Enhanced production of hydroxymethylfurfural from fructose with solid acid catalysts by simple water removal methods

This paper demonstrates two simple ways to increase 5-hydroxymethylfurfural (HMF) yield (selectivity) in fructose dehydration with various solid acid catalysts. One is a water removal from the reaction mixture by a mild evacuation at 0.97 × 10⁵ Pa; it increases HMF yield for various catalysts (heteropoly acid, zeolite, and acidic resin). The removal of water suppresses two undesired reactions: the hydrolysis of HMF to levulinic acid and the reaction of partially dehydrated intermediates to condensation products. The other method is a decrease in the particle (bead) size of the resin (Amberlyst-15). The crushed and sieved Amberlyst-15 powder in a size of 0.15–0.053 mm shows 100% HMF yield at high fructose concentration (50 wt.% in DMSO), which is to our knowledge the highest yield to date. Near-infrared spectroscopic characterization of adsorbed water suggests that the enhanced yield can be caused by an improved removal of adsorbed water in a small-size resin particle.     

Evaluation of selective plating media for the detection of heat- or freeze-injured Staphylococcus aureus

The efficacy of Baird-Parker (BP) agar, mannitol-salt-egg yolk (MSEY) agar and mannitol salt (MS) agar in detecting Staphylococcus aureus FRI-100 heated at 52 degrees C for 20 min in 100 mmol/L potassium phosphate buffer was determined. Brain heart infusion agar with 1% pyruvate (BHIP agar) supported the highest recovery of injured cells and was used as the control medium. Of the three selective media, significantly higher recovery of heat-injured cells was observed on BP agar than MSEY agar, and the poorest recovery was observed on MS agar (p < 0.05). Low recovery of unheated cells was obtained for MS compared with other media (p < 0.05). A reduction in populations occurred gradually in reagent-grade water stored for 14 days at -20 degrees C. There was no significant difference between BHIP agar and MS agar in the number of freeze-injured cells recovered from 1 to 14 days.     

PACVD-Beschichtung von Druckgußwerkzeugen unter ökonomischen und ökologischen Gesichtspunkten

Application of Wear Resistant PACVD-Coatings in Aluminium Diecasting under Economical and Ecological Aspects Aluminium pressure diecasting is a frequently applied manufacturing process for the near netshape production of precision parts. State of the art production techniques still demand considerable amounts of die lubricants. But the side effects of these lubricants include a decrease in surface quality of the cast part as well as a prolongation of the casting cycle time. The job quality decreases and the waste and exhaust disposal during production and application of lubricants is ecologically risky. In this study different wear resistant coating systems have been developed in order to minimize the use of die lubricants in the casting process while at the same time increasing the service life of the diecasting tools. Nitrides, carbides and borides of titanium were synthesized by means of DC-pulse-PACVD. The influence of the process parameters gas composition, pressure, voltage and pulse/pulse repetition ratio was investigated. Compositional analysis was performed by analytical methods such as XRD, EDS, WDS and SIMS. Hardness, adhesion and friction behaviour of the layers were determined in order to describe their mechanical properties. The wetting angle was determined and the corrosion resistance was evaluated in dip tests in aluminium melt. A selection of the best coatings was then compared in diecasting praxis tests under tightened-up conditions reducing the amount of lubricants. TiN, Ti(B,N), TiC and multilayers of the system Ti-C-N were deposited exhibiting a wide range of stoichiometry. The coatings reached hardness values of up to 4400 HK0.005 and the friction coefficient μ was in the range of 0.3. In the diecasting praxis test the amount of die lubricant could be reduced by 97%. Under most severe conditions all layer types led to a minimum increase in the lifetime of the tool of factor 60 compared to an untreated dummy. A strong dependence on the layer type and on its stoichiometry could be observed. Ti(B,N) as the most successful coating in this study has not yet shown any sign of failure and already achieved an increase in lifetime of 300 times.     

Porcine enamel matrix derivative enhances the formation of reparative dentine and dentine bridges during wound healing of amputated rat molars

We examined the biological effects of porcine enamel matrix derivative (EMD; Emdogain) on the formation of reparative dentine and dentine bridges in rat molars after pulp amputation. The pulp chambers of upper molars of Wistar rats were perforated and the amputated pulp surfaces were directly capped with either EMD or its carrier propylene glycol alginate (PGA) as control. The cavities were then restored with glass-ionomer cement. On post-amputation days 4-30, the dissected maxillae were examined by light and electron microscopy. In PGA-capped pulp, reparative dentine had been formed over the dentine walls under the prepared cavity on day 7 post-amputation and its thickness extended until day 30. On day 30, as well as reparative dentine formation, diffuse calcification had occurred beneath the amputated wound surfaces. Dentine bridge formation under the amputated coronal pulp surface was observed in 18.2% of amputated pulp on day 30. In EMD-capped pulp, reparative dentine had already been formed by odontoblast-like cells over the dentine walls, already on day 4 post-amputation, and its thickness extended until day 30. The Ca and P weight % and Ca/P ratio of reparative dentine matrix were similar to those of pre-existing dentine matrix, and these values were not different between PGA and EMD-capped pulp. Dentine bridge formation was observed in 27.3% of EMD-capped pulp on day 30. Our results suggest that EMD enhances the formation of both reparative dentine and dentine bridges during wound healing of amputated rat molar pulp.     

