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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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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Puiggalí, Jordi

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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (6/6 displayed)

  • 2024Ultrasonic Molding of Poly(3-hydroxybutyrate) and Its Clay Nanocomposites: Efficient Microspecimens Production with Minimal Material Loss and Degradationcitations
  • 2021Efficient One‐Pot Preparation of Thermoresponsive Polyurethanes with Lower Critical Solution Temperatures4citations
  • 2020Thermoresponsive Shape‐Memory Hydrogel Actuators Made by Phototriggered Click Chemistry55citations
  • 2018Hybrid polypeptide/polylactide copolymers with short phenylalanine blocks9citations
  • 2017Preparation of Nanocomposites of Poly(ε-caprolactone) and Multi-Walled Carbon Nanotubes by Ultrasound Micro-Molding. Influence of Nanotubes on Melting and Crystallization24citations
  • 2016Synthesis of poly(ester amide)s composed of lactic acid and glycolic acid units by the bulk polycondensation of metal halide saltscitations

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Valle, Luis J. Del
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Pérez, Germán
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Fontdecaba, Enric
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Jin, Anyi
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Enshaei, Hamidreza
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Bonardd, Sebastián
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Franco, Lourdes
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Alemán, Carlos
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Murase, Sara K.
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Mayans, Enric
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Casas, María Teresa
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Martínez, Juan Carlos
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Amestoy Muñoz, Hegoi
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Sarasua Oiz, José Ramón
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Olmo, Cristian
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Co-Authors (by relevance)

  • Valle, Luis J. Del
  • Pérez, Germán
  • Fontdecaba, Enric
  • Jin, Anyi
  • Enshaei, Hamidreza
  • Bonardd, Sebastián
  • Franco, Lourdes
  • Alemán, Carlos
  • Díaz Díaz, David
  • Maiti, Binoy
  • Nandi, Mridula
  • Abramov, Alex
  • Cativiela, Carlos
  • Pérez-Madrigal, Maria M.
  • Murase, Sara K.
  • Mayans, Enric
  • Casas, María Teresa
  • Martínez, Juan Carlos
  • Amestoy Muñoz, Hegoi
  • Sarasua Oiz, José Ramón
  • Olmo, Cristian
OrganizationsLocationPeople

article

Synthesis of poly(ester amide)s composed of lactic acid and glycolic acid units by the bulk polycondensation of metal halide salts

  • Puiggalí, Jordi
  • Murase, Sara K.
Abstract

<jats:title>ABSTRACT</jats:title><jats:p>Thermal polycondensation of the potassium salt of <jats:italic>N</jats:italic>‐methylchloroacetyl‐6‐aminohexanoic acid (LAHK) was found to be effective in the preparation of a new poly(ester amide) based on lactic acid units with a high yield and a moderate molecular weight. The reaction started in the solid state and proceeded through the formation of potassium chloride salt as the driving force. The use of a monomer having an amide linkage diminished the secondary reactions previously found in the synthesis of polylactide from 2‐halogenopropionates. The polymerization of potassium salt of <jats:italic>N</jats:italic>‐chloroacetyl‐6‐aminohexanoic acid (GAHK) took place in a similar temperature range as that of the 2‐chloropropionyl derivative; in this way, it was possible to conduct the copolymerization processes. The polymerization kinetics of LAHK and its mixture with GAHK was studied by Fourier transform infrared spectroscopy. The bulk polycondensation reaction was faster for GAHK than for LAHK, but the kinetic differences were not significant enough to prevent copolymerization at a temperature close to 160°C. Therefore, new degradable materials with tuned properties according to the glycolic acid/lactic acid content were obtained. <jats:sup>1</jats:sup>H‐NMR spectroscopy was useful for following the time evolution of the copolymerization process and for determining the final composition. Calorimetric data showed that all of the samples were thermally stable and that decreases in the melting temperature and enthalpy were observed at intermediate compositions. The existence of an eutectic point became proof that effective copolymerization was achieved in the thermal polycondensation process. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. <jats:bold>2016</jats:bold>, <jats:italic>133</jats:italic>, 43197.</jats:p>

Topics
  • Potassium
  • molecular weight
  • Nuclear Magnetic Resonance spectroscopy
  • ester
  • Fourier transform infrared spectroscopy
  • melting temperature