An investigation of the chemical changes taking place in the mixed lime sulphur-lead arsenate spray

1925 ◽  
Vol 15 (3) ◽  
pp. 307-326 ◽  
Author(s):  
WM. Goodwin ◽  
H. Martin
Keyword(s):  
Carbon Dioxide ◽  
Chemical Properties ◽  
Oxidation Products ◽  
Chemical Changes ◽  
Lead Arsenate ◽  
Lime Sulphur ◽  
Main Decomposition ◽  
Hydrolysis Of ◽  
Sulphuretted Hydrogen

1. The reaction between lime sulphur and acid lead arsenate is shown to be small and to have little effect on the chemical properties of either material as a spray.2. It is shown that the oxidation of lime sulphur proceeds according to the empirical formula:CaS.Sx + 30 = CaS2O3 + Sx-1and that the calcium sulphides are hydrolysed in aqueous solution.3. The addition of lead arsenate has no effect on the amount of sulphur precipitated from the lime sulphur by oxidation or by the action of carbondioxide.4. Lead arsenate is only slightly decomposed by lime sulphur or by the oxidation products of lime sulphur, the main decomposition being due to the action of sulphuretted hydrogen formed by the hydrolysis of the calcium sulphides. This decomposition becomes marked in the presence of carbon dioxide which reacts on the calcium sulphide to form sulphuretted hydrogen.5. The fungicidal value of the mixed spray—as judged by the mildew killing properties of the polysulphides—is not less than that of lime sulphur alone. Additional fungicidal properties may be expected from the presence in the spray of soluble arsenates and thioarsenates.6. Judging by the chemical changes which take place in the mixed spray the insecticidal value of the lead arsenate would not appear to be greatly affected by the addition of lime sulphur.7. There is an increased amount of soluble arsenic formed by the action of carbon dioxide on the mixed spray which may prove sufficient in amount to cause spray injury.8. The A.O.A.C. method for the determination of sulphate sulphur in lime sulphur solutions is shown to be inaccurate. A method yielding more concordant results is proposed.

scholarly journals III. On the atomic weight of manganese

1883 ◽  
Vol 35 (224-226) ◽  
pp. 44-48
Keyword(s):  
Carbon Dioxide ◽  
Silver Chloride ◽  
Atomic Weight ◽  
Special Method ◽  
Its Analysis ◽  
A Current ◽  
Sulphuretted Hydrogen

Our attention has been directed for some time to a new determination of the atomic weight of manganese. This communication gives a succinct account of the results of the preliminary stages of such an inquiry, and although the further progress of the investigation may reveal some errors, still we feel convinced the final numbers can in no way differ materially from the present values, and therefore further delay in publication is unnecessary. The atomic weight of manganese has been determined by many chemists, but the resulting values vary considerably according to the special method selected. The results of the different investigators may be divided into two classes—those giving approximately 55 as the number, and those making it about 54. To the former class belong Turner, Berzelius, and Dumas, all of whom use the same method, viz., the determination of the silver chloride yielded by a weighed amount of chloride of manganese. Turner also made determinations from the analysis of the carbonate, and from the conversion of the monoxide into sulphate. Von Hauer used the same method as that employed by him in the determination of the atomic weight of cadmium, viz., the reduction of manganous sulphate to sulphide by ignition in a current of sulphuretted hydrogen. It is probable that this method is not very trustworthy, as, according to Schneider, the sulphide may be contaminated by oxysulphide. Schneider and Rawack belong to the second class of observers, the former employing the oxalate, and from its analysis calculating the atomic weight by deducting the weight of water and carbon dioxide obtained. Rawack, whose experiments were conducted in Schneider’s laboratory, weighed the water obtained by reducing manganoso-manganic oxide to manganous oxide.

