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Artykuły w czasopismach na temat "Green chemical reaction"
Nagieva, I. T., N. I. Ali-zadeh i T. M. Nagiev. "GAS-PHASE OXIDATION OF 2-PICOLINE BY “GREEN OXIDIZERS” H2O2 AND N2O". Azerbaijan Chemical Journal, nr 4 (14.11.2023): 13–20. http://dx.doi.org/10.32737/0005-2531-2023-4-13-20.
Pełny tekst źródłaSahoo, Tejaswini, Jagannath Panda, Jnanaranjan Sahu, Dayananda Sarangi, Sunil K. Sahoo, Braja B. Nanda i Rojalin Sahu. "Green Solvent: Green Shadow on Chemical Synthesis". Current Organic Synthesis 17, nr 6 (25.09.2020): 426–39. http://dx.doi.org/10.2174/1570179417666200506102535.
Pełny tekst źródłaIgarashi, Akira. "Catalytic Reaction Engineering toward Green Chemical Processes". JOURNAL OF CHEMICAL ENGINEERING OF JAPAN 38, nr 10 (2005): 779–84. http://dx.doi.org/10.1252/jcej.38.779.
Pełny tekst źródłaDe Martino, M. Teresa, Loai K. E. A. Abdelmohsen, Floris P. J. T. Rutjes i Jan C. M. van Hest. "Nanoreactors for green catalysis". Beilstein Journal of Organic Chemistry 14 (29.03.2018): 716–33. http://dx.doi.org/10.3762/bjoc.14.61.
Pełny tekst źródłaPrajapati, Pintu, Avani Sheth, Dhaval M. Patel, Advaita Patel i Priti Mehta. "Sonochemistry: Non-Classical Way of Synthesis". Journal of Drug Delivery and Therapeutics 9, nr 6-s (15.12.2019): 229–32. http://dx.doi.org/10.22270/jddt.v9i6-s.3691.
Pełny tekst źródłaDay, Daniel M., Thomas J. Farmer, Joe Granelli, Janice H. Lofthouse, Julie Lynch, Con R. McElroy, James Sherwood, Seishi Shimizu i James H. Clark. "Reaction Optimization for Greener Chemistry with a Comprehensive Spreadsheet Tool". Molecules 27, nr 23 (2.12.2022): 8427. http://dx.doi.org/10.3390/molecules27238427.
Pełny tekst źródłaLi, Yanlin, Shenghua Chen, Wenyuan Duan, Yanli Nan, Donghai Ding i Guoqing Xiao. "Research progress of vanadium pentoxide photocatalytic materials". RSC Advances 13, nr 33 (2023): 22945–57. http://dx.doi.org/10.1039/d3ra03648k.
Pełny tekst źródłaDaglia, M., A. Papetti i G. Gazzani. "Green and roasted coffee antiradical activity stability in chemical systems". Czech Journal of Food Sciences 22, SI - Chem. Reactions in Foods V (1.01.2004): S191—S194. http://dx.doi.org/10.17221/10658-cjfs.
Pełny tekst źródłaDomènech, Xavier, José A. Ayllón, José Peral i Joan Rieradevall. "How Green Is a Chemical Reaction? Application of LCA to Green Chemistry". Environmental Science & Technology 36, nr 24 (grudzień 2002): 5517–20. http://dx.doi.org/10.1021/es020001m.
Pełny tekst źródłaCunningham, Michael F. "Green Macromolecular Reaction Engineering". Macromolecular Reaction Engineering 16, nr 3 (czerwiec 2022): 2200033. http://dx.doi.org/10.1002/mren.202200033.
Pełny tekst źródłaRozprawy doktorskie na temat "Green chemical reaction"
Pradhan, Kiran. "Designing of green chemical reaction conditional using thermal analysis". Thesis, University of North Bengal, 2012. http://hdl.handle.net/123456789/1338.
Pełny tekst źródłaAllen, Andrew J. (Andrew John) 1978. "Green chemistry : dense carbon dioxide and water as environmentally benign reaction media". Thesis, Massachusetts Institute of Technology, 2004. http://hdl.handle.net/1721.1/28656.
Pełny tekst źródłaIncludes bibliographical references.
