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The Oseberg Viking ship burial is one of the most extensive collections of Viking wooden artefacts ever excavated in Norway. In the early twentieth century, many of these artefacts were treated with alum in order to preserve them, inadvertently leading to their current degraded state. It is therefore crucial to develop new bioinspired polymers which could be used to conserve these artefacts and prevent further disintegration. Two hydroxylated polymers were synthesised (TPA6 and TPA7), using α-pinene- and oleic acid-derived monomers functionalised with an acrylate moiety. Characterisation using biomolecular hydrodynamics (analytical ultracentrifugation and high precision viscometry) has shown that these polymers have properties which would potentially make them good wood consolidants. Conformation analyses with the viscosity increment (ν) universal hydrodynamic parameter and ELLIPS1 software showed that both polymers had extended conformations, facilitating in situ networking when applied to wood. SEDFIT-MSTAR analyses of sedimentation equilibrium data indicates a weight average molar mass Mw of (3.9 ± 0.8) kDa and (4.2 ± 0.2) kDa for TPA6 and TPA7 respectively. Analyses with SEDFIT (sedimentation velocity) and MultiSig however revealed that TPA7 had a much greater homogeneity and a lower proportion of aggregation. These studies suggest that both these polymers—particularly TPA7—have characteristics suitable for wood consolidation, such as an optimal molar mass, conformation and a hydroxylated nature, making them interesting leads for further research. [ABSTRACT FROM AUTHOR]

The iron‐containing imidazolium‐based ionic liquids (ILs) 1‐n‐butyl‐3‐methylimidazolium heptachlorodiferrate (BMI.Fe2Cl7) and 1‐n‐butyl‐3‐methylimidazolium tetrachloroferrate (BMI.FeCl4) are applied as catalysts in the homogeneous polymerization of n‐butyl vinyl ether. Both solventless conditions as well as using different organic solvents, catalyst concentrations, temperatures, and reaction times are tested to assess the polymerization conditions that lead to the highest molecular weights of poly(n‐butyl vinyl ether). The Lewis acidic IL BMI.Fe2Cl7 proves to be highly efficient, even at low catalyst concentrations. In bulk polymerization, polymers with 142 kg mol−1 are obtained using a 1:10000 molar ratio of catalyst to monomer. In solution polymerization, the monomer consumption is also rapid and the molecular weight of the polymer is related to the catalyst concentration used. These results indicate the potential of this catalyst for industrial applications. In contrast with the acidic IL, the neutral iron‐containing imidazolium‐based IL BMI.FeCl4 does not show any catalytic activity. [ABSTRACT FROM AUTHOR]

The current work describes the synthesis of a new polyHIPE‐like sulfonated poly(styrene‐co‐n‐acylglycerol) and its use as an efficient heterogeneous catalyst to convert oleic acid into methyl oleate in esterification reactions. This new environmentally friendly polymer incorporates n‐acylglycerol macromonomer as a versatile strategy for glycerol valorization. Macroporous micrometric polymer particles are synthesized through suspension polymerization process without using porogenic agents. polyHIPE‐like copolymers formed with different feed compositions of styrene and n‐acylglycerol are chemically modified via sulfonation reactions to form a highly efficient catalyst for esterification of oleic acid to methyl oleate, exhibiting conversions lying in the interval from 52% to 96%, depending mainly on the amount of n‐acylglycerol macromonomer into the copolymer chains. The experimental results indicate the great potential of this new heterogeneous catalyst based on modified poly(styrene‐co‐n‐acylglycerol) to be successfully employed in esterification reactions of vegetable oils intended for the production of long chain alkyl esters of carboxylic acids, widely used as biofuels. [ABSTRACT FROM AUTHOR]

Gas phase copolymerizations of ethylene and an α‐olefin comonomer are performed using a commercial Ziegler–Natta catalyst in the presence of different induced condensing agents (ICA). The impact of these factors on the yield and final polyethylene properties such as the melt flow index, crystallinity, and incorporation of comonomer is studied. It has been shown that the increase in the rate of polymerization is even more pronounced in the presence of ICA. It also appears that adding ICA to the copolymerizations changes the comonomer incorporation with respect to similar copolymerizations performed without ICA due to competing cosolubility effects. [ABSTRACT FROM AUTHOR]

Graphical abstract A biobased monomer acrylated ricinoleic acid was synthesized from castor oil and copolymerized with methyl methacrylate in miniemulsion forming polymeric nanoparticles. The addition of the biobased monomer led to a decrease in the glass transition temperature of the copolymer and to the formation of a small fraction of gel, resulting in materials with interesting properties for future applications. Highlights • A biobased monomer acrylated ricinoleic acid was synthesized from castor oil. • The biobased monomer was copolymerized with methyl methacrylate in miniemulsion forming polymeric nanoparticles. • Polymers with lower Tgs were obtained with the addition of the biobased monomer. • The copolymers exhibited interesting properties for future applications as adhesives. Abstract Vegetable oils-based polymers are promising materials with application in the industry of coatings and adhesives. Chemically-modified ricinoleic acid obtained from castor oil was used in this study to produce polymeric materials. The adopted strategy consisted in the epoxidation of the double bonds of ricinoleic acid, followed by the ring opening reaction in the presence of acrylic acid to form the acrylated ricinoleic acid (ARA). Free radical copolymerizations of ARA and methyl methacrylate (MMA) were carried out in miniemulsion, resulting in latexes stable over a long storage time. DLS measurements revealed the formation of submicron polymeric particles of different sizes strongly dependent on the fraction of the biobased monomer ARA, exhibiting diameters ranging from approximately 80 nm to 150 nm, as the ARA fraction was increased up to 80 wt%. It was possible to prepare polymers with broad ranges of mass-average molar masses in the range from 1137 kDa to 65 kDa and glass transition temperatures lying in the interval from approximately 124 °C–50 °C by varying the concentration of the comonomer ARA. Crosslinked copolymers were obtained by increasing the proportion of ARA. [ABSTRACT FROM AUTHOR]