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Статті в журналах з теми "Acrylates Synthesis"
Czachor-Jadacka, Dominika, Barbara Pilch-Pitera, Maciej Kisiel, and Justyna Gumieniak. "Hydrophobic UV-Curable Powder Clear Coatings: Study on the Synthesis of New Crosslinking Agents Based on Raw Materials Derived from Renewable Sources." Materials 14, no. 16 (August 20, 2021): 4710. http://dx.doi.org/10.3390/ma14164710.
Повний текст джерелаPARK, MI NA, YOUNG SOO KANG, SUN WHA OH, BYUNG HYUN AHN, and MYUNG JUN MOON. "SYNTHESIS AND CHARACTERIZATION OF POLYURETHANE ACRYLATES FOR UV CURABLE COATING AGENTS." Surface Review and Letters 14, no. 04 (August 2007): 713–17. http://dx.doi.org/10.1142/s0218625x07009980.
Повний текст джерелаAzad, Leila, Maryam Ghazvini, Haleh Sanaeishoar, and Issa Yavari. "Synthesis of functionalized 1,2-dihydroisoquinolines via one-pot reactions of isoquinoline, alkyl propiolate, and thiazolidin-2,4-dione." Journal of Chemical Research 43, no. 11-12 (August 30, 2019): 457–60. http://dx.doi.org/10.1177/1747519819871028.
Повний текст джерелаTasic, Srba, Branislav Bozic, and Branko Dunjic. "Hyperbranched urethane-acrylates." Chemical Industry 58, no. 11 (2004): 505–13. http://dx.doi.org/10.2298/hemind0411505t.
Повний текст джерелаCurci, Michele, Jean-Luc Mieloszynski, and Daniel Paquer. "SYNTHESIS OF FUNCTIONALIZED ACRYLATES." Organic Preparations and Procedures International 25, no. 6 (December 1993): 649–57. http://dx.doi.org/10.1080/00304949309356260.
Повний текст джерелаChen, Hsuan, Shyh-Yuan Lee, and Yuan-Min Lin. "Synthesis and Formulation of PCL-Based Urethane Acrylates for DLP 3D Printers." Polymers 12, no. 7 (July 5, 2020): 1500. http://dx.doi.org/10.3390/polym12071500.
Повний текст джерелаKlee, Joachim E., та Uwe Lehmann. "Novel 2-(ω-phosphonooxy-2-oxaalkyl)acrylate monomers for self-etching self-priming one part adhesive". Beilstein Journal of Organic Chemistry 6 (7 вересня 2010): 766–72. http://dx.doi.org/10.3762/bjoc.6.95.
Повний текст джерелаLai, Xiao Juan, Yi Ding Shen, and Lei Wang. "Synthesis and Properties of Waterborne Polyurethane-Acrylate Hybrid Emulsion Modified by Organic Silicane." Advanced Materials Research 287-290 (July 2011): 1532–37. http://dx.doi.org/10.4028/www.scientific.net/amr.287-290.1532.
Повний текст джерелаTzeng, Jy-Jiunn, Yi-Ting Hsiao, Yun-Ching Wu, Hsuan Chen, Shyh-Yuan Lee, and Yuan-Min Lin. "Synthesis, Characterization, and Visible Light Curing Capacity of Polycaprolactone Acrylate." BioMed Research International 2018 (2018): 1–8. http://dx.doi.org/10.1155/2018/8719624.
Повний текст джерелаLiu, Hong Bo, Wu Ying Zhang, and Feng Lin. "Synthesis and Property of Polyurethane Acrylates Modified Graphene Oxide." Key Engineering Materials 703 (August 2016): 273–77. http://dx.doi.org/10.4028/www.scientific.net/kem.703.273.
Повний текст джерелаДисертації з теми "Acrylates Synthesis"
Clayton, Anthony Brian. "Photopolymerised urethane acrylates /." Title page, contents and summary only, 1992. http://web4.library.adelaide.edu.au/theses/09PH/09phc622.pdf.
