Extraction and Characterization of Niobium(V) Thiocyanate Complexes

Extraction of niobium(V) from sulphuric and hydrochloric acid Solutions containing an excess of thiocyanate ions with tetraphenylphosphonium (TPP) and tetraphenylarsonium (TPA) chloride into chloroform was investigated. The maximum extraction of niobium from sulphuric acid Solutions was about 91% and from hydrochloric acid Solutions about 94%. Chloride ions produced a moderate synergistic effect. Niobium(V) was quantitatively extracted (over 99%) from sulphuric and hydrochloric solutions only if chloride ions were also in excess and a lower excess of thiocyanate and extractant was required than in extraction without addition of chloride. The optimal conditions for the quantitative extraction of niobium were 0.2-0.5 M H2SO4 or 0.2-4 M HCl, 0.2-0.7 M thiocyanate and more than 4 M chloride in the aqueous phase, and TPP (TPA) concentration in the organic phase higher than 3 x 10-3 M. The extracted complexes in chloroform had an absorption maximum at 390 nm or at 390 and 320 nm, depending on the composition of the aqueous phase. Absorption spectra were studied as a function of H2SO4, HCl, thiocyanate and chloride concentrations in the aqueous phase. The optimal conditions for the spectrophotometric determination of niobium by measuring the absorbances of the organic phase at 390 nm were 1-2 M HCl, 0.1-0.5 M thiocyanate and TPP (TPA) chloride in chloroform of at least 5 x 10-3 M. A total chloride concentration lower than 2.2 M had no effect on absorbance. The mechanism of extraction based on the formation of ion-associated compounds between the onium cation and the thiocyanatoniobate(V) or mixed ligand chlorothiocyanatoniobate(V) anion is discussed

Scope and limitations of sodium and potassium trimethylsilanolate as reagents for conversion of esters to carboxylic acids

Sodium or potassium trimethylsilanolate act as versatile and very powerful reagents for conversion of a wide variety of esters to carboxylic acids. The reactions were performed in tetrahydrofuran under mild reaction conditions with high to quantitative yields

Potassium Phosphate/Benzyltriethylammonium Chloride as Efficient Catalytic System for Transesterification

Potassium phosphate (K(3)PO(4)) in the presence of benzyltriethylammonium chloride have been found to catalyses the transesterifications of a wide variety of aliphatic and aromatic esters with primary and secondary alcohols affording the corresponding esters in good-to-excel lent yields

Scope and Limitations of Sodium and Potassium Trimethylsilanolate as Reagents for Conversion of Esters to Carboxylic Acids

Sodium or potassium trimethylsilanolate act as versatile and very powerful reagents for conversion of a wide variety of esters to carboxylic acids. The reactions were performed in tetrahydrofuran under mild reaction conditions with high to quantitative yields

Kemijski profil sedimenata Plominskog zaljeva

Granulometric, chemical, and leaching properties of sediments dredged in the Plomin Bay (Northern Adriatic Sea, Croatia) were investigated in order to asses the risk of remobilisation of heavy metals into the water column. In total 65 samples from 65 sampling sites were taken from different sediment depths within the bay. Analysis of variance confirmed the homogeneity of granulometric and elemental composition of the investigated sediment throughout its volume. Granulometric analysis showed that all samples corresponded to a pelitic fraction (<0.063 mm). Bulk elemental mass fractions in the sediments were similar to literature data on relatively unpolluted areas of the Adriatic Sea. High sedimentation rate caused by constant infl ow of material from the Boljunčica River drainage may be responsible for low levels of heavy metals and negligible infl uence of fl y and bottom ash from a nearby disposal site on the chemical composition of the sediments. In contact with sea water only 0.29 mg kg-1 of V, 0.04 mg kg-1 of Cr, 0.07 mg kg-1 of Ni, 0.33 mg kg-1 of Cu, 0.67 mg kg-1 of Zn and 0.06 mg kg-1 of Pb could be remobilised from sediment material into the water column. However, these values increased three to ten times in case of leaching with organic acids.Granulometrijska i kemijska svojstva te mogućnost otpuštanja teških metala ispitivani su u sedimentima Plominskog zaljeva (Sjeverni Jadran, Hrvatska) u svrhu utvrđivanja rizika od remobilizacije teških metala iz sedimenta u stupac vode. Uzeto je 65 uzoraka s različitih točaka i dubina unutar zaljeva. Analizom varijance potvrđena je granulometrijska i kemijska homogenost cijelog volumena sedimenta, što upućuje na jedan prevladavajući izvor tijekom cijeloga sedimentacijskog razdoblja. Granulometrijskom analizom je utvrđeno da u svim uzorcima prevladava sitnozrnata frakcija (<0,063 mm). Koncentracije elemenata u ukupnim uzorcima sedimenata slične su literaturnim vrijednostima objavljenim za relativno onečišćena područja Jadranskog mora. Velika brzina sedimentacije uzrokovana konstantnim donosom materijala iz slijevnog područja Boljunčice vjerojatan je uzrok niskih koncentracija teških metala i slabo vidljivog utjecaja odlagališta šljake i pepela na sastav sedimenata. U kontaktu s morskom vodom moguća je remobilizacija samo 0,29 mg kg-1 V, 0,04 mg kg-1 Cr, 0,07 mg kg-1 Ni, 0,33 mg kg-1 Cu, 0,67 mg kg-1 Zn i 0,06 mg kg-1 Pb iz sedimenta u stupac morske vode. Ipak ove vrijednosti su tri do deset puta povećane u slučaju izluživanja s pomoću organskih kiselina