Добірка наукової літератури з теми "Styrene monomers"

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Статті в журналах з теми "Styrene monomers"

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Mizutani, Masato, Kotaro Satoh, and Masami Kamigaito. "Construction of Vinyl Polymer and Polyester or Polyamide Units in a Single Polymer Chain via Metal-catalyzed Simultaneous Chain- and Step-growth Radical Polymerization of Various Monomers." Australian Journal of Chemistry 67, no. 4 (2014): 544. http://dx.doi.org/10.1071/ch13476.

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Анотація:
Metal-catalyzed simultaneous chain- and step-growth radical polymerization was examined to combine common conjugated vinyl monomers, such as various acrylates and styrene, as chain-growth monomers and various ester- or amide-linked monomers bearing both an unconjugated C=C bond and an active C–Cl bond as step-growth monomers. The CuCl/1,1,4,7,10,10-hexamethyltriethylenetetramine-catalyzed copolymerization of alkyl acrylates and various step-growth monomers at a 1 : 1-monomer feed ratio resulted in almost linear random copolymers that consisted of vinyl polymer and polyester units. Additional f
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Yohanala P. T., Flaviana, Restu Mulya Dewa, Karinda Quarta, Widiyastuti Widiyastuti, and Sugeng Winardi. "Preparation of Polystyrene Spheres Using Surfactant-Free Emulsion Polymerization." Modern Applied Science 9, no. 7 (2015): 121. http://dx.doi.org/10.5539/mas.v9n7p121.

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Polystyrene spheres have been synthesized using potassium persulphate (KPS) as initiators without using anysurfactant or stabilizing agent. Simple mixing method was used to synthesize styrene monomer into polystyrenespheres. The influences of mixing time, ammount of styrene monomers, and ammount of initiators were studiedin this research. Size measurement and its distribution were analyzed by Scanning Electron Microscopy (SEM).Monodisperse spheres and verry narrow size distribution are expected in this research. The results showed thatthe most optimum time to synthesize styrene monomer into po
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Yu, Xinliang, Wenhao Yu, Bing Yi, and Xueye Wang. "Prediction of monomer reactivity ratios in radical copolymerization of vinyl monomers." Collection of Czechoslovak Chemical Communications 74, no. 9 (2009): 1279–94. http://dx.doi.org/10.1135/cccc2008215.

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Quantitative structure-property relationship (QSPR) models are developed to predict monomer reactivity ratios (log r12) in radical copolymerization with monomers M1 (styrene, methyl methacrylate and acrylonitrile) and M2 (vinyl monomers). The quantum chemical descriptors are calculated by the density functional theory (DFT) at B3LYP level of theory with 6-31G(d) basis set. Stepwise multiple linear regression analysis and artificial neural network (ANN) were used to generate Model S (monomer 1: styrene), Model MM (monomer 1: methyl methacrylate) and Model A (monomer 1: acrylonitrile). Simulatio
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4

Engler, Anthony, Habin Park, Manas Madhira, et al. "Investigation on Tethered Anion Effects in Solid Polymer Electrolytes for Li-Ion Batteries." ECS Meeting Abstracts MA2022-02, no. 4 (2022): 521. http://dx.doi.org/10.1149/ma2022-024521mtgabs.

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Solid polymer electrolytes (SPEs) have been proposed to reduce concentration polarizations within batteries by immobilizing anions to the polymer matrix, which can help stabilize the electrodeposition process and extend Li-ion battery lifetime. Unfortunately, single-ion conducting SPEs continue to suffer from poor conductivity due to coupling with the slow segmental mobility of polymer chains and poor ion pair dissociation. Our group systematically investigated how different tethered anions affect the Li-ion conduction and polymer segmental mobility. Copolymers were synthesized using a common
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Desire, Christopher T., R. Dario Arrua, Fotouh R. Mansour, Stefan A. F. Bon, and Emily F. Hilder. "Styrene-based polymerised high internal phase emulsions using monomers in the internal phase as co-surfactants for improved liquid chromatography." RSC Advances 12, no. 16 (2022): 9773–85. http://dx.doi.org/10.1039/d1ra07705h.

