GLORIA

GEOMAR Library Ocean Research Information Access

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
Filter
  • spectroscopic  (3)
  • yttrium  (3)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of solution chemistry 11 (1982), S. 127-136 
    ISSN: 1572-8927
    Keywords: Lead ; lead bromide ; lead chloride ; mixed ligand ; complexation ; spectroscopic
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Experimentally and theoretically derived formation constants of mixed lead halide complexes are compared at 25.0°C and one molar ionic strength. The formation constant of PbBrCl, β11=79±10, is somewhat larger than the theoretical results, β11=55, predicted using the formation constants of PbBr2 and PbCl2. The molar absorptivity of PbBrCl was observed to be intermediate in character between the molar absorptivities of PbBr2 and PbCl2. Determinations of the formation constants of PbBr2Cl− and PbBrCl2 − are in reasonable agreement with the predictions based on the formation constants of PbBr3 − and PbCl3 −. Mixed ligand species dominated the complexation scheme of Pb(II) in our test media.
    Type of Medium: Electronic Resource
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Aquatic geochemistry 3 (1997), S. 99-115 
    ISSN: 1573-1421
    Keywords: rare earth elements ; copper ; complexation ; ionic strength effects ; nitrilotriacetic acid ; lanthanide ; yttrium
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract Observations of competitive complexation of NTA by Cu2+ and rare earth element (REE) ions are used to determine REE-NTA stability constants at ionic strengths between 0.1 and 5.0 molar. Although REE stability constants change markedly with ionic strength, differences in the ionic strength dependence of REE-NTA stability constants across the rare earth element series are small. The ionic strength dependence of logβ1 for Y and REEs with NTA at 25 °C can be described as: logβ1(M) = logβ1(M)0 - 9.198 I1/2/(1+B I1/2)+C I + D I3/2, where β1(M) = [MNTA°][M3+]-1[NTA3-]-1, I is ionic strength, B = 1.732, C = 0.1596, D = 0.0816, and logβ1(M)° is the metal-NTA stability constant at zero ionic strength.
    Type of Medium: Electronic Resource
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 3
    ISSN: 1572-8927
    Keywords: Coprecipitation ; rare earths ; lanthanides ; yttrium ; phosphate ; arsenate
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Coprecipitation of yttrium (Y) and rare earth elements (REEs) with phosphate and arsenate removes these elements from solution in variable proportions. During both phosphate and arsenate Coprecipitation, middle REEs (Sm and Eu) are progressively depleted in solution relative to heavier and lighter elements. Solution complexation by oxalate (Ox 2-) influences Y and REE removal patterns by strongly enhancing the retention of Y and the heaviest REEs in solution. The extent of this enhancement is well described by a quantitative account of the comparative solution complexation of Y and REEs as M(Ox)+ and M(Ox) $$_{\text{2}}^ - $$ . The comparative behavior of phosphate and arsenate coprecipitation exhibits both similarities and differences. During arsenate coprecipitation the light REEs are retained in solution, relative to the heavy REEs, to a greater extent than is the case for phosphate coprecipitation. Notable irregularities are observed in the comparative coprecipitation behavior of nearest-neighbor elements (e.g., Eu–Gd–Tb and Tm–Yb–Lu). Such irregularities are very similar for phosphate and arsenate coprecipitation in the absence and in the presence of solution complexation.
    Type of Medium: Electronic Resource
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Journal of solution chemistry 29 (2000), S. 1089-1099 
    ISSN: 1572-8927
    Keywords: Rare earth elements ; fluoride complexation ; stability constants ; sodium perchlorate ; ionic strength ; lanthanide ; yttrium
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Formation constants for the complexation of yttrium and rare earth elements(YREE) by fluoride ions have been measured at 25°C. The ionic strength (μ)dependence of YREE formation constants in perchlorate solution for ionicstrengths between 0 and 6 molar can be expressed aslogFβ1 (M, μ) =logFβ1 o (M) −3.066 μ0.5/(1 + 1.769 μ0.5)+ 0.1645 μwhere logFβ1 o(M) represents MF2+formation constants at zero ionic strength.The logFβ1 o(M) results obtained inthis work are: Y(4.46), La(3.62), Ce(3.86),Pr(3.84), Nd(3.82), Sm(4.15), Eu(4.27), Gd(4.24), Tb(4.37), Dy(4.39), Ho(4.28),Er(4.27), Tm(4.29), Yb(4.39), and Lu(4.25). The relative magnitudes of YREEformation constants are independent of ionic strength. The pattern oflogFβ1(M,μ),formation constants obtained in this work [relative magnitudes oflogFβ1 o (M)],exhibits a shallow minimum between Dy and Yb. In contrast to the smoothpattern of stability constants expected if fluoride were to interact with bare ions(with monotonically decreasing crystal radii between La and Lu), theinteractionof F− with YREEs, which have extensive hydration spheres[M(H2O)8–9 3+] resultsin a relatively complex pattern of lanthanide stability constants. The fluoridecomplexation behavior of yttrium differs distinctly from the behavior of any rareearth. Although the crystal radius of Y3;pl is approximately equalto that of Ho3+,differences in the covalence/ionicity of Y3+ relative to therare earths leads to aYF2+ stability constant that exceeds that of any rare earthelement (REE).
    Type of Medium: Electronic Resource
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Journal of solution chemistry 10 (1981), S. 243-251 
    ISSN: 1572-8927
    Keywords: Lead chloride ; molar absorptivity ; complexation ; medium dependence ; ultraviolet ; spectroscopic
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The molar absorptivities of Pb2+, PbCl+, PbCl2, and PbCl 3 − were obtained between 210 and 300 nm. Molar absorptivity data were used to determine lead speciation directly from Pb(II) absorbance characteristics in a variety of media including natural seawater. The absorbance characteristics of lead in a particular chloride medium reveal the lead chloride formation constants appropriate to that medium. Our analyses indicate that lead chloride formation constants are significantly smaller in MgCl2 media than in HCl at constant ionic strength.
    Type of Medium: Electronic Resource
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Journal of solution chemistry 7 (1978), S. 373-383 
    ISSN: 1572-8927
    Keywords: Ferric ; hydrolysis ; ionic strength ; temperature ; enthalpy ; ferric hydroxide ; ultraviolet ; spectroscopic
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Ultraviolet absorbance spectra of ferric ions in 0.68m NaClO4 were studied as a function of pH at 4.0, 14.9, and 25.0°C. The results provided an evaluation of the stability constant for the formation of FeOH2+ which is *β1=[FeOH +][H +]/[Fe 3+]. The enthalpy change for the reaction Fe3++H2O⇌ FeOH2++H+ was calculated as 10.0±0.3 kcal-mole−1. Increasing temperature was also found to promote the reaction Fe3++2H2O⇌ Fe(OH) 2 + +2H+. Our results were combined with the results of other to produce an expression describing the first hydrolysis equilibrium at ionic strengths between 0 and 3m and temperatures between 4.0 and 45.0°C at 1 atm total pressure. At 25°C and 0.68m the ionic strength *β1=1.90×10-3
    Type of Medium: Electronic Resource
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...