Littérature scientifique sur le sujet « Resin »
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Articles de revues sur le sujet "Resin"
Talango, Novriyanti, et Wawan Rauf. « ANALISIS KEKUATAN TARIK MATERIAL KOMPOSIT BERBAHAN SERAT BAMBU MAYAM ». JURNAL SIMETRIK 13, no 2 (18 janvier 2024) : 729–33. http://dx.doi.org/10.31959/js.v13i2.1897.
Texte intégralPatel, Hasmukh S., et Amel Muhson Naji. « Novel unsaturated polyester resins based on (maleated cyclohexanone-formaldehyde resin)-(epoxy resin) condensation ». International Journal of Plastics Technology 14, no 1 (juin 2010) : 17–37. http://dx.doi.org/10.1007/s12588-010-0012-4.
Texte intégralSanclimens, Glòria, Laia Crespo, Miquel Pons, Ernest Giralt, Fernando Albericio et Miriam Royo. « Saturated resins or stress of the resin ». Tetrahedron Letters 44, no 9 (février 2003) : 1751–54. http://dx.doi.org/10.1016/s0040-4039(03)00109-6.
Texte intégralPokonova, Yu V. « Resins and asphaltenes–modifiers for epoxy resin ». Chemistry and Technology of Fuels and Oils 43, no 2 (mars 2007) : 135–39. http://dx.doi.org/10.1007/s10553-007-0026-6.
Texte intégralThompson, Kim A., et Dennis G. Hall. « Resin-to-resin Petasis borono-Mannich reaction between dialkylamino resins and supported boronic acids ». Chemical Communications, no 23 (2000) : 2379–80. http://dx.doi.org/10.1039/b006279k.
Texte intégralHoshi, Ikuo. « Phenol-formaldehyde resin/epoxy resin. » Kobunshi 37, no 11 (1988) : 824–25. http://dx.doi.org/10.1295/kobunshi.37.824.
Texte intégralWatts, David C. « Resin composite or composite resin ? » Dental Materials 36, no 9 (septembre 2020) : 1115. http://dx.doi.org/10.1016/j.dental.2020.07.002.
Texte intégralMUSTATA, FANICA, et IOAN BICU. « Epoxy aniline formaldehyde resins modified with resin acids ». Polimery 46, no 07/08 (juillet 2001) : 534–39. http://dx.doi.org/10.14314/polimery.2001.534.
Texte intégralRobertson, Frank C. « Resin transfer moulding of aerospace resins—a review ». British Polymer Journal 20, no 5 (1988) : 417–29. http://dx.doi.org/10.1002/pi.4980200506.
Texte intégralCelik, Cigdem, Sevi Burcak Cehreli et Neslihan Arhun. « Resin composite repair : Quantitative microleakage evaluation of resin-resin and resin-tooth interfaces with different surface treatments ». European Journal of Dentistry 09, no 01 (janvier 2015) : 092–99. http://dx.doi.org/10.4103/1305-7456.149652.
Texte intégralThèses sur le sujet "Resin"
Nelson, Christopher Lee. « Resin ». NCSU, 2008. http://www.lib.ncsu.edu/theses/available/etd-05062008-125114/.
Texte intégralMarinho, Márcio Leandro Von Dreifus [UNESP]. « Influência da interposição de diferentes cerâmicas no grau de conversão de agentes cimentantes resinosos ». Universidade Estadual Paulista (UNESP), 2010. http://hdl.handle.net/11449/97357.
