2015-09-01

Controlled molecular reorientation enables strong cellulose fibers regenerated from ionic liquid solutions

Johan Sundberg, Valentina Guccini, Karl M.O. Håkansson, German Salazar-Alvarez, Guillermo Toriz, Paul Gatenholm

Polymer 75 (2015) 119-124.
DOI: 10.1016/j.polymer.2015.08.035

Highlights:
• Strong cellulose fibers spun from ionic liquid solution.
• Extrusion process simulated in silica based upon rheological measurements.
• Increased DO for fibers regenerated with ethanol stretched at high RH.
• Significant improvement of mechanical properties for re-oriented fibers.
• Mechanical properties comparable to commercially available fibers.

Abstract:
Cellulose is difficult to solubilize and undergoes thermal decomposition prior to melting. In recent years ionic liquids have been evaluated as solvents of cellulose. In the regeneration process the non-solvent governs the resulting material's crystallinity. Water adsorbs to amorphous cellulose, acts as plasticizer and lowers the Tg, hence the degree of crystallinity will affect the potential strain induced reorientation. We prepared regenerated cellulose fibers form ionic liquid using different non-solvents. The influence of shear forces upon cellulose chain alignment during extrusion was simulated in silica based upon rheological measurements. The regenerated fibers had different physical, morphological and mechanical properties. Molecular re-orientation in fibers induced by mechanical strain, at humidities above the Tg, resulted in much improved mechanical properties with the Young's modulus reaching 23.4 ± 0.8 GPa and the stress at break 504.6 ± 51.9 MPa, which is comparable to commercially available cellulose fibers.


2015-07-02

[OPEN ACCESS] Rod Packing in Chiral Nematic Cellulose Nanocrystal Dispersions Studied by Small-Angle X-ray Scattering and Laser Diffraction

Christina Schütz, Michael Agthe, Andreas B. Fall, Korneliya Gordeyeva, Valentina Guccini, Michaela Salajková, Tomás S. Plivelic, Jan P. F. Lagerwall, German Salazar-Alvarez, and Lennart Bergström
Langmuir 31 (2015) 6507–6513.
DOI: 10.1021/acs.langmuir.5b00924

Abstract
The packing of cellulose nanocrystals (CNC) in the anisotropic chiral nematic phase has been investigated over a wide concentration range by small-angle X-ray scattering (SAXS) and laser diffraction. The average separation distance between the CNCs and the average pitch of the chiral nematic phase have been determined over the entire isotropic–anisotropic biphasic region. The average separation distances range from 51 nm, at the onset of the anisotropic phase formation, to 25 nm above 6 vol % (fully liquid crystalline phase) whereas the average pitch varies from ≈15 μm down to ≈2 μm as ϕ increases from 2.5 up to 6.5 vol %. Using the cholesteric order, we determine that the twist angle between neighboring CNCs increases from about 1° up to 4° as ϕ increases from 2.5 up to 6.5 vol %. The dependence of the twisting on the volume fraction was related to the increase in the magnitude of the repulsive interactions between the charged rods as the average separation distance decreases.

2015-06-30

[OPEN ACCESS] Fabrication of nanocellulose–hydroxyapatite composites and their application as water-resistant transparent coatings

Mai Ishikawa, Yuya Oaki, Yoshihisa Tanaka, Hideki Kakisawa, German Salazar-Alvarez and    Hiroaki Imai

J. Mater. Chem. B, 2015, Advance Article
DOI: 10.1039/C5TB00927H


Abstract
Nanosized composite rods ~300 nm in length and ~20 nm in width were produced by deposition of 22–77 wt% of a c-axis-oriented hydroxyapatite (HA) on cellulose nanocrystals (CNCs). The CNCs functionalized with sulphonic groups were covered with the HA nanocrystals through controlled nucleation and growth under a moderately supersaturated condition in a solution system based on a simulated body fluid. Water-resistant transparent coatings 2–4 μm thick were obtained via evaporation-induced assembly of CNC–HA nanocomposites by casting their suspension on a glass substrate and the subsequent growth of HA nanocrystals by vapour hydrothermal treatment. The composite coatings exhibited improved mechanical strength compared to that of crustacean exoskeletons, and potential for bone regeneration.


