Academic literature on the topic 'CuWO4'
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Journal articles on the topic "CuWO4"
Peng, Ben, Mengyang Xia, Chao Li, Changshen Yue, and Peng Diao. "Network Structured CuWO4/BiVO4/Co-Pi Nanocomposite for Solar Water Splitting." Catalysts 8, no. 12 (December 17, 2018): 663. http://dx.doi.org/10.3390/catal8120663.
Full textLi, Chao, and Peng Diao. "Boosting the Activity and Stability of Copper Tungsten Nanoflakes toward Solar Water Oxidation by Iridium-Cobalt Phosphates Modification." Catalysts 10, no. 8 (August 10, 2020): 913. http://dx.doi.org/10.3390/catal10080913.
Full textThiruppathi, M., M. Vahini, P. Devendran, M. Arunpandian, K. Selvakumar, C. Ramalingan, M. Swaminathan, and E. R. Nagarajan. "CuWO4 Nanoparticles: Investigation of Dielectric, Electrochemical Behaviour and Photodegradation of Pharmaceutical Waste." Journal of Nanoscience and Nanotechnology 19, no. 11 (November 1, 2019): 7026–34. http://dx.doi.org/10.1166/jnn.2019.16601.
Full textAndrade Neto, N. F., Y. G. Oliveira, J. H. O. Nascimento, M. R. D. Bomio, and F. V. Motta. "Influence of pH variation on CuWO4, CuWO4/WO3 and CuWO4/CuO structures stabilization: study of the photocatalytic properties under sunlight." Journal of Materials Science: Materials in Electronics 31, no. 20 (September 8, 2020): 18221–33. http://dx.doi.org/10.1007/s10854-020-04371-x.
Full textGoncalves, Renato Vitalino, Lucas Gabriel Rabelo, Washington Santa Rosa, and Luis Zampaulo. "Ternary-Oxides CuWO4/BiVO4/FeCoOx Films for Photoelectrochemical Water Oxidation: Insights into the Photoinduced Charge Transfer Pathway." ECS Meeting Abstracts MA2022-01, no. 36 (July 7, 2022): 1585. http://dx.doi.org/10.1149/ma2022-01361585mtgabs.
Full textÁgoston, Áron, and László Janovák. "Hydrothermal Co-Crystallization of Novel Copper Tungstate-Strontium Titanate Crystal Composite for Enhanced Photocatalytic Activity and Increased Electron–Hole Recombination Time." Catalysts 13, no. 2 (January 27, 2023): 287. http://dx.doi.org/10.3390/catal13020287.
Full textDorfman, Leonid P., David L. Houck, Michael J. Scheithauer, Jeffrey N. Dann, and Harry O. Fassett. "Solid-phase synthesis of cupric tungstate." Journal of Materials Research 16, no. 4 (April 2001): 1096–102. http://dx.doi.org/10.1557/jmr.2001.0152.
Full textMathew, T., N. M. Batra, and S. K. Arora. "Electrical conduction in CuWO4 crystals." Journal of Materials Science 27, no. 15 (1992): 4003–8. http://dx.doi.org/10.1007/bf01105096.
Full textArora, S. K., and T. Mathew. "Dielectric studies of CuWO4 crystals." Physica Status Solidi (a) 116, no. 1 (November 16, 1989): 405–13. http://dx.doi.org/10.1002/pssa.2211160141.
Full textAbbas, Zaheer, Razium Ali Soomro, Nazar Hussain Kalwar, Mawada Tunesi, Magnus Willander, Selcan Karakuş, and Ayben Kilislioğlu. "In Situ Growth of CuWO4 Nanospheres over Graphene Oxide for Photoelectrochemical (PEC) Immunosensing of Clinical Biomarker." Sensors 20, no. 1 (December 25, 2019): 148. http://dx.doi.org/10.3390/s20010148.