Texte intégral3M ESPE
O objetivo deste estudo foi avaliar o grau de conversão de agentes cimentantes resinosos polimerizados sob diferentes espessuras de cerâmica feldspática e diferentes sistemas cerâmicos de mesma espessura. No primeiro estudo, oitenta amostras dos cimentos resinosos RelyX ARC (3M Espe) e RelyX Veneer (3M Espe) foram confeccionadas sob discos de cerâmica convencional Starlight (DeguDent) com espessuras de 0,5mm, 1,2mm, 1,8mm e 2,4mm. No segundo estudo, oitenta amostras dos cimentos resinosos RelyX ARC (3M Espe) e Maxcem Elite (Kerr) foram confeccionadas sob discos de diferentes sistemas cerâmicos: Starlight (DeguDent), Empress (Ivoclair Vivadent), E-max (Ivoclair Vivadent), In Ceram Alumina (Vita) e In Ceram Zircônia (Vita) com espessuras de 2,0mm. A leitura do grau de conversão dos cimentos resinosos foi realizada 10 minutos, 1 hora e 24 horas após a fotoativação dos cimentos, em espectrofotômetro FTIR Nexus 670 (Nicolet). Os resultados do primeiro estudo mostraram que o cimento resinoso dual RelyX ARC apresentou maior grau de conversão que o cimento fotoativado RelyX Veneer em todas as espessuras de cerâmica, inclusive sem interposição (p<0.0001). Os valores de grau de conversão obtidos após 1 hora e 24 horas não diferiram estatisticamente entre si (p=0.7433), mas foram superiores aos analisados após 10 minutos (p<0.0001). Para o cimento fotoativado, houve aumento gradativo no grau de conversão de 10 minutos até 24 horas (p<0.0001). No segundo estudo, os maiores valores de grau de conversão foram obtidos para as amostras polimerizadas sob as cerâmicas reforçadas por leucita e dissilicato de lítio, sem diferença estatisticamente significante entre si (p=0.1181), enquanto os menores valores do grau de conversão obtidos foram das amostras polimerizadas sob cerâmicas reforçadas por alumina e zircônia, sem diferença entre si (p=0.2374). Com base nos resultados destes...
The aim of this study was to evaluate the degree of conversion of resin cements polymerized under different thicknesses of feldspatic ceramic and different ceramic systems with the same thickness. In the first study, eighty samples of RelyX ARC (3M Espe) and RelyX Veneer (3M Espe) were polymerized under conventional ceramic discs (Starlight, DeguDent) with thickness of 0.5 mm 1.2 mm, 1.8 mm and 2.4 mm. In the second study, eighty samples of RelyX ARC (3M Espe) and Maxcem Elite (Kerr) resin cements were polymerized over ceramics systems: Starlight (DeguDent), Empress (Ivoclar Vivadent), E-max (Ivoclar Vivadent), In Ceram Alumina (Vita) and In Ceram Zircon (Vita) with 2.0 mm of thickness. The degree of conversion of the resin cements was calculated 10 minutes, 1 hour and 24 hours after the curing of cements using a Nexus 670 FTIR spectrophotometer (Nicolet). The RelyX ARC showed higher values of degree of conversion than RelyX Veneer considering all the ceramics thickness in the first study. The measurements obtained after 1 hour and 24 hours did not differ significantly (p=0.7433), but were higher than those analyzed after 10 minutes (p<0.0001). Comparing the ceramic systems in the second study, the highest degree of conversion were obtained for samples polymerized under Empress and e.max ceramics, without statistically difference between them (p= 0.1181) and the lower values of conversion were obtained for the samples polymerized under In Ceram Alumina and In Ceram Zircon ceramics (p= 0.2374). Based on the results of these studies, we can conclude that the thickness of feldspatic porcelain as well as the ceramic system itself could influence the degree of conversion of light- and dual-cured resin cements. All the resin cements showed an increase on the degree of conversion after 24 hours, which could create an especial guideline for the clinical procedures using resin cements
Avila, Gisseli Bertozzi de. « Resina industrial de poliuretano modificada com terra diatomácea para ser empregada na modelagem odontológica ». Universidade de São Paulo, 2009. http://www.teses.usp.br/teses/disponiveis/58/58131/tde-26032010-124102/.
