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31.
Applications of electronic speckle interferometry (ESI) techniques for spacecraft structural components 总被引:1,自引:0,他引:1
Laser-based electronic speckle interferometry (ESI) techniques, viz., electronic speckle pattern interferometry (ESPI) and electronic speckle shearographic interferometry (ESSI) are used for testing of spacecraft structural components. The combined ESPI and ESSI system developed in house was successfully used for the non-destructive evaluation (NDE) of honeycomb sandwich panels and propellant tanks of Indian Space Research Organization (ISRO). Debonds between face sheet and the honeycomb core were identified using (i) thermal and (ii) dual vacuum stressing methods. On-line NDE of the propellant tanks under internal pressure loading for identification of the minute cracks and thickness reduction areas were successfully implemented by ESI. 相似文献
32.
33.
Ross W. Mair David G. Cory Sharon Peled Ching-Hua Tseng Samuel Patz Ronald L. Walsworth 《Journal of magnetic resonance (San Diego, Calif. : 1997)》1998,135(2):478-486
Pulsed-field-gradient NMR techniques are demonstrated for measurements of time-dependent gas diffusion. The standard PGSE technique and variants, applied to a free gas mixture of thermally polarized xenon and O2, are found to provide a reproducible measure of the xenon diffusion coefficient (5.71 × 10−6m2s−1for 1 atm of pure xenon), in excellent agreement with previous, non-NMR measurements. The utility of pulsed-field-gradient NMR techniques is demonstrated by the first measurement of time-dependent (i.e., restricted) gas diffusion inside a porous medium (a random pack of glass beads), with results that agree well with theory. Two modified NMR pulse sequences derived from the PGSE technique (named the Pulsed Gradient Echo, or PGE, and the Pulsed Gradient Multiple Spin Echo, or PGMSE) are also applied to measurements of time dependent diffusion of laser polarized xenon gas, with results in good agreement with previous measurements on thermally polarized gas. The PGMSE technique is found to be superior to the PGE method, and to standard PGSE techniques and variants, for efficiently measuring laser polarized noble gas diffusion over a wide range of diffusion times. 相似文献
34.
Douglas M. Ruthven 《Adsorption》2007,13(3-4):225-230
Diffusion of benzene and the xylene isomers in silicalite/HZSM-5 has been studied by a wide range of different experimental
techniques. The available data are reviewed in an attempt to draw general conclusions concerning the intracrystalline diffusion
process. The results for benzene are remarkably consistent, and the conformity between transport and tracer diffusion and
between single crystal membrane and ZLC and frequency response data suggests that diffusion is essentially isotropic with
no significant difference between the self and “corrected” transport diffusivity. The situation is more complex for p-xylene
which shows clear evidence of non-isotropic behavior and a significant difference between tracer and transport diffusivities. 相似文献
35.
The recently proposed Harbola–Sahni local potential in its exchange-only version [Phys. Rev. Lett. 62 , 689 (1989)] is found to give the static dipole and quadrupole polarizabilities for the Neisoelectronic series in excellent agreement with the corresponding Hartree–Fock estimates. © 1992 John Wiley & Sons, Inc. 相似文献
36.
For any authentication code for k source states and v messages having minimum possible deception probabilities (namely, % MathType!MTEF!2!1!+-% feaafiart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr% 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq-Jc9% vqaqpepm0xbba9pwe9Q8fs0-yqaqpepae9qq-f0-yqaqVeLsFr0-vr% 0-vr0db8meaabaqaciGacaGaaeqabaWaaeaaeaaakeaacaWGqbWaaS% baaSqaaiaadsgaaeqaaOWaaSbaaSqaaiaaicdaaeqaaOGaeyypa0Za% aSGbaeaacaWGRbaabaGaamODaaaaaaa!3F28!\[P_d _0 = {k \mathord{\left/ {\vphantom {k v}} \right. \kern-\nulldelimiterspace} v}\] and % MathType!MTEF!2!1!+-% feaafiart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr% 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq-Jc9% vqaqpepm0xbba9pwe9Q8fs0-yqaqpepae9qq-f0-yqaqVeLsFr0-vr% 0-vr0db8meaabaqaciGacaGaaeqabaWaaeaaeaaakeaacaWGqbWaaS% baaSqaaiaadsgaaeqaaOWaaSbaaSqaaiaaigdaaeqaaOGaeyypa0Ze% xLMBb50ujbqeguuDJXwAKbacfaGae8hkaGIaam4AaiabgkHiTiaaig% dacqWFPaqkcqWFVaWlcqWFOaakcqWF2bGDcqGHsislcaaIXaGae8xk% aKIae8xkaKcaaa!4CD1!\[P_d _1 = (k - 1)/(v - 1))\], we show that there must be at least v encoding rules. (This can be thought of as an authentication-code analogue of Fisher's Inequality.) We derive several properties that an extremal code must satisfy, and we characterize the extremal codes for equiprobable source states as arising from symmetric balanced incomplete block designs. We also present an infinite class of extremal codes, in which the source states are not equiprobable, derived from affine planes.Dedicated to Gus Simmons 相似文献
37.
By means of exponential laws we show a Bianchi Type I model of the universe where we define overall deceleration and Hubble's parameters that have constant values. We employ a convenient relation for defining the radius of the universe. Pressure and density have constant values, too. 相似文献
38.
Gregory H. Robinson Fritz Moise William T. Pennington Samuel A. Sangokoya 《Journal of chemical crystallography》1988,18(4):387-393
The crystalline condensation product [Al(CH3)2]2[C10H22N4][Al(CH3)3]2 is prepared from reaction of the multidentate open-chain amine 1,4-bis(3-aminopropyl)piperazine with trimethylaluminum in methylene chloride. The compound crystallized in the monoclinic space groupC2/c with unit cell parametersa=25.166(12),b=7.268(4),c=17.316(4) Å,=115.3(4)°, andD
c
=1.06 g cm–3 forZ=4. Least-squares refinement based on 1054 observed reflections with intensitiesI 3(I) in the range 2<2<45° led to a finalR factor of 0.053 (R
w
=0.064). The title compound resides on a crystallographic center of symmetry with independent Al-N distances of 1.889(5), 2.058(5), and 2.030(5) Å. 相似文献
39.
40.
Summary The complexestrans-[Ru(NH3)4(H2O)PPh3](PF6)2 and [Ru(NH3)5L](PF6)2, (L=AsPh3 or SbPh3) have been isolated and characterized by microanalysis, cyclic voltammetry and ultraviolet-visible spectroscopy. The specific rate constants for the aquation of [Ru(NH3)5L]2+ totrans-[Ru(NH3)4L(H2O)]2+ are (2.5±0.1)×10–5s–1 and (1.8±0.1)×10–5s–1 for L=AsPh3 and SbPh3, respectively, at 25.0±0.1°C; =0.10 mol dm–3, NaO2CCF3. Under the same conditions, the second-order rate constants for the substitution of water intrans-[Ru(NH3)4(H2O)L]2+ by isonicotinamide (isn) are 1.2±0.1, (6.3±0.3)×10–2 and (3.8±0.2)×10–2
m
–1s–1 for L=PPh3, AsPh3, and SbPh3, respectively, suggesting that the order of decreasingtrans-effect is: PPh3AsPh3>SbPh3. The formation constants for thetrans-[Ru(NH3)4L(isn)]2+ complexes are 75±3, (1.40±0.01)×103 and (1.80±0.02)×103M–1 for L=PPh3, AsPh3, and SbPh3, respectively, suggesting that the order of increasingtrans-influence is: SbPh33PPh3. 相似文献