Добірка наукової літератури з теми "Double Oxygen Reduction"
Оформте джерело за APA, MLA, Chicago, Harvard та іншими стилями
Ознайомтеся зі списками актуальних статей, книг, дисертацій, тез та інших наукових джерел на тему "Double Oxygen Reduction".
Біля кожної праці в переліку літератури доступна кнопка «Додати до бібліографії». Скористайтеся нею – і ми автоматично оформимо бібліографічне посилання на обрану працю в потрібному вам стилі цитування: APA, MLA, «Гарвард», «Чикаго», «Ванкувер» тощо.
Також ви можете завантажити повний текст наукової публікації у форматі «.pdf» та прочитати онлайн анотацію до роботи, якщо відповідні параметри наявні в метаданих.
Статті в журналах з теми "Double Oxygen Reduction"
Mladenović, Dušan, Milica Vujković, Slavko Mentus, Diogo M. F. Santos, Raquel P. Rocha, Cesar A. C. Sequeira, Jose Luis Figueiredo, and Biljana Šljukić. "Carbon-Supported Mo2C for Oxygen Reduction Reaction Electrocatalysis." Nanomaterials 10, no. 9 (September 10, 2020): 1805. http://dx.doi.org/10.3390/nano10091805.
Повний текст джерелаYin, Jiao, Jianbo Jia, and Liande Zhu. "Double-template synthesis of platinum nanomaterials for oxygen reduction." Microchimica Acta 166, no. 1-2 (June 3, 2009): 151–56. http://dx.doi.org/10.1007/s00604-009-0178-7.
Повний текст джерелаLee, Dong-Gyu, Su Hwan Kim, Jiyun Lee, Seokmin Shin, Se Hun Joo, Yeongdae Lee, Chanhyun Park, Youngkook Kwon, Sang Kyu Kwak, and Hyun-Kon Song. "Double activation of oxygen intermediates of oxygen reduction reaction by dual inorganic/organic hybrid electrocatalysts." Nano Energy 86 (August 2021): 106048. http://dx.doi.org/10.1016/j.nanoen.2021.106048.
Повний текст джерелаKumar, Sachin, Monika Singh, Raj Pal, Uday Pratap Azad, Ashish Kumar Singh, Divya Pratap Singh, Vellaichamy Ganesan, Akhilesh Kumar Singh, and Rajiv Prakash. "Lanthanide based double perovskites: Bifunctional catalysts for oxygen evolution/reduction reactions." International Journal of Hydrogen Energy 46, no. 33 (May 2021): 17163–72. http://dx.doi.org/10.1016/j.ijhydene.2021.02.141.
Повний текст джерелаHORITA, Kiyoshi, Gentaro KANO, and Tomoo TAKASAWA. "Oxygen-reduction performance and wettability of double-layered gas diffusion electrodes." Journal of the Society of Materials Science, Japan 40, no. 448 (1991): 84–88. http://dx.doi.org/10.2472/jsms.40.84.
Повний текст джерелаOgasawara, H., L. A. Naslund, J. McNaughton, T. Anniyev, and Anders Nilsson. "Double Role of Water in the Fuel Cell Oxygen Reduction Reaction." ECS Transactions 16, no. 2 (December 18, 2019): 1385–94. http://dx.doi.org/10.1149/1.2981979.
Повний текст джерелаDevoille, Aline M. J., and Jason B. Love. "Double-pillared cobalt Pacman complexes: synthesis, structures and oxygen reduction catalysis." Dalton Trans. 41, no. 1 (2012): 65–72. http://dx.doi.org/10.1039/c1dt11424g.
Повний текст джерелаOgura, Hiroyuki, Yasoshi Ito, and Tamotsu Shirogami. "Oxygen Reduction Mechanism in Molten Carbonates by Current Double Pulse Method." IEEJ Transactions on Power and Energy 119, no. 3 (1999): 388–93. http://dx.doi.org/10.1541/ieejpes1990.119.3_388.
