Steven Armes

Last updated

Steve Armes

FRS
Professor Steven Armes FRS.jpg
Steve Armes at the Royal Society admissions day in 2014
Born
Steven Peter Armes

1962 (age 6061) [1]
Education Whitley Abbey Comprehensive School [2]
Alma mater University of Bristol (BSc, PhD)
Awards Tilden Prize [ when? ]
Scientific career
Institutions
Thesis Colloidal forms of conducting polymers  (1987)
Doctoral advisor Brian Vincent [3]
Website

Steven Peter Armes (born 1962) [1] FRS [4] is a Professor of polymer chemistry and colloid chemistry at the University of Sheffield. [5] [6]

Contents

Education

Armes was educated at Whitley Abbey Comprehensive School [2] [7] in Coventry and the University of Bristol where he was awarded a Bachelor of Science degree in 1983 followed by a PhD in 1987 for research supervised by Brian Vincent. [3] [2] [8]

Career and research

After a postdoctoral research at Los Alamos National Laboratory [9] Armes became a lecturer at the University of Sussex in 1989 [2] where he worked until 2004. He moved to Sheffield to become Professor of Polymer and Colloid Chemistry in 2004. [2] As of 2016, he is a director of Farapack Polymers Limited, [1] a corporate spin-off from the University of Sheffield. Armes group does research on polymer chemistry and colloid chemistry. [9] Using polymerisation techniques such as reversible addition−fragmentation chain-transfer polymerization (RAFT) and atom-transfer radical-polymerization (ATRP) his laboratory synthesises a wide range of polymers.

His research focuses on the synthesis and application of polymers – long-chain molecules formed from many repeating units known as monomers. In particular, Steven's research group has developed new ways to make water-soluble or water-dispersible polymers based on methacrylic monomers. [10]

A powerful approach is to use polymerization-induced self-assembly (PISA). [11] For example, a water-insoluble polymer can be grown from one end of a water-soluble polymer in aqueous solution. The growing hydrophobic chain leads to in situ self-assembly, forming copolymer nanoparticles of tuneable size and shape. [12] These nanoparticles have a wide range of potential applications, including as a long-term storage medium for stem cells, viscosity modifiers, novel microcapsules and nanoparticle lubricants. [10]

His other research interests include designing novel biocompatible copolymer gels and vesicles and developing microscopic nanocomposite particles, which have applications in paints and anti-reflective coatings. Steven also has a fruitful collaboration with space scientists based in the United Kingdom, Germany, and the United States, for whom he designs synthetic mimics to aid our understanding the behaviour of micrometeorites travelling at hypervelocities in outer space. [10] Armes has developed robust new synthetic routes to controlled-structure water-soluble polymers. He optimised the living radical polymerisation of hydrophilic methacrylates, discovered a new class of 'schizophrenic' diblock copolymers whose amphiphilicity can be switched on or off, and has designed a range of novel biocompatible block copolymer gels and vesicles. His work on water-borne polymer colloids has led to novel shell cross-linked micelles and nanocomposite particles, with applications in paints, anti-reflective coatings and as stimulus-responsive Pickering emulsifiers. [4]

Awards and honours

Armes was elected a Fellow of the Royal Society (FRS) in 2014. [10] More recently, he has pioneered polymerisation-induced self-assembly to produce a range of bespoke spherical, worm-like and vesicular nano-objects via RAFT dispersion polymerisation. [4] In 2013, Armes was awarded the Tilden Prize by the Royal Society of Chemistry. [13]

Related Research Articles

<span class="mw-page-title-main">Micelle</span> Group of fatty molecules suspended in liquid by soaps and/or detergents

A micelle or micella is an aggregate of surfactant amphipathic lipid molecules dispersed in a liquid, forming a colloidal suspension. A typical micelle in water forms an aggregate with the hydrophilic "head" regions in contact with surrounding solvent, sequestering the hydrophobic single-tail regions in the micelle centre.

