Littérature scientifique sur le sujet « Biomass derivatives »
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Articles de revues sur le sujet "Biomass derivatives"
Ge, Shaokui, Ming Xu, Gerald L. Anderson et Raymond I. Carruthers. « Estimating Yellow Starthistle (Centaurea solstitialis) Leaf Area Index and Aboveground Biomass with the Use of Hyperspectral Data ». Weed Science 55, no 6 (décembre 2007) : 671–78. http://dx.doi.org/10.1614/ws-06-212.1.
Texte intégralDutta, Saikat, Linglin Wu et Mark Mascal. « Production of 5-(chloromethyl)furan-2-carbonyl chloride and furan-2,5-dicarbonyl chloride from biomass-derived 5-(chloromethyl)furfural (CMF) ». Green Chemistry 17, no 7 (2015) : 3737–39. http://dx.doi.org/10.1039/c5gc00936g.
Texte intégralde Assis, Geovânia C., Igor M. A. Silva, Tiago G. dos Santos, Thatiane V. dos Santos, Mario R. Meneghetti et Simoni M. P. Meneghetti. « Photocatalytic processes for biomass conversion ». Catalysis Science & ; Technology 11, no 7 (2021) : 2354–60. http://dx.doi.org/10.1039/d0cy02358b.
Texte intégralLu, Xihong, Shilei Xie, Hao Yang, Yexiang Tong et Hongbing Ji. « Photoelectrochemical hydrogen production from biomass derivatives and water ». Chem. Soc. Rev. 43, no 22 (2014) : 7581–93. http://dx.doi.org/10.1039/c3cs60392j.
Texte intégralCottet, Celeste, Yuly A. Ramirez-Tapias, Juan F. Delgado, Orlando de la Osa, Andrés G. Salvay et Mercedes A. Peltzer. « Biobased Materials from Microbial Biomass and Its Derivatives ». Materials 13, no 6 (11 mars 2020) : 1263. http://dx.doi.org/10.3390/ma13061263.
Texte intégralLund, Torben, Henning Lund et Jyoti Chattopadhyaya. « Electrochemical Reduction of Furan Derivatives Derived from Biomass. » Acta Chemica Scandinavica 39b (1985) : 429–35. http://dx.doi.org/10.3891/acta.chem.scand.39b-0429.
Texte intégralZhao, Li, Niki Baccile, Silvia Gross, Yuanjian Zhang, Wei Wei, Yuhan Sun, Markus Antonietti et Maria-Magdalena Titirici. « Sustainable nitrogen-doped carbonaceous materials from biomass derivatives ». Carbon 48, no 13 (novembre 2010) : 3778–87. http://dx.doi.org/10.1016/j.carbon.2010.06.040.
Texte intégralONDA, Ayumu, Shuhei OGO et Kazumichi YANAGISAWA. « Catalytic Conversions of Biomass Derivatives Over Apatite Compounds ». Hyomen Kagaku 32, no 6 (2011) : 387–92. http://dx.doi.org/10.1380/jsssj.32.387.
Texte intégralUmerzakova, M. B., B. K. Donenov, R. B. Sarieva et Zh N. Kainarbaeva. « PREPARATION OF SULPHATED FATTY ACID DERIVATIVES OF SPIRULINA OIL ». Chemical Journal of Kazakhstan 73, no 1 (14 mars 2021) : 34–42. http://dx.doi.org/10.51580/2021-1/2710-1185.03.
Texte intégralLiu, Xiaoqing, Xiaoguang Duan, Wei Wei, Shaobin Wang et Bing-Jie Ni. « Photocatalytic conversion of lignocellulosic biomass to valuable products ». Green Chemistry 21, no 16 (2019) : 4266–89. http://dx.doi.org/10.1039/c9gc01728c.
Texte intégralThèses sur le sujet "Biomass derivatives"
Yin, Xiuli, et 陰秀麗. « Synthesizing methanol from biomass derived syngas ». Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2004. http://hub.hku.hk/bib/B31456844.
Texte intégralReocreux, Romain. « Biomass derivatives in heterogeneous catalysis : adsorption, reactivity and support from first principles ». Thesis, Lyon, 2017. http://www.theses.fr/2017LYSEN019/document.
