Speckle-pattern contrast of semiconductor laser propagating in a multimode optical fiber

Speckle patterns produced by coherent light from a GaA1As double-hetero-structure laser diode that has been transmitted through a multi-mode optical fiber are experimentally studied by analyzing the average contrast. It has been found that the speckle contrast observed in the far-field region is significantly lowered when the spectral width of a laser diode is as broad as a few tens of Angstroms.     

Nuclear magnetic resonance of poly-β-alanine

Nuclear magnetic resonance of poly-β-alanine samples differing in solubility in water was studied over a wide temperature range as part of an investigation of their physical properties. Water-soluble poly-β-alanine has more branches and a lower degree of crystallinity than water-insoluble poly-β-alanine. NMR spectra of poly-β-alanine show one component at 77°K. which splits into two components, broad and narrow, at room temperature. Two transition regions were observed in curves for line width and second moment versus temperature. The higher transition temperature, corresponding to the glass transition of the polymer, appears to decrease with increasing water content. The second moment for the water-soluble polymer differs from that of the water-insoluble polymer at 77°K. This is interpreted in terms of the difference in the degree of crystallinity of the polymers.     

Visible nonlinear band-edge luminescence in ZnSe and CdS excited by a mid-infrared free-electron laser

Visible nonlinear band-edge luminescence in ZnSe and CdS bulk crystals was observed upon excitation by a mid-infrared free-electron laser (mid-IR FEL) at approximately 9 mm. The emission intensity is proportional to the 74th and 45th powers of the excitation intensity for ZnSe and CdS, respectively. For ZnSe, the temporal profile of the emission intensity does not follow the profile of the excitation macropulse of the FEL, but sharply rises and decays only at the maximum of the macropulse profile. These features are in marked contrast to those of a previous report, where the emission profile follows that of the macropulse, and the emission intensity scales with the 4th power of the excitation intensity. The experimental observations were reproduced by a numerical simulation based on impact ionization and avalanche ionization by electrons accelerated by the optical electric field of the FEL. The large nonlinearity in the bandedge emission comes from the macropulse temporal structure, which consists of micropulses densely spaced to allow excited carriers to survive when the next micropulse arrives. They work as seed carriers in the next carrier multiplication step.     

Polypyrrole coating doped by molybdo-phosphate anions for corrosion prevention of carbon steels

The polypyrrole coating was prepared from phosphoric acid aqueous solution containing the hetero-polyanion and pyrrole monomer to make new coating for corrosion prevention of carbon steels. The coating thus formed in the phosphate acid solution was doped by and by . The coating was flexible enough to cover the steel homogeneously without cracks, although many cracks were observed on the coating formed in a neutral aqueous solution of Na₂MoO₂. The 5.1-μm-thick polypyrrole coating makes the steel maintain the passive state for 48 h in neutral 3.5 wt% NaCl solution at pH 5.3 and for 80 h in acidic 3.5 wt% NaCl solution at pH 1.9. The coating decreased the corrosion rate of the steel by 1/200 in the neutral NaCl solution and by 1/340 in the acidic NaCl solution, if compared with the rate of the bare steel. The dissolution current of the steel during the immersion remained at the level of the typical passive current in the respective solutions.     

Relaxational behavior of the piezoelectric constant and the electrostriction constant in polymers

Piezoelectricity in polymer films is classified by its mechanism into three groups: A-1, intrinsic piezoelectricity due to internal strain in nonpolar crystals; A-2, intrinsic piezoelectricity due to the strain-dependence of the spontaneous polarization in polar crystals; and B, piezoelectricity due to the heterogeneity of macroscopic strain.