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Poly(styrene-co-divinylbenzene)-based monoliths prepared from the polymerisation of water-in-monomer high internal phase emulsions, where water-soluble monomers acrylamide or poly(ethylene glycol) diacrylate (Mw 258) were included in internal phase.
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Yang, Ke, Hui Niu, Zhenghai Shi, et al. "Convenient synthesis of versatile syndiotactic polystyrene materials containing pendant alkenyl groups with a scandium catalyst system." Polymer Chemistry 9, no. 27 (2018): 3709–13. http://dx.doi.org/10.1039/c8py00607e.

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Анотація:
The syndioselective copolymerization of styrene with five alkenyl functionalized styrenic monomers, with the use of a scandium catalyst, produced a new family of versatile syndiotactic polystyrene materials with pendant alkenyl groups.
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Lyons, RA, and E. Senogles. "Reactivities of Monomers Towards the 1-Methyl-1-(methoxycarbonyl)ethyl Radical." Australian Journal of Chemistry 47, no. 12 (1994): 2201. http://dx.doi.org/10.1071/ch9942201.

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Анотація:
The relative reactivities of acrylonitrile, methyl acrylate , methyl methacrylate and styrene towards the 1-methyl-1-( methoxycarbonyl )ethyl radical have been determined at 60°C, and the results compared with those for the poly (methyl methacrylate ) radical. The results for methyl acrylate suggest that the copolymerization of this monomer with methyl methacrylate is adequately described by a terminal mechanism. Those for styrene show that the presence of a penultimate styrene or methyl methacrylate unit in a poly(methyl methacrylate ) radical leads to a slightly greater preference for this r
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Bauer, R. F. "A Two-Step Emulsion Polymerization Process Catalyzed by an Organic Diperoxide." Rubber Chemistry and Technology 77, no. 4 (2004): 776–90. http://dx.doi.org/10.5254/1.3547851.

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Abstract An emulsion polymerization process is described which consists of consecutively polymerizing at least two olefinic monomers using an organic diperoxide with two independently functioning peroxy groups, namely 2,5-dimethyl-2-t-butylperoxy-5-hydroxy hexane. In the first polymerization step, the hydroperoxide group is activated by a redox reaction at low temperatures without decomposing the t-butyl peroxide portion of the initiator molecule. After charging fresh monomer, the t-butyl peroxide can then be thermally activated to initiate a second-stage polymerization reaction. This polymeri
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Schovanec, Martin, Jiří Horálek, Štěpán Podzimek, and Jaromír Šňupárek. "Copolymerization of 2-[3-(2H-Benzotriazol-2-yl)-4-hydroxyphenyl]ethyl Methacrylate with Styrene." Collection of Czechoslovak Chemical Communications 72, no. 9 (2007): 1244–54. http://dx.doi.org/10.1135/cccc20071244.

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Radical copolymerization of 2-[3-(2H-benzotriazol-2-yl)-4-hydroxyphenyl]ethyl methacrylate (M1) with styrene (M2) at 70 °C in 1,4-dioxane was investigated and the reactivity ratios were determined. The copolymerization was carried out as batch copolymerization to a low conversion or as copolymerization with a continuous addition of monomers at higher instantaneous conversion. The monomer reactivity ratios of the copolymerizable UV stabilizer 2-[3-(2H-benzotriazol-2-yl)-4-hydroxyphenyl]ethyl methacrylate with styrene were determined using the Finemann-Ross plot for both copolymeration technique
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Gziut, Konrad, Agnieszka Kowalczyk, Beata Schmidt, Tomasz J. Idzik, and Jacek G. Sośnicki. "Influence of Methacrylate and Vinyl Monomers on Radical Bulk Photopolymerization Process and Properties of Epoxy-Acrylate Structural Adhesives." Polymers 15, no. 4 (2023): 926. http://dx.doi.org/10.3390/polym15040926.

