Evaluation of culture media for enumeration of Lactobacillus acidophilus, Lactobacillus casei and Bifidobacterium animalis in the presence of Lactobacillus delbrueckii subsp bulgaricus and Streptococcus thermophilus

The study compared the growth capability of probiotic (Lactobacillus acidophilus La05, Lactobacillus casei Lc01 and Bifidobacterium animalis Bb12) and non-probiotic (Lactobacillus delbrueckii subsp bulgaricus and Streptococcus thermophilus) cultures on twenty-one culture media grouped according to selectivity: non-selective agars, selective agars without antibiotics and MRS agars containing different combinations of lithium chloride, cystein, bile salts and antibiotics. Four of these media were selected for quantitative enumeration of L. acidophilus La05, L. casei Lc01, and B. animalis Bb12. The best culture media and incubation conditions for enumeration of the probiotic cultures were: B. animalis: MRS agar with dicloxacillin, 37 °C or 42 °C, anaerobiosis; L. acidophilus: MRS agar with bile salts, 37 °C or 42 °C, aerobiosis; L. casei: MRS agar with lithium chloride and sodium propionate, 37 °C or 42 °C, aerobiosis or anaerobiosis. Plating on MRS with glucose replaced by maltose, 37 °C or 42 °C, anaerobiosis, will distinguish probiotic from non-probiotic cultures. For enumeration of each probiotic in a mixed culture, the following media and incubation conditions were recommended: B. animalis: 4ABC-MRS, 42 °C, anaerobiosis, L. acidophilus: LC medium, 42 °C, aerobiosis or anaerobiosis and L. casei: LP-MRS, 42 °C, aerobiosis or anaerobiosis. In all experiments, differences in counts using pour plating or surface plating were not significant (P ≤ 0.05).     

The structural characterization of (NH4)2B10H10 and thermal decomposition studies of (NH4)2B10H10 and (NH4)2B12H12

The structure of (NH₄)₂B₁₀H₁₀ (1) was determined through powder XRD analysis. The thermal decomposition of 1 and (NH₄)₂B₁₂H₁₂ (2) was examined between 20 and 1000 °C using STMBMS methods. Between 200 and 400 °C a mixture of NH₃ and H₂ evolves from both compounds; above 400 °C only H₂ evolves. The dihydrogen bonding interaction in 1 is much stronger than that in 2. The stronger dihydrogen bond in 1 resulted in a significant reduction by up to 60 °C, but with a corresponding 25% decrease in the yield of H₂ in the lower temperature region and a doubling of the yield of NH₃. The decomposition of 1 follows a lower temperature exothermic reaction pathway that yields substantially more NH₃ than the higher temperature endothermic pathway of 2. Heating of 1 at 250 °C resulted in partial conversion of B₁₀H₁₀²⁻ to B₁₂H₁₂²⁻. Both 1 and 2 form an insoluble polymeric material after decomposition. The elements of the reaction network that control the release of H₂ from the B₁₀H₁₀²⁻ can be altered by conducting the experiment under conditions in which pressures of NH₃ and H₂ are either near, or away from, their equilibrium values.     

Layered double hydroxides as efficient drug delivery system of ciprofloxacin in the middle ear: an animal study in rabbits

Chronic otitis media is a common disease often accompanied by recurrent bacterial infections. These may lead to the destruction of the middle ear bones such that prostheses have to be implanted to restore sound transmission. Surface coatings with layered double hydroxides (LDHs) are evaluated here as a possibility for drug delivery systems with convenient advantages such as low cytotoxicity and easy synthesis. Male New Zealand White rabbits were implanted with Bioverit^® II middle ear prostheses coated with the LDH Mg₄Al₂(OH)₁₂(SO₄)₂·6H₂O impregnated with ciprofloxacin. 12 (group 1) were directly infected with Pseudomonas aeruginosa and another 12 (group 2) 1 week after the implantation. Clinical outcome, blood counts, histological analyses and microbiological examination showed an excellent antimicrobial activity for group 1, whereas this effect was attenuated in animals where infection was performed 1 week after implantation. This is the first study to demonstrate an efficient drug delivery system with an LDH coating on prostheses in the middle ear.     

Acoustic emission technique for online monitoring during cold forging of steel components: a promising approach for online crack detection in metal forming processes

The acoustic emission technique is a very promising non-destructive and online capable approach for the detection of damage events in metal forming processes. The feasibility of using this testing method for online monitoring of cold forging processes of the case hardening steel 1.7321 (20MoCr4) was experimentally proven. In this paper, exemplary upsetting tests under varying test conditions were continuously monitored to analyze the relationship between cracking and resulting AE as well as to determine ideal AE measuring parameters. Finally, the critical forming stage of an industrial cold forging process for manufacturing of drive bevel gears is examined by applying acoustic emission technique. Cracking and tool wear were detected by analyzing the distribution of the AE parameters energy, hits and amplitude over the forming process.     

