Functionalised nanostructured polyaniline? A new substrate for building adaptive sensing surfaces

A new method for covalently binding side-chains to the surface of solution based conducting polymer nanostructures is introduced in this paper. Modification of the structures is achieved by convenient reflux in the presence of a nucleophile, and post-functionalization purification is subsequently carried out by centrifugation. The entire process is easily scalable and hence suitable for bulk production of functionalized nanomaterials. In particular we focus on the modification of polyaniline nanofibres which can be synthesized by interfacial polymerization. Mercaptoundecanoic acid side-chains are attached to the polymer nanostructures, with the intrinsic nano-morphology of the material being maintained during the process. The modified PAni nanofibres provide a template for the attachment of other specific functional groups which could be used to target a particular species

Magnetoelectric Effect driven by Magnetic Domain Modification in LuFe2O4

Magneto-capacitance effect was investigated using the impedance spectroscopy on single crystals of LuFe2O4. The intrinsic impedance response could be separated from the interfacial response and showed a clear hysteresis loop below TFerri ~ 240 K under the magnetic field. The neutron diffraction experiment under the magnetic field proves the origin of dielectric property related to the motion of nano-sized ferromagnetic domain boundary. These results imply that the modification of the microscopic domain structure is responsible for the magnetoelectric effect in LuFe2O4.Comment: 9 pages, 5 figure

Contact mechanics with adhesion: Interfacial separation and contact area

We study the adhesive contact between elastic solids with randomly rough, self affine fractal surfaces. We present molecular dynamics (MD) simulation results for the interfacial stress distribution and the wall-wall separation. We compare the MD results for the relative contact area and the average interfacial separation, with the prediction of the contact mechanics theory of Persson. We find good agreement between theory and the simulation results. We apply the theory to the system studied by Benz et al. involving polymer in contact with polymer, but in this case the adhesion gives only a small modification of the interfacial separation as a function of the squeezing pressure.Comment: 5 pages, 4 figure

Comparative study of heat transfer and pressure drop during flow boiling and flow condensation in minichannels

This paper was presented at the 4th Micro and Nano Flows Conference (MNF2014), which was held at University College, London, UK. The conference was organised by Brunel University and supported by the Italian Union of Thermofluiddynamics, IPEM, the Process Intensification Network, the Institution of Mechanical Engineers, the Heat Transfer Society, HEXAG - the Heat Exchange Action Group, and the Energy Institute, ASME Press, LCN London Centre for Nanotechnology, UCL University College London, UCL Engineering, the International NanoScience Community, www.nanopaprika.eu.In the paper a method developed earlier by authors is applied to calculations of pressure drop and heat transfer coefficient for flow boiling and also flow condensation for some recent data collected from literature for such fluids as R245fa, R600a, R134a, R1234yf and other. The modification of interface shear stresses between flow boiling and flow condensation in annular flow structure is considered through incorporation of the so called blowing parameter. The shear stress between vapor phase and liquid phase is generally a function of non-isothermal effects. The mechanism of modification of shear stresses at the vapor-liquid interface has been presented in detail. In case of annular flow it contributes to thickening and thinning of the liquid film, which corresponds to condensation and boiling respectively. There is also a different influence of heat flux on the modification of shear stress in the bubbly flow structure, where it affects the bubble nucleation. In that case the effect of applied heat flux is considered. As a result a modified form of the two-phase flow multiplier is obtained, in which the non-adiabatic effect is clearly pronounced

Supported ITZ modification efficiencies via surface coating nanoparticles on aggregate and its influence on properties