Повний текст джерелаTrenor, Scott Russell. "Synthesis and Characterization of Tailored Photoactive Macromolecules." Diss., Virginia Tech, 2004. http://hdl.handle.net/10919/27314.
Повний текст джерелаPh. D.
Lessard, Benoît H. 1985. "Random controlled free radical copolymerization of acrylic acidstyrene and tert-butyl acrylatestyrene mixtures using nitroxide mediators." Thesis, McGill University, 2008. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=111944.
Повний текст джерелаEvans, Stacy Alexandria Banford. "Dithiafulvene (1,3-dithiole) and acrylate liquid crystals: Synthesis of monomers and polymers with possible electronic and electro-optic applications, and investigations in the synthesis of pure (meth)acrylates." Diss., The University of Arizona, 1989. http://hdl.handle.net/10150/184777.
Повний текст джерелаMange, Siyabonga. "Synthesis, polymerisation and characterisation of a novel olefin-modified acrylate monomer, 1-methyl-1-propyl-hexel acrylate." Thesis, Stellenbosch : Stellenbosch University, 2005. http://hdl.handle.net/10019.1/50459.
Повний текст джерелаENGLISH ABSTRACT: Finding use for byproducts from the chemical industry holds many advantages for a country's economy. Synthesis of new monomers from such byproducts adds value to otherwise otherwise low-value material. The synthesis of a new olefin-modified acrylate monomer, 1-methyl-1-propyl-hexyl acrylate (1-MPHA), derived from 1-pentene, is reported. Homopolymerisation of the monomer 1-MPHA was carried out in both benzene and in toluene. The products of full-conversion of the homopolymer poly-(1-MPHA) were characterised by GPC, NMR, TGA and DMA. Kinetic studies of the homopolymerisation process of 1- MPHAwere also undertaken. The monomer 1-methyl-1-propyl-hexyl acrylate (1-MPHA) was copolymerised with methyl methacrylate (MMA). Samples obtained from full conversion copolymerisations at various 1-MPHAIMMAfeed ratios were characterised by GPC, NMR, TGA and DMA. Reactivity ratios of the two monomers were obtained from in situ 1H NMR kinetic studies. 1-MPHA was also copolymerised with vinyl acetate (VAc). Samples obtained from full conversion copolymerisation with a 1-MPHA content ranging from 2 to 16 wt% were characterised by GPC, NMR, TGA and DMA. The solubility parameter and the hydrophobicity of the VAc/1-MPHA copolymers were also determined. Reactivity ratios of the two monomers were obtained from in situ 1HNMR kinetic studies. Further copolymerisation studies with styrene and glycidyl methacrylate as comonomers were undertaken. The chemical analysis and thermogravimetric analysis of the copolymers are reported. In conclusion, the use of 1-methyl-1-propyl-hexyl acrylate as a comonomer results in a reduction in the glass transition temperature, better thermal stability, increased hydrophobicity with an insignificant loss in stiffness of the copolymers. These properties are due to the long and branched chain structure of the 1-MPHA monomer.