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In this paper, epoxy-acrylate structural adhesives tapes (SATs) were obtained from Bisphenol A-based liquid epoxy resin and epoxy acrylic resins (EARs). A new method of EARs preparation, i.e., the free radical bulk photopolymerization process (FRBP), was studied in detail. The influence of methacrylic monomers (methyl methacrylate, ethyl methacrylate, butyl methacrylate, lauryl methacrylate, (2-acetoacetoxy)ethyl methacrylate) and vinyl monomers (N-vinylpyrrolidone and styrene) on the FRBP process of base monomers (i.e., butyl acrylate, glycidyl methacrylate and 2-hydroxyethyl acrylate) was in
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Дисертації з теми "Styrene monomers"

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Ma, Yinghua. "Living cationic polymerization of styrene monomers." Thesis, Aston University, 2000. http://publications.aston.ac.uk/9636/.

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This thesis describes an experimental investigation of synthesis of polystyrene under various polymerization conditions such as solvent polarity, temperature, initial concentrations of initiator, catalyst, monomer and added salts or co-catalyst, which was achieved using the living cationic polymerization technology in conjunction with gel permeation chromatography (GPC) and NMR spectroscopy. Polymerizations of styrene were conducted using 1-phenyl ethylchloride (1-PEC) as an initiator and tin tetrachloride (SnCI4) as a catalyst in the presence of tetra-n-Butylammonium chloride (nBu4NCI). Effec
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Bahrin, Nurfariza. "Renewable monomers for bio-styrene formation using phenolic acid decarboxylase." Thesis, University of Warwick, 2017. http://wrap.warwick.ac.uk/100542/.

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Lignocellulose is an abundant natural polymer on earth that contains renewable resource of aromatic compound, the lignin. Many industrially valuable chemicals can be developed from lignin and this can reduce the dependency on petrochemicals. Wheat straw contains ferulic acid as one of its building blocks, which can be accumulated as a major metabolite from growth with Rhodococcus jostii RHA1, a known lignin degrading bacteria in minimal media. Using the enzyme phenolic acid decarboxylase (PAD) in engineered E.coli, ferulic acid was converted into 4-vinylguaiacol (3-methoxy-4-hydroxystyrene). T
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Tichagwa, Lilian M. "Synthesis of acrylate-based polymeric and polymerisable surfactants and their application in the emulsion polymerisation of styrene." Thesis, Stellenbosch : University of Stellenbosch, 2006. http://hdl.handle.net/10019.1/1185.

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Thesis (PhD (Chemistry and Polymer Science))--University of Stellenbosch, 2006.<br>The study described in this dissertation examines the synthesis of mainly acrylate-based surfactants and their subsequent use as emulsifiers/stabilisers in the emulsion polymerisation of styrene. Some acrylamide-based surfactants were also studied, for comparison purposes only. Two major types of surfactants, polymerisable (surfactant monomers or surfmers) and polymeric, were synthesised, characterised and used in emulsion polymerisation reactions. The prepared polymerisable surfactants, 12-acryloyloxydodecanoic
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Clark, Darren Cameron. "Dual monomer grafting of styrene and maleic anhydride onto polyethylene, effect of polyethylene microstructure." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 2000. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape3/PQDD_0020/NQ54405.pdf.

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Levy, Florence. "Fonctionnalisation d'un latex de polystyrène par un monomère chloré : le bis 2 chloroéthyl-itaconate." Lyon 1, 1987. http://www.theses.fr/1987LYO10538.

