Oxyde de zinc

Résumé

L’oxyde de zinc est un composé chimique d'oxygène et de zinc, corps ionique de formule chimique . Présentation, préparation Cet oxyde quasiment insoluble dans l'eau se présente généralement sous la forme d'une poudre blanche infusible communément appelée « zinc blanc », « blanc de zinc » ou « fleur de zinc ». Ce corps blanc pulvérulent se nommait autrefois pour ses aspects floconneux et légers en latin pompholix, nihil album (blanc de rien des alchimistes), lana philosophica (laine philosophique). Il était alors considéré comme un corps "infusible et fixe". Au laboratoire, il peut s'obtenir par calcination de carbonate de zinc ou de nitrate de zinc, induisant un dégagement respectivement de dioxyde de carbone et de dioxyde d'azote, le dernier nettement plus explosif. : ZnCO → ZnO + CO Mais le simple chauffage du corps simple métal zinc au rouge, dans un creuset ouvert, donne par réaction exothermique des flocons d'oxyde de zinc, puisque la vapeur de zinc brûle à l'a

Source officielle

https://fr.wikipedia.org/wiki/Oxyde_de_zinc

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Effect of ZnO on the reactivity of cementitious systems

Andrea Eloisa Teixeira Pita

One of the biggest driving forces in cement research today is the mitigation of the CO2 emissions caused by its production. A potential solution to reduce the environmental impact is to replace cement with supplementary cementitious materials (SCMs). This replacement results in low strength at early ages because they are slow to react. The incorporation of minor elements has shown the potential to improve cement reactivity. A few percent of ZnO in C3S causes a signifi- cant increase in reactivity. This effect was related to the incorporation of zinc into the C-S-H struc- ture, which increases its needle length. This research investigates the effect of ZnO in more realis- tic systems such as alite, C3A-polyclinker, and C4AF-polyclinker. The positive effects observed in C3S are translated in the alite system, but differences were found in the polyclinkers, which have a prolonged induction period. This resulted due concentration of zinc in the interstitial phases and a small amount of zinc in alite phase. An amorphous phase was identified in the C3A polyclinker; it is believed to react rapidly with water, releasing Zn ions into the solution, which delays the reaction of alite. The addition of more gypsum controls the reaction of this phase, and thus the induction period is shortened.This work explores the possibilities of retaining Zn in alite to enhance the reactivity of more realis- tic cementitious systems. The cooling rate was critical, as a slow cooling rate promoted more Zn in the alite, less amorphous, and hence, an enhancement in the hydration of C3A-polyclinker doped with ZnO. The recalcination of this system did not affect the hydration of alite but increased the amount of crystalline C3A, which reacted faster. Thus, the amorphous phase was related to an aluminate phase. Moreover, a C4AF-polyclinker and a system with a lower amount of interstitial phase were investigated. The results showed a higher Zn concentration in alite but also extended induction periods. This was associated with the free ZnO and the amorphous content. Even when the hydration was delayed, the height of the alite peak increased with Zn doping, probably due to the incorporation of Zn into the C-S-H observed in pure C3S.In addition, the interaction between sulfates and zinc in the alite system doped with ZnO was in- vestigated. Severe retardation was observed, and the reason is proposed to be the formation of amorphous Zn compound. The presence of aluminum, ettringite formation, or an amorphous layer were discarded as the cause of the retardation.

EPFL2022

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Templated electrodeposition of thin oxide

José Antonio Gonzalez Martinez

EPFL2005

Chargement

We report the atmospheric pressure chemical vapour deposition (APCVD) of a dual layer transparent conductive oxide (TCO). This combines a fluorine doped tin oxide (FTO) base layer with a fluorine doped zinc oxide (FZO) top layer, where we seek to utilise the respective advantages of each material and the differences in their associated industrial deposition process technologies. Deposition of a 250 nm thick FZO layer on FTO was enough to develop features seen with FZO only layers. The crystallographic orientation determined by the FZO dopant concentration. Changes to the deposition parameters of the underlying FTO layer effected stack roughness and carrier concentration, and hence optical scattering and absorption. Photovoltaic cells have been fabricated using this TCO structure showing promising performance, with efficiencies as high as 10.21% compared to reference FTO only values of 9.02%. The bulk of the coating was FTO, providing the majority of conductivity and the large surface features associated with this material, whilst keeping the overall cost low by utilising the very fast growth rates achievable. The FTO was capped with a thinner FZO layer to provide a top surface suitable for wet chemical or plasma etching, allowing the surface morphology to be tuned for specific applications. (C) 2015 Elsevier B.V. All rights reserved.

Elsevier2015

Chargement

Effect of ZnO on the reactivity of cementitious systems

Andrea Eloisa Teixeira Pita

EPFL2022