Posts Tagged ‘Aalto University’

“Control my chirality, please,” said the carbon nanotube to the researchers

Tuesday, April 30th, 2013

A combined Finnish, Russian, and Danish team have found a way to control the chirality of single-walled carbon nanotubes according to an Apr. 30, 2013 news item on Azonano,

An ultimate goal in the field of carbon nanotube research is to synthesise single-walled carbon nanotubes (SWNTs) with controlled chiralities. Twenty years after the discovery of SWNTs, scientists from Aalto University in Finland, A.M. Prokhorov General Physics Institute RAS in Russia and the Center for Electron Nanoscopy of Technical University of Denmark (DTU) have managed to control chirality in carbon nanotubes during their chemical vapor deposition synthesis.

The Aalto University Apr. 29, 2013 news release, which originated the news item, goes on to explain,

 Over the years, substantial progress has been made to develop various structure-controlled synthesis methods. However, precise control over the chiral structure of SWNTs has been largely hindered by a lack of practical means to direct the formation of the metal nanoparticle catalysts and their catalytic dynamics during tube growth.

– We achieved an epitaxial formation of Co nanoparticles by reducing a well-developed solid solution in CO, reveals Maoshuai He, a postdoctoral researcher at Aalto University School of Chemical Technology.

– For the first time, the new catalyst was employed for selective growth of SWNTs, adds senior staff scientist Hua Jiang from Aalto University School of Science.

By introducing the new catalysts into a conventional CVD reactor, the research team demonstrated preferential growth of semiconducting SWNTs (~90%) with an exceptionally high population of (6,5) tubes (53%) at 500 °C. Furthermore, they also showed a shift of the chiral preference from (6,5) tubes at 500 °C  to (7, 6) and (9, 4) nanotubes at 400 °C.

– These findings open new perspectives both for structural control of SWNTs and for elucidating their growth mechanisms, thus are important for the fundamental understanding of science behind nanotube growth, comments Professor Juha Lehtonen from Aalto University.

For anyone like me who needs a description of chirality, there’s this from Wikipedia,

Chirality (pron.: /kaɪˈrælɪtiː/) is a property of asymmetry important in several branches of science. The word chirality is derived from the Greek, χειρ (kheir), “hand”, a familiar chiral object.

An object or a system is chiral if it is not identical to its mirror image, that is, it cannot be superposed onto it. A chiral object and its mirror image are called enantiomorphs (Greek opposite forms) or, when referring to molecules, enantiomers. A non-chiral object is called achiral (sometimes also amphichiral) and can be superposed on its mirror image.

Human hands are perhaps the most universally recognized example of chirality: The left hand is a non-superimposable mirror image of the right hand; no matter how the two hands are oriented, it is impossible for all the major features of both hands to coincide.[2] This difference in symmetry becomes obvious if someone attempts to shake the right hand of a person using his left hand, or if a left-handed glove is placed on a right hand. In mathematics chirality is the property of a figure that is not identical to its mirror image.

One of the researchers notes why they, or anyone else, would want to control the chirality of carbon nanotubes, from the news release,

– Chirality defines the optical and electronic properties of carbon nanotubes, so controlling it is a key to exploiting their practical applications, says Professor Esko I. Kauppinen, the leader of the Nanomaterials Group in Aalto University School of Science.

ETA Apr. 30, 2013 at 4:20 pm PDT: Here’s a link to and a citation for the team’s published paper,

Chiral-Selective Growth of Single-Walled Carbon Nanotubes on Lattice-Mismatched Epitaxial Cobalt Nanoparticles by Maoshuai He, Hua Jiang, Bilu Liu, Pavel V. Fedotov, Alexander I. Chernov, Elena D. Obraztsova, Filippo Cavalca, Jakob B. Wagner, Thomas W. Hansen, Ilya V. Anoshkin, Ekaterina A. Obraztsova, Alexey V. Belkin, Emma Sairanen, Albert G. Nasibulin,  Juha Lehtonen, & Esko I. Kauppinen. Scientific Reports 3, Article number 1460  doi:10.1038/srep01460 Published15 March 2013

This article is open access.

Protein cages, viruses, and nanoparticles

Thursday, December 20th, 2012

The Dec. 19, 2012 news release on EurekAlert about a study published by researchers at Aalto University (Finland) describes a project where virus particles are combined with nanoparticles to create new metamaterials,

Scientists from Aalto University, Finland, have succeeded in organising virus particles, protein cages and nanoparticles into crystalline materials. These nanomaterials studied by the Finnish research group are important for applications in sensing, optics, electronics and drug delivery.