Повний текст джерелаWu, Jianbo, Zhenmeng Peng, and Hong Yang. "Supportless oxygen reduction electrocatalysts of CoCuPt hollow nanoparticles." Philosophical Transactions of the Royal Society A: Mathematical, Physical and Engineering Sciences 368, no. 1927 (September 28, 2010): 4261–74. http://dx.doi.org/10.1098/rsta.2010.0128.
Повний текст джерелаOnaka-Masada, Ayumi, Takeshi Kadono, Ryosuke Okuyama, Ryo Hirose, Koji Kobayashi, Akihiro Suzuki, Yoshihiro Koga, and Kazunari Kurita. "Reduction of Dark Current in CMOS Image Sensor Pixels Using Hydrocarbon-Molecular-Ion-Implanted Double Epitaxial Si Wafers." Sensors 20, no. 22 (November 19, 2020): 6620. http://dx.doi.org/10.3390/s20226620.
Повний текст джерелаДисертації з теми "Double Oxygen Reduction"
Pahls, Dale R. "Pathways for C—H Activation and Functionalization by Group 9 Metals." Thesis, University of North Texas, 2015. https://digital.library.unt.edu/ark:/67531/metadc801909/.
Повний текст джерелаHELLER, LING NATHALIE, and Pierre Chartier. "Etude et realisation d'une cellule electrochimique a flux d'electrolyte et a double electrode. Applications a l'etude du mecanisme reactionnel de la reduction de l'oxygene sur differents oxydes mixtes de metaux de transition." Université Louis Pasteur (Strasbourg) (1971-2008), 1994. http://www.theses.fr/1994STR13107.
Повний текст джерелаChala, Soressa Abera, and Soressa. "Developing Advanced Bifunctional Oxygen Electrocatalysts Using Ni-based Layered Double Hydroxide: Investigating the Active Phases and Mechanisms for Oxygen Evolution and Reduction Reaction." Thesis, 2019. http://ndltd.ncl.edu.tw/handle/fbd6tj.
Повний текст джерела國立臺灣科技大學
化學工程系
107
Developing advanced nanomaterials and catalytically active materials is a substantial area of research to meet the growing global energy demand, given the central role that electrocatalytic reactions play in green sustainable energy generation, storage and conversion. However, development of catalytically active, operationally stable and inexpensive materials for the bifunctional oxygen evolution (OER) and reduction reaction (ORR) is one of the grand challenges in renewable energy storage and conversion technologies such as metal-air batteries and fuel cells due to the sluggish reaction kinetics of OER and ORR even when noble metal catalysts such as platinum with carbon support (Pt/C for ORR), ruthenium oxide (RuO2), and iridium oxide (IrO2) toward OER are applied. Consequently, a critical feature is to develop robust materials that have outstanding catalytic activity, cost-effective and promising durability for the more difficult ORR/OER process. Currently, transition metal hydroxides/oxides and Ni-based layered double hydroxides (LDHs) electrocatalysts are an interesting alternative to the novel metal-based electrodes in alkaline solutions due to their low cost, abundance, proven ability to catalyze the OER/ORR and operationally stable in high pH values of the electrolytes. To accelerate the development of Ni-based LDHs electrocatalysts with improved catalytic activities for the OER/ORR, it is essential to increase the understanding of the mechanisms, active sites at a fundamental level, and surface properties at relevant potentials during the OER and ORR operation and remains of great importance to the design of new electrocatalysts. This dissertation aims to develop endurable, inexpensive, and efficient bifunctional electrocatalysts for the OER and ORR operated under alkaline conditions at room temperature; investigate the mechanisms, active sites, and surface properties during the OER process using in situ spectro-electrochemical techniques. Accordingly, new classes of Ni-based LDHs electrocatalysts (NiRu-LDHs and NiMn-LDHs nanosheets) were developed and integrated with conductive supports (silver nanoparticles (Ag NPs) and silver nanowires (Ag NWs)) using decoration action and core-shelling strategies as efficient bifunctional electrocatalysts for OER and ORR. This approaches will have great benefits to design highly active and stable bifunctional electrocatalysts for the next-generation reversible oxygen electrodes involve the combination of less-expensive