Study of the structural, thermal, rheological and film properties of functional copolymers of hydroxyethyl acrylate and methyl methacrylate
New functional polymers will be prepared using alkyd resins having high solid content (environmentally friendly) and comb-type structural morphology. Different copolymers of hydroxyethyl acrylate and methyl methacrylate (HEMMA) were synthesized by solution polymerization using azo-bis-(isobutyronitr...
- Autores:
-
Murillo, Edwin A.
Mejia, Maria Cristina
- Tipo de recurso:
- Article of journal
- Fecha de publicación:
- 2016
- Institución:
- Universidad Francisco de Paula Santander
- Repositorio:
- Repositorio Digital UFPS
- Idioma:
- eng
- OAI Identifier:
- oai:repositorio.ufps.edu.co:ufps/1026
- Acceso en línea:
- http://repositorio.ufps.edu.co/handle/ufps/1026
https://doi.org/10.1590/0104-1428.1896
- Palabra clave:
- hydroxyethyl acrylate
methyl methacrylate
synthesis
copolymerization
properties
- Rights
- openAccess
- License
- Atribución 4.0 Internacional (CC BY 4.0)
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dc.title.eng.fl_str_mv |
Study of the structural, thermal, rheological and film properties of functional copolymers of hydroxyethyl acrylate and methyl methacrylate |
title |
Study of the structural, thermal, rheological and film properties of functional copolymers of hydroxyethyl acrylate and methyl methacrylate |
spellingShingle |
Study of the structural, thermal, rheological and film properties of functional copolymers of hydroxyethyl acrylate and methyl methacrylate hydroxyethyl acrylate methyl methacrylate synthesis copolymerization properties |
title_short |
Study of the structural, thermal, rheological and film properties of functional copolymers of hydroxyethyl acrylate and methyl methacrylate |
title_full |
Study of the structural, thermal, rheological and film properties of functional copolymers of hydroxyethyl acrylate and methyl methacrylate |
title_fullStr |
Study of the structural, thermal, rheological and film properties of functional copolymers of hydroxyethyl acrylate and methyl methacrylate |
title_full_unstemmed |
Study of the structural, thermal, rheological and film properties of functional copolymers of hydroxyethyl acrylate and methyl methacrylate |
title_sort |
Study of the structural, thermal, rheological and film properties of functional copolymers of hydroxyethyl acrylate and methyl methacrylate |
dc.creator.fl_str_mv |
Murillo, Edwin A. Mejia, Maria Cristina |
dc.contributor.author.none.fl_str_mv |
Murillo, Edwin A. Mejia, Maria Cristina |
dc.subject.proposal.eng.fl_str_mv |
hydroxyethyl acrylate methyl methacrylate synthesis copolymerization properties |
topic |
hydroxyethyl acrylate methyl methacrylate synthesis copolymerization properties |
description |
New functional polymers will be prepared using alkyd resins having high solid content (environmentally friendly) and comb-type structural morphology. Different copolymers of hydroxyethyl acrylate and methyl methacrylate (HEMMA) were synthesized by solution polymerization using azo-bis-(isobutyronitrile) (AIBN) as initiator and dimethylformamide as a solvent. The proportions utilized of AIBN were 0.5 (HEMMA1), 1.0 (HEMMA2), 1.5 (HEMMA3) and 2.0 wt. % (HEMMA4). The conversion percentage of the reaction was higher than 90%. The formation of the copolymers was evidenced by infrared analysis, hydroxyl value, and nuclear magnetic resonance. The intensity of OH group adsorption increased with the molecular weight and hydroxyl value. The polydispersity index was lower than 1.5. All copolymers exhibited a stable region on viscosity at a shear rate between 0.1 and 10 s–1. The copolymers exhibited good thermal stability, flexibility, and adherence. |
