Single-point determination of limiting viscosity numbers of polyacrylamides in water and 1 M sodium chloride solution

Polymer ◽  
1987 ◽  
Vol 28 (13) ◽  
pp. 2244-2247 ◽  
Author(s):  
M.H.Rafi'ee Fanood ◽  
Maurice H. George
1960 ◽  
Vol 38 (9) ◽  
pp. 1488-1494 ◽  
Author(s):  
E. J. Bounsall ◽  
W. A. E. McBryde

An analytical method is described for the determination of microgram amounts of silver in galena ores, based on the "reversion" of silver dithizonate. Silver is separated from relatively large amounts of lead by extraction as dithizonate into chloroform from an aqueous 1:99 nitric acid solution. Separation from mercury, which is also extracted under these conditions and would, if present, interfere in the analysis, is achieved by reverting the dithizonate solution with a 5% aqueous sodium chloride solution which is also 0.015 molar in hydrochloric acid. Following dilution of this aqueous solution and adjustment of pH, silver is again extracted into chloroform as the dithizonate, and determined absorptiometrically. Analyses of a number of galena ore samples showed a precision of within 3% for a silver content ranging from 0.03 to 0.4%.Some other methods for isolating silver from these samples, which were tried but found unsatisfactory, are discussed.


1920 ◽  
Vol 10 (1) ◽  
pp. 72-85 ◽  
Author(s):  
Donald J. Matthews

Ammonia can be recovered from soil with an efficiency of 98·5 to 99·5 per cent, in six hours in the apparatus described.For most purposes it is sufficient to aerate the soil for three hours.Highly dunged glasshouse soils undergo partial decomposition in the cold with magnesia. In such cases the soil should be aerated with magnesia and strong sodium chloride solution for a definite time, say three hours.The complete recovery of added ammonia from a calcareous soil is difficult unless the soil is finely ground.


1993 ◽  
Vol 76 (5) ◽  
pp. 1127-1132 ◽  
Author(s):  
Robert P Snell

Abstract A capillary gas chromatographic procedure is described for the determination of cyclohexanone leached from hemodialysis tubing by water. Recoveries were 100% at 2.0 mg/100 mL (20 ppm), 99.0% at 500 μg/100 mL (5 ppm), and 106% at 1.0 μg/100 mL (10 ppb). Reproducibility of the system was 0.152% for 3.0 μL injections of a solution containing cyclohexanone at 5.58 μg/mL. Correlation coefficients were 0.9983 for 0.3672-3.672 ng and 1.0000 for 3.672-367.2 ng. Twenty hemodialysis tubing sets from 4 manufacturers were examined. The leachable cyclohexanone ranged from 1.02 to 43.7 ppm per set. Rinsing the tubing with 1 L 0.9% sodium chloride solution did not remove significant amounts (P = 0.05) of leachable cyclohexanone.


1985 ◽  
Vol 68 (4) ◽  
pp. 750-753
Author(s):  
Promode C Bardalaye ◽  
Willis B Wheeler

Abstract Residue analysis of the herbicide prometryn (2,4-bis(isopropylamino)- 6-methylthio-l,3,5-triazine) is widely known, but an analytical method for determining its metabolities or degradation products in addition to the parent chemical has not yet been reported in the literature. The procedure reported here is for the extraction and determination of prometryn and 2 metabolites, 2-amino-4-isopropylamino-6-methylthio- l,3,5-triazine and 2,4-diamino-6-methylthio-l,3,5-triazine, in parsley. Crops were extracted with 2-propanol followed by concentration of the extract and partitioning with a minimum amount of hexane in the presence of a large excess of water to remove most of the green pigment. The aqueous phase was divided into 2 equal halves: (A) Onehalf portion was partitioned with dichloromethane in the presence of saturated sodium chloride solution, the dichloromethane phase was separated, and the aqueous phase was discarded. The organic solvent was evaporated, and the contents were reconstituted in petroleum ether before prometryn analysis. (B) The other half was made slightly alkaline with ammonium hydroxide solution and was partitioned with ethyl acetate in the presence of saturated sodium chloride solution. The ethyl acetate phase was concentrated, centrifuged to remove any turbidity, and analyzed for the 2 metabolities above. Fused silica capillary gas chromatography (GC) with nitrogen-phosphorus (N-P) detection was used for quantitation. The limit of detection was 0.05 mg/kg for all the compounds examined. Recoveries from fortified parsley samples ranged from 59 to 73% at fortification levels of 0.05 to 1.0 mg/kg.


