Exact(1)
A new mechanism is proposed for the copolymerization based on the results from both video camera and Raman spectroscopy.
Similar(59)
A novel highly hydrophilic polymethacrylate-based monolithic stationary phase based on the copolymerization of 2-acrylamido-2-methyl-1-propanesulfonic acid (AMPS) and pentaerythritol triacrylate (PETA) was designed for pressurized capillary electrochromatography.
A novel cationic hydrophilic interaction monolithic stationary phase based on the copolymerization of 2- methacryloyloxy)ethyltrimethylammonium methyl sulfate (META) and pentaerythritol triacrylate (PETA) in a binary porogenic solvent consisting of cyclohexanol/ethylene glycol was designed for performing capillary liquid chromatography.
Based on the copolymerization data of St/MA and St/BA in emulsion and microemulsion polymerization, the mechanism of microemulsion polymerization was discussed.
The mechanisms of the copolymerization and O/S ER were proposed based on the ESI-MS, GC MS and FT-IR spectra.
The relationship between the residual monomer composition and the product composition can be modelled satisfactorily using a mathematical model based on the instantaneous copolymerization equation and Arrhenius relationships for the reactivity ratios.
In this article, a detailed fundamental model is developed to describe the chemical and physical phenomena in this gel dosimeter, based on the radiation-induced copolymerization of acrylamide and bisacrylamide monomers in water and gelatin.
Based on the X-ray crystal structure and results of copolymerization of CO2 with CHO, the copolymerization mechanism is examined as well.
The copolymer showed moderate to high sulphate scale inhibition activities based on the amount of curcumin used during copolymerization.
A direct synthetic method was employed and photo-active STEM gels based on (meth)acrylates were synthesized by free radical copolymerization of different monomers, a crosslinker, and a photo-active dormant initiator/monomer (inimer) based on the radical photoinitiator 2-hydroxy-4′- 2-hydroxyethoxy -2-methylpropiophenone 2-hydroxy-4′- 2-hydroxyethoxy -2-methylpropiophenone 2-hydroxy-4′- 2-hydroxyethoxy -2-methylpropiophenone 2-hydroxy-4′- 2-hydroxyethoxy -2-methylpropiophenone 2-hydroxy-4′- 2-hydroxyethoxy -2-methylpropiophenone 2-hydroxy-4′- 2-hydroxyethoxy -2-methylpropiophenone 2-hydroxy-4′- 2-hydroxyethoxy -2-methylpropiophenone
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