Scientific Program

Conference Series Ltd invites all the participants across the globe to attend 7th World Nano Conference Cape Town, South Africa.

Day 1 :

Keynote Forum

Suprakas Sinha Ray

Chief Research Scientist and Director, DST-CSIR National Centre for Nanostructured Materials, South Africa

Keynote: Nanoclay minerals and plastics: tiny particles deliver big impact

Time : 10:00-10:30

Conference Series Nano 2016 International Conference Keynote Speaker Suprakas Sinha Ray photo
Biography:

Suprakas Sinha Ray was born in 1973 in India and completed his PhD studies at the University of Calcutta in 2001, and then postdoctoral fellow at ToyotarnTechnological Institute and Laval University studying the structure-property relationship in nanoclay-containing polymer nanocomposites. He started working onrnfundamental understanding to real applications of polymer-based nanostructured materials when he joined the CSIR as a group leader. These studies advancedrnand broadened when he appointed as a chief researcher and director of the DST-CSIR National Centre for Nanostructured Materials and growing to the presentrntime with postdoctoral fellows, students, collaborators and industrial partners worldwide. Currently, more than 80 researchers, engineers and technologists arernworking with him. Prof. Ray is one of the most active and highly cited authors (his articles have been cited more than 14700 times, google scholar, h factor 44),rnin the field of polymer nanocomposite materials and his work has been featured on various international journal cover pages on 14 different occasions. He is thernauthor of 2 books, co-author of 3 edited books, 15 book chapters on various aspects of polymer-based nano-structured materials & their applications, and authorrnand co-author of 250 articles. He also has 4 patents and 7 new demonstrated technologies shared with colleagues, collaborators and industrial partners. His teamrnalso commercialized 16 different grades of polylactide nanocomposites.

Abstract:

Modern technology continuously requires new, enhanced materials with special combinations of properties. In recentrnyears, researchers have managed to develop new materials at the nanoscale with excellent combinations of properties.rnThese new materials, called nanocomposites, possess enhanced properties and promise to soon replace classical materials usedrnin industry. With nanoclay minerals, it becomes possible to create plastics, for instance, that are not only stronger and lighter,rnbut are also scratch, ultraviolet and fire-resistant. This enables various advanced modern uses for plastics, such as lighter,rnstronger plastic parts for motor vehicles. Another application is using enhanced plastics for meat and other food packaging.rnTraditionally packaging plastic is made up of up to nine thin layers. With nanocomposite plastics, only three layers are neededrnwhich dramatically reduces the amount of plastic required. During nanocomposite formulation, nano-level dispersion is thernmost important characteristic to achieve, in order to have increased surface area for polymer-filler interaction, improvedrnco-operative phenomena among dispersed particles, and/or a higher degree of confinement effects. However, the primaryrnchallenge is to find the right chemistry to provide the best favorable driving force to disperse fillers at a nano-level. What thisrnmeans is that one needs to determine the right temperature, pressure and environmental conditions needed to successfully andrnoptimally allow a nanoclay to mix with a polymer. The DST-CSIR Nanocentre’s work in nanoclay minerals focuses primarilyrnon South African nanoclay mineral-enhanced plastics and efforts to create awareness of polymer nanocomposites (PNCs) inrnindustry as well as the development of products that will benefit the industry. The DST-CSIR Nanocentre is also putting furtherrnresearch efforts into processing and characterization techniques, properties and applications, and key research challenges andrnfuture outlooks in the development of South African nanoclay minerals-based multifunctional PNCs.

Keynote Forum

Malik Maaza

UNESCO UNISA Africa Chair in Nanosciences & Nanotechnology

Keynote: Nano-structured materials for energy efficiency & MINERAL BENEFICIATION WITHIN THE SOUTH AFRICAN LANDSCAPE

Time : 9:45 - 10:15

Conference Series Nano 2016 International Conference Keynote Speaker Malik Maaza photo
Biography:

Prof Dr M Maaza, holds an UG/PG degrees in Solid State Physics & Photonics from University of Oran-Algeria & Paris VI-France University Marie Curie. He holds a PhD in Quantum Neutron Optics, from the University of Paris VI-France. He has about 2-decades of experience in nano-sciences with a focus on nano-photonics applications. His interests include investigation of surface-interface phenomena, low dimensional systems and nano-materials using optical based spectroscopies & large facilities such as synchrotrons and neutron research reactors while in France, Austria, Russia & Germany mainly. Prof. Maaza has produced numerous formal scientific publications mentored several postgraduates. He has co-initiated the South African National Laser Centre (NLC) & was instrumental in initiating & implementing the African Laser Centre(ALC). Likewise, he has initiated the South African Nanotechnology Initiative (SANi) as well as the Nanosciences African Network (NANOAFNET) supported by the ICTP & UNESCO, IAEA and for which he is the chairman elect. Currently, he is the UNESCO-UNISA Africa Chair in Nanosciences & Nanotechnology. Prof. M. Maaza is a fellow of the African Academy of Science, fellow of the Royal Society of Chemistry-London, fellow of the Islamic Academy of Science as well as the New York academy of Science. Being a joint staff of UNISA & NRF, he is in charge of the Africa & International Relations desk of iThemba LABS-National Research Foundation. Prof. M. Maaza seats in several national and international commissions including the UNESCO-l’Oreal international award jury, the AU Obasanjo Africa award as well as the AU Nkwame Nkrumah African award in STI.

Abstract:

Nano-structured materials for energy efficiency & MINERAL BENEFICIATION WITHIN THE SOUTH AFRICAN LANDSCAPErn

Keynote Forum

Vladimir G. Chigrinov

Professor, University of Science and Technology.

Keynote: Liquid Crystal Alignment by Photoinduced Nanolayers

Time : 10:50

Conference Series Nano 2016 International Conference Keynote Speaker Vladimir G. Chigrinov photo
Biography:

Professor Vladimir G. Chigrinov is Professor of Hong Kong University of Science and Technology since 1999. He is an Expert in Flat Panel Technology in Russia, recognized by the World Technology Evaluation Centre, 1994, and SID Fellow since 2008. He is an author of 6 books, 25 reviews and book chapters, about 245 journal papers, more than 575 Conference presentations, and 102 patents and patent applications including 20 US patents in the field of liquid crystals since 1974. He got Excellent Research Award of HKUST School of Engineering in 2012.