single-function OER and ORR electrocatalysts into one hybrid system. The first approach (Chapter 4) investigated in this dissertation “Site activity and population engineering of NiRu-layered double hydroxide nanosheets decorated with conductive silver nanoparticles for oxygen evolution and reduction reaction”. This work focuses on the development of new electrocatalyst; NiRu-LDHs decorated with Ag NPs (Ag NP/NiRu-LDHs) as efficient and stable bifunctional electrocatalyst toward the OER and ORR and intended to distinguish the site activity and site population associated to the overall catalytic activity. The higher ORR activity of Ag NP/NiRu-LDHs was mainly attributed to the increased Ag site activity and accessible Ag site populations. The increased Ag site activity is extensively contributed from the charge polarization occurring on the Ag sites responsible for weakening the adsorption of OH on the Ag sites and the presence of LDHs helps to remove the adsorbed OH from the surface of Ag. Furthermore, the decoration strategy enhances the dispersion of Ag and considerably increased the accessible site populations. These strong synergetic effects between Ag and LDHs significantly enhanced the catalytic activity of the ORR. Interestingly, engineering multiple vacancies (metal and oxygen vacancies) which causes the structural disorder and defects through the introduction of Ru and decorating NiRu-LDHs nanosheets with conductive Ag NPs (improve the intrinsically poor conductivity of LDHs) tunes the intrinsic properties of the Ni sites which in turn enhances the OER site activity and site populations. The strong synergetic effects of silver nanoparticles and metal LDHs engineer the active site activity and populations on both Ag and Ni in the bifunctional electrocatalysts for ORR and OER, respectively. The as-prepared Ag NP/NiRu-LDH shows substantially marvelous catalytic activity toward both OER and ORR features with low onset overpotential of 0.21 V and -0.27 V, respectively, with 0.76 V overvoltage difference between OER and ORR with excellent durability, demonstrating the preeminent bifunctional electrocatalyst reported to date. This work provides a new strategy to improve the intrinsic properties of LDHs and engineering multivacancies to enhance the site activity and populations associated with the overall bifunctional activity of the electrocatalysts. The second study (Chapter 5) aims to develop “hierarchical 3D NiMn-layered double hydroxide (NiMn-LDHs) shells grown on conductive silver nanowires (Ag NWs) cores as efficient ORR/OER bifunctional electrocatalysts”. As a result, the hierarchical 3D architectured Ag NW@NiMn-LDHs catalysts exhibit superb OER/ORR activities in alkaline condition. The outstanding bifunctional activities of Ag NW@NiMn-LDHs are essentially attributed to the synergistic contributions from the hierarchical 3D open-pores structure of the LDHs shells, improved electrical conductivity and small thickness of the LDHs shells associated to more accessible site populations. Moreover, the charge transferring effect between Ag cores and metals of LDHs shells, the formation of less coordinated Ni and Mn sites causes defective and distorted sites that strongly tune the intrinsic activity of the site activity and hence attaining enhanced catalytic activities. Thus, Ag NW@NiMn-LDH hybrids exhibit 0.75 V overvoltage difference between ORR and OER with excellent durability for 30 h, demonstrating the distinguished bifunctional electrocatalyst reported to date. Thus, the concept of the hierarchical 3D architecture of Ag NW@NiMn-LDHs considerably advances comprehensive research towards water electrolysis and oxygen electrocatalyst. The third approach (chapter 6) of this dissertation is to investigate the mechanisms, probe the active sites and surface properties of NiMn-LDHs and β-Ni(OH)2 electrocatalysts during the OER operation using in situ spectro-electrochemical techniques. Ni-based layered double hydroxides (LDHs) materials are highly active and cost-effective electrocatalysts that can be potentially used for efficient water oxidation process and extensively used toward sustainable energy