Differential thermal analysis of polyester/cotton blends treated with Thpc—urea—poly(vinyl bromide)

Differential thermal analyses (DTA) were made on a series of polyester/cotton blend fabrics before and after treatment with Thpc—urea—poly(vinyl bromide). This flame retardant did not affect the polyester melting endotherm, which was proportional to the polyester content and appeared at approximately 250°C. In nitrogen atmosphere, DTA of the treated blends showed exothermic peaks at 285°C for the cotton decomposition. and at 415°C for the polyester decomposition. In air, DTA of the treated blends showed exothermic peaks at 333°C for cellulose decomposition, at 431°C for polyester decomposition and at 490°C for char decomposition. The Thpc-urea component of the flame retardant is effective on the cotton cellulose portion of the blend; the poly(vinyl bromide) appears to decompose and act in the vapor state on the polyester.     

Psychophysical recovery from pulse-train forward masking in electric hearing

Psychophysical pulse-train forward-masking (PTFM) recovery functions were measured in fifteen subjects with the Nucleus mini-22 cochlear implant and six subjects with the Clarion cochlear implant. Masker and probe stimuli were 500-Hz trains of 200- or 77-micros/phase biphasic current pulses. Electrode configurations were bipolar for Nucleus subjects and monopolar for Clarion subjects. Masker duration was 320 ms. Probe duration was either 10 ms or 30 ms. Recovery functions were measured for a high-level masker on a middle electrode in all 21 subjects, on apical and basal electrodes in 7 of the Nucleus and 3 of the Clarion subjects, and for multiple masker levels on the middle electrode in 8 Nucleus subjects and 6 Clarion subjects. Recovery functions were described by an exponential process in which threshold shift (in microA) decreased exponentially with increasing time delay between the offset of the masker pulse train and the offset of the probe pulse train. All but 3 of the 21 subjects demonstrated recovery time constants on a middle electrode that were less than 95 ms. The mean time constant for these 18 subjects was 54 ms (s.d. 17 ms). Three other subjects tested on three electrodes exhibited time constants larger than 95 ms from an apical electrode only. Growth-of-masking slopes depended upon time delay, as expected from an exponential recovery process, i.e., progressively shallower slopes were observed at time delays of 10 ms and 50 ms. Recovery of threshold shift (in microA) for PTFM in electrical hearing behaves inthe same way as recovery of threshold shift (in dB) for pure-tone forward masking in acoustic hearing. This supports the concept that linear microamps are the electrical equivalent of acoustic decibels. Recovery from PTFM was not related to speech recognition in a simple manner. Three subjects with prolonged PTFM recovery demonstrated poor speech scores. The remaining subjects with apparently normal PTFM recovery demonstrated speech scores ranging from poor to excellent. Findings suggest that normal PTFM recovery is only one of several factors associated with good speech recognition in cochlear-implant listeners. Comparisons of recovery curves for 10- and 30-ms probe durations in two subjects showed little or no temporal integration at time delays less than 95 ms where recovery functions have steep slopes. The same subjects exhibited large amounts of temporal integration at longer time delays where recovery slopes are more gradual. This suggests that probe detection depends primarily on detection of the final pulses in the probe stimulus and supports the use of offset-to-offset time delays for characterizing PTFM recovery in electric hearing.     

119Sn mössbauer,IR, 1H NMR spectroscopic and thermal decomposition studies on organotin(IV) adducts with glycylglycine

The complexes R₂SnCl₂·(H₂glygly), (H₂glygly = glycylglycine) (R = Me, Buⁿ, Octⁿ, Ph) and RSnCl₃·(H₂glygly)     

Determination of silver in ores, concentrates, zinc process solutions, copper metal and copper-base alloys by atomic-absorption spectrophotometry after separation by extraction of the tribenzylamine-silver bromide complex

