ORCID Profile
0000-0003-3149-4464
Current Organisation
University of New South Wales
Does something not look right? The information on this page has been harvested from data sources that may not be up to date. We continue to work with information providers to improve coverage and quality. To report an issue, use the Feedback Form.
In Research Link Australia (RLA), "Research Topics" refer to ANZSRC FOR and SEO codes. These topics are either sourced from ANZSRC FOR and SEO codes listed in researchers' related grants or generated by a large language model (LLM) based on their publications.
Macromolecular and Materials Chemistry | Synthesis of Materials | Colloid and Surface Chemistry | Polymerisation Mechanisms | Nanomaterials | Nanomedicine | Nanotechnology | Materials engineering | Polymerisation mechanisms | Synthesis Of Macromolecules | Condensed Matter Physics | Colloid And Surface Chemistry | Polymerisation Mechanisms | Polymers and plastics | Nanoscale Characterisation | Surfaces and Structural Properties of Condensed Matter | Nanobiotechnology | Condensed Matter Characterisation Technique Development |
Plastics in Primary Forms | Paints | Plastic Products (incl. Construction Materials) | Paints | Plastic products (incl. Construction materials) | Plastics in primary forms | Organic Industrial Chemicals (excl. Resins, Rubber and Plastics) | Expanding Knowledge in the Medical and Health Sciences | Expanding Knowledge in Technology | Mining and Extraction of Titanium Minerals, Zircon, and Rare Earth Metal Ores (e.g. Monazite) | Expanding Knowledge in the Chemical Sciences | Industrial Chemicals and Related Products not elsewhere classified | Expanding Knowledge in the Physical Sciences | Management of Greenhouse Gas Emissions from Manufacturing Activities | Coated Metal and Metal-Coated Products
Publisher: Royal Society of Chemistry (RSC)
Date: 2013
DOI: 10.1039/C3PY00305A
Publisher: American Chemical Society (ACS)
Date: 05-04-2021
Publisher: Elsevier BV
Date: 02-2007
Publisher: Royal Society of Chemistry (RSC)
Date: 2022
DOI: 10.1039/D1PY01661J
Abstract: Poly(methyl methacrylate) based polymeric nanofillers are prepared via polymerization induced self-assembly (PISA). Nanofillers with worm-morphology result in more significant improvement in mechanical properties than spherical nanofillers.
Publisher: Royal Society of Chemistry (RSC)
Date: 2020
DOI: 10.1039/D0NA00534G
Abstract: The study focussed on synthesis of colloidally stable diamine functionalised graphene oxide (GO) with dangling free amine groups, and exhibited physicochemical and electrical properties of these functionalised sheets in a polymer-based nanocomposite.
Publisher: Elsevier BV
Date: 07-2008
Publisher: Wiley
Date: 06-09-2004
Publisher: Wiley
Date: 19-04-2018
Publisher: Wiley
Date: 1997
DOI: 10.1002/(SICI)1097-0126(199701)42:1<1::AID-PI636>3.0.CO;2-L
Publisher: American Chemical Society (ACS)
Date: 19-07-2021
Publisher: American Chemical Society (ACS)
Date: 13-01-2010
DOI: 10.1021/MA902309A
Publisher: American Chemical Society (ACS)
Date: 03-2022
Publisher: Informa UK Limited
Date: 09-2003
Publisher: American Chemical Society (ACS)
Date: 09-04-2021
Publisher: Royal Society of Chemistry (RSC)
Date: 2023
DOI: 10.1039/D2CS00115B
Abstract: Emulsion polymerization mediated by RAFT confers a plenty of advantages for the synthesis of multiblock copolymers, including but not limited to control over particle morphology, molecular weight, livingness, composition, and time.
Publisher: Wiley
Date: 20-02-2014
Publisher: Royal Society of Chemistry (RSC)
Date: 2017
DOI: 10.1039/C6PY02062C
Abstract: In this communication, we report the successful synthesis of gradient morphology nanoparticles composed of poly(styrene- co -methyl methacrylate) and their characterisation using X-Ray Photoelectron Spectroscopy (XPS).
Publisher: Wiley
Date: 29-04-2020
Publisher: Bentham Science Publishers Ltd.
Date: 05-2013
Publisher: Wiley
Date: 29-04-2017
DOI: 10.1002/POLA.28613
Publisher: Wiley
Date: 21-10-2004
DOI: 10.1002/POLA.20332
Publisher: Royal Society of Chemistry (RSC)
Date: 2013
DOI: 10.1039/C2PY20560B
Publisher: Wiley
Date: 29-10-2003
DOI: 10.1002/POLA.10972
Publisher: Wiley
Date: 11-10-2006
Publisher: Royal Society of Chemistry (RSC)
Date: 2015
DOI: 10.1039/C5SM02075A
Abstract: The synthesis of polymeric nanocapsules in the approximate diameter range 40–100 nm (TEM/SEM) using catanionic surfactant vesicle templates stabilized by subcritical CO 2 is demonstrated.
Publisher: Elsevier BV
Date: 12-2010
Publisher: Wiley
Date: 29-09-2006
Publisher: Elsevier BV
Date: 03-2008
Publisher: Elsevier BV
Date: 11-2005
Publisher: American Chemical Society (ACS)
Date: 16-03-2023
Publisher: American Chemical Society (ACS)
Date: 02-01-2018
Publisher: Wiley
Date: 26-02-2017
DOI: 10.1002/POLA.28509
Publisher: Elsevier BV
Date: 05-2003
Publisher: Wiley
Date: 22-04-2003
DOI: 10.1002/PI.1129
Publisher: American Chemical Society (ACS)
Date: 17-06-2010
DOI: 10.1021/MA101001J
Publisher: Wiley
Date: 12-08-2010
Abstract: Compartmentalization effects in the nitroxide‐mediated radical polymerization of butyl acrylate in a dispersed system using the nitroxide 2,2,6,6‐tetramethylpiperidine‐ N ‐oxyl (TEMPO) at 130 °C have been examined by means of modeling and simulations employing modified Smith–Ewart equations that account for compartmentalization effects on both propagating radicals and free nitroxide species. TEMPO‐mediated acrylate polymerization is known to be problematic, speculated to be mainly related to excessive accumulation of free TEMPO with increasing conversion. The present theoretical results indicate that it may be possible to at least partially overcome this difficulty by careful exploitation of compartmentalization effects in nanoreactors. magnified image
Publisher: Wiley
Date: 15-09-2021
Abstract: Synthesis of multicompositional polymeric nanoparticles of diameters 100–150 nm comprising well‐defined multiblock copolymers reaching from the particle surface to the particle core was conducted using surfactant‐free aqueous macroRAFT emulsion polymerization. The imposed constraints on chain mobility as well as chemical incompatibility between the blocks result in microphase separation, leading to formation of an onion‐like multilayered particle morphology with in idual layer thicknesses of approximately 20 nm. The approach provides considerable versatility in particle morphology design as the composition of in idual layers as well as the number of layers can be tailored as desired, offering more complex particle design compared to approaches relying on self‐assembly of preformed diblock copolymers within particles. Microphase separation can occur in these systems under conditions where the corresponding bulk system would not theoretically result in microphase separation.