publishDate |
2016 |
dc.date.issued.none.fl_str_mv |
2016-08-04 |
dc.date.accessioned.none.fl_str_mv |
2021-11-16T21:52:56Z |
dc.date.available.none.fl_str_mv |
2021-11-16T21:52:56Z |
dc.type.spa.fl_str_mv |
Artículo de revista |
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publishedVersion |
dc.identifier.uri.none.fl_str_mv |
http://repositorio.ufps.edu.co/handle/ufps/1026 |
dc.identifier.doi.none.fl_str_mv |
https://doi.org/10.1590/0104-1428.1896 |
url |
http://repositorio.ufps.edu.co/handle/ufps/1026 https://doi.org/10.1590/0104-1428.1896 |
dc.language.iso.spa.fl_str_mv |
eng |
language |
eng |
dc.relation.ispartof.none.fl_str_mv |
Polímeros |
dc.relation.citationedition.spa.fl_str_mv |
Vol.26 No.3.(2016) |
dc.relation.citationendpage.spa.fl_str_mv |
261 |
dc.relation.citationissue.spa.fl_str_mv |
3 (2016) |
dc.relation.citationstartpage.spa.fl_str_mv |
254 |
dc.relation.citationvolume.spa.fl_str_mv |
26 |
dc.relation.cites.none.fl_str_mv |
Mejia, M., & Murillo, E. (2016). Study of the structural, thermal, rheological and film properties of functional copolymers of hydroxyethyl acrylate and methyl methacrylate. Polímeros, 26, 254-261. |
dc.relation.ispartofjournal.spa.fl_str_mv |
Polímeros |
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Atribución 4.0 Internacional (CC BY 4.0) |
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openAccess |
rights_invalid_str_mv |
Atribución 4.0 Internacional (CC BY 4.0) http://purl.org/coar/access_right/c_abf2 |
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Polimeros |
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Brasilia, Brasil |
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https://www.scielo.br/j/po/a/mhF8mjqL4MHvGHW4xQqJHFS/?format=html&lang=en |
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Universidad Francisco de Paula Santander |
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Murillo, Edwin A.7ab07880daea21ce0ce8b90d2f638d95600Mejia, Maria Cristina8a8ce8f0830abed95afd783486e4a3f82021-11-16T21:52:56Z2021-11-16T21:52:56Z2016-08-04http://repositorio.ufps.edu.co/handle/ufps/1026https://doi.org/10.1590/0104-1428.1896New functional polymers will be prepared using alkyd resins having high solid content (environmentally friendly) and comb-type structural morphology. Different copolymers of hydroxyethyl acrylate and methyl methacrylate (HEMMA) were synthesized by solution polymerization using azo-bis-(isobutyronitrile) (AIBN) as initiator and dimethylformamide as a solvent. The proportions utilized of AIBN were 0.5 (HEMMA1), 1.0 (HEMMA2), 1.5 (HEMMA3) and 2.0 wt. % (HEMMA4). The conversion percentage of the reaction was higher than 90%. The formation of the copolymers was evidenced by infrared analysis, hydroxyl value, and nuclear magnetic resonance. The intensity of OH group adsorption increased with the molecular weight and hydroxyl value. The polydispersity index was lower than 1.5. All copolymers exhibited a stable region on viscosity at a shear rate between 0.1 and 10 s–1. The copolymers exhibited good thermal stability, flexibility, and adherence.application/pdfengPolimerosBrasilia, BrasilPolímerosVol.26 No.3.