(cont.) was investigated in scCO₂, and the cycloaddition between cyclopentadiene and methyl vinyl ketone (MVK) was studied in an scCO₂/liquid water environment. Nitrogen chemistry, specifically the synthesis of nitrogen heterocycles from amines, was also studied in scCO₂ and scCO₂/liquid water systems. The objective of studying the Diels-Alder cycloaddition of 9-hydroxymethylanthracene with N-ethylmaleimide in scCO₂ was to demonstrate the ability of scCO₂ to dramatically accelerate the rate of this reaction when compared to conventional solvents. Using spectroscopy to track the disappearance of the 9-hydroxymethylanthracene peak, it was found that this reaction proceeds at rates in scCO₂ that are significantly faster than in traditional organic solvents. It was also observed that the reaction rate constant increased with decreasing density, opposite the trend normally observed for most reactions conducted in scCO₂. On the basis of the low solubility of 9-hydroxymethylanthracene in scCO₂ and similar results observed in fluorocarbon solvents (fluorocarbons and scCO₂ are known to behave similarly as solvents), a solvophobic mechanism was inferred as the cause of the rate acceleration observed for this particular reaction in scCO₂. In order to utilize the complementary solvation powers of scCO₂ and water, a second Diels-Alder reaction, cyclopentadiene with MVK, was studied in an scCO₂/liquid water mixture. Specifically, the effect of MVK concentration on the selectivity and conversion was studied under both silent and sonicated conditions ...
With an ever increasing focus on reducing the environmental impact of solvent releases on human health and the environment, the replacement of conventional, organic solvents with alternative compounds that are inherently benign has attracted much attention in both industry and academia. Supercritical carbon dioxide (scCO₂) and water are two alternative compounds that are of particular interest because they are non-toxic, non-flammable, readily available, and cheap. Although scCO₂ has been successfully used in industry as a solvent for selective extraction (e.g. extraction of caffeine from coffee beans), development of scCO₂ as a reaction solvent has been less successful due to its limited solvation power for many organic reagents of interest. In addition scCO₂ has generally been shown to reduce both the reaction rate and selectivity of many reactions when compared to conventional solvents. Unlike scCO₂, water is known to significantly accelerate reaction rates and improve selectivities over that obtainable in conventional solvents. However, most organic compounds are insoluble in water which has limited its use as a reaction solvent for industrial-scale processes. In order to replace conventional solvents with scCO₂ and/or water, significant technological advantages resulting from the use of these compounds will have to be demonstrated. This research attempts to demonstrate some potential advantages of using scCO₂ and scCO₂/water as reaction media for several synthetic transformations of interest. The Diels-Alder cycloaddition of 9-hydroxymethylanthracene and N-ethylmaleimide
by Andrew J. Allen.
S.M.
Bassolino, Giovanni. "Tuning ultrafast chemical reaction dynamics in photoactive proteins". Thesis, University of Oxford, 2015. http://ora.ox.ac.uk/objects/uuid:42c19c5c-c6df-48e9-bb1c-8a7098eca8b4.
Pełny tekst źródłaCiccolini, Rocco P. "Carbon-nitrogen bond-forming reactions in supercritical and expanded-liquid carbon dioxide media : green synthetic chemistry with multiscale reaction and phase behavior modeling". Thesis, Massachusetts Institute of Technology, 2008. http://hdl.handle.net/1721.1/43203.
Pełny tekst źródłaIncludes bibliographical references.
The goal of this work was to develop a detailed understanding of carbon-nitrogen (C-N) bond-forming reactions of amines carried out in supercritical and expanded-liquid carbon dioxide (CO2) media. Key motivations behind this study were the importance of nitrogen-containing compounds in the pharmaceutical and fine chemical industries and a growing commercial interest in utilizing environmentally-friendly syntheses and processing with cost-efficient, green solvents. The thermodynamics and reaction engineering characteristics associated with the synthesis of several model C-N bond-forming reactions were examined both experimentally and theoretically. Operating conditions and engineering correlations were identified that will facilitate process scale-up and potential commercialization of these and other fundamentally-important CO2-based processes. Amine chemistry in CO2-based media was complicated by the facility of nucleophilic amines to react with carbon dioxide to form carbamic acids, which sometimes interfered with desired reaction pathways. Experimental observations and a complimentary ab initio quantum chemical calculation study revealed that carbamic acid formation was suppressed when adding bulky N-substituents to primary amines and when operating at low pressures and/or high temperatures. With a firm understanding of amine-CO2 chemistry, we developed a synthetic protocol that produced classes of pharmacologically-significant nitrogen heterocycles known as tetrahydroisoquinolines and tetrahyrdo-carbolines. Our method involved (1) the in situ carbamation of amines from their reaction with carbon dioxide and a dialkyl carbonate and (2) the Pictet-Spengler cyclization of these carbamates by their reaction with an aldehyde in the presence of acid. The conversion of amines to their carbamate derivatives offered suitable N-protection against carbamic acid formation.
