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Статті в журналах з теми "Furans Conversion"
Rivas, Sandra, María Jesús González-Muñoz, Valentín Santos, and Juan Carlos Parajó. "Production of furans from hemicellulosic saccharides in biphasic reaction systems." Holzforschung 67, no. 8 (December 1, 2013): 923–29. http://dx.doi.org/10.1515/hf-2013-0017.
Повний текст джерелаYuliati, Frita, Peter J. Deuss, Hero J. Heeres, and Francesco Picchioni. "Towards Thermally Reversible Networks Based on Furan-Functionalization of Jatropha Oil." Molecules 25, no. 16 (August 10, 2020): 3641. http://dx.doi.org/10.3390/molecules25163641.
Повний текст джерелаYang, Yanliang, Dongsheng Deng, Dong Sui, Yanfu Xie, Dongmi Li, and 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 (November 28, 2019): 1698. http://dx.doi.org/10.3390/nano9121698.
Повний текст джерелаMao, Yanli, and François Mathey. "The Conversion of Furans into Phosphinines." Chemistry – A European Journal 17, no. 38 (August 11, 2011): 10745–51. http://dx.doi.org/10.1002/chem.201100834.
Повний текст джерелаKumar, Hemant, and Marco Fraaije. "Conversion of Furans by Baeyer-Villiger Monooxygenases." Catalysts 7, no. 6 (June 7, 2017): 179. http://dx.doi.org/10.3390/catal7060179.
Повний текст джерелаHu, Xun, Roel J. M. Westerhof, Liping Wu, Dehua Dong, and 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.
Повний текст джерелаWang, Ting, Xianming Guo, Tao Chen, and 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.
Повний текст джерелаGuillard, Jér̂ome, Otto Meth-Cohn, Charles W. Rees, Andrew J. P. White, and David J. Williams. "Direct conversion of macrocyclic furans into macrocyclic isothiazoles." Chemical Communications, no. 3 (January 17, 2002): 232–33. http://dx.doi.org/10.1039/b110287g.
Повний текст джерелаPelter, Andrew, and Martin Rowlands. "The conversion of furans to 2(3H)-butenolides." Tetrahedron Letters 28, no. 11 (January 1987): 1203–6. http://dx.doi.org/10.1016/s0040-4039(00)95326-7.
Повний текст джерелаXu, Lujiang, Yuanye Jiang, Qian Yao, Zheng Han, Ying Zhang, Yao Fu, Qingxiang Guo, and 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.
Повний текст джерелаДисертації з теми "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.
Повний текст джерелаHoward, 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.
Повний текст джерелаAit, 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.
Повний текст джерелаThis 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], and 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.
Повний текст джерелаMuralidhara, 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.
Повний текст джерелаThe 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.
Повний текст джерелаЧастини книг з теми "Furans Conversion"
Nussbaumer, T., and P. Hasler. "Formation and Reduction of Polychlorinated Dioxins and Furans in Biomass Combustion." In Developments in Thermochemical Biomass Conversion, 1492–506. Dordrecht: Springer Netherlands, 1997. http://dx.doi.org/10.1007/978-94-009-1559-6_117.
Повний текст джерелаOhyama, Junya, and Atsushi Satsuma. "Reductive Conversion of 5-Hydroxymethylfurfural in Aqueous Solutions by Furan Ring Opening and Rearrangement." In 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.
Повний текст джерелаChatterjee, Amrita, Xijun Hu, and Frank L. Y. Lam. "Case Study 2: Development of Hydrothermally Stable Functional Materials for Sustainable Conversion of Biomass to Furan Compounds." In Sustainable Catalysis, 251–72. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2018. http://dx.doi.org/10.1002/9783527693030.oth2.
Повний текст джерелаTaber, Douglass. "Preparation of Heteroaromatics." In Organic Synthesis. Oxford University Press, 2011. http://dx.doi.org/10.1093/oso/9780199764549.003.0068.
Повний текст джерелаPal, Priyanka, and S. Saravanamurugan. "Conversion of cellulosic biomass to furanics." In Biomass, Biofuels, Biochemicals, 339–72. Elsevier, 2022. http://dx.doi.org/10.1016/b978-0-12-824419-7.00021-2.
Повний текст джерелаLambert, Tristan H. "Advances in Heterocyclic Aromatic Construction." In Organic Synthesis. Oxford University Press, 2015. http://dx.doi.org/10.1093/oso/9780190200794.003.0068.
Повний текст джерелаZhang, Ke, Quanxing Zheng, Zhongya Guo, Lili Fu, Qi Zhang, and Bing Wang. "Study on Pyrolysis Behaviors of Various Plant Fibers." In Cellulose - Fundamentals and Conversion Into Biofuel and Useful Chemicals [Working Title]. IntechOpen, 2022. http://dx.doi.org/10.5772/intechopen.109294.
Повний текст джерелаSmith, Eric C. "“Comforts and mercies, losses and crosses”." In Oliver Hart and the Rise of Baptist America, 199–221. Oxford University Press, 2020. http://dx.doi.org/10.1093/oso/9780197506325.003.0010.
Повний текст джерелаMitchell, Jennifer. "Mythologizing Masochisms." In Ordinary Masochisms, 21–32. University Press of Florida, 2020. http://dx.doi.org/10.5744/florida/9780813066677.003.0002.
Повний текст джерелаLambert, Tristan H. "Synthesis of Heteroaromatics." In Organic Synthesis. Oxford University Press, 2015. http://dx.doi.org/10.1093/oso/9780190200794.003.0069.
Повний текст джерелаТези доповідей конференцій з теми "Furans Conversion"
Kessler, Travis, Eric R. Sacia, Alexis T. Bell, and J. Hunter Mack. "Predicting the Cetane Number of Furanic Biofuel Candidates Using an Improved Artificial Neural Network Based on Molecular Structure." In ASME 2016 Internal Combustion Engine Division Fall Technical Conference. American Society of Mechanical Engineers, 2016. http://dx.doi.org/10.1115/icef2016-9383.
Повний текст джерелаDuo, Wenli, Ibrahim Karidio, Larry Cross, and Bob Ericksen. "Combustion and Emission Performance of a Hog Fuel Fluidized Bed Boiler With Addition of Tire Derived Fuel." In 17th International Conference on Fluidized Bed Combustion. ASMEDC, 2003. http://dx.doi.org/10.1115/fbc2003-016.
Повний текст джерелаLei, Hanwu, Shoujie Ren, James Julson, Lu Wang, Quan Bu, and Roger Ruan. "Microwave Torrefaction of Corn Stover and Tech-Economic Analysis." In ASME 2011 International Manufacturing Science and Engineering Conference. ASMEDC, 2011. http://dx.doi.org/10.1115/msec2011-50230.
Повний текст джерелаDe Oliveira Vigier, Karine, Christophe Coutanceau, and 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." In 2022 AOCS Annual Meeting & Expo. American Oil Chemists' Society (AOCS), 2022. http://dx.doi.org/10.21748/olba8004.
Повний текст джерелаЗвіти організацій з теми "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), January 2019. http://dx.doi.org/10.2172/1593368.
Повний текст джерелаCoulombe, S., G. Jean, P. Chantal, and 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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