A method for determining 0.1 μg/g or more of silver in ores and concentrates and 0.001 μg/ml or more of silver in zinc process solutions is described. Silver is separated from the matrix elements by chloroform extraction of the tribenzylamine—silver bromide ion-association complex from 0.08M potassium bromide—2M sulphuric acid and stripped with 9M hydrobromic acid. This solution is evaporated to dryness and organic material is destroyed with nitric and perchloric acids. Silver is determined by atomic-absorption spectrophotometry in an air—acetylene flame, at 328.1 nm, in a 10% v/v hydrochloric acid—1% v/v diethylenetriamine medium. Cadmium, bismuth and molybdenum are partly co-extracted but do not interfere. The method is also applicable to copper metal and copper-base alloys. Results obtained by this method are compared with those obtained by a fire-assay/atomic-absorption method.     

Adsorption and desorption of ammonia,hydrogen, and nitrogen on ruthenium (0001)

The adsorption of ammonia, hydrogen, and nitrogen on a Ru(0001) surface have been investigated by Auger electron spectroscopy, low-energy electron diffraction, and thermal flash desorption. The adsorption of ammonia on Ru(0001) can be divided into a low temperature mode (100 K) and a higher temperature mode (300–500 K). For a crystal temperature of 100 K the ammonia adsorbs into two weakly bound molecular γ states with s = 0.2. The ammonia desorbs as NH₃ molecules with desorption energies of 0.32 and 0.46 eV. At 300–500 K adsorption occurs via an activated process with a low sticking probability (s ? 2 × 10^?4).This adsorption is accompanied by dissociation and formation of an apparent (2 × 2) LEED pattern. Hydrogen adsorbs readily (s = 0.4) on Ru(0001) at 100 K and desorbs with 2nd order kinetics in the temperature range 350–450 K. Nitrogen does not appreciably adsorb on Ru(0001) even at 100 K; maximum nitrogen coverage obtained was estimated to be <2% of a monolayer. Changes in the ammonia flash desorption spectra after hydrogen preadsorption at 100 K will be discussed.     

Ermittelung metallischer Gifte

Ohne Zusammenfassung     

Boundary value problems for Yang—Mills fields

This paper investigates boundary value problems for Hermitian Yang—Mills equations over complex manifolds. The main result is the unique solubility of the Dirichlet problem for the Hermitian Yang—Mills equation. Connections with a number of topics are found, including the link with loop groups.     

Unsteady-state temperature distribution in a convecting fin of constant area

A solution for the unsteady-state temperature distribution in a fin of constant area dissipating heat only by convection to an environment of constant temperature, is obtained. The partial differential equation is separated into an ordinary differential equation with position as the independent variable, and a partial differential equation with position and time as the independent variables. The problem is solved for either a step function in temperature or a step function in heat flow rate, for zero time, at one boundary while the other boundary is insulated. The initial condition is taken as an arbitrary constant. The unspecified boundary values (temperature or heat flow rate) are presented for both cases by utilizing dimensionless plots. Experimental verification is presented for the case of constant heat flow rate boundary condition.     

Reactivity of acyclic (pentadienyl)iron(1+) cations: synthetic studies directed toward the frondosins

A short, 4-step route to the scaffold of frondosin A and B is reported. The [1-methoxycarbonyl-5-(2',5'-dimethoxyphenyl)pentadienyl]Fe(CO)(3)(+) cation was prepared in two steps from (methyl 6-oxo-2,4-hexadienoate)Fe(CO)(3). Reaction of this cation with isopropenyl Grignard or cyclohexenyllithium reagents affords (2-alkenyl-5-aryl-1-methoxycarbonyl-3-pentene-1,5-diyl)Fe(CO)(3) along with other addition products. Oxidative decomplexation of these (pentenediyl)iron complexes, utilizing CuCl(2), affords 6-aryl-3-methoxycarbonyl-1,4-cycloheptadienes via the presumed intermediacy of a cis-divinylcyclopropane.