(cont.) For nearly all reactions studied, the Pictet-Spengler step proceeded nearly quantitatively. The efficiency of amine carbamation via the CO2/dimethyl (cont) carbonate (DMC) reaction system was highly sensitive to process operating conditions. Phase behavior, amine conversion, and carbamate yield and selectivity all varied appreciably with temperature, pressure, and amine feed concentration. For example at 130 oC, carbamate selectivity increased from 50 to 75% with increasing pressure up to the mixture critical pressure of the CO2/DMC binary system (P, mixco2/DMC ). Selectivity decreased to 55% for ... mix of the entire reaction system (P,mixsystem). Above Pmixsytem,, selectivity increased to 80%. At 105 bar, decreasing temperature from 150 to 100 oC led to an increase in carbamate selectivity by 25%. Finally, decreasing the amine feed concentration from 4 to 1 M resulted in an increase in carbamate selectivity by 30%. Mixture critical pressures (Pc,mix) and liquid-phase densities, species concentrations, and volume expansion were measured for the CO2/DMC system over a wide range of operating conditions. Importantly, we developed an equation-of-state (EOS) model and several empirical engineering correlations that were used to predict vapor-liquid equilibrium properties in P-T-xi regimes for which data were not available. Deviations from experimental data and empirical correlations were typically less than 9%. Pmix CO2/DMC data were measured for 37 < T < 150 oC and were correlated well by a third-order polynomial. Liquid-phase carbon dioxide concentration ([CO2]I) varied linearly with pressure for 37 to 100 oC. Liquid-phase volume expansion (AV/) measured for the same temperature range increased exponentially with increasing pressure. Maximum-possible values of [C02]1 and AVI decreased with increasing temperature. [CO211 was 2 to 4 times larger than that of pure CO2 when compared at the same Tand P.
(cont.) We also developed and optimized a practical and high atom-economy C02-based synthetic protocol that afforded amides via the amination of ketenes generated in situ from the thermolysis of 1-alkynyl ethers. A variety of amines, 1-alkynyl ethers, and ketenes participated efficiently in the reaction and produced amides in yields comparable to those of conventional solvents. Experimental phase partitioning observations agreed well with EOS-based predictions and aided in the determination of process operating conditions. Amide yield varied in the order secondary > branched-primary > primary amines, which suggested that carbamic acid formation may have diminished reaction efficiency. t-butoxy-substituted 1-alkynyl ethers produced ketenes at rates faster than ethoxy-substituted ethers and allowed for a considerable reduction in operating temperature. Extension of the amide synthesis protocol to an intramolecular variant that afforded lactams resulted in a significant decrease in selectivity when compared to conventional solvents. We suspected that multi-phasic behavior led to this discrepancy and were able to increase selectivity by 25% using CO2/co-solvent mixtures. Finally, an ab initio quantum chemical kinetic model was developed and was capable of qualitatively predicting observed amide formation dynamics. Product selectivity and amine consumption rate predictions, for example, agreed well with experimental data.
by Rocco P. Ciccolini.
Ph.D.
Rahm, Martin. "Green Propellants". Doctoral thesis, KTH, Fysikalisk kemi, 2010. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-25835.
Pełny tekst źródłaQC 20101103
Dakkoune, Amine. "Méthodes pour l'analyse et la prévention des risques d'emballement thermique Zero-order versus intrinsic kinetics for the determination of the time to maximum rate under adiabatic conditions (TMR_ad): application to the decomposition of hydrogen peroxide Risk analysis of French chemical industry Fault detection in the green chemical process : application to an exothermic reaction Analysis of thermal runaway events in French chemical industry Early detection and diagnosis of thermal runaway reactions using model-based approaches in batch reactors". Thesis, Normandie, 2019. http://www.theses.fr/2019NORMIR30.