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Анотація:
Fonctionnalisation superficielle du polystyrene par bis 2-chloro ethyl-itaconate. Determination des constantes cinetiques et physicochimiques. Etude de la copolymerisation avec le styrene et l'acrylate de butyle
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Srichan, Sansanee. "Synthesis of sequence-controlled polymers by copolymerization of para-substituted styrenic derivatives and N-substituted maleimides." Thesis, Strasbourg, 2015. http://www.theses.fr/2015STRAF005/document.

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Анотація:
Dans ce travail, les copolymérisations radicalaires contrôlées de monomères donneurs (dérivés du styrène) et accepteurs (maleimides N-substitués) ont été effectuées afin de préparer des polymères à séquences contrôlées. Ces macromolécules ont été préparées par polymérisation radicalaire contrôlée par la voie des nitroxides en utilisant le SG1 comme agent de contrôle. Des polymères ayant des microstructures bien définies ont été obtenus par le contrôle du temps de l’addition d’une petite quantité de monomère accepteur au cours de la polymérisation d’un large excès de monomère de type donneur. D
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Applin, Samantha. "Surfactant Free Emulsion Polymerization of Poly(Styrene-Co-Methyl Methacrylate): Correlation of Microsphere Characteristics with Monomer Reactivity and Water Solubility." W&M ScholarWorks, 2017. https://scholarworks.wm.edu/etd/1530192354.

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Polymeric microspheres have been used in a broad range of applications from chromatographic separation techniques to analysis of air flow over aerodynamic surfaces. The preparation of microspheres from many polymer families has consequently been extensively studied using a variety of synthetic approaches. Although there are a myriad of polymeric microsphere synthesis methods, free-radical initiated emulsion polymerization is one of the most common techniques. In this work, poly(styrene-co-methyl methacrylate) microspheres were synthesized via surfactant-free emulsion polymerization. The effect
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Drockenmuller, Eric. "Synthèse de nouveaux nitroxydes et alcoxyamines fonctionnalisés. Application à la polymérisation radicalaire vivante/contrôlée de monomères vinyliques." Université Louis Pasteur (Strasbourg) (1971-2008), 2002. http://www.theses.fr/2002STR13071.

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Анотація:
Les travaux effectués au cours de cette thèse concernent la polymérisation radicalaire vivante/contrôlée de monomères vinyliques par les nitroxydes. Le principe de ce type de polymérisation repose sur l'établissement d'un équilibre entre espèces dormantes (ou alcoxyamines) et espèces actives (radicaux alkyle et nitroxyle). Afin d'abaisser la température de ce procédé et de l'étendre à d'autres monomères, nous avons modifié la réactivité du nitroxyde en introduisant divers substituants de polarité et d'encombrement stérique variables. Ainsi, une nouvelle classe de nitroxydes (b-sulfinyl nitroxy
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Malek, Fouad. "Synthèse de nouveaux monomères à chaînes latérales pyrazole et bipyrazole et leurs polymérisations." Montpellier 2, 1992. http://www.theses.fr/1992MON20140.

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Анотація:
Ce travail concerne la synthese et la caracterisation des polymeres et copolymeres obtenus par polymerisation de nouveaux monomeres styreniques, vinyliques, maleimiques et methacryliques porteurs des cycles pyridine, pyrazole et bipyrazole. Une discussion sur la copolymerisation de ces monomeres avec d'autres monomeres conduisant a des systemes accepteur-donneur est presentee. En plus, des comparaisons entre la structure et les proprietes, notamment thermiques, sont abordees. Enfin deux applications ont ete etudiees: la premiere concerne les resines acetylantes selectives, la seconde l'obtenti
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Ramirez, Marquez Walter. "Relations procédé de synthèse microstructure-morphologie-propriétés des copolymères acrylate de méthyle-styrène." Lyon 1, 1987. http://www.theses.fr/1987LYO19025.

