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Статті в журналах з теми "COPOLYMER RESINS"
Kizilcan, N., and B. Erson. "Novel phenylacetylene based ketonic resins." Pigment & Resin Technology 44, no. 4 (July 6, 2015): 198–204. http://dx.doi.org/10.1108/prt-07-2014-0052.
Повний текст джерелаLee, Pilwoo, Hunsang Jung, Chan-Sei Yoo, and Hyun Ho Lee. "Low Dielectric Constant Characteristics of Styrene and Maleimide Anhydride Copolymer with Modification for High Frequency Application of Printed Circuit Board." Polymers 15, no. 9 (April 27, 2023): 2078. http://dx.doi.org/10.3390/polym15092078.
Повний текст джерелаBienek, Diane R., Anthony A. Giuseppetti, Stanislav A. Frukhtbeyn, Rochelle D. Hiers, Fernando L. Esteban Florez, Sharukh S. Khajotia, and Drago Skrtic. "Physicochemical, Mechanical, and Antimicrobial Properties of Novel Dental Polymers Containing Quaternary Ammonium and Trimethoxysilyl Functionalities." Journal of Functional Biomaterials 11, no. 1 (December 18, 2019): 1. http://dx.doi.org/10.3390/jfb11010001.
Повний текст джерелаMachado, Marina, Mateus Hofmann, Mário Garrido, João R. Correia, João C. Bordado, and Inês C. Rosa. "Incorporation of Lignin in Bio-Based Resins for Potential Application in Fiber–Polymer Composites." Applied Sciences 13, no. 14 (July 19, 2023): 8342. http://dx.doi.org/10.3390/app13148342.
Повний текст джерелаKhatiwada, Shankar P., Sabu Thomas, Jean Marc Saiter, Ralf Lach, and Rameshwar Adhikari. "Mechanical and thermal properties of triblock copolymer modified epoxy resins." BIBECHANA 16 (November 22, 2018): 196–203. http://dx.doi.org/10.3126/bibechana.v16i0.21651.
Повний текст джерелаAteş, Esin, Nilgün Kizilcan, and Merve İstif. "New comonomer synthesis from thiophene-2-carbonyl chloride and cyclohexanone formaldehyde resin." Pigment & Resin Technology 44, no. 2 (March 2, 2015): 79–86. http://dx.doi.org/10.1108/prt-10-2013-0091.
Повний текст джерелаNandekar, Kamlakar. "Novel Applications of Some Organic Copolymers Derived From Phenolic and Nitrogen-Containing Compounds- A Review." Journal of ISAS 2, no. 1 (July 31, 2023): 15–26. http://dx.doi.org/10.59143/isas.jisas.2.1.kdqi5413.
Повний текст джерелаBabayev, E. R., I. I. Safiullina, E. Kh Karimov, I. Z. Mukhametzyanov, A. Yu Bakhtina, and E. M. Movsumzade. "Acrylic polymers for conditions of weakly acid conversion to resins, complex syntheses." SOCAR Proceedings, no. 4 (December 31, 2020): 84–94. http://dx.doi.org/10.5510/ogp20200400469.
Повний текст джерелаFainleib, A. M. "Copolymers and interpenetrating polymer networks of thermoreactive nitrogen-containing resins. Mini review." Polymer journal 42, no. 4 (December 10, 2020): 245–53. http://dx.doi.org/10.15407/polymerj.42.04.245.
Повний текст джерелаLi, Wei, Da Hong Li, Jian Ping Cao, Xiang Jun Yun, and Pawan Kunmar. "Study on the Transparent Electronic Isolation Layer Material - A Photoresist Composition which is Stable at High Temperature and Humidity." Materials Science Forum 980 (March 2020): 44–57. http://dx.doi.org/10.4028/www.scientific.net/msf.980.44.
Повний текст джерелаДисертації з теми "COPOLYMER RESINS"
Richards, Mark Ian. "Refined methods in solid (gel) phase peptide synthesis." Thesis, University of Wolverhampton, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.343258.
Повний текст джерелаAraujo, Renata Bastos de. "Preparação e avaliação de resinas biocidas impregnadas com iodo a partir de resinas comerciais de estireno e divinilbenzeno." Universidade do Estado do Rio de Janeiro, 2013. http://www.bdtd.uerj.br/tde_busca/arquivo.php?codArquivo=5197.