Texte intégralThis study evaluated the high performance polyurethane resin 6470 and hardener Dt 082 (Huntsman Advanced Materials Química Brasil Ltda., supplied by Maxepoxi, Santo Amaro, São Paulo, Brazil) loaded with 30 % diatomite, for use in dental modeling. The material was manipulated in the ratio of 1:8 between resin and hardener, with the addition of the polyurethane accelerator in the proportion of one drop for each 200 grams of resin. Samples of pure resin, modified with diatomite type IV plaster (Fuji Rock EP), GC America Inc-USA, were obtained for the following tests: resistance to compression; diametral compression test ASTM D 695 2(a) to obtain tensile strength, and resistance to fracture by impact ISO 179-1: 2000., three point bending flexural test (ISO 1567:1999); resistance to wear by abrasion, Standard ASTM D 4060. Samples were analyzed with regard to dimensional behavior in a profile projector (Mitutoyo PJ-A3000 Japan); surface roughness Ra, and capacity to copy details were analyzed in a Roughness meter (Mitutoyo Surftest SJ-301 - Japan), surface hardness was analyzed in a Sussen Wolpert durometer Type Tester HT1, with the Rockwell Hardness method. The compatibility of the resin with molding elastomers was analyzed by the criteria of modeling material adherence to the mold and color alteration of the model obtained. The resistance to compression test and diametral compression test for tensile strength were performed in a Universal Test Machine EMIC DL2000, with a 2000 Kgf load cell and speed of 1.3 mm/min. The bending flexural test was performed in the same equipment with a distance of 52 mm between the supports, 2000 Kgf load cell and speed of 5 mm/min. The resistance to fracture by impact was tested in a CEAST Impact Machine model Resil 25 using the Charpy type test. The test for resistance to wear by abrasion was performed in a TABER abrasimeter, which determines the loss of mass per 1000 cycles, using the standard CS-17 abrasive wheel (grindstone) with a 1000g load, ASTM D 4060. The data obtained were statistically analyzed by the analysis of variance and Tukey tests at the level of significance of 95%, and it was verified that: The pure or diatomite-modified polyurethane resin, considering the two criteria adopted, is compatible with condensation and addition silicone; the copying capacity of the resin was reduced with the addition of diatomite, but remained superior to that of type IV plaster; the diatomite interfered in the surface roughness of the polyurethane resin, but the values were lower than those presented by the type IV plaster; diatomite added to the polyurethane resin increased the surface hardness, resistance to compression, traction resistance to diametral compression, resistance to wear by abrasion, impact, and to three point bending flexure. The pure and diatomite-modified polyurethane resin were superior to type IV plaster for resistance to compression, traction resistance to diametral compression, resistance to wear by abrasion, impact and three point bending flexure. Similar dimensional behavior was verified for type IV plaster and diatomite-modified polyurethane resin; the pure resin contracted, and the diatomite reduced polyurethane resin contraction. Conducting this study enabled the following conclusions to be drawn: The pure or diatomite-modified polyurethane resin is compatible with the condensation and addition silicone elastomers; the diatomite load of silicone percent increases the surface hardness, resistance to compression, traction resistance to diametral compression, resistance to fracture by impact, resistance to three point bending flexure, and resistance to wear by abrasion of polyurethane resin; when polyurethane resin is modified with 30% diatomite it has a dimensional behavior similar to that of type IV plaster; the diatomite reduced the polyurethane resin capacity to copy and increased its surface roughness, but the loaded resin presented less surface roughness and greater capacity to copy than the type IV plaster; in view of the results found by modifying the polyurethane resin with 30% diatomite, it is feasible to use this material in dental modeling.
Hill, David John. « Microwave preheating of thermosetting resin for resin transfer moulding ». Thesis, University of Nottingham, 1993. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.300723.
Texte intégralLongo, Daniele Lucca. « Avaliação da citotoxicidade e expressão de citocinas induzidas por resina composta fotopolimerizável ». Universidade de São Paulo, 2013. http://www.teses.usp.br/teses/disponiveis/58/58135/tde-22072013-112353/.
