Determination of corrosion rate of molybdenum, rhenium and their alloys in sodium chloride solution by the method of Tafel extrapolation

2014 ◽  
Vol 50 (10) ◽  
pp. 994-998 ◽  
Author(s):  
V. S. Shaldaev ◽  
A. N. Malofeeva ◽  
A. D. Davydov
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.


1998 ◽  
Vol 47 (4) ◽  
pp. 254-259 ◽  
Author(s):  
Yasuyuki Takatani ◽  
Tsuyoshi Masugata ◽  
Kazuo Fujiwara ◽  
Koichi Shinkai ◽  
Koichi Hayashi

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.


2014 ◽  
Vol 893 ◽  
pp. 440-443
Author(s):  
Li Na Zhang ◽  
Jerzy A. Szpunar ◽  
Jian Xin Dong ◽  
Mai Cang Zhang

The influence of ions chloride concentration and pH value on the corrosion resistance of high-alloyed material UNS N08028 in the sodium chloride solution is investigated. Results show that the corrosion potential is active cathodically with the increase of chloride concentration. The current density and corrosion rate both increase with increasing chloride concentration and decreasing pH value.


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.


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