generation. However, the mechanisms at a fundamental level, active phases and the processes occurring on the surface of Ni-based LDHs materials during the OER operation are not clearly known. Accordingly, the evidence from in situ Raman features provide that the Ni(OH)2 phases in both NiMn-LDHs and β-Ni(OH)2 get oxidized to NiOOH species as the electrode voltage increasing and NiOOH intermediate species deprotonated and get charged prior to the real water oxidation, suggesting that the formation of “active oxygen” species and hence acts as a precursors for the OER. We therefore propose that the identity of the “active oxygen” species is nickel superoxidic or peroxidic nature. The in situ XANES spectra provides the evidence that the Ni K-edge significantly shifted to higher energy upon the electrode potential increased, suggesting the redox transition of Ni(OH)2 in NiMn-LDHs to NiOOH upon anodization that constitutes the catalytic activity of OER active center. The in situ EXAFS spectra of Ni K-edge indicates that the intensity of both Ni−O (R =1.53 Å) and Ni−M (R =2.73 Å) coordination spheres gradually decreases as the applied electrode potentials increase prior to the OER whereas the formation of new peaks at 1.44 Å and 2.42 Å corresponding to the coordination sphere of Ni−O and Ni−M, suggesting the formation of new phases existing in different environment due to the redox transition of Ni(OH)2 to NiOOH occurs. The intensity of these peaks substantially increased as the voltage of electrode increased. However, the intensity and peak positions of Mn K-edge collected at different potentials are almost similar and remain unchanged, suggesting no transformation of Mn sites during the OER process. We therefore conclude that Ni constitutes the active center and evidently the active site for the OER whereas the introduction of Mn atom promotes synergistically the OER activity. We also present a systematic studies of guest anion effect on the number of active sites and site activity of NiMn-LDHs and Ni(OH)2 catalysts during the OER process using electrochemical, in situ spectro-electrochemical techniques and in situ XRD measurements, which in turn used to probe the active sites and structural change during the OER process. Evidently, the NiMn-LDHs exhibited incredible OER activity after guest anions (bromide and chloride) introduced and the OER activity gradually increased as the concentration of guest anions increased. These observations suggest that the active site activity originated from the less-stacking and plentiful exposed active edge sites due to the expansion of interlayer spaces of LDHs structure (confirmed by the in situ XRD measurement) promotes the OER activity. Unlike NiMn-LDHs, both the redox transition of Ni(OH)2/NiOOH and the OER activity of β-Ni(OH)2 catalyst is significantly affected after guest anions introduced and suppressed to higher overpotential. These results suggest that since β-Ni(OH)2 is structurally close-packed, the guest anions have only one possibility to interact with Ni(OH)2 and that is attacking the Ni sites which certainly accounts for the declined OER activity. In general, integrating LDHs with conductive Ag NPs and Ag NWs through decoration and core-shelling strategies engineers multiple vacancies which cause the structural disorder and defects essentially enhances bifunctional properties of the hybrids, conductivity, stability during OER and ORR operation. The discussed in situ spectro-electrochemical characterization of NiMn-LDHs catalysts with high OER activity demonstrates that the Ni sites constitute the active center and the presence of Mn atom promotes synergistically the OER activity. Although the recent studies are limited to investigate the active sites and surface properties of LDHs for oxygen electrocatalysis, these considerations are also anticipated to extend to other LDHs catalysts and electrochemical reactions.
Ibrahim, Kassa Belay, and Kassa Belay Ibrahim. "Conductive and Robust Magneli-phase Ti4O7 Decorated Ni-based Layered Double Hydroxides towards Oxygen Evolution and Reduction Reaction." Thesis, 2018. http://ndltd.ncl.edu.tw/handle/emsqzs.
