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      Raman analysis of inverse vulcanised polymers

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          Abstract

          Raman analysis has been found to provide otherwise hard to obtain information on inverse vulcanised polymers, including their homogeneity, sulfur rank, and unpolymerised sulfur content.

          Abstract

          Inverse vulcanised polymers have received significant research attention on account of their easy, modifiable, and low-cost synthesis. These polymers are synthesized from the industrial by-product, elemental sulfur, resulting in a high sulfur content, which has many influences on the polymers’ behavior, and gives them their wide variety of valuable properties. Because of this, inverse vulcanised polymers have many industrially attractive applications, however the high sulfur content that is directly responsible for this, also makes the polymers challenging to analyse. As such, the structure of inverse vulcanised polymers is poorly understood, and although sensible theories exist, there is a lack of direct evidence derived from a complete understanding of the polymers’ bonding level structure. Presented here is the use of Raman spectroscopy to scrutinise better the nature of inverse vulcanised polymers. Several Raman spectroscopic techniques have been compared and contrasted, revealing what information can be obtained from Raman spectroscopy in regard to these otherwise difficult to analyse polymers. Method optimisations are presented alongside computational studies and model compounds, all of which benefit the understanding of spectral information obtained from Raman spectroscopy. It was found that Raman spectroscopy is capable of providing several key pieces of information about inverse vulcanised polymers in a rapid and non-destructive way. These include, calculating the amorphous elemental sulfur content, assessing the homogeneity, tracking reactions in progress, and most crucially, identifying the proportions of different sulfur ranks of the polymer, which has thus far eluded all other analytical techniques.

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          Most cited references36

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          Effect of the damping function in dispersion corrected density functional theory.

          It is shown by an extensive benchmark on molecular energy data that the mathematical form of the damping function in DFT-D methods has only a minor impact on the quality of the results. For 12 different functionals, a standard "zero-damping" formula and rational damping to finite values for small interatomic distances according to Becke and Johnson (BJ-damping) has been tested. The same (DFT-D3) scheme for the computation of the dispersion coefficients is used. The BJ-damping requires one fit parameter more for each functional (three instead of two) but has the advantage of avoiding repulsive interatomic forces at shorter distances. With BJ-damping better results for nonbonded distances and more clear effects of intramolecular dispersion in four representative molecular structures are found. For the noncovalently-bonded structures in the S22 set, both schemes lead to very similar intermolecular distances. For noncovalent interaction energies BJ-damping performs slightly better but both variants can be recommended in general. The exception to this is Hartree-Fock that can be recommended only in the BJ-variant and which is then close to the accuracy of corrected GGAs for non-covalent interactions. According to the thermodynamic benchmarks BJ-damping is more accurate especially for medium-range electron correlation problems and only small and practically insignificant double-counting effects are observed. It seems to provide a physically correct short-range behavior of correlation/dispersion even with unmodified standard functionals. In any case, the differences between the two methods are much smaller than the overall dispersion effect and often also smaller than the influence of the underlying density functional. Copyright © 2011 Wiley Periodicals, Inc.
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            The use of elemental sulfur as an alternative feedstock for polymeric materials.

            An excess of elemental sulfur is generated annually from hydrodesulfurization in petroleum refining processes; however, it has a limited number of uses, of which one example is the production of sulfuric acid. Despite this excess, the development of synthetic and processing methods to convert elemental sulfur into useful chemical substances has not been investigated widely. Here we report a facile method (termed 'inverse vulcanization') to prepare chemically stable and processable polymeric materials through the direct copolymerization of elemental sulfur with vinylic monomers. This methodology enabled the modification of sulfur into processable copolymer forms with tunable thermomechanical properties, which leads to well-defined sulfur-rich micropatterned films created by imprint lithography. We also demonstrate that these copolymers exhibit comparable electrochemical properties to elemental sulfur and could serve as the active material in Li-S batteries, exhibiting high specific capacity (823 mA h g(-1) at 100 cycles) and enhanced capacity retention.
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              Inverse Vulcanization of Elemental Sulfur to Prepare Polymeric Electrode Materials for Li–S Batteries

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                Author and article information

                Contributors
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                Journal
                PCOHC2
                Polymer Chemistry
                Polym. Chem.
                Royal Society of Chemistry (RSC)
                1759-9954
                1759-9962
                March 21 2023
                2023
                : 14
                : 12
                : 1369-1386
                Affiliations
                [1 ]University of Liverpool, School of Physical Sciences, Department of Chemistry, Crown Street, Liverpool, L697ZD, Merseyside, UK
                [2 ]University of Liverpool, Centre for Metabolomics Research, Department of Biochemistry and Systems Biology, Institute of Systems, Molecular and Integrative Biology, Crown Street, Liverpool, L697BE, Merseyside, UK
                [3 ]University of Liverpool, Stephenson Institute for Renewable Energy, Chadwick Building, Peach Street, Liverpool, L697ZF, Merseyside, UK
                [4 ]University College London, Department of Chemistry, Gower Street, London, WC1E6BT, UK
                [5 ]University of Bristol, HH Wills Physics Laboratory, Tyndall Avenue, Bristol, BS81TL, UK
                Article
                10.1039/D2PY01408D
                c2b2a1eb-7420-4141-a994-c108fbcb2b1e
                © 2023

                http://creativecommons.org/licenses/by/3.0/

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