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Water three-layer

Kitamura and coworkers demonstrated the photocyanation of pyrene by manipulating stable organic/aqueous (oil/water) laminar flow inside the microchannel (polystyrol microchannel chip with a channel, 100 pm wide, 20 pm deep and 350 mm long) [46], This two-layer oil/water system gave only 28% of the desired cyanated pyrene in 210 s under irradiation by a 300 W high-pressure Hg lamp (Scheme 4.32). However, the yield was improved (73%) by using a water/oil/water three-layer flow system. The 2.5-fold increase in yield was attributed to the greater surface area-to-volume ratio in the three-layer system. [Pg.74]

If you netralize the formic acid mix with 25% NaOH the layers separate out nicely. It takes 75 / of 25% NaOH to neutralize the soln for 150grm 88% formic, so you ll need a big sepatory funnel. After you hit ph 4.5 add it rery carefully cause it ll run away to 9+ real quick. You can then back extract the water with DCM, or I guess preferably ether. If you use too much DCM when extracting it sinks to the bottom and some product floats on the top, so you end up with three layers... But then my lab tech SUXSI (not that I d partake in iilegal activities. p"... [Pg.56]

The reaction solution is washed once with water, three times with 5% NaOH and once more with water. The benzene layer is dried through Na2S04 and distilled with no vacuum collecting the fraction between 150-170°C. This fraction is then redistilled and the fraction coming over at 154-157°C is the pure bromobenzene. [Pg.253]

The existence of tridymite as a distinct phase of pure crystalline siUca has been questioned (42,58—63). According to this view, the only tme crystalline phases of pure siUca at atmospheric pressure are quart2 and a highly ordered three-layer cristobaUte having a transition temperature variously estimated from 806 250°C to about 1050°C (50,60). Tridymites are considered to be defect stmctures in which two-layer sequences predominate. The stabihty of tridymite as found in natural samples and in fired siUca bricks has been attributed to the presence of foreign ions. This view is, however, disputed by those who cite evidence of the formation of tridymite from very pure siUcon and water and of the conversion of tridymite M, but not tridymite S, to cristobahte below 1470°C (47). It has been suggested that the phase relations of siUca are deterrnined by the purity of the system (42), and that tridymite is not a tme form of pure siUca but rather a soHd solution of minerali2er and siUca (63). However, the assumption of the existence of tridymite phases is well estabUshed in the technical Hterature pertinent to practical work. [Pg.475]

At low temperature, nonionic surfactants are water-soluble but at high temperatures the surfactant s solubUity in water is extremely smaU. At some intermediate temperature, the hydrophile—Hpophile balance (HLB) temperature (24) or the phase inversion temperature (PIT) (22), a third isotropic Hquid phase (25), appears between the oil and the water (Fig. 11). The emulsification is done at this temperature and the emulsifier is selected in the foUowing manner. Equal amounts of the oil and the aqueous phases with aU the components of the formulation pre-added are mixed with 4% of the emulsifiers to be tested in a series of samples. For the case of an o/w emulsion, the samples are left thermostated at 55°C to separate. The emulsifiers giving separation into three layers are then used for emulsification in order to find which one gives the most stable emulsion. [Pg.201]

In the studies by Skipper et al. the number of water layers (and thus molecules) was fixed on the basis of experimental evidence consequently, the stable states or degrees of swelhng were presumed. Quite differently, Karaborni et al. [44] determined, by means of a combination of GCMC and MD, the number of water molecules directly from a series of simulations in which the distance between montmorillonite planes was varied systematically. They observed that swelling proceeded from the dry state through the formation of one, three, and then five layers of water. This is very different from the usually beheved hydration sequence from one layer to two, then to three layers, and so on, which has been intrinsically assumed by Skipper and coworkers. The authors conclude that the complex swelling behavior accounts for many of the experimental facts. This work demonstrates impressively the power of the grand canonical simulation method. [Pg.378]

Schimmel Co. attempted to acetylise the alcohol by means of acetic anhydride, but the reaction product only showed 5 per cent, of ester, which was not submitted to further examination. The bulk of the alcohol had been converted into a hydrocarbon, with loss of water. Ninety per cent, formic acid is most suitable for splitting off water. Gne hundred grams of the sesquiterpene alcohol were heated to boiling-point with three times the quantity of formic acid, well shaken, and, after cooling, mixed with water. The layer of oil removed from the liquid was freed fi-om resinous impurities by steam-distillation, and then fractionated at atmo.spheric pressure. It was then found to consist of a mixture of dextro-rotatory and laevo-rotatory hydrocarbons. By repeated fractional distillation, partly in vacuo, partly at ordinary pressure, it was possible to separate two isomeric sesquiterpenes, which, after treatment with aqueous alkali, and distillation over metallic sodium, showed the following physical constants —... [Pg.158]

The mixture is heated at reflux for two hours with continual agitation and there is then added dropwise a solution of 2-methyl-3-dimethylaminopropyl chloride in an equal volume of Xylene. The mixture is then heated for fifteen hours, after which time it is cooled and decomposed by the cautious addition of ice water. The layers are separated and the aqueous layer extracted with ether. The combined organic layers are next extracted with 10% hydrochloric acid and the acidic extracts then rendered alkaline by the addition of ammonium hydroxide. The precipitated oil is extracted three times with chloroform. The chloroform extracts are dried and concentrated in vacuo, the residue being distiiled to yield the product. [Pg.213]

