silicon and stearic-acid

This report represents the conclusions of a Joint FAO/WHO Expert Committee convened to evaluate the safety of various food additives and contaminants and to prepare specifications for identity and purity. The first part of the report contains a brief description of general considerations addressed at the meeting, including updates on matters of interest to the work of the Committee. A summary follows of the Committee's evaluations of technical, toxicological and/or dietary exposure data for seven food additives (benzoates; lipase from Fusarium heterosporum expressed in Ogataea polymorpha; magnesium stearate; maltotetraohydrolase from Pseudomonas stutzeri expressed in Bacillus licheniformis; mixed β-glucanase, cellulase and xylanase from Rasamsonia emersonii; mixed β-glucanase and xylanase from Disporotrichum dimorphosporum; polyvinyl alcohol (PVA)- polyethylene glycol (PEG) graft copolymer) and two groups of contaminants (non-dioxin-like polychlorinated biphenyls and pyrrolizidine alkaloids). Specifications for the following food additives were revised or withdrawn: advantame; annatto extracts (solavnt extracted bixin, ad solvent-extracted norbixin); food additives containing aluminium and/or silicon (aluminium silicate; calcium aluminium silicate; calcium silicate; silicon dioxide, amorphous; sodium aluminium silicate); and glycerol ester of gum rosin. Annexed to the report are tables or text summarizing the toxicological and dietary exposure information and information on specifications as well as the Committees recommendations on the food additives and contaminants considered at this meeting.

Topics: alpha-Glucosidases; Aluminum; Benzoates; Cellulases; Diet; Endo-1,4-beta Xylanases; Food Additives; Food Contamination; Food Safety; Fusarium; Humans; Lipase; Polychlorinated Biphenyls; Polyethylene Glycols; Polyvinyl Alcohol; Pseudomonas; Pyrrolizidine Alkaloids; Recombinant Proteins; Silicon; Stearic Acids; World Health Organization

In this work, we investigate the adsorption process of two carboxylic acids (stearic and undecylenic) on a H-Si(111) surface via the calculation of structural and energy changes as well as the simulation of their IR and Raman spectra. The two molecules adsorb differently at the surface since the stearic acid simply physisorbs while the undecylenic acid undergoes a chemical reaction with the hydrogen atoms of the surface. This difference is observed in the change of geometry during the adsorption. Indeed, the chemisorption of the undecylenic acid has a bigger impact on the structure than the physisorption of the stearic acid. Consistently, the former is also characterized by a larger value of adsorption energy and a smaller value of the tilting angle with respect to the normal plane. For both the IR and Raman signatures, the spectra of both molecules adsorbed at the surface are in a first approximation the superposition of the spectra of the Si cluster and of the carboxylic acid considered individually. The main deviation from this simple observation is the peak of the stretching Si-H (ν(Si-H)) mode, which is split into two peaks upon adsorption. As expected, the splitting is bigger for the chemisorption than the physisorption. The modes corresponding to atomic displacements close to the adsorption site display a frequency upshift by a dozen wavenumbers. One can also see the disappearance of the peaks associated with the C=C double bond when the undecylenic acid chemisorbs at the surface. The Raman and IR spectra are complementary and one can observe here that the most active Raman modes are generally IR inactive. Two exceptions to this are the two ν(Si-H) modes which are active in both spectroscopies. Finally, we compare our simulated spectra with some experimental measurements and we find an overall good agreement.

Topics: Adsorption; Hydrogen; Models, Molecular; Molecular Conformation; Silicon; Spectrophotometry, Infrared; Spectrum Analysis, Raman; Stearic Acids; Surface Properties; Undecylenic Acids; Vibration

Self-assembled monolayers of fatty acids were formed on stainless steel by room-temperature solution deposition. The acids are covalently bound to the surface as carboxylate in a bidentate manner. To explore the effect of saturation in the carbon backbone on friction in sliding tribology, we study the response of saturated stearic acid (SA) and unsaturated linoleic acid (LA) as self-assembled monolayers using lateral force microscopy and nanotribometry and when the molecules are dispersed in hexadecane, using pin-on-disc tribometry. Over a very wide range (10 MPa-2.5 GPa) of contact pressures it is consistently demonstrated that the unsaturated linoleic acid molecules yield friction which is significantly lower than that of the saturated stearic acid. It is argued, using density functional theory predictions and XPS of slid track, that when the molecular backbone of unsaturated fatty acids are tilted and pressed strongly by a probe, in tribological contact, the high charge density of the double bond region of the backbone allows coupling with the steel substrate. The interaction yields a low friction carboxylate soap film on the substrate. The saturated fatty acid does not show this effect.