Abstract:

Photoalignment possesses obvious advantages in comparison with the usually “rubbing” treatment of the substrates of liquid crystal display (LCD) cells [1]. The liquid crystal photoalignment is nano-technology, as the thickness of the alignment layer is about 2-15 nm. The photoalignment materials can be very useful for the new generation of the liquid crystals displays and photonics devices [2]:rnPhotoalignment possesses obvious advantages in comparison with the usually “rubbing” treatment of the substrates of liquid crystal display (LCD) cells. Possible benefits for using this technique include:rn(i) Potential increase of manufacturing yield, especially in LCDs with active matrix addressing, where fine tiny pixels of a high resolution LCD screen are driven by thin film transistors on a silicone substrate;rn(ii) New advanced applications of LC in fiber communications, optical data processing, holography and other fields, where the traditional rubbing LC alignment is not possible due to the sophisticated geometry of LC cell and/or high spatial resolution of the processing system;rn(iii) Ability for efficient LC alignment on curved and flexible substrates;rn(iv) Manufacturing of new optical elements for LC technology, such as patterned polarizers and phase retarders, high resolution optical sensors, tunable optical filters, polarization non-sensitive optical lenses, with voltage controllable focal distance, patterned nano-rods structures etc.rnNanolayer photoalignment can be very useful for the new generation of the liquid crystals devices as well as in new photovoltaic, optoelectronic and photonic devices based on highly ordered thin organic layers. Examples of such applications are light emitted diodes (OLED), solar cells, optical data storage, nano-rods and holographic memory devices. The novel and highly ordered layer structures of organic molecules may exhibit certain physical properties, which are similar to the aligned LC layers.rn The physical mechanisms and characterization of the photoaligning technique, as well as the application for liquid crystal devices, including displays and photonic devices will be reviewed. rn

  • Track 1: Nanomaterials Particles and Applications, Track 4: Nano Electronics, Track 5: Molecular Nanotechnology, Track 9: Reinforcements in Nanotechnology
Location: DoubleTree by Hilton Hotel Cape Town
Speaker

Chair

Bonex W Mwakikunga

DST/CSIR National Centre for Nano-Structured Materials, South Africa

Speaker

Co-Chair

Annie Chimphango

Stellenbosch University, South Africa

Speaker
Biography:

Yoshio Kobayashi received his B. S. (1988), M. S. (1990), and Ph. D. (1993) degrees from Tohoku University. He worked as a Research Associate at Tohoku University (1993-1997), as a Postdoctoral Researcher at Colorado State University (1997-1998), as a Postdoctoral Researcher at Kansas State University (1998-1999), as a Visiting Researcher at Universidade de Vigo (1999-2001), as a Research Associate at Tohoku University (2001-2002), and as an Associate Professor at Tohoku University (2002-2006). He is a Professor of Ibaraki University, and has published more than 150 papers in reputed journals.

Abstract:

X-ray imaging of mice using a colloid solution of Au nanoparticles that were coated with silica and subsequently surface-modified with carboxymethylcellulose (CMC) (Au/SiO2/CMC) was performed in this work. The silica-coating for Au nanoparticles and the amination for silica-coated particles were simultaneously performed in the presence of the Au nanoparticles with a size of 17.9 nm, which were prepared by reducing Au ions (III) with sodium citrate in water at 80°C and by surface-modifying the Au nanoparticles with (3-aminopropyl)-trimethoxysilane, by a sol-gel process using tetraethylorthosilicate, (3-aminopropyl)-triethoxysilane, water and sodium hydroxide (Au/SiO2-NH2). The surface modification of Au/SiO2-NH2 particles with CMC was performed by simply adding CMC with carboxyl groups that react with an amino group to the Au/SiO2-NH2 particle colloid solution. The as-prepared the Au/SiO2/CMC particle colloid solution was concentrated by centrifugation for measurements using computed tomography (CT). Figure 1 shows a photograph of the concentrated particle colloid solution and a transmittance electron microscopy image of the Au/SiO2/CMC particles in the concentrated colloid solution. Most particles contained a single core of the Au nanoparticles. Their particle size was 67.4±5.4 nm. A CT value of the Au/SiO2/CMC particle colloid solution with a Au concentration of 0.043 M was as high as 344±12 Hounsfield units (HU). This value corresponded to 8.0×103 HU/M with respect to the Au concentration, which was larger than that of Iopamiron 300, a commercial X-ray contrast agent. Mouse tissues were imaged following injection of the Au/SiO2/CMC particle colloid solution.

Zenixole R Tshentu

Nelson Mandela Metropolitan University, South Africa

Title: Polymer nanofibers for desulfurization of fuels
Biography:

Prof. Dr. Zenixole R. Tshentu is currently an associate professor of analytical/inorganic chemistry at the Nelson Mandela Metropolitan University (NMMU) in South Africa. He completed his PhD studies in Inorganic Chemistry at NMMU in 2005 and was offered a lectureship position at the Rhodes University Chemistry Department where he remained for 7 years until his move back to NMMU in 2013 as associate professor. He has published 64 articles in peer-reviewed national and international journals as well as three book chapters. He has experience in the solid state and solution studies of transition metals chemistry as well as using inorganic/organic polymer materials in separation technology and in heterogeneous catalysis. He has been involved in several projects such as designing organic extractants for the separation of base metals and platinum group metals via solvent extraction and ion exchange processes, designing ligands for the stabilization of therapeutic metals in biological systems, and designing catalysts for selective oxidation of sulfur compounds in fuels followed by selective adsorption of sulfones using molecularly imprinted polymers. The functional chemistry is typically hosted in microscale materials as well as nanomaterials such as nanofobers. He terms his philosophy “the quest for selectivity and specificity”.

Abstract:

This presentation will uncover progress in the fabrication and catalytic applications of various metal-based catalysts immobilized unto nanofibers. It will also highlight the challenges associated with the use of electrospun nanofibers in catalysis. Herein, we also explore the possible use of polymer-supported oxovanadium(IV)-based catalysts for the oxidation of organosulfur compounds in hydro treated fuel followed by adsorption of polar sulfone compounds using molecularly imprinted polymers in a form of nanofibers. The application of the oxidation and the adsorption steps to a mildly hydro-treated diesel sample has been demonstrated to reach less than 2 ppm S content.

