Oxide Film Formation on Metals and Alloys by Thermal, Electrochemical and Plasma Oxidation and Prediction of Resulting Structures

1999 ◽  
Vol 574 ◽  
Author(s):  
D. L. Cocke ◽  
S. Promreuk ◽  
R. Schennach ◽  
M. Y. Mollah ◽  
D. G. Naugle
Keyword(s):  
Electric Fields ◽  
Film Formation ◽  
Complex Oxide ◽  
Metals And Alloys ◽  
Plasma Oxidation ◽  
Chemical Mechanisms ◽  
Physical Chemical ◽  
Layer Structures ◽  
Wide Range ◽  
Physical And Chemical

AbstractMulticomponent oxide films are needed to meet the increasing demands of the electronics industry. Three main methods that involve oxidation of a metallic substrate are thermal, anodic and plasma oxidation. Today we do not have an adequate fundamental physical-chemical model of how multicomponent oxides evolve on alloys under these oxidizing conditions to design a wide range of materials for electronic devices. The three methods will be discussed in terms of physical/chemical parameters that influence the chemical nature and structure of the resulting oxides. By using surface studies of the oxidation behavior of numerous metals and alloys we have been able to delineate the factors which are most important to the oxide formation process and provide insight into the prediction of oxide layer structures. The electrochemical processes that occur during the materials reaction with a chosen environment will be used to discuss the physical and chemical mechanisms involved. Intrinsic and extrinsic electric fields will be shown to influence the chemical and structural nature of the resulting oxide structures. Examples will be presented from a number of metal and alloy systems that have been examined in our laboratory. These include Al, Ti, Zr, Nb, Mn, Cu and Ni and some of their selected alloys. The models that have developed from these studies are providing some predictive power in how the complex oxide overlayer will be chemically speciated and on its structure.

scholarly journals EUCLIDEAN RESONANCE: APPLICATION TO PHYSICAL AND CHEMICAL EXPERIMENTS

2006 ◽  
Vol 20 (06) ◽  
pp. 627-658 ◽  
Author(s):  
B. IVLEV
Keyword(s):  
Electric Fields ◽  
Isotope Separation ◽  
Nuclear Fission ◽  
Particle Decay ◽  
Semiclassical Methods ◽  
Wide Range ◽  
Tunnel Barriers ◽  
Physical And Chemical ◽  
Nuclear Processes ◽  
Complex Trajectories

The phenomenon of Euclidean resonance (a strong enhancement of quantum tunneling through a nonstationary potential barrier) is applied to disintegration of atoms and molecules through tunnel barriers formed by applied constant and time-dependent electric fields. There are two different channels for such disintegration, electronic and ionic. The electronic mechanism is associated with the ionization of a molecule into an electron and a positive ion. The required frequencies are in a wide range between 100 MHZ and infrared. This mechanism may constitute a method of selective destruction of chemical bonds. The ionic mechanism consists of dissociation of a molecule into two ions. Since an ion is more massive than an electron, the necessary frequency is about 1 MHZ. This provides a theoretical possibility of a different method of isotope separation by radio frequency waves. The small sub-barrier tunneling probability of nuclear processes can be dramatically enhanced by collision with incident charged particles. Semiclassical methods of theory of complex trajectories have been applied to nuclear tunneling, and conditions for the effect have been obtained. The enhancement of α particle decay by incident proton with energy of about 0.25 MeV has been demonstrated. The general features of this process are common for other sub-barrier nuclear processes and can be applied to nuclear fission.

Seasonal Changes in the Limnology of Some Meromictic Lakes in Southern British Columbia

1969 ◽  
Vol 26 (7) ◽  
pp. 1763-1787 ◽  
Author(s):  
T. G. Northcote ◽  
T. G. Halsey
Keyword(s):  
Seasonal Changes ◽  
Specific Conductivity ◽  
Solid Content ◽  
Lake Basin ◽  
Physical Chemical ◽  
Morphometric Features ◽  
Wide Range ◽  
Sulphur Bacteria ◽  
Total Dissolved Solid ◽  
Physical And Chemical

Seasonal changes in physical, chemical, and biological features are described in four small lakes which show different types and degrees of meromixis. There is a wide range in total dissolved solid content between lakes as well as within lakes (surface to near-bottom): Yellow, 282 (surface) to 337 (bottom); White, 6229–7918; Mahoney, 10,003–86,906; Lyons, 12,116–222,195 mg/liter, but no marked seasonal changes. In Yellow Lake meromixis is probably maintained by morphometric features of the lake basin rather than a strong chemocline; in the other lakes complete mixing is inhibited by chemical density gradients, those in Mahoney and Lyons being especially sharp.Summer, autumn, winter (under ice), and spring vertical profiles are presented for temperature, dissolved oxygen, pH, alkalinity, specific conductivity; differences within and between lakes are discussed. Other physical–chemical characteristics are given in less detail.Purple sulphur bacteria occur in three of the lakes (White, Mahoney, Lyons) and in the latter two form discrete "plates" detectable by high frequency echo sounding (confirmed by sampling). Seasonal changes in depth of the bacterial plates are considered in relation to some physical and chemical parameters. Phytoplankton, zooplankton, and benthos communities are discussed in relation to the degree of meromixis shown by the lakes.

