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For the efficient removal of some anionic dyes, a novel adsorbent was developed. The adsorbent was prepared by coating a synthetic polymer on magnetite nanosphere surface as a magnetic carrier. The synthesized nano-adsorbent was fully characterized using Fourier transform infrared spectroscopy (FT-IR), vibrating sample magnetometer, X-ray diffractometer, scanning electron microscope, and transmission electronic microscopy measurements. The synthesized nano-adsorbent showed high adsorption capacity towards removal of some anionic dyes (221.4, 201.6, and 135.3 mg g À1 for reactive red 195, reactive yellow 145, and reactive blue 19 dye, respectively) from aqueous samples. The dye adsorption was thoroughly studied from both kinetic and equilibrium points of view. It was found that the Langmuir isotherm showed a better correlation with the experimental data. The kinetic data showed that the process was very fast, and the adsorption process followed pseudo-second order kinetic models for the modified magnetic nano-adsorbent. Furthermore, the results showed that a stable and reusable (up to 20 cycles) nano-adsorbent for dye removal purposes was synthesized.

The ability of molecules and systems to make copies of themselves and the ability of molecules to fold into stable, well-defined three-dimensional conformations are of considerable importance in the formation and persistence of life. The question of how, during the emergence of life, oligomerization reactions become selective and channel these reactions toward a small number of specific products remains largely unanswered. Herein, we demonstrate a fully synthetic chemical system where structurally complex foldamers and self-replicating assemblies emerge spontaneously and with high selectivity from pools of oligomers as a result of forming noncovalent interactions. Whether foldamers or replicators form depends on remarkably small differences in building block structures and composition and experimental conditions. We also observed the dynamic transformation of a foldamer into a replicator. These results show that the structural requirements/design criteria for building blocks that lead to foldamers are similar to those that lead to replicators. What determines whether folding or replication takes place is not necessarily the type of noncovalent interaction, but only whether they occur intra- or intermolecularly. This work brings together, for the first time, the fields of replicator and foldamer chemistry.