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dc.contributor.CRUESPUNIVERSIDADE ESTADUAL DE CAMPINASpt_BR
dc.contributor.authorunicampMelo Junior, Mauricio Alves de-
dc.contributor.authorunicampPires, Cleo Thomas Gabriel Vilela Menegaz Teixeira-
dc.contributor.authorunicampAiroldi, Claudio-
dc.typeArtigopt_BR
dc.titleThe influence of the leaving iodine atom on phyllosilicate syntheses and useful application in toxic metal removal with favorable energetic effectspt_BR
dc.contributor.authorMelo Jr., Maurício A.-
dc.contributor.authorPiresa, Cleo T. G. V. M. T.-
dc.contributor.authorAiroldi, Claudio-
dc.subjectFilossilicatopt_BR
dc.subject.otherlanguagePhyllosilicatept_BR
dc.description.abstractNovel nanostructured 2 : 1 hybrid cobalt and nickel phyllosilicates containing attached diethyl iminodiacetate moieties within the interlamellar spaces were synthesized using a mild non-hydrothermal sol–gel methodology. The organofunctionalization of these hybrids was achieved using silylating agents formed by the reaction of 3-chloropropyltriethoxysilane or 3-iodopropyltrietoxysilane with diethyl iminodiacetate, whereas 3-iodopropyltriethoxysilane was synthesized from the reaction of 3-chloropropyltriethoxysilane with NaI. The degrees of functionalization of the new materials are associated with the nucleophilic displacement of the halide atom by the nitrogen basic center of diethyl iminodiacetate during the silylating agents' syntheses. The incorporation of an iodine atom favored the introduction of bulky basic moieties in the pendant chain. For example, the degree of functionalization for the nickel phyllosilicate functionalized from 3-iodopropyltriethoxysilane, (1.83 ± 0.01) mmol g−1, was higher than that of the nickel phyllosilicate functionalized from 3-chloropropyltriethoxysilane, (0.59 ± 0.02) mmol g−1. Infrared spectroscopy combined with 13C and 29Si NMR spectroscopy confirmed the attachment of organic moieties covalently bonded to the silicon sheet network, and the lamellar 2 : 1 trioctahedral phyllosilicate structures were confirmed by XRD. Further characterization was provided by thermogravimetry, SEM and TEM, which exhibited thermally stable hybrids presenting well-formed particles with a homogeneous distribution of cobalt, nickel, and nitrogen. The attached basic centers have the ability to sorb lead and cadmium from aqueous solution. The sorption data fit the Langmuir model and indicated maximum lead sorption values of (2.11 ± 0.16) mmol g−1 for the cobalt phyllosilicate functionalized from 3-iodopropyltriethoxysilane and (1.99 ± 0.11) mmol g−1 for the hybrid prepared from 3-chloropropyltriethoxysilane, for example, reflecting the higher degree of functionalization of the former. All of the other hybrids exhibited the same tendency, even for cadmium sorption. The thermodynamic data obtained from calorimetric titration revealed the spontaneity of these chelating interactive processes, which are enthalpically and entropically favorable for the proposed cation-basic center interactions at the solid–liquid interfacept_BR
dc.relation.ispartofRSC advancespt_BR
dc.relation.ispartofabbreviationRSC adv.pt_BR
dc.publisher.cityCambridge, MApt_BR
dc.publisher.countryEstados Unidospt_BR
dc.publisherRoyal Society of Chemistrypt_BR
dc.date.issued2014-
dc.language.isoengpt_BR
dc.description.volume4pt_BR
dc.description.issuenumber77pt_BR
dc.description.firstpage41028pt_BR
dc.description.lastpage41038pt_BR
dc.rightsFechadopt_BR
dc.sourceSCOPUSpt_BR
dc.identifier.eissn2046-2069pt_BR
dc.identifier.doi10.1039/c4ra06615dpt_BR
dc.identifier.urlhttps://pubs.rsc.org/en/content/articlelanding/2014/RA/C4RA06615Dpt_BR
dc.date.available2020-11-13T19:04:37Z-
dc.date.accessioned2020-11-13T19:04:37Z-
dc.description.provenanceSubmitted by Sanches Olivia (olivias@unicamp.br) on 2020-11-13T19:04:37Z No. of bitstreams: 0. Added 1 bitstream(s) on 2021-02-11T21:14:09Z : No. of bitstreams: 1 2-s2.0-84907143935.pdf: 895140 bytes, checksum: 683974ea79d889d67cd79c185b118e45 (MD5)en
dc.description.provenanceMade available in DSpace on 2020-11-13T19:04:37Z (GMT). No. of bitstreams: 0 Previous issue date: 2014en
dc.identifier.urihttp://repositorio.unicamp.br/jspui/handle/REPOSIP/352323-
dc.contributor.departmentsem informaçãopt_BR
dc.contributor.departmentsem informaçãopt_BR
dc.contributor.departmentDepartamento de Química Inorgânicapt_BR
dc.contributor.unidadeInstituto de Químicapt_BR
dc.contributor.unidadeInstituto de Químicapt_BR
dc.contributor.unidadeInstituto de Químicapt_BR
dc.identifier.source2-s2.0-84907143935pt_BR
dc.creator.orcidsem informaçãopt_BR
dc.creator.orcid0000-0001-8330-2642pt_BR
dc.creator.orcid0000-0003-0463-6826pt_BR
dc.type.formArtigopt_BR
dc.description.otherSponsorshipsem informaçãopt_BR
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