AFRIKAANSE OPSOMMING: Gebruik van byprodukte van die chemiese nywerheid hou groot voordele in vir die land se ekonomie. Sintese van nuwe monomere vanuit sulke byprodukte dra by tot waardetoevoeging tot andersins lae-waarde byprodukte. Die sintese van 'n nuwe olefien-gewysigde akrilaatmonomeer afkomstig van 1-penteen, naamlik 1-metiel-1-propiel-heksielakrilaat (1-MPHA), word hier beskryf. Homopolimerisasie van die monomeer 1-MPHA is uitgevoer in beide benseen en tolueen. Die produkte van die volledige omskakeling van die homopolimeer is met behulp van GPC, KMR, TGA en DMA gekarakteriseer. Die reaksiekinetika van die homopolimerisasie van 1-MPHA is ook ondersoek. Die monomeer 1-MPHA is met metielmetakrilaat (MMA) gekopolimeriseer. Monsters van die volledig omgeskakelde kopolimere met verskeie 1- MPHNMMA voerverhoudings is m.b.v. GPC, KMR,' TGA en DMA gekarakteriseer. Die reaktiwiteitsverhoudings van die twee monomere is vanaf 1HKMR-studies bepaat. 1-MPHA is ook met vinielasetaat (VAc) gekopolimeriseer. Monsters van die produk van die volledige kopolimerisasie met 1-MPHA , met 'n inhoud van 2- 16 massa 0/0, is ook m.b.v. GPC, KMR, TGA en DMA gekarakteriseer. Die 1- MPHA het die hidrofobisiteit van VAc/1-MPHA aansienlik verhoog. Die reaktiwiteitsverhoudings van die twee monomere is vanaf in situ 1H KMRstudies bepaal. Verdere kopolimerisasiestudies met stireen en glisidielmetakrilaat as komonomere is onderneem. Chemiese- en termogravimetriese analises van die kopolimere is gedoen en gerapporteer. Ter afsluiting, die gebruik van 1-metiel-1-propiel-heksielakrilaat as komonomeer het 'n verlaging in die glasoorgangstemperatuur, verhoogde termiesestabiliteit, verhoogde hidrofobisiteit, en 'n klein verlies in die stewigheid (Eng. stiffness) van die kopolimeer tot gevolg. Hierdie eienskappe is as gevolg van die lang, vertakte kettingstruktuur van die 1-MPHA monomeer.
Sung, Jonggeun. "Design and synthesis of plant oil-based UV-curable acrylates for sustainable coating applications." Diss., Kansas State University, 2018. http://hdl.handle.net/2097/38657.
Повний текст джерелаDepartment of Grain Science and Industry
X. Susan Sun
A demand in sustainable polymers has been increased because of the environment concerns and saving finite petroleum resources. Plant oils are promising renewable resources to produce environmentally friendly polymer applications. Soybean oil-based resins such as epoxidized soybean oil (ESO) and acrylated epoxidized soybean oil (AESO) have been well-known functionalized plant oils, but relatively low performances of their polymers and a competition with food production have been disadvantages. Thus, in this study, we designed new plant oil-based acrylates using non-food resources and achieved excellent properties of the acrylates for coatings and thermoset applications. Firstly, we developed coating materials with high mechanical, thermal and coating performances using acrylated epoxidized camelina oil (AECO) as a main acrylate monomer with various meth(acrylates) as reactive diluents Next, acrylated epoxidized cardanol modified fatty acids from camelina oil (AECFA) was successfully synthesized, and a phenolic structure with long aliphatic side chains with acrylic groups was obtained. The novel structure of AECFA provided rigidity into its polymer maintained with flexibility, and AECFA coating material showed better performances in terms of all properties such as mechanical, thermal, viscoelastic, and coating performances, as compared to commercial AESO resin. Finally, acrylated epoxidized allyl 10-undecenoate (AEAU) was developed from 10-undecenoic acid, castor oil derivative. The single fatty ester structure with di-functional acrylates of AEAU had very lower viscosity and showed better thermoset performances than those of triglyceride-based acrylates such as AESO and AECO. Thus, AEAU had a potential to an alternative to AESO for thermoset applications.
Bagoury, Mohamed al. "Synthesis of aqueous polymer colloids based on saccharide monomers and alkyl acrylates through emulsion polymerization." [S.l. : s.n.], 2005. http://deposit.ddb.de/cgi-bin/dokserv?idn=974074527.
Повний текст джерелаLi, Peichun. "Synthesis of poly(ε-caprolactone) based copolymers in molten state by living polymerization". Saint-Etienne, 2009. http://www.theses.fr/2009STET4001.
