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Synthesis and structural characterisation of solid titanium(iv) phosphate materials by means of X-ray absorption and NMR spectroscopy
SunCarbon AB, P. O. Box 726, SE-941 28 Piteå, Sweden.
Department of Corrosion, RISE KIMAB, Isafjordsgatan 28A, SE-164 40 Kista, Sweden.ORCID-id: 0000-0002-4533-3920
Synchrotron Light Research Institute, 111 Moo 6, University Ave., Muang, Nakhon Ratchasima, 30000, Thailand.ORCID-id: 0000-0003-2568-9441
Synchrotron Light Research Institute, 111 Moo 6, University Ave., Muang, Nakhon Ratchasima, 30000, Thailand.
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2022 (Engelska)Ingår i: Dalton Transactions, ISSN 1477-9226, E-ISSN 1477-9234, Vol. 51, nr 21, s. 8192-8207Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

Solid titanium phosphate, TiP, materials hold great promise for wastewater treatment for removal of metal ions and complexes. A series of TiP materials, synthesised at mild conditions and short reaction times, have been structurally characterised using solid-state X-ray absorption spectroscopy, phosphorus and titanium K edge XANES and EXAFS, and 31P and 47/49Ti NMR spectroscopy. The titanium K edge EXAFS data of α-Ti(HPO4)2·H2O (α-TiP) revealed octahedral coordination of oxygens around titanium. Repeated washing of primary β-/γ-TiP with hydrochloric acid results in formation of a weakly ordered solid, TiO(OH)(H2PO4)·H2O, TiP1-H. The structure of TiP1-H is shown by Ti EXAFS to be a titanyl compound, containing a short Ti O bond. The analogous data for linked titanium phosphate compounds (LTP) disclosed that inter-linkage occurs between α-TiP and titanyl phosphate units, supported by 31P–31P NOESY NMR data. 47/49Ti NMR and Ti pre-edge XANES show evidence of two different titanium environments in LTP, one very similar to that observed in TiP1-H and a second more symmetric octahedral environment. Data are discussed in terms of induced acidic hydrolyses of titanium(IV) and phosphate counterpart during washings with hydrochloric acid and water. A straightforward relation between synthesis parameters/post synthetic treatment and structural re-arrangement in the materials is established.

Ort, förlag, år, upplaga, sidor
Royal Society of Chemistry, 2022. Vol. 51, nr 21, s. 8192-8207
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URN: urn:nbn:se:ltu:diva-90682DOI: 10.1039/d2dt00902aISI: 000797039400001PubMedID: 35583237Scopus ID: 2-s2.0-85132007265OAI: oai:DiVA.org:ltu-90682DiVA, id: diva2:1659556
Forskningsfinansiär
Europeiska regionala utvecklingsfonden (ERUF)Kempestiftelserna, JCK-1306 and JCK-1433Swedish Research Council for Environment, Agricultural Sciences and Spatial PlanningWallenbergstiftelserna
Anmärkning

Validerad;2022;Nivå 2;2022-05-31 (joosat);

Funder: EPSRC and BBSRC (grant no. EP/T015063/1); University of Warwick; Advantage West Midlands (AWM)

Tillgänglig från: 2022-05-20 Skapad: 2022-05-20 Senast uppdaterad: 2023-09-05Bibliografiskt granskad

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Antzutkin, Oleg

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Trublet, MylèneKlysubun, WantanaIuga, DinuDupree, RayAntzutkin, OlegPersson, Ingmar
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