Speaker
Biography:

Rodrigo Segura received his PhD. Degree in Chemistry at the Universidad de Concepción in 2004. Since 2009, Rodrigo Segura is Professor of Inorganic Chemistry in the Institute of Chemistry and Biochemistry at the Universidad de Valparaíso. His main fields of research encompass Synthesis, Characterization and Properties of Nanomaterials. Lasts years He has been devoted to the study of Carbon Nanostructures, specially the synthesis of carbon nanotubes alloyed with metal and semiconductor nanoparticles for sensing and energy applications.

Abstract:

Graphene layers represent a good candidate to develop composed photocatalysts. Due to its high electronic conductivity It can prevent the recombination of the electron-hole pair and act as a doping agent and even extend the range of light absorption of a semiconductor such as the TiO2. In this contribution thin TiO2 layers were grown on few layers graphene (FLG) in order to prepare hybrid photocatalysts with the properties of both materials. FLGs were synthesized by chemical vapor deposition (CVD) at 1000 °C using acetylene as carbon source and copper as substrate. After synthesis the FLGs were transferred to silicon substrates and TiO2 layers were deposited on FLG by decomposition of titanium tetraisopropoxide in a CVD system. The photocatalytic performances of these materials were evaluated by measurements of photocurrent in a 3-electrode cell assembly by using a solar simulator and a potentiostat. The photocurrent results show that the FLG is very electroactive presenting a similar behaviour under both dark and illumination; on the other hand the TiO2 layers grown over silicon show the typical behaviour of a photoactive semiconductor since these samples exhibit a raise in the current with the applied potential only when It is illuminated. The hybrid Si-FLG-TiO2 material present in principle a similar behaviour of Si-FLG but when we made a chronoamperometry alternating dark and light cycles an discounting the dark response It is possible to observe a similar performance than Si-TiO2 sample. Both materials graphene and titanium dioxide have preserved their properties after the assembly. The authors acknowledge the financial support of Fondecyt 1121203.

Shivani Bhardwaj Mishra

University of South Africa, South Africa

Title: Nanoscale sovereignty for waste water remediation

Time : 12:05-12:30

Speaker
Biography:

Prof. Shivani Bhardwaj Mishra has completed her PhD at the age of 30 years from Jamia Millia Islamia, New Delhi and postdoctoral studies from University of the Free State & University of Johannesburg. She is the Professor of Nanotechnology at University of South Africa which is a premier University. She has published 2 books, 30 book chapters and around 65 papers in reputed journals and also serving as reviewer and member of scientific board of repute.

Abstract:

Nanomaterials offer unique and unexpected material properties and this is due to the fact that at nanoscale, materials can be ‘tuned’ to build faster, lighter, stronger, more efficient and stimuli responsive materials. Such properties of nanomaterials provide a platform for eco-toxicological based research investigations. Presently, there is limited knowledge and understanding for a number of major uncertainties with respect to chemical behavior, chemical and biological interactions and toxicological properties of engineered nanomaterials. Clean water is always essential which often calls for a cheap and efficient water purification system. Nanomaterials are being used to develop more cost-effective and high-performance water treatment systems. Remediation is the process of pollutant transformation from toxic to less toxic in water. The focus of the talk will be the recent advancement and development of the nanoscale sovereignty for the waste water remediation.

Arjun Maity

DST/CSIR Innovation Centre, South Africa

Title: Water Purification using Nanotechnology
Speaker
Biography:

Dr. Arjun Maity earned his PhD degree in chemistry from University of Calcutta, India. After that he joint at DST/CSIR National Centre for Nanostructured Materials (NCNSM), Materials Science and Manufacturing, Council for Scientific and Industrial Research (CSIR), as a post-doctoral fellow. In 2009, he joint at Polymers and Composites department, CSIR, as a senior Researcher. Currently he is principal researcher at NCNSM, CSIR. His research interests are synthesis and engineering of nanocomposites for environmental applications. He has published more than 88 papers in reputed journals.

Abstract:

In recent years, extensive efforts have been devoted to develop nanostructured materials with unique reactivity and functionality for environmental clean-up. The presence of heavy metals such as Cr, Hg, As, Pb, Ni, Co etc. in both fresh water sources and industrial wastewater, is a critical health and environmental issue due to their high toxicity and bioaccumulation through the food chain and hence in the human body. Nowadays, smart polymeric nanostructured materials based on polyaniline and polypyrrole are promising materials in water treatment because they are cheap, easy to prepare, non-toxic, it displays high adsorption capacity and it also has ion exchange property. Recently, we have developed conducting polymer based nanocomposites via in-situ polymerization technique, for the removal of highly toxic pollutants. Adsorption of pollutants on the surface of the adsorbent was confirmed by the ATR-FTIR and XPS. XPS studies also provided mechanistic aspects in detailed. Desorption studies showed that in spite of the limited recovery of the adsorbate form the adsorbent; the regenerated adsorbent could be reused successfully without appreciable loss of its original capacity. On the other hand, spent adsorbents could be re-used for different applications: catalysis, antimicrobial activity and gas sensor.

Speaker
Biography:

Dr. Annie Chimphango is a Senior Lecture at Stellenbosch University, Department of Process Engineering. She holds a Master Degree in Agricultural and Bioresource Engineering from McGill University, Canada and a PhD in Chemical Engineering from Stellenbosch University.. She has published papers in reputable Journals on enzymatic modification of hemicelluloses to form nano-hydrogels and their application in pulp and paper and their use as encapsulation matrix for bioactive substances . Her research focus is on value addition to agro-residues and process waste through production of high value materials such as hydrogels and nanocellulose using biological methods.

Abstract:

Xylan solubility properties were modified using enzymatic and chemical methods to produce nanohydrogels. The enzymatic modification involved recombinant α-L-arabinofuranosidase that selectively removed arabinose side chains whereas the chemical method involved the coacervation through neutralization process that involved hydrochloric acid and sodium hydroxide. Furthermore, the effect of time, xylan concentration and presence of plasticizers, thus polyethylene glycol 1000 (PEG 1000), polyoxyethylene (20) sorbitan monolaurate [Tween 20], on particle size, surface charge and stability was investigated. The mean particle diameter, zeta potential, were measured by a Zetasizer Nano ZS90 that used Dynamic light scattering. In addition, the morphological profile of the particles was assessed using a microscope equipped with a micrometer grid, connected to a camera. The sugars from the enzymatic hydrolysis were analyzed using the High Performance Liquid Chromatography, Doinex Ultimate 3000, equipped with Prevail Carbohydrate ES analytical column, and ELS2100 Evaporative Light Scattering detector. Tween 20 plasticizer prevented aggregation of the particles. Over 80% of the particles formed using the chemical method attained a mean diameter ranged from 153- 853 nm and a zeta potential of -28mV. On the other hand the nano particles with sizes as low as 21 nm were produced by enzymatic method with Zeta potential of close to -20 mV. The presence of plasticisers during formation of nano particles to some extent prevented aggregation behavior of the nano-particlesr. In enzymatic production, size distribution was dependent on xylan concentration. These results demonstrates the potential to diversify industrial application of xylan.