Повний текст джерелаDans cette thèse, nous étudions la synthèse de poly(ε-caprolactone) (PCL) fonctionnelle ainsi que la copolymérisation contrôlée de l'ε-caprolactone (CL) avec l'acrylate de butyle (BA) dans une matrice polymère thermoplastique via l'extrusion réactive. Dans la première partie, l'initiateur de formule Ti[O(CH2)4OCH=CH2]4 a été synthétisé dans le but d'élaborer de la PCL fonctionnelle. La cinétique de polymérisation par ouverture de cycle (ROP) initiée par Ti[O(CH2)4OCH=CH2]4 a été étudiée. Par ailleurs, un processus de gélification a été mis en évidence par rhéologie lors de la polymérisation simultanée de l'ε-caprolactone et de l'acrylate de butyle. Dans un second temps, ces réseaux ont été élaborés dans une matrice de poly (methyl methacrylate) (PMMA) par voie fondue. Dans la deuxième partie, un initiateur schématisé par Ti[OCH2CCl3]4 a été synthétisé dans le but de coupler 2 techniques de polymérisations contrôlées, à savoir la polymérisation par ROP de l'ε-caprolactone et la polymérisation radicalaire par transfert d'atomes (ATRP) de l'acrylate de butyle. Les cinétiques de polymérisation ont été évaluées et des copolymères PCL-bloc-PBA ont été élaborés. Parallèlement, un macro initiateur porteur de chaînes de polybutylacrylate a été synthétisé par ATRP à partir de Ti(OCH2CCl3)4. Ce dernier a permis d'élaborer un copolymère avec de l'ε-caprolactone dans une matrice PMMA en mélangeur interne. L'objectif de cette dernière partie étant de synthétiser, in situ et en voie fondue dans une matrice thermoplastique, un matériau de structure contrôlée afin d'améliorer les propriétés de la matrice
Lee, Jehoon. "Synthesis, characterization, and applications of the low cross-link density poly acrylate elastomers using direct reversible addition fragmentation chain transfer cross-linker." University of Akron / OhioLINK, 2018. http://rave.ohiolink.edu/etdc/view?acc_num=akron149798302050725.
Повний текст джерелаHinojosa, Barbara R. "Nanoparticles Engineered to Bind Serum Albumin: Microwave Assisted Synthesis, Characterization, and Functionalization of Fluorescently-Labeled, Acrylate-Based, Polymer Nanoparticles." Thesis, University of North Texas, 2010. https://digital.library.unt.edu/ark:/67531/metadc30466/.
Повний текст джерелаКниги з теми "Acrylates Synthesis"
Oh, Jung Kwon. Synthesis and characterization of dye-labeled poly(vinyl acetate-butyl acrylate) latex particles and their application to film formation and polymer interdiffusion. 2004.
Знайти повний текст джерелаЧастини книг з теми "Acrylates Synthesis"
Grishin, Dmitry F., Elena V. Kolyakina, Marina V. Pavlovskaya, Mikhail A. Lazarev, and Alexander A. Shchepalov. "New Nitroxide Mediators for Controlled Synthesis of Polystyrene, Poly(meth)acrylates and Their Copolymers." In ACS Symposium Series, 95–114. Washington, DC: American Chemical Society, 2009. http://dx.doi.org/10.1021/bk-2009-1024.ch007.
Повний текст джерелаKeul, Helmut, Dirk Achten, Birte Reining, and Hartwig Höcker. "Synthesis of Oligomers by Stable Free Radical Polymerization of Acrylates, Methacrylates, and Styrene with Alkoxyamine Initiators." In ACS Symposium Series, 408–26. Washington, DC: American Chemical Society, 2000. http://dx.doi.org/10.1021/bk-2000-0768.ch029.
Повний текст джерелаGrevels, F. W., J. G. A. Reuvers, J. Takats, and B. F. G. Johnson. "Tetracarbonyl(η2 -Methyl Acrylate)Ruthenium." In Inorganic Syntheses, 176–80. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132555.ch51.
Повний текст джерелаGrevels, F. W., J. G. A. Reuvers, J. Takats, and B. F. G. Johnson. "Tetracarbonyl(η2 -Methyl Acrylate)Ruthenium." In Inorganic Syntheses, 47–51. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132593.ch10.