The checkers often obtained a thick emulsion which separated into three layers after standing for ca. 2 hours. When this occurred, the mixture was poured into 500 ml. of water, and the product was extracted with three 150-ml. portions of pentane. [Pg.7]

Tomato root growth bloassay of leaf extracts. Three hundred mg samples of fully expanded leaves were taken from each plant studied. Each sample was ground with a Polytron1 in 30 ml of distilled water and the extract was filtered. Five ml aliquots of each extract were pipetted onto three layers of germination paper in a 10 by 10 by 1.5 cm plastic petri dish. Distilled water was used as a control treatment. Twelve tomato seeds were placed in a 3x4 array in each dish, and incubated at 20C for 168 hours, prior to root measurement. The experimental design was a completely randomized design with five replications (dishes) per treatment except the control which had 10 replications. The experiment was repeated each week for 9 weeks. [Pg.223]

The heat store of 120 cm height and 20 cm diameter is divided into 12 layers, each one 10 cm thick. Each layer is represented by one knot with one temperature. The top three layers contain the PCM module which is represented similar to the water layers. [Pg.297]

The design and implementation of a portable fiber-optic cholinesterase biosensor for the detection and determination of pesticides carbaryl and dichlorvos was presented by Andreou81. The sensing bioactive material was a three-layer sandwich. The enzyme cholinesterase was immobilized on the outer layer, consisting of hydrophilic modified polyvinylidenefluoride membrane. The membrane was in contact with an intermediate sol-gel layer that incorporated bromocresol purple, deposited on an inner disk. The sensor operated in a static mode at room temperature and the rate of the inhibited reaction served as an analytical signal. This method was successfully applied to the direct analysis of natural water samples (detection and determination of these pesticides), without sample pretreatment, and since the biosensor setup is fully portable (in a small case), it is suitable for in-field use. [Pg.371]

Procedure Ten radish seeds (80 5 mg) were sown in each Petri dish (9-cm diameter) on three layers of filter paper (Whatman No. 3) previously moistened either with 7 ml of distilled water (control) or 7 ml of rue infusion (treated). Eighteen hours after sowing, control and rue treated radish seeds were differently moistened, having weight increases of 110 and 80 % respectively. The water uptake was evaluated as the difference in weight between moist and dry seeds (% of initial weight)(Fig.l.). [Pg.77]

The total volume of the world s oceans is 1.35 x 1031 1 with a total mass of 1.4 x 1031 kg compared with a fresh water mass of 1.26 x 1017 kg. The pH of the oceans, however, is moderated into layers because the oceans are not well mixed. There are essentially three layers - the surface layer, the mixed layer and the deep layer - and the volume of the mixed layer is 2.7 x 1019 1 to a mean depth of 75 m. The solubility of CO2 enables the precipitation of C032- to be estimated, from which an estimate (although it is fraught with approximations) of the total inorganic carbon in the world s mixed layer is 3.91 x 1016 kg. [Pg.235]

How come I got three layers Sometimes, when you pour fresh water or some other solvent into the funnel, you get a small amount hanging at the top, and it looks like there are three different layers. Yes, it looks as if there are three different layers, but there are not three different layers. Only two layers, where part of one has lost its way. Usually, this mysterious third layer looks just like its parent, and you might gently swirl the funnel and its contents to reunite the family. [Pg.115]

The CEC of clay minerals is partly the result of adsorption in the interlayer space between repeating layer units. This effect is greatest in the three-layer clays. In the case of montmorillonite, the interlayer space can expand to accommodate a variety of cations and water. This causes montmorillonite to have a very high CEC and to swell when wetted. This process is reversible the removal of the water molecules causes these clays to contract. In illite, some exchangeable potassium is present in the interlayer space. Because the interlayer potassium ions are rather tightly held, the CEC of this illite is similar to that of kaolinite, which has no interlayer space. Chlorite s CEC is similar to that of kaolinite and illite because the brucite layer restricts adsorption between the three-layer sandwiches. [Pg.358]

Clay minerals with their own surface properties affect the near surface water in different ways. The adsorbed water in the case of kaolinite consists only of water molecules ( pure water), whereas water adsorbed on a smectite-type mineral is an aqueous solution, due to the presence of exchangeable cations on the 2 1 layer sihcate. Sposito (1989) noted the generally accepted description that the spatial extent of adsorbed water on a phyUosilicate surface is about 1.0 nm (two to three layers of water molecules) from the basal plane of the clay mineral. [Pg.20]

Over 50 different pyridazin-3-ones were evaluated for biological activity in a wheat (Triticum aestivum L.) test system described previously (1). Briefly, seeds were germinated in 9-cm petri dishes on three layers of filter paper. Pyridazinones were dissolved in acetone and the filter papers were impregnated with 1 ml of acetone solution. After the soluent evaporated, 10 ml of distilled water were added to form an inhibitor concentration of 100 yM. Seeds were planted directly on the moist papers and germinated for 4 days in a controlled environment chamber on a 16-hr photoperiod with 27+lC day temperature and 21+lC night temperature. Light intensity from both fluorescent and incandescent bulbs was 28 klux at dish level. Lipids were extracted and recovered from 1 g of lyophilized shoot tissue, separated into membrane and non-membrane lipids, and analyzed by gas chromatography as described (1). [Pg.146]

Operating as described, cylindrical three-layer tablets were prepared, weighing about 900 mg and having two layers of active substance separated by a barrier layer of water swellable polymer mixture (granulate B). [Pg.82]


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Water layers

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