scholarly journals Nanosonotechnology: the next challenge in cancer sonodynamic therapy

2012 ◽  
Vol 1 (2) ◽  
pp. 173-182 ◽  
Author(s):  
Loredana Serpe ◽  
Federica Foglietta ◽  
Roberto Canaparo
Keyword(s):  
Chemical Structure ◽  
Chemical Compounds ◽  
Acoustic Cavitation ◽  
Sonodynamic Therapy ◽  
Chemical Mechanisms ◽  
Physical Chemical ◽  
Anticancer Treatment ◽  
Ultrasound Bioeffects ◽  
Ultrasound Energy ◽  
Physical And Chemical

AbstractSonodynamic therapy (SDT) is a newly developed anticancer treatment where ultrasound is used to trigger the cytotoxic effect of chemical compounds, known as sonosensitizers. Although SDT is similar to photodynamic therapy (PDT), SDT activates the chemical compounds through energy transfer using ultrasound rather than light. Moreover, SDT can focus the ultrasound energy onto malignant sites situa\xadted deeply within tissues, thus overcoming the main drawback linked to the use of PDT. Several physical and chemical mechanisms underlying ultrasound bioeffects and anticancer SDT take advantage of the non-thermal effect of acoustic cavitation generated by selected pulsed or continuous ultrasound. As the physical-chemical structure of the sonosentizer is essential for the success of SDT, we believe that the different aspects related to nanotechnology in medicine might well be able to improve the triggering effect ultrasound has on sonosensitizing agents. Therefore, the aim of this review is to focus on how nanotechnology might improve this innovative anticancer therapeutic approach.

Substituent Effects on the Thermal Decomposition of Phosphate Esters on Ferrous Surfaces

2019 ◽  
Author(s):  
James Ewen ◽  
Carlos Ayestaran Latorre ◽  
Arash Khajeh ◽  
Joshua Moore ◽  
Joseph Remias ◽  
...  
Keyword(s):  
Thermal Decomposition ◽  
Film Formation ◽  
Substituent Effects ◽  
Vapour Phase ◽  
Industrial Applications ◽  
Phosphate Esters ◽  
Antiwear Additives ◽  
Formation Mechanisms ◽  
Phosphate Ester ◽  
Wide Range

<p>Phosphate esters have a wide range of industrial applications, for example in tribology where they are used as vapour phase lubricants and antiwear additives. To rationally design phosphate esters with improved tribological performance, an atomic-level understanding of their film formation mechanisms is required. One important aspect is the thermal decomposition of phosphate esters on steel surfaces, since this initiates film formation. In this study, ReaxFF molecular dynamics simulations are used to study the thermal decomposition of phosphate esters with different substituents on several ferrous surfaces. On Fe<sub>3</sub>O<sub>4</sub>(001) and α-Fe(110), chemisorption interactions between the phosphate esters and the surfaces occur even at room temperature, and the number of molecule-surface bonds increases as the temperature is increased from 300 to 1000 K. Conversely, on hydroxylated, amorphous Fe<sub>3</sub>O<sub>4</sub>, most of the molecules are physisorbed, even at high temperature. Thermal decomposition rates were much higher on Fe<sub>3</sub>O<sub>4</sub>(001) and particularly α-Fe(110) compared to hydroxylated, amorphous Fe<sub>3</sub>O<sub>4</sub>. This suggests that water passivates ferrous surfaces and inhibits phosphate ester chemisorption, decomposition, and ultimately film formation. On Fe<sub>3</sub>O<sub>4</sub>(001), thermal decomposition proceeds mainly through C-O cleavage (to form surface alkyl and aryl groups) and C-H cleavage (to form surface hydroxyls). The onset temperature for C-O cleavage on Fe<sub>3</sub>O<sub>4</sub>(001) increases in the order: tertiary alkyl < secondary alkyl < primary linear alkyl ≈ primary branched alkyl < aryl. This order is in agreement with experimental observations for the thermal stability of antiwear additives with similar substituents. The results highlight surface and substituent effects on the thermal decomposition of phosphate esters which should be helpful for the design of new molecules with improved performance.</p>

scholarly journals Palladium and Copper: Advantageous Nanocatalysts for Multi-Step Transformations

