José Fabián Schneider

Dr. José Fabián Schneider

orcid

Research Focus & Metrics

Academic Career Length

35Years (1992-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 July 2001 in Cement and Concrete Research
Verified
Journal Article
Closed access
JSJosé Fabián Schneider
José Fabián Schneider
MCM.A Cincotto
M.A Cincotto
HPH Panepucci
H Panepucci

1 April 2005 in Journal of Non-Crystalline Solids
Verified
Journal Article
Closed access
Juliana MarchiJuliana Marchi
Juliana Marchi
DMD.S. Morais
D.S. Morais
JSJosé Fabián Schneider
José Fabián Schneider
JBJ.C. Bressiani
J.C. Bressiani
ABA.H.A. Bressiani
A.H.A. Bressiani

1 August 2000 in Journal of Non-Crystalline Solids
Verified
Journal Article
Closed access
JSJosé Fabián Schneider
José Fabián Schneider
VMValmor Mastelaro
Valmor Mastelaro
HPH. Panepucci
H. Panepucci
EZEdgar Zanotto
Edgar Zanotto

1 September 2003 in Journal of Non-Crystalline Solids
Verified
Journal Article
Closed access
JSJosé Fabián Schneider
José Fabián Schneider
VMValmor Mastelaro
Valmor Mastelaro
EZEdgar Zanotto
Edgar Zanotto
BSBoris A. Shakhmatkin
Boris A. Shakhmatkin
NVNatalia M. Vedishcheva
Natalia M. Vedishcheva
HPH. Panepucci
H. Panepucci

1 October 2015 in International Materials Reviews
Verified
Journal Article
Closed access
EZEdgar Zanotto
Edgar Zanotto
Jefferson Esquina TsuchidaJefferson Esquina Tsuchida
Jefferson Esquina Tsuchida
JSJosé Fabián Schneider
José Fabián Schneider
HEH. Eckert
H. Eckert
Over the past three decades, researchers have investigated the existence of possible relationships between crystal nucleation kinetics and the atomic-scale structure of silicate glasses. The main driving force for this quest was the fact that while the vast majority of glass-forming substances only undergo surface (heterogeneous) nucleation when sufficiently heated, a few systems also show the thermodynamically less favourable case of internal (homogeneous) nucleation on laboratory time/length scales. For such glass systems, various macroscopic properties, such as densities, configurational entropies and frozen-in birefringence, have suggested that the structure in the glassy state shows a closer resemblance to the structure of the phase formed upon crystallisation than in the case of glass systems only undergoing heterogeneous nucleation. However, the specific structural features and their length scales have remained uncertain. In this article, we review and discuss the research investigating relationships between the occurrence of internal nucleation and structural parameters related to various different length scales. The latter include (1) short-range order, concerning both network modifier cation-oxygen distances and coordination numbers as well as network former Q n distributions, (2) intermediate range order describing network former connectivities, network former/network modifier correlations, and network modifier distance distributions, and (3) medium range order as reflected by silicate tetrahedral ring-size statistics. Inspection of this data for several stoichiometric oxide glasses and their respective isochemical crystals suggests a positive correlation between homogeneous nucleation ability and structural similarity at the level of short- and intermediate-range order of the network modifier cations. In contrast, no correlation can be found with regard to any structural parameters describing the local structures of the network former species ( Q n distributions). Based on the limited set of data available, we develop concrete recommendations for future experiments to test this hypothesis.

1 October 2018 in Journal of Petroleum Science and Engineering
Verified
Journal Article
Closed access
MPMaria D.M. Paiva
Maria D.M. Paiva
ESEmílio C.C.M. Silva
Emílio C.C.M. Silva
DMDulce M.A. Melo
Dulce M.A. Melo
AMAntônio E. Martinelli
Antônio E. Martinelli
JSJosé Fabián Schneider
José Fabián Schneider