Biography:

Ololade Olatunji is a Lecturer at the University of Lagos, Nigeria. She completed ar PhD in chemical engineering department Loughborough University UK. She has a number of publication in the area of microneedles for transdermal drug delivery and is recently editor of the book Natural Polymers industry techniques and application, Published by Springer (in production). She is also guest editor of the special Issue on Microneedles in the MDPI journal of Pharmaceutics. She previously served as Senior Research officer at the Federal Institute of Industrial Research Oshodi (FIIRO) in Lagos, Nigeria.

Abstract:

A fish scale biopolymer blended with nanocellulose crystals is used for production of microneedles by appliying mechanical press microfabrication, and the effect of nanocelullose on the microfabrication, water absorption, moisture stability and mechanical properties of the microneedles are reported. The results show that microneedles produced from the nanocellulose loaded fish scale biopolymer requires higher temperature for micromoulding (80 o C + 5 o C) than microneedles from only fish scale biopolymer which were mouldable at 50 o C + 5 o C. The mechanical properties of the fish scale biopolymer nanocellulose (FSBPNC) films showed that the addition of nanocellulose (NC) resulted in lower elongation and higher tensile stress compared to fish scale biopolymer (FSBP) films. The nanocellulose also prevented dissolution of the needles and absorbed up to 300 % and 234 % its own weight in water (8 and 12 % w/w NC/FSBP), whereas FSBP films dissolved completely within 1 minute, indicating that the FSBPNC films can be used to produce microneedles with prolonged dissolution rate. FTIR spectrometry of the FSBP films was compared with the FSBPNC films and the NC gels. The FTIR showed typical peaks for fish scale polymer and nanocellulose with evidence of interactions. SEM micrographs showed relatively good dispersion of NC in FSBP at both NC contents corresponding to 8% and 12% w/w NC/FSBP respectively.

Speaker
Biography:

Kaviyarasu obtained his Master of Science (M.Sc.) & Master of Philosophy (M.Phil.) degree in Physics from Loyola College (Autonomous), Chennai, affiliated to the University of Madras, India. He has carried out research on Semiconductor Metal Oxide Nanocrystals & Synthesis and characterization of Hybrid Nanomaterials for energy applications. During the course of his research work, he has published 33 papers in International/National Journals and presented 35 papers in National and International conferences. Currently his a Postdoctoral researcher at UNESCO-UNISA Africa Chair in Nanosciences/Nanotechnology Laboratories, College of Graduate Studies, University of South Africa (UNISA), South Africa. My research is directed primarily toward developing and applying modern material design for the understanding and prediction of Physico - Chemical processes ranging from the molecular to the nanoscale to full-size engineering applications, using a multidisplinary approach that Physics, Chemistry, and Materials science. Work is closely coupled with synthesis and characterization of Hybrid Nanomaterials at the Center for Nanoscience and Nanotechnology, where scientific focus is on using theory and multiscale simulations and modeling for providing interpretive and predictive frameworks for virtual design and understanding of novel nanoscale materials with specific and/or emergent properties. This vision is possible through a multi-pronged, holistic, and tight integration with Materials Research Division (MRD) distinctive capabilities in precision experimental synthesis and characterization alongside leadership class computing. Understanding how atomic scale structure, confinement, and quantum mechanical effects impact electronic processes within these nanostructures and across interfaces to enable the design and synthesis of materials with prescribed functional (physio-chemical) properties. Very thin sheets of a material can exhibit greatly enhanced properties such as increased electrical conductivity as compared with the bulk and are well suited for applications in new electronic devices. Our goal is to understand how to design and control the nanoscale organization of macromolecular nanomaterials and their nanocomposites in order to achieve improved structure, properties, and functionality. The iThemba Laboratory for Accelerator-Based Sciences (iThemba LABS) where he studies materials for energy applications. His research interests include bulk and nanoscaled materials for solidstate- physics, and multifunctional metal oxide nanomaterial.

Abstract:

In the present work, we synthesized ZrO2:PbO2 nanorods samples were prepared by solvothermal process and the physiochemical properties of ZrO2:PbO2 nanoparticles were determined by using X-ray diffraction (XRD), ultraviolet–visible spectroscopy (UV– vis), Transmission electron microscope (TEM), Energy dispersive X-ray spectrometer (EDX) and X-ray photoelectron spectroscopy (XPS). The photocatalytic activity was evaluated by the degradation of methylene blue (MB) dye under UV and visible light irradiation. The solvothermal made ZrO2 treated PbO2 nanorods showed the highest photocatalytic activity under both UV and visible light irradiation. The addition of the ZrO2:PbO2 resulted in the formation of partial monolayer of ZrO2 doped ZrO2:PbO2 nanorods and an increase of the anatase phase stability. The XPS results reveal that the calcinated ambiance affected the distribution concentration of surface and interface species in ZrO2 and Zr-doped PbO2, such as surface oxygen and Pb3þ sites, thus improving photo catalytic activity.

Speaker
Biography:

Bella Mellisani completed her undergraduate program in Chemistry at Tanjungpura University. Currently, she is working on her MSc Program in Chemistry at Gadjah Mada University Yogyakarta, Indonesia. She receives scholarships from The Indonesia Endowment Fund for Education, Ministry of the Finance Republic of Indonesia. Her work focuses on the synthesis of functional nanoparticles.

