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  • 1.
    Lindman, Björn
    et al.
    Mittuniversitetet, Fakulteten för naturvetenskap, teknik och medier, Avdelningen för kemiteknik. Lunds Universitet.
    Medronho, Bruno
    University of Algarve, Faro, Portugal.
    Alves, Luís
    University of Coimbra, Portugal.
    Costa, Carolina
    Mittuniversitetet, Fakulteten för naturvetenskap, teknik och medier, Avdelningen för kemiteknik.
    Edlund, Håkan
    Mittuniversitetet, Fakulteten för naturvetenskap, teknik och medier, Avdelningen för kemiteknik.
    Norgren, Magnus
    Mittuniversitetet, Fakulteten för naturvetenskap, teknik och medier, Avdelningen för kemiteknik.
    The relevance of structural features of cellulose and its interactions to dissolution, regeneration, gelation and plasticization phenomena2017Inngår i: Physical Chemistry, Chemical Physics - PCCP, ISSN 1463-9076, E-ISSN 1463-9084, Vol. 19, nr 35, s. 23704-23718Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Cellulose is the most abundant polymer and a very important renewable resource. Since cellulose cannot be shaped by melting, a major route for its use for novel materials, new chemical compounds and renewable energy must go via the solution state. Investigations during several decades have led to the identification of several solvents of notably different character. The mechanisms of dissolution in terms of intermolecular interactions have been discussed from early work but, even on fundamental aspects, conflicting and opposite views appear. In view of this, strategies for developing new solvent systems for various applications have remained obscure. There is for example a strong need for using forest products for higher value materials and for environmental and cost reasons to use water-based solvents. Several new water-based solvents have been developed recently but there is no consensus regarding the underlying mechanisms. Here we wish to address the most important mechanisms described in the literature and confront them with experimental observations. A broadened view is helpful for improving the current picture and thus cellulose derivatives and phenomena such as fiber dissolution, swelling, regeneration, plasticization and dispersion are considered. In addition to the matter of hydrogen bonding versus hydrophobic interactions, the role of ionization as well as some applications of new knowledge gained are highlighted.

  • 2.
    Niga, Petru
    Mittuniversitetet, Fakulteten för naturvetenskap, teknik och medier, Institutionen för informationsteknologi och medier.
    Crown ethers at the aqueous solution–air interface: 1. Assignments and surface spectroscopy2011Inngår i: Physical Chemistry, Chemical Physics - PCCP, ISSN 1463-9076, E-ISSN 1463-9084, Vol. 13, nr 17, s. 7930-7938Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    The surface of aqueous solutions of 4-Nitro Benzo-15-Crown-5 (NB15C5) and Benzo-15-Crown-5 (B15C5) has been studied using the surface sensitive technique vibrational sum frequency spectroscopy (VSFS). The NO, CN, COC and CH vibrational modes of these compounds at the air–water interface as well as OH vibrational modes of the surface water hydrating this compound have been targeted in order to obtain molecular information about arrangement and conformation of the adsorbed crown ether molecules at the air–water interface. The CH2 vibrational modes of crown ethers have been identified and found to be split due to interaction with ether oxygen. The spectra provide evidence for the existence of a protonated crown complex moiety at the surface leading to the appearance of strongly ordered water species. The interfacial water species are influenced by the resulting charged interface and by the strong Zundel polarizability due to tunneling of the proton species between equivalent sites within the crown ring.

  • 3.
    Niga, Petru
    Mittuniversitetet, Fakulteten för naturvetenskap, teknik och medier, Institutionen för informationsteknologi och medier.
    Crown ethers at the aqueous solution–air interface. Part 2. Electrolyte effects, ethylene oxide hydration and temperature behaviour2011Inngår i: Physical Chemistry, Chemical Physics - PCCP, ISSN 1463-9076, E-ISSN 1463-9084, Vol. 13, nr 17, s. 7939-7947Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    Vibrational Sum Frequency Spectroscopy (VSFS) was employed to study adsorbing films of 4-Nitro Benzo-15-Crown-5 (NB15C5) and Benzo-15-Crown-5 (B15C5) at the aqueous solution–air interface. The surface of the solution is strongly influenced by the presence of crown ether species. Changes in the orientation of NB15C5 were monitored as a function of solution concentration, by targeting the ratio of peak intensities of the CN and NO2 vibrational modes. The water of hydration has also been probed as a function of crown concentration, salt concentration, and temperature. The latter study strongly suggests that the surface can be treated as a charged interface, and that the associated ordered water decreases with increasing ionic strength of the bulk solution.

  • 4. Nozière, Barbara
    et al.
    Dziedzic, Pawel
    Córdova, Armando
    Mittuniversitetet, Fakulteten för naturvetenskap, teknik och medier, Institutionen för naturvetenskap, teknik och matematik.
    Common Inorganic Ions Catalyze Chemical Reactions of Organic Compounds in Atmospheric Aerosols2010Inngår i: Physical Chemistry, Chemical Physics - PCCP, ISSN 1463-9076, E-ISSN 1463-9084, Vol. 12, s. 3864-Artikkel i tidsskrift (Fagfellevurdert)
  • 5.
    Wakeham, D.
    et al.
    Centre for Organic Electronics, University of Newcastle, Callaghan, NSW 2308, Australia.
    Niga, Petru
    Mittuniversitetet, Fakulteten för naturvetenskap, teknik och medier, Institutionen för informationsteknologi och medier. KTH Royal Inst Technol, Dept Chem Surface & Corros Sci, SE-10044 Stockholm, Sweden.
    Ridings, C
    Centre for Nano Scale Science and Technology, Flinders University, SA 5001, Australia.
    Andersson, G
    Centre for Nano Scale Science and Technology, Flinders University, SA 5001, Australia.
    Nelson, A
    Bragg Institute, Australian Nuclear Science and Technology Organisation, PMB 1, Menai, NSW 2234, Australia.
    Warr, G
    School of Chemistry, University of Sydney, NSW 2006, Australia.
    Baldelli, S
    Department of Chemistry, University of Houston, Houston, TX 77204-5003, United States.
    Rutland, M
    Department of Chemistry, Surface and Corrosion Science, KTH Royal Institute of Technology, Drottning Kristinas Väg 51, SE-100 44 Stockholm, Sweden.
    Atkin, R
    Centre for Organic Electronics, University of Newcastle, Callaghan, NSW 2308, Australia.
    Surface structure of a "non-amphiphilic" protic ionic liquid2012Inngår i: Physical Chemistry, Chemical Physics - PCCP, ISSN 1463-9076, E-ISSN 1463-9084, Vol. 14, nr 5, s. 5106-5114Artikkel i tidsskrift (Fagfellevurdert)
    Abstract [en]

    The nanostructure of the ethanolammonium nitrate (EtAN)-air surface has been investigated using X-ray reflectometry (XRR), vibrational sum frequency spectroscopy (VSFS) and neutral impact collision ion scattering spectroscopy (NICISS). The XRR data decays more rapidly than expected for a perfectly sharp interface, indicating a diffuse electron (scattering length) density profile. Modelling of the XRR data using three different fitting routines produced consistent interfacial profiles that suggest the formation of interfacial EtAN clusters. Consistent with this, VSFS reveals that the EtAN surface is predominantly covered by -CH 2- moieties, with the -NH 3 + and -OH groups of the cation buried slightly deeper in the interface. The elemental profiles determined using NICISS also show enrichment of carbon relative to nitrogen and oxygen in the outermost surface layer, which is consistent with the surface cation orientation deduced from VSFS, and with the presence of EtAN aggregates at the liquid surface. © 2012 the Owner Societies.

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