Characterization of Sorption of Endosulfan Isomers and Chlorpyrifos on Container Walls Using Mixed Solvent Systems

2010 ◽  
Vol 58 (13) ◽  
pp. 7902-7907 ◽  
Author(s):  
J. Wasswa ◽  
P. Nkedi-Kizza ◽  
B. T. Kiremire
2014 ◽  
Vol 898 ◽  
pp. 322-325
Author(s):  
Xue Jun Wang ◽  
Tao Lou ◽  
Zhen Yang ◽  
Kun Peng He

Scaffold plays an important role in tissue engineering. In this study, porous PLGA scaffold was successfully prepared by mixed solvent systems using the thermally induced phase separation method. The PLGA scaffold shows fibrous matrix and interconnective pores, and the scaffold has high porosity and compressive modulus with dioxane/THF solvent system, which could be a very promising scaffold for tissue engineering.


RSC Advances ◽  
2014 ◽  
Vol 4 (79) ◽  
pp. 42029-42034 ◽  
Author(s):  
Mariano G. S. Vieira ◽  
Nilce V. Gramosa ◽  
Nágila M. P. S. Ricardo ◽  
Gareth A. Morris ◽  
Ralph W. Adams ◽  
...  

Brij surfactant micelles in mixed solvent systems aid resolution of natural product NMR signals in diffusion-ordered spectroscopy.


2020 ◽  
Vol 10 (3) ◽  
pp. 5355-5360

The study of ion- solvent interaction is of much importance to investigate the nature of different solutions. Measurement of electrical conductivity and evaluation of physico-chemical properties, such as molar conductance, limiting molar conductance, ion-pair association, Walden product etc. shade light on different intermolecular interactions present in electrolyte solutions. Solvation properties can be varied by mixing two or more solvents. An extensive literature survey on conductometric studies has been carried out on different electrolytes dissolved in a wide range of mixed solvent systems. The reported results show that strong solute-solute, solute-solvent and solvent-solvent interactions are responsible for the physico- chemical behavior of a solution in mixed solvents.


Author(s):  
Rashmi D ◽  
Sharmila T ◽  
Sushama Patil ◽  
Onkar Apine ◽  
Srinivas Sistla ◽  
...  

Syringolin A is a non-ribosomal virulence factor secreted by few Pseudomonas strains. Syringolin A is an well known irreversible proteasome inhibitor and antitumor compound. The present study is focused on the extraction of Syringolin A through a non-tedious and economical process. Syringolin A is extracted from culture supernatants by the immiscible organic layer by mixing of dichloromethane or chloroform (trichloromethane). Syringolin A was identified by the characteristic peak at 350 nm by UV spectra. The compound was further characterized by Thin Layer Chromatography (TLC) with the retention value, Rf was found to be in the range of 0.78-0.83 run using a combination of solvent systems water and methanol.  The molecular weight of the compound was found to be 492.2614 g mol-1 identified and analyzed by UHPLC–QTOF-MS analysis. Due to its significant pharmacological importance in proliferative diseases, further studies on production and optimization of these compounds are necessary.   


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