Microwave-hydrothermal synthesis and characterization of nanostructured copper substituted ZnM2O4 (M = Al, Ga) spinels as precursors for thermally stable Cu catalysts

Nanostructured Cu(x)Zn(1-x)Al(2)O(4) with a Cu:Zn ratio of ?:? has been prepared by a microwave-assisted hydrothermal synthesis at 150 °C and used as a precursor for Cu/ZnO/Al(2)O(3)-based catalysts. The spinel nanoparticles exhibit an average size of approximately 5 nm and a high specific surface area (above 250 m(2) g(-1)). Cu nanoparticles of an average size of 3.3 nm can be formed by reduction of the spinel precursor in hydrogen and the accessible metallic Cu(0) surface area of the reduced catalyst was 8 m(2) g(-1). The catalytic performance of the material in CO(2) hydrogenation and methanol steam reforming was compared with conventionally prepared Cu/ZnO/Al(2)O(3) reference catalysts. The observed lower performance of the spinel-based samples is attributed to a lack of synergetic interaction of the Cu nanoparticles with ZnO due to the incorporation of Zn(2+) in the stable spinel lattice. Despite its lower performance, however, the nanostructured nature of the spinel catalyst was stable after thermal treatment up to 500 °C in contrast to other Cu-based catalysts. Furthermore, a large fraction of the re-oxidized copper migrates back into the spinel upon calcination of the reduced catalyst, thereby enabling a regeneration of sintered catalysts after prolonged usage at high temperatures. Similarly prepared samples with Ga instead of Al exhibit a more crystalline catalyst with a spinel particle size around 20 nm. The slightly decreased Cu(0) surface area of 3.2 m(2) g(-1) due to less copper incorporation is not a significant drawback for the methanol steam reforming.     

The return of degraded stream ecosystems by using positive impacts from near‐natural sections: a new practical guide for restorations

Streams in North Rhine‐Westphalia (Germany) are frequently impacted by hydromorphological degradation leading to a loss of sensitive species and a reduction in diversity. These findings mean that the final objective of the European Water Framework Directive to achieve the good ecological status will be failed for a large number of streams. In a holistic approach, a new concept, considering the cost efficiency, has been developed to enhance habitats by morphological changes. This guide serves as a basis for stream restoration projects. The theoretical background is that near‐natural sections influence adjacent sections of medium habitat quality positively by migration of type‐specific sensitive organisms. The preconditions are a local taxa richness in the catchment area, the reduction of nutrients and organic matter, and the guarantee of free movement. This so‐called ‘spreading effect’ can be measured upstream and downstream. The length of by these means valourized sections depends on the stream type and on the biological quality component.     

Nanostructured supported palladium catalysts—Non-oxidative methane coupling

The Pd on α-Al₂O₃ catalysts with Pd particles in the low nanometer range have been prepared by a sonochemical reduction and a colloidal method, respectively. The two catalysts differ in their particle size, the widths of their particle size distributions and the amount of carbon incorporation in the Pd lattice.The adsorptive properties of the Pd/Al₂O₃ samples are different as a result of the different preparation methods. The methane adsorption capacity of that sample with smaller particles is lower than that of the catalyst with larger particles and the energy of activation is nearly doubled. DRIFTS and TPD results of CO adsorption supported by transmission electron microscopy data indicate that the PdSON catalyst with smaller and more homogeneous particles than PdCOL is highly dispersed which influences the coupling-hydrogenolysis process.The catalytic activity evidenced the formation of different adspecies during methane coupling and chemisorption on both catalysts. During the hydrogenation the carbon adspecies formed mainly methane at low adsorption temperatures. The significant amount of adsorbed methane at 773 K is governed by the highly active coordination unsaturated sites at the surface.     

Production of Strong Steel‐Aluminum Composites by Formation of Intermetallic Phases in Compound Forging

In times of increasing energy costs automotive light weight construction is gaining more importance. The production of hybrid compounds by forging is a promising method to successfully manufacture functional parts by applying resource‐saving process steps. However, in compound forging of steel‐aluminum parts shrinking gaps may form because of the different thermal expansion coefficients. To avoid these unwanted gaps, it is necessary to achieve a firmly bonded joint e.g. by intermetallic phases. This paper deals with the investigation of the influences of different sample preparations, process parameters and true strains on the formation of intermetallic phases. Thus, the optimum production parameters for compound forging of steel‐aluminum parts will be determined.     

Three-dimensional titania pore structures produced by using a femtosecond laser pulse technique and a dip coating procedure

In this work, the preparation of three-dimensional hierarchical pore structures by a combination of laser-based templates and the self-organization process of mesostructured titania is presented. For this purpose macrostructured polymers produced by two-photon polymerization act as a template for the deposition of a mesostructured titania film from a solution containing an amphiphilic block copolymer by dip coating. A carefully applied calcination procedure removes both the macrotemplating polymer and the mesotemplating surfactant molecules so that a replica of the initial polymer structure with a hierarchical (macro- and meso-) pore system is obtained. In addition, the titania, which is amorphous after deposition, is transferred into crystalline anatase during calcination. Materials with dual pore systems are interesting for possible applications in catalysis and sorption, and three-dimensional crystalline structures from materials with high refraction index are attractive for photonic applications, for example as photonic crystals.