Materials Map

Discover the materials research landscape. Find experts, partners, networks.

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The Materials Map is an open tool for improving networking and interdisciplinary exchange within materials research. It enables cross-database search for cooperation and network partners and discovering of the research landscape.

The dashboard provides detailed information about the selected scientist, e.g. publications. The dashboard can be filtered and shows the relationship to co-authors in different diagrams. In addition, a link is provided to find contact information.

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Materials Map under construction

The Materials Map is still under development. In its current state, it is only based on one single data source and, thus, incomplete and contains duplicates. We are working on incorporating new open data sources like ORCID to improve the quality and the timeliness of our data. We will update Materials Map as soon as possible and kindly ask for your patience.

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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (5/5 displayed)

  • 2021Multifunctional lignin-based nanocomposites and nanohybrids185citations
  • 2021Toward waste valorization by converting bioethanol production residues into nanoparticles and nanocomposite films28citations
  • 2020Three-Dimensional Printed Cell Culture Model Based on Spherical Colloidal Lignin Particles and Cellulose Nanofibril-Alginate Hydrogel106citations
  • 2019Strong, Ductile, and Waterproof Cellulose Nanofibril Composite Films with Colloidal Lignin Particles263citations
  • 2018Elucidating enzymatic polymerisations50citations

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Balakshin, Mikhail
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Greca, Luiz G.
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Tardy, Blaise L.
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Puglia, Debora
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Lizundia, Erlantz
1 / 22 shared
Rojas, Orlando J.
1 / 51 shared
Farooq, Muhammad
3 / 12 shared
Koivula, Hanna
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Pandard, Pacal
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Pion, Florian
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Liao, Xun
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Jayabalan, Thangavelu
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Österberg, Monika
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Rivière, Guillaume
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Marlair, Guy
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Baumberger, Stephanie
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Ajdary, Rubina
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Linder, Markus B.
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Jonkergouw, Christopher
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Ora, Ari
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Huan, Siqi
1 / 3 shared
Morits, Maria
1 / 6 shared
Zhang, Xue
1 / 6 shared
Valle-Delgado, Juan José
1 / 8 shared
Zou, Tao
1 / 3 shared
Farmer, Thomas James
1 / 12 shared
Clark, James Hanley
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Maneffa, Andrew J.
1 / 2 shared
Comerford, James William
1 / 7 shared
Pellis, Alessandro
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2020
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Co-Authors (by relevance)

  • Balakshin, Mikhail
  • Greca, Luiz G.
  • Tardy, Blaise L.
  • Puglia, Debora
  • Lizundia, Erlantz
  • Rojas, Orlando J.
  • Farooq, Muhammad
  • Koivula, Hanna
  • Pandard, Pacal
  • Pion, Florian
  • Liao, Xun
  • Jayabalan, Thangavelu
  • Österberg, Monika
  • Rivière, Guillaume
  • Marlair, Guy
  • Baumberger, Stephanie
  • Ajdary, Rubina
  • Linder, Markus B.
  • Jonkergouw, Christopher
  • Ora, Ari
  • Huan, Siqi
  • Morits, Maria
  • Zhang, Xue
  • Valle-Delgado, Juan José
  • Zou, Tao
  • Farmer, Thomas James
  • Clark, James Hanley
  • Maneffa, Andrew J.
  • Comerford, James William
  • Pellis, Alessandro
OrganizationsLocationPeople

article

Elucidating enzymatic polymerisations

  • Farmer, Thomas James
  • Clark, James Hanley
  • Sipponen, Mika H.
  • Maneffa, Andrew J.
  • Comerford, James William
  • Pellis, Alessandro
Abstract

<p>The sustainable synthesis of polymers is a field with growing interest due to the need of modern society to preserve the environment whilst making used products and food sustainable for the future generations. In this work we investigate the possibility of synthesizing aliphatic polyesters derived from various dicarboxylic acid diesters and diols in a solvent-free reaction system. Candida antarctica lipase B was selected as biocatalyst and its selectivity towards the carbon and ester chain length were elucidated. The selected enzyme was able to synthesize various polyesters combining C<sub>4</sub>-C<sub>10</sub> diesters and C<sub>4</sub>-C<sub>8</sub> diols. All combinations led to monomer conversions above 90% in 24 h with the best number average molecular weights (M<sub>n</sub>) being obtained through the combination of dimethyl adipate and 1,8-octanediol leading to a M<sub>n</sub> of 7141 Da. Differential scanning calorimetry analysis shows a clear trend with an increase in melting temperature of the polymers that correlates with both the increase of the M<sub>n</sub> or of the polymer's constitutional repeat unit carbon chain length. Thermogravimetric analysis and rheology measurements performed on selected samples also confirm the trend showing a variation of the polymer's degradation temperatures and viscosity profiles.</p>

Topics
  • impedance spectroscopy
  • polymer
  • Carbon
  • viscosity
  • thermogravimetry
  • differential scanning calorimetry
  • molecular weight
  • ester
  • melting temperature
  • degradation temperature