Publisher: Royal Society of Chemistry (RSC)
Date: 2017
DOI: 10.1039/C7PY00552K
Abstract: It is demonstrated how the morphology of polymeric nanoparticles produced via polymerization-induced self-assembly (PISA) in dispersion can be conveniently tuned via the pH and ionic strength.
Publisher: Royal Society of Chemistry (RSC)
Date: 2017
DOI: 10.1039/C7RE00032D
Abstract: Polymeric nano-objects of a range of morphologies have been prepared using a novel approach based on the use of microporous membranes for mixing of a solvent (containing a diblock copolymer) and a non-solvent.
Publisher: American Chemical Society (ACS)
Date: 09-02-2023
Publisher: Royal Society of Chemistry (RSC)
Date: 2020
DOI: 10.1039/D0PY00925C
Abstract: The effectiveness of carboxylated graphene quantum dots (cGQDs) as sole surfactants have been investigated in miniemulsion polymerization of 8 different vinyl monomers, initiated by oil-soluble initiator AIBN and water-soluble initiator VA-044.
Publisher: Wiley
Date: 13-07-2011
Abstract: A novel method for synthesis of ultrafine polymeric nanoparticles of diameters less than 20 nm has been developed. The method is based on miniemulsion polymerization exploiting combination of the in situ surfactant generation approach (whereby the surfactant is formed at the oil-water interface by reaction between an organic acid and a base) and ultrasonication. Conventional radical polymerization and nitroxide-mediated radical polymerization of styrene have been conducted in miniemulsion using oleic acid otassium hydroxide, demonstrating that particles with diameters less than 20 nm can be obtained by this approach at surfactant contents much lower than traditionally required in microemulsion polymerizations.
Publisher: American Chemical Society (ACS)
Date: 12-06-2019
Publisher: Society of Polymer Science, Japan
Date: 2003
Publisher: Royal Society of Chemistry (RSC)
Date: 2018
DOI: 10.1039/C8PY00667A
Abstract: Polystyrene/graphene oxide (PSt/GO) nanocomposite latexes have been prepared by Pickering miniemulsion polymerization in the presence of the conventional surfactant sodium dodecyl sulfate (SDS) in order to investigate its influence on the polymerization mechanism.
Publisher: Springer Science and Business Media LLC
Date: 22-04-2012
DOI: 10.1038/NCHEM.1331
Abstract: Segregation and templating approaches have been honed by billions of years of evolution to direct many complex biological processes. Nature uses segregation to improve biochemical control by organizing reactants into defined, well-regulated environments, and the transfer of genetic information is a primary function of templating. The ribosome, wherein messenger RNA is translated into polypeptides, combines both techniques to allow for ideal biopolymer syntheses. Herein is presented a biomimetic segregation/templating approach to synthetic radical polymerization. Polymerization of a nucleobase-containing vinyl monomer in the presence of a complementary block copolymer template of low molecular weight yields high molecular weight (M(w) up to ~400,000 g mol(-1)), extremely low polydispersity (≤1.08) daughter polymers. Control is attained by segregation of propagating radicals in discrete micelle cores (via cooperative assembly of dynamic template polymers). Significantly reduced bimolecular termination, combined with controlled propagation along a defined number of templates, ensures unprecedented control to afford well-defined high molecular weight polymers.
Publisher: Wiley
Date: 28-01-2008
Publisher: Wiley
Date: 13-01-2023
DOI: 10.1002/POL.20220766
Abstract: Amphiphilic boronic acid (BA)‐substituted block copolymers have been utilized in biomedical applications through binding to saccharides, including to glucose whereas binding to the anaerobically produced metabolite lactate is unreported. Glucose requires basic conditions, while lactate binding occurs at neutral physiological conditions. Herein, BA binding to glucose and lactate is used for the first time to convert solvated hydrophobic homopolymer and hydrophobic block copolymers to hiphilic core‐shell nanoparticle spheres and worms.
Publisher: Elsevier BV
Date: 06-2005
Publisher: Wiley
Date: 09-06-2005
Publisher: American Chemical Society (ACS)
Date: 27-08-2015
DOI: 10.1021/CR500625K
Publisher: American Chemical Society (ACS)
Date: 31-07-2009
DOI: 10.1021/MA9012829
Publisher: Elsevier BV
Date: 06-2007
Publisher: American Chemical Society (ACS)
Date: 06-09-2006
DOI: 10.1021/MA061154N
Publisher: Royal Society of Chemistry (RSC)
Date: 2022
DOI: 10.1039/D2PY01005D
Abstract: Employing RAFT PISA emulsion polymerization to synthesize high molecular weight hexablock multiblock copolymers.
Publisher: American Chemical Society (ACS)
Date: 14-05-2014
DOI: 10.1021/MA402435N
Publisher: Springer Science and Business Media LLC
Date: 19-02-2008
Publisher: Royal Society of Chemistry (RSC)
Date: 2016
DOI: 10.1039/C6SM00269B
Abstract: Polymeric nanoparticles containing reduced graphene oxide (rGO) nanosheets have been prepared by aqueous miniemulsion radical polymerization of methyl methacrylate (MMA) utilizing poly(ionic liquid) (PIL) as stabilizer to effectively disperse the rGO nanosheets in the monomer phase. The PIL that gave the best results in terms of rGO dispersibility was a block copolymer of the ionic liquid monomer 1-(2-methacryloyloxyethyl)-3-butylimidazolium bis(trifluoromethanesulfonyl)amide ([Mbim][TFSA]) and MMA, the concept being that the MMA units impart solubility in the MMA monomer droplets whereas the IL units act as adsorption sites for rGO. The rGO dispersibility in vinyl monomer was demonstrated to be superior using the above PIL block copolymer compared to the corresponding statistical copolymer or PIL homopolymer. Overall, the approach developed demonstrates how PILs can be employed to conveniently switch (turn ON/OFF) the dispersibility of PIL/rGO via anion exchange reactions, which can be an efficient strategy for synthesis of polymer/rGO nanocomposite materials.