DETERMINATION OF MICRO-AMOUNTS OF 5β-PREGNAN-3α-OL-20-ONE IN URINE USING INFRARED-SPECTROMETRY

1962 ◽  
Vol 41 (2) ◽  
pp. 234-246 ◽  
Author(s):  
H. J. van der Molen
Keyword(s):  
Infrared Spectrum ◽  
Quantitative Determination ◽  
Acid Hydrolysis ◽  
Chromatographic Separation ◽  
Pure Form ◽  
Infrared Spectrometry ◽  
Hydrolysis Of

ABSTRACT A procedure for the quantitative determination of 5β-pregnan-3α-ol-20-one in urine is described. After acid hydrolysis of the pregnanolone-conjugates in urine, the free steroids are extracted with toluene. Pregnanolone is isolated in a pure form as its acetate; after chromatographic separation of the free steroids on alumina, the fraction containing pregnanolone is acetylated and rechromatographed on alumina. Quantitative determination of the isolated pregnanolone-acetate is carried out with the aid of the infrared spectrum recorded by a micro KBr-wafermethod. The reliability of the method under various conditions is discussed under the headings, specificity, accuracy, precision and sensitivity. It is possible to determine 30–40 μg pregnanolone in a 24-hours urine portion with a precision of 25%.

EINE CHEMISCHE METHODE ZUR BESTIMMUNG VON 16-EPI-ÖSTRIOL IM URIN DES MENSCHEN

1963 ◽  
Vol 44 (1) ◽  
pp. 47-66 ◽  
Author(s):  
W. Nocke ◽  
H. Breuer
Keyword(s):  
Melting Point ◽  
Phosphoric Acid ◽  
Aqueous Alkali ◽  
Percentage Error ◽  
Organic Layer ◽  
Maximum Percentage ◽  
Chemical Determination ◽  
Routine Assay ◽  
Hydrolysis Of

ABSTRACT A method for the chemical determination of 16-epi-oestriol in the urine of nonpregnant women with a qualitative sensitivity of less than 0.5 μg/24 h is described. The separation of 16-epi-oestriol and oestriol is accomplished by converting 16-epi-oestriol into its acetonide, a reaction which is stereoselective for cis-glycols and therefore not undergone by oestriol as a trans-glycol. Following partition between chloroform and aqueous alkali, the acetonide of 16-epi-oestriol is completely separated with the organic layer whereas oestriol as a strong phenol remains in the alkaline phase. 16-epi-oestriol is chromatographed on alumina as the acetonide and determined as a Kober chromogen. This procedure can easily be incorporated into the method of Brown et al. (1957 b) thus making possible the simultaneous routine assay of oestradiol-17β, oestrone, oestriol and 16-epi-oestriol from one sample of urine. The specificity of the method was established by separation of 16-epi-oestriol from nonpregnancy urine as the acetonide, hydrolysis of the acetonide by phosphoric acid, isolation of the free compound by microsublimation and identification by micro melting point, colour reactions and chromatography. The accuracy of the method is given by a mean recovery of 64% for pure crystalline 16-epi-oestriol when added to hydrolysed urine in 5–10 μg amounts. The precision is given by s = 0.24 μg/24 h. For the duplicate determination of 16-epi-oestriol the qualitative sensitivity is 0.44 μg/24 h, the maximum percentage error being ± 100% The quantitative sensitivity (±25% error) is 1.7 μg/24 h.

INDIREKTE PAPIERCHROMATOGRAPHISCHE METHODE ZUR BESTIMMUNG DER HARNOESTROGENE

1961 ◽  
Vol 38 (4) ◽  
pp. 545-562 ◽  
Author(s):  
L. Kecskés ◽  
F. Mutschler ◽  
I. Glós ◽  
E. Thán ◽  
I. Farkas ◽  
...  
Keyword(s):  
Pregnant Women ◽  
Granulosa Cell ◽  
Iron Content ◽  
List Type ◽  
Granulosa Cell Tumour ◽  
Hydrolysis Of ◽  
Phenol Fraction ◽  
Qualitative Determination

