EMPRESS : A European project to enhance process control through improved temperature measurement

A new European project called EMPRESS, funded by the EURAMET program ‘European Metrology Program for Innovation and Research,’ is described. The 3 year project, which started in the summer of 2015, is intended to substantially augment the efficiency of high-value manufacturing processes by improving temperature measurement techniques at the point of use. The project consortium has 18 partners and 5 external collaborators, from the metrology sector, high-value manufacturing, sensor manufacturing, and academia. Accurate control of temperature is key to ensuring process efficiency and product consistency and is often not achieved to the level required for modern processes. Enhanced efficiency of processes may take several forms including reduced product rejection/waste; improved energy efficiency; increased intervals between sensor recalibration/maintenance; and increased sensor reliability, i.e., reduced amount of operator intervention. Traceability of temperature measurements to the International Temperature Scale of 1990 (ITS-90) is a critical factor in establishing low measurement uncertainty and reproducible, consistent process control. Introducing such traceability in situ (i.e., within the industrial process) is a theme running through this project

Direct extreme UV-lithographic conversion of metal xanthates into nanostructured metal sulfide layers for hybrid photovoltaics

We present a versatile strategy toward the preparation of nanostructured metal sulfide layers, which exploits the photosensitivity of metal xanthates as a powerful tool for lithographic structuring. Using extreme ultraviolet interference lithography (EUV-IL), we successfully realized well-defined column and comb nanostructures. This approach provides new pathways to fabricate highly ordered structured metal sulfide layers with periodicities far below 100 nm for potential application in hybrid solar cells. © 2013 The Royal Society of Chemistry

Surfactant behavior of sodium dodecylsulfate in deep eutectic solvent choline chloride/urea

Deep eutectic solvents (DES) resemble ionic liquids but are formed from an ionic mixture instead of being a single ionic compound. Here we present some results that demonstrate that surfactant sodium dodecyl sulfate (SDS) remains surface-active and shows self-assembly phenomena in the most commonly studied DES, choline chloride/urea. X-ray reflectivity (XRR) and small angle neutron scattering (SANS) suggest that the behavior is significantly different from that in water. Our SANS data supports our determination of the critical micelle concentration using surface-tension measurements and suggests that the micelles formed in DES do not have the same shape and size as those seen in water. Reflectivity measurements have also demonstrated that the surfactants remain surface-active below this concentration

Voltammetric optimisation of TEMPO-mediated oxidations at cellulose fabric

A simple method for rapid voltammetric screening of N-oxyl based mediators and reaction conditions for electrochemical oxidation of cellulose is described. Using immobilised cellulose (cotton cloth) the screening requires small quantities of mediator and yet yields information about relative efficiency of mediator, optimum pH, and preferred buffer identity.</p

Two-vibron bound states in alpha-helix proteins : the interplay between the intramolecular anharmonicity and the strong vibron-phonon coupling

The influence of the intramolecular anharmonicity and the strong vibron-phonon coupling on the two-vibron dynamics in an $\alpha$-helix protein is studied within a modified Davydov model. The intramolecular anharmonicity of each amide-I vibration is considered and the vibron dynamics is described according to the small polaron approach. A unitary transformation is performed to remove the intramolecular anharmonicity and a modified Lang-Firsov transformation is applied to renormalize the vibron-phonon interaction. Then, a mean field procedure is realized to obtain the dressed anharmonic vibron Hamiltonian. It is shown that the anharmonicity modifies the vibron-phonon interaction which results in an enhancement of the dressing effect. In addition, both the anharmonicity and the dressing favor the occurrence of two different bound states which the properties strongly depend on the interplay between the anharmonicity and the dressing. Such a dependence was summarized in a phase diagram which characterizes the number and the nature of the bound states as a function of the relevant parameters of the problem. For a significant anharmonicity, the low frequency bound states describe two vibrons trapped onto the same amide-I vibration whereas the high frequency bound states refer to the trapping of the two vibrons onto nearest neighbor amide-I vibrations.Comment: may 2003 submitted to Phys. Rev.