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Copolymerisation en emulsion. Par le procede en reacteur ferme, l'existence d'azoetropes plus nombreux qu'en solution ou en masse confirme que les taux de reactivite sont des grandeurs cinetiques apparentes. Synthese de copolymeres a composition et a structuration controlees, par des procedes semicontinu, batch corrige et core-shell
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Книги з теми "Styrene monomers"

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Ltd, ICON Group. TAIWAN STYRENE MONOMER CORP: Labor Productivity Benchmarks and International Gap Analysis (Labor Productivity Series). 2nd ed. Icon Group International, 2000.

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Ltd, ICON Group. TAIWAN STYRENE MONOMER CORP: International Competitive Benchmarks and Financial Gap Analysis (Financial Performance Series). 2nd ed. Icon Group International, 2000.

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Частини книг з теми "Styrene monomers"

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Hirao, Akira, and Katsuhiko Takenaka. "Nonpolar Monomers: Styrene and 1,3-Butadiene Derivatives." In Anionic Polymerization. Springer Japan, 2015. http://dx.doi.org/10.1007/978-4-431-54186-8_3.

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Tanaka, Ryo, and Takeshi Shiono. "Coordination Polymerization (Styrene and Polar Vinyl Monomers)." In Encyclopedia of Polymeric Nanomaterials. Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-642-36199-9_180-1.

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Tanaka, Ryo, and Takeshi Shiono. "Coordination Polymerization (Styrene and Polar Vinyl Monomers)." In Encyclopedia of Polymeric Nanomaterials. Springer Berlin Heidelberg, 2015. http://dx.doi.org/10.1007/978-3-642-29648-2_180.

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Jiang, David, and Charles A. Wilkie. "Graft Copolymerization of Vinyl Monomers onto Polymers Containing Styrene." In Polymer Modification. Springer US, 1997. http://dx.doi.org/10.1007/978-1-4899-1477-4_10.

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Hampton, Kenneth W., and Warren T. Ford. "Synthesis and Emulsion Copolymerizations of Styrene Sulfonate Monomers for Cross-Linked Polyampholyte Latexes." In ACS Symposium Series. American Chemical Society, 2000. http://dx.doi.org/10.1021/bk-2000-0755.ch003.

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Wilén, Carl-Eric. "Synthesis of Antioxidant Monomers Based on Sterically Hindered Phenols, α-Tocopherols, Phosphites and Hindered Amine Light Stabilizers (HALS) and their Copolymerization with Ethylene, Propylene or Styrene." In Antioxidant Polymers. John Wiley & Sons, Inc., 2012. http://dx.doi.org/10.1002/9781118445440.ch12.

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Seymour, Raymond B. "Styrene-Maleic Anhydride-Vinyl Monomer Terpolymers and Blends." In High Performance Polymers: Their Origin and Development. Springer Netherlands, 1986. http://dx.doi.org/10.1007/978-94-011-7073-4_13.

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Krishnamurti, Chandrasekhar, Saurabh Dalai, and Mounika Jonnavittula House Surgeon. "An Incident of Styrene Monomer Gas Poisoning at Visakhapatnam." In 5th World Congress on Disaster Management. Routledge, 2022. http://dx.doi.org/10.4324/9781003341932-48.

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Hovhannisyan, A. A., M. Khaddaj, I. A. Gritskova, G. K. Grigoryan, N. G. Grigoryan, and A. G. Nadaryan. "Peculiarities of Polymerization of Vinyl Acetate and Styrene in Static Heterogeneous Monomer: Water System in the Absence of Emulsifier." In Science and Technology of Polymers and Advanced Materials. Apple Academic Press, 2019. http://dx.doi.org/10.1201/9780429425301-14.

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Stein, Judith, and Slawomir Rubinsztajn. "Silane Functionalired Styrene Monomers and Their Polymerization." In Silicon-Containing Polymers. Royal Society of Chemistry, 1995. http://dx.doi.org/10.1039/9781837672448-00187.