Texte intégralThe aim of this study was to evaluate in vitro the cytotoxicity and the production of cytokines induced by resin-based restorative materials containing new monomers KaloreTM (GC FUJI) and FiltekTM Silorane (3M ESPE) compared with conventional composite resins Charisma® (Heraeus-Kulzer) and FiltekTM Z250 (3M ESPE), in mice L929 fibroblast and RAW 264.7 macrophages culture. Cells were stimulated with the composite resins, light-cured or not, by indirect contact or extraction during 15, 45, and 120 days. After incubation for 6, 12, and 24 hours, cell viability was assessed by MTT assay and production of cytokines was investigated by enzyme-linked immunosorbent assay (ELISA). Data obtained were analyzed using oneway analysis of variance (ANOVA) and Tukey post-test ( α = 0.05). Production of TNF-α and IL-6 was not detected in L929 fibroblasts either 6, 12 or 24 hours following indirect contact with the KaloreTM and FiltekTM Silorane composite resins. On the other hand, the production of TNF-α was detected in RAW 264.7 macrophages, but was not influenced by indirect contact with composite resins, with the exception of the FiltekTM Silorane resin that inhibited the production of TNF-α, after 12 hours of incubation. The extracts obtained from incubation for 15 days with composite resins KaloreTM and FiltekTM Silorane were more cytotoxic than extracts incubated for 45 and 120 days. Cytotoxicity of composite KaloreTM was not influenced by light curing while cytotoxicity of FiltekTM Silorane resin was higher in the group that not received light-cure. Extracts of Charisma® and FiltekTM Z250 composite resins, obtained at 15, 45, and 120 days of incubation, were not cytotoxic 24 hours after stimulation of the cells. Also, FiltekTM Silorane, light-cured or not, stimulated the production of IL-6 following 45 days of incubation. KaloreTM resin extract for 15 days, unlike FiltekTM Silorane resin, stimulated the production of IL-10. However, during periods of 45 days of extraction, KaloreTM resin, light-cured, inhibited the production of IL-10, after 12 hours of incubation, and 120 days of extraction there was no detectable production of IL-10 in any of the groups.
Short, Christina Kaye. « Characterization of Epoxy Resins for use in the Resin Transfer Molding Process ». W&M ScholarWorks, 1993. https://scholarworks.wm.edu/etd/1539625806.
Texte intégralEsmeraldo, Milena Alencar. « PreparaÃÃo de novos compÃsitos suportados em matriz de fibra vegetal/natural ». Universidade Federal do CearÃ, 2006. http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=1450.
Texte intégralNos Ãltimos anos, houve um acelerado desenvolvimento na Ãrea de compÃsitos reforÃados por fibras naturais, como (juta, sisal, coco, linho etc.) Fibras naturais sÃo uma importante alternativa, pois apresentam as seguintes vantagens: abundÃncia, biodegrabilidade, baixo peso, regenerabilidade, nÃo sÃo tÃxicas, apresentam baixo custo de aplicaÃÃo comparado com as fibras sintÃticas e podem ser modificadas por tratamento quÃmico. O presente trabalho teve por objetivo a preparaÃÃo e caracterizaÃÃo de compÃsitos suportados, em matriz fenÃlica derivadas do LCC, reforÃados por fibras naturais de coco e juta. Foram conduzidas modificaÃÃes superficiais nas fibras atravÃs de tratamento alcalino (mercerizaÃÃo) NaOH nas concentraÃÃes 5% e 10% (75 0C) e branqueamento com hipoclorito de sÃdio (NaClO/H20 1:1) (60 0C). Os compÃsitos foram preparados por moldagem aberta com fibras de coco e juta para todos os tratamentos. As propriedades mecÃnicas, tÃrmicas, dielÃtricas bem como as investigaÃÃes superficiais das fibras antes e apÃs o tratamento quÃmico e interface dos compÃsitos foram investigados pelas tÃcnicas de ensaios de traÃÃo (elongaÃÃo à ruptura, mÃdulo elÃstico, resistÃncia à ruptura); TG/DTG (Termogravimetria/Derivada); DSC (Calorimetria ExploratÃria Diferencial); DRX (Difratograma de Raios X); propriedades dielÃtricas, (Perda DielÃtrica, Condutividade DielÃtrica) e MEV (Microscopia de Varredura EletrÃnica). Fibras de coco, juta e compÃsitos apresentaram um aumento global das