(2016)2613 (2016)25426Mejia, M., & Murillo, E. (2016). Study of the structural, thermal, rheological and film properties of functional copolymers of hydroxyethyl acrylate and methyl methacrylate. Polímeros, 26, 254-261.PolímerosThis is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.info:eu-repo/semantics/openAccessAtribución 4.0 Internacional (CC BY 4.0)http://purl.org/coar/access_right/c_abf2https://www.scielo.br/j/po/a/mhF8mjqL4MHvGHW4xQqJHFS/?format=html&lang=enStudy of the structural, thermal, rheological and film properties of functional copolymers of hydroxyethyl acrylate and methyl methacrylateArtículo de revistahttp://purl.org/coar/resource_type/c_6501http://purl.org/coar/resource_type/c_2df8fbb1Textinfo:eu-repo/semantics/articlehttp://purl.org/redcol/resource_type/ARTinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/version/c_970fb48d4fbd8a85hydroxyethyl acrylatemethyl methacrylatesynthesiscopolymerizationpropertiesMurillo, E. A., López, B. L., & Hess, M.(2004). Synthesis and characterization of a pressure-sensitive adhesive based on an isobutyl acrylate / 2-ethylhexyl acrylate copolymer. e-polymer, 28, 1-10.Silvestri, D., Gagliardi, M., Cristallini, C., Barbani, N., & Giusti, P. (2009). Different composition poly (methyl methacrylate-co-butyl methacrylate) copolymers through seeded semi-batch emulsion polymerization. Polymer Bulletin, 63(3), 423-439. http://dx.doi.org/10.1007/s00289-009-0095-2Yeon, K., Yeon, J., Choi, Y., & Min, S. (2014). Deformation behavior of acrylic polymer concrete: Effects of methacrylic acid and curing temperature. Construction & Building Materials, 63, 125-131. http://dx.doi.org/10.1016/j.conbuildmat.2014.04.051Chen, J. J., Ahmad, A. L., & Ooi, B. S. (2014). Thermo-responsive properties of poly(N-isopropylacrylamide-co-acrylic acid) hydrogel and its effect on copper ion removal and fouling of polymer-enhanced ultrafiltration. Journal of Membrane Science, 469, 73-86. http://dx.doi.org/10.1016/j.memsci.2014.05.062Murillo, E. A., & López, B. L. (2011). Novel waterborne hyperbranched acrylated-maleinized alkyd resins. Progress in Organic Coatings, 72(4), 731-738. http://dx.doi.org/10.1016/j.porgcoat.2011.08.004Miller, K. R., & Soucek, M. D. (2012). Photopolymerization of biocompatible films containing poly(lactic acid). European Polymer Journal, 48(12), 2107-2116. http://dx.doi.org/10.1016/j.eurpolymj.2012.08.006Çaykara, T., Özyürek, C., Kantoğlu, Ö., & Erdoğan, B. (2003). Thermal behavior of poly(2-hydroxyethyl methacrylate-maleic acid) networks. Polymer Degradation & Stability, 80(2), 339-343. http://dx.doi.org/10.1016/S0141-3910(03)00018-1Taghizadeh, S. M., & Ghasemi, D. (2010). Synthesis and optimization of a four-component acrylic-based copolymer as pressure sensitive adhesive. Iranian Polymer Journal, 19, 343-352.Kowalczyk, K., Spychaj, T., Ubowska, A., & Schmidt, B. (2014). Industrially applicable methods of poly(methyl methacrylate)/organophilic montmorillonite nanocomposites preparation: processes and cast materials characterization. Applied Clay Science, 97, 96-103. http://dx.doi.org/10.1016/j.clay.2014.05.011Ozbay, S., & Erbil, H. Y. (2014). Solution copolymerization of perfluoroalkyl ethyl methacrylate with methyl methacrylate and butyl acrylate: synthesis and surface properties. Colloids and Surfaces. A, Physicochemical and Engineering Aspects, 452, 9-17. http://dx.doi.org/10.1016/j.colsurfa.2014.03.054Shan, X., Liu, Y. C., & Lam, Y. C. (2008). Studies of polymer deformation and recovery in micro hot embossing. Microsystem Technologies, 14(7), 1055-1060. http://dx.doi.org/10.1007/s00542-007-0486-yMoayed, S. H., Fatemi, S., & Pourmahdian, S. (2007). Synthesis