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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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (3/3 displayed)

  • 2024Virus adsorbent systems based on Amazon holocellulose and nanomaterials.citations
  • 2023Extraction and Modification of Cellulose Microfibers Derived from Biomass of the Amazon Ochroma pyramidale Fruit3citations
  • 2022Head-to-Tail and Head-to-Head Molecular Chains of Poly(p-Anisidine): Combined Experimental and Theoretical Evaluation2citations

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Inada, Natalia
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Lalwani, Pritesh Or Jaychand Pritesh, Lalwani
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Macalia, Celio Matias Airone
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Sanches, Edgar
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Ţălu, Ştefan
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Soares, Juliana
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Bezerra, Jaqueline De Araújo
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Coatrini Soares, Andrey
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Martins, Xaiane
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Souza, Sérgio Michielon De
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De Andrade Feitosa, Bianca
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Silva, Kalil Araújo Da
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Nunes, Ronald Zico De Aguiar
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Rocha, Ana Luisa Farias
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Macalia, Célio Matias Airone
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Co-Authors (by relevance)

  • Inada, Natalia
  • Lalwani, Pritesh Or Jaychand Pritesh, Lalwani
  • Macalia, Celio Matias Airone
  • Sanches, Edgar
  • Ţălu, Ştefan
  • Soares, Juliana
  • Bezerra, Jaqueline De Araújo
  • Pinto, Camila
  • Arc, Barbosa
  • Coatrini Soares, Andrey
  • Martins, Xaiane
  • Souza, Sérgio Michielon De
  • De Andrade Feitosa, Bianca
  • Silva, Kalil Araújo Da
  • Nunes, Ronald Zico De Aguiar
  • Dias, Cleverton Oliveira
  • Rocha, Ana Luisa Farias
  • Macalia, Célio Matias Airone
  • Feitosa, Bianca De Andrade
OrganizationsLocationPeople

article

Extraction and Modification of Cellulose Microfibers Derived from Biomass of the Amazon Ochroma pyramidale Fruit

  • Souza, Sérgio Michielon De
  • De Andrade Feitosa, Bianca
  • Silva, Kalil Araújo Da
  • Nunes, Ronald Zico De Aguiar
  • Sanches, Edgar
  • Dias, Cleverton Oliveira
  • Carolino, Adriano De Souza
  • Rocha, Ana Luisa Farias
  • Bezerra, Jaqueline De Araújo
  • Macalia, Célio Matias Airone
  • Feitosa, Bianca De Andrade
Abstract

<jats:p>Microfibers are important to several areas of human lifestyle, and the knowledge about their physicochemical characteristics allows for proposing new technological applications. The in natura microfiber of Ochroma pyramidale fruit (IN sample) and its extracted pulp (PU sample) were evaluated by X-ray Diffraction (XRD), Scanning Electron Microscopy (SEM), Fourier Transform Infrared Spectroscopy (FTIR) and Thermogravimetry and Differential Scanning Calorimetry (TG/dTG and DSC). Microfibers were composed mainly of (68 ± 1)% holocellulose, (35.8 ± 0.1)% cellulose, (32 ± 3)% lignin and (3.7 ± 0.3)% extractives. The XRD pattern of the PU sample revealed that the mercerization process resulted in the change of the cellulose crystal structure from Iα type (triclinic) to type II (monoclinic). The SEM technique showed that the IN sample presented regular cylindrical/hollow-shaped wire-like microfibers with diameters ranging from 5 µm to 25 µm. However, the mercerization process changed their natural morphology. A significant change in the FTIR spectra after the removal of hemicellulose and lignin components was observed: weak bands at 1739 cm−1 (C=O stretching of lignin and hemicellulose fractions), 1463 cm−1 (CH3 of lignin) and 1246 cm−1 (C-O of lignin) were still observed in the PU sample, indicating that the lignin was not completely removed due to the natural difficulty of isolating pure cellulose. The TG/dTG and DSC evaluation revealed a temperature increase of the second thermal event (starting at 235 °C) in the PU sample, which was assigned to the cellulose and residual hemicellulose degradation. Then, this work aimed to disseminate and characterize a microfiber with unusual characteristics still little explored by the scientific community, as well as its cellulosic pulp, providing information that may be useful in its application in different industries, enabling the positive development of new biocompatible, renewable and sustainable materials.</jats:p>

Topics
  • scanning electron microscopy
  • x-ray diffraction
  • extraction
  • thermogravimetry
  • lignin
  • differential scanning calorimetry
  • cellulose
  • wire
  • Fourier transform infrared spectroscopy