Повний текст джерела國立臺灣科技大學
應用科技研究所
106
Abstract We are in the era of seeking renewable energy to substitute fossil fuels due to the increasing demand for energy of the modern society, global warming, and depletion of natural sources. Therefore, globalization of advanced energy conversion technologies like rechargeable metal-air batteries (MAB’s), water-splitting, and regenerated fuel cells (RFCs) devices are highly regarded by the scientists as an environmentally friendly power source with global commercial viability. One of the most important challenges for electrochemically energy conversion and storage devices is to increase the efficiencies of both oxygen evolution reaction (OER) and oxygen reduction reaction (ORR), which will require the development of efficient and stable electrocatalysts. So far, Pt, Pd, IrO2, and RuO2 noble metal catalysts have acceptable kinetics. However, other electrocatalysts usually have high overpotential and sluggish kinetics and they give unsatisfactory ORR/OER performance. Further, limited reserves of noble-metal-based catalysts have precluded these renewable energy technologies from large-scale commercial applications. In many cases, how to improve both the activity and stability of an electrocatalyst is still an important challenge, especially under harsh alkaline conditions. The objectives of this dissertation are to tackle the challenge by developing new electrocatalysts and introducing robust and conductive support. The introduced materials are robust and conductive Magnéli phase Ti4O7 decorated in 3D-FL-NiRu-LDH and NiFe-LDH as ORR and OER electrocatalyst, respectively. This will have a great impact on lengthening the lifetime and reduce cost in energy conversion devices. The first part of the dissertation emphasizes “Robust and conductive Magnéli Phase Ti4O7 decorated on 3D-nanoflower NiRu-LDH (3D-FL-NiRu-LDH/Ti4O7) as high-performance oxygen reduction electrocatalyst”. This work has intended to discuss two basic issues and challenges in ORR electrocatalysts, namely increasing site population and enhancing the stability. The site population of the NiRu-LDH increased by engineering the morphology from 2D to 3D flowerlike material and the approach resulted in more surfaces exposed to the electrolyte. The second main challenge is to improve the intrinsically poor conductivity of LDHs and their short durability. In order to address this issue, we introduce robust, conductive and stable Magnéli phase Ti4O7 nano-pillar into flower-like NiRu-LDH through an easy in situ growth approach for the first time. The decoration of Magnéli phase Ti4O7 not only significantly improves the activity but also the stability of LDH nanosheet catalyst. The as-synthesized materials retain 98% of the activity after 45 h which surpasses all the reported LDH catalysts for oxygen reduction reaction under alkaline media. The key roles of Ti4O7 are to provide the effective charge transfer networks of LDH catalyst and prevent agglomeration of LDH catalysts though strongly coupled interactions evidenced by XPS. Therefore, the developed catalyst demonstrates promising conductivity, together with durability. The reported approach of introducing a robust and conductive pillar coupled with LDH catalysts provides a novel pathway for developing a highly efficient and durable electrocatalyst. The second part of this work is mediate extension of the first work but with some modification material for the application. Based on this, it is concerned with NiFe-LDH decorated by Magnéli phase Ti4O7 for OER electrocatalyst. An earth-abundant and highly efficient electrocatalyst are essential for OER due to its poor kinetics. NiFe-LDH is most promising OER catalysts, which perform best in alkaline electrolytes. However, the poor conductivity and the stacking structure of LDH limit its activity and exposure of active site, respectively. Therefore, we decorate LDH with highly conductive and robust Magnéli phase Ti4O7 in order to both boost conductivity and generate more dangling bonds and disordered structure that would result in vacancy and expose more active site on NiFe-LDH. In this work, a series of analyses reveal that the improved OER performances of NiFe-LDH-Ti4O7 compared to previously published works. This series improved performance is originated from the charge transfer effect, and strain effect between Ti4O7 and NiFe-LDH that results in structural deformation. Based on this, the as-synthesized NiFe-LDH-Ti4O7 nano-sheet exhibit an excellent catalytic activity for OER with ultra-small onset potential of only 1.42 and retain 100% of the current density after 30 hr. Furthermore, the presence of Fe3+ ions in the solution could bond with the Ti4O7 generating heterogeneous NiFe-LDH sites decorated with Ti4O7. These NiFe-LDH-Ti4O7 sites exhibited markedly an improved OER activity. In general, the use of Ti4O7 to decorate LDHs mainly enhances conductivity, stability (relative to carbon supports) and stacking between LDH layers during OER and ORR measurement. Additionally, it can also electronic and strain effect in the material that will result in vacancy and disordered in a structure of LDHs.