of a latex with bimodal particle size distribution for coating applications using acrylic monomers. Progress in Organic Coatings, 60(4), 312-319. http://dx.doi.org/10.1016/j.porgcoat.2007.07.023Park, S. G., Kwak, N. S., Hwang, C. W., Park, H., & Hwang, T. S. (2012). Synthesis and characteristics of aminated vinylbenzyl chloride-co-styrene-co-hydroxyethyl acrylate anion-exchange membrane for redox flow battery applications. Journal of Membrane Science, 423, 429-437. http://dx.doi.org/10.1016/j.memsci.2012.08.040Dziczkowski, J., & Soucek, M. D. (2012). Factors influencing the stability and film properties of acrylic/alkyd water-reducible hybrid systems using a response surface technique. Progress in Organic Coatings, 73(4), 330-343. http://dx.doi.org/10.1016/j.porgcoat.2011.03.005Harakawa, H., Kasari, A., Tominaga, A., & Yabuta, M. (1998). The rheological properties of an aqueous acrylic dispersion suitable for automotive waterborne basecoats. Progress in Organic Coatings, 34(1-4), 84-90. http://dx.doi.org/10.1016/S0300-9440(98)00003-4Gómez, J. L., Monleón, M., Gallego, G., Peidro, N., Pérez, V., Pissis, P., & Kyritsis, A. (1999). Poly(methyl acrylate)/poly(hydroxyethyl acrylate) sequential interpenetrating polymer networks. Miscibility and water sorption behavior. Journal of Polymer Science. Part B, Polymer Physics, 37, 1587-1599. http://dx.doi.org/10.1002/(SICI)1099-0488(19990715)37:14<1587Pourjavadi, A., Samadi, M., & Ghasemzadeh, H. (2008). Fast-swelling superabsorbent hydrogels from poly(2-hydroxy ethyl acrylate-co-sodium acrylate) grafted on starch. Stärke, 60(2), 79-86. http://dx.doi.org/10.1002/star.200700666Sahloul, N., Emwas, A., Power, W., & Penlidis, A. (2005). Ethyl acrylate‐hydroxyethyl acrylate and hydroxyethyl acrylate‐methacrylic acid: reactivity ratio estimation from cross‐linked polymer using high resolution magic angle spinning spectroscopy. Journal of Macromolecular Science, Part A: Pure and Applied Chemistry, 42(10), 1369-1385. http://dx.doi.org/10.1080/10601320500205558Mun, G. A., Nurkeeva, Z. S., Dergunov, S. A., Nam, I. K., Maimakov, T. P., Shaikhutdinov, E. M., Lee, S. C., & Park, K. (2008). Studies on graft copolymerization of 2-hydroxyethyl acrylate onto chitosan. Reactive & Functional Polymers, 68(1), 389-395. http://dx.doi.org/10.1016/j.reactfunctpolym.2007.07.012Lee, J. H., & Kim, J. J. (2014). Poly(hydroxyethyl acrylate-co-coumaryl acrylate) as a photo-responsive amphiphile. Journal of Industrial and Engineering Chemistry, 20(5), 3075-3080. http://dx.doi.org/10.1016/j.jiec.2013.11.046Henini, G., Souahi, F., & Laidani, Y. (2012). Tracking offline conversion solution polymerization of methyl methacrylate / vinyl acetate in toluene in a reactor calorimeter. Procedia Engineering, 33, 225-233. http://dx.doi.org/10.1016/j.proeng.2012.01.1198Murillo, E. A., Vallejo, P. P., & López, B. L. (2010). Synthesis and characterization of hyperbranched alkyd resins based on tall oil fatty acids. Progress in Organic Coatings, 69(3), 235-240. http://dx.doi.org/10.1016/j.porgcoat.2010.04.018Murillo, E. A., Vallejo, P. P., & López, B. L. (2011). Effect of tall oil fatty acids content on the properties of novel hyperbranched alkyd resins. Journal of Applied Polymer Science, 112(6), 3151-3158. http://dx.doi.org/10.1002/app.33502Murillo, E. A., López, B. L., & Brostow, W. (2011). Synthesis and characterization of novel alkyd–silicone hyperbranched nanoresins with high solid contents. Progress