Relevant bibliographies by topics / Styrene derivatives

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters
  4. Conference papers

Academic literature on the topic 'Styrene derivatives'

Author: Grafiati
Published: 5 June 2025
Last updated: 1 August 2025

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Journal articles on the topic "Styrene derivatives"

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Fujita, Morifumi, Koki Miura, and Takashi Sugimura. "Enantioselective dioxytosylation of styrenes using lactate-based chiral hypervalent iodine(III)." Beilstein Journal of Organic Chemistry 14 (March 20, 2018): 659–63. http://dx.doi.org/10.3762/bjoc.14.53.

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A series of optically active hypervalent iodine(III) reagents prepared from the corresponding (R)-2-(2-iodophenoxy)propanoate derivative was employed for the asymmetric dioxytosylation of styrene and its derivatives. The electrophilic addition of the hypervalent iodine(III) compound toward styrene proceeded with high enantioface selectivity to give 1-aryl-1,2-di(tosyloxy)ethane with an enantiomeric excess of 70–96% of the (S)-isomer.
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Madahi, Meysam, Dadkhoda Ghazanfari, and Sayed Ali Ahmadi. "Theoretical Study of the Chemical Properties and the Reaction Pathway of Decarbonylative Alkylative Esterification of Styrenes with Aliphatic Aldehydes." Journal of Chemistry 2022 (February 18, 2022): 1–11. http://dx.doi.org/10.1155/2022/4842630.

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Using inexpensive and available aliphatic aldehydes as an alkyl source is a useful and cost-effective way to extend the chain of benzyl esters; this decarbonylative alkylative esterification of styrene derivatives has been used for organic synthesis and medical chemistry. A cocatalyzed decarbonylative alkylative esterification of styrene derivatives with aliphatic aldehydes and iodobenzenediacetate to provide chain elongated benzoates was investigated by the density functional theory, and quantum theory of atoms in molecules analysis has been used. The chemical properties and the reaction path
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Duarte, Tiago A. G., Ana C. Estrada, Mário M. Q. Simões, et al. "Homogeneous catalytic oxidation of styrene and styrene derivatives with hydrogen peroxide in the presence of transition metal-substituted polyoxotungstates." Catalysis Science & Technology 5, no. 1 (2015): 351–63. http://dx.doi.org/10.1039/c4cy00702f.

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Spurcaciu, Bogdan, Lorena Iancu, Mircea Filipescu, et al. "Polymeric Nanofibers Manufactured by Electrospinning of Styrene-Ethylene-Butylene-Styrene (SEBS) Composites." Proceedings 29, no. 1 (2019): 84. http://dx.doi.org/10.3390/proceedings2019029084.

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The study aimed to synthesize nanofibers based on styrene-ethylene-butylene-styrene block-copolymers (SEBS) [1] and its composite derivatives, through the electrospinning (Figure 1) process [2]. [...]
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Iatsyshyn, Oksana, Michael Bratychak, Olena Shyshchak, Nataliya Mitina, and Olexander Zaichenko. "Copolymerization of Peroxy Derivatives of Dioxydiphenylpropane Diglycidyl Ether Monomethacrylate with Styrene." Chemistry & Chemical Technology 9, no. 3 (2015): 293–300. http://dx.doi.org/10.23939/chcht09.03.293.

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Mu, Xiaochun, and Yang Li. "Syndiospecific coordination (Co)polymerization of carbazole-substituted styrene derivatives using the scandium catalyst system." Polymer Chemistry 12, no. 43 (2021): 6291–99. http://dx.doi.org/10.1039/d1py00896j.

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Perfect syndiospecific polymerization of carbazole-substituted styrene derivatives was achieved using a rare-earth metal catalyst. Also copolymerization of FSt with styrene afforded copolymers with gradient sequence distributions and easily tunable incorporation rate.
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Wei, Xudong, Paul Johnson, and Richard J. K. Taylor. "Organolithium addition to styrene and styrene derivatives: scope and limitations." Journal of the Chemical Society, Perkin Transactions 1, no. 7 (2000): 1109–16. http://dx.doi.org/10.1039/a910195k.

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Mu, Xiaochun, Xuefei Leng, Chuanchuan Liu, Qiang Yao, and Yang Li. "Terpolymerization of Ethylene with Hexene and Styrene Derivatives by Half-Sandwich Scandium Catalyst." Polymers 16, no. 16 (2024): 2290. http://dx.doi.org/10.3390/polym16162290.