Publisher: American Chemical Society (ACS)
Date: 20-02-2023
Publisher: American Chemical Society (ACS)
Date: 23-07-2019
DOI: 10.1021/ACSMACROLETT.9B00534
Abstract: Multiblock copolymers are a class of polymeric materials with a range of potential applications. We report here a strategy for the synthesis of multiblock copolymers based on methacrylates. Reversible addition-fragmentation chain transfer (RAFT) polymerization is implemented as an emulsion polymerization to generate seed particles as nanoreactors, which can subsequently be employed in sequential RAFT emulsion polymerizations. The segregation effect allowed the synthesis of a high molar mass (>100,000 g·mol
Publisher: Wiley
Date: 14-07-2009
Abstract: Modeling and simulations employing modified Smith‐Ewart equations have been performed to elucidate compartmentalization effects (the segregation effect and the confined space effect) in nitroxide‐mediated polymerization of styrene at 125 °C in dispersed systems using the nitroxides TEMPO and TIPNO. By proper choice of particle size, it is possible to improve both the level of control and livingness relative to the corresponding homogeneous (bulk/solution) systems. magnified image
Publisher: Elsevier BV
Date: 06-2013
Publisher: Royal Society of Chemistry (RSC)
Date: 2012
DOI: 10.1039/C2PY20434G
Publisher: Royal Society of Chemistry (RSC)
Date: 2021
DOI: 10.1039/D0PY01311K
Abstract: It is demonstrated that the nature of the Z-group of trithiocarbonate RAFT agents can have a major effect on the nucleation step of aqueous RAFT PISA performed as emulsion polymerization.
Publisher: Royal Society of Chemistry (RSC)
Date: 2014
DOI: 10.1039/C3PY01441J
Publisher: American Chemical Society (ACS)
Date: 03-09-2020
Publisher: Wiley
Date: 30-09-2019
Abstract: Production of aqueous dispersions of polymeric nanoparticles via heterogeneous radical polymerization in emulsion-type systems is of enormous commercial importance. The ability to reversibly destabilize such a latex is highly desirable, for ex le, to save transportation costs. Herein, a method for synthesis of photo-responsive polymer latexes that can be destabilized (leading to sedimentation) by only using UV irradiation (no addition of chemicals or change in the experimental conditions) and subsequently redispersed by stirring under visible light irradiation is described. The destabilization/redispersion mechanism relies on photoinduced trans-cis isomerization of the cationic diazene surfactant 2-(4-(4-butylphenyl)diazenylphenoxy)ethyltrimethylammonium bromide (C4AzoTAB) used in conjunction with the anionic surfactant sodium dodecyl sulfate. It is demonstrated that reversible destabilization can be achieved very rapidly (90 s residence time) employing continuous flow technology.
Publisher: American Chemical Society (ACS)
Date: 23-09-2013
DOI: 10.1021/MZ4004198
Abstract: The synthesis of well-defined high molecular weight block copolymers by sequential in situ chain extensions via Cu(0)-mediated living radical polymerization is reported. Optimal conditions for iterative high molecular weight block formation were determined using model homopolymer quasiblock systems, including methyl acrylate (MA), ethyl acrylate (EA), and
Publisher: Elsevier BV
Date: 11-2013
Publisher: Elsevier BV
Date: 07-2009
Publisher: American Chemical Society (ACS)
Date: 23-06-2011
DOI: 10.1021/MA200859S
Publisher: Royal Society of Chemistry (RSC)
Date: 2016
DOI: 10.1039/C6PY01447J
Abstract: The preparation of polymer-silica hybrid nanoparticles of various morphologies is reported.
Publisher: American Chemical Society (ACS)
Date: 18-08-2011
DOI: 10.1021/MA201531W
Publisher: Wiley
Date: 05-2022
Abstract: Synthesis of light polymer nanocomposites with high strength and toughness has been a significant interest for its potential applications in industry. Herein, the authors have synthesized polymerization‐induced self‐assembly (PISA) derived nanodimensional polymeric worm (fiber) reinforced polymer nanocomposites by a simple and environmentally friendly synthesis process without the addition of volatile organic compounds. PISA‐derived worms with a core‐forming block of low glass transition temperature ( T g ≈ 27.1 °C) comprising poly(styrene‐ stat ‐ n ‐butyl acrylate) have been employed as reinforcing filler. The influence of core‐segment cross‐linking on reinforcement efficiency has been explored by comparing noncross‐linked worms, and worms cross‐linked with a small amount of ethylene glycol diacrylate introduced at t = 0 h or t = 2 h of polymerization. Upon addition of 1 wt% of noncross‐linked, t = 0 h cross‐linked, and t = 2 h cross‐linked worms, toughness of polymer nanocomposites can be enhanced by 62%, 114%, and 120%, respectively. The results suggest that the reinforcement efficiency of worms is significantly influenced by the cross‐linking of core‐segments regardless of cross‐linking methods. This work broadens the understanding in application of PISA‐derived worms as reinforcing filler by demonstrating the efficient reinforcement with low T g worms.
Publisher: American Chemical Society (ACS)
Date: 23-09-2015
Publisher: Wiley
Date: 13-04-2007
DOI: 10.1002/POLA.21986
Publisher: Springer Science and Business Media LLC
Date: 06-2003
Publisher: Elsevier BV
Date: 12-2005
Publisher: American Chemical Society (ACS)
Date: 09-01-2014
DOI: 10.1021/MA402286E
Publisher: Wiley
Date: 15-09-2021
Abstract: Synthesis of multicompositional polymeric nanoparticles of diameters 100–150 nm comprising well‐defined multiblock copolymers reaching from the particle surface to the particle core was conducted using surfactant‐free aqueous macroRAFT emulsion polymerization. The imposed constraints on chain mobility as well as chemical incompatibility between the blocks result in microphase separation, leading to formation of an onion‐like multilayered particle morphology with in idual layer thicknesses of approximately 20 nm. The approach provides considerable versatility in particle morphology design as the composition of in idual layers as well as the number of layers can be tailored as desired, offering more complex particle design compared to approaches relying on self‐assembly of preformed diblock copolymers within particles. Microphase separation can occur in these systems under conditions where the corresponding bulk system would not theoretically result in microphase separation.