in Organic Coatings, 72(3), 292-298. http://dx.doi.org/10.1016/j.porgcoat.2011.04.019Chen, S., Hu, T., Tian, Y., Chen, L., & Pojman, J. A. (2007). Facile synthesis of poly(hydroxyethyl acrylate) by frontal free-radical polymerization. Journal of Polymer Science. Part A, Polymer Chemistry, 45(5), 873-881. http://dx.doi.org/10.1002/pola.21865Moad, G., Rizzardo, E., & Thang, S. H. (2005). Living radical polymerization by the RAFT process. Australian Journal of Chemistry, 58(6), 379-410. http://dx.doi.org/10.1071/CH05072Jain, M., Vora, R. A., & Satpathy, U. S. (2003). Kinetics of emulsion copolymerization of methylmethacrylate and ethylacrylate: effect of type and concentration of initiator in unseeded polymerization system. European Polymer Journal, 39(10), 2069-2076. http://dx.doi.org/10.1016/S0014-3057(02)00347-6Xu, M., Yan, X., Cheng, R., & Yu, X. (2001). Investigation into the solution properties of hyperbranched polymer. Polymer International, 50(12), 1338-1345. http://dx.doi.org/10.1002/pi.740Murillo, E. A., Vallejo, P. P., Sierra, L., & López, B. L. (2009). Characterization of hyperbranched polyol polyesters based on 2,2-bis (methylol propionic acid) and pentaerythritol. Journal of Applied Polymer Science, 112(1), 200-207. http://dx.doi.org/10.1002/app.29397Murillo, E. A., Cardona, A., & López, B. L. (2011). Rheological behavior in the molten state and solution of hyperbranched polyester of fourth and fifth generation. Journal of Applied Polymer Science, 119(2), 929-935. http://dx.doi.org/10.1002/app.32774Murillo, E. A., Vallejo, P. P., & López, B. L. (2010). Characterization of hydroxylated hyperbranched polyesters of fourth and fifth generation. Polymer, 10(1), 1347-1358. http://dx.doi.org/10.1515/epoly.2010.10.1.1347Perera, D., & Shanks, R. A. (1995). Synthesis and rheological properties of soluble poly(hydroxyethyl methacrylate) and some copolymers. Polymer International, 36(4), 303-308. http://dx.doi.org/10.1002/pi.1995.210360401McManus, N. T., Kim, J. D., & Penlidis, A. (1998). Observations on styrene-hydroxyethyl acrylate and styrene-hydroxyethyl acrylate-ethyl acrylate polymerizations. Polymer Bulletin, 41(6), 661-668. http://dx.doi.org/10.1007/s002890050415Peykova, Y., Lebedeva, O. V., Diethert, A., Müller-Buschbaum, P., & Willenbacher, N. (2012). Adhesive properties of acrylate copolymers: effect of the nature of the substrate and copolymer functionality. International Journal of Adhesion and Adhesives, 34, 107-116. http://dx.doi.org/10.1016/j.ijadhadh.2011.12.001LICENSElicense.txtlicense.txttext/plain; charset=utf-814828https://repositorio.ufps.edu.co/bitstream/ufps/1026/2/license.txt2f9959eaf5b71fae44bbf9ec84150c7aMD52open accessORIGINALStudy of the structural, thermal, rheological and film properties of functional copolymers of hydroxyethyl acrylate and methyl methacrylate.pdfStudy of the structural, thermal, rheological and film properties of functional copolymers of hydroxyethyl acrylate and methyl methacrylate.pdfapplication/pdf1705448https://repositorio.ufps.edu.co/bitstream/ufps/1026/1/Study%20of%20the%20structural%2c%20thermal%2c%20rheological%20and%20film%20properties%20of%20functional%20copolymers%20of%20hydroxyethyl%20acrylate%20and%20methyl%20methacrylate.pdf8674e85fb282859a85c6827e7a046120MD51open accessTEXTStudy of the structural, thermal, rheological and film properties of functional copolymers of hydroxyethyl acrylate 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 incorporada en las Obras Colectivas.

