Littérature scientifique sur le sujet « Furans Conversion »
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Articles de revues sur le sujet "Furans Conversion"
Rivas, Sandra, María Jesús González-Muñoz, Valentín Santos et Juan Carlos Parajó. « Production of furans from hemicellulosic saccharides in biphasic reaction systems ». Holzforschung 67, no 8 (1 décembre 2013) : 923–29. http://dx.doi.org/10.1515/hf-2013-0017.
Texte intégralYuliati, Frita, Peter J. Deuss, Hero J. Heeres et Francesco Picchioni. « Towards Thermally Reversible Networks Based on Furan-Functionalization of Jatropha Oil ». Molecules 25, no 16 (10 août 2020) : 3641. http://dx.doi.org/10.3390/molecules25163641.
Texte intégralYang, Yanliang, Dongsheng Deng, Dong Sui, Yanfu Xie, Dongmi Li et Ying Duan. « Facile Preparation of Pd/UiO-66-v for the Conversion of Furfuryl Alcohol to Tetrahydrofurfuryl Alcohol under Mild Conditions in Water ». Nanomaterials 9, no 12 (28 novembre 2019) : 1698. http://dx.doi.org/10.3390/nano9121698.
Texte intégralMao, Yanli, et François Mathey. « The Conversion of Furans into Phosphinines ». Chemistry – A European Journal 17, no 38 (11 août 2011) : 10745–51. http://dx.doi.org/10.1002/chem.201100834.
Texte intégralKumar, Hemant, et Marco Fraaije. « Conversion of Furans by Baeyer-Villiger Monooxygenases ». Catalysts 7, no 6 (7 juin 2017) : 179. http://dx.doi.org/10.3390/catal7060179.
Texte intégralHu, Xun, Roel J. M. Westerhof, Liping Wu, Dehua Dong et Chun-Zhu Li. « Upgrading biomass-derived furans via acid-catalysis/hydrogenation : the remarkable difference between water and methanol as the solvent ». Green Chemistry 17, no 1 (2015) : 219–24. http://dx.doi.org/10.1039/c4gc01826e.
Texte intégralWang, Ting, Xianming Guo, Tao Chen et Juan Li. « The Pd(0) and Pd(ii) cocatalyzed isomerization of alkynyl epoxides to furans : a mechanistic investigation using DFT calculations ». Dalton Transactions 49, no 27 (2020) : 9223–30. http://dx.doi.org/10.1039/d0dt00965b.
Texte intégralGuillard, Jér̂ome, Otto Meth-Cohn, Charles W. Rees, Andrew J. P. White et David J. Williams. « Direct conversion of macrocyclic furans into macrocyclic isothiazoles ». Chemical Communications, no 3 (17 janvier 2002) : 232–33. http://dx.doi.org/10.1039/b110287g.
Texte intégralPelter, Andrew, et Martin Rowlands. « The conversion of furans to 2(3H)-butenolides ». Tetrahedron Letters 28, no 11 (janvier 1987) : 1203–6. http://dx.doi.org/10.1016/s0040-4039(00)95326-7.
Texte intégralXu, Lujiang, Yuanye Jiang, Qian Yao, Zheng Han, Ying Zhang, Yao Fu, Qingxiang Guo et George W. Huber. « Direct production of indoles via thermo-catalytic conversion of bio-derived furans with ammonia over zeolites ». Green Chemistry 17, no 2 (2015) : 1281–90. http://dx.doi.org/10.1039/c4gc02250e.
Texte intégralThèses sur le sujet "Furans Conversion"
ZHANG, WENWEN. « Catalytic Conversion of Sugar Mixtures into Furan Products in Ionic Liquid Media with Organic Solvent Extraction ». University of Toledo / OhioLINK, 2012. http://rave.ohiolink.edu/etdc/view?acc_num=toledo1341540235.
Texte intégralHoward, Joshua M. « Catalytic conversion of sugar manufacturing by-products to 5-(chloromethyl) furfural and 5-(hydroxymethyl) furural ». Thesis, Queensland University of Technology, 2017. https://eprints.qut.edu.au/107143/2/Joshua_Howard_Thesis.pdf.
Texte intégralAit, Rass Hicham. « Transformation chimique du furfural en acide 2,5-furane dicarboxylique par catalyse hétérogène ». Thesis, Lyon 1, 2014. http://www.theses.fr/2014LYO10198/document.