Abstract:

Colloidal Ag nanoparticles are of interest for many researchers due to their vast potential applications. In this work, the colloidal Ag nanoparticles were prepared in the polyvinyl alcohol (PVA) solution as a capping agent using ascorbic acid as reducing agent. PVA with a molecular weight of 13,000-23,000 (PVA-I) and 145,000 (PVA-II) was used. The concentration of silver nitrate and ascorbic acid was set at 3.0 x 10-4 mol L-1 and 6.0 x 10-4 mol L-1, respectively. The reaction between Ag+ ion and ascorbic acid in PVA was performed at 80°C. After 5 min of heating, the solution color changed from colorless to yellow to indicate the formation of silver nanoparticles. The optimum concentration of PVA-I and PVA-II was found to be 1.0% and 0.25%, respectively. The surface plasmon resonance (SPR) absorbance of the colloid in PVA-I has λ-max of 416 nm, with full-width-half-maximum of 94 nm. The SPR absorbance of the colloid in PVA-II has λ-max of 413 nm, with full-width-half-maximum of 73 nm. The colloids are stable for four weeks, which show a decrease in the SPR absorbance by 10.57% in PVA-I and 8.45% in PVA-II. Using PVA-II, the synthesis required a lower concentration than that of using PVA-I. The colloidal Ag nanoparticles in PVA with high molecular weight have smaller particle size than that in PVA with lower molecular weight.

Biography:

Aline Simo has completed her PhD at the age of 29 years from Western Cape University and was awarded the l`Oreal Unesco For Women in Science. She is currently doing her postdoctoral studies at UNISA University, College of Graduate Studies. She is working on various V-based systems functional materials and she has bringing new insight regarding the potential sensing application aspect of the vanadium oxide material at room temperature

Abstract:

Porous polycrystalline resistors made of metal oxides are highly demanded as semiconductor gas sensors. The operating at low temperature requires narrow band gap resistive gas sensors amongst which vanadium oxides have been found to be suitable for gas sensing materials. This is due to their ability to be used as catalysts in oxidation reaction and to form different lower oxides stoichiometry of the VO cubic lattice derived from V2O5. Hydrogen (H2) is one of the attractive energy sources to succeed the current carbon based energy, with the highest specific energy content of 141.79 MJ/kg and high risk of explosions while handling its storage and usage. In relation to H2 economy, various 1-D nanomaterials have been investigated as ideal candidates for gas sensing applications. Well established gas sensing materials such as SnO2, ZnO, WO3, have shown higher sensitivity and selectivity efficiency at high temperature resulting in significant power consumption with addition to their complexities in device integration. VO2 oxide nanobelts are demonstrated to be effective hydrogen gas sensors at room temperature with sensitivity as low as 14 ppm. The nanobelts (ultralong belt-like) nanostructures could be an ideal system for fully understanding dimensionally confined transport phenomena in functional oxides and for building functional devices based on individual nanobelts.

Biography:

B.T. holds a PhD in Chemistry from the University of the Western Cape, South Africa. He is currently a DST-NRF Innovatiuon Postdoctoral fellow at the UNESCOUNISA Africa Chair for Nanosciences & Nanotechnology, and is hosted by the Materials Research Dept’t of iThemba LABS. He has published more than 16 papers and proceedings in ISI peer reviewed journals and conference proceedings. His interests lie in the area of gas sensing, electrochromism, energy storage, solar cells.

Abstract:

P-type Bunsenite NiO powders with an average crystallite size of 21 nm (as shown by x-ray diffraction analysis) were produced via biosynthesis and heat treatment, using aqueous extracts from flowers of the plant Callistemon viminalis. SEM showed that the NiO powders consisted of particles with sizes in the 20-35 nm range while XPS confirmed the formation of highly pure NiO. From Raman spectroscopy, strong 1 phonon vibration at 507.4 cm-1and the existence of a broadened 2-phonon band of reduced intensity at 1096 cm-1 confirmed that biosynthesized NiO powders were not only defect-rich/ rich in surface effects but were also nanosized with dimensions less than 100 nm. Using UV-Vis-NIR spectroscopy the optical band gap for a spin coated thin film of NiO obtained by spin coating unto glass the green coloured Ni2+-containing aqueous extract of Callistemon viminalis red flowers, then annealing in air, was calculated to be 3.35 eV. A cyclic voltammetric study of the redox processes in thin films of the NiO nanopowders on Ni showed the redox processes to be quasi-reversible with the films showing good potential for pseudocapacitance. From our calculations the specific capacitance of the NiO thin films on Ni was estimated at 101 F/g, a value close to that reported in the literature. This method demonstrates that the use of natural plant extracts can be a cost-effective and environmentally friendly alternative to preparing Nickel oxide nanoparticles that can be of use in a variety of energy storage applications.

Speaker
Biography:

Sanele Nyembe has completed his Msc from University of Witwatersrand, Johannesburg and currently doing his PhD with the same university. He works as a Scientist at Mintek-Nanotechnology Innovation Centre, Research and Development. He has published 2 papers in reputed journals from his PhD work and 1 publication from other projects.

Abstract:

Temperature Programmed Desorption (TPD) is crucial spectroscopic method used to determine thermodynmic and kinetic parameters of desorption processes. Sorption of gases from Group III-V semiconductor nanowires is a fascinating area of nanoscience, because they reveal potential of gas sensing. These nanowires have a potential to be used in various applications such as photonics, electronics including micro and nanoelectromechanical systems (MEMS and NEMS). They have relatively tuneable small direct bandgaps (Indium Phosphide (InP) = 1.34 eV) which makes them suitable for use in optoelectronic devices as well. InP surface in particular, has an interesting electron reach/deficiant active sites that could form part of the gas binding sites. The sorption of gases such as Methane (CH4), Carbon Monoxide (CO) and Nitric Oxide (NO) were studied using TPD. In this study, it was discovered that InP nanowires binds through chermisoption to both CO and NO and binds very weakly through physisorption to CH4. The heat of desorption enthalpies were found to be 140 kJ/mol, 80 kJ/mol and 48 kJ/mol for CO, NO and CH4 respectively. The experimental enthalpies were compared to the theoretical values (binding energies) obtained through molecular modelling. The binding modes of the gases to the surface of InP nanowires were studied by Diffuse Reflectance Infrared Fourie Transorm Spectroscopy (DRIFTS) together with adsorption modelling. This study reveals the nature and strength of interaction between NO, CO, CH4 gas molecules on the surface of InP nanowires and the sorption temperature range.