Study of local intracellular signals regulating axonal morphogenesis using a microfluidic device

The establishment and maintenance of axonal patterning is crucial for neuronal function. To identify the molecular systems that operate locally to control axonal structure, it is important to manipulate molecular functions in restricted subcellular areas for a long period of time. Microfluidic devices can be powerful tools for such purposes. In this study, we demonstrate the application of a microfluidic device to clarify the function of local Ca²⁺ signals in axons. Membrane depolarization significantly induced axonal branch-extension in cultured cerebellar granule neurons (CGNs). Local application of nifedipine using a polydimethylsiloxane (PDMS)-based microfluidic device demonstrated that Ca²⁺ entry from the axonal region via L-type voltage-dependent calcium channels (L-VDCC) is required for branch extension. Furthermore, we developed a method for locally controlling protein levels by combining genetic techniques and use of a microfluidic culture system. A vector for enhanced green fluorescent protein (EGFP) fused to a destabilizing domain derived from E. coli dihydrofolate reductase (ecDHFR) is introduced in neurons by electroporation. By local application of the DHFR ligand, trimethoprim (TMP) using a microfluidic device, we were able to manipulate differentially the level of fusion protein between axons and somatodendrites. The present study revealed the effectiveness of microfluidic devices to address fundamental biological issues at subcellular levels, and the possibility of their development in combination with molecular techniques.     

Study on the determination of pesticide residues in crops by ion-trap GC/MS/MS

Ion-trap GC/MS/MS was evaluated for the multi-residue determination of pesticides in agricultural products. Matrices were extracted from samples (spinach, carrot, onion and brown rice) with acetone and submitted to gel permeation chromatography, followed by a clean-up step through a graphite carbon cartridge. Thirty-five pesticides were added to either matrix, and analyzed by GC/MS/MS. Detection limits of pesticides by GC/MS/MS was almost the same as those by GC/MS (SIM). Coefficients of variation of peak area in 5 measurements of each pesticide at 0.1 microgram/mL or 0.05 microgram/mL with or without matrices were mostly acceptable, though those of 20 pesticides out of 35 were higher than 10% at a concentration of 0.02 microgram/mL. It was indicated that matrix artifacts, which interfere with GC/MS-Scan analysis, could be eliminated in some cases by using GC/MS/MS.     

Magnetic properties and phase diagram of Ni50Mn50−xGax ferromagnetic shape memory alloys

We present the magnetic properties and the magnetic phase diagram of Ni₅₀Mn_50?xGa_x ferromagnetic shape memory alloys across a wide concentration range. Martensitic transformation, intermediate transformation, B2–L2₁ order–disorder transformation, Néel and Curie temperatures are determined for the prepared samples. The martensitic transformation temperature decreases with increasing Ga concentration and bends two times when crossing the Curie temperature and the intermediate-phase transformation temperature. Spontaneous magnetization and its composition dependence were also investigated. Composition dependence of the transformation temperatures and the spontaneous magnetization in the martensite phase of Ni₅₀Mn_50?xGa_x are compared with those of Ni₅₀Mn_50?xIn_x and Ni₅₀Mn_50?xSn_x, revealing a similarity in the NiMn-based alloy systems.     

Corrosion properties of titanium based hard coatings on steel

Titanium nitride TiN, titanium boronitride Ti(B,N) and titanium carbonitride Ti(C,N) coatings were deposited by PA-CVD on tempering and stainless steel substrates. The deposition process can be supervised by OES. The coatings were characterized XRD, SEM and WDS as well as hardness, adhesion and friction tests. Electrochemical impedance measurements and cyclic voltammetry in praxis relevant media were carried out. Mechanical and corrosion properties of the coatings can be controlled by the PA-CVD process parameters. The incorporation of chlorine in the coating can be varied by the process parameters with TiCl₄ or completely avoided using metallo-organic precursors. No influence of the chlorine content on the corrosion behavior was observed. Even coatings with extremely high chlorine content still exhibit an excellent corrosion resistance. Thus, the microstructure of the coating is the key to the corrosion properties of hard coatings on steel. A new micro electrochemical scanning droplet technique with a lateral resolution of 150 μm allows the investigation of TiN-coated substrates of complex geometry. The PA-CVD technique permits the deposition of dense and pinhole free coatings. On structures with simulated aspect ratios less than 3, a dense protective coating is proved. However, if the formation of micro pores is not suppressed by the optimal choice of deposition parameters, low-alloyed steel substrates corrode through pores, causing a detachment of the coating. On layers deposited on stainless steel, no sign of substrate corrosion could be detected. A model for the corrosion mechanism is given in Fig. 17.