Texte intégralThis thesis reports a study of heterogeneously catalyzed conversion of furfural (biobased product formed from the acid-catalyzed dehydration of xylose) into 2,5-furane dicarboxylique acid (FDCA, possible replacement monomer for terephtalic acid for the production of polyethylene terephtalate). This transformation has been considered in two catalytic steps: 1) hydroxymethylation of furfural with aqueous formaldehyde or trioxane into 5-hydroxymethylfurfural (HMF) in the presence of solid acids. The maximum yields of 40% have been obtained using aqueous formaldehyde in the presence of nanoparticles of ZSM-5. The main problem was the lack of stability of furfural and HMF in reaction conditions. 2) aerobic oxidation of HMF into FDCA. HMF was oxidized in alkaline aqueous solutions over Pt-based catalysts using dioxygen from air. Promotion of the catalyst with bismuth and the presence of a weak base (Na2CO3) yielded a catalytic system with a remarkable activity and selectivity. HMF was completely and exclusively converted to FDCA within 2,5 h. The catalyst could be recovered by simple filtration and reused several times without significant loss of activity and with no platinum or bismuth leaching
Ulbrich, Kathrin [Verfasser], et Oliver [Akademischer Betreuer] Reiser. « The conversion of furan derivatives from renewable resources into valuable building blocks and their application in synthetic chemistry / Kathrin Ulbrich. Betreuer : Oliver Reiser ». Regensburg : Universitätsbibliothek Regensburg, 2014. http://d-nb.info/1068055839/34.
Texte intégralMuralidhara, Anitha. « Physico-chemical safety issues pertaining to biosourced furanics valorization with a focus on humins as biomass resource ». Thesis, Compiègne, 2019. http://www.theses.fr/2019COMP2508.
Texte intégralThe present research work was integrated as part of the EU-funded project named HUGS (HUmins as Green and Sustainable precursors for eco-friendly building blocks and materials), involving 5 main partners (Institut national de l'environnement industriel et des risques - France, Avantium - the Netherlands, Institut de Chimie de Nice - France, Universidad De Cordoba- Spain and Leibniz - Institut Fur Katalyse Ev An Der Universitat Rostock- Germany). The project is essentially supported through five European Industrial Doctorate fellowships put in place when the HUGS-MSCA-ITN-2015 program was launched in 2016. The primary objective of the HUGS project was to explore several valorization pathways of so-called “humins” in order to add value and create better business cases. Humins (and similarly lignins) are the side products that may become low-cost feedstock resulting from a number of future biorefineries and sugar conversion processes. Humins are complex residues resulting from the Acid-Catalyzed Dehydration and condensation of sugars, having furan-rings in their polymeric structures. The work presented in this specific part of the HUGS project is essentially focusing on safety-related topics of all components and subsequent applications related to sugar dehydration technology. Priority actions were devoted to a first insight on the characterization of physicochemical safety profiles of the side-product humins and main (parent) furanic products. Some members of this large family of compounds (e.g. RMF and FDCA) have high volume potential which results in opening new doors towards the development of furanbased building blocks and a bio-based economy. Humins are residues or side products which can be burnt for energy. However, its safe and sustainable use in high-value applications could also become a key milestone in the so-called circular economy. In practice, the work has been developed in two main locations: primarily at the INERIS lab, located in Verneuil-en-Halatte and at Avantium, located in Amsterdam. Nearly all experimental research after the production of the components at Avantium was performed at INERIS. This involved the evaluation of physicochemical hazards of both humins (crude industrial humins and humin foams obtained by thermal curing) and a series of furanic compounds. Avantium is involved in the commercialization of humins, furanics and furanic polymers/materials as novel chemicals and materials. The work has encompassed: An extensive bibliographical review of humins, furanics, and their related products (polymers, composites) resulted in the following main conclusions o A lack of physicochemical safety-oriented studies for many furanic compounds and for humins was observed as these products are still in the early stage of development and only a few may be commercialized in the next 5 years.o Despite the limited availability of safety-related data, more studies on toxicity aspects have been conducted for a selected number of furanics than physicochemical safety-related aspects. o A few furanic family members that have been evaluated as biofuel components were found to have given better emphasis on addressing some physicochemical safety attributes. o Every modification of the process for acid-catalyzed sugar dehydration (such as solvent, temperature, residence time and sugar concentration) will result in different humins, which would certainly demand further characterization and safety profiling of the resulting humins. • Analytical development integrating the first examination of flash point distribution versus the Net Heating Values, and analysis of total heats of combustion of furanic compounds. • Design and development of experimental plan addressing the safety-related key parameters such as thermal stability, self-heating risks, fire-risk-assessment and flammability limits depending on the need for specific tests and availability of the test samples
Cheng, Yu-Ting. « Catalytic fast pyrolysis of furan over ZSM-5 catalysts : A model biomass conversion reaction ». 2012. https://scholarworks.umass.edu/dissertations/AAI1530357.
Texte intégralChapitres de livres sur le sujet "Furans Conversion"
Nussbaumer, T., et P. Hasler. « Formation and Reduction of Polychlorinated Dioxins and Furans in Biomass Combustion ». Dans Developments in Thermochemical Biomass Conversion, 1492–506. Dordrecht : Springer Netherlands, 1997. http://dx.doi.org/10.1007/978-94-009-1559-6_117.
