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Plant oils: The perfect renewable resource for polymer science?!

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TLDR
In this paper, the authors provide an overview of the present situation with special attention to the use of olefin metathesis and thiol-ene chemistry as synthetic methods and as polymerization techniques.
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This article is published in European Polymer Journal.The article was published on 2011-05-01 and is currently open access. It has received 551 citations till now.

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Rigid polyurethane foams obtained from tall oil and filled with natural fibers: Application as a support for immobilization of lignin-degrading microorganisms

TL;DR: In this article, the first topic of the research activity is forest biomass as an abundant, renewable, non-food competition, and low-cost resource that can play an alternative role to petro-resources.

Effect of the Addition of Tall Oil-Based Polyols on the Thermal and Mechanical Properties of Ureaurethane Elastomers

Abstract: As part of this work, the test results for ureaurethane elastomers (PUURs) manufactured with the use of tall oil (TO)-based polyols with a rosin acid content ranging from 2 to 20% are presented. The goal of this study was to verify the thermal and mechanical properties of bio-based PUURs. The physicomechanical properties of PUURs were tested along with the strength (static tensile test) and thermal properties: thermogravimetry (TGA), differential scanning calorimetry (DSC) and dynamic mechanical thermal analysis (DMTA). A structural analysis of the materials was also carried out via Fourier transform infrared (FTIR) spectroscopy. The replacement of the chain extender with tall oil-based polyols resulted in materials with different properties, different chemical constitutions and different thermal decomposition patterns. PUURs with TO polyols had a higher thermal resistance, and this resistance increased for higher isocyanate numbers (INCO). The thermal decomposition of the tested PUURs with TO polyols increased with the increase in the rosin acid content. The mechanical properties of the PUURs show that changing the chain extender with the TO polyols causes an increase in the storage modulus.
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Enhanced interfacial and mechanical performance of styrene-butadiene rubber/silica composites compatibilized by soybean oil derived silanized plasticization

TL;DR: In this paper, the effect of additive bioplasticizers on the performance of styrene-butadiene rubber (SBR)/silica composites for green tire manufacturing was investigated.
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NMR analysis of roasted coffee lipids and development of a spent ground coffee application for the production of bioplastic precursors

TL;DR: Multinuclear and multidimensional NMR spectroscopy was applied as a robust and rapid tool for the analysis of several classes of non-polar compounds in roasted coffee beans, coffee beverage and spent coffee grounds.
References
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Journal ArticleDOI

Thiol–Ene Click Chemistry

TL;DR: The radical-mediated thiol-ene reaction has all the desirable features of a click reaction, being highly efficient, simple to execute with no side products and proceeding rapidly to high yield.
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Recent developments in the chemistry of halogen-free flame retardant polymers

TL;DR: An overview of recent developments of the chemistry of halogen-free flame retardant polymers is presented in this article, along with their thermal stabilities and flame-retardant properties.
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Thiol-ene “click” reactions and recent applications in polymer and materials synthesis

TL;DR: In this paper, a review highlights examples of recent applications of both the radical-mediated and base/nucleophile-initiated thiol-ene reactions in polymer and materials synthesis.
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Plant oil renewable resources as green alternatives in polymer science

TL;DR: The synthesis of monomers as well as polymers from plant fats and oils has already found some industrial application and recent developments in this field offer promising new opportunities, as is shown within this contribution.
Journal ArticleDOI

Click Chemistry beyond Metal-Catalyzed Cycloaddition

TL;DR: This Minireview discusses the success and applicability of new, in particular metal-free, click reactions, which expand the opportunities for synthesizing small organic compounds as well as tailor-made macromolecules and bioconjugates.
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