Improving Stability of Vitamin B5 Through Double Salt Formation

Author(s):  
Xuan Liang ◽  
Qi Zhang ◽  
Zaiyong Zhang ◽  
Qiaoce Ding ◽  
Xuefeng Mei
2020 ◽  
Vol 59 (17) ◽  
pp. 12200-12208
Author(s):  
Stipe Lukin ◽  
Tomislav Stolar ◽  
Ivor Lončarić ◽  
Igor Milanović ◽  
Nikola Biliškov ◽  
...  
Keyword(s):  

1979 ◽  
Vol 10 (10) ◽  
Author(s):  
H. MOEHRLE ◽  
C. KAMPER ◽  
J. HERBKE ◽  
H. J. NOWAK ◽  
D. WENDISCH ◽  
...  

2000 ◽  
Vol 131 (10) ◽  
pp. 1019-1023 ◽  
Author(s):  
Todora Ojkova ◽  
Donka Stoilova ◽  
Dimitar Barkov
Keyword(s):  

1995 ◽  
Vol 36 (34) ◽  
pp. 6083-6086 ◽  
Author(s):  
Yoshikatsu Ito ◽  
Bozena Borecka ◽  
James Trotter ◽  
John R Scheffer

1980 ◽  
Vol 58 (5) ◽  
pp. 539-545 ◽  
Author(s):  
Elinor M. Kartzmark

The double salt formation between indium chloride and the chlorides of Groups IIa and IIb has been investigated, and a comparison is made with the double salts of the Group I chlorides and indium trichloride. Three double salts of formula 2BeCl2•InCl3•(4–5)H2O, MgCl2•InCl3•(6–8)H2O, and CaCl2•InCl3•7H2O were found. The phase diagrams of the chlorides of Groups IIa and IIb with indium trichloride and water prove that the double salts MgCl2•2InCl3•10H2O, 2MgCl2•InCl3•12H2O, CaCl2•2InCl3•12H2O, 3CaCl2•4InCl3•30H2O, SrCl2•2InCl3•8H2O, SrCl2•InCl3•8H2O, ZnCl2•2InCl3•8H2O, and 2ZnCl2•InCl3•5H2O reported by Ensslin etal. (1) and recorded in Solubility of inorganic and metal organic compounds by Linke and Seidell (2) do not exist.


2013 ◽  
Vol 12 ◽  
pp. 351-358 ◽  
Author(s):  
Keling Zhang ◽  
Xiaohong S. Li ◽  
Yuhua Duan ◽  
David L. King ◽  
Prabhakar Singh ◽  
...  

1998 ◽  
Vol 63 (12) ◽  
pp. 2036-2043 ◽  
Author(s):  
Violeta Z. Vassileva

By solubility method in the Ca(HCOO)2-Cd(HCOO)2-H2O system at 25 and 50 °C, the formation of a double salt CaCd(HCOO)4 and mixed crystals Ca1-xCdx(HCOO)2 was established. The double salt formation is explained by the electronic configuration of the metal ions involved. Formation of the mixed crystals, possessing the α-Ca(HCOO)2 structure, is attributed to the ability of the Cd2+ ions to accept the coordination environment, characteristic of the Ca2+ ions in α-Ca(HCOO)2.


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