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A multitechnique study of the interactions between H+, Na+, Ca2+ and Cu2+, and two types of softwood Kraft fibre materials
Umeå universitet, Teknisk-naturvetenskapliga fakulteten, Kemiska institutionen.ORCID-id: 0000-0002-1705-5249
Umeå universitet, Teknisk-naturvetenskapliga fakulteten, Kemiska institutionen.
Umeå universitet, Teknisk-naturvetenskapliga fakulteten, Kemiska institutionen.
2008 (Engelska)Ingår i: Journal of Colloid and Interface Science, ISSN 0021-9797, E-ISSN 1095-7103, Vol. 328, nr 2, s. 248-56Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

Aiming for a better understanding of the interactions between water suspended cellulose fibres and metal ions, this study was focused on characterising the interactions between Ca2+, Cu2+ and two different fibre materials—a fully bleached softwood Kraft pulp, and a chemically modified fully bleached softwood Kraft fibre material. The study was conducted as a function of pH (2–7), and both in the absence and presence of an excess of Na+ ions, 0–100 mM Na(Cl). For both fibre materials, adsorption data collected in the absence of Na+ were fully explained by the unspecific Donnan ion-exchange model. However, in an excess of Na(Cl), data clearly indicated that higher amounts of divalent metal ions adsorbed, than predicted by the Donnan model. Therefore, to model these data, specific metal ion–fibre surface complexes were assumed to form, in addition to the Donnan ion-exchange. A neutral surface species involving two surface carboxylate groups and one metal ion was, for both metal ions, found to yield a good description of data at all ionic strengths. In the case of Cu2+, the existence of this complex was corroborated by Cu K-edge EXAFS data, suggesting that copper ions interacts directly with carboxyl groups present int the fibres. EXAFS data also indicate that one Cu2+ interacts with two carboxyls.

Graphical abstract

In combination with unspecific Donnan interactions, specific interactions between divalent metal ions (Ca2+ and Cu2+) and cellulose fibre carboxylic groups were evidenced from both macroscopic adsorption data and spectroscopic measurements.

Ort, förlag, år, upplaga, sidor
2008. Vol. 328, nr 2, s. 248-56
Nyckelord [en]
Metal ions, Kraft fibres, Donnan, Adsorption, Ion exchange, Surface complexes, EXAFS, Affinity
Nationell ämneskategori
Kemi
Identifikatorer
URN: urn:nbn:se:umu:diva-10631DOI: 10.1016/j.jcis.2008.09.027ISI: 000260845300005PubMedID: 18849049Scopus ID: 2-s2.0-75749137588OAI: oai:DiVA.org:umu-10631DiVA, id: diva2:150302
Tillgänglig från: 2008-12-15 Skapad: 2008-12-15 Senast uppdaterad: 2023-03-24Bibliografiskt granskad
Ingår i avhandling
1. Cation adsorption properties of substituted kraft fibres: an experimental and thermodynamic modelling study
Öppna denna publikation i ny flik eller fönster >>Cation adsorption properties of substituted kraft fibres: an experimental and thermodynamic modelling study
2008 (Engelska)Doktorsavhandling, sammanläggning (Övrigt vetenskapligt)
Abstract [en]

Acid/base and metal ion adsorption properties have been investigated for a range of chemically modified bleached Kraft fibre materials (pulps). The studies were performed via potentiometric titrations, Flame Atomic Absorbtion (and Emission) Spectroscopy, Inductively Coupled Plasma Optical Emission Spectroscopy and Extended X-ray Absorbtion Fine Structure measurements. As a result of a chemical modification procedure, the total concentration of acidic carboxylate groups in the fibre materials ranged between 43 and 590 μmol/g.

The preferable surface potential model for modelling the ionic strength dependent acid/base properties of fibre materials with low charge densities, i.e. unmodified fully bleached Kraft fibre materials, was found to be the Basic Stern Model. For fibre materials with high total charge, ≳100 μmol/g, this model resulted in poor fits to data, and for such materials a number of Constant Capacitance Models, one at each ionic strength, must be recommended.

With respect to metal ion adsorption, the results have indicated that the unspecific Donnan theory could correctly model the simultaneous adsorption of several metal ions, i.e. K+, Na+, Mg2+, Ca2+ and Cu2+, provided that the salt concentration in the fibre suspension is low. In suspensions of high salt concentration it was, however, found that this very same model strongly underestimated the adsorption of Ca2+ and Cu2+. Here, the Donnan model had to be complemented by specific ion exchange equilibria. These results were corroborated by spectroscopic evidence of specific interactions between Cu2+-ions and fibres. The spectroscopic indication of a complex formed between two fibre surface carboxylate groups and one Cu2+-ion, agree with the specific ion exchange model. It was therefore concluded that specific metal ionfibre interactions cannot be neglected, especially at high salt concentrations.

The interactions occurring between the polycation GaO4Al12(OH)24(H2O)127+ and fibre materials were studied by both adsorption and spectroscopic measurements. These indicate that GaO4Al12(OH)24(H2O)127+ is surprisingly stable in fibre suspensions and that intact GaO4Al12(OH)24(H2O)127+- ions are strongly adsorbed onto the fibres. Also for this ion, specific interactions has to be considered, since the strong adsorption registered was too strong to be explained by Donnan equilibria. In the thesis, the stochiometric composition and an equilibrium constant characterising these interactions is presented.

Ort, förlag, år, upplaga, sidor
Umeå: Kemi, 2008. s. 49
Nyckelord
Kraft fibres, Donnan equilibria, ion exchange, acid/base properties, potentiometric titrations, thermodynamic modelling, NPEs, GaAl12 7+, EXAFS
Nationell ämneskategori
Annan medicinsk grundvetenskap
Identifikatorer
urn:nbn:se:umu:diva-1891 (URN)987-91-7264-672-8 (ISBN)
Disputation
2008-11-14, KB3A9, KBC-Huset, Umeå Universitet, Umeå, 10:00 (Engelska)
Opponent
Handledare
Tillgänglig från: 2008-10-24 Skapad: 2008-10-24 Senast uppdaterad: 2022-03-02Bibliografiskt granskad

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Sundman, OlaPersson, PerÖhman, Lars-Olof

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Sundman, OlaPersson, PerÖhman, Lars-Olof
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