b.	Distribuir copias o fonogramas de las Obras, exhibirlas públicamente, ejecutarlas públicamente y/o ponerlas a disposición pública, incluyéndolas como incorporadas en Obras Colectivas, según corresponda.

c.	Distribuir copias de las Obras Derivadas que se generen, exhibirlas públicamente, ejecutarlas públicamente y/o ponerlas a disposición pública.
Los derechos mencionados anteriormente pueden ser ejercidos en todos los medios y formatos, actualmente conocidos o que se inventen en el futuro. Los derechos antes mencionados incluyen el derecho a realizar dichas modificaciones en la medida que sean técnicamente necesarias para ejercer los derechos en otro medio o formatos, pero de otra manera usted no está autorizado para realizar obras derivadas. Todos los derechos no otorgados expresamente por el Licenciante quedan por este medio reservados, incluyendo pero sin limitarse a aquellos que se mencionan en las secciones 4(d) y 4(e).

4. Restricciones.
La licencia otorgada en la anterior Sección 3 está expresamente sujeta y limitada por las siguientes restricciones:

a.	Usted puede distribuir, exhibir públicamente, ejecutar públicamente, o poner a disposición pública la Obra sólo bajo las condiciones de esta Licencia, y Usted debe incluir una copia de esta licencia o del Identificador Universal de Recursos de la misma con cada copia de la Obra que distribuya, exhiba públicamente, ejecute públicamente o ponga a disposición pública. No es posible ofrecer o imponer ninguna condición sobre la Obra que altere o limite las condiciones de esta Licencia o el ejercicio de los derechos de los destinatarios otorgados en este documento. No es posible sublicenciar la Obra. Usted debe mantener intactos todos los avisos que hagan referencia a esta Licencia y a la cláusula de limitación de garantías. Usted no puede distribuir, exhibir públicamente, ejecutar públicamente, o poner a disposición pública la Obra con alguna medida tecnológica que controle el acceso o la utilización de ella de una forma que sea inconsistente con las condiciones de esta Licencia. Lo anterior se aplica a la Obra incorporada a una Obra Colectiva, pero esto no exige que la Obra Colectiva aparte de la obra misma quede sujeta a las condiciones de esta Licencia. Si Usted crea una Obra Colectiva, previo aviso de cualquier Licenciante debe, en la medida de lo posible, eliminar de la Obra Colectiva cualquier referencia a dicho Licenciante o al Autor Original, según lo solicitado por el Licenciante y conforme lo exige la cláusula 4(c).

