Numerical model of a planar jet wiping system for continuous strip lines

Journal of Mechanical Science and Technology - The present study focuses on the numerical modelling of gas-jet wiping process. Many processes involving liquids are necessary during steel...     

Colloidal thiophosphorus calcium salt as antiwear additive

This paper describes the synthesis of an oil-soluble colloidal calcium thiophosphate by a direct route. It consists of the reaction of calcium oxide or hydroxide with tetraphosphorus decasulphide and water in the presence of a surfactant such as a calcium alkylaryl sulphonate in an organic medium. Reaction and micellisation occurred simultaneously according to a one-step process. The product is characterised by a high calcium, phosphorus and sulphur content. The colloidal nature of the product has been confirmed by dialysis. The ³¹P-NMR spectrum showed signals characteristic of a blend of different calcium thiophosphates, plus calcium phosphate. The product could be defined as a core of different calcium (thio)phosphates surrounded by a calcium alkylaryl sulphonate shell, according to a reverse micelle type association in oil. This compound was evaluated as an antiwear additive in a 130 Neutral Solvent mineral oil by anti-wear and extreme-pressure four-ball tests. The extreme-pressure characteristics depend on the concentration of mineral colloidal core in oil. The antiwear properties are a function not only of the concentration, but also of the colloidal core/surfactant shell ratio. Thermogravimetric analysis of these colloidal species shows a weight loss in the 350°C to 450°C range, due to surfactant degradation. The further evolution of weight loss up to 900°C demonstrates the high thermal stability of the colloidal calcium (thio)phosphate core.     

Polymeric materials as anion-exchange membranes for alkaline fuel cells

After summarizing the different fuel cells systems, including advantages and drawbacks, this review focuses on the preparation of copolymers and polymeric materials as starting materials for solid alkaline fuel cells membranes. The requirements for such membranes are also summarized. Then, different strategies are given to synthesize anion-exchange polymeric materials containing cationic (especially ammonium) groups. The first pathway focuses on heterogeneous membranes that consist in: (i) polymer blends and composites based on poly(alkene oxide)s and hydroxide salts or polybenzimidazole doped with potassium hydroxide, (ii) organic–inorganic hybrid membranes especially those synthesized via a sol–gel process, and (iii) (semi)interpenetrated networks based on poly(epichlorhydrine), poly(acrylonitrile) and polyvinyl alcohol for example, that have led to new polymeric materials for anion-exchange membranes. The second and main part concerns the homogeneous membranes divided into three categories. The first one consists in materials synthesized from (co)polymers obtained via direct (co)polymerization, for example membranes based on poly(diallyldimethylammonium chloride). The second pathway concerns the modification of polymeric materials via radiografting or chemical reactions. These polymeric materials can be hydrogenated or halogenated. The radiografting of membranes means the irradiation via various sources – electron beam, X and γ rays, ⁶⁰Co and ¹³⁷Cs that lead to trapped radicals or macromolecular peroxides or hydroperoxides, followed by the radical graft polymerization of specific monomers such as chloromethyl styrene. The third route deals with the chemical modifications of commercially available hydrogenated aliphatic and aromatic (co)polymers, and the syntheses of fluorinated (co)polymers such as carboxylic and sulfonic perfluoropolymers. In addition, several approaches for the crosslinking of above-mentioned polymeric materials are also reported as this process enhances the properties of the resulting membranes. Moreover, electrochemical and thermal properties of various above ionomers are given and discussed.     

Dye–fiber interactions in PET fibers: Hydrogen bonding studied by IR‐spectroscopy

Dye–fiber interactions are studied in poly (ethylene terephthalate) fibers by FT‐IR spectroscopy. It is shown for the first time that DRIFTS (diffuse reflectance infrared Fourier transform spectroscopy) serves as an easy applicable and accurate technique for the study of fibrous structures. This article focuses on the possible hydrogen bond interactions in the dye–fiber system, where the PET fibers are dyed with anthraquinone‐based disperse dyes. The dyes and related anthraquinone structures are studied in both the dilute solution state, the solid state, and as present in the PET fibers. It is proven that 1‐amino anthraquinones show strong “chelate‐type” intramolecular hydrogen bonding in all three states. In the fibers an important supplementary intermolecular hydrogen bonding with the C?O groups in the PET fiber is observed. The extend of hydrogen bonding seems to be prone to dye concentration variations. Further analysis by modulated differential scanning calorimetry links the hydrogen bonding to an intrinsic plasticizing effect of the dyes affecting the dye diffusion process. This thus offers a tool for the fundamental understanding of the dyeing process and possible observed differences in dyeing behavior in dye–fiber systems. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007     

Numerical simulation of dilute turbulent gas‐particle flow with turbulence modulation

A numerical study of a dilute turbulent gas‐particle flow with inelastic collisions and turbulence modulation in an Eulerian framework is described. A new interpretation is provided for the interaction/coupling terms, based on a fluctuating energy transfer mechanism. This interpretation provides for a new robust closure model for the interaction terms with the ability to predict the turbulence dampening as well as the turbulence enhancement phenomenon. Further, the model developed herein is investigated along with a variety of other published closure models used for the interaction/coupling terms, particle drag, and solid stress. The models are evaluated against several sets of benchmark experiments for fully‐developed, turbulent gas‐solid flow in a vertical pipe. © 2011 American Institute of Chemical Engineers AIChE J, 2012     

Farbmeßgeräte für transparente Flüssigkeiten sichern die Qualität in der chemischen Industrie – Qualitätskontrolle an transparenten Flüssigkeiten

Colour Measuring Instruments for Transparent Liquids Safeguard the Quality in the Chemical Industry – Quality Control of Transparent Liquids In many areas of the chemical industry a complete product specification comprises – besides various other parameters – the colour characteristics as well. The colour of transparent liquids is still frequently determined by visual comparison of the product with e.g. iodine, Hazen- or Gardner colour standard solutions or appropriate colourfilter discs. In 1989 a new DIN 53995 standard for instrumental colour assessment of transparent liquids was introduced to replace the error-prone, subjective methods of visual comparisons. Dr. Lange GmbH, Düsseldorf, has developed the LICO 200 spectrophotometer under consideration of the new DIN 53995 for objective colour assessment in compliance with the iodine, Hazen and Gardner colour scales.