Publisher: Elsevier BV
Date: 10-2006
Publisher: Elsevier BV
Date: 12-2017
Publisher: American Chemical Society (ACS)
Date: 27-08-2008
DOI: 10.1021/CR800242X
Publisher: American Chemical Society (ACS)
Date: 02-08-2013
DOI: 10.1021/MA401250F
Publisher: Wiley
Date: 07-2003
Publisher: American Chemical Society (ACS)
Date: 18-02-2005
DOI: 10.1021/MA048154C
Publisher: American Chemical Society (ACS)
Date: 12-03-2013
DOI: 10.1021/MA4002148
Publisher: Royal Society of Chemistry (RSC)
Date: 2019
DOI: 10.1039/C9NR00816K
Abstract: A facile method to synthesize colloidally stable polymer nanoparticles decorated with GO sheets via miniemulsion polymerization, which enables the preparation of electrically conductive films using a simple dropcasting method.
Publisher: Royal Society of Chemistry (RSC)
Date: 2017
DOI: 10.1039/C7CC06347D
Abstract: We introduce the facile synthesis of segmented copolymers via a catalyst-free Diels–Alder (DA) reaction at ambient temperature via step-growth polymerization and subsequent reversible addition fragmentation chain transfer (RAFT) polymerization.
Publisher: American Chemical Society (ACS)
Date: 14-09-2002
DOI: 10.1021/MA020695J
Publisher: Royal Society of Chemistry (RSC)
Date: 2022
DOI: 10.1039/D1PY01636A
Abstract: Synthesis of nanodimensional polymeric worms of low glass transition temperature using aqueous polymerization-induced self-assembly.
Publisher: American Chemical Society (ACS)
Date: 06-07-2018
Publisher: Wiley
Date: 28-07-2011
Publisher: Wiley
Date: 08-02-2011
DOI: 10.1002/POLA.24580
Publisher: Royal Society of Chemistry (RSC)
Date: 2015
DOI: 10.1039/C4PY01632G
Abstract: A novel method for synthesis of polymeric nano-objects via polymerization-induced self-assembly in a CO 2 -expanded medium has been developed.
Publisher: Wiley
Date: 13-10-2010
DOI: 10.1002/POLA.24343
Publisher: Wiley
Date: 23-03-2007
Publisher: American Chemical Society (ACS)
Date: 05-01-2021
Publisher: Elsevier BV
Date: 03-2002
Publisher: CSIRO Publishing
Date: 2010
DOI: 10.1071/CH10063
Abstract: Compartmentalization of a nitroxide-mediated radical polymerization system can lead to improved levels of both control and livingness, but at the cost of a reduced polymerization rate. Improved control is a result of the confined space effect on deactivation, whereas improved livingness stems from the segregation effect on bimolecular termination. Modelling and simulations have been carried out for the systems styrene/2,2,6,6-tetramethylpiperidine-N-oxyl (TEMPO) and styrene/2,2,5-trimethyl-4-phenyl-3-azahexane-3-oxy (TIPNO) using the respective nitroxide-based polystyrene macroinitaitors (alkoxyamines) at 125°C to elucidate whether similar benefits can be obtained in the corresponding bulk polymerizations by merely diluting the systems or by addition of extra free nitroxide. The results have shown that neither approach leads to simultaneous improvement in control and livingness relative to the corresponding bulk systems, thus accentuating the merits of compartmentalization in nanoreactors.
Publisher: American Chemical Society (ACS)
Date: 26-02-2021
Publisher: American Chemical Society (ACS)
Date: 05-11-2021
Publisher: Wiley
Date: 08-05-2012
DOI: 10.1002/POLA.26094
Publisher: Wiley
Date: 12-2006
Publisher: Royal Society of Chemistry (RSC)
Date: 2017
DOI: 10.1039/C7SM01521F
Abstract: Soft polyhedral particles based on variations of the cubic symmetry group are produced from a precursor emulsion by extracting solvent to grow facets on the droplets.
Publisher: American Chemical Society (ACS)
Date: 24-10-2007
DOI: 10.1021/MA0712403
Publisher: Wiley
Date: 02-2003
Publisher: Informa UK Limited
Date: 2002
Publisher: Wiley
Date: 30-01-2018
DOI: 10.1002/POLA.28958
Publisher: Wiley
Date: 21-04-2004
Publisher: MDPI AG
Date: 20-02-2018
Publisher: Wiley
Date: 21-07-2017
Abstract: The catalytic polymerization of ethylene is performed in water pressurized with CO
Publisher: Wiley
Date: 18-09-2007
DOI: 10.1002/POLA.22294
Publisher: American Chemical Society (ACS)
Date: 04-09-2014
DOI: 10.1021/MZ5005019
Publisher: American Chemical Society (ACS)
Date: 22-02-2005
DOI: 10.1021/MA047894I
Publisher: American Chemical Society (ACS)
Date: 13-03-2009
DOI: 10.1021/MA900035X
Publisher: American Chemical Society (ACS)
Date: 08-08-2002
DOI: 10.1021/MA020325V
Publisher: Royal Society of Chemistry (RSC)
Date: 2019
DOI: 10.1039/C9PY00498J
Abstract: Polymerization-induced self-assembly (PISA) based on ATRP has been successfully conducted in scCO 2 resulting in polymer particles of high order morphology.
Publisher: Elsevier BV
Date: 09-2018
Publisher: Elsevier BV
Date: 08-2019
Publisher: Wiley
Date: 28-02-2001
DOI: 10.1002/POLA.1100
Publisher: Wiley
Date: 09-10-2013
DOI: 10.1002/POLA.26947
Publisher: Elsevier BV
Date: 12-2008
Publisher: Elsevier BV
Date: 12-1996
Publisher: Wiley
Date: 28-01-2009
Publisher: Wiley
Date: 10-06-2009
DOI: 10.1002/POLA.23432
Publisher: American Chemical Society (ACS)
Date: 03-02-2016
Publisher: American Chemical Society (ACS)
Date: 05-07-2013
DOI: 10.1021/MZ400280T
Abstract: In this letter, we report a simple and unexpected method of producing polymer-graphene oxide (GO) composite materials via ab initio emulsion polymerization in water. On the basis of the recent reports concerning the surfactant-like behavior of GO for stabilizing oil-in-water emulsions, we prepared exfoliated GO sheets with lateral dimension approximately 200 nm for use as surfactant in the emulsion polymerization of styrene. We observed an expected "classic" surfactant behavior to produce stable nanoparticles at extremely low GO loadings (<0.1% w/w) however, at higher concentrations a highly aggregated, fibrous morphology was formed. This morphology is predominantly due to the electrolyte concentration (ionic strength) of the aqueous phase resulting in heterocoagulation of growing oligomers with dispersed GO sheets, which offers a convenient route toward preparing hybrid materials.