Full textDissertations / Theses on the topic "CuWO4"
POLO, ANNALISA. "TERNARY OXIDE SEMICONDUCTOR PHOTOANODES FOR SOLAR ENERGY CONVERSION." Doctoral thesis, Università degli Studi di Milano, 2021. http://hdl.handle.net/2434/827287.
Full textTimofejeva, Oksana. "Nuosėdų formavimosi sistemose CuSO4 – K4P2O7 – H2O ir CuSO4 – (NH4)4P2O7 – H2O mechanizmo tyrimas." Doctoral thesis, Lithuanian Academic Libraries Network (LABT), 2009. http://vddb.library.lt/obj/LT-eLABa-0001:E.02~2009~D_20090526_111134-61644.
Full textAt least three poorly soluble compounds can be formed in the CuSO4 – K4P2O7 – H2O system: a single salt Cu2P2O7.5H2O and two dimorph’s both having chemical formula Cu3K2(P2O7)2.3H2O. A previously known form of Cu3K2(P2O7)2.3H2O (we named it Dimorph A) transforms into a novel Dimorph B, which has a different structure. The similarities between the XRD patterns and vibrations spectra of copper–ammonium and copper–potassium Dimorph’s B imply that they are isostructural. The values of the angle for copper–potassium and copper–ammonium salts and Cu2P2O7.5H2O are relatively low and vary within a narrow range (123.1 – 127.1°). The formation of the compounds significantly depends on the conditions of the experiment. A double salt in the CuSO4 – K4P2O7 – H2O system may be formed after some time in the reaction mixture as a result of the following heterogeneous reaction: 3Cu2P2O7∙5H2O↓ + H2P2O72– + 4K+ → 2Cu3K2(P2O7)2∙3H2O↓ + 2H+ + 9H2O This reaction has not been previously described for any polyphosphate system. Therefore, novel results of scientific investigation are presented. The rate, duration and yield of heterogeneous reaction substantially depend on pH of the solution, [Cu2+ + P2O74–] and n ([P2O74–] / [Cu2+]). At a relatively low pH the induction time is high, the reaction rate is low and duration is long. The maximal yields close to 100% can be achieved when [Cu2+ + P2O74–] = 0.1 M. At increased pH values, the induction time, the yield and duration of the reaction diminish... [to full text]
Timofejeva, Oksana. "Formation of Barely Soluble Compounds in the CuSO4 – K4P2O7 – H2O and CuSO4 – (NH4)4P2O7 – H2O Systems." Doctoral thesis, Lithuanian Academic Libraries Network (LABT), 2009. http://vddb.library.lt/obj/LT-eLABa-0001:E.02~2009~D_20090526_111121-30909.
Full textNaudojant IR-spektrometrijos, rentgenofazinės analizės, atominės absorbcinės spektroskopijos, kolorimetrijos analizės metodus buvo ištirta sistemose CuSO4 – K4P2O7 – H2O ir CuSO4 – (NH4)4P2O7 – H2O susidarančių mažai tirpių junginių sudėtis, jų susidarymo dėsningumai ir vykstančios reakcijos, įvairių veiksnių įtaką nuosėdų sudėčiai ir struktūrai. Nustatyta, kad sistemoje CuSO4 – K4P2O7 – H2O, be jau žinomų mažai tirpių junginių (paprastosios druskos Cu2P2O7 ∙ 5H2O ir dvigubosios druskos Cu3K2(P2O7)2 ∙ 3H2O), susidaro ir naujas mokslinėje literatūroje neaprašytas junginys (Dimorfas B), dvigubajai druskai patiriant polimorfinį perėjimą. Polimorfinio perėjimo trukmė labai priklauso nuo pH ir reaguojančių jonų koncentracijų. FTIR duomenų analizė parodė, kad difosfato jonų energetinė būsena Cu – K ir Cu – NH4 Dimorfuose B panaši. Jų rentgenogramos yra panašios, tikėtina, kad šie junginiai – izostruktūriniai, jų kristalinės gardelės tipas – monoklininis. Naudojant Lazarevo lygtį, bei Rulmonto priklausomybę buvo apskaičiuoti Cu – K ir Cu – NH4 Dimorfų A ir B bei paprastosios druskos P – O – P kampai, gauta, kad jie mažai keičiasi siaurame 123,1 – 127,1 º intervale. Nustatyta, kad dviguboji druska susidaro iš paprastosios, vykstant heterogeninei reakcijai: 3Cu2P2O7 ∙ 5H2O↓ + H2P2O72– + 4K+ → 2Cu3K2(P2O7)2∙ 3H2O↓ + 2H++ 9H2O. Mokslinėje literatūroje tokia reakcija neaprašyta jokiai difosfatų sistemai, jos tyrimo duomenys yra nauji. Taip pat nustatyta, kad heterogeninės reakcijos... [toliau žr. visą tekstą]
Rüdow, Lina. "Miljöpåverkan av Cu från mjölkkors klövbad." Thesis, Linnéuniversitetet, Institutionen för biologi och miljö (BOM), 2015. http://urn.kb.se/resolve?urn=urn:nbn:se:lnu:diva-43724.