Texte intégralMoving away from fossil ressources is currently being accompanied by the increasing exploitation of biomass.This shift requires the development of new processes, in particular in heterogeneous catalysis. Chemists are nowfacing two major challenges: (i) deoxygenate biomass (cellulose/lignin) to produce platform intermediates with aeel-known chemistry (ii) make catalysts resistant to water, ubiquitous within the context of biomass.Within a collaboration with experimentalists at the University of Ottawa, we have first studied the deoxygenationof lignin-like aromatics. From an ab initio (DFT) inspection, we have characterized and described the adsorptionof such aromatic oxygenates on Pt(111) with simple molecular descriptors. We have then investigated thedecomposition mechanism of anisole and 2-phenoxyethanol. For these two model compounds, we have showedthe significance of hydrogen and carbonaceous species to have the deoxygenation reaction proceed properly.Meanwhile, we have examined the stability, in water, of γ-alumina, a major support in heterogeneous catalysis.The necessity to perform ab initio molecular dynamics simulations makes the modeling of such a systemparticularly challenging computationally. The simulations have nevertheless enabled us to characterize thestructuration of liquid water in contact with alumina and the significance of solvation on surface aluminol groups.Using rare-event methods (constrained dynamics, metadynamics) we have eventually been able to probe thereactivity of alcohols and water with hydrated alumina. We have then identified the first steps of hydration andgained insights on how to limit them
Shaheed, Abdul. « Coconut oil and its derivatives as a renewable alternative diesel fuel for use in the Maldives ». Thesis, Loughborough University, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.299675.
Texte intégralAbaye, Daniel. « Lipid derivatives and the relationships between microbial biomass, community structure and activity in soils ». Thesis, University of Nottingham, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.324119.
Texte intégralAlipour, Siamak. « Conversion of Cellulose from Plant Biomass to 5-(hydroxymethyl)furfural (HMF) and its Derivatives in Ionic Liquid Media ». University of Toledo / OhioLINK, 2015. http://rave.ohiolink.edu/etdc/view?acc_num=toledo1429780958.
Texte intégralSCELFO, SIMONE. « Metal oxides catalysts for the synthesis of value-added chemicals from 2nd generation sugars and sugar derivatives ». Doctoral thesis, Politecnico di Torino, 2017. http://hdl.handle.net/11583/2675152.
Texte intégralStüke, Caroline Ziegler. « Prospecção fitoquímica e atividade biológica de plantas medicinais da família asteraceae do bioma pampa ». Universidade Federal de Santa Maria, 2012. http://repositorio.ufsm.br/handle/1/4226.
Texte intégralThe species selected for this study were: Pluchea sagittalis, Baccharis pentodonta and Baccharidastrum triplinervium, all belonging to the Asteraceae family. The extracts and fractions from leaves and roots of three species of medicinal plants in Rio Grande do Sul were obtained by different extraction processes (cold, the hot water extraction and soxhlet) and subjected to HPLC analysis. These extracts and fractions were subjected to different fractionations were isolated where some secondary metabolites (chlorogenic acid derivatives and flavonoids). In the leaves of Pluchea sagittalis were isolated the secundary metabolites 3,4- dicaffeoylquinic acid, 3,5-dicaffeoylquinic acid and 4,5-dicaffeoylquinic acid. The crude extract of the root of the same species were isolated the same three metabolites 3,4-dicaffeoylquinic acid, 3,5-dicaffeoylquinic acid and 4,5-dicaffeoylquinic acid and the 1,3, 5-tricaffeoylquinic acid. Baccharis pentodonta were isolated metabolites 5,7,4'- trihydroxy-6-methoxy-luteolin and 5,7,3,4 - tretrahydroxy-6-methoxy-flavon for leaves and their metabolites 3,4-dicaffeoylquinic acid, 3,5-dicaffeoylquinic acid, 4,5- dicaffeoylquinic acid and 3-feruloyl-5-caffeoylquinic acid. The root Baccharidastrum triplinervium were isolated metabolites 3,4-dicaffeoylquinic acid, 3,5-dicaffeoylquinic acid and 4,5-dicaffeoylquinic acid already isolated from other species previously worked. The structures of these metabolites isolated was characterized by NMR analysis and high resolution mass. Additionally extracts and fractions obtained were tested in vitro and to determine their antimicrobial, antioxidant and enzyme inhibition against the enzyme DPP IV and POP. Most of the extracts and fractions tested showed antimicrobial activity by the method of microdilution around 0,5 mg ml-1 and moderate antioxidant activity by the method of free radical (DPPH) and the ethyl acetate fraction showed the highest potential. Among the activities of enzyme inhibition, the activity was more pronounced compared to POP, with only the crude extracts of the roots of B. pentodonta and B. triplinervium presented themselves as potential inhibitors of the enzyme DPP IV.
