Found 109 results
Author Title Type [ Year(Asc)]
Filters: Keyword is parker solar probe  [Clear All Filters]
1986
Authors: Brucker G. J., Herbert J., Stewart R., and Plus D.
Title: Sapphire Photocurrent Sources and Their Impact on RAM Upset
Abstract:

This paper reports on the transient photocurrent measurements made with test structures fabricated on sapphire substrates, and the computer simulation model which was developed to use the test results. Predictions of logic upset for a 4 K RAM CMOS/SOS compared with measured upset rates showed agreement within a factor of 2. The test structure results indicate that the sapphire photoconductance is 6.3 x 10 to the -19th mhos/(rads/s)-micron. The use of this value in the present simulation model will increase the predicted upset rate, and thus, increase the disagreement by more than a factor of two.


Date: 12/1986 Publisher: IEEE Transactions on Nuclear Science Pages: 1377 - 1380 DOI: 10.1109/TNS.1986.4334608 Available at: http://ieeexplore.ieee.org/document/4334608/http://xplorestaging.ieee.org/ielx5/23/4334557/04334608.pdf?arnumber=4334608
More Details
1982
Authors: Stewart R.G., and Plus D.
Title: A 40 ns CMOS E/SUP 2/PROM
Abstract:

New high-performance CMOS circuit techniques have been developed and used to build an 8K E/SUP 2/PROM with an access time of 38 ns at 5 V. Using standard CMOS/SOS technology, the device dissipates only 0.8 mW quiescent power at 5 V and 60 mW at 1 MHz. A midpoint precharge and sense technique permits operation form a supply voltage of 4-12 V.


Date: 10/1982 Publisher: IEEE Journal of Solid-State Circuits Pages: 841 - 846 DOI: 10.1109/JSSC.1982.1051828 Available at: http://ieeexplore.ieee.org/document/1051828/http://xplorestaging.ieee.org/ielx5/4/22585/01051828.pdf?arnumber=1051828
More Details
1976
Authors: Plus R.
Title: Utilisation des isotopes D, 15N, 26Mg pour l'étude vibrationnelle de Mg(NH3)6Cl2.
Abstract:

The following substituted magnesium chloride hexa-ammines: 24Mg( 14NH 3) 6Cl 2; 26Mg( 14NH 3) 6Cl 2; 24Mg( 15NH 3) 6Cl 2; 24Mg( 14ND 3) 6Cl 2; 24Mg( 14ND 3) 6Cl 2 have been studied by i.r. and Raman spectroscopy. The frequency shifts have been measured for all active vibrational bands predicted by group theory analysis. The results show that measurements made on isotopically substituted compounds can provide confirmation of assignments of vibrational bands previously proposed [2].


Date: 01/1976 Publisher: Spectrochimica Acta Part A: Molecular Spectroscopy Pages: 263 - 268 DOI: 10.1016/0584-8539(76)80076-1 Available at: http://linkinghub.elsevier.com/retrieve/pii/0584853976800761http://api.elsevier.com/content/article/PII:0584853976800761?httpAccept=text/xmlhttp://api.elsevier.com/content/article/PII:0584853976800761?httpAccept=text/plain
More Details
1975
Authors: Plus R., and Lutz M.
Title: Resonance Raman Scattering of Mesoporphyrin IX Dimethylester in Solution
Abstract:

Resonance Raman spectra of Mesoporphyrin IX dimethylester in solution were obtained using various wavelengths in the region of electronic band IV. Vibrational data, as well as variations in the depolarization ratios and the band intensities with excitation wavelengths were compared to those previously obtained for porphin. The new data provide confirmation of the existence of three, most probably purely electronic transitions in band IV of both Mesoporphyrin IX dimethylester and porphin.


Date: 01/1975 Publisher: Spectroscopy Letters Pages: 119 - 139 DOI: 10.1080/00387017508067314 Available at: https://www.tandfonline.com/doi/full/10.1080/00387017508067314https://www.tandfonline.com/doi/pdf/10.1080/00387017508067314
More Details
1974
Authors: Plus R., and Lutz M.
Title: Resonance Raman Spectroscopy of Porphin
Abstract:

We report and discuss Raman spectra of porphin. These were obtained by resonance effect, irradiating in the electronic band IV. Unexpected variations of vibrational band intensities and depolarization ratios were recorded on changing the excitation wavelength. Some implications on the symmetry types of the vibrations are discussed. Results are compared with current data from quasi-linear electronic spectra.