Publisher: MDPI AG
Date: 30-07-2019
DOI: 10.3390/JFB10030033
Abstract: Poly(d,l–lactide–co–glycolide) (PLGA) has been extensively explored for bone regeneration applications however, its clinical use is limited by low osteointegration. Therefore, approaches that incorporate osteoconductive molecules are of great interest. Graphene oxide (GO) is gaining popularity for biomedical applications due to its ability to bind biological molecules and present them for enhanced bioactivity. This study reports the preparation of PLGA microparticles via Pickering emulsification using GO as the sole surfactant, which resulted in hybrid microparticles in the size range of 1.1 to 2.4 µm based on the ratio of GO to PLGA in the reaction. Furthermore, this study demonstrated that the hybrid GO-PLGA microparticles were not cytotoxic to either primary human fetal cartilage rudiment cells or the human osteoblast-like cell line, Saos-2. Additionally, the GO-PLGA microparticles promoted the osteogenic differentiation of the human fetal cartilage rudiment cells in the absence of exogenous growth factors to a greater extent than PLGA alone. These findings demonstrate that GO-PLGA microparticles are cytocompatible, osteoinductive and have potential as substrates for bone tissue engineering.
Publisher: Wiley
Date: 02-2010
Publisher: Royal Society of Chemistry (RSC)
Date: 2017
DOI: 10.1039/C7PY00939A
Abstract: Methodology for the successful implementation of RAFT (4-cyano-4[(dodecylsulfanylthiocarbonyl)sulfanyl]pentanoic acid (CDTPA)) iniferter polymerization of butyl methacrylate in miniemulsion using visible light (green light λ max = 530 nm) has been developed.
Publisher: Wiley
Date: 09-12-2002
DOI: 10.1002/POLA.10582
Publisher: Elsevier BV
Date: 03-2015
DOI: 10.1016/J.JCIS.2014.11.047
Abstract: Two-dimensional nanoparticles such as graphene oxide (GO) can serve as emulsion stabilizers due their ability to adsorb at oil-water (o/w) interfaces with high atom efficiency. The ability for GO to act as a surfactant is hypothesized to be highly dependent on the nature (i.e. polarity) of the oil phase, which has not considered previously. The stabilization energy associated with adsorption of GO sheets at an o/w interface was modelled as a function of the polarity of the oil phase using surface tension contributions terms and Hansen solubility parameters (HSPs). Oil-in-water (o/w) miniemulsions were prepared via ultrasonication in the presence of GO for a variety of different oil phases, and were studied using dynamic light scattering (DLS). The stabilization energy associated with GO adsorption was greater for non-polar oil phases compared to more polar oils. This behaviour is driven by the significant reduction in the oil-water interfacial tension as the polarity of the oil increases, to the point where GO adsorption is no longer thermodynamically favourable. This was verified by DLS measurements experiments, as GO-stabilized emulsion were successfully prepared for hydrophobic and aromatic oil phases (e.g. styrene), but not for polar oil phases such as methyl methacrylate.
Publisher: Royal Society of Chemistry (RSC)
Date: 2012
DOI: 10.1039/C2CC36116G
Abstract: Hollow polymeric nanoparticles with a hydrophilic liquid core have been synthesized in a one-pot approach via a novel inverse miniemulsion periphery RAFT polymerization process. Successful encapsulation and release of a model protein is reported as a potential application.
Publisher: Wiley
Date: 27-10-2003
DOI: 10.1002/PI.1291
Publisher: Wiley
Date: 27-10-2003
DOI: 10.1002/PI.1292
Publisher: Wiley
Date: 27-10-2003
DOI: 10.1002/PI.1293
Publisher: Wiley
Date: 10-08-2007
Publisher: Elsevier BV
Date: 10-2006
Publisher: American Chemical Society (ACS)
Date: 07-10-2019
Publisher: American Chemical Society (ACS)
Date: 17-05-2018
DOI: 10.1021/ACS.LANGMUIR.8B00554
Abstract: Copolymer/water interfacial tensions of statistical copolymers of styrene/ n-butyl acrylate were estimated by pendant drop tensiometry using an "inverse" configuration according to which a drop of water was formed in toluene/copolymer solutions. The study first involved the precise measurement of copolymer solutions density using pycnometry. Subsequently, interfacial tensions of copolymer solutions against water were plotted as a function of copolymer concentration in toluene. Several methods were explored to fit the experimental data and obtain estimates of copolymer/water interfacial tensions at 100% copolymer concentration in toluene by extrapolation. The Belton-Evans extrapolation resulted in the best fit with the experimental data. When plotted as a function of the styrene composition of the copolymer, the interfacial tensions estimates followed an additivity relationship. This enabled estimation of the copolymer/water interfacial tensions directly from their respective homopolymer/water interfacial tensions values. These results are particularly useful for the prediction of composite particle morphology involving copolymerization of multiple monomers.
Publisher: Elsevier BV
Date: 2002
Publisher: Elsevier BV
Date: 08-2014
Publisher: Elsevier BV
Date: 08-2020
Publisher: American Chemical Society (ACS)
Date: 29-09-2001
DOI: 10.1021/MA010560Y
Publisher: Springer Science and Business Media LLC
Date: 02-2016
DOI: 10.1038/NCOMMS10514
Abstract: Precise control over the location of monomers in a polymer chain has been described as the ‘Holy Grail’ of polymer synthesis. Controlled chain growth polymerization techniques have brought this goal closer, allowing the preparation of multiblock copolymers with ordered sequences of functional monomers. Such structures have promising applications ranging from medicine to materials engineering. Here we show, however, that the statistical nature of chain growth polymerization places strong limits on the control that can be obtained. We demonstrate that monomer locations are distributed according to surprisingly simple laws related to the Poisson or beta distributions. The degree of control is quantified in terms of the yield of the desired structure and the standard deviation of the appropriate distribution, allowing comparison between different synthetic techniques. This analysis establishes experimental requirements for the design of polymeric chains with controlled sequence of functionalities, which balance precise control of structure with simplicity of synthesis.
