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Titration Toluene

The procedure is to pass purified hydrogen through a hot solution of the pure acid chloride in toluene or xylene in the presence of the catalyst the exit gases are bubbled through water to absorb the hydrogen chloride, and the solution is titrated with standard alkali from time to time so that the reduction may be stopped when the theoretical quantity of hydrogen chloride has been evolved. Further reduction would lead to the corresponding alcohol and hydrocarbon ... [Pg.691]

Trialkylammonium salts, such as lidocaine hydrochloride, are titrated in an aqueous solution containing a surfactant. The presence of the surfactant increases the trialkylammonium salt s K , giving a titration curve with a more pronounced break. The effect of adding an immiscible organic solvent, such as methylene chloride or toluene, also is demonstrated. [Pg.359]

Thiosulfate titration of iodine is limited to an iodine concentration of 7.5 fig/mL (69). The use of organic solvents such as benzene, toluene, chloroform, and carbon tetrachloride as indicators in the titration of iodine have been proposed (70—72). These procedures increase the sensitivity of the titration so that 6.0 fig/mL of iodine can be detected, although a sensitivity of 2 fig/mL has been claimed (73). [Pg.364]

To approximately 20 ml of a 1 1 mixture of toluene (xylene) isopropyl alcohol, add 1 ml of oil-base mud and 75 to 100 ml of distilled water. Add 8 to 10 drops of phenolphthalein indicator solution and stir vigorously with a stirring rod (the use of a Hamilton Beach mixer is suggested). Titrate slowly with H SO, (N/10) until red (or pink) color disappears permanently from the mixture. Report the alkalinity as the number of ml of H SO (N/10) per ml of mud. Lime content may be calculated as... [Pg.662]

Calcium Chloride [25]. Calcium chloride estimation is based on calcium titration. To 20 ml of 1 1 mixture of toluene (xylene) isopropyl alcohol, add a 1-ml (or 0.1-ml, if calcium is high) sample of oil-base mud, while stirring. Dilute the mixture with 75 to 100 ml of distilled water. Add 2 ml of hardness buffer solution and 10 to 15 drops of hardness indicator solution. Titrate mixture with standard versenate solution until the color changes from wine-red to blue. If common standard versenate solution (1 ml = 20 g calcium ions) is used, then... [Pg.662]

Titration A process in which one reagent is added to another with which it reacts an indicator is used to determine the point at which equivalent quantities of the two reagents have been added, 84-85,92 Toluene, 589... [Pg.698]

Determination of carboxy groups. Esterification or polyesterification kinetics is usually followed by this titration which is both easy and accurate. Each sample is dissolved in a solvent or a mixture of solvents (CHCI3, QH /EtOH or MeOH, toluene/EtOH or MeOH...) and then titrated with alcoholic KOH. The end point is determined either with an indicator (in most cases phenolphthalein) or with a pH-meter. An accuracy of about 0.1-1% can generally be achieved. [Pg.56]

A sample of polyester (ca. 1 g, exactly weighed) is dissolved in 20 mL toluene-ethanol mixture (1/1 vol.) and titrated by a solution of KOH in ethanol (0.05 mol/L) using a potentiometric titrator. A blank titration must be performed under the same conditions. Hardly soluble polyesters (e.g., PET) must be dissolved in an o-cresol-chloroform mixture or in hot benzyl alcohol.417 The result (acid content) is normally expressed in mmol COOH/g polyester but may also be given as the acid number, defined as the number of milligrams of KOH required to neutralize 1 g of polyester. [Acid number = (number of mmol COOH/g polyester) x 56.106.]... [Pg.94]

Toluene and THF were purchased from Fisher Scientific and dried over 4A molecular sieves overnight prior to use. The water content of the solvents was <50 pg/mL by Karl Fischer titration. [Pg.46]

The checkers purchased [(COD)RuCl2]n from Fluka (purum quality), BINAP from Aldrich (97 %), and toluene (HPLC grade) and triethylamine (reagent grade) from Fisher Scientific the latter was distilled from CaH2 under Ar prior to use. The submitters dried toluene and triethylamine over 4 A molecular sieves. Karl-Fischer titration indicated <200 pg/mL water. [Pg.94]

Griffin and Albaugh [102] describe a procedure whereby the neutral AOS product is converted to the parent acids by cation exchange and then titrated potentiometrically. A dilute aqueous solution of AOS is passed through cationic ion exchange resin in acid form. The acids are eluted with small portions of water and titrated potentiometrically using tetrabutylammonium hydroxide solution in a solvent mixture of 70 30 benzene/methanol. It is probable that the benzene can be replaced with toluene for safety reasons or that ASTM titration solvent (ASTM D664 toluene/propan-2-ol/water) can be used. [Pg.433]

Procedure. Concentration of n-BuLi in the feed was measured by titration (15). The reactor was filled completely with styrene monomer solution in toluene initially. Time was measured from the moment initiator and monomer feed was initiated. The reaction was... [Pg.381]