Speaker
Biography:

Nolubabalo Matinise has completed her PhD in 2014 at the University of the Western Cape under electrochemistry in Sensorlab research group. Her PhD research involves sensors and applied electrodynamics of nanomaterials. She is a postdoctoral fellow for two years now at iThemba labs under material research department. Her research interests include morphologically, optical, surface modification and dimensionally controlled synthesis and characterization of nanomaterials, bimetallic, polymers, development of new high efficiency and low cost transitional metal nanoscale catalysts, as well as investigation of the relationships between their structures and properties, and exploring their applications in heterogeneous catalysis, electrochemistry, energy conversion or nanoscale electronic devices.

Abstract:

The research work involves the development of better, inexpensive, reliable, easily and accurate method for the fabrication of novel metal oxide nanoparticles-based nanocomposite materials through green synthetic method. The characterization of the nanostructured nanocomposite materials will use various techniques, including High Resolve Transmission Electron Microscope (HRTEM) technique for the physical property such as morphology, particle size, structure and particle distribution; Fourier transform infrared spectroscopy (FTIR) for the composition and purity of the product; Ultraviolet-vis spectroscopy (UV/Vis spectra) Photoluminescence (PL) analysis for optical studies; X-ray diffraction (XRD) for purity and crystalline structure; Thermal studies by DSC/TGA technique for change phases and weight loss and Electrochemical methods such as cyclic, square wave voltammetry and electrochemical impedance spectroscopy for the evaluating the electrochemical activities. The electrochemical dynamics as a sensor or electrochemical catalyst of the nanostructured crystalline multi-metallic will be studied using cyclic voltammetry and Electrochemical Impedance Spectroscopy (EIS). The development of electrodes is prepared by drop coating the metal oxide nanoparticles-based nanocomposite materials on the surface area of electrode (Glassy carbon/Platinum) electrode for electrochemical application.

Speaker
Biography:

Xolile Fuku is a Chemist and obtained his PhD in 2014 at the University of the Western Cape, SensorLab Research Group. Presently, he doing his Post-doctoral studies at iThemba LABS under UNISA/UNESCO African chair. His research platform is in nanotechnology, material science and electro-analytical chemistry, which focuses on fundamental and applied electrodynamics of materials and sensors.

Abstract:

Bimetallic nano-oxides on polyvinylpyrrolidone will be synthesised by simple and facile green route. The green synthesised nanocomposite will be characterised by different techniques and methods. Detailed structural, compositional, optical, photoelectrochemical and electrochemical properties of the obtained nanomaterials will be analysed by X-ray diffraction (XRD), high resolution-transmission electron microscopy (HR-TEM), ultraviolet-visible spectroscopy (UV-Vis), impedance spectroscopy (EIS), cyclic voltammetry (CV), galvanostatic charge-discharge (CDG) and FTIR spectroscopy techniques. Ni substrate and boron doped diamond (BDD) will be used as electrochemical transducer for the fabrication of the potential energy storage devices. Furthermore, the nanocomposites will be used as a catalyst and in other applications such as solar absorbers.

Biography:

Ms.Denisha Gounden has completed her undergraduate (BSc. Biochemistry, Chemistry) and honors (BSc. (Hons) Chemistry) degrees at the University of KwaZulu-Natal (2010-2014). She is currently pursuing her MSc. degree. Her first scientific paper was published in 2015, which was based upon her honors research entitled, the “Impact of spiked concentrations of Cd, Pb, As and Zn in growth medium on elemental uptake of Nasturtium officinale (Watercress)”.

Abstract:

Electrochemistry has been widely recognized as a simple and yet highly efficient method for the fabrication of low cost, portable sensors for onsite detection of heavy metals. This study explores the use of iron oxide nanoparticles incorporated with metallophthalocyanines for the selective detection of heavy metal ions from aqueous solution. The iron oxide nanoparticles (NPs, Fig 1a) were synthesized using a co-precipitation method and later coated with silica via a modified Stober method. The synthesized nanoparticles were characterized using IR, EDX, SEM, TEM, XRD, XPS and Mossbauer spectroscopy. These characterization techniques confirmed NP formation, silica coating and super paramagnetism. Phthalocyanines have been reported to enhance electrochemical sensitivity of numerous electrochemical reactions due to their extensive π-system. The Pcs were synthesized and characterized using IR, UV-vis, MCD and MALDI-TOF. It is expected that the impressive properties of iron oxide nanoparticles coupled with the electro-active Pcs will have a synergistic effect that will enhance the sensitivity of heavy metal detection. The electrochemical performance of this hybrid system towards the selective detection of heavy metals is explored.

Phumlani Tetyana

Mintek Nanotechnology Inovation Centre, South Africa

Title: Aqueous Synthesis of Copper Sulfide Nanoparticles for Biological Applications
Biography:

Phumlani works as a research scientist in the DST/Mintek Nanotechnology Inovation Centre (DST/Mintek NIC), at Mintek. He holds an MSc degree in Physiology and is currently registered for a PhD degree in Chemistry and Nanosciences at the University of Witwatersrand.

Abstract:

Innovation in the field of nanotechnology has shown potential to unlock key advances in the detection, diagnosis, treatment and management of infectious diseases. Nanotechnology has pioneered the miniaturization of structures and materials to a nanometre scale, forming nanostructures that are suitable to explore biological processes. Amongst nanomaterials, quantum dots (QDs) are gaining popularity in biological applications. Quantum dots have been applied in biological assays as fluorescent probes for disease diagnosis in vitro and imaging replacing conventional fluorophores (organic dyes and fluorescent proteins) thereby improving assay sensitivity. Amongst these QDs, Copper Sulfide (CuxS) nanoparticles have been the most widely used nanomaterial since they are non-toxic, inexpensive and stable under ambient conditions. Herein, we report the synthesis of glutathione (GSH) capped copper sulfide quantum dots for use in biological applications. Biocompatible copper sulfide nanoparticles of different shapes and sizes were synthesised in aqueous media using a one pot hydrothermal synthesis route. These nanoparticles were found to be less toxic when tested on mammalian cells in the MTS assay, and therefore qualify for use as targeting agents in biological assays.

Biography:

Fredrick Okumu is a 31 years old doctoral student at Cape Peninsula University of Technology (CPUT), faculty of applied science and has recently submitted his PhD thesis for examination. He is currently working as student support staff at CPUT as a retention officer. He has published 6 papers in reputed journals.