2021 ◽  
Vol 1 (11) ◽  
pp. 47-52
Author(s):  
Andrey K. Martusevich ◽  
◽  
Ivan V. Bocharin ◽  
Marina N. Ivashchenko ◽  
◽  
...  

The aim of the work was to clarify the crystallogenic properties of pseudomonads under the action of an antiseptic. The material for the study was 8 strains of Ps. aeruginosa. In accordance with the purpose and objectives of the study, the work was carried out in 3 stages: assessment of the biological properties of the isolated pseudomonas strains; determination of sensitivity to disinfectants by the squares method; assessment of the crystallogenic (initiating) the activity of pseudomonads in an individual and joint form with a disinfectant. The tested antiseptic was "Desam" in the form of a standard 1% solution. Most of the analyzed strains turned out to be sensitive to the applied working concentration of the tested disinfectant and are active initiators of the crystallogenesis of sodium chloride solution. The revealed significant differences in the tesigraphic test conducted with pseudomonas strains sensitive and resistant to the studied disinfectant create prerequisites for the development of a new express method for determining the sensitivity of microorganisms to disinfectants.


2019 ◽  
Vol 8 (2) ◽  
pp. 109-116
Author(s):  
Maskur Maskur ◽  
◽  
Enny Lestari ◽  
Amal Rezka Putra ◽  
Dede Kurniasih ◽  
...  

The more efficient and effective quality control techniques for 99mTc-DTPA are needed because 99mTc has a short half-life of around 6.0 hours. We have succeeded in developing a one-system of Thin Layer Chromatography (TLC) for radiochemical purity testing system that is faster and more practical. Two-system method of TLC for radiochemical purity testing uses mobile phase of methyl ethyl ketone indicated as system A and 0.9% sodium chloride solution indicated as system B. One-system method uses the mobile phase of a mixture solution of acetone and 0.9% sodium chloride. In this study, the determination of radiochemical purity of the one-system of TLC has been successfully developed using the Whatman-1 paper stationary phase and the mixture of mobile phase between acetone and 0.9% sodium chloride solution. The mobile phase of acetone: 0.9% sodium chloride with a ratio of 9:1 shows the most optimum results. This phase can separate 99mTc-DTPA (Rf = 0.4-0.6) from 99mTcO4- (Rf = 0.9-1.0) and 99mTcO2 (Rf = 0.0-0.1) as radiochemical impurities. This result shows that the one-system of TLC method can be used for radiochemical purity testing of 99mTc-DTPA radiopharmaceutical kits. This method can completely separate the product compound (99mTc-DTPA) from its impurities (99mTcO2 and 99mTcO4-).


The Analyst ◽  
2012 ◽  
Vol 137 (2) ◽  
pp. 481-484 ◽  
Author(s):  
Bao D. Q. Nguyen ◽  
Margarita S. Chernov'yants ◽  
Igor V. Burykin

1986 ◽  
Vol 64 (3) ◽  
pp. 484-487 ◽  
Author(s):  
P. V. R. Rao ◽  
S. K. Gupta ◽  
T. S. B. Narasaraju

The solubility products of phosphate and vanadate apatites of lead and seven of their solid solutions, spread over the entire compositional range, were determined in 0.165 M sodium chloride solution at 37 °C. These solubility products decreased with an increase in vanadium content. A theoretical interpretation was advanced based on changes in lattice and hydration energies resulting from isomorphous ionic substitutions. The aim of the studies was the understanding of the toxic effects of lead and vanadium on the human skeletal system.


Sign in / Sign up

Export Citation Format

Share Document