C, which leads to a break in the pressure-composition curve at BF3 Ir = 2 1. The formation of the 1 1 complex in solution is indicated by titrations. Insertion of InCl into the Fe—Fe bond in boiling dioxane yields [T7 -C CO)2Fe]2lnCl in 55% yield. The only group-VIIA compound that forms an addition compound with a group-lIIB halide, namely with BF3, is [(i7 -Cp)2ReH]The formation of (t -Cp),ReH BF3 is established when (T7 -Cp),ReH is titrated tensimetrically in toluene with BF3 at 0°C. [Pg.56]

Examples of BXg-group-VIA element adducts include (i7 -Cp)2MoH2, which adds BF3, and (Tj -Cp)2WH2, which adds BF3 as well as BClj. A tensimetric titration of BF3 with (tj -Cp)2MoH2 in toluene indicates a 1 1 adduct, and (17 -Cp)2WH2 reacts with BF3 gas both in the solid state (33.6°C, 3 d) and in toluene solution, whereby (tj -Cp)2WH2 BF3 precipitates immediately. Similarly, if a (tj -... [Pg.56]

An analytical solution for molecules with alkaline functionality is acid/base titration. In this technique, the polymer is dissolved, but not precipitated prior to analysis. In this way, the additive, even if polymer-bound, is still in solution and titratable. This principle has also been applied for the determination of 0.01 % stearic acid and sodium stearate in SBR solutions. The polymer was diluted with toluene/absolute ethanol mixed solvent and stearic acid was determined by titration with 0.1 M ethanolic NaOH solution to the m-cresol purple endpoint similarly, sodium stearate was titrated with 0.05 M ethanolic HC1 solution [83]. Also long-chain acid lubricants (e.g. stearic acid) in acrylic polyesters were quantitatively determined by titration of the extract. [Pg.155]

CHARACTERIZATION. The intrinsic viscosity of the soluble fractions was determined in toluene at 30 C. The MAH content of the soluble fractions was determined by heating a 0.5-1.0g portion in refluxing water-saturated xylene for 1 hr and titrating the hot solution with 0.05N ethanolic KOH using 1% thymol blue in DMF as indicator. [Pg.439]

Other methods have involved compleximetric titration, nephelom-etry, potentiometric titration, and gravimetric methods. In 1981, a paper by Mayanna and Jayaram11 outlined the determination of caffeine in a wide variety of products including pharmaceuticals and food products using sodium N-chloro-p-toluene-sulphonamide (chloramine-T) in a titri-metric procedure. [Pg.28]

Optimal Salinities Phase inversions at optimal salinity were assessed routinely by salt titrations into systems maintained at constant temperature. For the Leonox IOS surfactant system, increasing levels of salinity were necessary to cause the emulsion state to phase invert as the alkane molecular weight increased (Figure 11). Ihe initial conductivity value at the condition where zero salt had been added may in part reflect the salt contamination naturally present within the supplied formulation. Ihe internal olefin sulphonate species again revealed a linear relationship between EACN and optimal salinity as did all ionic formulations under test (see Figures 12 and 13, plus Table III). Ihe estimation of EACN values for both toluene... [Pg.315]

Procedure The apparatus shown in Figure 5.1, is employed for the standardization of 0.1 N methoxide solution. Transfer 10 ml of DMF in a conical flask and add to it 3 to 4 drops of thymol blue and first neutralize the acidic impurities present in DMF by titrating with 0.1 N lithium methoxide in toluene-methanol. Quickly introduce 0.06 g of benzoic acid and titrate immediately with methoxide in toluene-methanol. [Pg.117]

Thioetherification of PECH is feasibly performed in DA-solvents as already described in the patent (20J. For example, the highest substitution was obtained by the reaction of P(ECH-EO)(1 1 copolymer of epichloro-hydrin and ethylene oxide) and equimolar thiophenoxide in HMPA at 100°C for 10 h as DS 83% for sodium and 93% for potassium salts. The DS in our nucleophilic substitution was estimated by the elemental analysis as well as the titration of liberated chloride ion with mercuric nitrate (21). In the latter method, reacted medium was pretreated with hydrogen peroxide when the reductive nucleophiles which can react with mercuric ion were used. As described before for PVC, thiolation was also achieved conveniently with iso-thiuronium salt followed by alkaline hydrolysis without the direct use of ill-smelling thiolate. The thiolated PECH obtained are rubbery solids, soluble in toluene, methylene chloride, ethyl methyl ketone and DMF and insoluble in water, acetone, dioxane and methanol. [Pg.52]

The submitters used butyllithium in hexane available from Janssen Chimica and standardized before use by titration against a solution of benzylic alcohol in toluene and cuproine (2,2 -biquinoline). The checkers used butyllithium (1.6 M in hexane) available from Aldrich Chemical Company, Inc., which was standardized before use by titration with diphenylacetic acid in THF. [Pg.122]


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