Повний текст джерелаIn this study, we employed two commercial resins strongly basic character. Both based on copolymers of styrene and divinylbenzene (DVB), and the VPOC 1950 contains in its composition quaternary ammonium groups of the type 1 (has three methyl groups) and VPOC 1960 quaternary ammonium groups of the type 2 (where a group ethanol replaces one of the methyl groups). The aforementioned commercial resins were chosen because they have a high ion exchange capacity, stability and functional groups of interest for impregnation with iodine. The resins were impregnated with iodine by three different methodologies, a methanol solution of 0.08 mol/L iodine with and without 0.14 mol/L potassium iodide and 0.08 mol/L iodine in heptane. The resins were characterized by surface area, pore volume, degree of swelling, optical microscopy, infrared spectroscopy by Fourier transform (FTIR), elemental analysis, thermogravimetry, scanning electron microscopy and determination of iodine prescribed by iodometry. The biocidal activity evaluation was performed by the method of plate counting, using a strain of Escherichia coli ATCC11775 at concentrations 103-107 cells/ml. All resins impregnated showed significant bactericidal activity due to the presence of iodine correlated characteristics of the resin, such as functional groups, size and shape of the pores. For comparison, tests were performed with bactericidal resins departure for confirmation or not of bactericidal only be attributed to iodine
Abreu, Iury Körting de. "Estudos dos efeitos da adição de copolímeros em blocos em nanocompósitos de matriz epoxídica reforçados com nanoplateletes de grafeno e nanotubos de carbono." Universidade do Estado de Santa Catarina, 2015. http://tede.udesc.br/handle/handle/1677.
Повний текст джерелаConselho Nacional de Desenvolvimento Científico e Tecnológico
O estado de dispersão das nanopartículas na matriz está diretamente ligado às propriedades físicas dos nanocompósitos. Assim técnicas que visam um estado de dispersão mais homogêneo das nanopartículas na matriz são constantemente estudadas. Funcionalização não covalente, ou física, é uma técnica que utiliza-se de interações Coulombianas e/ou barreira estérica com o objetivo de estabilizar a interação entre nanopartícula/matriz e consequentemente obter um estado de dispersão homogêneo. Utilizando copolímero em bloco BYK- 9077® como agente funcionalizante não covalentemente, este trabalho teve como objetivo produzir nanocompósitos de matriz epoxídica Novolac® reforçados com nanoplateletes de grafeno ou nanotubos de carbono funcionalizados não covalentemente. Foram analisadas a influência da adição do copolímero em bloco nas propriedades mecânicas, térmicas e morfológicas dos nanocompósitos produzidos. Utilizou-se frações volumétricas de nanopartículas nos valores de 0,15%, 0,50% e 1,50%. A partir destes valores foi adicionado copolímero em bloco nas quantidades de 1, 5 e 10 vezes a quantidade em massa das nanopartículas. Foram realizadas espectroscopia Raman para caracterização das nanopartículas, verificando o grau de pureza das mesmas, assim como o número de plateletes empilhados. Analisando os resultados, estado de dispersão das nanopartículas na matriz sem a adição de copolímero em bloco não foi homogêneo, assim foram encontrados aglomerados de nanopartículas em Microscopia Eletrônica de Transmissão. Também os valores de Tg s não variaram significativamente em comparação com a resina pura, indicando dispersão não homogênea. Já ao adicionar copolímero em bloco, em quantidades baixas, 1x, foi possível observar aumentos de 8% no módulo de elasticidade, indicativo de que a adição de copolímero em bloco nesta quantidade tornou a dispersão das nanopartículas mais homogênea na matriz. Esta afirmação foi verificada em Microscopia Eletrônica de transmissão. Em contrapartida, conforme foi aumentado a quantidade de copolímero em bloco, 5 e 10x, foram observadas formação de uma segunda fase, que por consequência diminuiu o módulo de elasticidade, tensão de ruptura e Tg.
Arnold, Cynthia A. "Structure-property behavior of polyimide homopolymers, copolymers, and blends." Diss., This resource online, 1990. http://scholar.lib.vt.edu/theses/available/etd-09162005-115012/.
Повний текст джерелаHudda, Laila B. "Origin of limiting conversion phenomenon in alkyd/acrylate graft copolymerization systems." Thesis, Georgia Institute of Technology, 2003. http://hdl.handle.net/1853/10960.
Повний текст джерелаStein, Jasmin. "Toughening of highly crosslinked epoxy resin systems." Thesis, University of Manchester, 2013. https://www.research.manchester.ac.uk/portal/en/theses/toughening-of-highly-crosslinked-epoxy-resin-systems(de1605b9-d14d-43f1-83a1-dc13a7530179).html.