Chen, Pei-Wen, and 陳姵妏. "Study on bifunctional catalyst derived from NiFe layered double hydroxides decorated with Ag nanowires for oxygen evolution and reduction reactions in alkaline media." Thesis, 2019. http://ndltd.ncl.edu.tw/handle/53hhw6.
Повний текст джерела國立臺灣科技大學
化學工程系
107
Recently years, the rechargeable zinc-air batteries have its attracted much attention owing to high energy density and economic viability. In air electrode, a bifunctional electrocatalyst is desirable since the dual functionality of the oxygen evolution reaction (OER) and oxygen reduction reaction (ORR) are required on the same electrode under charging and discharging processes, respectively. Unfortunately, both commonly used catalysts: Pt/C in ORR and IrO2 in OER have no bifunctional property while the scarcity and cost of the metals limit its large-scale application for the electrolysis. In this work, the NiFe layered double hydroxides (Ni3Fe LDH) decorated with Ag nanowires (Ag NWs), as a bifunctional catalyst, was applied in oxygen reduction reaction and oxygen evolution reaction under alkaline media. First, the Ag nanowires were prepared via a polyol reduction method, and to optimize their linewidth and shape by changing the stirring rate and the precursor dropping rate. The Ni3Fe LDH was then deposited on the Ag nanowires by a hydrothermal process. As the results in surface morphology, the linewidth of Ag NWs was shortened with increasing stirring rate and precursor dropping rate. In FTIR analysis, a few residual PVP was still observed on Ag NWs while the intercalation anions of CO32- and NO3- were identified. As characterized in XPS and XAS, it was found that Fe sites in decorated Ni3Fe LDH were strongly influenced by Ag NWs, including the electronic effect (binding energy positively shifts) and the local structure environment (shorter Fe-O and Fe-M bond length). In OER performance, a mass activity of 432 mA mg-1LDH was reached by S-Ni3Fe LDH/Ag NWs-F(2:1)-10mL, much better than Ni3Fe LDH (121 mA mg-1LDH) and IrO2 (149 mA mg-1catalyst), attributed to a large number of accessible active sites on the catalytic surface. However, the ORR activities of the Ni3Fe LDH/Ag NWs catalysts showed no advantage compared to as-synthesized Ag NWs and commercial Pt/C catalyst, which may be attributed to a few residual of PVP and too thick of LDH layer on Ag surface thereby inhibit O2 diffusion. In OER stability test, a chronoamperometric method was used for 24 hours, S-Ni3Fe LDH/Ag NWs-F(2:1)-10mL showed current retention by 92.6%, better than Ni3Fe LDH (76.3%) and IrO2 (91.6%), more suitable as an OER catalyst.
Частини книг з теми "Double Oxygen Reduction"
Djellali, Meriem, Mostefa Kameche, Hakima Kebaili, Abdallah Benhamou, Mustapha Bouhent, and Christophe Innocent. "Utilization of Double-Layered Hydroxides for Enhancement of Dissolved Oxygen Reduction in Microbial Fuel Cell: An Approach for the Evaluation of Coulomb Efficiency." In ICREEC 2019, 239–44. Singapore: Springer Singapore, 2020. http://dx.doi.org/10.1007/978-981-15-5444-5_30.
Повний текст джерелаSenzaki, Tatsuya, Michiaki Matsukawa, Takanori Yonai, Haruka Taniguchi, Akiyuki Matsushita, Takahiko Sasaki, and Mokoto Hagiwara. "Functional Materials Synthesis and Physical Properties." In Recent Perspectives in Pyrolysis Research. IntechOpen, 2022. http://dx.doi.org/10.5772/intechopen.100241.