As espécies selecionadas para este estudo foram: Pluchea sagittalis, Baccharis pentodonta e Baccharidastrum triplinervium, todas pertencentes a família Asteraceae. Os extratos e frações das folhas e raízes destas três espécies de plantas medicinais do Rio Grande do Sul foram obtidos por diferentes processos de extração (a frio, a quente em soxhlet e extração aquosa) e submetidos à análise por CLAE. Estes extratos e frações obtidos foram submetidos a diferentes fracionamentos de onde foram isolados alguns metabólitos secundários (derivados do ácido clorogênico e flavonóides). Das folhas de Pluchea sagittalis foram isolados os metabólitos ácido 3,4-dicafeoilquínico, ácido 3,5-dicafeoilquínico e ácido 4,5-dicafeoilquínico. Do extrato bruto da raiz desta mesma espécie foram isolados os mesmos três metabólitos ácido 3,4-dicafeoilquínico, ácido 3,5-dicafeoilquínico e ácido 4,5-dicafeoilquínico além do ácido 1,3,5- tricafeoilquínico. De Baccharis pentodonta foram isolados os metabólitos 5,7,4 - triidroxi-6-metoxi-luteonina e 5,7,3,4 - tretrahidroxi-6-metoxi-flavona de suas folhas e os metabólitos ácido 3,4-dicafeoilquínico, ácido 3,5-dicafeoilquínico, ácido 4,5- dicafeoilquínico e ácido 3-feruloil-5-cafeoilquínico. Da raiz de Baccharidastrum triplinervium foram isolados os metabólitos ácido 3,4-dicafeoilquínico, ácido 3,5- dicafeoilquínico, ácido 4,5-dicafeoilquínico já isolados anteriormente das outras espécies trabalhadas. A elucidação estrutural desses metabólitos isolados se deu por RMN e por análises de massa de alta resolução. Adicionalmente os extratos e frações obtidos foram submetidos a testes in vitro e para determinação de suas atividades antimicrobiana, antioxidante e de inibição enzimática frente às enzimas POP e DPP IV. A maioria dos extratos e frações testados apresentou atividade antimicrobiana pelo método de microdiluição em caldo por volta de 0,5 mg mL-1 e atividade antioxidante moderada pelo método do radical livre (DPPH) sendo a fração acetato de etila a que apresentou maior potencial. Dentre as atividades de inibição enzimática, as atividade mais pronunciadas foram frente a POP, sendo que apenas os extratos brutos das raízes de B. pentodonta e B. triplinervium apresentaram-se como potenciais inibidores da enzima DPP IV.
Shen, Qun. « Utilization of biomass derivatives from waste sugar acids ». 1989. http://catalog.hathitrust.org/api/volumes/oclc/19476155.html.
Texte intégralTypescript. eContent provider-neutral record in process. Description based on print version record. Includes bibliographical references (leaves 89-93).
Zeng, Yan-Ru, et 曾彥儒. « Butanol fermentation from lignocellulosic biomass hydrolysate : effectof phenolic derivatives ». Thesis, 2018. http://ndltd.ncl.edu.tw/handle/a9yu9t.