ABSTRACT 1. An indirect paperchromatographic method is described for separating urinary oestrogens; this consists of the following steps: acidic hydrolysis, extraction with ether, dissociation of phenol-fractions with partition between the solvents. Previous purification of phenol fraction with the aid of paperchromatography. The elution of oestrogen containing fractions is followed by acetylation. Oestrogen acetate is isolated by re-chromatography. The chromatogram was developed after hydrolysis of the oestrogens 'in situ' on the paper. The quantity of oestrogens was determined indirectly, by means of an iron-reaction, after the elution of the iron content of the oestrogen spot, which was developed by the Jellinek-reaction. 2. The method described above is satisfactory for determining urinary oestrogen, 17β-oestradiol and oestriol, but could include 16-epioestriol and other oestrogenic metabolites. 3. The sensitivity of the method is 1.3–1.6 μg/24 hours. 4. The quantitative and qualitative determination of urinary oestrogens with the above mentioned method was performed in 50 pregnant and 9 non pregnant women, and also in 2 patients with granulosa cell tumour.

THE IMPORTANCE OF THE RED BOOK OF SOILS FOR MONITORING AND JUSTIFICATION OF CONSERVATION MEASURES

2020 ◽  
Author(s):  
O.S. Bezuglova ◽  
Keyword(s):  
Chemical Properties ◽  
Natural State ◽  
Soil Maps ◽  
Rostov Region ◽  
Conservation Measures ◽  
Background Data ◽  
The Russian Federation ◽  
Physical And Chemical ◽  
And Chemical Properties

Rostov Region belongs to the highly protected natural territories characterized by the continuous plowing. There territories are the only reserves with the soils preserved in their natural state. However, these areas often lack detailed information about the soils quality and composition. Surveying soils on these territories is crucial for determination of their basic physical and chemical properties. The resulted compilation of soil maps could lay a foundation for creating the Red Book of Soils and the formation of a section in the soil-geographical database of the Russian Federation. Subsequently, such information can be used as a background data for the main types of soils in the region. It will be also valuable during monitoring and justification of conservation measures.

Determination of δ-hexadecansultone in sodium α-olefinesulphonates and liquid detergents using gas chromatography-mass spectrometry (GC/MS)

2019 ◽  
Vol 85 (7) ◽  
pp. 16-21
Author(s):  
Liliya R. Mubarakova ◽  
German K. Budnikov
Keyword(s):  
Multicomponent Mixture ◽  
Operating Mode ◽  
Complete Separation ◽  
Gas Chromatography Mass Spectrometry ◽  
Liquid Detergent ◽  
Cyclic Esters ◽  
Alcohol Water ◽  
Household Chemicals ◽  
Hydrolysis Of

Sultones are cyclic esters of hydroxysulfonic acids, which are formed in the process of sulfonation of α-olefins with sulfur trioxide gas. More stable sultones may be present in the final product — an anionic surfactant — sodium α-olefin sulfonate (AOC-Na). AOC-Na is widely used in the production of household chemicals and cosmetic products, including liquid dishwashing detergents. Sultones are strong skin sensitizers, their level in AOC-Na should be strictly controlled and not exceed 5 ppm. Operational and strict control of the sultone content upon AOC-Na production allows timely adjustment at the stage of hydrolysis, which leads to a more complete disclosure of the sultone cycle with the formation of the corresponding olefin sulfonates and hydroxyalkanesulfonates. We propose a method for determining δ-hexadecansultone in liquid dishwashing detergents and sodium α-olefinsulfonates obtained on the basis of α-olefins of C14 – C16 fractions using GC/MS, which provides shortening of sample preparation and keeps the sensitivity with a detection limit of 0.02 mg/kg. The effect of various weakly polar and non-polar organic solvents used for Sultone extraction from AOC-Na and liquid detergent on liquid extraction based on the dispersion of the extractant in an alcohol/water phase is studied. When selecting the solvent we have shown that the use of diethyl ether provided the best extraction of the analyte. Determination of the analyte extraction recovery was performed using the reaction of hydrolysis of the extracted mixture. We specified the operating mode of the device which provided complete separation of the components of the analyzed compounds including the samples of liquid detergent for dishes being a multicomponent mixture of complex composition.

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