Повний текст джерелаAkkol, EsraKüpeli, and OzlemBahadır Acıkara. "Phytosterols in the Treatment of Gastrointestinal Tract Cancers." In Phytonutrients in the Treatment of Gastrointestinal Cancer, 231–62. BENTHAM SCIENCE PUBLISHERS, 2023. http://dx.doi.org/10.2174/9789815049633123010013.
Повний текст джерелаTaber, Douglass F. "C–O Natural Products: (–)-Hybridalactone (Fürstner), (+)-Anthecotulide (Hodgson), (–)-Kumausallene (Tang), (±)-Communiol E (Kobayashi), (–)-Exiguolide (Scheidt), Cyanolide A (Rychnovsky)." In Organic Synthesis. Oxford University Press, 2015. http://dx.doi.org/10.1093/oso/9780190200794.003.0051.
Повний текст джерелаUshakumari, Deepu S., and Stephanie Rayos Callison. "Thoracoabdominal surgeries in obese patients." In Oxford Textbook of Anaesthesia for the Obese Patient, edited by Ashish C. Sinha, 111–26. Oxford University Press, 2021. http://dx.doi.org/10.1093/med/9780198757146.003.0012.
Повний текст джерела"The Chemical Logic for Major Reaction Types." In Natural Product Biosynthesis, 22–46. The Royal Society of Chemistry, 2022. http://dx.doi.org/10.1039/bk9781839165641-00022.
Повний текст джерелаLambert, Tristan H. "Total Synthesis of C–O Natural Products." In Organic Synthesis. Oxford University Press, 2017. http://dx.doi.org/10.1093/oso/9780190646165.003.0049.
Повний текст джерелаТези доповідей конференцій з теми "Double Oxygen Reduction"
Gitzhofer, F., M.-E. Bonneau, and M. Boulos. "Double Doped Ceria Electrolyte Synthesized by Solution Plasma Spraying with Induction Plasma Technology." In ITSC2001, edited by Christopher C. Berndt, Khiam A. Khor, and Erich F. Lugscheider. ASM International, 2001. http://dx.doi.org/10.31399/asm.cp.itsc2001p0061.
Повний текст джерелаAlhazmi, Waleed, and Maher Alabdullatif. "Smart SRUs Pre-Investment Utilizing Oxygen Enrichment Technology." In SPE Middle East Oil & Gas Show and Conference. SPE, 2021. http://dx.doi.org/10.2118/204756-ms.
Повний текст джерелаWire, Gary L., and William J. Mills. "Fatigue Crack Propagation from Notched Specimens of 304 SS in an Elevated Temperature Aqueous Environment." In ASME 2002 Pressure Vessels and Piping Conference. ASMEDC, 2002. http://dx.doi.org/10.1115/pvp2002-1232.
Повний текст джерелаYoung, E. D., A. J. Andrews, and D. W. Coutts. "Oxygen Isotope Ratio Analysis of Silicate and Oxide Minerals by UV Ablation with a Frequency-Doubled Copper Vapour Laser." In The European Conference on Lasers and Electro-Optics. Washington, D.C.: Optica Publishing Group, 1996. http://dx.doi.org/10.1364/cleo_europe.1996.cwf71.
Повний текст джерелаSohnemann, Jens, Walter Scha¨fers, and Armin Main. "Waste Combustion Technology and Air Emission Control Developments by Fisia Babcock Environment." In 19th Annual North American Waste-to-Energy Conference. ASMEDC, 2011. http://dx.doi.org/10.1115/nawtec19-5418.
Повний текст джерелаAl-Sabouni, O., D. J. Stephenson, J. R. Nicholls, and G. Creffield. "Reactive Plasma Spraying of 80:20 Ni/Cr and Mcraly Powders with Hydrocarbon Reactive Gases." In ITSC 1998, edited by Christian Coddet. ASM International, 1998. http://dx.doi.org/10.31399/asm.cp.itsc1998p1315.
Повний текст джерела