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Статті в журналах з теми "Dissolved CO₂":
Cohen, Yossi, and Daniel H. Rothman. "Mechanisms for mechanical trapping of geologically sequestered carbon dioxide." Proceedings of the Royal Society A: Mathematical, Physical and Engineering Sciences 471, no. 2175 (March 2015): 20140853. http://dx.doi.org/10.1098/rspa.2014.0853.
Akanishi, Yuya, Els Kesters, Quoc Toan Le, and Frank Holsteyns. "Corrosion of Co in BEOL interconnects in dilute HF solution." Solid State Phenomena 282 (August 2018): 256–62. http://dx.doi.org/10.4028/www.scientific.net/ssp.282.256.
Dang, Jie, Ning Wang, and Hasan K. Atiyeh. "Review of Dissolved CO and H2 Measurement Methods for Syngas Fermentation." Sensors 21, no. 6 (March 19, 2021): 2165. http://dx.doi.org/10.3390/s21062165.
Bown, J., M. Boye, P. Laan, A. R. Bowie, Y. H. Park, C. Jeandel, and D. M. Nelson. "Imprint of a dissolved cobalt basaltic source on the Kerguelen Plateau." Biogeosciences 9, no. 12 (December 19, 2012): 5279–90. http://dx.doi.org/10.5194/bg-9-5279-2012.
Bundy, Randelle M., Alessandro Tagliabue, Nicholas J. Hawco, Peter L. Morton, Benjamin S. Twining, Mariko Hatta, Abigail E. Noble, et al. "Elevated sources of cobalt in the Arctic Ocean." Biogeosciences 17, no. 19 (October 1, 2020): 4745–67. http://dx.doi.org/10.5194/bg-17-4745-2020.
Afrida, Yenni, and Fitriono. "Analisa Kondisi Minyak Trafo Berdasarkan Hasil Uji Dissolved Gas Analisys Pada Trafo Daya #1 Di PT.PLN (PERSERO) GARDU INDUK KOTABUMI." Electrician 16, no. 3 (September 30, 2022): 355–58. http://dx.doi.org/10.23960/elc.v16n3.2408.
Fu, An Qing, Yang Zhou, Ming Jie Zhu, Yao Rong Feng, Xun Ji Li, Feng Shou Shangguan, Cheng Xian Yin, and Zhen Quan Bai. "CO2 Permeability Characterization of High Performance Composite Coating." Applied Mechanics and Materials 529 (June 2014): 117–21. http://dx.doi.org/10.4028/www.scientific.net/amm.529.117.
Tovar-Sanchez, A., and S. A. Sañudo-Wilhelmy. "Influence of the Amazon River on dissolved and intra-cellular metal concentrations in <i>Trichodesmium</i> colonies along the western boundary of the sub-tropical North Atlantic Ocean." Biogeosciences Discussions 7, no. 4 (August 27, 2010): 6523–43. http://dx.doi.org/10.5194/bgd-7-6523-2010.
Tovar-Sanchez, A., and S. A. Sañudo-Wilhelmy. "Influence of the Amazon River on dissolved and intra-cellular metal concentrations in <i>Trichodesmium</i> colonies along the western boundary of the sub-tropical North Atlantic Ocean." Biogeosciences 8, no. 1 (January 28, 2011): 217–25. http://dx.doi.org/10.5194/bg-8-217-2011.
Hart, Barry T., and Tina Hines. "Geochemistry of Cu, Zn and Fe in the Tambo River, Australia I. Oxidation of Fe(II)-rich water entering the river." Marine and Freshwater Research 59, no. 1 (2008): 72. http://dx.doi.org/10.1071/mf07056.
Дисертації з теми "Dissolved CO₂":
Stubbins, Aron Paul. "Aspects of aquatic CO photoproduction from CDOM." Thesis, University of Newcastle Upon Tyne, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.369787.
Randi, Aurélien. "Modélisation expérimentale de l’injection de solutions enrichies en CO₂ dans un doublet géothermique. Étude des impacts géochimiques en proche puits." Electronic Thesis or Diss., Université de Lorraine, 2021. http://www.theses.fr/2021LORR0087.