Full textThe hoof disease digital dermatitis rise pain with the cows as well as production disruption. To prevent and treat the hoof disease different substances are used, including CuSO4 solutions. The purpose of this study is to examine if, and in that case in which incidence, the spread of copper contaminated manure affects the copper content in agricultural land. The study was performed sampling two independent agricultural areas. One of the areas was fertilized with copper contaminated manure. The results show that agricultural land where CuSO4 has been spread with the manure has a significant higher content of Cu in the upper level of the soil, 0-25 cm.
Campos, ClÃudio Valadares Farias. "Suscetibilidade à CorrosÃo Sob TensÃo Dos AÃos AISI 321 E 347 Em Meio De H2so4 + Cuso4." Universidade Federal do CearÃ, 2003. http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=7323.
Full textOs aÃos inoxidÃveis austenÃticos tÃm sido bastante utilizados em equipamentos de utilidades de dessulfurizaÃÃo de petrÃleo devido à sua boa resistÃncia à corrosÃo em temperatura elevada.Contudo, esses materiais estÃo sujeitos a sensitizaÃÃo (deficiÃncia em cromo na regiÃo vizinha ao contorno de grÃo) quando expostos a temperaturas de 425 a 815ÂC, durante a operaÃÃo ou processos de fabricaÃÃo. A sensitizaÃÃo torna o equipamento suscetÃvel à corrosÃo sob tensÃo causada por aÃos politiÃnicos, formados pela interaÃÃo de compostos sulforoso, umidade e ar em temperatura ambiente. A resistÃncia à corrosÃo sob tensÃo de amostras de aÃo inoxidÃvel austenÃtico AISI 321 e 347, removidas de um tubo, foi investigada atravÃs do procedimento ASTM 262 Pr. E â ensaio alternativo e de execuÃÃo mais fÃcil do que a simulaÃÃo dos aÃos politiÃnicos. Os corpos de prova foram submetidos aos tratamentos tÃrmicos de estabilizaÃÃo (900ÂC, durante 75 minutos) e de sensitizaÃÃo (600ÂC, durante 20, 40, 80, 120 e 140 horas), apÃs o que foram expostos ao meio corrosivo de CuSO4 + H2SO4 durante 72 horas e depois dobradas, nÃo apresentando trincamento. A agressividade do meio utilizado no ensaio foi verificada atravÃs da utilizaÃÃo de amostras de aÃo AISI 304L sensitizadas (600ÂC, 24, 28 e 72 horas e 677ÂC durante 4, 45 e 72 horas). Neste caso, somente as amostras com acabamento superficial feito com lixa n 100 sofreram um intensivo processo corrosivo.