In order to modify the porous interfacial transition zone (ITZ) microstructure of concrete more efficiently, a method of coating aggregate surfaces by using several nanoparticles was evaluated in this study. The compressive strength, chloride penetration of sound, and pre-loading samples were assessed in relation to the type of coating materials used (slag, nano-CaCO3, and nano-SiO2) and the designed coating thickness (5, 10, and 15 mu m). The ITZ microstructure was quantitatively determined via Backscattered electron (BSE) image analysis. Results showed that the overall performance of concrete is highly dependent on the coating materials and the designed coating thickness. Increasing the coating thickness of slag and nano-SiO2 could improve the chloride penetration resistance but decrease the compressive strength. Using nano-CaCO3 to coat the aggregate leads to a significant reduction in the properties of the so-prepared concrete. Though coating inert fine particles around aggregate could disturb the initial particle packing and modify the ITZ, it is not able to improve the overall concrete properties. Coating aggregate could determine the ITZ microstructure, especially within the region that is around 30 mu m away from aggregate surface

Nanocellulose as building block for novel materials

This thesis describes the fabrication of novel green materials using nanocellulose as the building block. Bacterial cellulose (BC) was used as the nanocellulose predominantly in this work. BC is highly crystalline pure cellulose with an inherent fibre diameter in the nano-scale. A single BC nanofibre was found to possess a Young’s modulus of 114 GPa. All these properties are highly favourable for using BC as a nanofiller/reinforcement in green nanocomposite materials. In this work, the surface of BC was rendered hydrophobic by grafting organic acids with various aliphatic chain lengths. These surface-modified BC was used as nanofiller for poly(L-lactide) (PLLA). Direct wetting measurements showed that the BC nanofibre-PLLA interface was improved due to the hydrophobisation of BC with organic acids. This led to the production of BC reinforced PLLA nanocomposites with improved tensile properties. Nanocellulose can also be obtained by grinding of wood pulp, producing nanofibrillated cellulose (NFC). The surface and bulk properties of one type of NFC and BC were compared in this work. Furthermore, the reinforcing ability of NFC and BC was also studied and it was observed that there is no significant difference in the mechanical performance of NFC or BC reinforced nanocomposites. A novel method based on slurry dipping to coat sisal fibres with BC was developed to modify the surface of natural fibres. This method can produce either (i) a densely BC coating layer or (ii) “hairy” BC coated sisal fibres. Randomly oriented short BC coated sisal fibre reinforced hierarchical composites were manufactured. It was found that hierarchical (nano)composites containing BC coated sisal fibres and BC dispersed in the matrix were required to produce composites with improved mechanical properties. This slurry dipping method was also extended to produce robust short sisal fibre preforms. By infusing this preform with a bio-based thermosetting resin followed by curing, green composites with significantly improved mechanical properties were produced. BC was also used as stabiliser and nano-filler for the production of macroporous polymers made by frothing of acrylated epoxidised soybean oil followed by microwave curing

Nanoscale Voltage Enhancement at Cathode Interfaces in Li-ion Batteries

Interfaces are ubiquitous in Li-ion battery electrodes, occurring across compositional gradients, regions of multiphase intergrowths, and between electrodes and solid electrolyte interphases or protective coatings. However, the impact of these interfaces on Li energetics remains largely unknown. In this work, we calculated Li intercalation-site energetics across cathode interfaces and demonstrated the physics governing these energetics on both sides of the interface. We studied the olivine/olivine-structured LixFePO4/LixMPO4 (x=0 and 1, M=Co, Ti, Mn) and layered/layered-structured LiNiO2/TiO2 interfaces to explore different material structures and transition metal elements. We found that across an interface from a high- to low-voltage material the Li voltage remains constant in the high-voltage material and decays approximately linearly in the low-voltage region, approaching the Li voltage of the low-voltage material. This effect ranges from 0.5-9nm depending on the interfacial dipole screening. This effect provides a mechanism for a high-voltage material at an interface to significantly enhance the Li intercalation voltage in a low-voltage material over nanometer scale. We showed that this voltage enhancement is governed by a combination of electron transfer (from low- to high-voltage regions), strain and interfacial dipole screening. We explored the implications of this voltage enhancement for a novel heterostructured-cathode design and redox pseudocapacitors