The Role of the Specific Surface Area of an Adsorbent in the Optimization of Mixture Separation Conditions in Thin-Layer Chromatography

1983 ◽  
Vol 6 (14) ◽  
pp. 2665-2677 ◽  
Author(s):  
Jan K. Rozyło ◽  
Irena Malinowska ◽  
Małgorzata Poniewaz
Author(s):  
Changjian Xie ◽  
Yuhui Ma ◽  
Peng Zhang ◽  
Junzhe Zhang ◽  
Xiaowei Li ◽  
...  

With the increasing environmental application and discharge of nano cerium dioxide (nano-CeO2), it is urgent to fully understand its ecotoxicological effects on the aquatic environment. This study for the first...


2019 ◽  
Vol 43 (33) ◽  
pp. 13217-13224 ◽  
Author(s):  
Xieyi Huang ◽  
Peng Wang ◽  
Zhichao Zhang ◽  
Shaoning Zhang ◽  
Xianlong Du ◽  
...  

Thin-layer SiOx matrix anchored nickel catalysts with high specific surface area and a unique electronic/geometric structure were fabricated for efficient CO2 methanation.


Author(s):  
Mouhammad Abu Rasheed ◽  
Ahmad Alshaghel ◽  
Amir Alhaj Sakur

Metal organic frameworks (MOFs) are a variety of micro-porous materials which have high surface area, and permanent porosity making them possible options as chromatographic stationary phases. Herein we reported the synthesis and characterization of a new MOF structure and its utilization as a stationary phase for thin layer chromatography (TLC). [Zn(BMAB).DMF]n is a zinc-based MOF with an organic linker consists of chemically distinct binding groups which is 4-{[(1h-1,2,3-benzotriazol-1-yl)methyl]amino}benzoic acid (BMAB). This MOF was synthesized using ultra sound assisted reaction process, then activated via solvent exchange protocol to preserve its porous structure. FT-IR, UV-diffuse reflection spectroscopy (UV-DRS) and differential scanning calorimetry (DSC) were performed to characterize the synthesized MOF. Integrated data from "loss on desolvation" and atomic absorption spectrophotometry (AAS) measurements were used to define the chemical composition of the synthesized material. A specific surface area of 122.9 m2/g was determined for the activated MOF using methylene blue langmuir isotherm method. TLC plates were prepared from the activated form of the structure to investigate its chromatographic characteristics by utilizing it to separate a model mixture of benzidine and o-tolidine using n-propanol: Chloroform: Acetonitrile (50:30:20, v/v/v) as a mobile phase. The retardation factors (Rf), separation factor, and resolution (Rs) were determined via densitometric method at 310 nm to be 0.45 and 0.63 (α=2.08, Rs=1.61) for o-tolidine and benzidine; respectively. The plate was then visualized using iodine chamber method to confirm a successful separation.


1984 ◽  
Vol 18 (1) ◽  
pp. 37-40 ◽  
Author(s):  
S. M. Petrović ◽  
L. A. Kolarov ◽  
Julijana A. Petrović

Author(s):  
Olga Voronina ◽  
Maria Malysheva ◽  
Liudmyla Nosach ◽  
Eugeny Voronin ◽  
Vladimir Gun’ko ◽  
...  

In this work, a role of the number of free silanol groups at a nanosilica surface (specific surface area S<sub>BET</sub> = 250 m<sup>2</sup>/g, initial amount of silanols α<sub>ОН</sub> = 0.60-0.62 mmol/g) was analyzed in interaction with poly(vinyl pyrrolidone) (PVP) vs. the degree (Q<sub>TMS</sub>) of silica hydrophobization by hexamethyldisilazane at 100 <sup>o</sup>C. The value of Q<sub>TMS</sub> was 0.07, 0.42, 0.67, 0.81, 0.82, and 1.0. Adsorption of PVP onto a nanosilica surface was carried out from a water and water-ethanol (1:1) solutions of the polymer. It was shown that free silanol groups play a crucial role in the adsorption of poly(vinyl pyrrolidone). The value of the maximal adsorption (monolayer capacity) on completely hydrophobic nanosilica surface is approximately by 6.5 times lower than that for unmodified nanosilica


1984 ◽  
Vol 39 (2) ◽  
pp. 186-189
Author(s):  
Takaya Iida ◽  
Kaname Ito

The volume ratios of the mobile and stationary phases in thin layer chromatography, and the partition coefficients of halide and halate anions and some other anions between these phases were obtained by developing the ions simultaneously with a series of metaphosphates. The water contents of the developing solvents influenced the volume ratios very much, but not so much the partition coefficients. The logarithm of the partition coefficient of the halide anions is proportional to the reciprocal of their ionic radius, and that of the halate anions and oxoanions to the partial charge on the oxygens of them.


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