Pieter Thyssen

The block universe theory of time is commonly held to be incompatible with temporal becoming. This confuses Maudlin who upholds both eternalism and passage. The aim of this paper is to answer Maudlin’s plea for clarification by distinguishing four degrees of temporal becoming: (1) absolute becoming, (2) relational becoming, (3) presentist becoming, and (4) dynamic becoming. After discussing their respective compatibility with the block universe, I argue that Maudlin subscribes to a much more deflated form of temporal becoming as compared to most philosophers of time. Consequently, his form of becoming is compatible with the block universe, whereas the stronger forms of becoming are not.

Are acids natural kinds? Or are they merely relevant kinds? Although acidity has been one of the oldest and most important concepts in chemistry, surprisingly little ink has been spilled on the natural kind question. I approach the question from the perspective of microstructural essentialism. After explaining why both Brønsted acids and Lewis acids are considered functional kinds, I address the challenges of multiple realization and multiple determination. Contra Manafu and Hendry, I argue that the stereotypical properties of acids are not multiply realized. Instead, given the equivalence between the proton-donating and electron-accepting mechanisms of Brønsted and Lewis, respectively, I show that acidity as a property type can be identified with a unique microstructural property, namely the presence of a LUMO or other low energy empty orbital. In doing so, I defend the view that the Lewis theory encompasses Brønsted–Lowry, and that all Brønsted acids are also Lewis acids. Contra Hacking and Chang, I thus maintain that the different concepts of acidity do not crosscut, and that the hierarchy requirement is met. Finally, by characterizing natural kinds as powerful objects and by adopting a dispositional view of functions, I illustrate how the microessentialist can make sense of the latent and relational character of most acids. In sum, I contend that acids are genuine natural kinds, even for the microstructural essentialist.

Since Mendeleev’s discovery in 1869, the periodic table has figured as the ultimate paper tool in chemical research. It has proved to be a vital research instrument in the arsenal of the chemical community. No chemistry textbook, lecture theatre or scientific laboratory is complete without a copy of the periodic table of the elements. This however, should not necessarily imply that the periodic table has never had to contend with problems. In this thesis, the history of the accommodation of the rare-earth elements in the periodic table will be addressed. When Mendeleev published his periodic table in 1869, the rare earths already constituted a major obstacle. Mendeleev was able to include only four members of the rare earths and he experienced great difficulties in positioning these elements. Question marks and wrong atomic weights reigned in the last rows of Mendeleev’s system. This problematic accommodation quickly grew into one of the most serious threats for the periodic law. For over fifty years, chemists continually struggled with the placement of these maddeningly similar elements. As a consequence, a lot of chemists started to question the validity of the periodic law, but others took it as a sign that the concept of a chemical element had to be reconsidered. As a result, this work intends to retrace the mutual influence of the philosophical ideas about the nature of chemical elements and the development of the periodic table from its inception in 1869 to the discovery of Moseley’s law in 1913 and Bohr’s publication of his landmark paper On the Constitution of Atoms and Molecules. The aim of this thesis is to show how, on the one hand, the periodic table (as a research instrument) helped in reformulating the contemporary ideas about chemical elements, and how it aided in developing a new research program in order to resolve the rare earth crisis. On the other hand, the question will be taken up to what extent Crookes’ evolutionary ideas about meta elements helped in saving the periodic table from a severe downfall by solving the gnawing problem of the rare-earth elements. In particular, this work will also focus on the investigations of the Czech chemist, Bohuslav Brauner. It will be shown how Brauner, under the influence of Crookes’ ideas, was led to his formulation of the Asteroid Hypothesis, according to which all the rare-earth elements should be placed in a single case of the periodic table.

This review paper provides a detailed overview and critical analysis of the philosophical literature on the Rietdijk–Putnam–Maxwell argument for the four-dimensionality of the world. After briefly introducing the debate on the dimensionality of the world, I present the arguments by Rietdijk, Putnam and Maxwell, and highlight the differences between them. I subsequently raise a total of eleven objections against the Rietdijk–Putnam–Maxwell argument, and conclude that its validity is underdetermined by the formalism of special relativity.

At the heart of chemistry lies the periodic system of chemical elements. Despite being the cornerstone of modern chemistry, the overall structure of the periodic system has never been fully understood from an atomic physics point of view. Group-theoretical models have been proposed instead, but they suffer from several limitations. Among others, the identification of the correct symmetry group and its decomposition into subgroups has remained a problem to this day. In an effort to deepen our limited understanding of the periodic law, we have extended the traditional Lie algebraic framework to account for the peculiar degeneracy structure of the periodic system. Starting from the four-dimensional hidden symmetry and accidental degeneracy of the hydrogen atom, as first revealed by Fock in 1935, our research has mainly focussed on the way this SO(4) symmetry of the Coulomb potential gets broken in the periodic system as a consequence of the transformation of the hydrogenic (n, l) filling order to the Madelung (n+l, n) order due to electronic repulsions, relativistic effects and spin-orbit couplings. In this PhD dissertation, a new left-step format of the periodic table is first proposed on the basis of the Madelung rule. Following the particle physics tradition, the chemical elements are then considered as various states of some 'atomic matter', which is described by a non-compact spectrum-generating dynamical Lie group. The chemical elements are shown to form a basis for a single infinite-dimensional degeneracy space of the SO(4,2) ⊗ SU(2) group. An explanation for the period doubling is then proposed in terms of a particular symmetry breaking of the SO(4,2) group to the anti de Sitter SO(3,2) group. The Madelung rule is rationalised on the basis of nonlinear Lie algebras which reflect the screening of the Coulomb hole. This opens new perspectives for a symmetry-based understanding of how the periodic law emerges from its quantum mechanical foundations, and holds the future promise of complementing our current phenomenological approach by a direct atomic physics approach.