Publisher: American Chemical Society (ACS)
Date: 21-05-2012
DOI: 10.1021/MZ3001786
Abstract: Modeling and simulations of compartmentalization effects in tandem with nitroxide exit and entry have been performed for the nitroxide-mediated radical polymerization (NMP) of styrene in an aqueous dispersed system employing 2,2,6,6-tetramethylpiperidinyl-1-oxy (TEMPO) at 125 °C. It is demonstrated that, even for a relatively water-insoluble nitroxide like TEMPO, exit and entry can strongly influence the polymerization kinetics in submicrometer-size droplets articles. In such systems, the polymerization is expected to proceed at a markedly higher rate than the corresponding bulk system at the expense of control/livingness. Depending on the deactivator water solubility, these findings will apply qualitatively to all controlled/living radical polymerization systems governed by the persistent radical effect [e.g., NMP and atom transfer radical polymerization (ATRP)].
Publisher: Wiley
Date: 14-02-2005
Publisher: American Chemical Society (ACS)
Date: 18-11-2009
DOI: 10.1021/MA9022179
Publisher: Wiley
Date: 04-12-2007
Publisher: Wiley
Date: 04-2004
Publisher: Wiley
Date: 17-04-2015
Abstract: Currently available methods for synthesis of polymeric nanocapsules only offer limited control over the shell thickness, even though it is an important parameter for various applications. Furthermore, suitable methods to critically measure this parameter in a facile way are still nonexistent. Here, lab-scale small-angle X-ray scattering (SAXS) is utilized to in situ measure the evolution of shell thickness during nanocapsule synthesis via inverse miniemulsion periphery reversible addition-fragmentation chain transfer (RAFT) polymerization (IMEPP). The measured shell thickness is consistent with estimates from the commonly used transmission electron microscopy (TEM) technique. Moreover, the in idual thicknesses of two concentric shells comprising different polymeric materials (the outer shell formed via IMEPP chain extension of the inner shell) can be determined, thus further demonstrating the versatility of this approach.
Publisher: Wiley
Date: 04-12-2007
Publisher: Wiley
Date: 10-2003
Publisher: American Chemical Society (ACS)
Date: 07-02-2019
Publisher: Royal Society of Chemistry (RSC)
Date: 2011
DOI: 10.1039/C0PY00247J
Publisher: Wiley
Date: 28-12-2018
DOI: 10.1002/POLA.29313
Publisher: American Chemical Society (ACS)
Date: 02-03-2004
DOI: 10.1021/MA0352734
Publisher: Royal Society of Chemistry (RSC)
Date: 2016
DOI: 10.1039/C6CS00253F
Abstract: We review the range of CLRP-controlled syntheses of block copolymer particles in dispersed systems, which are being exploited to create new opportunities for the design of nanostructured soft materials.
Publisher: Springer Science and Business Media LLC
Date: 30-09-2013
DOI: 10.1038/NCOMMS3505
Abstract: A long-standing challenge in polymer chemistry has been to prepare synthetic polymers with not only well-defined molecular weight, but also precisely controlled microstructure in terms of the distribution of monomeric units along the chain. Here we describe a simple and scalable method that enables the synthesis of sequence-controlled multiblock copolymers with precisely defined high-order structures, covering a wide range of functional groups. We develop a one-pot, multistep sequential polymerization process with yields >99%, giving access to a wide range of such multifunctional multiblock copolymers. To illustrate the enormous potential of this approach, we describe the synthesis of a dodecablock copolymer, a functional hexablock copolymer and an icosablock (20 blocks) copolymer, which represents the largest number of blocks seen to date, all of very narrow molecular weight distribution for such complex structures. We believe this approach paves the way to the design and synthesis of a new generation of synthetic polymers.
Publisher: Rubber Division, ACS
Date: 05-2003
DOI: 10.5254/1.3547757
Abstract: In order to investigate the effects of storage and service on passenger car tire performance, two separate sets of s les were characterized: (i) tires stored at a temperature of 45–50 °C for different time periods, and (ii) used tires of different mileage. The tires were analyzed with respect to the performance of the tread rubber as manifested in the modulus at 200% elongation, the tensile strength at break, the elongation at break, the hardness, the viscoelasticity of the rubber, swelling, and the oil component content. The change in the properties of the tires as functions of increasing storage time and mileage indicated a marked deterioration in performance. The rate of change in these properties was found to be markedly enhanced by the extra stimuli provided by service, as demonstrated by comparing tires of similar age but different mileage. The results were analyzed and rationalized in terms of the change in the degree of crosslinking and transfer of oil components from the tread rubber to the inner part of the tire or to the surroundings.
Publisher: American Chemical Society (ACS)
Date: 03-2008
DOI: 10.1021/MA702645B
Publisher: Wiley
Date: 21-11-2017
DOI: 10.1002/POLA.28911
Publisher: Wiley
Date: 05-02-2019
DOI: 10.1002/POLA.29329
Publisher: Elsevier BV
Date: 12-2015
Publisher: American Chemical Society (ACS)
Date: 19-06-2020
Publisher: American Chemical Society (ACS)
Date: 15-10-2018
DOI: 10.1021/ACS.LANGMUIR.8B02638
Abstract: Soft, rotationally symmetric particles of dispersed hexagonal liquid crystalline phase are produced using a method previously developed for cubosome microparticle production. The technique forms hexosome particles via removal of ethanol from emulsion droplets containing monoolein, water, and one of the various hydrophobic molecules: vitamin E, hexadecane, oleic acid, cyclohexane, or inylbenzene. The unique rotational symmetry of the particles is characterized by optical microscopy and small-angle X-ray scattering to link particle phase, shape, and structure to composition. Rheology of the soft particles can be varied independently of shape, enabling control of transport, deformation, and biological response by controlling composition and molecular structure of the additives. The direct observations of formation, and the resultant hexosome shapes, link the particle-scale and mesoscale properties of these novel self-assembled particles and broaden their applications. The micron-scale hexosomes provide a route to understanding the effects of particle size, crystallization rate, and rheology on the production of soft particles with liquid crystalline structure and unique shape and symmetry.
Publisher: Royal Society of Chemistry (RSC)
Date: 2022
DOI: 10.1039/D2PY00530A
Abstract: For the unprotected monomer, the boroxine core of nanoparticles allows transitions to higher order morphologies, while worms and vesicles are yielded directly from PISA of the pinacol ester-protected monomer.
