Preparation method of magnetic porous adsorbent by suspension polymerization
A porous adsorbent, suspension polymerization technology, applied in chemical instruments and methods, adsorption water/sewage treatment, other chemical processes, etc., can solve problems such as damage and high toxicity of chlorophenol, achieve good magnetic response performance, increase adsorption The effect of high capacity and mechanical strength
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Embodiment 1
[0034] 1. A method for preparing magnetic porous adsorbent by suspension polymerization, the preparation method is carried out according to the following steps:
[0035] (1) Synthesis of porous phenethyl-divinylbenzene (St-DVB) nanoparticles:
[0036]Dissolve 5 ml styrene (St), 7.5 ml divinylbenzene (DVB), 0.25 g azobisisobutyronitrile (AIBN) and 6.3 ml cyclohexanol in 4.2 ml toluene to form an organic phase, and 1.5 g chloride Sodium (NaCl) and 0.9 g of hydroxyethylcellulose (HEC) were dissolved in 70 ml of deionized water to form the aqueous phase. After thorough stirring, the two phases were mixed under ultrasonic conditions for 15 min to form an emulsion. The emulsion was transferred to a 250 ml three-neck flask equipped with a condenser and a nitrogen device, stirred for 1 h under the protection of nitrogen, and then the temperature was raised from room temperature to 70 °C. The reaction was continued for 24 h under high-speed stirring at 800 rpm / min. Finally, a porous...
Embodiment 2
[0049] 1. A method for preparing magnetic porous adsorbent by suspension polymerization, the preparation method is carried out according to the following steps:
[0050] (1) Synthesis of porous phenethyl-divinylbenzene (St-DVB) nanoparticles:
[0051] Dissolve 5.3 ml of styrene (St), 7.8 ml of divinylbenzene (DVB), 0.2 g of azobisisobutyronitrile (AIBN) and 6.5 ml of cyclohexanol in 4.3 ml of toluene to form an organic phase, and 1.57 g of chlorine Sodium chloride (NaCl) and 1.1 g of hydroxyethylcellulose (HEC) were dissolved in 75 ml of deionized water to form the aqueous phase. After thorough stirring, the two phases were mixed under ultrasonic conditions for 30 min to form an emulsion. The emulsion was transferred to a 250 ml three-neck flask equipped with a condenser and a nitrogen device, stirred for 2 h under the protection of nitrogen, and then the temperature was raised from room temperature to 70 °C. The reaction was continued for 24 h under a high-speed stirring co...
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