Повний текст джерелаJothi Rajan, M. A., T. Mathavan, T. S. Vivekanandam, S. Umapathy, V. Ganesan, G. S. Okram, and Ajay Soni. "Sonochemical Synthesis of Poly (Methyl Acrylate)." In Solid State Phenomena, 175–90. Stafa: Trans Tech Publications Ltd., 2008. http://dx.doi.org/10.4028/3-908451-50-7.175.
Повний текст джерелаJinger, Suman, and Jyoti Chaudhary. "Homopolymer, Copolymers, and Terpolymer Synthesis Via Esterification-Cum-Addition of N-Substituted Phthalimide with Acrylates: Studies on Influences of Macromolecule Compositions on Thermal and Microbial Performances." In Advances in Polymer Sciences and Technology, 231–46. Singapore: Springer Singapore, 2018. http://dx.doi.org/10.1007/978-981-13-2568-7_20.
Повний текст джерелаJerome, R., R. Forte, S. K. Varshney, R. Fayt, and Ph Teyssie. "The Anionic Polymerization of Alkyl Acrylates : A Challenge." In Recent Advances in Mechanistic and Synthetic Aspects of Polymerization, 101–17. Dordrecht: Springer Netherlands, 1987. http://dx.doi.org/10.1007/978-94-009-3989-9_8.
Повний текст джерелаBrookhart, Maurice, Elisabeth Hauptman, and Sylviane Sabo-Etienne. "Rh(III) Catalysts for Tail-to-Tail Dimerization of Methyl Acrylate." In Organic Synthesis via Organometallics (OSM 4), 69–77. Wiesbaden: Vieweg+Teubner Verlag, 1993. http://dx.doi.org/10.1007/978-3-322-84062-2_6.
Повний текст джерелаWang, Yuxiu, Guangxue Chen, Minghui He, and Qifeng Chen. "Synthesis of Novel Hyperbranched Polyurethane Acrylate Based on Pentaerythritol." In Lecture Notes in Electrical Engineering, 657–64. Singapore: Springer Singapore, 2018. http://dx.doi.org/10.1007/978-981-10-7629-9_82.
Повний текст джерелаSpaltenstein, A., and J. J. Leban. "A new approach to “carba”-peptide isosteres: Synthesis of Boc-(S)-PheΨ[CH2CH2]-(R/S)Val and Boc-(S)-TrpΨ[CH2CH2]-(R/S)-Val via Michael addition of sulfone-stabilized anions to acrylates." In Peptides, 74–76. Dordrecht: Springer Netherlands, 1994. http://dx.doi.org/10.1007/978-94-011-0683-2_18.
Повний текст джерелаТези доповідей конференцій з теми "Acrylates Synthesis"
Zailani, N. A. M., F. A. Latif, A. M. M. Ali, M. A. A. Rani, and M. Z. A. Yahya. "Synthesis of flexible acrylates films." In GREEN DESIGN AND MANUFACTURE: ADVANCED AND EMERGING APPLICATIONS: Proceedings of the 4th International Conference on Green Design and Manufacture 2018. Author(s), 2018. http://dx.doi.org/10.1063/1.5066760.
Повний текст джерелаXu, Lei, Min Wang, Xi-Zhi Jiang, and Yong-Fu Zhao. "Synthesis and Characterization of Polysiloxane and Acrylate Elastomer Material." In 2015 International Conference on Material Science and Applications (icmsa-15). Paris, France: Atlantis Press, 2015. http://dx.doi.org/10.2991/icmsa-15.2015.188.
Повний текст джерелаHwang, 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.
Повний текст джерелаOstrauskaitė, Jolita, Auksė Navaruckienė, and Greta Motiekaitytė. "Vanillin Acrylate-Based Photocross-Linked Polymers: Synthesis and Investigation of Properties." In The First International Conference on “Green” Polymer Materials 2020. Basel, Switzerland: MDPI, 2020. http://dx.doi.org/10.3390/cgpm2020-07205.