Publisher: American Chemical Society (ACS)
Date: 11-1999
DOI: 10.1021/MA9910078
Publisher: Royal Society of Chemistry (RSC)
Date: 2023
DOI: 10.1039/D2PY01425D
Abstract: The effect of monomer droplet size on the particle formation mechanism in aqueous heterogeneous polymerization using a hydrophilic macroRAFT agent has been investigated.
Publisher: Royal Society of Chemistry (RSC)
Date: 2012
DOI: 10.1039/C1PY00384D
Abstract: A new iterative copper(0)-mediated radical polymerization approach is presented that represents a significant advance in the synthesis of high order multi-block star copolymers. The synthesis of these materials can now be achieved in high yield and with controlled structural complexity, with purification only required at the last step. The approach is general, facile and offers the opportunity to synthesize new copolymer stars.
Publisher: American Chemical Society (ACS)
Date: 02-03-2022
Publisher: Elsevier BV
Date: 09-2011
Publisher: American Chemical Society (ACS)
Date: 17-02-2011
DOI: 10.1021/MA102689D
Publisher: Wiley
Date: 02-09-2018
Abstract: Polymerization-induced self-assembly of 2-hydroxypropyl methacrylate is conducted in water and water/MeOH using a CO
Publisher: American Chemical Society (ACS)
Date: 22-11-2006
DOI: 10.1021/MA060841B
Publisher: Elsevier BV
Date: 02-2008
Publisher: Wiley
Date: 12-01-2006
Publisher: Royal Society of Chemistry (RSC)
Date: 2020
DOI: 10.1039/D0PY00654H
Abstract: Synthesis of polymeric nanoparticles of adjustable size in the submicron-range 200–950 nm has been conducted via membrane emulsification combined with photoinduced miniemulsion polymerization in a continuous tubular flow reactor.
Publisher: Wiley
Date: 21-04-2004
DOI: 10.1002/POLA.20127
Publisher: Wiley
Date: 14-09-2013
DOI: 10.1002/POLA.26341
Publisher: Wiley
Date: 15-05-2017
DOI: 10.1002/POLA.28644
Publisher: American Chemical Society (ACS)
Date: 07-09-2014
DOI: 10.1021/MA501379Q
Publisher: American Chemical Society (ACS)
Date: 06-2012
DOI: 10.1021/MZ300213J
Abstract: A novel approach is presented whereby nitroxide-mediated radical polymerization (NMP) is conducted in an aqueous heterogeneous system at an initial polymerization rate an order of magnitude greater than the corresponding bulk system, accompanied by an improvement in the level of control over the molecular weight distribution. NMP of styrene mediated by
Publisher: Royal Society of Chemistry (RSC)
Date: 2020
DOI: 10.1039/D0PY00523A
Abstract: Controlling polymer molecular weight by topochemical polymerisation inside nanoreactors.
Publisher: American Chemical Society (ACS)
Date: 17-06-2015
Publisher: Wiley
Date: 27-11-2008
Publisher: American Chemical Society (ACS)
Date: 20-11-2019
Abstract: Electrically conductive polymer/rGO (reduced graphene oxide) films based on styrene and
Publisher: Royal Society of Chemistry (RSC)
Date: 2021
DOI: 10.1039/D1PY01163D
Abstract: We report a method to efficiently prepare multisegmented polymers via a combination of step-growth (SG) and reversible addition-fragmentation chain transfer (RAFT) polymerization.
Publisher: Royal Society of Chemistry (RSC)
Date: 17-09-0006
DOI: 10.1039/C4PY00855C
Publisher: Royal Society of Chemistry (RSC)
Date: 2016
DOI: 10.1039/C6PY01584K
Abstract: Synthesis of polymeric capsules with good control over the particle size and size distribution is demonstrated via a novel approach involving SPG membrane emulsification.
Publisher: American Chemical Society (ACS)
Date: 25-06-2015
DOI: 10.1021/ACS.BIOMAC.5B00545
Abstract: Encapsulation of hydrophilic cancer drugs in polymeric nanocapsules was achieved in a one-pot process via the inverse miniemulsion periphery RAFT polymerization (IMEPP) approach. The chosen guest molecule was gemcitabine hydrochloride, which is used as the first-line treatment of pancreatic cancer. The resulting nanocapsules were confirmed to be ∼200 nm, with excellent encapsulation (∼96%) and loading (∼12%) efficiency. Postpolymerization reaction was successfully conducted to create glyocopolymer nanocapsules without any impact on the loads as well as the nanocapsules size or morphology. The loaded nanocapsules were specifically designed to be responsive in a reductive environment. This was confirmed by the successful disintegration of the nanocapsules in the presence of glutathione. The gemcitabine-loaded nanocapsules were tested in vitro against pancreatic cancer cells (AsPC-1), with the results showing an enhancement in the cytotoxicity by two fold due to selective accumulation and release of the nanocapsules within the cells. The results demonstrated the versatility of IMEPP as a tool to synthesize functionalized, loaded-polymeric nanocapsules suitable for drug-delivery application.
Publisher: Wiley
Date: 26-02-2017
DOI: 10.1002/POLA.28538
Publisher: Wiley
Date: 03-2011
DOI: 10.1002/POLA.24612
Publisher: Royal Society of Chemistry (RSC)
Date: 2017
DOI: 10.1039/C7PY00998D
Abstract: Polymerization-induced self-assembly (PISA) is conducted based on “non-living” radical dispersion polymerization in the form of addition–fragmentation chain transfer (AFCT) polymerization.
Publisher: Elsevier BV
Date: 11-2009
Publisher: American Chemical Society
Date: 2014
Publisher: Royal Society of Chemistry (RSC)
Date: 2019
DOI: 10.1039/C9PY00166B
Abstract: Polymerization-induced self-assembly (PISA) via PhotoRAFT (photoinduced reversible addition–fragmentation radical transfer) was investigated in polar solvents via continuous flow reactors.
Publisher: Wiley
Date: 13-05-2015
DOI: 10.1002/POLA.27688
Publisher: American Chemical Society (ACS)
Date: 16-09-2021
Publisher: Royal Society of Chemistry (RSC)
Date: 30-06-2014
DOI: 10.1039/C4NR01175A
Abstract: The preparation of hybrid hollow capsules consisting of a cross-linked polymer shell and a coating of graphene oxide (GO) is demonstrated. The capsules are prepared by Pickering miniemulsion polymerization, exploiting the surface activity of GO for its use as a colloidal surfactant. This approach represents a simple and convenient route towards hollow carbon nanostructures for a variety of applications. The incorporation of surface-modified TiO2 nanoparticles into the interior of these capsules was also demonstrated.