Because of their resistance to high temperature corrosion by hydrogen sulfide, austenitic stanless steels are commonly used for equipment in desulfurization process. However, these materials are subject to sensitization (chromium carbide precipitation) from exposure in the temperature range 425 to 815ÂC during fabrication or operation. Sensitization makes the equipment susceptible to failure from intergranular stress corrosion cracking caused by polythionic acid. Polythionic acid is formed by sulfur compounds, moisture, and air at ambient temperature. The main goal of the present work is to investigate the stress corrosion cracking susceptibility of stainless steels AISI 321 and 347 in polythionic acids using an alternative process that is to submit the samples to cooper-cooper sulfate-16% sulfuric acid test (ASTM A262 Pr.E). After the stabilization heat treatment at 900ÂC for 75 minutes, samples were heat treated at 600ÂC during 20, 40, 80, 120 and 140 hours and then exposed to boiling acidified copper sulfate solution for 72 hours. After exposure, the specimens were bent. The appearance of fissures or cracks was not observed in AISI 321 and 347 samples. The effectiveness of the solution has been made by submitting AISI 304L samples to the same environment . The AISI 304L samples with higher finishing have been cracked. The ones with fine-ground finishing have not been attacked.
Because of their resistance to high temperature corrosion by hydrogen sulfide, austenitic stanless steels are commonly used for equipment in desulfurization process. However, these materials are subject to sensitization (chromium carbide precipitation) from exposure in the temperature range 425 to 815ÂC during fabrication or operation. Sensitization makes the equipment susceptible to failure from intergranular stress corrosion cracking caused by polythionic acid. Polythionic acid is formed by sulfur compounds, moisture, and air at ambient temperature. The main goal of the present work is to investigate the stress corrosion cracking susceptibility of stainless steels AISI 321 and 347 in polythionic acids using an alternative process that is to submit the samples to cooper-cooper sulfate-16% sulfuric acid test (ASTM A262 Pr.E). After the stabilization heat treatment at 900ÂC for 75 minutes, samples were heat treated at 600ÂC during 20, 40, 80, 120 and 140 hours and then exposed to boiling acidified copper sulfate solution for 72 hours. After exposure, the specimens were bent. The appearance of fissures or cracks was not observed in AISI 321 and 347 samples. The effectiveness of the solution has been made by submitting AISI 304L samples to the same environment . The AISI 304L samples with higher finishing have been cracked. The ones with fine-ground finishing have not been attacked.
Campos, Cláudio Valadares Farias. "Suscetibilidade à corrosão sob tensão dos aços AISI 321 e 347 em meio de H2SO4 + CuSO4." reponame:Repositório Institucional da UFC, 2003. http://www.repositorio.ufc.br/handle/riufc/2527.
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Because of their resistance to high temperature corrosion by hydrogen sulfide, austenitic stanless steels are commonly used for equipment in desulfurization process. However, these materials are subject to sensitization (chromium carbide precipitation) from exposure in the temperature range 425 to 815ºC during fabrication or operation. Sensitization makes the equipment susceptible to failure from intergranular stress corrosion cracking caused by polythionic acid. Polythionic acid is formed by sulfur compounds, moisture, and air at ambient temperature. The main goal of the present work is to investigate the stress corrosion cracking susceptibility of stainless steels AISI 321 and 347 in polythionic acids using an alternative process that is to submit the samples to cooper-cooper sulfate-16% sulfuric acid test (ASTM A262 Pr.E). After the stabilization heat treatment at 900ºC for 75 minutes, samples were heat treated at 600ºC during 20, 40, 80, 120 and 140 hours and then exposed to boiling acidified copper sulfate solution for 72 hours. After exposure, the specimens were bent. The appearance of fissures or cracks was not observed in AISI 321 and 347 samples. The effectiveness of the solution has been made by submitting AISI 304L samples to the same environment . The AISI 304L samples with higher finishing have been cracked. The ones with fine-ground finishing have not been attacked.