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Тези доповідей конференцій з теми "Styrene monomers"

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Kass, Michael, Jiheon Jun, Christopher Janke, Gavin Warrington, Dino Sulejmanovic, and James Keiser. "Swell Behavior of Elastomers with a Hydrothermal Liquefaction Bio-Crude and a Fast Pyrolysis Bio-Oil." In CORROSION 2021. AMPP, 2021. https://doi.org/10.5006/c2021-16565.

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Abstract The compatibility of seventeen elastomer materials with two heavy biofuels (fast pyrolysis bio-oil and hydrothermal liquefaction (HTL) bio-crude) and diesel was assessed through volume change measurements. The elastomers included two fluorocarbons, six acrylonitrile rubbers (NBRs), and one each of fluorosilicone, neoprene, polyurethane, silicone, epichlorohydrin rubber (ECO), a blend of polyvinyl chloride and NBR (OZO), styrene butadiene rubber (SBR), hydrogenated NBR (HNBR) and ethylene propylene diene monomer (EPDM). The specimens were immersed in each test fuel for four weeks at 50
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Kass, Michael D., Christopher J. Janke, Samuel A. Lewis, James R. Keiser, and Raynella M. Connatser. "Elastomer Compatibility with a Pyrolysis-derived Bio-oil." In CORROSION 2020. NACE International, 2020. https://doi.org/10.5006/c2020-14613.

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Abstract The compatibility of fueling infrastructure elastomers in bio-oil and diesel fuel was determined by measuring the volume swell and hardness before and after drying. The bio-oil was produced via fast pyrolysis from a blend of pine feedstocks. The elastomer materials included two fluorocarbons, six acrylonitirile butadiene rubbers (NBRs), fluorosilicone, styrene butadiene rubber, neoprene, polyurethane, neoprene, silicone, ethylene propylene diene monomer (EPDM), hydrogenated acrylonitrile butadiene rubber (HNBR), a blend of NBR and PVC (OZO), and a blend of epichlorohydrin and ethylene
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Kokol, Nino, Tomaž Pirman, Martin Ocepek, and Robin A. Hutchinson. "High-Temperature Radical Copolymerization of Dibutyl Itaconate With N-Butyl Acrylate, Methyl Methacrylate and Styrene." In TBMCE, International Conference on Technologies & Business Models for Circular Economy. University of Maribor Press, 2025. https://doi.org/10.18690/um.fkkt.1.2025.5.

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The homopolymerization of itaconates results in relatively short polymer chains and low monomer conversions. To study whether copolymerization provides a more favorable result, dibutyl itaconate was copolymerized with n-butyl acrylate, methyl methacrylate and styrene. In addition to representing the most commercially preferred monomer families, these co-monomers were also chosen due to the differences in the secondary reactions that occur during polymerization at elevated temperatures. Experiments were conducted under semi-batch operating conditions at 110 °C with equal molar ratios of the co-
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Caillol, Sylvain. "Plant oil based radically polymerizable monomers for sustainable polymers." In 2022 AOCS Annual Meeting & Expo. American Oil Chemists' Society (AOCS), 2022. http://dx.doi.org/10.21748/kypx2569.

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We have focuses our studies on the synthesis of novel biobased monomers designed for free radical polymerization which could increase the biomass carbon content pursuing to equal or improve the performance of existing polymers from non-renewable sources. Cardanol, which is a natural phenolic oil, is issued from Cashew Nutshell Liquid (CNSL), a non-edible renewable resource, co-produced from cashew industry in large commercial volumes (1Mt p.a.). Cardanol is non-toxic and particularly suitable for the addition of aromatic renewable resources in polymers and materials. We recently reported vario
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Pantić, Olga. "Biobased composite materials obtained from unsaturated polyester resins and waste coffee." In 35th International Congress on Process Industry. SMEITS, 2022. http://dx.doi.org/10.24094/ptk.022.041.