This work was conducted in the framework of the technical assessment of a novel Carbon Capture and Storage (CCS) concept integrating aqueous dissolution of CO2 and injection via a geothermal doublet. This study focuses on i) the quantification and modelling of the hydrodynamic and geochemical impact induced by the injection of a CO2-laden solution in a reservoir rock and ii) the evaluation of long term integrity of the well materials (cement, steel casing) in order to ensure a safe injection protocol. A dedicated experimental device named MIRAGES.2 was developed to mimic, at the lab scale, the continuous radial injection of a CO2-enriched solution under realistic conditions of a geological reservoir. The miniature well consists in a steel tube that is cemented to the core plug with a class G Portland cement. The test bench is divided in two parts: the first one is devoted to the CO2-solution mixing process, and the second one enables to perform the injection of the solution in the core-plug. In addition, the implementation of original in situ measurement techniques (in-situ HP/HT Raman and pH probes, flowmeter) was carried out in order to ensure optimal acquisition of physical and chemical data (pressure, temperature, pH, concentrations of different species in solution...) during the experiments. A method of image processing acquired on post-experimental samples by X-ray micro-tomography has been developed. This technique revealed the 3D architecture of the mesoscopic porous network. This experimental protocol revealed the physicochemical evolution of: the different interfaces between cement and steel, and between cement and reservoir ; the near-well region of the reservoir ; The injected fluid. A set of 7 experiments was performed. The injection duration (12 h, 24 h, 2.5 d, 10 d and 21 d), the fluid salinity and the core drilling inclination with respect to the bedding were investigated. The experiments demonstrate the non-uniform propagation of the acidic solution from the injection point in the form of preferential pathways called « wormholes ». Once a single wormhole breaks through the core-plug, all the other competing wormholes stop growing and their density tend to decrease as the solution is injected. Despite a predominant localized phenomenon, changes in petrophysical properties of the rock in regions far from the wormholes was observed. Following the continuous renewal of the acidic solution, a uniform dissolution in the upper part of the injection well was also highlighted. Roughness surface measurements coupled with microscopic observations have revealed the presence of calcite precipitation which induces the clogging of secondary wormholes. Cement ageing in contact with the reactive solution induces localized chemical imbalances. Changes in magnesium concentration, inhibitor of calcite precipitation, released during cement alteration, govern the local calcite saturation states of the interstitial solution. These phenomena could explain the observed precipitation in a medium mainly undersaturated with respect to the calcite. The experiments also demonstrated the important role of the salinity of the injected solution, which dissolves up to five times more host rock than a freshwater solution. Finally, a multi-scale structural study was carried out and established the close relationship between the distribution of structural defects generated by regional tectonics and the orientation of the dissolution networks observed in our experiments. These results refine the analysis and assessment of environmental impacts and risks in the context of the CO2 injection in a geothermal doublet. They demonstrate the discontinuities present in the rock control the dissolution paths at the reservoir scale
Tsai, Meng Jung, and 蔡孟容. "Electrooxidation of Dissolved CO and Methanol on gold Electrodes." Thesis, 2013. http://ndltd.ncl.edu.tw/handle/80014689106580706572.
長庚大學
化工與材料工程學系
101
The electrochemical oxidation of dissolved CO on gold electrode was studied by using rotating disk electrode forced convection approaches and the limiting currents of CO oxidation demonstrate negligible influence of adsorbed CO. The electrooxidation of dissolved CO by using gold-microelectrode also demonstrate similar limiting currents phenomena without rotating disk approach. By adding less than 1 x 10-3 M methanol in saturated CO electrolyte, we will be able to increase the dissolved CO concentrations because of the stepwise oxidation of methanol and the CO-like intermediates. The simultaneously oxidation of CO and methanol was studies by using rotating disk electrode forced convection approaches in cyclic voltammograms. The limiting currents of simultaneously oxidation of CO and methanol were not proportional to the expecting higher dissolved bulk CO concentrations. The simultaneously oxidation of CO and methanol demonstrates the retardation effect of surface adsorbed species on the dissolved CO limiting currents.
Hegele, Paul. "Gas Dynamics during Bench-Scale Electrical Resistance Heating of Water, TCE and Dissolved CO2." Thesis, 2014. http://hdl.handle.net/1974/8674.