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The terpolymerization of ethylene with hexene and styrene derivatives was achieved with a rare earth metal catalyst (C5Me4SiMe3)Sc(CH2C6H4NMe2-o)2 to prepare functional polyethylene. The catalyst system exhibited high activity in the terpolymerization of ethylene with hexene and amine-substituted styrene, affording terpolymers a moderate molecular weight and a unimodal molecular weight distribution. In addition, the comonomer content of the terpolymers can be controlled by changing the feeding ratio of monomers. The aliphatic region of the 13C NMR spectra reveals that the structural units of t
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Abdallah, Dalia, Mohmad Asri Abd Ghani, Michael F. Cunningham, Peter M. Kazmaier, Barkev Keoshkerian, and Erwin Buncel. "Multi-armed, TEMPO-functionalized unimolecular initiators for starburst dendrimer synthesis via stable free radical polymerization. 1. Tri azo-functionalized unimer." Canadian Journal of Chemistry 82, no. 9 (2004): 1393–402. http://dx.doi.org/10.1139/v04-107.

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The synthesis of azobenzene-functionalized multi-armed unimolecular initiators or "unimers" that can be polymerized using styrene or styrenic derivatives via TEMPO (2,2,6,6-tetramethylpiperidenyl-1-oxyl) mediated stable free radical polymerization (SFRP) is described. The unimers are composed of an azobenzene-functionalized core and a TEMPO-modified unit. Homopolymers and copolymers of styrene and acetoxystyrene were synthesized using the mono-and trifunctionalized unimers as initiators under bulk conditions with average molecular weights and polydispersities reported. The studies lay the grou
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Potapov, Vladimir A., Roman S. Ishigeev, Lyudmila A. Belovezhets, Irina V. Shkurchenko, and Svetlana V. Amosova. "New Water-Soluble Condensed Heterocyclic Compounds with Antimicrobial Activity Based on Annulation Reactions of 8-Quinolinesulfenyl Halides with Natural Products and Alkenes." Applied Sciences 11, no. 18 (2021): 8532. http://dx.doi.org/10.3390/app11188532.

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The annulation reactions of 8-quinolinesulfenyl halides with natural products and alkenes affording new water-soluble [1,4]thiazino[2,3,4-ij]quinolin-4-ium derivatives in high or quantitative yields are developed in this study. The reactions with styrene derivatives and terminal alkenes including allyl arenes proceed in a regioselective manner but with the opposite regiochemistry. The reactions with terminal alkenes including allyl arenes occur in an anti-Markovnikov fashion (regarding addition of the 8-quinolinesulfenyl electrophile to the double bond) to give 2-organyl-2H,3H-[1,4]thiazino[2,
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Dissertations / Theses on the topic "Styrene derivatives"

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Mpitso, Khotso. "Synthesis and characterization of styrene – maleic anhydride copolymer derivatives." Thesis, Stellenbosch : University of Stellenbosch, 2009. http://hdl.handle.net/10019.1/1972.

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Thesis (MSc (Chemistry and Polymer Science))--University of Stellenbosch, 2009.<br>ENGLISH ABSTRACT: In this study, a functional styrene – maleic anhydride copolymer (SMA) was synthesized via reversible addition-fragmentation chain transfer mediated polymerization (RAFT). The obtained copolymer had an alternating structure with well controlled molecular weight. The structure of the copolymer was found to alternating when characterized by NMR and MALDI-Tof-MS. SMA copolymer is functional polymer due to the presence of reactive maleic anhydride moiety in its backbone. The SMA copolymer wa
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Yeniay, Secil. "Sulfonated Styrene-co-maleic Acid And Its Derivatives As Superplasticizers In Concrete." Master's thesis, METU, 2008. http://etd.lib.metu.edu.tr/upload/2/12609455/index.pdf.

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In the past three decades, a new group of concrete admixtures, termed &ldquo<br>superplasticizers&rdquo<br>, were introduced to the concrete industry. They have gained wide acceptance because of their many advantages. The addition of superplasticizers to concrete improves the workability and strength of concrete. In this study, the effect of the chemical structure of poly (4-styrenesulfonic acid-co-maleic acid) sodium salt (SSAMA), which contains both sulfonic and carboxylic acid groups, which is a new superplasticizer, was analyzed. Two different molecular weights of PEG (polyethylene glycol
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Penner, Alexander [Verfasser], and H. A. [Akademischer Betreuer] Wagenknecht. "Photocatalytic nucleophilic additions to styrene derivatives / Alexander Penner. Betreuer: H.-A. Wagenknecht." Karlsruhe : KIT-Bibliothek, 2014. http://d-nb.info/1053703953/34.