propriedades mecÃnicas apÃs o tratamento quÃmico com NaOH 5% e 10% .Os melhores resultados foram aqueles observados para os compÃsitos de juta apÃs tratamento com NaOH 5% onde se observou um aumento de 28% na resistÃncia à ruptura, jà para os compÃsitos de coco os melhores resultados foram os apÃs tratamento com NaOH 10% com aumento de 48%. Os resultados de anÃlise termogravimÃtrica em atmosfera inerte mostraram processos de estabilidade tÃrmica para as fibras e compÃsitos apÃs o II tratamento quÃmico com NaOH 5% e 10 % respectivamente. Para as fibras de juta observou-se um aumento de (218-228 0C) para as de coco o aumento foi de (259- 276 0C). Os compÃsitos de juta e coco tambÃm apresentaram um aumento na estabilidade tÃrmica apÃs o tratamento quÃmico, onde os melhores resultados obtidos foram: compÃsitos de juta (302-3060C) apÃs tratamento com NaOH 5%, e os de coco (288-310 0C) apÃs tratamento com NaOH 10%. Esses resultados comprovaram que o tratamento alcalino de fato proporcionou uma melhora da estabilidade tÃrmica dos compÃsitos. As anÃlises de investigaÃÃo superficial das fibras de juta e coco apresentaram claramente modificaÃÃes estruturais como conseqÃÃncia da remoÃÃo parcial de constituintes apÃs o tratamento quÃmico. Para os compÃsitos dessas fibras, foi observado que apÃs o tratamento quÃmico, com a remoÃÃo de componentes nÃo celulÃsicos, ocorreu de fato uma melhor adesÃo, ou seja, interface agente de reforÃo/matriz fenÃlica.
In recent years there was a rapid development in the field of composites reinforced by natural fibers like (jute, sisal, coir, hemp etc). Natural fibers are an important alternative, offering several advantages such their abundant, biodegrability, light weight, renewability, are not toxic, presents low cost application compared with synthetic fibers and may be easily modified by chemical treatment. The present work aimed the study, preparation and characterization of composites of phenolic resin (matriz) based on CNSL, reinforced by natural fibers of coir and jute. Superficial modification on the fibers were carried out through alkali treatment (mercerization) NaOH 5% and NaOH 10% (75 0C) and bleaching with sodium hipoclorite (NaClO/H20 1:1) (60 0C). All the fibers composites were prepared by open mold. The composites and fibers were characterized by analysis techniques such mechanical tensile strength (elongation at break, youngâs modulus, resistant at break); TG/DTG (Thermogravimetry); DSC (Differential Scanning Calorimetric); DRX (Difractrogram X - Ray); dielectric properties (Dielectric Conductivity, Dielectric Loss) and SEM (Scanning Electron Microscopy) investigation on the surface modification in fibers and composites after chemical treatment. The results to coir and jute fibers composites showed an increase of mechanical properties. The best mechanical performance was generally obtained for composites of jute and coir after NaOH 5% and NaOH 10% showing an enhancement of mechanical properties resistant at break (28%) and (48%) respectively. IV The thermal degradation behavior of composites and coir - jute fibers under a nitrogen atmosphere showed an increase of thermal stability after alkaline treatment NaOH 5% e 10 % compared with untreated fibers. To jute fibers it was observed an improvement of (218-228 0C) to coir fibers this increased it was (259- 276 0C). The same thermal stability was evaluated to composites of theses fibers after alkaline treatment NaOH 5% and NaOH 10%. To jute fibers composites the best results were (302-3060C) while coir composites were (288-310 0C). From the results obtained, it is possible to conclude that alkaline treatment contribute to significant improvement of thermal behaviour of the composites The SEM investigation showed significant improvement on surfaces of jute and coir fibers after chemical treatment. The alkali treatment, removed non-celluloic components from fibers surface, expoding their internal fibrillar structure. As a consequence the treatment promoted an increase on interfacial adhesion between coir and jute fibers reinforced phenolic resin composite.