Повний текст джерелаRoyston, Gareth John. "Modification of epoxy resins with block copolymers of poly(ethylene oxide) and poly(butylene oxide)." Thesis, University of Sheffield, 2007. http://etheses.whiterose.ac.uk/15156/.
Повний текст джерелаMiles, Andrew. "Copolymers of methacrylic acid and itaconic acid derivatives as thermally crosslinkable electron resists." Thesis, University of Stirling, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.236050.
Повний текст джерелаLascu, Claudia M. "Block Copolymers via Reverse Addition-Fragmentation Chain Transfer Polymerization as a Viable Resin for Packaging Coatings." University of Cincinnati / OhioLINK, 2015. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1428070054.
Повний текст джерелаCheng, Jing. "Toward sub-10 nm lithographic processes: epoxy-based negative tone molecular resists and directed self-assembly (DSA) of high χ block copolymers". Diss., Georgia Institute of Technology, 2013. http://hdl.handle.net/1853/49113.
Повний текст джерелаКниги з теми "COPOLYMER RESINS"
Budkowski, A., I. W. Hamley, and T. Koike. Interfaces Crystallization Viscoelasticity. Springer London, Limited, 2003.
Знайти повний текст джерела(Contributor), A. Budkowski, I. W. Hamley (Contributor), and T. Koike (Contributor), eds. Interfaces/Crystallization/Viscoelasticity (Advances in Polymer Science). Springer, 1999.
Знайти повний текст джерелаBudkowski, A., I. W. Hamley, and T. Koike. Interfaces Crystallization Viscoelasticity. Springer Berlin / Heidelberg, 2013.
Знайти повний текст джерелаЧастини книг з теми "COPOLYMER RESINS"
Gooch, Jan W. "Ethylene–Acid Copolymer Resins." In Encyclopedic Dictionary of Polymers, 278. New York, NY: Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_4557.
Повний текст джерелаH. Builes, Daniel. "Chapter 7 Nanostructuration of Unsaturated Polyester Resins Using Block Copolymers." In Block Copolymer Nanocomposites, 225–64. Penthouse Level, Suntec Tower 3, 8 Temasek Boulevard, Singapore 038988: Pan Stanford Publishing Pte. Ltd., 2016. http://dx.doi.org/10.1201/9781315364834-8.
Повний текст джерелаLi, Guizhi, and Charles U. Pittman. "Polyhedral Oligomeric Silsesquioxane (POSS) Polymers, Copolymers, and Resin Nanocomposites." In Macromolecules Containing Metal and Metal-Like Elements, 79–131. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2005. http://dx.doi.org/10.1002/0471712566.ch5.
Повний текст джерелаJurek, M. J., and Elsa Reichmanis. "Lithographic Evaluation of Phenolic Resin—Dimethyl Siloxane Block Copolymers." In ACS Symposium Series, 158–74. Washington, DC: American Chemical Society, 1989. http://dx.doi.org/10.1021/bk-1989-0412.ch010.
Повний текст джерелаHse, Chung-Yun, and QiQing Hong. "Effects of Phenol-Formaldehyde Copolymer on Gluebond Performance of Lignin-Phenolic Resin Systems." In ACS Symposium Series, 96–109. Washington, DC: American Chemical Society, 1989. http://dx.doi.org/10.1021/bk-1989-0385.ch008.
Повний текст джерелаPionteck, Jürgen. "pVT Analysis of the Effect of Addition of Thermoplastics, Block-Copolymers, or Rubbers on the Curing Behavior and Shrinkage of Epoxy Resins." In Handbook of Epoxy Blends, 799–823. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-40043-3_44.
Повний текст джерелаPionteck, Jürgen. "pVT Analysis of the Effect of Addition of Thermoplastics, Block-Copolymers, or Rubbers on the Curing Behavior and Shrinkage of Epoxy Resins." In Handbook of Epoxy Blends, 1–26. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-18158-5_44-1.
Повний текст джерела"Ethylene-acid copolymer resins." In Encyclopedic Dictionary of Polymers, 372. New York, NY: Springer New York, 2007. http://dx.doi.org/10.1007/978-0-387-30160-0_4494.
Повний текст джерелаFoster, R. "Ethylene Vinyl Alcohol Copolymer (EVOH) Resins." In Coatings Technology Handbook, Third Edition, 57–1. CRC Press, 2005. http://dx.doi.org/10.1201/9781420027327.ch57.