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Анотація:
Replacing styrene with biobased monomers to produce fully biobased unsaturated polyester resins (UPRs) turned out to be quite a challenging task. Styrene has been recognized as a hazardous and a potentially carcinogenic substance for human health. Using dimethyl itaconate as an alternative reactive diluent to styrene, which can be obtained from renewable resources, enables low viscosity for easy manipulation of mentioned UPRs. Fully biobased UPRs in question were based on itaconic acid, succinic acid, and propylene glycol, which were then diluted with dimethyl itaconate. Having in mind that UP
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Jung, D., A. Hegeman, N. R. Sottos, P. H. Geubelle, and S. R. White. "Self-Healing Composites Using Embedded Microspheres." In ASME 1997 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 1997. http://dx.doi.org/10.1115/imece1997-0673.

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Abstract A self-repairing polyester matrix composite material is described which utilizes embedded polyoxymethylene urea (PMU) microspheres to store a crack filling agent to be released into the crack and rebond the crack faces. The developed repair mechanism uses naturally occurring functional sites in the polyester matrix network to trigger the repair action. The repair agent is mostly composed of styrene monomers and high molecular weight polystyrene. Microscopic observations of the microsphere/crack interaction are presented. Of particular interest is the process with which the microsphere
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7

Kratzok, Max, Anil Saigal, and Michael Zimmerman. "Temperature-Dependent Impact Properties of ABS Polymer." In ASME 2021 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 2021. http://dx.doi.org/10.1115/imece2021-71382.

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Abstract Polymeric materials are composed of chains of molecules known as monomers which are held together by secondary bonds. Amorphous polymers have a glass transition temperature above which their behavior transitions from glassy to viscoelastic, meaning they act like both a viscous liquid and an elastic solid. This concept may seem familiar to anyone who has used Silly Putty®; bouncing a ball of Silly Putty causes the material to behave elastically whereas it will flow into a puddle if left on a table overnight. Time temperature superposition (TTS) describes the dependence of viscoelastic
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8

Febriansyar, Rosyad Adrian, Nadya Ummi Azizah, and Widayat. "Optimization heat integration of preliminary plant design of styrene monomer into polystyrene." In 1ST INTERNATIONAL CONFERENCE ON TECHNOLOGY, INFORMATICS, AND ENGINEERING. AIP Publishing, 2022. http://dx.doi.org/10.1063/5.0094754.

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9

Cheng, X., L. Yang, and Y. Zhang. "A Novel Styrene-Assisted Monomer Route for Polymer Derived Macroporous SiBCN Ceramic Monolith." In MS&T19. TMS, 2019. http://dx.doi.org/10.7449/2019mst/2019/mst_2019_1336_1342.

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10

Cheng, X., L. Yang, and Y. Zhang. "A Novel Styrene-Assisted Monomer Route for Polymer Derived Macroporous SiBCN Ceramic Monolith." In MS&T19. TMS, 2019. http://dx.doi.org/10.7449/2019/mst_2019_1336_1342.

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Звіти організацій з теми "Styrene monomers"

1

Moore, Brian, Timothy Haddad, Rene Gonzalez, and Constance Schlaefer. Reactivity Ratios of Isobutyl POSS-Styrene and Styrene Monomers. Defense Technical Information Center, 2004. http://dx.doi.org/10.21236/ada422517.

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2

Saiwan, Chintana. Mesostructural ultra thin silica film formation through admicellar technique. Chulalongkorn University, 2003. https://doi.org/10.58837/chula.res.2003.78.

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Thin silica film formation from adsolubilization of inorganic silica precursors, letra-n-butoxysilane (TBOS) and tetraethyl orthosilicate (TBOS) in admicellar polymerization were studies. Cetyltrimethylammonium bromide (CTAB) at 700 uM and octyl phenol ethoxylate or Triton X-100 at 200 uM were used as surfactant templates for adsolubilizates TBOS and TBOS respectively. For the TBOS/CTAB system, the atomic force microscopy (AFM) topographic images showed fibers, hemispheres and flat layers existing along with increase of surface coverge on the mica surface as the TBOS feed concentration was inc
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