The presence of and interactions between structural defects, fluids, and trace elements during deformation play a vital role in the manner in which materials respond to an applied stress. Although the links between crystal defects and trace element mobility have been lying at the frontier of research in Earth sciences, the role of fluids and the underlying physico-chemical processes linking them remain poorly understood. Investigation of these nanometer scale processes requires a correlative approach combining high-spatial resolution analytical techniques. This thesis integrates novel 2D and 3D structural and geochemical mapping methods such as electron channeling contrast imaging, electron backscatter diffraction, scanning transmission electron microscopy (STEM) and atom probe tomography (APT) to interrogate the atomic structure and composition of geomaterials in an attempt to better understand long-standing questions in Earth sciences and build bridges between materials science and geoscience. The processes investigated in this thesis include: 1) the underlying diffusion processes that mobilize trace elements into deformation-induced nanostructures; 2) the mechanisms of trace element segregation associated with fluid inclusions; 3) the influence of fluid inclusions on the mobility of structural defects and trace element mobility; and 4) the initial stages of bubble nucleation in the presence of nanoscale chemical heterogeneities. Ultimately, this research interrogates the feedbacks between deformation and trace element diffusion processes, fundamentally investigating their impact on rheology. More specifically, the thesis investigates the influence of deformation and associated nanostructures on the remobilization of trace elements and, in turn, the influence of trace elements on the nucleation and mobility of nanostructures. The combined work successfully identified two diffusion mechanisms for deformation-induced trace element mobility, characterized fluid-inclusions in APT data, documented two processes that led to proposing a new fluid inclusion-induced hardening model, and documented direct evidence of bubble nucleation on the surface of nanoscale chemical heterogeneities. This work not only pushes the limits of high-spatial resolution analytical techniques including STEM and APT, but the results have significant transdisciplinary implications in the fields of geoscience, materials science, engineering, and analytical microscopy.

京都大学 / 新制・課程博士 / 博士(工学) / 甲第23891号 / 工博第4978号 / 新制||工||1777(附属図書館) / 京都大学大学院工学研究科材料工学専攻 / (主査)教授 辻 伸泰, 教授 乾 晴行, 教授 安田 秀幸 / 学位規則第4条第1項該当 / Doctor of Philosophy (Engineering) / Kyoto University / DFAM

The thesis is concerned with relationships between progressive technological processes of spheroidal graphite cast iron’s production and their structural properties. The aim of the work is to explain causal relationship between parameters of the proposed manufacturing technology of the iron type given (involving selected variants of modification and inoculation of melt and the parameters of melt crystallization, solidification and cooling down in a mould), their structure and even chemical heterogeneity of elements in this structure. For close specification of presented relationships three-dimensional model of spheroidal graphite growth was used, which was developed at the Brno University of Technology, Faculty of Mechanical Engineering. Its usability in praxis has been verified on the basisis of the application of this model on experimentally acquired data. The U GRAFIT 20 model of the authors Stránský and Million counting segregation in the frame of eutectic cell has not still been used for prediction of segregation in real condition in greater extent. On the basis of the above mentioned model microsegregation within “on average” of the cell has been discovered during experimental melts. Microsegregation has been described by segregation and heterogeneity indexes. Calculated values of segregation and heterogeneity indexes have been compared with experimentally verified values. On the basis of comparison of calculated and measured values the possibility of further usage of the mentioned model in praxis has been explored.