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Gülak, Samet [Verfasser]. "Olefin-Assisted Iron and Cobalt Catalyzed Cross-Coupling Reactions for the Synthesis of Highly Functionalized Styrene Derivatives / Samet Gülak." München : Verlag Dr. Hut, 2013. http://d-nb.info/1043892397/34.

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Li, Haoran. "Pd-catalyzed C-H bond functionalizations of (hetero)arenes and alkenes : A one step access to poly(hetero)aromatics and styrene derivatives." Thesis, Rennes, Ecole nationale supérieure de chimie, 2020. http://www.theses.fr/2020ENCR0068.

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Afin d'expliquer le contexte de mon travail de recherche, j'ai résumé dans le premier chapitre des informations mécanistiques générales sur l'arylation des liaisons C-H catalysée par le palladium et j'ai détaillé certains travaux sur l'arylation directe en relation avec mes travaux. Mes objectifs étaient d'étudier la réactivité de nouvelles unités synthétiques permettant l'accès direct à des composés bi-(hétéro)aryls ou à des dérivés du styrène. Ensuite, dans les chapitres 2 à 6, j'ai résumé mes travaux de recherche. J'ai étudié l’arylation directes en C2 du Methoxsalen par des chlorures de be
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Trejo, O'Reilly José Antonio. "Synthèse d'agents de couplage, réactions de greffage en surface de fibres cellulosiques et propriétés d'interface fibres-matrices dans des matériaux composites à base de polystyrène." Grenoble INPG, 1997. http://www.theses.fr/1997INPG0019.

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L’objectif principal de ce travail est la modification chimique des fibres cellulosiques, afin d'améliorer leurs propriétés interfaciales lors de leur utilisation comme renforts dans des matériaux composites à matrice polymère organique (polystyrène). La synthèse d'un nouvel agent de couplage pour le système cellulose-polystyrène a été entreprise par la voie de copolymérisation cationique. Une caractérisation complète de cet agent de couplage a été faite par ftir, analyse élémentaire, #1h-nmr, calorimétrie différentielle (dsc) et chromatographie par exclusion stérique (ces). La réactivité de c
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Goussé, Cécile. "Applications de la réaction de Diels-Alder aux polymères furaniques." Grenoble INPG, 1997. http://www.theses.fr/1997INPG0007.

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Certains derives furaniques, obtenus a partir de la biomasse, se comportent comme d'excellents dienes vis a vis de la reaction de diels-alder. Dans cette perspective, l'application de cette reaction aux polymeres furaniques peut etre envisagee sous deux aspects. Le premier consiste en la modification de polymeres tels l'alcool polyvinylique ou le polystyrene par greffage de groupements pendants furaniques, qui seront ensuite mis en reaction avec des mono ou bismaleimides conduisant respectivement a des polyadduits ou des gels. Le second concerne la synthese et la polycondensation de monomeres
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Mansri, Ali. "Synthese et etude de polymeres styreniques porteurs de chaines laterales polycetoniques." Le Mans, 1987. http://www.theses.fr/1987LEMA1025.

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Synthese de nouveaux polymeres styreniques portant en chaine laterale soit des motifs dicetoniques-1,5, soit des motifs di et tricetoniques-1,3. Synthese des monomeres par photoaddition d'acylindanedione ou de tricetone-1,3 sur le styrene et le paradivinylbenzene. Polymerisation et copolymerisation radicalaire des monomeres. Etude physicochimique des polymeres
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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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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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Raihane, Mustapha. "Copolymérisation du méthyl cyanure de vinylidène (MVCN) avec l'acétate de vinyle et des styrènes substitués : synthèses, microstructures, propriétés et dégradation thermique." Saint-Etienne, 1993. http://www.theses.fr/1993STET4017.