Thesis (Master, Civil Engineering) -- Queen's University, 2014-03-27 15:26:30.683
Wang, Chun Chieh, and 王俊傑. "To Study the Electrochemical oxidation of Dissolved CO in Acidic and Alkaline By Using Au-RDE and Au-Microelectrode." Thesis, 2010. http://ndltd.ncl.edu.tw/handle/05016264458450047801.
長庚大學
化工與材料工程學系
98
The electrochemical oxidation of solution phase CO on Au electrode indicates the less positive potentials due to negligible influence of surface adsorbed CO in comparison of the adsorbed CO oxidation on Pt electrode in either in acidic or alkaline electrolyte. The study of electroxidation of dissolved CO by using rotation gold disk electrode in acidic or alkanline system indicates mass transfer diffusion which determined the rate law for the electrochemical oxidation of dissolved CO. A gold Microelectrode was used to study the rate of mass transfer diffusion of the dissolved CO electrocatalysis in acidic or alkaline system. The cyclic voltammograms data shows the onset potential of dissolved CO oxidation increases in the order 100μm-Au microelectrode, Au-RDE and 10μm-Au microelectrode in acidic system. In alkaline system, the onset potential of dissolved CO oxidation of Au-RDE and 10μm-Au microelectrode were similarly with 0V(v.s RHE). The rate law of dissolved CO oxidation was determined with mass transfer diffusion by using Au-RDE and 10μm-Au microelectrode in alkaline system, and in acidic system, results indicate electrode kinetic and diffusion mixed control by using 10μm-Au microelectrode. The cyclic voltammograms of the oxidation potentials of dissolved CO by using rotation disk gold electrode and 10μm microelectrode indicate the potential windows of gold oxides regions may affect the starting oxidation potentials of the dissolved CO and the electrodes surface treatments and conditions may also affect the starting oxidation potentials of the dissolved CO. The cyclic voltammetry confirms that the gold surface oxides, surface pre-treatments and the electrolytes of acidic and alkaline determine the electrochemical oxidation potentials of dissolved CO.
Chou, Chih Han, and 周志翰. "The Effects of Dissolved Oxygen and Different Immobilization Carriers for Ethanol Production from Carboxymethylcellulose using a Novel Co-Culture-Cell Bioreactor." Thesis, 2010. http://ndltd.ncl.edu.tw/handle/90469086854016578085.
長庚大學
生化與生醫工程研究所
98
There were more than 1600 thousand tons of rice straw agricultural wastes produced in Taiwan every year. Produce bioethanol from rice straw not only regenerates the agriculture waste into bioenergy, but also solves the problem of environmental pollution by rice straw burning. Cellulose is the main component of rice straw. However, it is difficult to hydrolyze the lignocellulose to glucose by enzymes, bio-ethanol produced by lignocellulose still expensive when compared to sugar or starch substrate. Using the technology of cell immobilization might lower the cost by repeat immobilized cells utilization; process of cellulose hydrolysis and glucose fermentation combination, and co-culture system. In this study, we investigated the bio-ethanol production of our new co-culturing immobilized cells system reactor with dissolved oxygen monitored by different immobilization carriers in different aeration or the agitation speed condition. We also study the aerobic/anaerobic zone construction in ethanol production. In the shaking flask research, the enzyme activities of immobilized cells on different carriers showed that loofah sponge performs well in both one stage and two stage immobilize strategy, but decomposed. The loofah sponge decomposed slower when culturing in the bioreactor Besides, suspended culturing in the shaking flask, 2 days preculture could reach highest value summarized enzyme activity in both carboxymethylcellulose and rice straw substrate. We also found the aerobic/anaerobic zones constructed well under the aeration rate of 2L / min. The loofah sponge immobilization carriers, had yield of ethanol concentration reached 825 ppm after 8 hrs fermentation. The aeration rate of 2 L /min performed better than the others. The dissolved oxygen (DO) was affected by different agitation speeds, the DO value rose with the agitation speed. The agitation speed of 150 rpm could maintain the DO level stably with the ethanol concentration reached 934 ppm after 8hrs fermentation. Higher substrate concentration 20g/L of caboxymethylcellulose(CMC) could achieve the ethanol concentration of 1080 ppm after 8 hrs fermentation. Three repeated batches of substrate concentration 10 g/L CMC could reach the ethanol concentration of 2650 after 9 hrs fermentation. These results showed that our immobilized co-culture-cell bioreactor system had high potential of continuous and stable bio-ethanol production.