Nanomaterials ◽  
2021 ◽  
Vol 11 (8) ◽  
pp. 1891
Author(s):  
Antonio Reina ◽  
Trung Dang-Bao ◽  
Itzel Guerrero-Ríos ◽  
Montserrat Gómez
Keyword(s):  
Chemical Properties ◽  
Added Value ◽  
Solid Supports ◽  
Nanosized Materials ◽  
Nano Structures ◽  
Liquid Phases ◽  
Wide Range ◽  
Synthetic Methodologies ◽  
Physical And Chemical ◽  
A Current

Metal nanoparticles have been deeply studied in the last few decades due to their attractive physical and chemical properties, finding a wide range of applications in several fields. Among them, well-defined nano-structures can combine the main advantages of heterogeneous and homogenous catalysts. Especially, catalyzed multi-step processes for the production of added-value chemicals represent straightforward synthetic methodologies, including tandem and sequential reactions that avoid the purification of intermediate compounds. In particular, palladium- and copper-based nanocatalysts are often applied, becoming a current strategy in the sustainable synthesis of fine chemicals. The rational tailoring of nanosized materials involving both those immobilized on solid supports and liquid phases and their applications in organic synthesis are herein reviewed.

Nanobiotechnology: Nature-inspired silver nanoparticles towards green synthesis

2021 ◽  
pp. 0958305X2198988
Author(s):  
Nur Syakirah Rabiha Rosman ◽  
Noor Aniza Harun ◽  
Izwandy Idris ◽  
Wan Iryani Wan Ismail
Keyword(s):  
Electrical Conductivity ◽  
Silver Nanoparticles ◽  
Green Synthesis ◽  
Metal Nanoparticles ◽  
Current Trend ◽  
Biological Properties ◽  
Noble Metal Nanoparticles ◽  
Current Application ◽  
Physical Chemical ◽  
Physical And Chemical

The emergence of technology to produce nanoparticles (1 nm – 100 nm in size) has drawn significant researchers’ interests. Nanoparticles can boost the antimicrobial, catalytic, optical, and electrical conductivity properties, which cannot be achieved by their corresponding bulk. Among other noble metal nanoparticles, silver nanoparticles (AgNPs) have attained a special emphasis in the industry due to their superior physical, chemical, and biological properties, closely linked to their shapes, sizes, and morphologies. Proper knowledge of these NPs is essential to maximise the potential of biosynthesised AgNPs in various applications while mitigating risks to humans and the environment. This paper aims to critically review the global consumption of AgNPs and compare the AgNPs synthesis between conventional methods (physical and chemical) and current trend method (biological). Related work, advantages, and drawbacks are also highlighted. Pertinently, this review extensively discusses the current application of AgNPs in various fields. Lastly, the challenges and prospects of biosynthesised AgNPs, including application safety, oxidation, and stability, commercialisation, and sustainability of resources towards a green environment, were discussed.

scholarly journals Hybrid Acrylated Chitosan and Thiolated Pectin Cross-Linked Hydrogels with Tunable Properties

Polymers ◽  
2021 ◽  
Vol 13 (2) ◽  
pp. 266
Author(s):  
Shaked Eliyahu ◽  
Alexandra Galitsky ◽  
Esther Ritov ◽  
Havazelet Bianco-Peled
Keyword(s):  
Electrostatic Interactions ◽  
Profile Analysis ◽  
Hybrid Hydrogel ◽  
Texture Profile ◽  
Ph Values ◽  
X Ray Scattering ◽  
Wide Range ◽  
Michael Type Addition ◽  
Physical And Chemical ◽  
Hydrogel System

We developed and characterized a new hydrogel system based on the physical and chemical interactions of pectin partially modified with thiol groups and chitosan modified with acrylate end groups. Gelation occurred at high pectin thiol ratios, indicating that a low acrylated chitosan concentration in the hydrogel had a profound effect on the cross-linking. Turbidity, Fourier transform infrared spectroscopy, and free thiol determination analyses were performed to determine the relationships of the different bonds inside the gel. At low pH values below the pKa of chitosan, more electrostatic interactions were formed between opposite charges, but at high pH values, the Michael-type addition reaction between acrylate and thiol took place, creating harder hydrogels. Swelling experiments and Young’s modulus measurements were performed to study the structure and properties of the resultant hydrogels. The nanostructure was examined using small-angle X-ray scattering. The texture profile analysis showed a unique property of hydrogel adhesiveness. By implementing changes in the preparation procedure, we controlled the hydrogel properties. This hybrid hydrogel system can be a good candidate for a wide range of biomedical applications, such as a mucosal biomimetic surface for mucoadhesive testing.

scholarly journals Changes in Optical Properties upon Dye–Clay Interaction: Experimental Evaluation and Applications

