Carbonaceous deposits on heterogeneous catalysts are traditionally associated with catalyst deactivation. However, they can play a beneficial role in many catalytic processes, e.g. dehydrogenation, hydrogenation, alkylation, isomerisation, Fischer–Tropsch, MTO etc. This review highlights the role and mechanism by which coke deposits can enhance catalytic performance.

BackgroundBiological fluids often have interesting and unusual physical properties to adapt them for their specific purpose. Laboratory-based rheometers can be used to characterise the viscoelastic properties of such fluids. This, however, can be challenging as samples often do not retain their natural properties in storage while conventional rheometers are fragile and expensive devices ill-suited for field measurements. We present a portable, low-cost extensional rheometer designed specifically to enable in situ studies of biological fluids in the field. The design of the device (named Seymour) is based on a conventional capillary break-up extensional rheometer (the Cambridge Trimaster). It works by rapidly stretching a small fluid sample between two metal pistons. A battery-operated solenoid switch triggers the pistons to move apart rapidly and a compact, robust and inexpensive, USB 3 high speed camera is used to record the thinning and break-up of the fluid filament that forms between the pistons. The complete setup runs independently of mains electricity supply and weighs approximately 1 kg. Post-processing and analysis of the recorded images to extract rheological parameters is performed using open source software.ResultsThe device was tested both in the laboratory and in the field, in Brunei Darussalam, using calibration fluids (silicone oil and carboxymethyl cellulose solutions) as well as Nepenthes pitcher plant trapping fluids as an example of a viscoelastic biological fluid. The fluid relaxation times ranged from 1 ms to over 1 s. The device gave comparable performance to the Cambridge Trimaster. Differences in fluid viscoelasticity between three species were quantified, as well as the change in viscoelasticity with storage time. This, together with marked differences between N. rafflesiana fluids taken from greenhouse and wild plants, confirms the need for a portable device.ConclusionsProof of concept of the portable rheometer was demonstrated. Quantitative measurements of pitcher plant fluid viscoelasticity were made in the natural habitat for the first time. The device opens up opportunities for studying a wide range of plant fluids and secretions, under varying experimental conditions, or with changing temperatures and weather conditions.Electronic supplementary materialThe online version of this article (doi:10.1186/s13007-015-0059-5) contains supplementary material, which is available to authorized users.

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The impact of the chemical and physical composition of biochar catalysts is demonstrated in the carboxylation of glycerol with carbon dioxide for the first time, using acetonitrile as a dehydrating agent. Biochars are an important emerging class of catalytic material that can readily be produced from low-value biomass residues; however, the impact of feedstock choice is often overlooked. The ash content of biochar from three different feedstocks is shown to be catalytically active for the production of glycerol carbonate and triacetin, whilst low-ash catalysts such as soft wood biochar and commercial activated charcoal are inactive. Following treatment with hydrochloric acid, yields of glycerol carbonate over ash were reduced by over 94%, and triacetin was no longer produced. This has been attributed to the loss of potassium content. Carbon content was shown to be catalytically active for the synthesis of diacetin, and graphitic carbon may be beneficial. Through the development of structure–performance relationships, biomass feedstocks with the most suitable properties can therefore be selected to produce biochars for specific catalytic applications. This would expand the range of reactions which can be effectively catalysed by these materials and enhance the development of a more circular and sustainable chemicals industry.

Samples of synchronously growing cultures of Escherichia coli B/r removed at predetermined time intervals after synchronization were added to solutions containing bactericidal concentrations of tetra‐cycline. Three active antibacterials, 7‐nitro‐6‐demethyl‐6‐deoxytetracycline, 9‐amino‐6‐demethyl‐6‐deoxytetracycline and 6‐demethyl‐6‐deoxytetracycline, and one inactive compound, 7‐chloroisotetra‐cycline, were studied. Survival curves for the active agents, determined using samples of culture differing in age, were of constant slope for a given tetracycline. It is concluded that interruption of protein synthesis is the primary mode of action at bactericidal concentrations of tetracyclines, the same process as has been established for the action of the tetracyclines at the lower bacteriostatic concentrations.