Investigation of the spectral content of a cw CO laser output using a high-resolution scanning Fabry-Perot interferometer

The use of a scanning Fabry-Perot interferometer of variable length (variable resolution) for investigating the output of a cw CO laser is reported. Under experimental conditions required to achieve maximum power it was found that the laser output consisted of two or more simultaneously occuring transitions due to the overlapping nature of the vibration- rotation bands. The frequency differences between these transitions were measured to an accuracy of 0.01 cm^-1. Operation of the CO laser on a single vibration-rotation transition was obtained by controlling the laser gain with the experimental variables of discharge pressure, gas temperature, and optical alignment. An alternative approach of obtaining monochromatic radiation, by using a Fabry-Perot interferometer as a frequency selective filter external to the CO laser, is reported.     

Lagerhaltung als ein Regelungsproblem

Zusammenfassung An Hand von einfachen Modellen wird gezeigt, daß man die Theorie der Automatik auf das Gebiet der Lagerhaltung anwenden kann. Ein kontinuierliches lineares System und ein diskretes System werden untersucht. Für das erste System wird dieLaplace-Transformation verwendet, für das zweite diez- und modifiziertez-Transformation. Schließlich wird die Zeitbereichmethode eingeführt und eine Anwendung davon gezeigt.

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Summary By means of simple models, it is shown that control theory can be applied to inventory control problems. TheLaplace transform is used in the study of a linear continuous system. Thez and modifiedz transforms are employed in the study of a discrete system. Finally, the state space approach is introduced and is applied to a model with multirate sampling.

     

Carbon-13 spin–lattice relaxation in some polyfluoroaromatic compounds

Carbon-13 chemical shifts, spin-lattice relaxation times and nuclear Overhauser enhancement factors are reported for five polyfluoroaromatic compounds at 28°C. In all cases the relaxation of the fluorine bearing carbon is predominantly dipolar. Effective correlation times are smaller than those of the analogous benzene derivatives by a factor of 3–4, in qualitative agreement with predictions from the Stokes–Einstein diffusion theory. The T₁ values for the para-carbon of monosubstituted fluorobenzenes is clearly shorter than the T₁ values for the ortho- and meta-carbons. This phenomenon was traced to anisotropic tumbling, and D∥ and D⊥ diffusion coefficients were computed using Woessner's equations for molecules assumed to behave like symmetric rotors about their C₂ in-plane principal symmetry axis. Equal tumbling ratios, D∥/D⊥, were found in this way for toluene and perfluorotoluene.     

Kinetics and mechanism of the reactions of Pd(II) complexes with azoles and diazines. Crystal structure of [Pd(bpma)(H2O)](ClO4)2.2H2O

Substitution reactions of the complexes [Pd(bpma)(H2O)]2+, [Pd(bpma)Cl]+, [Pd(dien)(H2O)]2+ and [Pd(dien)Cl]+, where bpma = bis(2-pyridylmethyl)amine and dien = diethylentriamine or 1,5-diamino-3-azapentane, with some nitrogen-donor ligands such as triazole, pyrazole, pyrimidine, pyrazine and pyridazine, were studied in an aqueous 0.10 M NaClO4 at pH 2.8 using variable-temperature and -pressure stopped-flow spectrophotometry. The second-order rate constants indicate that the Pd(II) complexes of bpma, viz. [Pd(bpma)(H2O)]2+ and [Pd(bpma)Cl]+, are more reactive than the complexes of dien, viz. [Pd(dien)(H2O)]2+ and [Pd(dien)Cl]+. Also, the aqua complexes, [Pd(bpma)(H2O)]2+ and [Pd(dien)(H2O)]2+, are much more reactive than the corresponding chloro complexes. The most reactive nucleophile of the five-membered rings is triazole and for the six-membered rings the most reactive one is pyridazine. Activation parameters were determined for all reactions and the negative entropies and volumes of activation (Delta S++, Delta V++) support an associative ligand substitution mechanism. The crystal structure of [Pd(bpma)(H2O)](ClO4)2.2H2O was determined by X-ray diffraction. Crystals are monoclinic with the space group P2(1)/c. The coordination geometry of [Pd(bpma)(H2O)]2+ is distorted square-planar. The Pd-N (central) bond distance, 1.958(5) A, is shorter than the other two Pd-N distances, 2.007(5) and 2.009(5) A. The Pd-O distance is 2.043(5) A.     

Regularization and Fourier Series for Fredholm Integral Equations of the Second Kind with a Weakly Singular Kernel

To compute an approximate solution, of a weakly singular integral equation, we first regularize the kernel, and then truncate the associated Fourier series. An application to an astrophysical transfer equation is presented.     

Effects of Microstructural Defects on Ion-Irradiated Type-316 Stainless Steel

Microstructure defects play a very important role in the swelling of irradiated stainless steel. This work is a parametric study of the effects of microstructural defects on the swelling of ion-irradiated steel. For simplicity, vacancy loop effects were neglected. Cold working was found to play a complicated role in the swelling behavior. On one hand, it increase the bias to interstitial absorption due to the increase in dislocation density. On the other hand, it decreases the total flux of point defects to voids by the decrease of the point defect concentrations. Grain size has also a strong effect on swelling. It was found that large gain sizes produces higher swelling and vise versa, i.e. the larger the surface of grain boundaries the less the irradiation-produced swelling. Similar effects were found for precipitates.     

Occupied and Unoccupied Orbitals of C60 and C70

Abstract

The full spectrum of occupied and unoccupied σ and π orbitals is presented for solid C₆₀, C₇₀, and graphite, using Cls emission and absorption spectroscopy. There are significant diffcrences between C₆₀ and C₇₀, and even larger changes relative to their infinite analog graphite (C∝). A comparison is made with photocmission and inverse photoemission results, along with first principles quasiparticle calculations.     

Cycloaddition of Aroyl Isothiocyanate: A Novel Synthesis of Triazine,Oxazine, Pyrimidine,and Pyridine Derivatives

A simple and direct synthetic methodology for a novel series of azines and their annulated systems was performed. Heterocyclization of acyl isothiocyanate 2 with urea or malononitrile gave s‐triazine 4 and 1,3‐oxazine 7 derivatives, respectively. The reaction of heteroallene 1 with acetylacetone tolerated 2‐thioxopyridine derivative 9 . The latter compound underwent heterocyclization with urea, hydrazine hydrate, or phenyl hydrazine to give the annulated pyridines 10 – 12 . Pyrimidinethione 14 was resulted from reaction of acylisothiocyanate with enamine 13 . Condensation of compound 14 with hydrazine hydrate, phenyl hydrazine, urea, and 3‐nitrobenzaldehyde in the presence of ethyl cyanoacetate or sodium hydroxide afforded 15 – 20 , respectively.     

Band gap and band offsets of GaNAsBi lattice matched to GaAs substrate

In this paper, we calculate the band gap and the band discontinuities of a GaN _y AsBi _x structure lattice matched to GaAs substrate using the conduction and the valence band anticrossing models at the same time. The results obtained show a good agreement with experiment. The nitrogen and the bismuth concentrations leading to a wavelength emission of 1.55 μm have been determined (x = 3.5%, y = 2%). This structure shows a good electron confinement resulting in a high characteristic temperature.