A method for the study of surface corrosion beneath protective layers

This work is concerned with the development of a technique to observe the onset of corrosion as it occurs beneath a temporary protective layer. Such temporary protectives include paints, varnishes, greases and oils that are applied to metal surfaces to give short-term protection from corrosion. The objective of this project was to develop a technique that could be used to evaluate the effectiveness of various temporary protectives in different environments, without the need to remove the protective layer, thus eliminating the possibility of any chemical changes or loss of corrosion products occurring as a result of removal. The temporary protective layers are typically 25Μm for paints and 15Μm per layer for varnishes. The 6.3 keV fluorescence X-ray is able to penetrate such layers, but the large escape depth (∼10Μm) of the X-rays means that for a thin protective layer a large proportion of the X-rays detected will originate from deep within the substrate and the resultant spectrum will be representative of the bulk rather than the surface. To enhance the surface sensitivity of the CXMS technique, the near surface region must be enriched in the isotope Fe-57. To achieve this, Fe-57 was vacuum evaporated onto the surface of mild steel substrates and subsequently diffused into the near surface region. An approximate 20 nm Fe-57 layer was deposited onto mild steel samples. The surface enriched samples were then annealed to allow the Fe-57 to diffuse into the near surface region of the mild steel substrate, and also to allow back diffusion of the substrate. A diffusion model was developed to predict the surface distribution of Fe-57 as a function of annealing parameters. The computer diffusion model allowed the ideal annealing conditions to be estimated to obtain a required near surface environment. It was essential that the annealing conditions did not result in any surface oxidation, and did result in a surface that was characteristic of mild steel. CEMS and CXMS spectra were recorded of samples before and after annealing, and also dynamic Secondary Ion Mass Spectrometry (SIMS) was used to monitor the enrichment and diffusion process. Energy Dispersive X-ray Analysis (EDXA) was also used to characterize the surface. A number of enriched samples were prepared and treated with a variety of surface temporary protectives. The CXMS spectra were recorded before and after exposure of the coated samples to various aggressive environments.     

UnyLinker dimer impurity characterization and process improvement

Herein, we describe the isolation and characterization of a UnyLinker dimer which, if left uncontrolled, can become incorporated in oligonucleotide products. The dimer is formed as a result of an unusual intermolecular osmium-catalyzed etherification. We demonstrate that by simply replacing H₂O₂ as the co-oxidant with NMO, none of the UnyLinker dimer impurity is formed.     

A computational investigation of the nitrogen-boron interaction in o-(N,N-dialkylaminomethyl)arylboronate systems

o-(N,N-Dialkylaminomethyl)arylboronate systems are an important class of compounds in diol-sensor development. We report results from a computational investigation of fourteen o-(N,N-dialkylaminomethyl)arylboronates using second-order M?ller-Plesset (MP2) perturbation theory. Geometry optimizations were performed at the MP2/cc-pVDZ level and followed by single-point calculations at the MP2/aug-cc-pVDZ(cc-pVTZ) levels. These results are compared to those from density functional theory (DFT) at the PBE1PBE(PBE1PBE-D)/6-311++G(d,p)(aug-cc-pVDZ) levels, as well as to experiment. Results from continuum PCM and CPCM solvation models were employed to assess the effects of a bulk aqueous environment. Although the behavior of o-(N,N-dialkylaminomethyl) free acid and ester proved to be complicated, we were able to extract some important trends from our calculations: (1) for the free acids the intramolecular hydrogen-bonded B-O-H···N seven-membered ring conformers 12 and 16 are found to be slightly lower in energy than the dative-bonded N→B five-membered ring conformers 10 and 14 while conformers 13 and 17, with no direct boron-nitrogen interaction, are significantly higher in energy than 12 and 16; (2) for the esters where no intramolecular B-O-H···N bonded form is possible, the N→B conformers 18 and 21 are significantly lower in energy than the no-interaction forms 20 and 23; (3) H(2)O insertion reactions into the N→B structures 10, 14, 18, and 21 leading to the seven-membered intermolecular hydrogen-bonded B···OH(2)···N ring structures 11, 15, 19, and 22 are all energetically favorable.     

Cold nuclear matter effects on J/ψ yields as a function of rapidity and nuclear geometry in d+A collisions at sqrt[s(NN)]=200 GeV

We present measurements of J/ψ yields in d+Au collisions at sqrt[s(NN)]=200 GeV recorded by the PHENIX experiment and compare them with yields in p+p collisions at the same energy per nucleon-nucleon collision. The measurements cover a large kinematic range in J/ψ rapidity (-2.2相似文献   

Floating Electrode Dielectric Barrier Discharge Plasma in Air Promoting Apoptotic Behavior in Melanoma Skin Cancer Cell Lines

Initiation of apoptosis, or programmed cell death, is an important issue in cancer treatment as cancer cells frequently have acquired the ability to block apoptosis and thus are more resistant to chemotherapeutic drugs. Targeted and perhaps selective destruction of cancerous tissue is desirable for many reasons, ranging from the enhancement of or aid to current medical methods to problems currently lacking a solution, i.e., lung cancer. Demonstrated in this publication is the inactivation (killing) of human Melanoma skin cancer cell lines, in vitro, by Floating Electrode Dielectric Barrier Discharge (FE-DBD) plasma. Not only are these cells shown to be killed immediately by high doses of plasma treatment, but low doses are shown to promote apoptotic behavior as detected by TUNEL staining and subsequent flow cytometry. It is shown that plasma acts on the cells directly and not by “poisoning” the solution surrounding the cells, even through a layer of such solution. Potential mechanisms of interaction of plasma with cells are discussed and further steps are proposed to develop an understanding of such systems.     

System size and energy dependence of jet-induced hadron pair correlation shapes in Cu+Cu and Au+Au collisions at square root sNN=200 and 62.4 GeV

We present azimuthal angle correlations of intermediate transverse momentum (1-4 GeV/c) hadrons from dijets in Cu+Cu and Au+Au collisions at square root sNN=62.4 and 200 GeV. The away-side dijet induced azimuthal correlation is broadened, non-Gaussian, and peaked away from Delta phi=pi in central and semicentral collisions in all the systems. The broadening and peak location are found to depend upon the number of participants in the collision, but not on the collision energy or beam nuclei. These results are consistent with sound or shock wave models, but pose challenges to Cherenkov gluon radiation models.     

J/psi production versus centrality, transverse momentum, and rapidity in Au+Au collisions at square root sNN=200 GeV

The PHENIX experiment at the BNL Relativistic Heavy Ion Collider (RHIC) has measured J/psi production for rapidities -2.2相似文献