Abstract:

Core shell bimetallic nanoparticles of Ag-Pt of varying ratios (1:1, 1:3 and 3:1) band gaps were studied using UV-visible spectroscopy (UV) and cyclic voltammetry (CV) and further characterized using X-ray diffraction (XRD) technique. Tauc’s model was employed for optical band gap studies typical of direct band gaps while electrochemical band gap was investigated under CV based on Breda’s equation. Band gap of nanoparticles were found in the range of 3.55 eV to 4.02 eV for optical and 1.45 eV to 1.80 eV for electrochemical measurements. The expansion in each case could be attributed to quantum size effect. Band gap increase in the bimetallic nanoparticles ratios was consistent in both electrochemical and optical results relative to monometallics. The fact that electrochemical band gaps were found to be smaller than the optical band gaps with an average factor difference above 1 was attributed to solvation and electrode surface coverage effects. These band gap values suggest better electroactivity of the nanoparticles. Although the electrochemically determined band gaps were found to be lower than the optical band gap, in most cases values portrayed similar trends. These results depict nanoparticles with band gaps within semiconductor range for most materials. XRD patterns depicted crystallinity in all the synthesized NPs with confirmation of the face centred cubic structure. Comparison of transmission electron microscope (TEM) data showed that the band gaps were nanoparticle size-dependent with an inverse relationship observed and this was attributed to the quantum confinement effect.

Chiara Busa

University of Birmingham, UK

Title: Low Temperature Mechanical Press Method
Speaker
Biography:

Chiara Busa’ completed her scientifically oriented secondary school in 2005; she obtained her BSc in 2009 in Chemistry and Master in Chemical Science, graduating in 2012, at university of Florence(IT); She moved to Sweden, where she was consulting in Applied Physics at Chalmers University of Technology(SE); in 2014, she joined Pola Goldberg-Oppenheimer group(Advanced Nano-Materials, Structures and Application) to undertake her PhD in Chemical Engineering at the University of Birmingham(UK).

Abstract:

DNA nanotechnologies had a major development during the last two decades. Their real potential and versatility began to be investigated and understood with the synthesis of a polyhedron-structured DNA molecule. Due to the intrinsic properties of DNA and developments in sequence design, different polyhedral, either in shape and/or dimensions were synthesised. Custom-tailored properties and high yields are characteristic of these structures. In this project, the main work was represented by the disposition, anchoring and imaging of self-annealed DNA polyhedron, with high yield and stability of the molecules. The last step consists in formation a gold layer on top of the pre-annealed DNA polyhedron, in order to build a specifically-patterned gold materials with optical responses. According to previous studies, specific strands of DNA sequence were designed, to anneal and form a geometric 3D tetrahedron, with >90% yield. The anchoring of the DNA structures was carried out on TEM carbon grids, where the structures where demonstrated to firmly immobilise on the surface. Hence, the gold layer deposition was carried out by electroplating, due to the conductive nature of the TEM grid employed. AFM and TEM are the predominant techniques carried out for characterizing the structures and their disposition on the substrates in each stage of this work.

Speaker
Biography:

Aruna completed her MSc in Manchester working on a project titled “Synthesis of organelle-specific inhibitors of Deubiquitinating enzymes” in 2013. She is currently a BBSRC funded PhD student on the Doctoral Training Partnership also at the University of Manchester under the supervision of Dr Louise Natrajan and Dr Sam Hay. Aruna has also spent time at the National Nuclear Laboratory for several months working on separation of radionuclides.

Abstract:

Upconverting nanophosphors (UCNPs) are typically composed of an inorganic lattice doped with luminescent lanthanide ions and demonstrate the ability to convert long-wavelength excitation in the near-infrared (with wavelengths of typically 800-1000 nm) into higher energy visible luminescence. Such materials display several advantages in analytical applications, in comparison to other fluorophores, including low autofluorescence and scattering of excitation radiation, reducing background noise. Lanthanides display multiple very specific emission bands allowing careful tuning of the emission profile of the UCNPs. These properties make then suitable candidates as the donor species in luminescence resonance energy transfer (LRET) in chemical sensors and biosensors. This project details the design of a chemical sensor based on Gd4O2S:Yb,Tm and Gd4O2S:Yb,Er UCNPs. A proof of principle technique for the detection of uranyl(VI) species in aqueous solutions has been developed. Luminescence resonance energy transfer efficiency is used to sense these species. Tm3+ and Er3+ doped upconversion nanophosphors exhibit emission bands at 475 nm and 410 nm respectively, which can be monitored by ratiometric analysis, relative to other emission bands. Recent work consists of improving the sensitivity of the current system to detect lower concentration of uranyl(VI) species.

Speaker
Biography:

Chloë is a final year PhD student of the North West Nanoscience Doctoral Training Centre (NoWNano DTC) at The University of Manchester, UK. She currently has two publications and was awarded the TA Students Application Award in 2014. Chloë also has industrial experience working in pharmaceutical R&D on the development of inhaled therapeutics to reduce rejection in lung transplant patients and monitoring drug manufacture for the Indian sites of a large generic pharmaceutical company.

Abstract:

Rare-earth upconversion nanophosphors (UCNPs) are rapidly emerging as an important class of nanoparticles with potential uses in bioimaging, biosensing and therapeutics. When UCNPs are excited with near infra-red (NIR) light they exhibit efficient photoluminescence in the visible spectrum due to photon upconversion (UC). Their emission spectrum can be tuned by doping the UCNPs with various lanthanides, allowing for multiple sharp, line-like emission bands, long emissive lifetimes and, as a consequence of their UC, no autofluorescence. These properties make UCNPs particularly promising as biosensing probes. The aim of this project is to develop sensitive and selective UCNP-based biosensing systems. Preliminary work involved investigation of the interaction between the flavin-containing enzyme pentaerythritol tetranitrate reductase (PETNR) and the UCNPs. Promising results have been obtained from this system; UCNPs are able to detect the presence of FMN, the intrinsic cofactor of PETNR, through energy transfer. Using this energy transfer process enzyme turnover can be indirectly monitored by ratiometric methods due to the multiple bands in the UCNP emission spectra. Work is now focused on improving the sensitivity of this UCNP-enzyme biosensing system.

Speaker
Biography:

Dr. Siek-Ting Yong obtained her Ph.D. degree in Chemical Engineering from the National University of Singapore. She is a senior lecturer in Monash University Malaysia Campus. Her research interests include fuel reforming, direct carbon fuel cell, carbon capture, and membrane separation.