McNeil, BIB. "Carbon export and the uptake of anthropogenic CO\(_2\) in the Southern Ocean using stable carbon isotopes of dissolved inorganic carbon." Thesis, 2001. https://eprints.utas.edu.au/20500/1/whole_McNeilBenjaminIvanBarry2001_thesis.pdf.
Almada-Calvo, Fernando. "Effect of temperature, dissolved inorganic carbon and light intensity on the growth rates of two microalgae species in monocultures and co-cultures." Thesis, 2014. http://hdl.handle.net/2152/25053.
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Wei, Ming-hui, and 魏明輝. "Determination of Dissolved Trace Metal (Cd, Co, Cu, Ni and Zn) Partitioning in Natural Water by a Two-Column Ion Exchange Method." Thesis, 2014. http://ndltd.ncl.edu.tw/handle/11607461175472020448.
國立中山大學
海洋科學系研究所
103
In this study, experiments were carried out using a two-column (Chelex-100 and AG MP-1 resin) ion exchange technique, operated in different sequences (Chelex-AG MP1, normal phase, or AG MP1-Chelex, reversed phase). The model solutions, containing various concentrations of metal complexing agents (humic acid, HA and/or ethylenediaminetetraacetic acid, EDTA), of different pH were prepared in Milli-Q water and seawater, and then passed through the column sets, in order to investigate the variations in trace metal (Cd, Co, Cu, Ni and Zn) partitioning. Chelex-100 is a cation exchange resin, and AG MP-1 is an anion exchange resin. The fractions obtained were operationally defined as Chelex-labile, AG MP-labile, non-labile and zwitterionic (retained by both Chelex-100 and AG MP-1 resins, obtained by calculation). Experimental results showed that: (1) Cd, Co, Ni and Zn were mostly present as Chelex-labile fraction, while Cu was equivalently present as Chelex-labile and AG MP-labile fractions. When the column sequence was reversed, Cd was not retained by Chelex-100 resin, and some can be retained by AG MP-1 resin in seawater medium, suggesting the predominant fraction of Cd being non-labile fraction (probably CdCl2). Solutions with higher pH (8.0) showed enhanced AG MP-labile metal fractions, indicating organic complexation, than those at pH 5.5 in freshwater medium; (2) Organic complexes in model solutions were retained mostly by AG MP-1 resin, with a small part being retained by Chelex-100 resin. In addition, part of non-labile fraction exhibited organic complex characteristics; (3) AG MP-labile metal concentrations and the concentration of humic acid had a positive correlation, indicating the complexation with humic acid for different metals is in the following order: Cu &;gt; Ni &;gt; Co &;gt; Zn &;gt; Cd; (4) When model solutions contain only trace metals and EDTA, and the total metal concentration was lower than the complexation capacity of EDTA, Cd (89~92%), Co (77~83%), Cu (92~96%), Ni (88~93%) and Zn (80~83%) were predominantly present as AG MP-labile fraction (negatively charged M-EDTA complexes, MHEDTA-) in freshwater model solutions, and a minor were present as non-labile fraction (neutrally charged M-EDTA complexes, MH2EDTA). Fe was equivalently present as AG MP-labile and non-labile fractions in model solutions, comparing with other metals, and accounted for most of the non-labile fraction (FeHEDTA) among the elements determined. In seawater model solutions, Cd, Co, Cu, Ni and Zn were present mostly as Chelex-labile and non-labile fractions. Fe was equivalently present as Chelex-labile, AG MP-labile and non-labile fractions in model solutions. It was found that metal-organic complexes could present in different terms of metal speciation in model solutions (MHEDTA-, MH2EDTA); (5) Metal-EDTA complexes showed stronger complexation than those of metal-HA. This analytical scheme was applied to estuarine and coastal waters. Results showed that, column yields had comparable trends of differences between operation modes (normal and reversed), and between samples in natural pH (~8.0) and buffered (5.5) when compared with lab experiments. Metal concentrations in the coastal and estuarine waters were in general lower than those in model solutions prepared in the lab, thus the distributions of metal species derived from the dual-column preconcentration technique represent results closer to natural waters. Results obtained in this study suggest that column yields vary when the dual-column preconcentration technique is operated under different column sequences. Modification of sample/solution, especially pH, results in shifts of metal species. Therefore, the use of technique with multiple preconcentration resins requires more careful definition of operating conditions and result interpretation.
