R. Teets. Epoxy Functionalized Hyberbranched Polymer/Epoxy Blends. Fort Belvoir, VA: Defense Technical Information Center, December 1999. http://dx.doi.org/10.21236/ada372416.

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Rafailovich, M., and J. Sokolov. Surface and interfacial properties of polymer blends. Office of Scientific and Technical Information (OSTI), November 1991. http://dx.doi.org/10.2172/6048397.

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Czarnecki, Lech, Andrzej Garbacz, Pawel Lukowski, and James R. Clifton. Optimization of polymer concrete composites:. Gaithersburg, MD: National Institute of Standards and Technology, 1999. http://dx.doi.org/10.6028/nist.ir.6361.

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Florio, John, Henderson Jr., Test Jack B., and Frederick L. Thermal Analysis of Polymer Composites. Fort Belvoir, VA: Defense Technical Information Center, December 1989. http://dx.doi.org/10.21236/ada216947.

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Baer, E., and A. Hiltner. New Microlayer and Nanolayer Polymer Composites. Fort Belvoir, VA: Defense Technical Information Center, December 1998. http://dx.doi.org/10.21236/ada396499.

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Madhukar, Madhu S. Cure Cycle Optimization in Polymer Composites. Fort Belvoir, VA: Defense Technical Information Center, April 2000. http://dx.doi.org/10.21236/ada379701.

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Fabish, T. J., W. F. Lynn, R. J. Passinault, A. Vreugdenhil, and B. Metz. High Performance Flat Coatings Through Compatibilized Immiscible Polymer Blends. Fort Belvoir, VA: Defense Technical Information Center, July 1999. http://dx.doi.org/10.21236/ada375878.

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Chu, B. Phase transition in polymer blends and structure of ionomers. Office of Scientific and Technical Information (OSTI), January 1989. http://dx.doi.org/10.2172/5362446.

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Jeong, Wonje. ROMP-based polymer composites and biorenewable rubbers. Office of Scientific and Technical Information (OSTI), January 2009. http://dx.doi.org/10.2172/967070.

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