Enhancing process efficiency through improved temperature measurement : the EMPRESS projects

EMPRESS 2 is a European project to enhance the efficiency of high value manufacturing processes by improving temperature measurement and control capability. This project seeks to address four contemporary thermometry challenges in this sector, and new developments from this and its predecessor project, EMPRESS, will be described: • Below 1000°C many industrial processes require reliable surface thermometry e.g. welding, coating, forging and forming. Conventional non-contact surface thermometry techniques e.g. thermal imaging are prone to large errors (tens of degrees) due to reflected thermal radiation and unknown emissivity. Contact thermometry approaches are prone to similarly large errors. Traceable imaging phosphor thermometry is being developed to overcome these difficulties, and is being combined with quantitative thermography to determine emissivity for thermometry over wide fields of view. • Above 1300°C sensor drift is a significant unaddressed issue for casting, forging and heat treatment, causing large errors. There is a need for more stable sensors and standardisation of at least one new thermocouple type to fill the gap from 1300°C to 1800°C. This is being addressed through improved Pt-Rh thermocouples and optimisation of double-walled mineral insulated, metal sheathed thermocouples by mitigating insulation breakdown and drift effects. • Combustion temperature measurement is very challenging and traceability is almost non-existent; for example, thermocouple measurements of flame temperatures can be in error by hundreds of degrees. A ‘standard flame’ that can be transported to users’ sites has been developed, and is being deployed in several high value manufacturing and industrial applications to a) demonstrate the possibility of reducing flame temperature uncertainties by at least an order of magnitude and b) for the first time to demonstrate in-situ traceability to the International Temperature Scale of 1990 (ITS-90). • Many processes are not amenable to any conventional thermometry techniques due to inaccessibility, ionising radiation, electromagnetic interference, and contamination; here methods based on optical fibres are ideal but there are no traceable calibration techniques for such sensors currently available. A suite of different fibre-optic thermometers and calibration techniques is being developed to address this. In some cases (ionising radiation) darkening of the fibre is a problem, and this is being overcome by the development of novel thermometry approaches based on practical ‘hollow core’ fibres

Submesoscale physicochemical dynamics directly shape bacterioplankton community structure in space and time

Submesoscale eddies and fronts are important components of oceanic mixing and energy fluxes. These phenomena occur in the surface ocean for a period of several days, on scales between a few hundred meters and few tens of kilometers. Remote sensing and modeling suggest that eddies and fronts may influence marine ecosystem dynamics, but their limited temporal and spatial scales make them challenging for observation and in situ sampling. Here, the study of a submesoscale filament in summerly Arctic waters (depth 0–400 m) revealed enhanced mixing of Polar and Atlantic water masses, resulting in a ca. 4 km wide and ca. 50 km long filament with distinct physical and biogeochemical characteristics. Compared to the surrounding waters, the filament was characterized by a distinct phytoplankton bloom, associated with depleted inorganic nutrients, elevated chlorophyll a concentrations, as well as twofold higher phyto- and bacterioplankton cell abundances. High-throughput 16S rRNA gene sequencing of bacterioplankton communities revealed enrichment of typical phytoplankton bloom-associated taxonomic groups (e.g., Flavobacteriales) inside the filament. Furthermore, linked to the strong water subduction, the vertical export of organic matter to 400 m depth inside the filament was twofold higher compared to the surrounding waters. Altogether, our results show that physical submesoscale mixing can shape distinct biogeochemical conditions and microbial communities within a few kilometers of the ocean. Hence, the role of submesoscale features in polar waters for surface ocean biodiversity and biogeochemical processes need further investigation, especially with regard to the fate of sea ice in the warming Arctic Ocean

Versatile thiol-based reactions for micrometer- and nanometer-scale photopatterning of polymers and biomolecules

Thiol-based chemistry provides a mild and versatile tool for surface functionalization. In the present work, mercaptosilane films were patterned by utilizing UV-induced photo-oxidation of the thiol to yield sulfonate groups via contact and interferometric lithography (IL). These photo-generated sulfonic acid groups were used for selective immobilization of amino-functionalized molecules after activation with triphenylphosphine ditriflate (TPPDF). Moreover, protein-resistant poly(oligoethyleneglycolmethacrylate) (POEGMA) brushes were grown from the intact thiol groups by a surface-induced polymerization reaction. Exploiting both reactions it is possible to couple amino-labelled nitrilotriacetic acid (NH2-NTA) to sulfonate-functionalized regions, enabling the site-specific binding of green fluorescent protein (GFP) to regions defined lithographically, while exploiting the protein-resistant character of POEGMA brushes to prevent non-specific protein adsorption to previously masked areas. The outstanding reactivity of thiol groups paves the way towards novel strategies for the fabrication of complex protein nanopatterns beyond thiol–ene chemistry