Topics: Alkanes; Fatty Acids; Friction; Linoleic Acid; Lubrication; Microscopy, Atomic Force; Silicon; Spectrometry, X-Ray Emission; Spectroscopy, Fourier Transform Infrared; Stainless Steel; Stearic Acids

We present results concerning the formation of Langmuir-Blodgett (LB) films of a class I hydrophobin from Pleurotus ostreatus at the air-water interface, and their structure as Langmuir-Blodgett (LB) films when deposited on silicon substrates. LB films of the hydrophobin were investigated by atomic force microscopy (AFM). We observed that the compressed film at the air-water interface exhibits a molecular depletion even at low surface pressure. In order to estimate the surface molecular concentration, we fit the experimental isotherm with Volmer's equation describing the equation of state for molecular monolayers. We found that about (1)/ 10 of the molecules contribute to the surface film formation. When transferred on silicon substrates, compact and uniform monomolecular layers about 2.5 nm thick, comparable to a typical molecular size, were observed. The monolayers coexist with protein aggregates, under the typical rodlet form with a uniform thickness of about 5.0 nm. The observed rodlets appear to be a hydrophilic bilayer and can then be responsible for the surface molecular depletion.

Topics: Air; Ferric Compounds; Fungal Proteins; Lipid Bilayers; Microscopy, Atomic Force; Molecular Conformation; Pleurotus; Proteins; Silicon; Stearic Acids; Surface Properties; Temperature; Time Factors; Water; X-Rays

The effect of electric and magnetic fields on the sandwich structure Pt/hydrogenated amorphous silicon (a-Si:H)/stearic acid monolayer/Langmuir-Blodgett film of Ag/Co nanoparticles encapsulated in an organic envelope is studied. This structure is used as a working electrode in an electrochemical cell filled with NaCl solution (1 mM) and equipped with an Ag/AgCl reference electrode. Reversible changes in voltammograms are observed due to treatments (negative or positive bias voltage and simultaneous laser irradiation) applied to the designed structure before measurements. As an explanation of the observed phenomena we suggest that both the Co-up and Ag-up (on the a-Si:H surface) orientation orderings of nanoparticle Ag/Co cores are repeatedly reached. The role of the photovoltaic material (a-Si:H) in the observed behavior is explained. Voltammetric measurements with an applied magnetic field support our idea about the orientation ordering of nanoparticle cores.

Topics: Cobalt; Electrochemistry; Electrodes; Magnetics; Metal Nanoparticles; Platinum; Silicon; Silver; Stearic Acids; Surface Properties

Upon exposure to blood, rapid adsorption of proteins is the initial event at the contacting surface, followed by the adhesion of platelets and other blood components. Surfaces absorbing albumin appear to possess antithrombotic character in discouraging adhesion of platelets. Therefore, for the development of a blood contacting device, the interfacial events are extremely important and need serious investigation. We have attempted to observe the variations in competitive adsorption of fibrinogen and albumin onto the polyetherurethane urea (PEUU) surface in the presence of external lubricant, such as calcium stearate and silicone fluid coating. It seems, in the presence of such mediators, that fibrinogen adsorption is increased relatively with reduction in albumin at the surface.

Topics: Adsorption; Animals; Biocompatible Materials; Blood Proteins; Fibrinogen; Humans; In Vitro Techniques; Lubrication; Polymers; Polyurethanes; Serum Albumin; Silicon; Silicones; Stearic Acids; Surface Properties; Time Factors