Texte intégral國立宜蘭大學
環境工程學系碩士班
106
With the growth of population, the problem of environment and energy shortage has attracted people's attention, and bioenergy is one of the most effective way to solve the problem. Bioethanol is the first to be studied and discussed in bioenergy, but biobutanol has more advantages than bioethanol such as more rich energy , less volatile , less corrosive and easier to purify than bioethanol。It can solve the environmental problems and re-use it for energy production by using waste containing lignocellulose as a substrate. Lignocellulose has a structure that is difficult to be decomposed by microorganisms , so before use must be subjected to hydrolysis pretreatment. In addition to saccharides for microorganisms by hydrolysis , other inhibitory byproducts are also produced. These inhibitory by-products are classified as furan derivatives, carboxylic acid compounds and phenolic compounds. Among them, the phenolic compounds than the other two byproducts to suppress the effect of strong, the most complex types. The effects of phenolic byproducts have been extensively discussed in biomass ethanol, but not in biomass butanol. In this study, common lignocellulose hydrolyzed phenolic compounds vanillin, 4-hydroxyhydroxyoic acid (4-HBA) and syringaldehyde were added to different concentrations of C.saccharoperbutylacetonicum N1- 4 (ATCC 27021) fed-batch culture. The results of the study found that: The inhibitory effect of vanillin on the product increased with increasing concentration , at 0.5 g / L, the cell growth was increased by 9.5% compared with the control group , the 1.5 g / L cell growth ratio higher than 8% at 1.0 g/L; Until the complete inhibition of the product and cells was achieved at 8.0 g / L. The inhibition of cell growth was increased with the increase of 4-HBA concentration. The inhibitory effect of product and cell growth did not increase with the concentration of clove aldehyde , such as syringaldehyde concentration 1.0 g/L and 1.5 g/L were 12.1% , 42.2% and 33.7% , 50.1%;at 0.5 g/L glucose utilization increased 13% than the control group. According to the results, the vanillin inhibition mechanism was judged to inhibit the production of coenzyme by inhibiting the production of the product; Syringaldehyde inhibit the production of cells by inhibiting cells. Three compounds in the 1.0 g / L production inhibition of more than 80%, the cell growth inhibition of more than 60%, but less than or greater than 1.0 g / L concentration will be different according to different compounds have different inhibitory effect.
Kupeta, Albert Jerry Kafushe. « Synthesis of cross-linked pine cone biosorbent and its applications in industrial wastewater treatment ». Thesis, 2014. http://hdl.handle.net/10352/340.
Texte intégralThe widespread use of phenols and phenolic derivatives in industrial applications has resulted in their discharge as part of industrial wastewater. These chemicals are toxic and need to be removed from the aqueous environment. Amongst the available pollutant removal technologies, adsorption has been widely used due to its simplicity, ease of operation, cost-effectiveness and ability to sequester pollutants at very low concentrations. Different adsorbents have been applied for removal of phenols and their derivatives. Use of agricultural waste as adsorbents seems to offer a much cheaper alternative in pollutant removal. This study examines the synthesis of a hydrophobic biomaterial composite by cross-linking of Fenton treated pine cone and applying the prepared adsorbent for 2-nitrophenol removal from aqueous solution. Pine cone biomass, in its raw and modified forms was tested for its ability to remove 2-nitrophenol from simulated industrial wastewater. The experimental procedure is divided into two main parts: (1) pine cone modification using Fenton’s reagent and 1.6-hexamethylene diisocyanate and (2) application of the prepared hydrophobic adsorbent for 2-nitrophenol removal from wastewater. Fenton’s reagent was used to remove pigments, extractives and other soluble organic compounds from the raw pine. FTIR spectroscopy showed an increase in magnitude of oxygenated surface groups which resulted in a decrease in pHpzc. The effect of Fenton treatment on further modification of the pine biomass via cross-linking using 1.6-hexamethylene diisocyanate was investigated. Optimum reaction variables for the cross-linking using dibutyltin dilaurate as catalyst under an inert nitrogen gas atmosphere in anhydrous hexane solvent were determined using FTIR spectroscopy. Success of the cross-linking procedure was confirmed by use of analytical techniques (XRD, TGA, SEM, EDX and BET surface area) and weight percent gain calculations. Pine and modified pine biomass were tested for their ability to sequester 2-nitrophenol via batch adsorption technique. The effect of pine modification on affinity for the biosorbate was investigated. The mechanism of the adsorption process was determined via use of kinetic, diffusion and equilibrium isotherm models. Two error functions (coefficient of determination and percent variable error) were employed to substantiate the model showing a good fit to the experimental adsorption data. The experimental adsorption kinetic data was fit to the