Sas, Hatice Sinem. « Modeling Of Particle Filled Resin Impregnation In Compression Resin Transfer Molding ». Master's thesis, METU, 2010. http://etd.lib.metu.edu.tr/upload/12612158/index.pdf.
Texte intégralAzzam, Mai Ahmed. « Flexural strength comparison of monolayer resin composite to bilayer resin/ liner composite ». Thesis, Connect to resource online, 2009. http://hdl.handle.net/1805/2077.
Texte intégralTitle from PDF t. p. (viewed Feb. 5, 2010) Advisor(s): Jeffrey A. Platt, Chair of the Research Committee, Joseph Legan, Carl J. Andres, David Brown, Burak Taskonak . Curriculum vitae. Includes abstract. Includes bibliographical references (leaves 45-52).
Spence, Deborah-Ann C. (Deborah-Ann Candice). « Rigid silicone resin studies ». Thesis, Massachusetts Institute of Technology, 1996. http://hdl.handle.net/1721.1/42581.
Texte intégralLivres sur le sujet "Resin"
Resin : Poems. Baton Rouge : Louisiana State University Press, 2005.
Trouver le texte intégralSoul resin. Normal, Ill : FC2, 2002.
Trouver le texte intégralDoran, Geri. Resin : Poems. Baton Rouge, LA : Louisiana State University Press, 2004.
Trouver le texte intégralAssociation, European Resin Manufacturers. European resin directory. Redhill, Surrey : ERMA, 1992.
Trouver le texte intégralPotter, Kevin. Resin Transfer Moulding. Dordrecht : Springer Netherlands, 1997. http://dx.doi.org/10.1007/978-94-009-0021-9.
Texte intégral(Firm), Knovel, dir. Resin transfer moulding. London : Chapman & Hall, 1997.
Trouver le texte intégralP, Benjamin William, et Beckwith Scott W, dir. Resin transfer molding. Covina, CA : SAMPE, 1999.
Trouver le texte intégralPotter, Kevin. Resin Transfer Moulding. Dordrecht : Springer Netherlands, 1997.
Trouver le texte intégralResin transfer moulding. London : Chapman & Hall, 1997.
Trouver le texte intégralResin from the rain. Seattle, Wash : Rose Alley Press, 2002.
Trouver le texte intégralChapitres de livres sur le sujet "Resin"
Suriano, Raffaella, Andrea Mantelli, Gianmarco Griffini, Stefano Turri et Giacomo Bonaiti. « Styrene-Free Liquid Resins for Composite Reformulation ». Dans Systemic Circular Economy Solutions for Fiber Reinforced Composites, 99–123. Cham : Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-031-22352-5_6.
Texte intégralGooch, Jan W. « Resin ». Dans Encyclopedic Dictionary of Polymers, 623–24. New York, NY : Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_9936.
Texte intégralBährle-Rapp, Marina. « Resin ». Dans Springer Lexikon Kosmetik und Körperpflege, 474. Berlin, Heidelberg : Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_8856.
Texte intégralPengelly, Andrew. « Resins and cannabinoids. » Dans The constituents of medicinal plants, 112–22. 3e éd. Wallingford : CABI, 2021. http://dx.doi.org/10.1079/9781789243079.0007.
Texte intégralJolanki, Riitta, et Kristiina Alanko. « Epoxy Resin ». Dans Management of Positive Patch Test Reactions, 105–9. Berlin, Heidelberg : Springer Berlin Heidelberg, 2003. http://dx.doi.org/10.1007/978-3-642-55706-4_25.
