i-propylammonium lead chloride based perovskite photocatalysts for depolymerization of lignin under UV light

Lignin depolymerization for the purpose of synthesizing aromatic molecules is a growing focus of research to find alternative energy sources. In current studies, the photocatalytic depolymerization of lignin has been investigated by two new iso-propylamine-based lead chloride perovskite nanomaterial...

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Published in:Molecules
Main Author: Kausar S.; Altaf A.A.; Hamayun M.; Rasool N.; Hadait M.; Akhtar A.; Muhammad S.; Badshah A.; Shah S.A.A.; Zakaria Z.A.
Format: Article
Language:English
Published: MDPI AG 2020
Online Access:https://www.scopus.com/inward/record.uri?eid=2-s2.0-85089131022&doi=10.3390%2fmolecules25153520&partnerID=40&md5=24769a27d6919fb5ee3bb02dc1353a72
id 2-s2.0-85089131022
spelling 2-s2.0-85089131022
Kausar S.; Altaf A.A.; Hamayun M.; Rasool N.; Hadait M.; Akhtar A.; Muhammad S.; Badshah A.; Shah S.A.A.; Zakaria Z.A.
i-propylammonium lead chloride based perovskite photocatalysts for depolymerization of lignin under UV light
2020
Molecules
25
15
10.3390/molecules25153520
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85089131022&doi=10.3390%2fmolecules25153520&partnerID=40&md5=24769a27d6919fb5ee3bb02dc1353a72
Lignin depolymerization for the purpose of synthesizing aromatic molecules is a growing focus of research to find alternative energy sources. In current studies, the photocatalytic depolymerization of lignin has been investigated by two new iso-propylamine-based lead chloride perovskite nanomaterials (SK9 and SK10), synthesized by the facile hydrothermal method. Characterization was done by Powder X-Ray Diffraction (PXRD), Scanning Electron Microscopy (SEM), UV-Visible (UV-Vis), Photoluminescence (PL), and Fourier-Transform Infrared (FTIR) Spectroscopy and was used for the photocatalytic depolymerization of lignin under UV light. Lignin depolymerization was monitored by taking absorption spectra and catalytic paths studied by applying kinetic models. The %depolymerization was calculated for factors such as catalyst dose variation, initial concentration of lignin, and varying temperatures. Pseudo-second order was the best suited kinetic model, exhibiting a mechanism for lignin depolymerization that was chemically rate controlled. The activation energy (Ea) for the depolymerization reaction was found to be 15 kJ/mol, which is remarkably less than conventional depolymerization of the lignin, i.e., 59.75 kJ/mol, exhibiting significant catalytic efficiencies of synthesized perovskites. Products of lignin depolymerization obtained after photocatalytic activity at room temperature (20 ◦C) and at 90 ◦C were characterized by GC-MS analysis, indicating an increase in catalytic lignin depolymerization structural subunits into small monomeric functionalities at higher temperatures. Specifically, 2-methoxy-4-methylphenol (39%), benzene (17%), phenol (10%) and catechol (7%) were detected by GC-MS analysis of lignin depolymerization products. © 2020 by the authors. Licensee MDPI, Basel, Switzerland.
MDPI AG
14203049
English
Article
All Open Access; Gold Open Access
author Kausar S.; Altaf A.A.; Hamayun M.; Rasool N.; Hadait M.; Akhtar A.; Muhammad S.; Badshah A.; Shah S.A.A.; Zakaria Z.A.
spellingShingle Kausar S.; Altaf A.A.; Hamayun M.; Rasool N.; Hadait M.; Akhtar A.; Muhammad S.; Badshah A.; Shah S.A.A.; Zakaria Z.A.
i-propylammonium lead chloride based perovskite photocatalysts for depolymerization of lignin under UV light
author_facet Kausar S.; Altaf A.A.; Hamayun M.; Rasool N.; Hadait M.; Akhtar A.; Muhammad S.; Badshah A.; Shah S.A.A.; Zakaria Z.A.
author_sort Kausar S.; Altaf A.A.; Hamayun M.; Rasool N.; Hadait M.; Akhtar A.; Muhammad S.; Badshah A.; Shah S.A.A.; Zakaria Z.A.
title i-propylammonium lead chloride based perovskite photocatalysts for depolymerization of lignin under UV light
title_short i-propylammonium lead chloride based perovskite photocatalysts for depolymerization of lignin under UV light
title_full i-propylammonium lead chloride based perovskite photocatalysts for depolymerization of lignin under UV light
title_fullStr i-propylammonium lead chloride based perovskite photocatalysts for depolymerization of lignin under UV light
title_full_unstemmed i-propylammonium lead chloride based perovskite photocatalysts for depolymerization of lignin under UV light
title_sort i-propylammonium lead chloride based perovskite photocatalysts for depolymerization of lignin under UV light
publishDate 2020
container_title Molecules
container_volume 25
container_issue 15
doi_str_mv 10.3390/molecules25153520
url https://www.scopus.com/inward/record.uri?eid=2-s2.0-85089131022&doi=10.3390%2fmolecules25153520&partnerID=40&md5=24769a27d6919fb5ee3bb02dc1353a72
description Lignin depolymerization for the purpose of synthesizing aromatic molecules is a growing focus of research to find alternative energy sources. In current studies, the photocatalytic depolymerization of lignin has been investigated by two new iso-propylamine-based lead chloride perovskite nanomaterials (SK9 and SK10), synthesized by the facile hydrothermal method. Characterization was done by Powder X-Ray Diffraction (PXRD), Scanning Electron Microscopy (SEM), UV-Visible (UV-Vis), Photoluminescence (PL), and Fourier-Transform Infrared (FTIR) Spectroscopy and was used for the photocatalytic depolymerization of lignin under UV light. Lignin depolymerization was monitored by taking absorption spectra and catalytic paths studied by applying kinetic models. The %depolymerization was calculated for factors such as catalyst dose variation, initial concentration of lignin, and varying temperatures. Pseudo-second order was the best suited kinetic model, exhibiting a mechanism for lignin depolymerization that was chemically rate controlled. The activation energy (Ea) for the depolymerization reaction was found to be 15 kJ/mol, which is remarkably less than conventional depolymerization of the lignin, i.e., 59.75 kJ/mol, exhibiting significant catalytic efficiencies of synthesized perovskites. Products of lignin depolymerization obtained after photocatalytic activity at room temperature (20 ◦C) and at 90 ◦C were characterized by GC-MS analysis, indicating an increase in catalytic lignin depolymerization structural subunits into small monomeric functionalities at higher temperatures. Specifically, 2-methoxy-4-methylphenol (39%), benzene (17%), phenol (10%) and catechol (7%) were detected by GC-MS analysis of lignin depolymerization products. © 2020 by the authors. Licensee MDPI, Basel, Switzerland.
publisher MDPI AG
issn 14203049
language English
format Article
accesstype All Open Access; Gold Open Access
record_format scopus
collection Scopus
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