Abstract:

It is crucial to achieve high purity of Hydrogen for the use in renewable energy industry. Purification of Hydrogen using dense hollow fiber is one of the common ways employed. The transport mechanism of Hydrogen from one side of the membrane to the other side involves a series of sequntial steps. It started with the adsorption and dissociation of Hydrogen molecules, then absorption and diffusion of protons, followed by recombination and desorption of Hydrogen molecules. The dissociation of Hydrogen molecules on the membrane surface plays the most critical role in the overall trasnport mechanism. In this work, a novel post-treatment method using aluminium nitrate solution was developed. The objective is to achive high Hydrogen permeability and ideal selectiviy in parallel by improving the morphology of hollow fiber via mobility control of polymer chain. Morphologies analyses including FTIR-ATR, DSC and EDX were carried out and the mechanism of chemical surface modification was proposed.

Speaker
Biography:

Devika chitrani has completed his PhD from University of Toronto. She was avarded the faculty gold medal and gold medal for physics at her BSc convocation. She is the director of Nanoscience and Technology Development Laboratory at Ryerson University. He has published more than 30 papers in reputed journals in few years time and has been serving as an editorial board member for six Nano journals. Her work was featured on the cover of radiation research and Nan-Micro letters. Her group is very dynamic and published 14 papers and 3 book chapters in last two years alone. Her publications has received over 4000 citations in the last few years.

Abstract:

The interface between nanotechnology and biology needs to be well understood for improved outcome in medical applications. In other words, we need to know the interaction of nanoparticles with individual cells and tissue for improved outcome in diagnosis, imaging and therapeutic techniques. Among other nanoparticles, gold nanoparticles (GNPs) are emerging as a novel tool to improve existing cancer therapeutics. GNPs are being used as radiation dose enhancers in radiation therapy and as well as an anticancer drug carrier in chemotherapy. However the success of GNP-based therapeutics depends on their ability to penetrate and distribute homogenously in tumor tissue. In this work, multicellular layers (MCLs) were grown to model the post-vascular tumor environment. GNPs of 20 nm and 50 nm diameters were used to elucidate the effects of size on the GNP penetration and distribution dynamics. Though the GNPs were able to penetrate into the tumor tissue, their penetration was inversely proportional to the GNP size. Similar to in vivo tissue, the MCLs exhibited a much more extensive extracellular matrix (ECM) than monolayer cell cultures. This increased ECM created a barrier for NP transport. Smaller NPs penetrated better compared to larger NPs. This model tissue structures are better tools to optimize NP transport through tissue before using them in animal models. This work highlights the importance of both the improved tissue model provided by MCLs as well as the importance of GNP functionalization in cancer therapeutics. A multifunctional platform based on gold nanostructures holds an array of promising directions for cancer research.

Speaker
Biography:

Mike Scurrell has worked extensively in catalysis for over 40 years and has published some 170 papers in various areas. He is Emeritus Professor of Chemistry at the University of the Witwatersrand in Johannesburg and is also Research Professor at the University of South Africa in Johannesburg in South Africa. He held previous positions at the University of Edinburgh, Scotland, the Technical University of Denmark, the CSIR, South Africa and at Anglo American Research Laboratories. His current interests are in improving heterogeneous catalysts through the use of innovative approaches in nanosynthesis.

Abstract:

Gold catalysts for CO oxidation have been very well studied, particularly using titania as a support. Small nanoparticles of gold are implicated in the catalysis and support effects must also be present because there is a marked activity dependence of the support. Only gold-perovskites appear to show activity essentially identical to that of Au/titania, depending on the nature of the A and B elements present in the Au/ABO3 structure. The low temperature activity of gold for the oxidation of hydrocarbons has also been demonstrated and it has been suggested that gold may well form the basis for active autoemission control catalysts for use at low temperatures, under cold start conditions. The economics of using gold rather than the platinum group elements are also considered to be attractive. Gold anions are associated with the defect sites present in titania, but undergo spontaneous partial reduction so that a variety of oxidation states may coexist in solid catalysts. The +1 oxidation state appears to correlate best with CO oxidation activity but a role for zerovalent gold may also be contemplated. It seems possible to thrift gold by the judicious use of cyanide extraction though this reaction is not simple. High temperature applications of gold catalysts such as autoemission control catalysts have been discussed but the simultaneous use of platinum complicates the understanding of just which entities are responsible for catalysis. Nanogold particle growth must be stopped ar, at least controlled. Recently the4 use of nanoaligned rutile rods as a support for gold appears to offer a very convenient method for stabilizing nanogold. These catalysts show very limited growth of gold up to about 800 °C and offer a very real chance of designing gold only-based catalysis for emission control. The oxidation of CO remains very high even after exposure of the solids to high temperatures. The activity of gold for hydrocarbon oxidation is also well known, but the behaviour of gold in effecting NOx removal, though claimed, is less well studied. Applications in diesel exhaust systems, where device temperatures are likely to be lower are probably more immediately realizable than 3-way systems for gasoline emission control applications.

Speaker
Biography:

Miss Abongile Ndamase is currently studying masters in polymer technology at Tshwane University of technology. She has a BTech Biotechnology that she obtained from the Vaal University of Technology. In 2014 she did an internship and counsel of scientific and industrial research (CSIR), that is when she became a co-author to a publication.

Abstract:

Drug delivery, using polymers as carriers, is one of the important areas of research that scientists are uncovering due to the belief that they help improve drug efficacy. Chemotherapy is an effective treatment for breast cancer, but due to the side effects that result from the drug not only targeting the cancerous cells but also the quick dividing cells of the system, patients become extremely sick before they could get cured. In this paper, we investigate the hypothesis that pamidronate and platinum complexes could be conjugated with linear poly(amidoamine)s (PAMAM) in order to improve drug efficacy and this is a possibility because of the physicochemical properties of PAMAM such as: they are pH-responsive, precise direct targeting of the drug to the infected cells, meaning that only the infected cells would be treated. The conjugates were synthesised by Michael-addition process and characterised using SEM; TEM; AFM; FTIR and EDS in order to determine the occurrence of conjugation. In-vitro viability assay was done using HeLa and MCF-7 cell lines. EDS and FTIR confirmed the conjugation of the drugs to the polymer and viability assay confirmed that the conjugates are not toxic to the cells. Therefore, the results obtained from this experiment prove that there is potential for PAMAM to be used as drug delivery for cancer cells, however further characterisation and in-vitro tests would need to be conducted before further steps are taken.