Texte intégralKnop, Andre, et Louis A. Pilato. « Resin Production ». Dans Phenolic Resins, 91–102. Berlin, Heidelberg : Springer Berlin Heidelberg, 1985. http://dx.doi.org/10.1007/978-3-662-02429-4_5.
Texte intégralGooch, Jan W. « Butylated Resin ». Dans Encyclopedic Dictionary of Polymers, 101. New York, NY : Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_1734.
Texte intégralGooch, Jan W. « Acrylate Resin ». Dans Encyclopedic Dictionary of Polymers, 14. New York, NY : Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_182.
Texte intégralGooch, Jan W. « Acrylic Resin ». Dans Encyclopedic Dictionary of Polymers, 15. New York, NY : Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_194.
Texte intégralGooch, Jan W. « Casting Resin ». Dans Encyclopedic Dictionary of Polymers, 123. New York, NY : Springer New York, 2011. http://dx.doi.org/10.1007/978-1-4419-6247-8_2029.
Texte intégralActes de conférences sur le sujet "Resin"
Skobeltsyn, Gleb, Flavio Junqueira, Vassilis Plachouras et Ricardo Baeza-Yates. « ResIn ». Dans the 31st annual international ACM SIGIR conference. New York, New York, USA : ACM Press, 2008. http://dx.doi.org/10.1145/1390334.1390359.
Texte intégralIndriasari, Indriasari, Suppachai Sattayanurak, Riastuti Fidyaningsih, Ade Sholeh Hidayat, Mahendra Anggaravidya, Dewi Kusuma Arti, Akhmad Amry et al. « The Effect of Oligomeric Resins on Tire Traction of SBR/BR-Based Rubber Blends ». Dans 6th International Conference on Advanced Materials Science. Switzerland : Trans Tech Publications Ltd, 2024. http://dx.doi.org/10.4028/p-sk0hzu.
Texte intégralLi, Junfeng, et Jianlong Wang. « Cementation of Radioactive Waste Resin by Calcium Sulfoaluminate Cement ». Dans 17th International Conference on Nuclear Engineering. ASMEDC, 2009. http://dx.doi.org/10.1115/icone17-75197.
Texte intégralBondaletov, Vladimir G., Aleksandr V. Vosmerikov, Lyudmila I. Bondaletova, Nguyen Van Thanh et Anna V. Bondaletova. « Protective bitumen-resin coatings based on aromatic petroleum resin ». Dans PROCEEDINGS OF THE ADVANCED MATERIALS WITH HIERARCHICAL STRUCTURE FOR NEW TECHNOLOGIES AND RELIABLE STRUCTURES. Author(s), 2018. http://dx.doi.org/10.1063/1.5083280.
Texte intégralSAITO, TAKUYA, KENJI MIZUTANI, HIROSHI SAITO et ISAO KIMPARA. « EVALUATION OF EFFECT OF SURFACE MODIFICATION ON CORRELATION BETWEEN PERMEABILITY OF GLASS FIBER/RESIN AND CAPILLARY NUMBER ». Dans Thirty-sixth Technical Conference. Destech Publications, Inc., 2021. http://dx.doi.org/10.12783/asc36/35896.
Texte intégralDENG, KAIYUE, CHUNYAN ZHANG et KUN (KELVIN) FU. « 3D PRINTING OF THERMALLY CURABLE RESIN/CONTINUOUS CARBON FIBER COMPOSITES WITH INTERPENETRATING POLYMER INTERLAYER ». Dans Proceedings for the American Society for Composites-Thirty Eighth Technical Conference. Destech Publications, Inc., 2023. http://dx.doi.org/10.12783/asc38/36520.
Texte intégralZhou, Yan, et Haifeng Zhang. « Design and Research of Spent Resin Conical Dryer Device ». Dans 2017 25th International Conference on Nuclear Engineering. American Society of Mechanical Engineers, 2017. http://dx.doi.org/10.1115/icone25-66008.