b.	Usted no puede ejercer ninguno de los derechos que le han sido otorgados en la Sección 3 precedente de modo que estén principalmente destinados o directamente dirigidos a conseguir un provecho comercial o una compensación monetaria privada. El intercambio de la Obra por otras obras protegidas por derechos de autor, ya sea a través de un sistema para compartir archivos digitales (digital file-sharing) o de cualquier otra manera no será considerado como estar destinado principalmente o dirigido directamente a conseguir un provecho comercial o una compensación monetaria privada, siempre que no se realice un pago mediante una compensación monetaria en relación con el intercambio de obras protegidas por el derecho de autor.

c.	Si usted distribuye, exhibe públicamente, ejecuta públicamente o ejecuta públicamente en forma digital la Obra o cualquier Obra Derivada u Obra Colectiva, Usted debe mantener intacta toda la información de derecho de autor de la Obra y proporcionar, de forma razonable según el medio o manera que Usted esté utilizando: (i) el nombre del Autor Original si está provisto (o seudónimo, si fuere aplicable), y/o (ii) el nombre de la parte o las partes que el Autor Original y/o el Licenciante hubieren designado para la atribución (v.g., un instituto patrocinador, editorial, publicación) en la información de los derechos de autor del Licenciante, términos de servicios o de otras formas razonables; el título de la Obra si está provisto; en la medida de lo razonablemente factible y, si está provisto, el Identificador Uniforme de Recursos (Uniform Resource Identifier) que el Licenciante especifica para ser asociado con la Obra, salvo que tal URI no se refiera a la nota sobre los derechos de autor o a la información sobre el licenciamiento de la Obra; y en el caso de una Obra Derivada, atribuir el crédito identificando el uso de la Obra en la Obra Derivada (v.g., "Traducción Francesa de la Obra del Autor Original," o "Guión Cinematográfico basado en la Obra original del Autor Original"). Tal crédito puede ser implementado de cualquier forma razonable; en el caso, sin embargo, de Obras Derivadas u Obras Colectivas, tal crédito aparecerá, como mínimo, donde aparece el crédito de cualquier otro autor comparable y de una manera, al menos, tan destacada como el crédito de otro autor comparable.

d.	Para evitar toda confusión, el Licenciante aclara que, cuando la obra es una composición musical:

i.	Regalías por interpretación y ejecución bajo licencias generales. El Licenciante se reserva el derecho exclusivo de autorizar la ejecución pública o la ejecución pública digital de la obra y de recolectar, sea individualmente o a través de una sociedad de gestión colectiva de derechos de autor y derechos conexos (por ejemplo, SAYCO), las regalías por la ejecución pública o por la ejecución pública digital de la obra (por ejemplo Webcast) licenciada bajo licencias generales, si la interpretación o ejecución de la obra está primordialmente orientada por o dirigida a la obtención de una ventaja comercial o una compensación monetaria privada.

ii.	Regalías por Fonogramas. El Licenciante se reserva el derecho exclusivo de recolectar, individualmente o a través de una sociedad de gestión colectiva de derechos de autor y derechos conexos (por ejemplo, los consagrados por la SAYCO), una agencia de derechos musicales o algún agente designado, las regalías por cualquier fonograma que Usted cree a partir de la obra (“versión cover”) y distribuya, en los términos del régimen de derechos de autor, si la creación o distribución de esa versión cover está primordialmente destinada o dirigida a obtener una ventaja comercial o una compensación monetaria privada.

e.	Gestión de Derechos de Autor sobre Interpretaciones y Ejecuciones Digitales (WebCasting). Para evitar toda confusión, el Licenciante aclara que, cuando la obra sea un fonograma, el Licenciante se reserva el derecho exclusivo de autorizar la ejecución pública digital de la obra (por ejemplo, webcast) y de recolectar, individualmente o a través de una sociedad de gestión colectiva de derechos de autor y derechos conexos (por ejemplo, ACINPRO), las regalías por la ejecución pública digital de la obra (por ejemplo, webcast), sujeta a las disposiciones aplicables del régimen de Derecho de Autor, si esta ejecución pública digital está primordialmente dirigida a obtener una ventaja comercial o una compensación monetaria privada.

5. Representaciones, Garantías y Limitaciones de Responsabilidad.
A MENOS QUE LAS PARTES LO ACORDARAN DE OTRA FORMA POR ESCRITO, EL LICENCIANTE OFRECE LA OBRA (EN EL ESTADO EN EL QUE SE ENCUENTRA) “TAL CUAL”, SIN BRINDAR GARANTÍAS DE CLASE ALGUNA RESPECTO DE LA OBRA, YA SEA EXPRESA, IMPLÍCITA, LEGAL O CUALQUIERA OTRA, INCLUYENDO, SIN LIMITARSE A ELLAS, GARANTÍAS DE TITULARIDAD, COMERCIABILIDAD, ADAPTABILIDAD O ADECUACIÓN A PROPÓSITO DETERMINADO, AUSENCIA DE INFRACCIÓN, DE AUSENCIA DE DEFECTOS LATENTES O DE OTRO TIPO, O LA PRESENCIA O AUSENCIA DE ERRORES, SEAN O NO DESCUBRIBLES (PUEDAN O NO SER ESTOS DESCUBIERTOS). ALGUNAS JURISDICCIONES NO PERMITEN LA EXCLUSIÓN DE GARANTÍAS IMPLÍCITAS, EN CUYO CASO ESTA EXCLUSIÓN PUEDE NO APLICARSE A USTED.