Texte intégralOhyama, Junya, et Atsushi Satsuma. « Reductive Conversion of 5-Hydroxymethylfurfural in Aqueous Solutions by Furan Ring Opening and Rearrangement ». Dans Production of Biofuels and Chemicals with Bifunctional Catalysts, 159–85. Singapore : Springer Singapore, 2017. http://dx.doi.org/10.1007/978-981-10-5137-1_5.
Texte intégralChatterjee, Amrita, Xijun Hu et Frank L. Y. Lam. « Case Study 2 : Development of Hydrothermally Stable Functional Materials for Sustainable Conversion of Biomass to Furan Compounds ». Dans Sustainable Catalysis, 251–72. Weinheim, Germany : Wiley-VCH Verlag GmbH & Co. KGaA, 2018. http://dx.doi.org/10.1002/9783527693030.oth2.
Texte intégralTaber, Douglass. « Preparation of Heteroaromatics ». Dans Organic Synthesis. Oxford University Press, 2011. http://dx.doi.org/10.1093/oso/9780199764549.003.0068.
Texte intégralPal, Priyanka, et S. Saravanamurugan. « Conversion of cellulosic biomass to furanics ». Dans Biomass, Biofuels, Biochemicals, 339–72. Elsevier, 2022. http://dx.doi.org/10.1016/b978-0-12-824419-7.00021-2.
Texte intégralLambert, Tristan H. « Advances in Heterocyclic Aromatic Construction ». Dans Organic Synthesis. Oxford University Press, 2015. http://dx.doi.org/10.1093/oso/9780190200794.003.0068.
Texte intégralZhang, Ke, Quanxing Zheng, Zhongya Guo, Lili Fu, Qi Zhang et Bing Wang. « Study on Pyrolysis Behaviors of Various Plant Fibers ». Dans Cellulose - Fundamentals and Conversion Into Biofuel and Useful Chemicals [Working Title]. IntechOpen, 2022. http://dx.doi.org/10.5772/intechopen.109294.
Texte intégralSmith, Eric C. « “Comforts and mercies, losses and crosses” ». Dans Oliver Hart and the Rise of Baptist America, 199–221. Oxford University Press, 2020. http://dx.doi.org/10.1093/oso/9780197506325.003.0010.
Texte intégralMitchell, Jennifer. « Mythologizing Masochisms ». Dans Ordinary Masochisms, 21–32. University Press of Florida, 2020. http://dx.doi.org/10.5744/florida/9780813066677.003.0002.
Texte intégralLambert, Tristan H. « Synthesis of Heteroaromatics ». Dans Organic Synthesis. Oxford University Press, 2015. http://dx.doi.org/10.1093/oso/9780190200794.003.0069.
Texte intégralActes de conférences sur le sujet "Furans Conversion"
Kessler, Travis, Eric R. Sacia, Alexis T. Bell et J. Hunter Mack. « Predicting the Cetane Number of Furanic Biofuel Candidates Using an Improved Artificial Neural Network Based on Molecular Structure ». Dans ASME 2016 Internal Combustion Engine Division Fall Technical Conference. American Society of Mechanical Engineers, 2016. http://dx.doi.org/10.1115/icef2016-9383.
Texte intégralDuo, Wenli, Ibrahim Karidio, Larry Cross et Bob Ericksen. « Combustion and Emission Performance of a Hog Fuel Fluidized Bed Boiler With Addition of Tire Derived Fuel ». Dans 17th International Conference on Fluidized Bed Combustion. ASMEDC, 2003. http://dx.doi.org/10.1115/fbc2003-016.
Texte intégralLei, Hanwu, Shoujie Ren, James Julson, Lu Wang, Quan Bu et Roger Ruan. « Microwave Torrefaction of Corn Stover and Tech-Economic Analysis ». Dans ASME 2011 International Manufacturing Science and Engineering Conference. ASMEDC, 2011. http://dx.doi.org/10.1115/msec2011-50230.
Texte intégralDe Oliveira Vigier, Karine, Christophe Coutanceau et Steve Baranton. « Electro-oxidation of glycerol and diglycerol in the presence of Pt or Pd-based electrocatalyst follows by the reductive amination of the products obtained ». Dans 2022 AOCS Annual Meeting & Expo. American Oil Chemists' Society (AOCS), 2022. http://dx.doi.org/10.21748/olba8004.
Texte intégralRapports d'organisations sur le sujet "Furans Conversion"
Chadderdon, Xiaotong Han. Electrochemical conversion of biomass-derived furanics for production of renewable chemicals and fuels. Office of Scientific and Technical Information (OSTI), janvier 2019. http://dx.doi.org/10.2172/1593368.
Texte intégralCoulombe, S., G. Jean, P. Chantal et S. Kaliaguine. Characterization of products from the conversion of furanic compounds to hydrocarbons on zeolite using gas chromatography/mass spectrometry and gas chromatography/Fourier transform infrared spectrometry. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 1985. http://dx.doi.org/10.4095/302618.
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