Texte intégralRuiz-Limón, B., G. B. J. Wetzel, A. Olivares Pérez, E. L. Ponce-Lee, R. Ramos-Garcia, S. Toxqui López, M. P. Hernández-Garay et I. Fuentes-Tapia. « Epoxy resin holograms ». Dans Integrated Optoelectronic Devices 2006, sous la direction de Hans I. Bjelkhagen et Roger A. Lessard. SPIE, 2006. http://dx.doi.org/10.1117/12.647143.
Texte intégralKEMPPAINEN, JOSH, IVAN GALLEGOS, PRATHAMESH DESHPANDE, JACOB GISSINGER et GREGORY ODEGARD. « MOLECULAR DYNAMICS SIMULATIONS OF FURAN RESIN (POLYFURFURYL ALCOHOL) : PREDICTING MECHANICAL PROPERTIES ». Dans Thirty-sixth Technical Conference. Destech Publications, Inc., 2021. http://dx.doi.org/10.12783/asc36/35847.
Texte intégralZhang, Dongxu, Qiyu Huang, Rongbin Li, Danfu Cao et Huiyuan Li. « Hydrate Formation in Water-in-Oil Emulsions in the Presence of Resins ». Dans 2020 13th International Pipeline Conference. American Society of Mechanical Engineers, 2020. http://dx.doi.org/10.1115/ipc2020-9350.
Texte intégralRapports d'organisations sur le sujet "Resin"
Dynes, Paul J. Emerging Resin Characterization. Fort Belvoir, VA : Defense Technical Information Center, avril 1989. http://dx.doi.org/10.21236/ada208173.
Texte intégralPowell, K. R. Resin Longevity Studies. Office of Scientific and Technical Information (OSTI), mai 2002. http://dx.doi.org/10.2172/799356.
Texte intégralOrhan, Nilüfer, Burak Temiz, Hale Gamze Ağalar et Gökalp İşcan. Boswellia serrata Oleogum Resins and Extracts Laboratory Guidance Document. ABC-AHP-NCNPR Botanical Adulterants Prevention Program, août 2022. http://dx.doi.org/10.59520/bapp.lgd/mqgn3574.
Texte intégralBibler, J. P. EP-toxicity test of saturated GT-73 resin and resin in grout. Office of Scientific and Technical Information (OSTI), avril 1985. http://dx.doi.org/10.2172/10134258.
Texte intégralLee, Yongwoo, R. Kovar, U. Shin, N. Francis, W. Collins et L. Renna. Environmentally Compliant Vinyl Ester Resin (VER) Composite Matrix Resin Derived from Renewable Resources. Fort Belvoir, VA : Defense Technical Information Center, novembre 2011. http://dx.doi.org/10.21236/ada557369.
Texte intégralMay, Clayton A. Ambient Temperature Storable Thermoset Resin. Fort Belvoir, VA : Defense Technical Information Center, avril 1995. http://dx.doi.org/10.21236/ada294775.
Texte intégralHayes, Brian S., et Doyle Dixon. New Low Cost Resin Systems. Fort Belvoir, VA : Defense Technical Information Center, février 2004. http://dx.doi.org/10.21236/ada422011.
Texte intégralLeung, C. Acetylene Terminated Resin Mechanical Characterization. Fort Belvoir, VA : Defense Technical Information Center, mai 1986. http://dx.doi.org/10.21236/ada172623.
Texte intégralMcConnell, Jr, J W et Sanders, Sr, R D. EPICOR-II resin degradation results from first resin samples of PF-8 and PF-20. Office of Scientific and Technical Information (OSTI), décembre 1985. http://dx.doi.org/10.2172/6391311.
Texte intégralBannochie, C. J. FB-Line resin testing final report. Office of Scientific and Technical Information (OSTI), janvier 1992. http://dx.doi.org/10.2172/7190212.
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