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Le méthyl cyanure de vinylidène (MVCN) est un nouveau monomère préparé en une seule étape selon la méthode de Knoevenagel à partir de produits commerciaux. Ce monomère n'homopolymérise pas. Sa copolymérisation avec l'acétate de vinyle et des styrènes substitués est effectuée par voie radicalaire. Ces copolymères ont été caractérisés par les méthodes classiques d'analyse (IR, RMN, GPC, DSC, microanalyse. . . ). La microstructure de ces copolymères a été aussi étudiée par RMN #1h et #1#3C pour déterminer la répartition des stéréoséquences dans ces copolymères. Le mécanisme de copolymérisation a
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Book chapters on the topic "Styrene derivatives"

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Greenhalgh, Mark. "Iron-Catalysed Hydromagnesiation of Styrene Derivatives." In Iron-Catalysed Hydrofunctionalisation of Alkenes and Alkynes. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-33663-3_4.

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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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Bennetau, B. "By Hydrosilylation of Styrene Derivatives." In Compounds of Groups 15 (As, Sb, Bi) and Silicon Compounds. Georg Thieme Verlag KG, 2002. http://dx.doi.org/10.1055/sos-sd-004-00904.

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Kostikov, R. R. "Styrene Synthesis with Perfluoroalk-1-enylzinc Derivatives." In Three Carbon-Heteroatom Bonds: Ketenes and Derivatives. Georg Thieme Verlag KG, 2006. http://dx.doi.org/10.1055/sos-sd-024-00136.

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Nishimura, Naoya, Katsuya Maeyama, and Akinori Toyota. "Copolymerization of Styrene Derivatives and Cycloolefin with Ni Compound/MAO Catalyst." In Studies in Surface Science and Catalysis. Elsevier, 2006. http://dx.doi.org/10.1016/s0167-2991(06)80455-6.

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Taber, Douglass. "Enantioselective Construction of Alkylated Stereogenic Centers." In Organic Synthesis. Oxford University Press, 2011. http://dx.doi.org/10.1093/oso/9780199764549.003.0038.

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The enantioselectivity of alkene reduction usually depends on the geometric purity of the alkene. Bruce H. Lipshutz of the University of California, Santa Barbara used ( Organic Lett. 2007, 9, 4713) carboalumination of the alkyne 1 to prepare 2, which was selectively reduced to 3 in high ee. André B. Charette of the Université de Montréal reported ( Angew. Chem. Int. Ed. 2007, 46, 5955) a related reduction of unsaturated sulfones such as 4. Juan C. Carretero of the Universidad Autónoma de Madrid has developed ( J. Org. Chem. 2007, 72, 9924) a complementary route to enantiomerically-enriched su
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Hiney, Rachel M., Arne Ficks, Helge Müller-Bunz, Declan G. Gilheany, and Lee J. Higham. "Air-stable chiral primary phosphines part (i) synthesis, stability and applications." In Organometallic Chemistry. The Royal Society of Chemistry, 2011. http://dx.doi.org/10.1039/bk9781849731379-00027.

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This article reviews recent findings from our research groups on the preparation and utility of air-stable chiral primary phosphines. Enantiopure primary phosphines (R)-2 and (S)-3 have been synthesized and are remarkably stable to air-oxidation in both the neat state and in solution, by virtue of the extended π-ring system of the binaphthyl backbone. The extent of conjugation was found to be critical to their stability rather than the presence of bulky groups or heteroatoms. Despite this oxidative resistance, the ability to functionalize these atropisomeric primary phosphines remains, and the
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Beletskaya, I. P. "Organotin and organosilicon compounds in cross-coupling, aromatic nucleophilic substitution, and addition reactions." In Chemistry and Technology of Silicon and Tin. Oxford University PressOxford, 1992. http://dx.doi.org/10.1093/oso/9780198555803.003.0009.

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Abstract Abstract The reactions of organotin compounds with organic halides and acid halides catalysed by palladium complexes without phosphine ligands have been carried out under very mild conditions. These reactions afford biaryls, tolans, styrenes, dienes, and unsymmetrical ketones having various substituents. The synthesis of organotin compounds may be realized through the reactions of organic halides with hexaaryldistannanes catalysed by palladium and nickel complexes. The palladium-catalysed carbonylation of organic halides in the presence of organotin compounds of the series Alk SnNu (N
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Lambert, Tristan H. "Synthesis and Reactions of Alkenes." In Organic Synthesis. Oxford University Press, 2015. http://dx.doi.org/10.1093/oso/9780190200794.003.0032.