Pełny tekst źródłaThe history of accidental events in chemical industries shows that their human, environmental and economic consequences are often serious. This thesis aims at proposing an approach of detection and diagnosis faults in chemical processes in order to prevent these accidental events. A preliminary study serves to identify the major causes of chemical industrial events based on experience feedback. In France, according to the ARIA database, 25% of the events are due to thermal runaway because of human errors. It is therefore appropriate to develop a method for early fault detection and diagnosis due to thermal runaway. For that purpose, we develop an approach that uses dynamical thresholds for the detection and collection of measurements for diagnosis. The localization of faults is based on a classification of the statistical characteristics of the temperature according to several defectives modes. A multiset of linear classifiers and binary decision diagrams indexed with respect to the time are used for that purpose. Finally, the synthesis of peroxyformic acid in a batch and semi batch reactor is considered to validate the proposed method by numerical simulations and then experiments. Faults detection performance has been proved satisfactory and the classifiers have proved a high isolability rate of faults
Wigley, Max Merlin. "Fluid-mineral reactions in an exhumed CO2-charged aquifer, Green River, Utah, USA". Thesis, University of Cambridge, 2013. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.608145.
Pełny tekst źródłaVam, Albert. "Kinetics of the Hydro-Deoxygenation of Stearic Acid over Palladium on Carbon Catalyst in Fixed-Bed Reactor for the Production of Renewable Diesel". University of Dayton / OhioLINK, 2013. http://rave.ohiolink.edu/etdc/view?acc_num=dayton1373313020.
Pełny tekst źródłaProsa, Nicolo. "Synthèse supportée d'hétérocycles en milieux éco-compatibles : étude des conditions par lots et en flux continu. Purification par ultrafiltration en phase aqueuse". Phd thesis, Université Paris Sud - Paris XI, 2011. http://tel.archives-ouvertes.fr/tel-00664999.
Pełny tekst źródłaDrouet, Fleur. "Synthèse énantiosélective d'1,2 et 1,3-diamines et Développement de réactions multicomposants dans des conditions oxydantes". Phd thesis, Université Paris Sud - Paris XI, 2011. http://tel.archives-ouvertes.fr/tel-00823407.
Pełny tekst źródłaKsiążki na temat "Green chemical reaction"
author, Zhang Shufen 1960, red. Gao xiao fan ying ji shu yu lü se hua xue: Highly Efficient Reaction Technologies & Green Chemistry. Beijing Shi: Zhongguo shi hua chu ban she, 2012.
Znajdź pełny tekst źródłaTundo, Pietro, i Vittorio Esposito, red. Green Chemical Reactions. Dordrecht: Springer Netherlands, 2008. http://dx.doi.org/10.1007/978-1-4020-8457-7.
Pełny tekst źródła1945-, Tundo Pietro, i Esposito Vittorio, red. Green chemical reactions. Dordrecht: Springer, 2008.
Znajdź pełny tekst źródła1961-, Abraham Martin A., Moens Luc 1957-, American Chemical Society. Division of Industrial and Engineering Chemistry i American Chemical Society Meeting, red. Clean solvents: Alternative media for chemical reactions and processing. Washington, DC: American Chemical Society, 2002.
Znajdź pełny tekst źródłaB, Zwanenburg, Mikołajczyk Marian 1937- i Kiełbasiński Piotr, red. Enzymes in action: Green solutions for chemical problems. Boston: Kluwer Academic Publishers, 2000.
Znajdź pełny tekst źródłaservice), SpringerLink (Online, red. Adsorption of Reactive Red 158 Dye by Chemically Treated Cocos Nucifera L. Shell Powder: Adsorption of Reactive Red 158 by Cocos Nucifera L. Dordrecht: The Author(s), 2011.
Znajdź pełny tekst źródłaSartori, Giovanni. Advances in Friedel-Crafts Acylation Reactions: Catalytic and Green Processes. CRC, 2009.
Znajdź pełny tekst źródłaMaggi, Raimondo, i Giovanni Sartori. Advances in Friedel-Crafts Acylation Reactions: Catalytic and Green Processes. Taylor & Francis Group, 2009.
Znajdź pełny tekst źródłaMaggi, Raimondo, i Giovanni Sartori. Advances in Friedel-Crafts Acylation Reactions: Catalytic and Green Processes. Taylor & Francis Group, 2009.
Znajdź pełny tekst źródłaMaggi, Raimondo, i Giovanni Sartori. Advances in Friedel-Crafts Acylation Reactions: Catalytic and Green Processes. Taylor & Francis Group, 2017.
Znajdź pełny tekst źródłaCzęści książek na temat "Green chemical reaction"
Sheldon, Roger A. "Reaction Efficiencies and Green Chemistry Metrics of Biotransformations". W Biocatalysis for Green Chemistry and Chemical Process Development, 67–88. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2011. http://dx.doi.org/10.1002/9781118028308.ch4.