pseudo-first-order and pseudo-second-order kinetic models. Due to the large size of the pollutant molecules diffusion process analysis was also conducted. The effect of pine modification on kinetic and diffusion parameters was determined. The experimental equilibrium adsorption data was fit to the Freundlich, Redlich-Peterson and Hill isotherm models. The initial shapes of the adsorption isotherms for 2-nitrophenol adsorption onto pine and modified pine biomass determined the type of equilibrium isotherm models to fit the experimental data to. Thermodynamic parameters were calculated to determine the spontaneity, feasibility and energy changes associated with the adsorption process. The degree of disorder at the solid/liquid interface after the adsorption was determined. The effect of temperature on the adsorption process was used to show whether the adsorption is physical or chemical. The effect of pine modification on equilibrium isotherm parameters was determined. The study is divided into seven chapters: Chapter 1: The chapter covers the introduction, problem statement, aim and objectives of the research. It gives an insight into the research project. Chapter 2: The literature review of pollutants in industrial wastewater and methods of their removal is dealt with in this chapter. Adsorption is introduced as an alternative technique for pollutant removal from aqueous systems. An in-depth review of various adsorbents (including pine cone), their merits and limitations are also discussed together with methods of modifying and use of modified adsorbents. Equilibrium, kinetic and thermodynamic models used to treat adsorption experimental data are presented. Chapter 3: The experimental procedures on the synthesis, characterization and application of the hydrophobic biosorbent in the removal of 2-nitrophenol from aqueous solution are presented. Kinetic and equilibrium experiments are described in detail. Chapter 4: It describes the first part of the results and discussions. The chapter focuses on optimization of reaction variables and characterization (using various analytical techniques) of the hydrophobic biomaterial composite. Chapter 5 The chapter discusses the second part of the results. It focuses on magnitude of surface charge, pHpzc and kinetic studies. Fitting of the adsorption experimental data to kinetic and diffusion models is presented together with the error functions. Chapter 6 The chapter discusses part three of the results on equilibrium studies. The adsorption experimental data is fitted to equilibrium isotherm equations and error determination is presented. Thermodynamic parameters are calculated and interpreted. Chapter 7: Conclusion and recommendations are presented. The optimum reaction variables for cross-linking of Raw and Fenton treated pine cone were determined using FTIR analysis and found to be: 0.2 g pine biomass, 3.5 cm3 1.6-hexamethylene diisocyanate cross-linker, 50 cm3 anhydrous hexane solvent, 1.5 cm3 dibutyltin dilaurate catalyst, temperature of 50 °C and a reaction time of 4 hours. The pine surface showed an increase in phenolic, lactonic and carboxylic acid groups due to the modification. The pHpzc showed a decrease due to modification of the pine cone biomass. The pHpzc values for the pine and modified pine cone biomass were found to be: Raw = 7.49, Raw-HMDI modified = 6.68, Fenton treated pine = 5.40 and Fenton-HMDI modified = 6.12. The optimum pH for the adsorption of 2-nitrophenol onto raw pine and modified pine cone biomass was determined to be 6. The optimum adsorbent dosage was determined as 1.5 g/dm3. The adsorption kinetics show a good fit with the pseudo-second-order model. This suggests that surface adsorption is the controlling step in the adsorption of 2-nitrophenol onto pine cone biomass. The analysis of diffusion processes showed that the initial rapid stage during the adsorption is due to external mass transfer processes. The adsorption experimental data also showed that pore diffusion was rate-limiting amongst the diffusion processes. Pine modification using Fenton’s reagent and 1.6-hexamethylene diisocyanate increased magnitude of kinetic and diffusion parameters. Experimental data for 2-nitrophenol adsorption onto pine and modified pine cone biomass showed better correlation with the Redlich-Peterson and Hill isotherm models and poor correlation with the Freundlich isotherm model. This suggests that the mechanism does not show complete multilayer coverage with cooperative phenomena between adsorbate molecules. Thermodynamic parameters showed that the adsorption is feasible, spontaneous, and exothermic and results in a decrease in degree of disorder at the solid/liquid interface. An increase in temperature resulted in a decrease in adsorption capacity showing that the adsorption is physical. Pine modification using Fenton’s reagent and 1.6-hexamethylene diisocyanate increased magnitude of kinetic, diffusion and isotherm parameters. The kinetic and equilibrium results show that the adsorption of 2-nitrophenol onto pine cone biomass follows the order: Fenton treated-HMDI > Fenton treated > Raw-HMDI > Raw. Hence, it can be concluded that Fenton treatment and HMDI cross-linking modification did increase the adsorptive capabilities of the pine cone biomass.