… biohybrid superlattices of nanoparticles and proteins would allow the best features of both particle types to be combined. They would comprise the versatility of synthetic nanoparticles and the highly controlled assembly properties of biomolecules.

The gold nanoparticles and viruses adopt a special kind of crystal structure. It does not correspond to any known atomic or molecular crystal structure and it has previously not been observed with nano-sized particles.

Virus particles – the old foes of mankind – can do much more than infect living organisms. Evolution has rendered them with the capability of highly controlled self-assembly properties. Ultimately, by utilising their building blocks we can bring multiple functions to hybrid materials that consist of both living and synthetic matter, Kostiainen [Mauri A. Kostiainen, postdoctoral researcher] trusts.

The article which has been published in Nature Nanotechnology is free,

Electrostatic assembly of binary nanoparticle superlattices using protein cages by Mauri A. Kostiainen, Panu Hiekkataipale, Ari Laiho, Vincent Lemieux, Jani Seitsonen, Janne Ruokolainen & Pierpaolo Ceci in Nature Nanotechnology (2012) doi:10.1038/nnano.2012.220  Published online 16 December 2012

There’s a video demonstrating the assembly,

From the YouTube page, here’s a description of what the video is demonstrating,

Aalto University-led research group shows that CCMV virus or ferritin protein cages can be used to guide the assembly of RNA molecules or iron oxide nanoparticles into three-dimensional binary superlattices. The lattices are formed through tuneable electrostatic interactions with charged gold nanoparticles.

Bravo and thank  you to  Kostiainen who seems to have written the news release and prepared all of the additional materials (image and video). There are university press offices that could take lessons from Kostiainen’s efforts to communicate about the work.

Nanocellulose at the American Chemical Society’s 243rd annual meeting

Tuesday, March 27th, 2012

Nanocellulose seems to be one of the major topics at the ACS’s (Americal Chemical Society) 243rd annual meeting themed Chemistry of Life  in San Diego, California, March 25-29, 2012. From the March 25, 2012 news item on Nanowerk,

… almost two dozen reports in the symposium titled, “Cellulose-Based Biomimetic and Biomedical Materials,” that focused on the use of specially processed cellulose in the design and engineering of materials modeled after biological systems. Cellulose consists of long chains of the sugar glucose linked together into a polymer, a natural plastic–like material. Cellulose gives wood its remarkable strength and is the main component of plant stems, leaves and roots. Traditionally, cellulose’s main commercial uses have been in producing paper and textiles –– cotton being a pure form of cellulose. But development of a highly processed form of cellulose, termed nanocellulose, has expanded those applications and sparked intense scientific research. Nanocellulose consists of the fibrils of nanoscale diameters so small that 50,000 would fit across the width of the period at the end of this sentence.

“We are in the middle of a Golden Age, in which a clearer understanding of the forms and functions of cellulose architectures in biological systems is promoting the evolution of advanced materials,” said Harry Brumer, Ph.D., of Michael Smith Laboratories, University of British Columbia, Vancouver. He was a co-organizer of the symposium with J. Vincent Edwards, Ph.D., a research chemist with the Agricultural Research Service, U.S. Department of Agriculture in New Orleans, Louisiana. “This session on cellulose-based biomimetic and biomedical materials is really very timely due to the sustained and growing interest in the use of cellulose, particularly nanoscale cellulose, in biomaterials.”

One of the presenters has a very charming way of describing the nanocellulose product his team is working on (from the news item),

Olli Ikkala, Ph.D., [Aalto University, Finland] described the new buoyant material, engineered to mimic the water strider’s long, thin feet and made from an “aerogel” composed of the tiny nano-fibrils from the cellulose in plants. Aerogels are so light that some of them are denoted as “solid smoke. [emphasis mine]” The nanocellulose aerogels also have remarkable mechanical properties and are flexible.

There were some 20 presentations in this symposium held under the auspices of the ACS annual meeting. Here’s a few of the presentations (some of these folks have been featured on this blog previously), from the news item,

Native cellulose nanofibers: From biomimetic nanocomposites to functionalized gel spun fibers and functional aerogels Olli Ikkala, Professor, PhD, Aalto University, P.O. Box 5100, Espoo, Finland, FIN-02015, Finland , 358-9-470 23154, olli.ikkala@aalto.fi Native cellulose nanofibers and whiskers attract interest even beyond the traditional cellulose community due to their mechanical properties, availability and sustainability. We describe biomimetic nanocomposites with aligned self-assemblies combining nanocellulose with nanoclays, polymers, block copolymer, or graphene, allowing exciting mechanical properties. Functional ductile and even flexible aerogels are presented, combining superhydrophobicity, superoleophobicity, oil-spill absorption, photocatalytics, optically switchable water absorption, sensing, and antimicrobial properties. Finally mechanically excellent fibers are gel-spun and functionalized for electric, magnetic, optical and drug-release properties.