Publisher: American Chemical Society (ACS)
Date: 02-04-2021
Publisher: Wiley
Date: 11-09-2007
Publisher: Wiley
Date: 2003
DOI: 10.1002/PI.1040
Publisher: Elsevier BV
Date: 07-1996
Publisher: Rubber Division, ACS
Date: 09-2003
DOI: 10.5254/1.3547783
Abstract: A new approach of preventing evaporation and migration of antioxidants in rubber is presented. The antioxidant N-1,3-dimethylbutyl-N'-phenyl-p-phenylenediamine (6PPD) was microencapsulated in silica (MC6PPD) prior to compounding with the rubber. The microencapsulated antioxidants were characterized by differential scanning calorimetry and thermogravimetric analysis, indicating reduced rates of evaporation compared to free antioxidant. The stress-strain properties, flex cracking resistance and discoloration of the rubber were examined as s les containing equal amounts of antioxidant but in the different forms of 6PPD and MC6PPD. The results clearly indicated superior rubber performance in the case of MC6PPD, suggesting that antioxidant encapsulation is an effective technique to prevent rubber degradation due to aging.
Publisher: American Chemical Society (ACS)
Date: 03-04-2019
Publisher: Wiley
Date: 16-12-2004
DOI: 10.1002/POLA.10803
Publisher: Wiley
Date: 31-08-2006
Publisher: Royal Society of Chemistry (RSC)
Date: 2020
DOI: 10.1039/D0PY00404A
Abstract: Carboxylated graphene quantum dots (cGQDs) were synthesized from dextrose and sulfuric acid via a hydrothermal process, and subsequently used as sole surfactant in miniemulsion polymerization of styrene.
Publisher: Wiley
Date: 10-08-2005
Publisher: Elsevier BV
Date: 10-2006
Publisher: Wiley
Date: 28-07-2011
DOI: 10.1002/POLA.24875
Publisher: Elsevier BV
Date: 07-2023
Publisher: American Chemical Society (ACS)
Date: 03-03-2022
Publisher: Elsevier BV
Date: 06-2019
DOI: 10.1016/J.JCIS.2019.03.069
Abstract: Cubic and hexagonal liquid crystalline particles, or cubosomes and hexosomes, are used as templates to polymerize various monomers to produce particles with unique micron-scale geometric shapes. Emulsion droplets containing water, ethanol, and the lipid glyceryl monooleate are suspended in a yield stress fluid and used to produce shapes based on cubic and hexagonal symmetry by slow crystallization. The underlying liquid crystalline ordering of the aqueous lipid system drives symmetric shape formation, while its hiphilicity allows incorporation of various organic monomers. Photopolymerization of monomers in the lipid templates creates polymeric particles shaped like polyhedra based on cubic symmetry as well as biconical cylinders based on hexagonal symmetry, and their shape is preserved after template removal. Product particle shapes are controlled by varying the structures and hydrophobicity of the monomers, as they control formation of different phases and microstructures. Monomer polarity determines whether the template can exhibit hexagonal phase, as when inylbenzene is used, or cubic phase, when di(ethylene glycol) dimethacrylate is used. The monomers also control the microstructure of the final particles produced, forming rigid shapes composed of linked polymer nanospheres when inylbenzene or di(ethylene glycol) dimethacrylate are used, and soft hydrogel particles when N,N'-methylenebisacrylamide is used.
Publisher: American Chemical Society (ACS)
Date: 27-03-2007
DOI: 10.1021/MA062786C
Publisher: Wiley
Date: 02-11-2004
Publisher: American Chemical Society (ACS)
Date: 16-05-2019
Publisher: Wiley
Date: 12-05-2014
DOI: 10.1002/POLA.27220
Publisher: Royal Society of Chemistry (RSC)
Date: 2014
DOI: 10.1039/C4PY00757C
Abstract: The first controlled/living precipitation NMP in supercritical carbon dioxide in the absence of nitroxide and comparisons with fluorinated alkoxyamines.
Publisher: Elsevier BV
Date: 03-2009
Location: United Kingdom of Great Britain and Northern Ireland
Start Date: 2014
End Date: 2017
Funder: Australian Research Council
View Funded ActivityStart Date: 2016
End Date: 2016
Funder: Australian Research Council
View Funded ActivityStart Date: 2016
End Date: 2016
Funder: Australian Research Council
View Funded ActivityStart Date: 2010
End Date: 2012
Funder: Australian Research Council
View Funded ActivityStart Date: 2011
End Date: 2015
Funder: Australian Research Council
View Funded ActivityStart Date: 2014
End Date: 2016
Funder: Australian Research Council
View Funded ActivityStart Date: 2005
End Date: 2006
Funder: Japan Society for the Promotion of Science
View Funded ActivityStart Date: 2007
End Date: 2008
Funder: Japan Society for the Promotion of Science
View Funded ActivityStart Date: 2005
End Date: 2006
Funder: Japan Society for the Promotion of Science
View Funded ActivityStart Date: 2008
End Date: 2009
Funder: Japan Society for the Promotion of Science
View Funded ActivityStart Date: 2005
End Date: 2007
Funder: Japan Society for the Promotion of Science
View Funded ActivityStart Date: 09-2014
End Date: 12-2017
Amount: $330,913.00
Funder: Australian Research Council
View Funded ActivityStart Date: 2019
End Date: 12-2022
Amount: $382,000.00
Funder: Australian Research Council
View Funded ActivityStart Date: 02-2016
End Date: 12-2017
Amount: $500,000.00
Funder: Australian Research Council
View Funded ActivityStart Date: 2014
End Date: 12-2017
Amount: $360,000.00
Funder: Australian Research Council
View Funded ActivityStart Date: 01-2010
End Date: 01-2013
Amount: $298,955.00
Funder: Australian Research Council
View Funded ActivityStart Date: 2012
End Date: 12-2015
Amount: $753,856.00
Funder: Australian Research Council
View Funded ActivityStart Date: 2017
End Date: 08-2020
Amount: $326,000.00
Funder: Australian Research Council
View Funded ActivityStart Date: 2016
End Date: 03-2017
Amount: $650,000.00
Funder: Australian Research Council
View Funded ActivityStart Date: 09-2023
End Date: 09-2026
Amount: $466,000.00
Funder: Australian Research Council
View Funded Activity