Chen, Kai-Yue, and 陳楷岳. "Effects of C/Fe ratios, pH, and Al on the Structures of Dissolved Organic Matter-Fe Hydroxides Co-precipitates and Cr(VI) Transformations." Thesis, 2018. http://ndltd.ncl.edu.tw/handle/4krcc9.
國立中興大學
土壤環境科學系所
106
Co-precipitation of dissolved organic matter (DOM) and Fe is an important process occurring naturally that may stabilize C and Fe in the soil systems. Aluminum ions are abundant in soils, and thus, the structural developments of DOM/Fe co-precipitates (DFC) can be greatly affected by the element. In addition, the nanosized DOM/Fe co-precipitates may be a potential scavenger of heavy metals, e.g., Cr(VI), in soils and sediments. Thus, the overall goal of this research was to determine the effects of C/Fe ratios, pH, and Al ions on the structures of DOM/Fe co-precipitates and Cr(VI) transformations. The specific objectives were: (1) to determine the structural development and stabilization of DOM/Fe co-precipitates in relation to the changes of pH and C/Fe molar ratios; (2) to understand the effects of Al ions on the structural stabilization of DOM-Fe co-precipitates accompanied with the changes of pH and Fe/Al molar ratios; and (3) to examine the mechanisms of Cr bonding/transformation on DOM/Fe co-precipitates as influenced by the changes of pH and C/Fe molar ratios. Results showed that rhe local structures of DFC samples could be classified into three categories depending on the molar ratios of C/(C+Fe): (1) the ferrihydrite-like domain with the C/(C+Fe) molar ratios ≤ 0.65 (DFC structure I); (2) the mixtures of the edge/corner-sharing FeO6 octahedra associated with Fe-C bonds and ferrihydrite-like domains with the C/(C+Fe) molar ratios between 0.71 and 0.89 (DFC structure II); and (3) the corner-sharing FeO6 octahedra associated with Fe-C bonds with the C/(C+Fe) molar ratios ≥ 0.92 (DFC structure III). Additionally, influences of Al ions on the co-precipitation behaviors of DOM and Fe in relation to the changes of pH and Fe/Al ratios were categorized into five types : (1) DOM/Fe co-precipitates were the dominant species with a Fe/(Fe+Al) molar ratios > 0.25 at pH 3.0; (2) the O-containing groups of DOM homogenously associated with Fe(III) and Al domains of co-precipitates with a Fe/(Fe+Al) molar ratio of 0.25 at pH ≤ 4.5; (3) the mixtures of homogeneous distributions of DOM/Fe co-precipitates with a smaller size of Fe domain, and the Fe domain was gradually covered by Al domains and DOM molecules with Fe/(Fe+Al) molar ratios > 0.25 and at pH 4.5; (4) Al hydroxides covered by the homogeneous distributions of DOM and FeO6 with a Fe/(Fe+Al) molar ratio of 0.25 at pH 6.0; and (5) when the Fe/(Fe+Al) molar ratios > 0.25 at pH 6.0, the association between Al domains and DOM may promote the formation of Fe core. Once the DFC was formed in soil, it became an important scavenger of Cr(VI). However, Cr(VI) transformations on the DFC depend greatly on the C/(C+Fe) molar ratios and solution pH. For instance, the Fe domains of the DFC adsorbed rapidly Cr(VI) when the bulk C/(C+Fe) molar ratios of DFC were less than 0.89. The amounts of Cr(VI) reductions were related to both DOM contents and solution pH, but the pH seemed to be the key factor of controlling Cr(VI) reduction. The reactive mechanisms of Cr(VI) with DFC could be grouped into four types depending on C/(C+Fe) molar ratios and pH values: (1) Nearly 100% of Cr(VI) were associated with ferrihydrite-like domains of DFC with the bulk C/(C+Fe) molar ratios ≤ 0.65; (2) The Fe hydroxides-Cr(VI) was the dominant species of Cr, and the reductive products of Cr(III) were associated with Fe hydroxides or DOM when the bulk C/(C+Fe) molar ratios were between 0.71 and 0.89; (3) With C/(C+Fe) molar ratios ≥ 0.89, Cr(VI) was reduced by DOM and then associated with Fe(III) hydroxides at pH 4.5 and 6.0; and (4) At pH 3.0 and the C/(C+Fe) molar ratios ≥ 0.92, the DOM-Cr(III) complexes became the dominant Cr species. In general, the studies show that C/Fe molar ratios control the structural developments of DFC, and both of C/Fe molar ratios and solution pH affect adsorption/reduction reactions of Cr(VI) on DFC. However, the pH may be a key factor of controlling the formation of DFC in the presence of Al ions and regulating Cr(VI) reduction behavior on DFC.