Date: 01/1974 Publisher: Spectroscopy Letters Pages: 133 - 145 DOI: 10.1080/00387017408067229 Available at: https://www.tandfonline.com/doi/full/10.1080/00387017408067229https://www.tandfonline.com/doi/pdf/10.1080/00387017408067229
More Details
Authors: Plus R., and Lutz M.
Title: Study of Band IV of Porphin by Resonance Raman Spectroscopy
Abstract:

Excitation spectra were obtained for 21 resonance Raman bands of porphin from 455 to 515 nm. Each of them exhibited one to three maxima which generally lay close to 453, 475 and 490 nm. These three resonance levels were tentatively attributed to the presence of pure electronic transitions in band IV. The few other maxima could be interpreted as resonance at vibrational sublevels of band III. The structure of band IV is thus shown to be of greater complexity than has been generally suspected up to now.


Date: 01/1974 Publisher: Spectroscopy Letters Pages: 73 - 84 DOI: 10.1080/00387017408067222 Available at: http://www.tandfonline.com/doi/abs/10.1080/00387017408067222http://www.tandfonline.com/doi/pdf/10.1080/00387017408067222
More Details
1973
Authors: Plus émi
Title: Étude par spectroscopie infrarouge des composés Mg(NH 3 ) 6 Cl 2 et Mg(ND 3 ) 6 Cl 2
Abstract:

The infrared spectra of pure Mg(NH3)6Cl2 and Mg(ND3)6Cl2 were recorded from 4 000 to 50 cm-1 at 40 and — 180 °C. The observed bands are assigned. The hydrogenated compound was studied by differential thermal analysis.

The observed infrared spectral data are compared with the previously reported experimental values for other divalent metals (Co2+, Ni2+, Fe2+, Mn2+). This comparison proves that (he coordination bond is stronger for Mg than for the other metals.


Date: 01/1973 Publisher: Journal de Chimie Physique Pages: 900 - 904 DOI: 10.1051/jcp/1973700900 Available at: http://jcp.edpsciences.org/10.1051/jcp/1973700900http://jcp.edpsciences.org/10.1051/jcp/1973700900/pdf
More Details
Authors: Plus émi
Title: Étude vibrationnelle de complexes du magnesium. Spectroscopie Raman de Mg(NH3)6Cl2et Mg(ND3)6Cl2
Abstract:

L'auteur a pu obtenir les fréquences des vibrations actives en diffusion Raman du chlorure de magnésium hexa‐amminé hydrogéné et deutérié à l'état cristallisé. Toutes les vibrations attendues ont pu être observées pour la première fois pour un composé de ce type (vibrations internes et vibrations externes). L'attribution de toutes les bandes du spectre est proposée. Ces résultats, rapprochés de ceux obtenus par spectroscopie infrarouge, permettent de connaître la structure vibrationnelle complète du complexe. L'éclatement de certaines vibrations montre que les coordinats ne sont pas en rotation libre et que leur orientation donne à l'ion complexe la symétrie du groupe ponctuel D3d.


Date: 12/1973 Publisher: Journal of Raman Spectroscopy Pages: 551 - 563 DOI: 10.1002/jrs.v1:610.1002/jrs.1250010605 Available at: https://onlinelibrary.wiley.com/doi/abs/10.1002/jrs.1250010605
More Details
1969
Authors: Lewis John S.
Title: Observability of spectroscopically active compounds in the atmosphere of Jupiter
Abstract:

The abundances of several hundred volatile compounds have been calculated at several different levels in the atmosphere of Jupiter. Complete chemical equilibrium has been assumed, and a solar-composition, adiabatic-equilibrium model of the atmospheric composition and structure is used throughout. The results which relate to upper limits on the abundances of spectroscopically active compounds in the upper atmosphere are, however, directly applicable to subadiabatic models. The principal results are that only H2, CH4, and NH3 are predicted to be observable with present techniques. These three species are in fact the only compounds conclusively identified in Jupiter spectra to date. A number of plausible previously suggested constituents of the upper atmosp. . .
Date: 05/1969 Publisher: Icarus Pages: 393 - 409 DOI: 10.1016/0019-1035(69)90094-3 Available at: https://linkinghub.elsevier.com/retrieve/pii/0019103569900943https://api.elsevier.com/content/article/PII:0019103569900943?httpAccept=text/xmlhttps://api.elsevier.com/content/article/PII:0019103569900943?httpAccept=text/plain
More Details

Pages