VUT Research Directorate
Livres sur le sujet "Biomass derivatives"
Licursi, Domenico, dir. Advances in the Catalytic Conversion of Biomass Components to Ester Derivatives : Challenges and Opportunities. MDPI, 2022. http://dx.doi.org/10.3390/books978-3-0365-4122-8.
Texte intégralChapitres de livres sur le sujet "Biomass derivatives"
Suflet, Dana M. « Curdlan Derivatives ». Dans Sustainability of Biomass through Bio-based Chemistry, 263–86. First edition. | Boca Raton : CRC Press, 2021. | Series : : CRC Press, 2021. http://dx.doi.org/10.1201/9780429347993-10.
Texte intégralThomas, John J., et Ronald G. Barile. « Biomass Derived Levulinic Acid Derivatives and Their Use as Liquid Fuel Extenders ». Dans Biomass Energy Development, 333–48. Boston, MA : Springer US, 1986. http://dx.doi.org/10.1007/978-1-4757-0590-4_28.
Texte intégralChoudhury, M. Jonayed, et G. M. Arifuzzaman Khan. « Utilization of Sawmill By-Product for Making Cellulose and Its Valuable Derivatives ». Dans Biomass and Bioenergy, 165–86. Cham : Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-07578-5_9.
Texte intégralChin, Kit-Ling, Paik-San H’ng et M. T. Paridah. « Unlocking the Destructive Powers of Wood-Eating Termites : From Pest to Biopolymer Derivatives Extractor ». Dans Biomass and Bioenergy, 307–21. Cham : Springer International Publishing, 2014. http://dx.doi.org/10.1007/978-3-319-07578-5_15.
Texte intégralManzer, Leo E. « Biomass Derivatives : A Sustainable Source of Chemicals ». Dans ACS Symposium Series, 40–51. Washington, DC : American Chemical Society, 2006. http://dx.doi.org/10.1021/bk-2006-0921.ch004.
Texte intégralKarmakar, Gobinda, Pranab Ghosh, Kirtika Kohli, Brajendra K. Sharma et Sevim Z. Erhan. « Chemicals from Vegetable Oils, Fatty Derivatives, and Plant Biomass ». Dans ACS Symposium Series, 1–31. Washington, DC : American Chemical Society, 2020. http://dx.doi.org/10.1021/bk-2020-1347.ch001.
Texte intégralMurthy, Hosakatte Niranjana, Chun-Hua Wu, Yong-Yi Cui et Kee-Yoeup Paek. « Production of Caffeic Acid Derivatives from Adventitious Root Cultures of Echinacea purpurea (L.) Moench ». Dans Production of Biomass and Bioactive Compounds Using Bioreactor Technology, 167–84. Dordrecht : Springer Netherlands, 2014. http://dx.doi.org/10.1007/978-94-017-9223-3_8.
Texte intégralMartín, A., M. D. Bermejo, E. Pérez, L. Quintana-Gómez, J. Queiroz, M. Andérez, J. I. del Río et M. Chinchilla. « Chapter 24. Hydrothermal CO2 Reduction Using Metals and Biomass Derivatives as Reductants ». Dans Green Chemistry Series, 520–43. Cambridge : Royal Society of Chemistry, 2022. http://dx.doi.org/10.1039/9781839167645-00520.
Texte intégralKuna, Ewelina, Ronan Behling, Sabine Valange, Gregory Chatel et Juan Carlos Colmenares. « Sonocatalysis : A Potential Sustainable Pathway for the Valorization of Lignocellulosic Biomass and Derivatives ». Dans Topics in Current Chemistry Collections, 1–20. Cham : Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-90653-9_1.
