INCENTIVE COMPATIBLE ENVIRONMENTAL REGULATIONS

This paper addresses the problem of designing environmental regulations when firms possess better information about the cost of pollution abatement than regulators. In the regulatory equilibrium derived in the paper, firms are induced to reveal the information they have concerning abatement costs through the judicious use of abatement standard-subsidy combinations. Offering firms a menu of regulatory contracts, each one specifying a required level of pollution abatement as well as a lump sum subsidy to be paid by the regulatory agency to the firm, is shown to be superior to optimal uniform standard-subsidy schemes. By appealing to the revelation principle and employing a second policy instrument (subsidies), albeit a costly one, in conjunction with an abatement standard, the incentive compatible approach to environmental regulation presented in the paper minimizes the economic inefficiency customarily attributable to a lack of initial information regarding pollution abatement costs.     

Fast switching ferroelectric side-chain liquid-crystalline polymer and copolymer

New ferroelectric side-chain liquid-crystalline polymers, a copolymer and a homopolymer, with siloxane backbone and a triaromatic mesogen as the side group have been synthesized. The materials exhibit a chiral smectic C phase over a large temperature range extending to room temperature. They possess high values of spontaneous polarization: 105 nC cm^-2 for the homopolymer and 180 nC cm^-2 for the copolymer. The electro-optic switching time in the chiral smectic C phase is extremely fast (150 μs). In the smectic A phase, an electroclinic effect with switching times less than 100 μs and with field induced tilt angles of 18° is observed.     

Synthesis of poly-yne polymers containing transition metals,disilane, disiloxane and phosphine groups in the main chain

The synthesis and characterization of metal poly-yne polymers containing disilane, disiloxane and phosphine groups in the main chain are described. The platinum and palladium poly-yne polymers were synthesized by polycondensation reactions between a metal chloride and an α, ω-bisethynyl complex in amines in the presence of cuprous iodide as a catalyst. The nickel poly-yne polymers were synthesized by an alkynyl ligand exchange reaction between a nickel acetylide and an α, ω-bisethynyl complex in diethylamine in the presence of cuprous iodide as a catalyst. The reaction of the platinum poly-yne polymer, containing disiloxane groups in the main chain, with copper (I) salts afforded adducts of η-²-bonded σ-acetylide polymer complexes. The reactions of the palladium poly-yne polymer, containing phosphine groups in the main chain, with transition-metal carbonyl complexes afforded polymer complexes which have phosphorus in the main chain-transition-metal bonds. A concentrated solution of the platinum poly-yne polymer containing disiloxane groups in the main chain forms a lyotropic liquid crystal in dichloromethane or 1, 2-dichloroethane.     

Magnetopause plasma transients: mapping into the auroral ionosphere

Attention is focused on a specific category of auroral event occurring predominantly during a southward directed interplanetary magnetic field (IMF). Coordinated observations from the ground and satellites in polar orbit have been used to study the temporal/spatial development of the events in relation to the background patterns of particle precipitation and ionospheric convection as well as the field-aligned current and ion drift characteristics of the individual events. Both prenoon and postnoon sector events are reported. In one case the auroral event was observed near the zero point potential line separating the morning and postnoon convection cells. The available data indicate that this auroral event sequence is a signature of quasi-periodic bursts of particle entry from the magnetosheath along flux tubes convecting into the polar cap, representing structures of enhanced IMF B_Y-related convection poleward of the persistent cleft aurora. Such events may be initiated by localized patches of enhanced merging rate at the dayside magnetopause     

Rotational Spectra of Argon Acetone: A Two-Top Internally Rotating Complex

The rotational spectra of the argon acetone weakly bound complex was studied by pulsed jet Fabry-Perot Fourier transform microwave spectroscopy. Over 500 transitions of the complex were measured between 5.5 and 26 GHz from J=2-1 to J=12-11. The two methyl groups undergo hindered internal rotation resulting in four or five internal rotation states. The microwave transitions are within these states, resulting in a splitting of each rotational transition into four and sometimes five distinct transitions. The three-fold barrier to internal rotation is determined to be 260 cm⁻¹, 2% less than the 266 cm⁻¹ barrier in acetone itself. The structure of the complex has the argon atom above the heavy atom plane of the acetone, 3.52 Å from the CO bond and approximately in the C_s plane, which is perpendicular to the CCC plane of acetone.     

Determination of the parameters of semiconductor quantum dots in glassy matrices from the absorption and luminescence spectra and from saturation of the optical absorption

Optical methods are described for determining the parameters of semiconducting quantum dots synthesized in a glassy borosilicate matrix. The limitations of these methods and the magnitudes of their errors are analyzed. The parameters of CdS_xSe_1−x nanocrystals in the commercial glasses KS-10, OS-12, Corning 2–61, and other experimental samples are determined. Fiz. Tverd. Tela (St. Petersburg) 39, 1865–1870 (October 1997)     

Dependence of impurity incorporation upon substrate misorientation during GaAs growth by metalorganic vapour phase epitaxy

Doping studies of the incorporation behaviour of three different dopants (Zn, In and Si) versus the misorientation of the (100) surface during MOVPE growth of GaAs have been carried out with diethylzinc, trimethylindium and disilane as precursors. The incorporation of the dopants has been studied as function of the input mole fraction dopant, growth temperature, degree and direction of misorientation. In order to explain the results we discuss the BCF theory and the nature of the steps as function of above mentioned parameters. It appears that the BCF theory alone cannot explain the results, a counteracting mechanism has been introduced based on preferential arsenic desorption from the step edges.