Absorption, experimental system used measurements

Figure 1. Experimental system used in the time resolved absorption measurements. (EL=excimer laser, KrF, 248nm DG=delay generator OMA=optical multichannel analyser MC=monochromator and gated diode array detector C=cell X=xenon flash lamp L=lenses )...

The complexation of Pu(IV) with carbonate ions is investigated by solubility measurements of 238Pu02 in neutral to alkaline solutions containing sodium carbonate and bicarbonate. The total concentration of carbonate ions and pH are varied at the constant ionic strength (I = 1.0), in which the initial pH values are adjusted by altering the ratio of carbonate to bicarbonate ions. The oxidation state of dissolved species in equilibrium solutions are determined by absorption spectrophotometry and differential pulse polarography. The most stable oxidation state of Pu in carbonate solutions is found to be Pu(IV), which is present as hydroxocarbonate or carbonate species. The formation constants of these complexes are calculated on the basis of solubility data which are determined to be a function of two variable parameters the carbonate concentration and pH. The hydrolysis reactions of Pu(IV) in the present experimental system assessed by using the literature data are taken into account for calculation of the carbonate complexation. 

New or improved methods are needed to measure local uptake experimentally. Such data can be used to verify the detailed dosage distribution predicted by the models. For example the retrograde catheter and tracheal cannula system used by Com et al. appears promising for transfer-coefficient measurements within segments of the tracheobronchial tree. A similar method was used by Battista and (3oyer to measure the absorption of acetaldehyde vapor in the dog lung. 

Figure 24.8 Experimental schematic of the multiplexed diode-laser sensor system used to measure CO, CO2, CH4, and H2O absorption by sampling hot combustion gases 1 ECDL 1.49-1.58 pm 2 optical isolator 3 — fiber coupler 4 — 1x2 fiber splitter 5 — etalon 6 — InGaAs detector 7 — DEB 1.65 pm 8 — 2 x 1 fiber combiner 9 optical fiber 10 fiber pitch 11 — concave mirror 12 — multipass...

In the preceding sections we presented descriptions of absorption spectroscopy systems that use folded optics and small sample chambers to achieve the desired measurements. Other experimenters have... 

Ultrasonic absorption measurements were carried out over the frequency range from 0 2 to 65 MHz. Three different techniques were used depending on the frequency ranges from 0 3 to 1.7 MHz, we used the plano-concave resonator method coupled with the optical detection techniques, from 2 to 7 MHz range we used the cylindrical resonator method and from 15 MHz to 65 MHz we used the pulse method. The details of the experimental system are described elsewhere. ... 

Although it is essentially a conductivity technique, the experimental setup is very similar to that used for optical absorption measurements. In simple terms, the attenuation of the amplitude of the microwave resulting from its passage through the irradiated system is measured. Actually, the microwaves are reflected back through the medium by a metal plate at the back of the cell, but because micro-waves undergo reflection at any dielectric discontinuity, such as the gas-liquid interface at the front of the cell, interference effects arise due to the coherent nature of the microwave radiation. 

The prepared catalysts and the chemical compositions measured by atomic absorption, are listed in Table 1. Complementary characterization experiments such as hydrogen chemisorption in a pulse apparatus and temperature-programmed reduction (TPR) were performed using experimental systems and methods described in detail elsewhere [10]. 

Solubilities of ammonia in ionic liquids, l-ethyl-3-methylimidazolium acetate ([EMIm]Ac), l-ethyl-3-methylimidazolium thiocyanate ([EMIm]SCN), l-ethyl-3-methylimidazolium ethylsulfate ([EMImJEtOSOs), and N,N-dimethy- lethanolammonium acetate ([DMEA]Ac) were measured for the first time by A.Yokozeki and M.B. Shiflett [7] in 2007. Six mixture compositions of each binary system were involved from about 30 to 85 mole% of ammonia. Pressure-temperature-composition (P-T-x) data were claimed at isothermal conditions of 283, 298, 323, 348, and 373 K. The observed solubility of ammonia in ionic liquids is very high, and all cases show negative deviations from ideal solution behavior. Experimental P-T-x data were successfully correlated with the equation-of-state (EOS) model [8]. The experimental data and fitting results are shown in Figure 5 8. The opportunity for the absorption cycle application using the ammonia-RTIL system, replacing the traditional ammonia-water system, has been discussed [7]. 

The several experimental methods allow a wide range of relaxation times to be studied. T-Jump is capable of measurements over the time range 1 to 10 s P-jump, 10 to 5 X 10" s electric field jump, 10 to 10 s and ultrasonic absorption, 10 to 10 " s. The detection method in the jump techniques depends upon the systems being studied, with spectrophotometry, fluorimetry, and conductimetry being widely used. 

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