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Chemistry World January 28, 2008 Lewis Brindley |
Graphene Sheets with Less Flap Researchers in Australia have developed a new way to make graphene, the atom-thin sheets that stack together to make the graphite found in pencil lead.  |
Chemistry World January 28, 2008 Lewis Brindley |
Colourful Crystals Monitor Humidity Chinese chemists have developed a material that changes color according to the humidity of the air around it.  |
Chemistry World January 25, 2008 Simon Hadlington |
Catalysis Probed with MRI Scientists have developed a way of peering into a microreactor to watch gases react on a solid catalyst.  |
Chemistry World January 23, 2008 James Mitchell Crow |
2008 Wolf Prize Winners Revealed US chemists William Moerner and Allen Bard have jointly been awarded the 2008 Wolf Prize for Chemistry, for their pioneering work on single molecule spectroscopy.  |
Chemistry World January 23, 2008 Michael Gross |
Turning Gas Into Fuel Cheaply Researchers in Japan have developed a fuel cell that can convert methane, the main component of natural gas, into methanol, a useful fuel, at moderate temperatures.  |
Chemistry World January 23, 2008 Lewis Brindley |
New Light on Fluorescent Gels Organic gels that fluoresce in a wide range of vibrant colors could one day be used in devices ranging from digital displays to photovoltaic cells.  |
Chemistry World January 16, 2008 Michael Gross |
Chemists Tame the Uranyl Ion UK chemists have devised a 'trap' in which to catch and modify the predominant form of uranium.  |
Chemistry World January 16, 2008 Jonathan Edwards |
Microneedles May Mean an End to Painful Injections Microneedles that could deliver drugs painlessly can be made more quickly and cheaply thanks to a laser polymerisation technique developed by US scientists.  |
Chemistry World January 14, 2008 Michael Gross |
Ice-Cream Without the Crunch A mixture of molecules obtained from gelatin could help to make food last longer in the freezer and make ice-cream creamier.  |
Chemistry World January 10, 2008 Jonathan Edwards |
Textbook Reaction Has a Subtle Twist The SN2 bimolecular nucleophilic substitution, a textbook reaction fundamental to organic synthesis, has a subtle twist, according to researchers.  |
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