Probe bath

Routine applications of the refrigerated immersion probe bath include low temperature synthesis, collection flask cooling (for low pressure distillations), and numerous manipulations involving... 

Two major sources of ultrasound are employed, namely ultrasonic baths and ultrasonic immersion hom probes [79, 71]- The fonuer consists of fixed-frequency transducers beneath the exterior of the bath unit filled with water in which the electrochemical cell is then fixed. Alternatively, the metal bath is coated and directly employed as electrochemical cell, but m both cases the results strongly depend on the position and design of the set-up. The ultrasonic horn transducer, on the other hand, is a transducer provided with an electrically conducting tip (often Ti6A14V), which is inuuersed in a three-electrode thenuostatted cell to a depth of 1-2 cm directly facing the electrode surface. 

Kaltwasser-bad. n. cold-water bath, -farbe,/. cold-water color or paint, -probe, /. cold-water test. -Strom, m. stream or current of cold water. 

B. (Z)-l-Iodo-l-heptene.2 A solution of 8.52 g of (112 mmol) of borane-dimethylsulfide complex (Note 13) in 100 mL of ether is added to a flame-dried, three-necked, 300-mL, round-bottomed flask equipped with stirbar, temperature probe, and N2 inlet. The solution is cooled to 5°C with an ice-bath. Cyclohexene (18.4 g, 224 mmol) (Note 14) is then added by syringe over 10 min while keeping the temperature below 15°C. The mixture is stirred at 5°C for 15 min. A white solid precipitates either towards the end of the addition or during the subsequent stirring period. The reaction mixture is allowed to warm to room temperature and is stirred for 1 hr. The non-homogeneous solution is cooled to 2-3°C... 

In the current work a Digital Instmments Dimension 3000 SPM was operated in force-volume mode using a probe with stiffness selected to match the stiffness of the sample. Standard silicon nitride probes with a nominal spring constant of 0.12 or 0.58 N/m were used for recombinant and native resilin samples. These samples were characterized in a PBS bath at a strain rate of 1 Hz. For synthetic rubbers, silicon probes with a nominal spring constant of 50 N/m were used and the material was characterized in air. Typically, at least three force-volume plots (16 X 16 arrays of force-displacement curves taken over a 10 X 10 p.m area) were recorded for each of the samples. 

Sonication of MLV dispersions above the Tc of the lipids results in the formation of SUV (Saunders, et al., 1962). Sonication can be performed with a bath sonicator (Papahadjopoulos and Watkins, 1967) or a probe sonicator (Huang, 1969). During sonication the MLV structure is broken down and small unilamellar vesicles with a high radius of curvature are formed. In case of SUV with diameters of about 20 nm (maximum radius of curvature), the outer monolayer can contain over 50% of the phospholipids and in the case of lipid... 

Anti-Stokes picosecond TR spectra were also obtained with pump-probe time delays over the 0 to 10 ps range and selected spectra are shown in Figure 3.33. The anti-Stokes Raman spectrum at Ops indicates that hot, unrelaxed, species are produced. The approximately 1521 cm ethylenic stretch Raman band vibrational frequency also suggests that most of the Ops anti-Stokes TR spectrum is mostly due to the J intermediate. The 1521 cm Raman band s intensity and its bandwidth decrease with a decay time of about 2.5 ps, and this can be attributed the vibrational cooling and conformational relaxation of the chromophore as the J intermediate relaxes to produce the K intermediate.This very fast relaxation of the initially hot J intermediate is believed to be due to strong coupling between the chromophore the protein bath that can enable better energy transfer compared to typical solute-solvent interactions. ... 

By using an identical radical clock substrate probe which did not rearrange upon hydroxylation with M. capsulatus (Bath), rearranged product was detected with MMO from AT. trichosporium 0B3b (59). From the ratio of unrearranged to rearranged products, a rebound rate constant was calculated to be 6 x 1012 s-1 at 30°C for this system. A separate study with another radical clock substrate probe with MMO from M. trichosporium 0B3b reported products consistent with both radical and cationic substrate intermediates (88). 