Nanomaterials ◽  
2021 ◽  
Vol 11 (1) ◽  
pp. 197
Author(s):  
Giorgia Giovannini ◽  
René M. Rossi ◽  
Luciano F. Boesel
Keyword(s):  
Optical Properties ◽  
Hybrid Materials ◽  
High Performance ◽  
Fluorescent Properties ◽  
Chemical Mechanisms ◽  
Strong Electrostatic Interaction ◽  
Potential Applications ◽  
Photochemical Properties ◽  
Physical And Chemical ◽  
The Relationship

The development of hybrid materials with unique optical properties has been a challenge for the creation of high-performance composites. The improved photophysical and photochemical properties observed when fluorophores interact with clay minerals, as well as the accessibility and easy handling of such natural materials, make these nanocomposites attractive for designing novel optical hybrid materials. Here, we present a method of promoting this interaction by conjugating dyes with chitosan. The fluorescent properties of conjugated dye–montmorillonite (MMT) hybrids were similar to those of free dye–MMT hybrids. Moreover, we analyzed the relationship between the changes in optical properties of the dye interacting with clay and its structure and defined the physical and chemical mechanisms that take place upon dye–MMT interactions leading to the optical changes. Conjugation to chitosan additionally ensures stable adsorption on clay nanoplatelets due to the strong electrostatic interaction between chitosan and clay. This work thus provides a method to facilitate the design of solid-state hybrid nanomaterials relevant for potential applications in bioimaging, sensing and optical purposes.

The Varied Causes of Color in Glass

1985 ◽  
Vol 61 ◽  
Author(s):  
K. Nassau
Keyword(s):  
Chalcogenide Glasses ◽  
Water Ligand ◽  
Ligand Field ◽  
Energy Bands ◽  
Metal Compounds ◽  
Chemical Mechanisms ◽  
Doped Glasses ◽  
Blue Eyes ◽  
Physical And Chemical ◽  
Ice Water

ABSTRACTAll but two of the fifteen physical and chemical mechanisms which are necessary to explain all the varied causes of color apply in one way or another to glass. These fifteen causes of color derive from a variety of physical and chemical mechanisms and are summarized in five groups with concentration on those mechanisms that apply to glass and the related glazes and enamels. Vibrations and simple excitations explain the colors of incandescence (e.g. flames, hot glass), gas excitations (neon tube, aurora), and vibrations and rotations (blue ice, water, glasses based on water). Ligand field effect colors are seen in transition metal compounds (turquoise, chrome oxide green, glasses based on copper sulfate) and impurities (ruby, emerald, many doped glasses). Molecular orbitals explain the colors of organic compounds (indigo, chlorophyll, organic glasses) and charge transfer compounds (blue sapphire, lapis lazuli, “beer-bottle” brown and chromate glasses). Energy bands are involved in the colors of metals and alloys (gold, brass, glassy metals), of semiconductors (cadmium yellow, vermillion, chalcogenide glasses), doped semiconductors (blue and yellow diamond), and color centers (amethyst, topaz, irradiated glass). Geometrical and physical optics are involved in the colors derived from dispersive refraction (rainbow, green flash, glass prism spectrum), scattering (blue sky, blue eyes, red sunset, ruby gold and opal glasses), interference (soap bubbles, iridescent beetles, cracks in glasses, interference filters), and diffraction (the corona aureole, diffraction grating spectrum).

The vibration of electrified water drops

1971 ◽  
Vol 322 (1551) ◽  
pp. 523-534 ◽  
Keyword(s):  
Electric Field ◽  
Electric Fields ◽  
Axial Ratio ◽  
Uniform Electric Field ◽  
Interferometric Technique ◽  
Photographic Analysis ◽  
Wide Range ◽  
Water Drops ◽  
Strength And Deformation ◽  
A Charge

Pressure has been used as the principal parameter in calculations of the fundamental vibrational frequencies of spherical drops of radius R , density ρ, and surface tension T carrying a charge Q or uncharged spheroidal drops of axial ratio a / b situated in a uniform electric field of strength E . Freely vibrating charged drops have a frequency f = f 0 ( 1 - Q 2 /16π R 3 T ) ½ , as shown previously by Rayleigh (1882) using energy considerations; f 0 is the vibrational frequency of non-electrified drops (Rayleigh 1879). The fundamental frequency of an uncharged drop in an electric field will decrease with increasing field strength and deformation a / b and will equal zero when E ( R )/ T ) ½ = 1.625 and a / b = 1.86; these critical values correspond to the disintegration conditions derived by Taylor (1964). An interferometric technique involving a laser confirmed the accuracy of the calculations concerned with charged drops. The vibration of water drops of radius around 2 mm was studied over a wide range of temperatures as they fell through electric fields either by suspending them in a vertical wind tunnel or allowing them to fall between a pair of vertical electrodes. Photographic analysis of the vibrations revealed good agreement between theory and experiment over the entire range of conditions studied even though the larger drops were not accurately spheroidal and the amplitude of the vibrations was large.

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