Книги з теми "Dissolved CO₂":
Richette, Pascal. Principles of gout management. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199668847.003.0044.
Johansen, Bruce, and Adebowale Akande, eds. Nationalism: Past as Prologue. Nova Science Publishers, Inc., 2021. http://dx.doi.org/10.52305/aief3847.
Частини книг з теми "Dissolved CO₂":
Xie, Bo, and Anthony Muscat. "Repair of Porous MSQ (p-MSQ) Films Using Monochlorosilanes Dissolved in Supercritical CO2." In Solid State Phenomena, 323–26. Stafa: Trans Tech Publications Ltd., 2005. http://dx.doi.org/10.4028/3-908451-06-x.323.
Brons, M. D. (Anne). "Cross-National Variation in the Link Between Parental Socio-Economic Status and Union Formation and Dissolution Processes." In Social Background and the Demographic Life Course: Cross-National Comparisons, 17–34. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-67345-1_2.
Bianchi, Thomas S. "Dissolved Gases in Water." In Biogeochemistry of Estuaries. Oxford University Press, 2006. http://dx.doi.org/10.1093/oso/9780195160826.003.0012.
N. Nweke, Eucheria, Victor U. Okechukwu, Daniel O. Omokpariola, Theresa C. Umeh, and Nwanneamaka R. Oze. "Pollution Evaluation of Industrial Effluents from Consolidated Breweries: A Case Study from Benue State, Nigeria." In River Basin Management - Under a Changing Climate [Working Title]. IntechOpen, 2022. http://dx.doi.org/10.5772/intechopen.105955.
Bühler, T. M., K. Burrell, H. U. Eggars, and R. J. R. Reed. "The application of membranes for new approaches to brewery operations." In European Brewery Convention, 691–700. Oxford University PressOxford, 1993. http://dx.doi.org/10.1093/oso/9780199634668.003.0076.
Papageorgiou, M., M. G. Gothard, L. E. Willoughby, S. Kasapis, R. K. Richardson, and E. R. Morris. "Rheology and structure of gellan-alginate co-gels." In Gums and Stabilisers for the Food Industry 7, 345–56. Oxford University PressOxford, 1994. http://dx.doi.org/10.1093/oso/9780199634651.003.0030.
Walker, James C. G. "The Carbon System and Several Useful Procedures." In Numerical Adventures with Geochemical Cycles. Oxford University Press, 1991. http://dx.doi.org/10.1093/oso/9780195045208.003.0007.
Nofar, Mohammadreza, and Chul B. Park. "Polylactide PVT, Solubility, and Interfacial Tension Behavior in Presence of Dissolved CO 2." In Polylactide Foams, 35–56. Elsevier, 2018. http://dx.doi.org/10.1016/b978-0-12-813991-2.00003-2.
Davies, Mark R. "The Potential Liability Of Solicitors For Costs." In Solicitors’ Negligence And Liability, 457–72. Oxford University PressOxford, 2008. http://dx.doi.org/10.1093/oso/9780199284399.003.0018.
Gorlizki, Yoram, and Oleg Khlevniuk. "The New Course." In Substate Dictatorship, 255–78. Yale University Press, 2020. http://dx.doi.org/10.12987/yale/9780300230819.003.0010.
Тези доповідей конференцій з теми "Dissolved CO₂":
Mukayama, Tomoyuki, Yoshitaka Hattori, Masaki Kuribayashi, Go Asai, Eriko Matsumura, and Jiro Senda. "Effects of Spray Internal EGR Using CO <sub>2</sub> Gas Dissolved Fuel on Combustion Characteristics and Emissions in Diesel Engine." In Small Engine Technology Conference & Exposition. 10-2 Gobancho, Chiyoda-ku, Tokyo, Japan: Society of Automotive Engineers of Japan, 2020. http://dx.doi.org/10.4271/2019-32-0592.