Since work with the radical clock substrate probes indicated important differences in the hydroxylation mechanisms for M. capsulatus (Bath) and M. trickosporium OB3b, work with (R) and (S)-[1-2H,1-3H]ethane with both enzymes was carried out (93, 94). With M. tri-chosporium OB3b, approximately 65% of the product displays retention of stereochemistry (93). A rebound rate constant of 2 - 6 x 1012 s-1 was calculated, assuming a free energy change of 0.5 kcal mole-1 for rotation about the C-C bond (94). This estimate approaches the value obtained from the radical clock substrate probe analysis (59). 

In summary, mechanistic studies have revealed intriguing differences between MMO from M. capsulatus (Bath) and MMO from M. triehosporium OB3b. With M. capsulatus (Bath), radical clock substrate probes indicated either that a substrate radical is not produced or that it reacts with a rate constant > 1013 s-1. With MMO from M. triehosporium OB3b, radical involvement was suggested from several experiments, and a rebound rate constant of 6 x 1012 s"1 was calculated for this system. 

We have observed a dependence of the yield, polymerization degree, and polydispersity of polysilanes on temperature and also on the power of ultrasonication. In the ultrasonication bath the simplest test of the efficiency of cavitation is the stability of the formed dispersion. It must be remembered that the ultrasonic energy received in the reaction flask placed in the bath depends on the position of the flask in the bath (it is not the same in each bath), on the level of liquid in the bath, on temperature, on the amount of solvent, etc. When an immersion probe is used the cavitation depends on the level of the meniscus in the flask as well. The power is usually adjusted close to 50% of the output level but it varies with the reaction volume, flask shape, and other rection conditions. The immersion-type probe is especially convenient at lower temperatures. 

In the preceding chapters many aspects of sonochemistry and its application have already been discussed in details and now to conclude, few experiments are being discussed here to make the beginners in the field of sonochemistry, especially the undergraduate students, to ride on the sound wave and begin their journey of sonochemistry with some of these experiments, which can be conveniently carried out with an ultrasonic cleaning bath (Fig. 15.1) or an ultrasonic probe (Fig. 15.2) of 20 kHz, available commercially abundantly. 

Crude material prepared in glass on 3 g mol scale was distilled uneventfully at 40°C/0.067 mbar from a bath at 70-80°C. A 30 mol batch prepared in a glass-lined vessel with a stainless steel thermo-probe (and later found to contain 15 ppm of iron) decomposed very violently dining distillation at 75°C/13 mbar from a bath at 130°C. Thermal analysis showed that the stability of the methyl (and ethyl) ester... 

Ellison EH, Moodley D, Hime J (2006) Fluorescence study of arene probe microenvironment in the intraparticle void volume of zeolites interfaced with bathing polar solvents. J Phys Chem B 110 4772 1781... 

Galvanostatic pulse plating techniques were used to probe the displacement or corrosion of A1 from Cu-Al by Cu+ in the AlCl3-EtMeImCl plating bath [103],... 

The simplest experimental arrangement (two-probe method) uses two thermometers one on the thermal bath at Ts, the second on the warm end of the sample together with the heater (see Fig. 11.1). Such configuration can be used when one is sure that contact resistances are negligible compared with the sample thermal resistance. This is seldom the case at very low temperature. A sample bath (and sample support) temperature drop ... 

Fig. 1. Capsule permeability as measured by the inverse GPC method. Capsules were made from 1.25% A-carrageenan (Fluka) and 0.02% carboxymethylcellulose (Aqualon) in 0.9% sodium chloride (core polymers) and 2% polydimethylamine-co-epichlorohydrin modified, quater-nized (Scientific Polymer Products) and a quaternary amine (Agefloc B50, CPS) in PBS (receiving bath) using a 3 min reaction time. The capsules were subsequently washed with PBS, coated for 15 min with 0.1% LV alginate (Kelco) and again washed in PBS. Two molecular size dex-trans were used to probe the capsule permeability. 170 kD dextran is almost totally excluded while the lower molar mass polymers permeated the membrane to varying extents...

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