Texte intégralAshter, Syed Ali. « Direct derivatives of polymers from biomass ». Dans Technology and Applications of Polymers Derived from Biomass, 179–91. Elsevier, 2018. http://dx.doi.org/10.1016/b978-0-323-51115-5.00009-8.
Texte intégralActes de conférences sur le sujet "Biomass derivatives"
HENRIQUE FREIRE ARAUJO, LUIZ, José Augusto Rosário Rodrigues, FABIO NASARIO et Paulo José Samenho Moran. « Biotransformation of Biomass Furan Derivatives ». Dans XXIV Congresso de Iniciação Científica da UNICAMP - 2016. Campinas - SP, Brazil : Galoa, 2016. http://dx.doi.org/10.19146/pibic-2016-51633.
Texte intégralXueqiong Wang, Yong Pang, Zhongjun Zhang et Yu Yuan. « Forest aboveground biomass estimation using SPOT-5 texture indices and spectral derivatives ». Dans IGARSS 2014 - 2014 IEEE International Geoscience and Remote Sensing Symposium. IEEE, 2014. http://dx.doi.org/10.1109/igarss.2014.6947065.
Texte intégralDeCorso, Mario, Richard Newby, Don Anson, Richard Wenglarz et Ian Wright. « Coal/Biomass Fuels and the Gas Turbine : Utilization of Solid Fuels and Their Derivatives ». Dans ASME 1996 International Gas Turbine and Aeroengine Congress and Exhibition. American Society of Mechanical Engineers, 1996. http://dx.doi.org/10.1115/96-gt-076.
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 intégralHarth, Florian M., Brigita Hočevar, Blaž Likozar et Miha Grilc. « A Novel Process to Produce Adipic Acid by Catalytic Dehydroxylation of Biomass-derived Mucic Acid ». Dans International Conference on Technologies & Business Models for Circular Economy. University of Maribor Press, 2022. http://dx.doi.org/10.18690/um.fkkt.3.2022.1.
Texte intégralAnson, Don, Mark A. Paisley et M. A. Ratcliff. « Conditioning and Detailed Analysis of Biomass Derived Fuel Gas Ongoing and Planned Work by Battelle ». Dans ASME 1999 International Gas Turbine and Aeroengine Congress and Exhibition. American Society of Mechanical Engineers, 1999. http://dx.doi.org/10.1115/99-gt-192.
Texte intégralKrasnoshtanova, Alla, et Elisaveta Borovkova. « OBTAINING NUCLEIC ACID PREPARATIONS AND THEIR HYDROLYSATES FROM BIOMASS OF METHANE-OXIDIZING BACTERIA ». Dans GEOLINKS Conference Proceedings. Saima Consult Ltd, 2021. http://dx.doi.org/10.32008/geolinks2021/b1/v3/14.
Texte intégralMoritz, Robert R. « Near Term Gas Turbine Program to Enable the Use of “Renewable” Fuels ». Dans ASME 1998 International Gas Turbine and Aeroengine Congress and Exhibition. American Society of Mechanical Engineers, 1998. http://dx.doi.org/10.1115/98-gt-271.
Texte intégralKwon, Eilhann, Kelly J. Westby et Marco J. Castaldi. « An Investigation Into the Syngas Production From Municipal Solid Waste (MSW) Gasification Under Various Pressures and CO2 Concentration Atmospheres ». Dans 17th Annual North American Waste-to-Energy Conference. ASMEDC, 2009. http://dx.doi.org/10.1115/nawtec17-2351.
Texte intégralCavarzere, A., M. Morini, M. Pinelli, P. R. Spina, A. Vaccari et M. Venturini. « Fuelling Micro Gas Turbines With Vegetable Oils : Part I — Straight and Blended Vegetable Oil Properties ». Dans ASME Turbo Expo 2012 : Turbine Technical Conference and Exposition. American Society of Mechanical Engineers, 2012. http://dx.doi.org/10.1115/gt2012-68238.
Texte intégralRapports d'organisations sur le sujet "Biomass derivatives"
Silks, III, Louis A. Catalytic Routes for the Conversion of Biomass Derivatives to Hydrocarbons and/or Platform Chemicals. Office of Scientific and Technical Information (OSTI), octobre 2015. http://dx.doi.org/10.2172/1223183.
Texte intégral