RUCL Institutional Repository

Solvent Extraction of Ti(IV) and V(IV) by Cyanex 301 and Cyanex 302 and Application of Yates Experimental Design

Show simple item record

dc.contributor.advisor Biswas, Ranjit Kumar
dc.contributor.author Karmaka, Aneek Krishna
dc.date.accessioned 2022-08-11T04:13:22Z
dc.date.available 2022-08-11T04:13:22Z
dc.date.issued 2012
dc.identifier.uri http://rulrepository.ru.ac.bd/handle/123456789/732
dc.description This thesis is Submitted to the Department of Applied Chemistry and Chemical Engineering, University of Rajshahi, Rajshahi, Bangladesh for The Degree of Doctor of Philosophy (PhD) en_US
dc.description.abstract The solvent extractions in (i) Ti(IV)-Cyanex 301 {HA), (ii) Ti{IY)-Cyanex 302 (H2A2), (iii) V(IV)-HA and (iv) V(IV) - H2A2 have been investigated from equilibrium and kinetic points of view. Yates Experimental Design has been made to the equilibrium and kinetic data for all systems. In system (i) and (ii), heptanol and hexanol (respectively) have been used as de-emulsifier. The equilibration times are 40, 30, 15 and 20 min, respectively. The extraction equilibria at 303 K can be expressed (respectively) as: Kcx = 101.1 17 = co (1+316.2 [Ti(IV)]) {I+ 0.794 [SO/] ([H+] + 229 [W]2) / [HA)to) K.x = 10°.339 = cD (I+ 141.3 [Ti(JV)]) (I+ 1.86 [SO/°]) ([H+)+58.88 [H+J2) I [H2A2Jtii1 K.x = 10·t.42 = cD [H+J2 / [HA)fo) (1+1.58 [SO/]) Kcx = cD [H+r (I +2.24 [SO/·]) / [H2 A2 lfo) [Kcx depends on 'x' and 'x' varies between 2 - OJ The processes are endothermic with 􀂨H values of -27, -50, -16 and -25 kJ/mol (at l.t.r and - 90 kJ/mol at h.t.r), respevtively. The loading capacities are 7.11, 5.08, 7.87 and 4.05 g/L respective metal ions/ 100 g respective extractant. Suitable diluents are chlorobenzene, n-heptane, kerosene and toluene (benzene) respectively, for systems (i), (ii), (iii) and (iv). The cited equilibrium expressions have been used to suggest equilibrium reactions. The extracted species are [TiOA2], [TiOA2.HA], [VOA2] and [VO(HA2)2] in respective systems; but the reacting metallic species depends on the aqueous pH and sulphate ion concentration ranges. The kinetics of forward extraction of the systems (i), (ii), (iii) and (iv) have been investigated by measuring initial flux of metal ion transfer in a Lewis cell operated at 3 Hz……………………………………… en_US
dc.language.iso en en_US
dc.publisher University of Rajshahi en_US
dc.relation.ispartofseries ;D3511
dc.subject Cyanex 301 en_US
dc.subject Cyanex 302 en_US
dc.subject Ti(IV), V(IV) Chemical Solvent en_US
dc.subject Yates en_US
dc.subject Applied Chemistry and Chemical Engineering en_US
dc.title Solvent Extraction of Ti(IV) and V(IV) by Cyanex 301 and Cyanex 302 and Application of Yates Experimental Design en_US
dc.type Thesis en_US


Files in this item

This item appears in the following Collection(s)

Show simple item record

Search DSpace


Browse

My Account