Повний текст джерелаJhaumeer-Laulloo, S., P. Ramasami, L. Rhyman, and J. Joule. "1,3-Dipolar Cycloaddition of 3-Oxidopyrazinium to Methyl Acrylate: An Experimental and Computational Investigation." In The 12th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2008. http://dx.doi.org/10.3390/ecsoc-12-01207.
Повний текст джерелаAvramenko, Valentin, Vitaly Mayorov, Dmitry Marinin, Alexander Mironenko, Marina Palamarchuk, and Valentin Sergienko. "Macroporous Catalysts for Hydrothermal Oxidation of Metallorganic Complexes at Liquid Radioactive Waste Treatment." In ASME 2010 13th International Conference on Environmental Remediation and Radioactive Waste Management. ASMEDC, 2010. http://dx.doi.org/10.1115/icem2010-40186.
Повний текст джерелаDeniau, Eric. "Total synthesis of (–)-herbaric acid through organocatalyzed asymmetric halolactonization of acrylate-type benzoic acids." In The 21st International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2017. http://dx.doi.org/10.3390/ecsoc-21-04725.
Повний текст джерелаSousa, Carlos, Cristina Freire, and José Rodriguez-Borges. "Synthesis and application of L-serine derivative ligands in Diels-Alder reaction between cyclopentadiene and methyl acrylate." In The 17th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2013. http://dx.doi.org/10.3390/ecsoc-17-a036.
Повний текст джерелаWang, Si-yuan, and Ying-quan Zou. "The study of synthesis and photocuring behaviors of organic silicon modified methylacrylate and acrylate." In SPIE Advanced Lithography, edited by Patrick P. Naulleau and Obert R. Wood II. SPIE, 2012. http://dx.doi.org/10.1117/12.916673.
Повний текст джерелаDeniau, Eric, Christophe Michon, Stéphane LEBRUN, and Francine Agbossou-Niedercorn. "Regioselective organocatalyzed asymmetric bromolactonization of aryl acrylate-type carboxylic acids. A new approach towards enantioenriched 3-substituted isobenzofuranones." In The 20th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2016. http://dx.doi.org/10.3390/ecsoc-20-a037.
Повний текст джерелаЗвіти організацій з теми "Acrylates Synthesis"
Gogate, M. R., J. J. Spivey, J. R. Zoeller, R. D. Colberg, G. N. Choi, and S. S. Tam. Synthesis of Acrylates and Methacrylates from Coal-Derived Syngas. Office of Scientific and Technical Information (OSTI), October 1997. http://dx.doi.org/10.2172/643566.
Повний текст джерелаTischer, R. E., and J. J. Spivey. Synthesis of acrylates and methacrlyates from coal-derived syngas. Quarterly technical progress report, January 1, 1995--March 31, 1995. Office of Scientific and Technical Information (OSTI), August 1995. http://dx.doi.org/10.2172/106469.
Повний текст джерелаSynthesis of acrylates. Quarterly report, 1996. Office of Scientific and Technical Information (OSTI), July 1996. http://dx.doi.org/10.2172/436453.
Повний текст джерелаSynthesis of acrylates. Quarterly report, 1996. Office of Scientific and Technical Information (OSTI), October 1996. http://dx.doi.org/10.2172/436456.
Повний текст джерелаSynthesis of acrylates and Methacrylates from Coal-Derived Syngas. Office of Scientific and Technical Information (OSTI), May 1997. http://dx.doi.org/10.2172/643526.
Повний текст джерелаSynthesis of acrylates. [Quarterly report], January 1, 1996--March 31, 1996. Office of Scientific and Technical Information (OSTI), April 1996. http://dx.doi.org/10.2172/274170.
Повний текст джерелаSynthesis of acrylates. Quarterly progress report, April 1, 1995--June 30, 1995. Office of Scientific and Technical Information (OSTI), September 1995. http://dx.doi.org/10.2172/181501.
Повний текст джерелаSynthesis of acrylates and methacrylates from coal-derived syngas. Quarterly report, October--December 1996. Office of Scientific and Technical Information (OSTI), May 1997. http://dx.doi.org/10.2172/510671.
Повний текст джерела