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Christine L. Willis and Varinder K. Aggarwal at the University of Bristol have developed (Angew. Chem. Int. Ed. 2012, 51, 12444) a procedure for the diastereodivergent synthesis of trisubstituted alkenes via the protodeboronation of allylic boronates, such as in the conversion of 1 to either 2 or 3. An alternative approach to the stereoselective synthesis of trisubstituted alkenes involving the reduction of the allylic C–O bond of cyclic allylic ethers (e.g., 4 to 5) was reported (Chem. Commun. 2012, 48, 7844) by Jon T. Njardarson at the University of Arizona. A novel synthesis of allylamines
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Conference papers on the topic "Styrene derivatives"

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Seijas, Julio, M. Vàsquez-Tato, and Luis Barreiro-Castro. "Reactivity of styrene derivatives: Nucleophilic addition versus 1,2-wittig rearrangement." In The 2nd International Electronic Conference on Synthetic Organic Chemistry. MDPI, 1998. http://dx.doi.org/10.3390/ecsoc-2-01670.

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Dolgin, I. S., Yu P. Zarubin та P. P. Purygin. "Synthesis and studying the values of dielectric permeability and tangens angles of dielectric losses for synthesized copolymers based on styrene and α-methylstyrene derivatives". У ACTUAL PROBLEMS OF ORGANIC CHEMISTRY AND BIOTECHNOLOGY (OCBT2020): Proceedings of the International Scientific Conference. AIP Publishing, 2022. http://dx.doi.org/10.1063/5.0070144.

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Castaldi, Marco J., and Eilhann Kwon. "An Investigation of the Thermal Degradation Mechanisms of a Waste Tire Through Chemical Analysis Including Hydrocarbons, Benzene Derivatives, and Polycyclic Aromatic Hydrocarbons (PAHs) at High Temperature." In 16th Annual North American Waste-to-Energy Conference. ASMEDC, 2008. http://dx.doi.org/10.1115/nawtec16-1914.

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Previous work has focused on a series of fundamental Thermal Gravimetric Analysis (TGA) studies using representative atmospheres found in Waste-to-Energy (WtE) boilers. Those studies were done for waste tires and their major constituents, such as Styrene-Butadiene Copolymer (SBR) and Poly-Isoprene (IR). The outcome has been the elucidation of the likely mechanism responsible for initial decomposition, final product and byproduct formation. To extend that understanding to a more practical level, a flow through apparatus has been used to test waste tire samples in the temperature range of 500°C–
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Kwon, Eilhann, Kelly J. Westby, and Marco J. Castaldi. "An Investigation Into the Syngas Production From Municipal Solid Waste (MSW) Gasification Under Various Pressures and CO2 Concentration Atmospheres." In 17th Annual North American Waste-to-Energy Conference. ASMEDC, 2009. http://dx.doi.org/10.1115/nawtec17-2351.

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The Municipal Solid Waste (MSW) gasification process is a promising candidate for both MSW disposal and syngas production. The MSW gasification process has been characterized thermo-gravimetrically under various experimental atmospheres in order to understand syngas production and char burnout. This preliminary data shows that with any concentration of carbon dioxide in the atmosphere the residual char is reduced about 20% of the original mass (in an inert atmosphere) to about 5%, corresponding to a significant amount of carbon monoxide production (0.7% of CO was produced from a 20mg sample wi
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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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Malik, Sanjay, Andrew J. Blakeney, Lawrence Ferreira, et al. "Lithographic properties of novel acetal-derivatized hydroxy styrene polymers." In Microlithography '99, edited by Will Conley. SPIE, 1999. http://dx.doi.org/10.1117/12.350222.

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Niino, Hiroyuki, Tatsuya Imura, Tsuguyori Ohana, Chiaki Nagai, and Akira Yabe. "Formation of radicals on the surface of polymer films by excimer laser ablation: Application to surface reaction of ablated polymer films with a styrene derivative." In Laser ablation: mechanisms and applications—II. AIP, 1993. http://dx.doi.org/10.1063/1.44856.

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Funes-Gallanzi, M. "A Novel Fluids Research Technique: Three-State Anemometry." In ASME 1996 International Gas Turbine and Aeroengine Congress and Exhibition. American Society of Mechanical Engineers, 1996. http://dx.doi.org/10.1115/96-gt-305.

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A new flow measurement technique is described which allows for the non-intrusive simultaneous measurement of flow velocity, density, and viscosity. The viscosity information can be used to derive the flow field temperature. The combination of the three measured variables and the perfect-gas law then leads to an estimate of the flow field pressure. Thus, the instantaneous state of a flow field can be completely described. Three-State anemometry (3SA), a derivative of PIV, which uses a combination of three monodisperse sizes of styrene seeding particles is proposed. A marker seeding is chosen to
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