Os aços inoxidáveis austeníticos têm sido bastante utilizados em equipamentos de unidades de dessulfurização de petróleo devido à sua boa resistência à corrosão em temperatura elevada. Contudo, este materiais estão sujeitos à sensitização (deficiência em cromo na região vizinha ao contorno de grão) quando expostos a temperaturas de 425 a 815°C, durante a operação ou processos de fabricação. A sensitização torna o equipamento suscetível à corrosão sob tensão na presença de tensões de tração e de ácidos politiônicos, formados pela interação de compostos sulfurosos, umidade e ar em temperatura ambiente. A resistência à corrosão sob tensão de amostras de aço inoxidável austenítico AISI 321 e 347, removidas de um tubo, foi investigada através do procedimento ASTM 262 Pr. E - ensaio alternativo e de execução mais fácil do que a simulação dos ácidos politiônicos. Os corpos de prova foram submetidos aos tratamentos térmicos de estabilização (900°C, durante 75 minutos) e de sensitização (600°C, durante 20, 40, 80, 120 e 140 horas), após o que foram expostos ao meio corrosivo de CuSO4 + H2SO4 durante 72 horas e depois submetidos ao ensaio de dobramento, não apresentando trincamento. A agressividade do meio utilizado no ensaio foi verificada através da utilização de amostras de aço AISI 304L sensitizadas durante 08, 14, 24 e 48 horas a 600°C e 24, 48 e 72 horas a 677°C. Verificou-se que somente as amostras com acabamento superficial feito com lixa n° 100 sofreram um intenso processo corrosivo.
Burrows, Oliver James. "Structural and magnetic properties of the geometrically frustrated 3d and 5d s = ½ Double Perovskites Sr₂CuWO₆, Ba₂YWO₆ and LaSrMgWO₆." Thesis, University of Edinburgh, 2017. http://hdl.handle.net/1842/22069.
Full textSosa, Filipe Hobi Bordón 1992. "Equilíbrio líquido-líquido de sistemas de duas fases aquosas (SDFA) formados por polímero (PEG ou PVP) e sal inorgânico (CuSO4 ou MnSO4) : determinação experimental e modelagem termodinâmica." reponame:Repositório Institucional da UFPR, 2017. http://hdl.handle.net/1884/46972.
Full textDissertação (mestrado) - Universidade Federal do Paraná, Setor de Tecnologia, Programa de Pós-Graduação em Engenharia Química. Defesa: Curitiba, 03/02/2017
Inclui referências
Resumo: Os sistemas de duas fases aquosas (SDFA) sao uma alternativa aos sistemas de extracao liquido-liquido convencionais. Estes sao formados atraves da adicao de solucoes aquosas de dois polimeros soluveis em agua, ou um polimero soluvel em agua e um componente de baixa massa molar, tal como sais inorganicos. Para aplicacoes industriais, sistemas formados por polimero, sal e agua sao de maior preferencia, uma vez, que apresentam baixa viscosidade, menor custo e menor tempo de separacao de fase. O conhecimento do comportamento termodinamico destes sistemas e de fundamental importancia para o projeto de unidades de extracao. Este trabalho teve como objetivo levantar dados experimentais e realizar a modelagem termodinamica do equilibrio liquido-liquido (ELL) dos sistemas de duas fases aquosas (SDFA) de PEG 2.000 e 6.000 + CuSO4 + H2O, PEG 2.000, 4.000 e 6.000 + MnSO4 + H2O e PVP 10.000 e 40.000 + MnSO4 + H2O em diferentes temperaturas (298,15, 318,15 e 338,15 K) utilizando o metodo de ponto de nevoa. Os dados de equilibrio obtidos para os SDFA demonstraram que o aumento de temperatura e da massa molar do polimero resultam em um aumento da regiao de duas fases dos sistemas, em um aumento da inclinacao e do comprimento das linhas de amarracao. Na analise do efeito de salting-out os sistemas compostos por sulfato de manganes obtiveram os maiores valores de coeficiente de salting-out devido a maior cosmotropicidade do cation Mn2+. A substituicao do polimero PEG pela polivinilpirrolidona (PVP) nos SDFA tambem foi avaliada. Os ajustes dos modelos termodinamicos NRTL e UNIQUAC foram eficazes para os sistemas formados por PEG, para os sistemas composto por PVP somente o UNIQUAC foi eficiente. Palavras Chaves: Sistemas de duas Fases Aquosas, Salting-out, Sais cosmotropicos, NRTL e UNIQUAC.
