Influence of the anionic part of the stabilizer on electroless nickel-boron plating

Selectivity and smooth operation of electroless nickel plating require that a stabilizing agent is used. It operates by blocking catalytic activity on unwanted germination sites and regulating the activity of the substrate. In the case of alkaline electroless nickel-boron plating systems, which use sodium (or potassium) borohydride as reducing agent, lead and thallium salts are the most popular stabilizers. However, there is little knowledge about the way the stabilizer acts. In this study, 4 different lead-based stabilizers (tungstate, sulphate, nitrate and chloride) have been used, all other things left constant, in electroless nickel-boron plating baths. The thickness, composition, roughness, morphology, hardness and structure of all the obtained coatings have been investigated. Chloride led to thinner deposits and the boron content varied between 5.5?wt.% for lead tungstate and 6.5?wt.% for lead nitrate and lead sulphate, with a lead content between 0.2 and 0.25?wt.%. Coatings obtained with a lead tungstate stabilized bath were thicker, harder and contained less boron and lead than the others. This shows the influence of the anionic part of the stabilizing agent on the plating process.     

Adhesion of resin cement to contemporary hybrid ceramic and polymeric CAD/CAM materials: effect of conditioning methods and ageing

This study assessed the effect of different surface conditioning methods and ageing protocols on adhesion of resin cement to hybrid ceramic and polymeric CAD/CAM materials. CAD/CAM materials (n?=?360, n?=?30 per group), namely (a) Lithium disilicate (IPS e.max CAD-LIS), (b) Zirconia (IPS e.max ZirCAD-ZIR), (c) Polymer (Lava Ultimate-LAV), (d) Polymer infiltrated ceramic network (Enamic-ENA), (e) Polymer infiltrated ceramic (Experimental-1-CS1), (f) Polymer infiltrated ceramic (Experimental-2-CS2), (g) Lithium disilicate reinforced alumina (n!ce-NIC) were cut into slices (3?×?6 × 8?mm³) and conditioned: (a) Method 1: 5% hydrofluoric acid etching (H)+silane and (b) Method 2: Silica coating (CoJet (A)+silane). Group LIS was conditioned with only Method 1 and Group ZIR only with Method 2 (control). Resin cement (Variolink Esthetic II) was bonded onto the conditioned specimens and photopolymerized. One-half of the specimens was subjected to ageing (thermocycling 5–55°, 5000 cycles) and the other half was stored in distilled water (37?°C, 24?h). The resin-substrate interface was loaded under shear forces in a Universal Testing Machine (1?mm/min). Data (MPa) were analyzed using two-way ANOVA and Tukey`s tests (α?=?0.05). Substrate type, conditioning method and ageing had a significant effect on adhesion values (p?<?.05). In aged conditions, ENA-H, ENA-A, LAV-H, LAV-A, CS2-A (15?±?4 – 11.6?±?5) showed no significant difference (p?>?.05), with the CS2-A (15?±?4) showing the least reduction (5.5%) compared to all other groups (5.8–62.6%). CS1-A (100%) followed by ENA-H, ENA-A (93%), CS2-A (80%) presented the highest incidence of cohesive failures after ageing.     

First isolation of Brevibacterium sp. pigments in the rind of an industrial red‐smear‐ripened soft cheese

The smear‐ripened soft cheeses are characterised by a surface orange‐red‐brown colour, which has a microbial origin. For a long time, this colouration was mainly imputed to Brevibacterium linens. However, the latest published works, based on molecular biology, have shown a minor role for this bacterium. This study shows the results obtained with an industrial cheese named Vieux‐Pané, which is characterised by the presence of carotenoids from Brevibacterium linens group at its surface. This demonstrates that, under certain conditions, the Brevibacterium linens group (Brevibacterium linens and Brevibacterium aurantiacum sp. nov.) is able to produce pigments and to colour cheeses effectively.     