2015-05-10

[REVIEW] [OPEN ACCESS] Mesocrystals in Biominerals and Colloidal Arrays

Lennart Bergström, Elena V. Sturm (née Rosseeva), German Salazar-Alvarez, and Helmut Cölfen
Accounts of Chemical Research (2015)


Abstract

Mesocrystals, which originally was a term to designate superstructures of nanocrystals with a common crystallographic orientation, have now evolved to a materials concept. The discovery that many biominerals are mesocrystals generated a large research interest, and it was suggested that mesocrystals result in better mechanical performance and optical properties compared to single crystalline structures. Mesocrystalline biominerals are mainly found in spines or shells, which have to be mechanically optimized for protection or as a load-bearing skeleton. Important examples include red coral and sea urchin spine as well as bones. Mesocrystals can also be formed from purely synthetic components. Biomimetic mineralization and assembly have been used to produce mesocrystals, sometimes with complex hierarchical structures. Important examples include the fluorapatite mesocrystals with gelatin as the structural matrix, and mesocrystalline calcite spicules with impressive strength and flexibility that could be synthesized using silicatein protein fibers as template for calcium carbonate deposition. Self-assembly of nanocrystals can also result in mesocrystals if the nanocrystals have a well-defined size and shape and the assembly conditions are tuned to allow the nanoparticles to align crystallographically. Mesocrystals formed by assembly of monodisperse metallic, semiconducting, and magnetic nanocrystals are a type of colloidal crystal with a well-defined structure on both the atomic and mesoscopic length scale.

Mesocrystals typically are hybrid materials between crystalline nanoparticles and interspacing amorphous organic or inorganic layers. This structure allows to combine disparate materials like hard but brittle nanocrystals with a soft and ductile amorphous material, enabling a mechanically optimized structural design as realized in the sea urchin spicule. Furthermore, mesocrystals can combine the properties of individual nanocrystals like the optical quantum size effect, surface plasmon resonance, and size dependent magnetic properties with a mesostructure and morphology tailored for specific applications. Indeed, mesocrystals composed of crystallographically aligned polyhedral or rodlike nanocrystals with anisotropic properties can be materials with strongly directional properties and novel collective emergent properties. An additional advantage of mesocrystals is that they can combine the properties of nanoparticles with a structure on the micro- or macroscale allowing for much easier handling.

In this Account, we propose that mesocrystals are defined as “a nanostructured material with a defined long-range order on the atomic scale, which can be inferred from the existence of an essentially sharp wide-angle diffraction pattern (with sharp Bragg peaks) together with clear evidence that the material consists of individual nanoparticle building units”. We will give several examples of mesocrystals and discuss the structural characteristics for biominerals, biomimetic materials, and colloidal arrays of nanocrystals. The potential of the mesocrystal materials concept in other areas will be discussed and future developments envisioned.

2015-01-07

[OPEN ACCESS] Origin of the Large Dispersion of Magnetic Properties in Nanostructured Oxides: FexO/Fe3O4 Nanoparticles as a Case Study


M. Estrader, A. López-Ortega, I. V. Golosovsky, S. Estradé, G. Salazar-Alvarez, Ll. López- Conesa, D. Tobia, E. Winkler, J. D. Ardisson, W.A.A. Macedo, M. Vasilakaki, K. N. Trohidou, R. D. Zysler, F. Peiró, L. Bergström, and J. Nogués

Nanoscale (2015)
DOI: 10.1039/C4NR06351A

Abstract:
The intimate relationship in transition-metal oxides between stoichiometry and physiochemical properties makes them appealing as tunable materials. These features become exacerbated when dealing with nanostructures. However, due to the complexity of nanoscale materials, establishing a distinct relationship between structure-morphology and functionalities is often complicated. In this regard, in the FexO/Fe3O4 system a largely unexplained broad dispersion of magnetic properties has been observed. Here we show, thanks to a comprehensive multi-technique approach, a clear correlation between magneto-structural properties in large (45 nm) and small (9 nm) FexO/Fe3O4 core/shell nanoparticles that can explain the spread of magnetic behaviors. The results reveal that while the FexO core in the large nanoparticles is antiferromagnetic and has bulk-like stoichiometry and unit-cell parameters, the FexO core in the small particles is highly non-stoichiometric and strained, displaying no significant antiferromagnetism. These results highlight the importance of ample characterization to fully understand the properties of nanostructured metal oxides.