Abstract: Aqueous two-phase systems (ATPS) are an alternative to conventional liquidliquid extraction systems. These are formed by the addition of aqueous solutions of two water soluble polymers, or a water soluble polymer and a low molar mass component, such as inorganic salts. For industrial applications, systems formed by polymer + salt + water are more favorite, once, they have low viscosity, lower cost and less time of phase separation. The knowledge of the thermodynamic behavior of these systems is of fundamental importance for the design of extraction units. The objective of this work was to obtain experimental data and thermodynamic modeling the liquid-liquid equilibrium (LLE) of aqueous two-phase systems of PEG 2,000 and 6,000 + CuSO4 + H2O, PEG 2,000, 4,000 and 6,000 + MnSO4 + H2O and PVP 10,000 e 40,000 + MnSO4 + H2O at different temperatures (298.15, 318.15 and 338.15 K) using the cloud point method.The equilibrium data obtained for SDFAs demonstrated that the increase in temperature and molar mass of the polymer results in an increase of the two-phase region of the systems in an increase of the slope and length of the tie-lines. In the analysis of the salting-out effect the systems composed of manganese sulfate obtained the highest values of the salting-out coefficient due, to the higher cosmotropicity of the cation Mn2+.The substitution of PEG polymer by polyvinylpyrrolidone (PVP) in SDFA was also evaluated.The adjustments of the thermodynamic models NRTL and UNIQUAC were effective for the systems formed by PEG, for systems composed of PVP only UNIQUAC was efficient. Keywords: Aqueous Two-Phase Systems, Salting-out, Cosmotropic Salts, NRTL and UNIQUAC.
Patabendige, Chami N. K. "Material characterisation, phase transitions, electrochemical properties and possible fuel cell applications of Nd₂₋ₓPrₓCuO₄ and Nd2-x-y LayPrₓCuO₄ systems." Thesis, University of St Andrews, 2012. http://hdl.handle.net/10023/3181.
Full textWang, Yuh Yuan, and 王裕淵. "Photoelectrochemical Reactions in CuSO4/MeOH/TiO2 Suspension Systems." Thesis, 1994. http://ndltd.ncl.edu.tw/handle/14679083229339852005.
Full text國立清華大學
化學工程研究所
82
The objective of this thesis is to study the characteristic of the photoelectrochemical reac- tions in the CuSO4/MeOH/TiO2 suspension systems. Reduction of cupric ions and oxidation of methanol are preceded on TiO2 simultaneously. Reaction curves of the cupric ion conversion with time show a two-stage behavior, which a slow stage is followed by a rapid stage. Besides,the rapid stage shows a little concavity. These characteristics were studied via product, nucleation and para- meters'' studies. The Cu2O being produced at high pH can retard electrons to penetrate the Cu2O/TiO2 interface. The metallic Cu being produced at low pH acts as an electron trap.It can increase the photoelectrochemical reaction too. Successive reduction of cupric ions is preceded at existed Cu nuclei. Results of mechanism study on MeOH oxidation demonstrate that the active sites of Ti2O are the defects and the undamaged surface. Absorption of MeOH on TiO2 is identified as physisorption. Film breakdown and S doping were found during the studies of Ti anodization in Na2SO4 solution. The discussion of nucleation is confirmed by photoelectrochemical study on the anodized TiO2 surface. Establishment of the electric field needs a certain distance for Cu nucleation.
Book chapters on the topic "CuWO4"
Holze, Rudolf. "Ionic conductance of CuSO4." In Electrochemistry, 874–75. Berlin, Heidelberg: Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-49251-2_822.