6. Limitación de responsabilidad.
A MENOS QUE LO EXIJA EXPRESAMENTE LA LEY APLICABLE, EL LICENCIANTE NO SERÁ RESPONSABLE ANTE USTED POR DAÑO ALGUNO, SEA POR RESPONSABILIDAD EXTRACONTRACTUAL, PRECONTRACTUAL O CONTRACTUAL, OBJETIVA O SUBJETIVA, SE TRATE DE DAÑOS MORALES O PATRIMONIALES, DIRECTOS O INDIRECTOS, PREVISTOS O IMPREVISTOS PRODUCIDOS POR EL USO DE ESTA LICENCIA O DE LA OBRA, AUN CUANDO EL LICENCIANTE HAYA SIDO ADVERTIDO DE LA POSIBILIDAD DE DICHOS DAÑOS. ALGUNAS LEYES NO PERMITEN LA EXCLUSIÓN DE CIERTA RESPONSABILIDAD, EN CUYO CASO ESTA EXCLUSIÓN PUEDE NO APLICARSE A USTED.

7. Término.

a.	Esta Licencia y los derechos otorgados en virtud de ella terminarán automáticamente si Usted infringe alguna condición establecida en ella. Sin embargo, los individuos o entidades que han recibido Obras Derivadas o Colectivas de Usted de conformidad con esta Licencia, no verán terminadas sus licencias, siempre que estos individuos o entidades sigan cumpliendo íntegramente las condiciones de estas licencias. Las Secciones 1, 2, 5, 6, 7, y 8 subsistirán a cualquier terminación de esta Licencia.

b.	Sujeta a las condiciones y términos anteriores, la licencia otorgada aquí es perpetua (durante el período de vigencia de los derechos de autor de la obra). No obstante lo anterior, el Licenciante se reserva el derecho a publicar y/o estrenar la Obra bajo condiciones de licencia diferentes o a dejar de distribuirla en los términos de esta Licencia en cualquier momento; en el entendido, sin embargo, que esa elección no servirá para revocar esta licencia o que deba ser otorgada , bajo los términos de esta licencia), y esta licencia continuará en pleno vigor y efecto a menos que sea terminada como se expresa atrás. La Licencia revocada continuará siendo plenamente vigente y efectiva si no se le da término en las condiciones indicadas anteriormente.

8. Varios.

a.	Cada vez que Usted distribuya o ponga a disposición pública la Obra o una Obra Colectiva, el Licenciante ofrecerá al destinatario una licencia en los mismos términos y condiciones que la licencia otorgada a Usted bajo esta Licencia.

b.	Si alguna disposición de esta Licencia resulta invalidada o no exigible, según la legislación vigente, esto no afectará ni la validez ni la aplicabilidad del resto de condiciones de esta Licencia y, sin acción adicional por parte de los sujetos de este acuerdo, aquélla se entenderá reformada lo mínimo necesario para hacer que dicha disposición sea válida y exigible.

c.	Ningún término o disposición de esta Licencia se estimará renunciada y ninguna violación de ella será consentida a menos que esa renuncia o consentimiento sea otorgado por escrito y firmado por la parte que renuncie o consienta.

d.	Esta Licencia refleja el acuerdo pleno entre las partes respecto a la Obra aquí licenciada. No hay arreglos, acuerdos o declaraciones respecto a la Obra que no estén especificados en este documento. El Licenciante no se verá limitado por ninguna disposición adicional que pueda surgir en alguna comunicación emanada de Usted. Esta Licencia no puede ser modificada sin el consentimiento mutuo por escrito del Licenciante y Usted.
0000-0002-0617-23277ab07880daea21ce0ce8b90d2f638d95600 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