Pełny tekst źródłaGore, B. L., L. B. Giorgi i G. Porter. "Picosecond Transient Absorption Spectroscopy of Green Plant Photosystem I Reaction Centres". W Springer Series in Chemical Physics, 398–401. Berlin, Heidelberg: Springer Berlin Heidelberg, 1986. http://dx.doi.org/10.1007/978-3-642-82918-5_106.
Pełny tekst źródłaNeumann, Karsten, Mirka-Kristin Verhoefen, Ingrid Weber, Clemens Glaubitz i Josef Wachtveitl. "Primary Reaction Dynamics of Green Absorbing Proteorhodopsin WT and D97N Mutant Observed by fs Infrared and Visible Spectroscopy". W Springer Series in Chemical Physics, 580–82. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-95946-5_188.
Pełny tekst źródłaSaluja, Pooja, Garima Khanna, Ankita Chaudhary i Jitender M. Khurana. "Synthesis of Spiro[Indene-2,2′-Naphthalene]-4′-Carbonitriles and Spiro[Naphthalene-2,5′-Pyrimidine]-4-carbonitriles via One-pot Three Component Reaction Using Task Specific Ionic Liquid". W Green Chemistry in Environmental Sustainability and Chemical Education, 111–18. Singapore: Springer Singapore, 2018. http://dx.doi.org/10.1007/978-981-10-8390-7_11.
Pełny tekst źródłaAkwi, Faith M., i Paul Watts. "The Role of Continuous Flow Processing in the Development of Green Chemical Syntheses". W Green Organic Reactions, 257–97. Singapore: Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-33-6897-2_15.
Pełny tekst źródłaArévalo, Maria José, Óscar López i Maria Victoria Gil. "Green Chemical Synthesis and Click Reactions". W Click Reactions in Organic Synthesis, 77–97. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2016. http://dx.doi.org/10.1002/9783527694174.ch3.
Pełny tekst źródłaKnez, Željko, Maja Leitgeb i Mateja Primožič. "Chemical Reactions in Subcritical Supercritical Fluids". W Green Chemistry and Chemical Engineering, 111–31. New York, NY: Springer New York, 2019. http://dx.doi.org/10.1007/978-1-4939-9060-3_1004.
Pełny tekst źródłaGupta, Meghavi, Noopur Ameta, Surbhi Benjamin i P. B. Punjabi. "Photo-Fenton Reactions: A Green Chemical Route". W Green Chemistry, 2nd edition, 323–57. Wyd. 2. New York: Apple Academic Press, 2024. http://dx.doi.org/10.1201/9781003431473-9.
Pełny tekst źródłaKokel, Anne, Christian Schäfer i Béla Török. "Microwave-Assisted Reactions in Green Chemistry". W Green Chemistry and Chemical Engineering, 573–612. New York, NY: Springer New York, 2019. http://dx.doi.org/10.1007/978-1-4939-9060-3_1008.
Pełny tekst źródłaKodolov, V. I., V. V. Kodolova-Chukhontseva, N. S. Terebova, I. N. Shabanova, Yu V. Pershin, R. V. Mustakimov i A. Yu Bondar. "Phenomena of Charge Quantization, Interference, and Annihilation in Chemical Reactions of Mesoparticles". W Green Materials and Environmental Chemistry, 163–77. Includes bibliographical references and index.: Apple Academic Press, 2021. http://dx.doi.org/10.1201/9780429330674-10.
Pełny tekst źródłaStreszczenia konferencji na temat "Green chemical reaction"
Du, Mei, Yiwei Jia i Graham R. Fleming. "Femtosecond Spectroscopic Studies of Barrierless Reaction of Triphenylmethane Dye Molecules in Alcohol Solutions". W International Conference on Ultrafast Phenomena. Washington, D.C.: Optica Publishing Group, 1994. http://dx.doi.org/10.1364/up.1994.thd.3.
Pełny tekst źródłaXie, Renchao, Tao Huang, F. Richard Yu i Yunjie Liu. "Caching Design in Green Content Centric Networking Based on Chemical Reaction Optimization". W 2013 IEEE International Conference on Green Computing and Communications (GreenCom) and IEEE Internet of Things(iThings) and IEEE Cyber, Physical and Social Computing(CPSCom). IEEE, 2013. http://dx.doi.org/10.1109/greencom-ithings-cpscom.2013.33.
