Analysis of dimensionally stable copolyimide with a low‐level residual stress

Copolyimide thin film, which has low‐level stress and stress relaxation induced by water sorption, was characterized for potential applications as an encapsulant, a stress‐relief buffer, and in interlayer dielectrics. The polyimides examined were poly(p‐phenylene pyromellitimide) (PMDA‐PDA) and poly(p‐phenylene biphenyltetracarboximide) (BPDA‐PDA) as well as their random copolyimides with various compositions. These copolyimide films exhibited good combinations of physical and mechanical properties with low thermal expansion coefficients, residual stress, and moisture‐induced stress–relaxation behavior by appropriately selecting the ratios of the dianhydride component. For these polyimides, the residual stress increased in the range of −8.1–7.5 MPa, whereas stress relaxation induced by water uptake decreased in the range of 10.3–4.7 MPa with increasing BPDA contents, respectively. The major factor in determining the magnitude of the stress behavior induced by both the thermal mismatch and water uptake in films should be the morphological factors such as chain rigidity, chain orientation, crystallinity, and microvoids. Their morphological structures were examined by wide angle X‐ray diffraction and a prism coupler, and the thermal properties were measured using a dynamic mechanical thermal analyzer as well as thermomechanical analysis. Overall, the candidate for the low level stress buffer application from the PMDA/BPDA‐PDA copolyimide was the 30/70 (= PMDA/BPDA in molar ratio) copolyimide. This copolyimide showed no residual stress after curing at 400 °C and relatively insensitive stress relaxation to ambient humidity. © 2001 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 39: 796–810, 2001     

Spectral,electrochemical and computational investigations on the host–guest interaction of Coumarin-460 with <Emphasis Type="Italic">p</Emphasis>-sulfonatocalix[4]arene

The supramolecular host–guest investigation of Coumarin 460 (C460), a salient coumarin family dye molecule is studied with a noteworthy host molecule, p-sulfonatocalix[4]arene (p-SC4). The investigation is carried out by both experimental and theoretical approach. The binding affinity of C460 with p-SC4 is experimentally studied using absorption, emission, excited state lifetime and Cyclic Voltammetry methods. The binding constant is around 10³ M^??1, which shows potent binding. The binding stoichiometry is 1:1. The binding orientations and binding energies are studied using computational simulations. The mode of binding is also established using NMR spectral techniques.     

TEMPO-Assisted Free Radical-Initiated Peptide Sequencing Mass Spectrometry (FRIPS MS) in Q-TOF and Orbitrap Mass Spectrometers: Single-Step Peptide Backbone Dissociations in Positive Ion Mode

The present study demonstrates that one-step peptide backbone fragmentations can be achieved using the TEMPO [2-(2,2,6,6-tetramethyl piperidine-1-oxyl)]-assisted free radical-initiated peptide sequencing (FRIPS) mass spectrometry in a hybrid quadrupole time-of-flight (Q-TOF) mass spectrometer and a Q-Exactive Orbitrap instrument in positive ion mode, in contrast to two-step peptide fragmentation in an ion-trap mass spectrometer (reference Anal. Chem. 85, 7044–7051 (30)). In the hybrid Q-TOF and Q-Exactive instruments, higher collisional energies can be applied to the target peptides, compared with the low collisional energies applied by the ion-trap instrument. The higher energy deposition and the additional multiple collisions in the collision cell in both instruments appear to result in one-step peptide backbone dissociations in positive ion mode. This new finding clearly demonstrates that the TEMPO-assisted FRIPS approach is a very useful tool in peptide mass spectrometry research.

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Layered perovskites with giant spontaneous polarizations for nonvolatile memories

A series of titanate-based layered perovskites having large values of the spontaneous polarization P(s) were developed for their applcations to nonvolatile ferroelectric random access memories. Among these, the Nd-modified bismuth titanate [Bi(4-x)Nd(x)Ti(3)O(12) (BNdT)] system exhibited the most remarkable ferroelectric properties. The c-axis oriented BNdT capacitor was characterized by a switchable remanent polarization 2P(r) of over 100 microC/cm(2) and imprinting and fatigue-free behavior. The active Ti site responsible for the giant P(s) was identified with the help of Rietveld analysis, x-ray absorption near-edge structure study, and ab initio quantum computations.     

Dynamic PIV measurement of a high-speed flow issuing from vent-holes of a curtain-type airbag

A curtain-type airbag is a safety device designed to protect passengers from the side collisions of a car. The curtain-type airbag system consists of an inflator, a fill-hose, and a curtain-airbag. The fill-hose is a passageway and distributor of the exploded gases from the inflator to the airbag through vent-holes. Although the design of vent-holes is important for proper deployment of the airbag, it is very difficult to measure the exceedingly high speed flow issuing from the vent-holes by using conventional measurement methods. In this study, we employed a dynamic PIV technique to measure the temporal evolution of instantaneous velocity fields of the flow ejecting from the vent-holes. From the velocity field data measured at a frame rate of 2000 fps, the temporal variation of the volume flux from vent-holes was also evaluated for the diagnosis of airbag performance. The flows ejecting from the vent-holes showed high velocity fluctuations, and the maximum velocity was about 480 m/s. The instantaneous velocity fields in the initial stage showed a swaying motion of a high-speed jet. The accumulated volume flux from the vent-holes was also compared at each vent-hole region.     

Some insight into the structure of the nuclei 19F, 19Ne, 21Ne, 21Na, 23Na and 23Mg through the generator coordinate method and the projected Hartree-Fock method

Structures of two sets of mirror nuclei ¹⁹Ne, ²¹Na, ²³Mg and ¹⁹F, ²¹Ne, ²³Na were studied comparatively by means of the electromagnetic properties of the even-parity states, calculated with the generator coordinate method and with mixing of projected Hartree-Fock determinants. The present results are compared with those of complete diagonalization. In particular, collective features of these nuclei are investigated by comparing the various microscopic results with the predictions of the simple rotational model.     

Proton transfer of excited 7-azaindole in reverse-micellar methanol nanopools: even faster than in bulk methanol

The methanol-catalyzed double-proton transfer of photoexcited 7-azaindole in the free cores of solvation-restricted reverse micelles takes place on the time scale of 90 ps, even shorter than in bulk methanol. This anomalous rate increase with a large kinetic isotope effect of 5 experimentally proves the widely discussed two-step model for the overall reaction of solvent-mediated proton transfer. On the other hand, the molecules in the bound layers and in the headgroup layers relax in 900 and 6000 ps, respectively, without going through proton transfer. The tautomerization and the relaxation of excited 7-azaindole can be exploited to probe the nanopools of methanol reverse micelles.     

Evidence for muon neutrino oscillation in an accelerator-based experiment

We present results for nu(mu) oscillation in the KEK to Kamioka (K2K) long-baseline neutrino oscillation experiment. K2K uses an accelerator-produced nu(mu) beam with a mean energy of 1.3 GeV directed at the Super-Kamiokande detector. We observed the energy-dependent disappearance of nu(mu), which we presume have oscillated to nu(tau). The probability that we would observe these results if there is no neutrino oscillation is 0.0050% (4.0 sigma).