Full textMorrison, Clyde Arthur. "La2-x Sr x CuO4." In Crystal Fields for Transition-Metal Ions in Laser Host Materials, 99–101. Berlin, Heidelberg: Springer Berlin Heidelberg, 1992. http://dx.doi.org/10.1007/978-3-642-95686-7_23.
Full textCastillo, V. M., R. D. Pochy, and L. Lam. "Pattern Changes in Electrodeposit of CuSO4." In Applications of Statistical and Field Theory Methods to Condensed Matter, 151–52. Boston, MA: Springer US, 1990. http://dx.doi.org/10.1007/978-1-4684-5763-6_14.
Full textBauer, Joseph, and Michael Moats. "Effective Copper Diffusion Coefficients in CuSO4–H2SO4 Electrowinning Electrolytes." In TMS 2020 149th Annual Meeting & Exhibition Supplemental Proceedings, 1237–47. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-36296-6_114.
Full textHayden, S. M. "Magnetic Excitations in La2-x (Ba,Sr) x CuO4." In Physics and Chemistry of Materials with Low-Dimensional Structures, 135–64. Dordrecht: Springer Netherlands, 1998. http://dx.doi.org/10.1007/978-94-015-1284-8_4.
Full textFujita, Toshizo, Minoru Nohara, Takashi Suzuki, Yoshiteru Maeno, Isao Tanaka, and Hironao Kojima. "Unusual Lattice Hardening below Tc in La2−xSr x CuO4." In Advances in Superconductivity VII, 219–24. Tokyo: Springer Japan, 1995. http://dx.doi.org/10.1007/978-4-431-68535-7_48.
Full textQi, Xiaoding, Zainovia Lockman, Masood Soorie, Yura Bugoslavsky, David Caplin, and Judith L. MacManus-Driscoll. "Growth of YBCO Thick Films on Nd2 CuO4 Buffered Substrates." In Ceramic Transactions Series, 103–9. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2012. http://dx.doi.org/10.1002/9781118405932.ch9.
Full textYu, Lianxu, Jun Xiao, Wenru Sun, Dandan Zheng, Weihong Zhang, Fang Liu, Xin Xin, Dan Jia, Feng Qi, and Zhuangqi Hu. "Surface Morphology Evolution of IN718 Alloy Etched by a CuSO4-HCl-H2SO4Etchant." In 8th International Symposium on Superalloy 718 and Derivatives, 777–86. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2014. http://dx.doi.org/10.1002/9781119016854.ch61.
Full textItoh, Mitsuru, Yue-Jin Shan, Shigeru Sakamoto, Osamu Ishiyama, Yoshiyuki Inaguma, and Tetsurō Nakamura. "Electrochemical Oxidation of La2-x Ba x CuO4 (0≤x≤0.145)." In Advances in Superconductivity VI, 391–94. Tokyo: Springer Japan, 1994. http://dx.doi.org/10.1007/978-4-431-68266-0_84.
Full textSchneider, Toni. "Thermal and Quantum Critical Properties of Overdoped La2−x Sr x CuO4." In High-Tc Copper Oxide Superconductors and Related Novel Materials, 299–305. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-52675-1_24.
Full textConference papers on the topic "CuWO4"
Müller, Sönke, Rainer Eichberger, Hannes Hempel, Daniel Peeters, Alexander Sadlo, James Hirst, Dariusz Mitoraj, et al. "The Transport Pathways of Charge Carriers in CuWO4 for Photocatalysis." In nanoGe Fall Meeting 2018. València: Fundació Scito, 2018. http://dx.doi.org/10.29363/nanoge.fallmeeting.2018.054.
Full textMüller, Sönke, Rainer Eichberger, Hannes Hempel, Daniel Peeters, Alexander Sadlo, James Hirst, Dariusz Mitoraj, et al. "The Transport Pathways of Charge Carriers in CuWO4 for Photocatalysis." In nanoGe Fall Meeting 2018. València: Fundació Scito, 2018. http://dx.doi.org/10.29363/nanoge.nfm.2018.054.
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