Hydrated polysaccharide systems primarily using xylans along with mutans and alternans were studied using long atomistic simulations over a few microseconds to analyse structure-function relationships and nanoscale interactions with moisture. The influence of various structural and chemical factors such as alignment, nature of glycosidic linkage, effect of moisture / chemical substitutions was explored with a focus on structure-dynamics correlations to aid in the effective functionalisation of biomaterials for the development of a green, circular bioeconomy. The effect of initial geometry in terms of alignment of the xylan chains was observed to affect xylan chain extension and water dynamics significantly. Xylan interaction with moisture studied at high and low moisture contents showed compression along with structural locking, and evolution into segregated water-rich and polymer-rich phases respectively. The effect of chemical heterogeneity in terms of substitutions appeared to improve xylan dispersion in water resulting in faster dynamics for substituted residues with reference to unsubstituted residues along a given polymer chain. In addition, significant correlations between local hydration and polymer dynamics / structure in terms of relaxation times and order parameters was observed across differently substituted hydrated xylan systems, such that the polymer dynamics could be expressed as a local hydration water dependent component and a second partially stochastic component. In addition, the molecular structure of mixed linkage (1,3 and 1,6) as well as 1,3 linked glucans elucidated the effect of the nature of glycosidic linkage on the molecular structure of glucan oligosaccharides. A combination of glucan linkages and the ratio of different conformation states of the hydroxymethyl dihedral angle was observed to yield linear, twisted and extended structures in mutans, or helical coils of varying pitch sizes in alternans. Further modeling of structure-dynamics dependencies in hydrated xylan systems and analysis of the effect of alignment / chemical substitutions at the nanoscale is to be correlated with scattering or related experimental techniques in the future to understand the dynamics of hydrated xylan aggregates in typically aqueous solutions at varying intermediate length / timescales. In addition, the methodologies derived in this work to identify atom-specific, temporally sensitive, structural / dynamical parameters for analysing structural / dynamical variations at the nanoscale can be extended to study other hydrated biopolymeric systems. The role of substitutions, involving its polar nature and interactions with other xylans, can be extended to neutral groups such as arabinose sugars to broaden knowledge in carbohydrate science as well as being analysed further to improve effective functionalisation for tailoring physical properties influencing phenomena like aggregation / dispersion. / Hydrerade polysackaridsystem som primärt använde xylaner, mutaner och alternaner studerades med hjälp av långa atomistiska simuleringar under några mikrosekunder för att analysera struktur-funktionsförhållanden och interaktioner med fukt i nanoskala. Inverkan av olika strukturella och kemiska faktorer såsom placering, karaktären av glykosidbindning, effekten avfukt/kemiska substitutioner undersöktes med fokus på struktur-dynamiska korrelationer för att hjälpa till med en effektiv funktionalisering av biomaterial för utvecklingen av en grön, cirkulär bioekonomi. Effekten av initial geometri i termer av placering av xylan-kedjorna observerades påverka xylan-kedjeförlängningen och vattendynamiken signifikant. Xylaninteraktionen medfukt studerades vid höga och låga fukthalter och visade kompression tillsammans med strukturell låsning och utveckling till segregerade vattenrika och polymerrika faser respektive. Effekten av kemisk heterogenitet i termer av substitutioner verkade förbättra dispersionen av xylan i vatten vilket resulterade i snabbare dynamik för substituerade delar jämfört med osubstituerade delar längs en given polymerkedja. Dessutom observerades signifikanta korrelationer mellan lokal hydratisering och polymerdynamik/struktur i termer av relaxationstider och ordningsparametrar över olika substituerade hydratiserade xylansystem, så att polymerdynamiken kunde uttryckas som en lokal hydreringsvattenberoende komponent och en andra delvis stokastisk komponent. Dessutom klargjorde den molekylära strukturen av blandad koppling (1,3 och 1,6) såväl som 1,3 länkade glukaner effekten av glykosidkopplingens natur på molekylstrukturen hos glukanoligosackarider. En kombination av glukanbindningar och förhållandet mellan olika konformationstillstånd för den hydroximetyldiedriska vinkeln observerades i linjära, vridna och utsträckta strukturer som i mutaner, eller som spiralformade spolar med varierande stigningsstorlekar i alternaner. Ytterligare modellering av struktur-dynamiska beroenden i hydratiserade xylansystem och analys av effekten av inriktning/kemiska substitutioner på nanoskala ska korreleras med spridning av relaterade experimentella tekniker i framtiden för att förstå dynamiken hos hydratiserade xylanaggregat i typiskt vattenhaltiga lösningar vid varierande medellängd /tidsskalor. Dessutom kan de metoder som härrör från detta arbete för att identifiera atomspecifika, tidsmässigt känsliga, strukturella/dynamiska parametrar för analys av strukturella/dynamiska variationer på nanoskala, utvidgas till att studera andra hydratiserade biopolymera system. Substitutionernas roll, som involverar dess polära natur och interaktioner med andra xylaner, kan utvidgas till neutrala grupper som arabinossocker för att bredda kunskapen inom kolhydratvetenskap samt analyseras ytterligare för att förbättra effektiv funktionalisering för att skräddarsy fysiska egenskaper som påverkar fenomen som aggregering / dispersion. / <p>QC 2023-05-22</p>