<span class="mw-page-title-main">Copolymer</span> Polymer derived from more than one species of monomer

In polymer chemistry, a copolymer is a polymer derived from more than one species of monomer. The polymerization of monomers into copolymers is called copolymerization. Copolymers obtained from the copolymerization of two monomer species are sometimes called bipolymers. Those obtained from three and four monomers are called terpolymers and quaterpolymers, respectively. Copolymers can be characterized by a variety of techniques such as NMR spectroscopy and size-exclusion chromatography to determine the molecular size, weight, properties, and composition of the material.

A drug carrier or drug vehicle is a substrate used in the process of drug delivery which serves to improve the selectivity, effectiveness, and/or safety of drug administration. Drug carriers are primarily used to control the release of drugs into systemic circulation. This can be accomplished either by slow release of a particular drug over a long period of time or by triggered release at the drug's target by some stimulus, such as changes in pH, application of heat, and activation by light. Drug carriers are also used to improve the pharmacokinetic properties, specifically the bioavailability, of many drugs with poor water solubility and/or membrane permeability.

Poloxamers are nonionic triblock copolymers composed of a central hydrophobic chain of polyoxypropylene flanked by two hydrophilic chains of polyoxyethylene. The word poloxamer was coined by BASF inventor, Irving Schmolka, who received the patent for these materials in 1973. Poloxamers are also known by the trade names Pluronic, Kolliphor, and Synperonic.

Small-angle X-ray scattering (SAXS) is a small-angle scattering technique by which nanoscale density differences in a sample can be quantified. This means that it can determine nanoparticle size distributions, resolve the size and shape of (monodisperse) macromolecules, determine pore sizes, characteristic distances of partially ordered materials, and much more. This is achieved by analyzing the elastic scattering behaviour of X-rays when travelling through the material, recording their scattering at small angles. It belongs to the family of small-angle scattering (SAS) techniques along with small-angle neutron scattering, and is typically done using hard X-rays with a wavelength of 0.07 – 0.2 nm. Depending on the angular range in which a clear scattering signal can be recorded, SAXS is capable of delivering structural information of dimensions between 1 and 100 nm, and of repeat distances in partially ordered systems of up to 150 nm. USAXS can resolve even larger dimensions, as the smaller the recorded angle, the larger the object dimensions that are probed.

<span class="mw-page-title-main">Janus particles</span> Type of nanoparticle or microparticle

Janus particles are special types of nanoparticles or microparticles whose surfaces have two or more distinct physical properties. This unique surface of Janus particles allows two different types of chemistry to occur on the same particle. The simplest case of a Janus particle is achieved by dividing the particle into two distinct parts, each of them either made of a different material, or bearing different functional groups. For example, a Janus particle may have one-half of its surface composed of hydrophilic groups and the other half hydrophobic groups, the particles might have two surfaces of different color, fluorescence, or magnetic properties. This gives these particles unique properties related to their asymmetric structure and/or functionalization.

<span class="mw-page-title-main">Temperature-responsive polymer</span> Polymer showing drastic changes in physical properties with temperature

Temperature-responsive polymers or thermoresponsive polymers are polymers that exhibit drastic and discontinuous changes in their physical properties with temperature. The term is commonly used when the property concerned is solubility in a given solvent, but it may also be used when other properties are affected. Thermoresponsive polymers belong to the class of stimuli-responsive materials, in contrast to temperature-sensitive materials, which change their properties continuously with environmental conditions. In a stricter sense, thermoresponsive polymers display a miscibility gap in their temperature-composition diagram. Depending on whether the miscibility gap is found at high or low temperatures, either an upper critical solution temperature (UCST) or a lower critical solution temperature (LCST) exists.

Richard John Puddephatt, was born 1943 in Aylesbury, England. He is a distinguished university professor in the department of chemistry at the University of Western Ontario, in London, Ontario, Canada. Richard is a former holder of a Canada research chair in material synthesis. He has been studying the fundamental chemistry of gold and other precious metals in the development of new materials for potential applications in health care and electronics. Puddephatt's research interests involve organometallic chemistry related to catalysis and materials science, and he is considered a world expert on platinum and gold chemistry. He has authored two books: The Chemistry of Gold and The Periodic Table of Elements.

