Olivier Boyron

Industrial kraft black liquor from maritime pine was oxidised in aqueous, alkaline medium, under air, at 150 °C, with or without a CuO/TiO 2 catalyst.

The relationship between the structure and the final properties of materials is an important issue in polymer science. In particular, the properties of polyolefins are impacted by their branching contents. A simple rheological method is presented to estimate the degree of short chain branching (SCB) in linear low‐density polyethylene (LLDPE). A range of ethylene‐1‐hexene copolymers is synthetized using a metallocene catalyst to obtain homogenous LLDPE models with various comonomer contents. The polymers are analyzed by size exclusion chromatography, 13 C NMR, and crystallization elution fractionation to determine both their molar masses and their chemical composition distributions. Subsequently, they are measured by rheology to assess the impact of SCB. This work provides calibration curves for rheology and proves that it is possible to predict the SCB content in LLDPE from the melt viscosity analysis.

para -Azaquinodimethane ( p -AQM) based quinoidal–donor (Q–D) polymers have been synthesized following a strategy for enhancing the backbone planarity and control the bond length alternation (BLA).

Over the past decade, halogenated semiconducting polymers have attracted considerable interest due to their outstanding optoelectronic properties. Thus, in most of today's organic photovoltaic devices benchmark organic semiconductors are halogenated materials, either electron donor polymers or non‐fullerene acceptor (NFA) small molecules. However, the nature and position of the substituted halogen atoms in halogenated semiconducting polymers impact, through self‐assembly modification, their optoelectronic properties in a way that is difficult to predict. Yet, the solid‐state self‐assembling of these materials has been shown to be a key parameter toward high charge transport properties and photovoltaic efficiencies. In this context, there is still a need to develop analytical methods that will enable an atomic‐scale structural characterization of these materials as a function of the halogenation. In this study, the solid‐state nuclear magnetic resonance (NMR) under magic angle spinning (MAS) is explored as a tool to investigate the local structure and supramolecular organization of a series of conjugated polymers, specially designed for this study. Through a comprehensive study using complementary techniques, including MAS–NMR, small and wide‐angle X‐ray scattering, and molecular modeling investigations, the molecular conformation of these polymers in relation to their chemical composition, is successfully determined.