Pełny tekst źródłaMenon, A. S., C. L. Hii, C. L. Law, S. Suzannah i M. Djaeni. "Effects of water blanching on polyphenol reaction kinetics and quality of cocoa beans". W INTERNATIONAL CONFERENCE OF CHEMICAL AND MATERIAL ENGINEERING (ICCME) 2015: Green Technology for Sustainable Chemical Products and Processes. AIP Publishing LLC, 2015. http://dx.doi.org/10.1063/1.4938291.
Pełny tekst źródłaWidiyastuti, W., Siti Machmudah, Kusdianto, Tantular Nurtono i Sugeng Winardi. "Characteristics of ZnO nanostructures synthesized by sonochemical reaction: Effects of continuous and pulse waves". W INTERNATIONAL CONFERENCE OF CHEMICAL AND MATERIAL ENGINEERING (ICCME) 2015: Green Technology for Sustainable Chemical Products and Processes. AIP Publishing LLC, 2015. http://dx.doi.org/10.1063/1.4938316.
Pełny tekst źródłaSchael, Frank, Krishna Nigam i Patrick Rojahn. "Green engineering approach with microstructured coiled flow inverter for CMF and HMF continuous flow synthesis". W 2022 AOCS Annual Meeting & Expo. American Oil Chemists' Society (AOCS), 2022. http://dx.doi.org/10.21748/ikvz3189.
Pełny tekst źródłaKumoro, Andri Cahyo, Diah Susetyo Retnowati, Ratnawati i Catarina Sri Budiyati. "Implementation of steady state approximation for modelling of reaction kinetic of UV catalysed hydrogen peroxide oxidation of starch". W INTERNATIONAL CONFERENCE OF CHEMICAL AND MATERIAL ENGINEERING (ICCME) 2015: Green Technology for Sustainable Chemical Products and Processes. AIP Publishing LLC, 2015. http://dx.doi.org/10.1063/1.4938340.
Pełny tekst źródłaHidayat, Arif, Rochmadi, Karna Wijaya i Arief Budiman. "Reaction kinetics of free fatty acids esterification in palm fatty acid distillate using coconut shell biochar sulfonated catalyst". W INTERNATIONAL CONFERENCE OF CHEMICAL AND MATERIAL ENGINEERING (ICCME) 2015: Green Technology for Sustainable Chemical Products and Processes. AIP Publishing LLC, 2015. http://dx.doi.org/10.1063/1.4938341.
Pełny tekst źródłaRamasamy, Jothibasu, i Mohammad K. Arfaj. "Sustainable and Green Drilling Fluid Additives Development". W Offshore Technology Conference Asia. OTC, 2022. http://dx.doi.org/10.4043/31350-ms.
Pełny tekst źródłaMurti, S. D. Sumbogo, Fusia Mirda Yanti, Atti Sholihah, Asmi Rima Juwita, Joni Prasetyo, Meyly Ekawati Thebora, Edwin Pramana i Hens Saputra. "Synthesis of green diesel through hydrodeoxygenation reaction of used cooking oil over NiMo/Al2O3 catalyst". W THE 5TH INTERNATIONAL CONFERENCE ON INDUSTRIAL, MECHANICAL, ELECTRICAL, AND CHEMICAL ENGINEERING 2019 (ICIMECE 2019). AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0000604.
Pełny tekst źródłaRohova, Maryna, Vladyslav Kovalenko, Volodymyr Tkachenko, Inna Lych i Iryna Voloshyna. "Green Biosynthesis of Zinc Nanoparticles". W The 9th International Conference on Advanced Materials and Systems. INCDTP - Leather and Footwear Research Institute (ICPI), Bucharest, Romania, 2022. http://dx.doi.org/10.24264/icams-2022.iv.12.
Pełny tekst źródłaRaporty organizacyjne na temat "Green chemical reaction"
Führ, Martin, Julian Schenten i Silke Kleihauer. Integrating "Green Chemistry" into the Regulatory Framework of European Chemicals Policy. Sonderforschungsgruppe Institutionenanalyse, lipiec 2019. http://dx.doi.org/10.46850/sofia.9783941627727.
Pełny tekst źródłaLucia, Lucian A., Dimitri S. Argyropoulos i Sanghamitra Sen. Feasibility Study for the Use of Green, Bio-Based, Efficient Reactive Sorbent Material to Neutralize Chemical Warfare Agents. Fort Belvoir, VA: Defense Technical Information Center, sierpień 2012. http://dx.doi.org/10.21236/ada582167.
Pełny tekst źródła