The relaxational behavior of piezoelectricity in Type A-1 is discussed for two cases: (a) the piezoelectric phase is relaxing, and (b) the piezoelectric phase is nonrelaxing but the nonpiezoelectric phase is relaxing. For Case a, a thermody-namic theory is developed, yielding relations among relaxation strengths of piezoelectric constant, dielectric constant, and elastic modulus. For Case b, on the other hand, the inequalities e″/e′ < 0 and d″/d′ > 0 are verified for a generalized composite model of two phases, where e′ — ie” and d′ — id″ are complex piezoelectric stress and strain constants, respectively.

Relaxational behavior of the piezoelectric constant for Type A-2 and Type B is expected to reflect that of the electrostriction constant as suggested by theories. The complex electrostriction constant in a range from 30 Hz to 500 kHz is presented for unrolled and rolled poly(vinylidene fluoride) films. The frequency dependence of the complex electrostriction constant can explain the relaxational behavior of the piezoelectric constant of Types A-2 and B, and at the same time gives a new aspect of the relaxational character of polymers, the strain-dependence of the relaxation time, and its anisotropy.     

Synthesis of novel thermosetting imide compounds having phenylethynyl carbonyl groups at both terminal ends and production of new network polymers based on the imide compounds

A novel thermosetting imide compound having a respective phenylethynyl carbonyl group at both terminal ends was newly synthesized from an acid anhydride having a phenylethynyl carbonyl group and various diamine compounds. The thermosetting behavior of the obtained novel thermosetting imide compound having phenylethynyl carbonyl groups was analyzed through differential scanning calorimetry measurements and infrared spectroscopic analysis. As a result, it became clear that a curing reaction of phenylethynyl carbonyl groups proceeds at approximately 200°C and that the curing reaction thereof proceeds at a temperature that is lower by 150°C or more compared with that of phenylethynyl groups. Examination of the polymerization reaction of the imide compounds having phenylethynyl carbonyl groups using model compounds revealed that a reaction that imparted an alkene C=C and polycyclic aromatic structure progressed. Moreover, a network polymer obtained from a thermosetting imide compound having respective phenylethynyl carbonyl groups at both terminal ends exhibited extremely superior heat resistance and thermal decomposition resistance. These superior thermal properties are thought to be due to the strong molecular interaction (molecular packing) that results from the polycyclic aromatic structures and alkenes produced through polymerization of the phenylethynyl carbonyl groups and to the suppression of the movement of the molecular chains.     

A Defect‐Free Ring Polymer: Size‐Controlled Cyclic Poly(tetrahydrofuran) Consisting Exclusively of the Monomer Unit

A series of size‐controlled, cyclic poly(tetrahydrofuran)s ( of 4 400–8 600) that consist exclusively of the monomer, i.e., oxytetramethylene, unit ( I ) have been prepared in high yield through the metathesis polymer cyclization of a telechelic precursor having allyl groups, 1 , in the presence of a Grubbs catalyst, and the subsequent hydrogenation of the linking, i.e., 2‐butenoxy, unit in the presence of an Adams' catalyst (PtO₂). A remarkable topology effect has subsequently been observed upon the isothermal crystallization of these two model polymers, showing distinctive spherulite growth rates and spherulite morphologies in comparison with the relevant linear poly(tetrahydrofuran) counterpart that has ethoxy end groups ( II ).

     

Measurements of the complex degree of spectral coherence by use of a wave-front-folded interferometer

A wave-front-folded interferometer composed of a K?sters prism and an image-forming lens provides a good way of measuring the complex degree of spectral coherence. Demonstrative experiments are implemented by incorporation of uncorrelated two-point spectral sources in the primary-source plane; these sources establish a spatially partially coherent wave field over the secondary source plane just in front of the interferometer. The complex degree of spectral coherence of the secondary source is successfully measured after an a priori calibration is made for the interferometer that was constructed.     

Eigenvalues of some distal functions

In this paper we construct distal functions of another type discussed by Salehi (1991). Let be an almost periodic function with the mean value 0, which has unbounded integral, and a continuous periodic function with the prime period 1. If satisfies some additional condition, then is a distal function, which is not almost periodic, and the set of eigenvalues of is the module of .