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Complete Column Trials for Water Refinement Using Titanium(IV) Phosphate Sorbents
Luleå tekniska universitet, Institutionen för samhällsbyggnad och naturresurser, Kemiteknik.ORCID-id: 0000-0002-4533-3920
Luleå tekniska universitet, Institutionen för samhällsbyggnad och naturresurser, Kemiteknik.
2018 (Engelska)Ingår i: ACS Sustainable Chemistry & Engineering, E-ISSN 2168-0485, Vol. 6, nr 5, s. 6157-6165Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

A titanium phosphate sorbent with linked active units (LTP) is synthesized. XRD, 31P MAS NMR, and TGA techniques are used to disclose the relation between the ion-exchange units of −HPO4 (crystalline α-TiP) and of −H2PO4 (amorphous TiP1) type. The reported kinetics data of TiP1 sorbent in batch mode have been reprocessed according to the nonlinear approach in order to explore further the sorption mechanism. It was found that the data could be well described by the pseudo-second-order model in the case of Ni2+ ions. Consequently, fixed-bed column sorption experiments of Ni2+ ions on LTP were designed, and the effects of both the amount of nickel(II) ions in the feed solution and the flow rates on the sorption equilibrium were studied. The ion-exchange capacity is estimated to be 1.6 meq·g–1 during the first four cycles before decreasing to 1.2 meq·g–1 for cycles five and six. The experimental data were simulated following the Thomas model, and desorption experiments with HCl were performed. Observations show that regeneration and reutilization of the LTP ion-exchanger are possible through at least six cycles. It is revealed that the sorption performances in column conditions could be undoubtedly predicted from the corresponding batch sorption data.

Ort, förlag, år, upplaga, sidor
American Chemical Society (ACS), 2018. Vol. 6, nr 5, s. 6157-6165
Nyckelord [en]
Column, Ion-exchanger, Nickel, Sorption, Titanium phosphate
Nationell ämneskategori
Fysikalisk kemi
Forskningsämne
Gränsytors kemi
Identifikatorer
URN: urn:nbn:se:ltu:diva-68298DOI: 10.1021/acssuschemeng.7b04823ISI: 000431927500054Scopus ID: 2-s2.0-85046747198OAI: oai:DiVA.org:ltu-68298DiVA, id: diva2:1197047
Anmärkning

Validerad;2018;Nivå 2;2018-05-23 (andbra)

Tillgänglig från: 2018-04-11 Skapad: 2018-04-11 Senast uppdaterad: 2018-08-10Bibliografiskt granskad
Ingår i avhandling
1. Titanium(IV) Phosphates: The Next Generation of Wastewater Sorbents
Öppna denna publikation i ny flik eller fönster >>Titanium(IV) Phosphates: The Next Generation of Wastewater Sorbents
2018 (Engelska)Doktorsavhandling, sammanläggning (Övrigt vetenskapligt)
Abstract [en]

Treatment of industrial waters containing heavy metal ions is essential before being discharged into the environment. Consequently, European regulations have been established to control and limit the amount of heavy metals released. There is a need to develop efficient water treatment techniques that can remove contaminants with respect to these EU regulations.

Ion-exchange is one of the processes that is being investigated due to fast kinetics, high treatment capacity and its ability to remove heavy metal ions present in trace amounts. Titanium phosphates (TiP) are a group of inorganic ion-exchangers that have demonstrated to be particularly selective towards transition metal ions in aqueous solutions. Two types of ion-exchange units are present in TiP material, which are –HPO4 and –H2PO4 groups. Their structural characteristic is highly dependent on the synthesis conditions, which include the source of titanium, temperature, reaction time and P2O5:TiO2 ratio. Most of the studies have been performed on amorphous TiP containing a mixture of both exchange units, with –HPO4 groups being predominant; as crystalline TiP and –H2PO4 based TiP  are often obtained in difficult conditions, high temperature (up to 250 °C) and/or long reaction time (up to 30 days) and/or using autoclave. Despite promising properties depicted in batch conditions, very few data in continuous flow systems (fixed-bed columns) have been reported.

In this work, amorphous TiP composed of entirely –H2PO4 ion-exchange units (TiP1) was synthesized at mild conditions using a TiOSO4 solution and HCl/deionized water as post-synthesis treatments. The sorbent was characterized using a range of techniques (solid-state 31P MAS NMR, Raman, XRD, TGA, BET, Elemental analysis, EXAFS and XANES,) and tested in batch and column set-ups towards single and multi-component waters. The chemical formula of TiP1 was established as TiO(OH)(H2PO4)·H2O and it was found that the synthesis of TiP1 was also dependent on the TiO2/H2SO4 content in the primary titanium solution.

The material displayed a high maximum exchange capacity of ca. 6.4 meq.g-1, expressed as the sodium uptake. The actual ion-exchange capacity towards divalent metal ions was calculated to be ca. 3.4 meq.g-1 in batch condition and up to 4.1 meq.g-1 in fixed-bed column, which is to date the highest recorded for TiP materials. Kinetics of the exchange processes have been studied and the equilibrium was reached within 5-20 minutes. Modeling of the breakthrough curves was achieved using the Thomas model, indicating that the rate driving forces of the processes follow second-order reversible kinetics. The TiP1 sorbent has shown to maintain a high selectivity towards heavy metal ions in multi-component systems (including closed-mine waters) when column studies were performed. The sorption behavior of TiP1 in batch experiments correlates very well with data obtained in fixed-bed column conditions, confirming that prediction of the sorption behavior on the basis of batch data is conceivable.

Another important aspect of this work also involves the mild syntheses of crystalline α-TiP, Ti(HPO4)·H2O, and LTP (Linked Titanium Phosphate) composed of α-TiP and TiP1, where the structural characteristics of these materials were investigated using solid-state NMR, XRD, TGA, EXAFS and XANES.

Ort, förlag, år, upplaga, sidor
Luleå: Luleå University of Technology, 2018
Serie
Doctoral thesis / Luleå University of Technology 1 jan 1997 → …, ISSN 1402-1544
Nationell ämneskategori
Kemiteknik Kemi Fysikalisk kemi
Forskningsämne
Gränsytors kemi
Identifikatorer
urn:nbn:se:ltu:diva-70326 (URN)978-91-7790-178-5 (ISBN)978-91-7790-179-2 (ISBN)
Disputation
2018-09-14, E632, Luleå, 09:00 (Engelska)
Opponent
Handledare
Tillgänglig från: 2018-08-13 Skapad: 2018-08-10 Senast uppdaterad: 2018-08-28Bibliografiskt granskad

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