Повний текст джерела"Ethylene Vinyl Alcohol Copolymer (EVOH) Resins." In Coatings Materials and Surface Coatings, 91–96. CRC Press, 2006. http://dx.doi.org/10.1201/9781420044058-16.
Повний текст джерелаТези доповідей конференцій з теми "COPOLYMER RESINS"
Miller, Tim, Fabio Aguirre, and Ray Hudack. "New Specialty Resins for High Performance Fusion Bonded Epoxy Coatings." In 2012 9th International Pipeline Conference. American Society of Mechanical Engineers, 2012. http://dx.doi.org/10.1115/ipc2012-90561.
Повний текст джерелаZhou, Hongfu, and Jianbin Wang. "Preparation of copper clad laminates with high performance bismaleimide-based copolymer matrix resins." In 2011 International Symposium on Advanced Packaging Materials (APM). IEEE, 2011. http://dx.doi.org/10.1109/isapm.2011.6105742.
Повний текст джерелаGabor, Allen H., Eric A. Lehner, Guoping Mao, Christopher K. Ober, Timothy E. Long, Brian A. Schell, and Richard C. Tiberio. "Hydrosiloxane-modified styrene-diene block copolymer resists." In SPIE'S 1993 Symposium on Microlithography, edited by William D. Hinsberg. SPIE, 1993. http://dx.doi.org/10.1117/12.154785.
Повний текст джерелаNamaste, Y. M. N., S. K. Obendorf, and F. Rodriguez. "Methacrylamide Copolymer Resists For Electron Beam Lithography." In 1986 Microlithography Conferences, edited by C. Grant Willson. SPIE, 1986. http://dx.doi.org/10.1117/12.963630.
Повний текст джерелаLi, Jiaxiong, Chao Ren, Kyoung-sik Moon, and Ching-ping Wong. "Epoxy/ Triazine Copolymer Resin System for High Temperature Encapsulant Applications." In 2019 IEEE 69th Electronic Components and Technology Conference (ECTC). IEEE, 2019. http://dx.doi.org/10.1109/ectc.2019.000-2.
Повний текст джерелаWakisaka, Yukiya, Tadayuki Fujiwara, Masayuki Tooyama, Hideaki Kuwano, and Koji Nishida. "Development of advanced ArF resist using alicyclic methacrylate copolymer: the optimum quenchers for this copolymer." In Microlithography 2000, edited by Francis M. Houlihan. SPIE, 2000. http://dx.doi.org/10.1117/12.388272.
Повний текст джерелаMertesdorf, Carlo, Bertholt Nathal, Norbert Muenzel, Heinz E. Holzwarth, and Hans-Thomas Schacht. "Deep-UV resists based on methacrylamide copolymers." In SPIE's 1994 Symposium on Microlithography, edited by Omkaram Nalamasu. SPIE, 1994. http://dx.doi.org/10.1117/12.175342.
Повний текст джерелаBinkley, E. S., and S. Nara. "Low Loss, Buried Channel Waveguides Fabricated From New, Fluorinated Polyimide Copolymers." In Organic Thin Films for Photonic Applications. Washington, D.C.: Optica Publishing Group, 1993. http://dx.doi.org/10.1364/otfa.1993.fa.4.
Повний текст джерелаMalhotra, Sandeep, Bernard C. Dems, Yarrow M. N. Namaste, Ferdinand Rodriguez, and S. K. Obendorf. "Modified maleic anhydride copolymers as e-beam resists." In Microlithography '90, 4-9 Mar, San Jose, edited by Douglas J. Resnick. SPIE, 1990. http://dx.doi.org/10.1117/12.20167.
Повний текст джерелаHartney, M. A., and A. E. Novembre. "Poly (Methylstyrene - Dimethylsiloxane) Block Copolymers As Bilevel Resists." In 1985 Microlithography Conferences, edited by Larry F. Thompson. SPIE, 1985. http://dx.doi.org/10.1117/12.947820.
Повний текст джерелаЗвіти організацій з теми "COPOLYMER RESINS"
Hubler, T. L., J. A. Franz, W. J. Shaw, M. O. Hogan, R. T. Hallen, G. N. Brown, and J. C. Linehan. Structure/function studies of resorcinol-formaldehyde (R-F) and phenol-formaldehyde (P-F) copolymer ion-exchange resins. Office of Scientific and Technical Information (OSTI), September 1996. http://dx.doi.org/10.2172/402296.
Повний текст джерела