John Texter is an American engineer, chemist, and educator. He is professor emeritus of polymer and coating technology at Eastern Michigan University (EMU) in Ypsilanti, Michigan, and managing consultant of Strider Research Corporation (SRC). He is best known for his work in applied dispersion technology, small particle science, and stimuli-responsive polymers based on ionic liquids, for his international conference organization activities, including Particles 2001, Particles 2002, etc., and the Gordon Research Conferences, Chemistry at Interfaces and Chemistry of Supramolecules and Assemblies, and for his editing of the Primers page for nanoparticles.org.

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<span class="mw-page-title-main">Self-assembly of nanoparticles</span>

Nanoparticles are classified as having at least one of its dimensions in the range of 1-100 nanometers (nm). The small size of nanoparticles allows them to have unique characteristics which may not be possible on the macro-scale. Self-assembly is the spontaneous organization of smaller subunits to form larger, well-organized patterns. For nanoparticles, this spontaneous assembly is a consequence of interactions between the particles aimed at achieving a thermodynamic equilibrium and reducing the system’s free energy. The thermodynamics definition of self-assembly was introduced by Professor Nicholas A. Kotov. He describes self-assembly as a process where components of the system acquire non-random spatial distribution with respect to each other and the boundaries of the system. This definition allows one to account for mass and energy fluxes taking place in the self-assembly processes.

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References

  1. 1 2 3 Anon (2016). "Steven Peter Armes: Farapack Polymers Limited (05063994)". London: Companies House. Archived from the original on 6 December 2016.
  2. 1 2 3 4 5 Anon (2017). "Armes, Prof. Steven Peter" . Who's Who (online Oxford University Press  ed.). Oxford: A & C Black. doi:10.1093/ww/9780199540884.013.U281967.(Subscription or UK public library membership required.)
  3. 1 2 Stephen Armes. "Polymerisation-Induced Self-Assembly" (PDF). Royalsociety.org. Retrieved 23 August 2018.
  4. 1 2 3 Anon (2014). "Professor Steven Armes FRS". London: Royal Society. Archived from the original on 2 May 2014.
  5. Steven Armes publications indexed by the Scopus bibliographic database. (subscription required)
  6. Armes, Steven (2016). "Armes lab group members". shef.ac.uk. Sheffield. Archived from the original on 27 January 2016.
  7. Anon (2016). "Whitley Academy Alumni: Professor Steven Armes". Coventry: whitleyacademy.com. Archived from the original on 3 March 2016.
  8. Armes, Steven Peter (1987). Colloidal forms of conducting polymers (PhD thesis). University of Bristol. OCLC   499867741. EThOS   uk.bl.ethos.483279.
  9. 1 2 Steven Armes ORCID   0000-0002-8289-6351
  10. 1 2 3 4 Anon (2014). "Professor Steven Armes FRS". London: Royal Society. Archived from the original on 17 November 2015. One or more of the preceding sentences incorporates text from the royalsociety.org website where:
    All text published under the heading 'Biography' on Fellow profile pages is available under Creative Commons Attribution 4.0 International License." -- "Royal Society Terms, conditions and policies". Archived from the original on 25 September 2015. Retrieved 9 March 2016.{{cite web}}: CS1 maint: bot: original URL status unknown (link)
  11. Blanazs, Adam; Armes, Steven P.; Ryan, Anthony J. (2009). "Self-Assembled Block Copolymer Aggregates: From Micelles to Vesicles and their Biological Applications". Macromolecular Rapid Communications. 30 (4–5): 267–277. doi:10.1002/marc.200800713. ISSN   1022-1336. PMID   21706604.
  12. Du, Jianzhong; Tang, Yiqing; Lewis, Andrew L.; Armes, Steven P. (2005). "pH-Sensitive Vesicles Based on a Biocompatible Zwitterionic Diblock Copolymer". Journal of the American Chemical Society . 127 (51): 17982–17983. doi:10.1021/ja056514l. ISSN   0002-7863. PMID   16366531. Closed Access logo transparent.svg
  13. "Armes, FRS, Steven P., Professor". The University of Sheffield. 14 December 2021. Retrieved 27 August 2022.

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