Preparation method of functional molecular sieves for adsorbing Pb (II) heavy metal ions
A technology of heavy metal ions and molecular sieves, applied in the directions of alkali metal compounds, chemical instruments and methods, alkali metal oxides/hydroxides, etc., can solve the problem that the functionalized MCM-41 mesoporous material has few types and the adsorption and removal of heavy metal lead ions is limited. , the preparation of equipment and materials are expensive, etc., to achieve the effect of convenient industrial production and promotion, regular and orderly microstructure, and easy preparation
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[0021]The present invention provides a technical solution: a method of adsorbing a functional molecular sieve of PB (II) heavy metal ions, including the following steps:
[0022]Step 1: Preparation of mesoporous molecular sieve MCM-41: dissolved from 1.0 g of hexadalkyltrimethyla bromine in 100 ml of deionized water, followed by adding 80 mL of concentrated ammonia water, and stirred vigorously at 65 ° C Hour, then the 5 mL of orthosable ethyl ester was then slowly added, and stirring was continued for three hours at a temperature of 65 ° C. After the mixture reacted, the product was transferred to the beaker, and the crystals were allowed to crystallize for four days, followed by filtration and Wash the powder sample and dried in a temperature of 90 ° C, then transfer the powder sample into the high temperature furnace temperature control temperature, the high temperature furnace controls to 700 ° C, and the surfactant is removed for five hours to obtain primary The mesoporous molecul...
Embodiment 1
[0027]Step 1: Preparation of MCM-41 of the mesoporous molecular sieve:
[0028]A 1.0 g of hexadalkyltrimethylammonium bromide was dissolved in 100 ml of deionized water, and 80 ml of concentrated concentrated ammonia was added vigorously stirred at 65 ° C for an hour, then slowly to add 5 ml of orthosilicate to the above mixed solution. After stirring at the above temperature, the product was transferred to a beaker at room temperature, and the powder sample was obtained by filtration and water, dried at 90 ° C, then shifted the sample into the program temperature control temperature. The furnace is heated to 700 ° C, and the surfactant is removed for 5 hours, and the primary mesoporous molecular sieve MCM-41 is obtained, and it is submitted as M-1;
[0029]Step 2: 3-mercaptopropyltrimethoxysilane and 3-aminopropyltrimethoxysilane prehydly:
[0030]Take 0.1 mol of 3-mercaptopropyltrimethoxysilane and 0.1 mol of water mixed with a molar ratio of 1: 1, then adding a pH of acetic acid to a pH o...
Embodiment 2
[0035]Step 1: Preparation of MCM-41 of the mesoporous molecular sieve:
[0036]A 1.6 g of hexadalkyltrimethylammonium bromide was dissolved in 100 ml of deionized water, and 120 ml of concentrated concentrated ammonia was added vigorously for 1.5 hours at 70 ° C, then, 8 ml of orthosilicate was added to the above mixed solution. After stirring at the above temperature, the product was transferred to the beaker at room temperature, and the powder sample was obtained by filtration and water, drying the sample at 100 ° C, then shifting the sample into the program temperature control. The high temperature furnace is heated to 750 ° C, and the surfactant is removed by 4.5 h, obtaining the primary mesoporous molecular sieve MCM-41, which will be submitted to M-1;
[0037]Step 2: 3-mercaptoethyltriethoxysilane and 3-aminopropyltriethoxysilane prehydly:
[0038]The 0.15 mol of 3-mercaptopropyltrimethoxysilane and 0.15 mol of water were mixed with a molar ratio of 1: 1, and then the pH of acetic acid...
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