Browsing by Author "Matos, Ana"
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- A bridge between liquid-liquid extraction and the use of bacterial communities for palladium and platinum recovery as nanosized metal sulphidesPublication . Assunção, Ana; Matos, Ana; Costa, Ana M. Rosa da; Candeias, Antonio; Costa, Maria ClaraThe Platinum Group Metals (PGM) are rare in the Earth's crust and in the past years their use had a considerable expansion limiting their availability, which justifies PGM's high commercial value and demand. Therefore, PGM recovery from secondary sources is very important from both economic and environmental points of view. In recent years, several methods for PGM removal have been investigated. Our research group has been studying the removal/recovery of PGM using both chemical (liquid liquid extraction) and biological methods (using anaerobic bacterial communities).The aim of this study was to combine these two chemical and biological approach technologies, for PGM recovery. For that purpose, Pd(II) and Pt(IV) present in aqueous phases, were extracted to organic phases composed by N,N'-dimethyl-N,N'-dicyclohexylsuccinamide (DMDCHSA) and N,N'-dimethyl-N,N'-dicyclohexyltetradecylmalonamide (DMDCHTDMA) in 1,2-dichloroethane, respectively, with an extraction efficiency of 79% for Pd(II) and 99% for Pt(IV). The metals in the loaded organic phases were then stripped with seawater, a low-cost solution largely available in nature, with efficiencies of 100% for Pd and 86% for Pt. Finally, the metals were precipitated and recovered using metabolic products produced by a community enriched for sulphate-reducing bacteria. The palladium precipitated completely, while 86% of platinum was precipitated. During the precipitation process sulphide concentration in the solution decreased and the analysis of the precipitates was consistent with the formation of nanosized PdS and PtS2.To our knowledge, this research shows, for the first time, the potential of combining liquid liquid extraction with the use of bacteria aiming platinum and palladium recovery, as metal sulphides, from aqueous media. (C) 2016 Elsevier B.V. All rights reserved.
- Dataset of the complete mitogenome of the deep-sea sailfin roughshark, Oxynotus paradoxus Frade, 1929Publication . Matos, Ana; Gomes-dos-Santos, André; Graça Aranha, Sofia; Dias, Ester; Veríssimo, Ana; Teodosio, Maria; Figueiredo, Ivone; Castro, L. Filipe C．; Froufe, ElsaChondrichthyans comprise a diverse group of vertebrate species with extraordinary ecological relevance. Yet, multiple members of this evolutionary lineage are associated with sig-nificant extinction risk. The sailfin roughshark Oxynotus para-doxus is a deep-water benthic shark currently listed as vul-nerable due to population declines in parts of its range. Here we provide the first complete mitochondrial genome of O. paradoxus, comprising also the first record for the genus and family Oxynotidae. These data can facilitate future monitor-ing of the genetic diversity in this and related species. Ge-nomic DNA was extracted from O. paradoxus collected in the eastern North Atlantic off western Portugal (37.59 degrees N, 9.51 degrees W) and sent for Illumina Paired-End (2 x 150 bp) library con-struction and whole genome sequencing on a Novaseq60 0 0 platform. Trimmomatic (version 0.38) was used to remove adapters and MitoZ (version 3.4) to assemble and anno-tate the mitogenome. This mitogenome with 17 100 bp has a total of 38 genes, 13 of which are protein-coding genes, 23 transfer RNA genes, and 2 ribosomal RNA genes. Eight transfer RNAs and 1 protein-coding gene (NADH de-hydrogenase subunit 6, NAD6) are in the complementary strand. In the provided phylogenetic inference, with all avail-able and verified Squalomorphii mitogenomes, the four or-ders are well separated, and as expected, O. paradoxus is placed in the Squaliformes order. This data reinforces the need for more genomic resources for the Oxynotidae family.(c) 2023 The Author(s). Published by Elsevier Inc. This is an open access article under the CC BY-NC-ND license ( http://creativecommons.org/licenses/by-nc-nd/4.0/ )