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Wyszukujesz frazę "Gotfryd, L." wg kryterium: Autor


Wyświetlanie 1-4 z 4
Tytuł:
Recovery of major components of spent zinc electrolyte with di(2-ethylhexyl)phosphoric acid (DEHPA) used as a zinc(II) extractant
Autorzy:
Gotfryd, L.
Pietek, G.
Szołomicki, Z.
Becker, K.
Powiązania:
https://bibliotekanauki.pl/articles/951834.pdf
Data publikacji:
2014
Wydawca:
Politechnika Wrocławska. Oficyna Wydawnicza Politechniki Wrocławskiej
Tematy:
zinc electrolyte
zinc solvent extraction
DEHPA
mineral fertilizer
Opis:
Industrial acidic zinc electrolyte has been treated with calcium compounds and/or concentrated ammonia solution and resulting crystalline phases as well as equilibrium mother liquors were analyzed in detail for dependence on preliminary dilution of electrolyte with water. Neutralized zinc electrolyte was an object of investigation in zinc(II) extraction with di(2-ethylhexyl)phosphoric acid (DEHPA) as an extractant. Dependencies of zinc(II) and contaminants extraction on equilibrium pH, isotherms of zinc(II) extraction and stripping have been studied. During simulated laboratory counter-current trial of zinc extraction a new zinc electrolyte (stripped solution) has been produced. Raffinates left after the process were purified and qualified as mineral magnesium-ammonium fertilizer solutions.
Źródło:
Physicochemical Problems of Mineral Processing; 2014, 50, 1; 311-325
1643-1049
2084-4735
Pojawia się w:
Physicochemical Problems of Mineral Processing
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Neodecanoic acid as extractant of selected non-ferrous metals
Autorzy:
Gotfryd, L.
Pietek, G.
Szołomicki, Z.
Becker, K.
Piwowońska, J.
Powiązania:
https://bibliotekanauki.pl/articles/109507.pdf
Data publikacji:
2015
Wydawca:
Politechnika Wrocławska. Oficyna Wydawnicza Politechniki Wrocławskiej
Tematy:
Versatic 10
neodecanoic acid
solvent extraction
non-ferrous metals
hydrometallurgy
Opis:
The paper presents results of studies on extracting properties of neodecanoic acid (Versatic 10) solutions. Neodecanoic acid was diluted in Exxsol D80 AZ to three concentrations: 7.5, 15, and 30 % (v/v). Tests were conducted using sulphate(VI) solutions of six ions: Zn(II), Ni(II), Cu(II), Co(II), Cd(II), Mn(II) and a nitrate(V) solution of Pb(II). All the aqueous solutions were prepared as 0.1 M concentration. For all combinations of the used solutions (organic and aqueous), direct methods of measuring and recording the pH of the biphasic mixture have been applied. The degrees of ions extraction, depending on equilibrium pH were also presented in the paper. Extraction and stripping isotherms of selected ions and organic phase were plotted for 7.5 and 30 % (v/v) of extractant solutions and Zn(II), Ni(II) and Cu(II) ions.
Źródło:
Physicochemical Problems of Mineral Processing; 2015, 51, 2; 435-445
1643-1049
2084-4735
Pojawia się w:
Physicochemical Problems of Mineral Processing
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Direct measurements of reaction time for extractive processes
Autorzy:
Gotfryd, L.
Becker, K.
Pietek, G.
Szołomicki, Z.
Piwowonska, J.
Powiązania:
https://bibliotekanauki.pl/articles/109772.pdf
Data publikacji:
2016
Wydawca:
Politechnika Wrocławska. Oficyna Wydawnicza Politechniki Wrocławskiej
Tematy:
reaction time
solvent extraction
viscosity
stripping rate
sulphuric acid
Opis:
Extraction times for selected metal cations (Mg2+, Al3+, Zn2+, Cd2+, Cu2+, Ni2+, Co2+, Mn2+, Fe2+ and Fe3+) have been measured using cation-exchanging extractants - Versatic 10 (neodecanoic acid), DEHPA (bis(2-ethylhexyl)phosphoric acid) and Cyanex 272 (bis(2,4,4-trimetylpentyl)phosphinic acid). Data was collected directly by measuring and recording pH of the two phase reaction mixture with maintaining continuity of the aqueous phase. Similarly, the stripping rate of selected cations (Mg2+, Al3+, Zn2+, Cu2+, Ni2+, Co2+) in a sulphuric acid solution was measured. Viscosities of organic phases, saturated with cations, were measured before their stripping. Additionally, the extraction dependence of Mg2+, Al3+, Fe2+ and Fe3+ on pH was measured using Versatic 10 at various concentrations (7.5, 15 and 30 %).
Źródło:
Physicochemical Problems of Mineral Processing; 2016, 52, 2; 909-919
1643-1049
2084-4735
Pojawia się w:
Physicochemical Problems of Mineral Processing
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Contaminants of post-leaching copper solutions and their behavior during extraction with industrial extractants
Autorzy:
Gotfryd, L.
Pietek, G.
Powiązania:
https://bibliotekanauki.pl/articles/109816.pdf
Data publikacji:
2013
Wydawca:
Politechnika Wrocławska. Oficyna Wydawnicza Politechniki Wrocławskiej
Tematy:
industrial copper extractants
copper contaminants
copper extraction isotherms
Opis:
Several copper extractants have been examined in laboratory glassware with a special attention paid to their behavior towards cations others than copper(II). In the studies 25 vol. percent of hydrocarbon (Exxsol D80 AZ) solutions of six industrial copper extractants have been used. They were mainly rea-gents of hydrooxime type (LIX 860N-IC, LIX 984, LIX 984N, LIX 84-I, Acorga M5640) and diketone type LIX 54-100. Individual isotherms of independent extraction of copper(II) and selected cations (Fe3+, Fe2+, Co2+, Ni2+, Zn2+, Mn2+, Cd2+, Mg2+) versus equilibrium pH have been compared. Investigations have been conducted with synthetic 0.1 mol/L solutions of their sulfates. The values of pH50% − parameter defined as an equilibrium pH at the moment of half-and-half extraction of the investigated cationic spe-cies have been presented. Also ΔpH50%, that is differences between values of pH50% for specific cation Me(II) and copper(II): ΔpH50% = pH50%(Me) − pH50%(Cu), have been given. In addition to that 25% LIX 984 has been used in counter-current pilot trials for copper(II) extraction from naturally contaminated solutions produced by bioleaching of industrial sulfide copper concentrate to observe behavior of investi-gated contaminants such as correlations between their real co-extraction with copper(II) and the position of their extraction on the pH scale. Copper electrolyte/strip solution, working alternately within close loop of coupled stripping - electrowinning system, has been analyzed during consecutive cycles to observe building up of the contaminants concentrations in the course of test.
Źródło:
Physicochemical Problems of Mineral Processing; 2013, 49, 1; 133-143
1643-1049
2084-4735
Pojawia się w:
Physicochemical Problems of Mineral Processing
Dostawca treści:
Biblioteka Nauki
Artykuł
    Wyświetlanie 1-4 z 4

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