Synthesis,characterization,and performance comparison of boron using adsorbents based on N-methyl-D-glucosamine

Using N-methyl-D-glucosamine(NMDG)as the functional monomer,glycidyl methacrylate(GMA)as the connecting monomer,functionalized Fe3O4 nano-particles(NPs)as the support,three adsorbents were prepared including direct polymer GMA-NMDG,magnetic GMA-NMDG polymer(MGN),and boron magnetic ion-imprinted polymer(BMIIP).Based upon the optimization of synthesis conditions,the prepared adsorbents and intermediate products were characterized using Fourier transform infrared spectroscopy,thermogravimetric analysis,scanning electron microscope,energy dispersive spectroscopy,X-ray diffraction,vibrating sample magnetometer,and Brunauer–Emmett–Teller to investigate the synthesis process,the morphological structure and the functional properties of the materials.The optimum performances of GMA-NMDG,MGN and BMIIP were obtained in the initial neutral solution(pH of 6.5).Moreover,GMANMDG and MGN reached the maximum adsorption capacity at 120 min,whereas BMIIP reached adsorption saturation at 60 min.The pseudo-second-order kinetic model was more suitable for the adsorption of boron using the adsorbents.The maximum adsorption capacity of GMA-NMDG was found to be 43.4 mg·g^(-1),while those of MGN and BMIIP were 32.5 and 28.3 mg·g^(-1),respectively.The Langmuir isotherm model was more appropriate to describe the adsorption process.The adsorbents maintained satisfactory adsorption performance within a certain temperature range.Competing ions had little effect on the adsorption of boron,and would be adsorbed simultaneously,due to which,the effect of co-adsorption can be considered.The adsorption capacity of GMA-NMDG was high,while the adsorption selectivity of BMIIP was much better.Furthermore,BMIIP showed good adsorption after five cycles of adsorption and desorption.The comparison of adsorbents showed that GMA-NMDG had the highest adsorption capacity and was suitable for co-adsorption.MGN had a high adsorption capacity,good comprehensive performance and magnetic properties.BMIIP had better adsorption rate,adsorption selectivity and recyclability.Through the optimization of synthesis conditions,the adsorption capacity of the traditional monomer NMDG polymer was increased,and the magnetism was given to facilitate rapid recovery.Combined with the ion imprinting technology,it showed higher boron adsorption selectivity in the presence of competitive ions.

Adsorption Properties of Phosphate by CaCl2-loaded Straw Microwave Charcoal

Phosphate is the main limiting factor of water eutrophication. In order to effectively control phosphorus pollution in water, straw microwave charcoal(CaCl2SBC) was prepared with straw after CaCl2activation and microwave biomass carbonization, and the adsorption effect of phosphate by CaCl2SBC was analyzed. The results showed that the prepared straw microwave charcoal contained hydroxyl and carbon-carbon double bonds, and CaCl2SBC had a very obvious adsorption effect on phosphate in eutrophic water. The optimum conditions for the adsorption of phosphate by CaCl2SBC are as follows: initial concentration of phosphate was 50 mg/L;adsorption time was 120 min;pH was 9;adsorption temperature was 25 ℃;CaCl2SBC dosage was 300 mg/L. Under the optimum conditions, the maximum removal rate can reach 99%. The prepared straw microwave charcoal can be used for phosphorus removal from eutrophic water.

Enhanced catalytic oxidation of dichloromethane by a surfactant-modified CeO_(2)@TiO_(2) core-shell nanostructured catalyst

Surfactant-modified CeO_(2)@TiO_(2) core-shell nanostructure catalysts were prepared by coprecipitation with the addition of sodium dodecyl sulfonate(SDS),and their catalytic oxidation of dichloromethane(DCM) was studied.A 90% DCM conversion efficiency is obtained at 300℃ with the CeO_(2)@TiO_(2)SDS catalyst,and its catalytic stability in the 55 h test period is better than that of Ce/TiO_(2) and CeO_(2)@TiO_(2).Based on the characterization of CeO_(2)@TiO_(2)SDS,the dispersion of active components is promoted due to the inhibition of crystal growth with the introduction of SDS.The improvement of surface acidity and redox capacity is beneficial to the enhancement of catalytic activity.The higher adsorbed oxygen content on the surface of the CeO_(2)@TiO_(2)SDS catalyst is responsible for the better catalytic stability.Generally,a novel method was developed to design catalytic oxidation catalysts for the treatment of chlorinated volatile organic compounds in future applications.