An improved water-filled impedance tube

A water-filled impedance tube capable of improved measurement accuracy and precision is reported. The measurement instrument employs a variation of the standardized two-sensor transfer function technique. Performance improvements were achieved through minimization of elastic waveguide effects and through the use of sound-hard wall-mounted acoustic pressure sensors. Acoustic propagation inside the water-filled impedance tube was found to be well described by a plane wave model, which is a necessary condition for the technique. Measurements of the impedance of a pressure-release terminated transmission line, and the reflection coefficient from a water/air interface, were used to verify the system.     

Sub- and above-barrier fusion of loosely bound 6Li with 28Si

Fusion excitation functions are measured for the system ⁶Li + ²⁸Si using the characteristic $ \gamma$ -ray method, encompassing both the sub-barrier and above-barrier regions, viz, E _lab = 7-24 MeV. Two separate experiments were performed, one for the above-barrier region ( E _lab = 11-24 MeV) and another for the below-barrier region ( E _lab = 7-10 MeV). The results were compared with our previously measured fusion cross-section for the ⁷Li + ²⁸Si system. We observed the enhancement of the fusion cross-section at sub-barrier regions for both ⁶Li and ⁷Li , but the yield was substantially larger for ⁶Li . However, for well-above-barrier regions, a similar type of suppression was identified for both the systems.     

Digital computation of transient characteristics of an induction motor on switched supply

A novel method of computing the nonlinear differential equations relating to the transient behaviour of an induction motor using a polynomial series, is presented. The stator and rotor currents and the angle of rotation are expressed as polynomial series dependent on time. These are then substituted into the differential equations of the induction motor to compute the polynomial coefficients and, consequently, the transient quantities. Since the equations are nonlinear, the computations are carried out using the step-by-step method. The stator and rotor currents, speed and torque are calculated for acceleration and braking conditions. The results are compared both analytically and experimentally.     

Dissociation constants of the ampholyte glycine in 50 mass % methanol-water from 5 to 55°C,with related thermodynamic quantities

The two thermodynamic dissociation constants of glycine at 11 temperatures from 5 to 55°C in 50 mass % methanol-water mixed solvent have been determined from precise emf measurements with hydrogen-silver bromide electrodes in cells without liquid junction. The first acidic dissociation constant (K ₁)for the process HG⁺H⁺+G^± is expressed as a function ofT(^oK) by the equation pK ₁ = 2043.5/T – 9.6504 + 0.019308T. At 25°C, pK ₁is 2.961 in the mixed solvent, as compared with 2.350 in water, with H°=1497 cal-mole^–1, G°=4038 cal-mole^–1, S°=–8.52 cal-°K^–1-mole^–1, and C _p ^o =–53 cal-°K^–1-mole^–1. The second acidic dissociation constant (K ₂)for the process G^±H⁺+G^– over the temperature range studied is given by the equation pK ₂ = 3627.1/T – 7.2371 + 0.015587T. At 25°C, pK ₂is 9.578 in MeOH–H₂O as compared with 9.780 in water, whereas H° is 10,257 cal-mole^–1, G° is 13,063 cal-mole^–1, S° is –9.41 cal-°K^–1-mole^–1, and C _p ^o is –43 cal-°K^–1-mole^–1. The protonated glycine becomes weaker in 50 mass % methanol-water, whereas the second dissociation process becomes stronger despite the lower dielectric constant of the mixed solvent (=56.3 at 25°C).     

EFFECT OF CHLORIDE AND BENZOATE ANIONS ON THE DELAYED LIGHT EMISSION IN DCMU-TREATED SPINACH CHLOROPLASTS

Abstract —Chloride anions, when added to DCMU [3-(3,4-dichlorophenyl)-1,1-dimethylurea]-treated spinach chloroplasts, change the rate of decay of the delayed light emission in the seconds region but do not change the shape or the temperature dependence of the decay. Benzoate anions, on the other hand, change both the rate and the shape of the decay of the delayed light emission. These results are consistent with a model in which the membrane potential and the structure of the reaction center affect the decay kinetics of the delayed light emission in the seconds region.     

Separation of lead sulphate from barium sulphate in their determination in glass

The conventional method for separation of lead from a combined lead and barium sulphate precipitate by extraction with ammonium acetate has been critically studied. The results show that quantitative separation of lead is possible only when the molar concentration ratio of barium to lead is 4.2 or above, but at ratios below 4.2 the method fails because of the formation of a solid solution of lead and barium sulphates which is maximal at initial mole-ratio 0.42. The lead in the solid solution, however, forms a strong soluble complex with EDTA and can be quantitatively separated. Based on this, a gravimetric method has been worked out for determination of lead and barium in glass.     

Rearrangement correction to higher polarizabilities of two-electron systems

In this paper we include the rearrangement correction (discussed in the preceding paper) in a coupled Hartree–Fock (CHF) calculation of atomic hyperpolarizabilities and other related properties. We have studied the effect of these corrections on properties like electric dipole hyperpolarizabilities, uniform electric field quadrupole polarizabilities and shielding factors in two-electron ions and have noticed significant changes in the computed values over the CHF results.     

Donor—acceptor interactions of substituted benzenes with molecular chlorine and carbon disulfide

CNDO molecular orbital calculations have been performed to analyze donor—acceptor interactions between molecular chlorine and benzene, toluene, mesitylene and hexamethylbenzene and the, as yet, unreported chlorine—hexafluorobenzene and carbon disulfide—benzene pairs. The stabilization energy and the dipole moment and its derivative (?p/?R_CICI) calculated for the benzene—chlorine complex are in good agreement with the estimated experimental values. The trends in the experimental stabilization energies and the Cl-Cl vibrational frequencies with increasing methyl substitution appear to be well reproduced by the calculations. The charge transferred from the benzene donor is polarized toward the outer chlorine atom or sulfur atom. For hexafluorobenzene-chlorine the direction of electronic charge polarization is reversed from that of the benzene and methylbenzene complexes. The calculated results are discussed within the framework of Muliiken's simplified resonance theory for complexes.