Optimisation of production conditions for 4-hydroxy-2,6-dioxabicyclo(3,3,0)octan-8-one[1S,4S,5R] by catalytic oxidation

The 4-Hydroxy-2,6-dioxabicyclo(3,3,0)Octan-8-one[1S,4S,5R], monoketone, is obtained by catalytic oxidation of isosorbide—or 2,6-dioxabicyclo(3,3,0)4,8-octandiol[1R,4S,5R,8R]—in an aqueous solution with a stream of oxygen and in the presence of a platinum on carbon catalyst. Setting up sequentially two experimental designs made it possible to study the three main factors which influence the monoketone formation in the case of two reactors of different size and profile. Optimisation of selective and/or quantitative conditions is carried out by comparing response surfaces. Several functional configurations for a discontinuous reactor under agitation are proposed as a function of the constraints chosen.     

Engagement et persuasion par la peur: Vers une communication engageante dans le domaine de la santé.

Evidence from psychological research has shown the importance of fear on attitude and/or behavior change. The experiment hereby quoted tests the influence of commitment (high vs. low) on an attempt of persuasive message for a forthcoming effect, that is, after reading an antialcohol message to subjects. The idea consists in inducing alcohol consumers toward modifying their attitude and behavioral intentions toward alcohol. As expected, the high committed drinkers (i.e., regular drinkers) resist persuasion (on the level of both attitude and intention). The low committed drinkers (i.e., occasional drinkers) do not resist persuasion but adopt further on a more favorable attitude toward alcohol. The drinkers who had read a strongly threatening, yet at the same time strongly reassuring, message express the strongest intention to reduce their alcohol consumption. Results are described with reference to Witte's (1998) extended parallel process model. A new perspective is presented at the end of our paper, that is, toward a "committing communication." (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Rational design, synthesis, and evaluation of nanomolar type II dehydroquinase inhibitors

The in silico design, synthesis, and biological evaluation of ten potent type II dehydroquinase inhibitors are described. These compounds contain an anhydroquinate core, incorporated as a mimic of the enolate reaction intermediate. This substructure is attached by a variety of linking units to a terminal phenyl group that binds in an adjacent pocket. Inhibitors were synthesised from (-)-quinic acid using palladium-catalysed Stille and carboamidation chemistry. Several inhibitors exhibited nanomolar inhibition constants against type II dehydroquinases from Streptomyces coelicolor and Mycobacterium tuberculosis. These are among the most potent inhibitors of these enzymes reported to date.     

Tracking a new cell-penetrating (W/R) nonapeptide, through an enzyme-stable mass spectrometry reporter tag

We have designed a mass stable reporter (msr) tag with m/z over 500, trifluoroacetyl(alpha,alpha-diethyl)Gly-Lys(Nepsilonbiotin)-(D)Lys-Cys, for the quantification of the uptake and study of the degradation processes of cell-penetrating peptides (CPP), by matrix assisted laser desorption/ionization time-of-flight (MALDI-TOF) mass spectrometry. This tag was found stable in cell lysis conditions. Using a quantitative MALDI-TOF mass spectrometry analysis based method, an accurate tracking of a new CPP and of its degradation products could be done. (1) The new msr(W/R) nonapeptide (H-RRWWRRWRR-NH2) enters chinese hamster ovary (CHO) K1 cells with a kinetic reaching a steady state after 30-60 min of incubation. This plateau was stable for 4 h and decreased slowly afterward. (2) The peptide msr(W/R) nonapeptide was not cytotoxic over 48 h incubation with CHO cells. (3) After 1 h incubation, the msr(W/R) nonapeptide accumulated with a 3-fold higher concentration than the extracellularly added concentration (7.5 microM). (4) The intracellular quantification was accurate with less than 3% of the quantified peptide being potentially membrane-bound. (5) There was no leakage of the full-length CPP outside the cells. And, finally, (6) analysis of the degradation process of this new CPP suggests that the peptide did not traffick to lysosomes.