Zhu, Chen, Guangmao Li, Shengya Qiao, Fuli Zheng, and Jianping Deng. "Detection of CO and CO2 Dissolved in Transformer Oil Based on Raman Spectroscopy and Neural Network." In 2021 11th International Conference on Power and Energy Systems (ICPES). IEEE, 2021. http://dx.doi.org/10.1109/icpes53652.2021.9683879.
Nenonen, Ville, Ralf Kaegi, Stephan Hug, Stefan Mangold, Jörg Göttlicher, Lenny Winkel, and Andreas Voegelin. "Phosphate co-precipitation with Fe(III) during Fe(II) oxidation: Effects of dissolved organic compounds." In Goldschmidt2023. France: European Association of Geochemistry, 2023. http://dx.doi.org/10.7185/gold2023.20443.
Mukayama, Tomoyuki, Ryota Nishigami, Annisa Bhikuning, Go Asai, Masaki Kuribayashi, Eriko Matsumura, and Jiro Senda. "Improvement of Spray and Combustion Process by Applying CO <sub>2</sub> Gas Dissolved Fuel." In JSAE/SAE Small Engine Technologies Conference & Exhibition. 10-2 Gobancho, Chiyoda-ku, Tokyo, Japan: Society of Automotive Engineers of Japan, 2017. http://dx.doi.org/10.4271/2017-32-0046.
Chatterjee, Nikitasha, Anil Gupta, Sameer Tiwari, Mohan Kuppusamy, and Kanishak Sharma. "Dissolved carbon system in the Bhagirathi basin, Uttarakhand, India: implications on CO2 degassing." In Goldschmidt2023. France: European Association of Geochemistry, 2023. http://dx.doi.org/10.7185/gold2023.14510.
Zhou, Qu, Weigen Chen, and Shudi Peng. "Study on sensing properties of Pt/Fe/Zn decorated SnO2 sensor for dissolved CO in transformer oil." In 2013 IEEE Conference on Electrical Insulation and Dielectric Phenomena - (CEIDP 2013). IEEE, 2013. http://dx.doi.org/10.1109/ceidp.2013.6748301.
Voigt, Martin, Chiara Marieni, Andre Baldermann, Iwona Galeczka, Domenik Wolff-Boenisch, Eric Oelkers, and Sigurdur Gislason. "Experimental characterisation of basalt carbonation by seawater-dissolved CO2 at 130 °C." In Goldschmidt2021. France: European Association of Geochemistry, 2021. http://dx.doi.org/10.7185/gold2021.5312.
Dellinger, Mathieu, Robert Hilton, Mateja Ogric, Kate Horan, A. Joshua West, Katherine Grant, and Guillaume Soulet. "Quantifying petrogenic organic carbon weathering fluxes and associated CO2 release using dissolved rhenium in rivers." In Goldschmidt2023. France: European Association of Geochemistry, 2023. http://dx.doi.org/10.7185/gold2023.17055.
Qiao, Wen, Deqiang Zhang, Yi Wang, Guangyu Bai, and Wei Sun. "Co-contamination of dissolved antimony, arsenic, and fluoride in mining-influenced aquifers from the Xikuangshan antimony mine, China." In Goldschmidt2023. France: European Association of Geochemistry, 2023. http://dx.doi.org/10.7185/gold2023.18048.
Absar, Saheem, Mujibur Khan, Kyle Edwards, and David Calamas. "Electrospinning of Cisplatin-Loaded Cellulose Nanofibers for Cancer Drug Delivery." In ASME 2014 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 2014. http://dx.doi.org/10.1115/imece2014-37182.
Звіти організацій з теми "Dissolved CO₂":
Chefetz, Benny, Baoshan Xing, and Yona Chen. Interactions of engineered nanoparticles with dissolved organic matter (DOM) and organic contaminants in water. United States Department of Agriculture, January 2013. http://dx.doi.org/10.32747/2013.7699863.bard.
Shiao, S. Y. Physical cleaning of waste coal by dissolved-CO{sub 2} flotation. Final technical report, September 1, 1992--August 31, 1993. Office of Scientific and Technical Information (OSTI), December 1993. http://dx.doi.org/10.2172/10132412.
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