Determination of Adsorbates on the Surface of Polymer with Low Absorption Capacity by Thermal Lens Spectrometry
- Authors: Nedosekin D.A.1, Mikheev I.V.2, Volkov D.S.2, Proskurnin M.A.2
- 
							Affiliations: 
							- Arkansas Nanomedicine Center
- Department of Chemistry
 
- Issue: Vol 73, No 7 (2018)
- Pages: 641-649
- Section: Articles
- URL: https://journals.rcsi.science/1061-9348/article/view/183086
- DOI: https://doi.org/10.1134/S1061934818070146
- ID: 183086
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Abstract
Thermal lens spectrometry in a coaxial configuration is used for the direct determination of adsorbates on a planar surface of polyethylene terephthalate (PET). A possibility of the direct measurement of the rate of adsorption from solutions and the determination of the parameters of the adsorbed layer is demonstrated by the example of an investigation of the adsorption of iron(II) tris(1,10-phenantrolinate) on a PET surface. The adsorption isotherm of iron(II) tris(1,10-phenantrolinate) on the PET surface is described by the Langmuir equation and is linear in the concentration range in solution from 0.02 to 0.7 mM. The method for calculating the thermal perturbation in surface-absorbing solids was used to interpret the results of the adsorption study, and a possibility of determining iron(II) tris(1,10-phenantrolinate) on the surface at a level smaller than a monolayer was shown. Thermal lens spectrometry enables the determination of the absorption of the surface layer at a level up to 5 × 10–5 absorbance units, which corresponds to the surface concentration of iron(II) tris(1,10-phenanthrolinate) 2 × 10–13 mol/cm2. Using the example of the adsorption of 4-(2-pyridylazo) resorcinol on the PET surface, it is demonstrated that, in the case of strong absorption of the surface layer, the thermal destruction of substance and the deformation of the substrate may occur. A local increase in temperature in the layer is also confirmed by theoretical calculations.
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About the authors
D. A. Nedosekin
Arkansas Nanomedicine Center
														Email: proskurnin@gmail.com
				                					                																			                												                	United States, 							Little Rock, AR, 72205						
I. V. Mikheev
Department of Chemistry
														Email: proskurnin@gmail.com
				                					                																			                												                	Russian Federation, 							Moscow, 119991						
D. S. Volkov
Department of Chemistry
														Email: proskurnin@gmail.com
				                					                																			                												                	Russian Federation, 							Moscow, 119991						
M. A. Proskurnin
Department of Chemistry
							Author for correspondence.
							Email: proskurnin@gmail.com
				                					                																			                												                	Russian Federation, 							Moscow, 119991						
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