Evaluation of skin tissue repair materials from bacterial cellulose Lina Fu, Miss, Huazhong University of Science & Technology, College of Life Science & Technology, 1037 Luoyu Road, Wuhan, Hubei, 430074, China , 86-18971560696, runa0325@gmail.com Bacterial cellulose (BC) has been reported as the materials in the tissue engineering fields, such as skin, bone, vascular and cartilage tissue engineering. Exploitation of the skin substitutes and modern wound dressing materials by using BC has attracted much attention. A skin tissue repair materials based on BC have been biosynthesized by Gluconacetobacter xylinus. The nano-composites of BC and chitosan form a cohesive gel structure, and the cell toxicity of the composite is excellent. Unlike other groups, which showed more inflammatory behavior, the inflammatory cells of the BC group were mainly polymorph-nuclear and showed few lymphocytes. The BC skin tissue repair material has an obviously curative effect in promoting the healing of epithelial tissue and reducing inflammation. With its superior mechanical properties, and the excellent biocompatibility, these skin tissue repair materials based on BC have great promise and potential for wound healing and very high clinical value.

….

New materials from nanocrystalline cellulose Mark MacLachlan [mentioned in my Nov. 18, 2010 posting], University of British Columbia, Department of Chemistry, 2036 Main Mall, Vancouver, BC, V6T 1Z1, Canada , 604-822-3070, mmaclach@chem.ubc.ca Nanocrystalline cellulose (NCC) is available from the acid-catalyzed degradation of cellulosic materials. NCC is composed of cylindrical crystallites with diameters of ca. 5-10 nm and large aspect ratios. This form of cellulose has intriguing properties, including its ability to form a chiral nematic structure. By using the chiral nematic organization of NCC as a template, we have been able to create highly porous silica films and carbon films with chiral nematic organization.1,2 These materials are iridescent and their structures mimic the shells of jewel beetles. In this paper, I will describe our recent efforts to use NCC to create new materials with interesting optical properties.

Factors influencing chiral nematic pitch and texture of cellulose nanocrystal films Derek G Gray, McGill University, Department of Chemistry, Pulp and Paper Building, 3420 University Street, Montreal, QC, H3A 2A7, Canada , 1-514-398-6182, derek.gray@mcgill.ca Appropriately stabilized cellulose nanocrystal (NCC) suspensions in water form chiral nematic liquid crystalline phases above some critical concentration. In the absence of added electrolye, the chiral nematic pitch of such suspensions is longer than that of visible light. Films prepared by evaporation from the suspensions also often display the characteristic fingerprint patterns characteristic of long-pitch chiral nematic phases, but the pitch values can be shifted into the visible range by adding small quantities of electrolyte to the evaporating suspension. The factors that control the final pitch have been the subject of some confusion. While still not well understood, it is clear that at high nanocrystal concentrations and in solid films, the pitch is not simply a reversible function of nanocrystal concentration. We examine some of the factors that control the pitch and liquid crystal texture during the drying of chiral nematic NCC films.

….

Bioprinting of 3D porous nanocellulose scaffolds for tissue engineering and organ regeneration Paul Gatenholm, Professor, [mentioned in my March 19, 2012 posting] Wallenberg Wood Science Center, Chalmers, Department of Chemical and Biological Engineering, Kemigarden 4, Goteborg, V. Gotaland, SE41296, Sweden , 46317723407, paul.gatenholm@chalmers.se Nanocellulose is a promising biocompatible hydrogel like nano-biomaterial with potential uses in tissue engineering and regenerative medicine. Biomaterial scaffolds for tissue engineering require precise control of porosity, pore size, and pore interconnectivity. Control of scaffold architecture is crucial to promote cell migration, cell attachment, cell proliferation and cell differentiation. 3D macroporous nanocellulose scaffolds, produced by unique biofabrication process using porogens incorporated in the cultivation step, have shown ability to attract smooth muscle cells, endothelial cells, chondrocytes of various origins, urethral cells and osteoprogenitor cells. We have developed bioprinter which is able to produce 3D porous nanocellulose scaffolds with large size and unique architecture. Surface modifications have been applied to enhance cell adhesion and cell differentiation. In this study we have focused on use of 3D porous Nanocellulose scaffolds for stem cell differentiation into osteogenic and chondral lineages.