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If you want to learn more about this compound(1-(2,4-Difluorophenyl)-2-(1H-1,2,4-triazol-1-yl)ethanone)Recommanded Product: 86404-63-9, you may wish to communicate with the author of the article,or consult the relevant literature related to this compound(86404-63-9).

Heterocyclic compounds can be divided into two categories: alicyclic heterocycles and aromatic heterocycles. Compounds whose heterocycles in the molecular skeleton cannot reflect aromaticity are called alicyclic heterocyclic compounds. Compound: 86404-63-9, is researched, Molecular C10H7F2N3O, about Preparation and adsorption properties of Ni(II) ion-imprinted polymers based on synthesized novel functional monomer, the main research direction is nickel imprinted polymer preparation adsorption property.Recommanded Product: 86404-63-9.

In this study, a novel functional monomer N-(1-(2,4-difluorophenyl)-2-(1H-1,2,4-triazol-1-yl)ethyl)acrylamide (NDTEA) was designed and synthesized, and was used to prepare Ni(II) ion-imprinted polymers (Ni(II)-IIPs). Sixteen kinds of Ni(II)-IIP (Ni(II)-IIP1 – 16) and corresponding non-imprinted polymers (NIP1 – 16) were prepared by precipitation polymerization method. After optimized condition experiment, Ni(II)-IIP5 possessed maximum adsorption capacity and better imprinting factor under optimal exptl. conditions which indicated by equilibrium adsorption experiments The morphol. and structural characteristics of Ni(II)-IIP5 were characterized by SEM and Brunauer-Emmett-Teller (BET). The adsorption selectivity of Ni(II)-IIP5 was analyzed by ICP-OES, and the results showed that Ni(II)-IIP5 had favorable selectivity recognition ability for Ni(II) when Cu(II), Co(II), and Cd(II) are used as competitive ions. The kinetic experiment indicated that the performance of Ni(II) adsorption on the surface of Ni(II)-IIP5 obeyed the pseudo-first-order model, and adsorption equilibrium was attained after 15 min. Isothermal adsorption process fitted to Langmuir and Freundlich isothermal adsorption models, simultaneously. The results showed that Ni(II)-IIP5 prepared by using a new functional monomer had better permeation selectivity and higher affinity for Ni(II), which also verified the rationality of the functional monomer design. At the same time, it also provided a broad application prospect for removal of Ni(II) in complex samples.

If you want to learn more about this compound(1-(2,4-Difluorophenyl)-2-(1H-1,2,4-triazol-1-yl)ethanone)Recommanded Product: 86404-63-9, you may wish to communicate with the author of the article,or consult the relevant literature related to this compound(86404-63-9).

Reference:
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics