Surface polymerization modified hydrotalcite material and preparation method thereof
A technology for modifying water and hydrotalcite, which can be used in fibrous fillers, dyed organosilicon compound treatment, dyed polymer organic compound treatment, etc. It can solve application limitations, prone to agglomeration, poor compatibility between hydrotalcite and polymers problem, to achieve the effect of improving dispersibility and improving compatibility
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0037] This embodiment discloses a method for preparing a surface polymerization modified hydrotalcite material, comprising the following steps:
[0038] Step A: Accurately weigh 0.01mol (2.5641g) of Mg(NO 3 ) 2 ·6H 2 O, 0.005mol (1.8756g) of Al(NO 3 ) 3 9H 2 O and 0.05mol (3g) of CO(NH 2 ) 2 , dissolved in 80mL deionized water. Using the urea method, the solution was transferred to a polytetrafluoroethylene lining, placed in an oven, and crystallized at 130 ° C for 24 hours. The product was centrifuged to separate the filter cake and used to remove CO 2 Wash with deionized water until the filtrate pH = 7, and dry for 12 hours to obtain the hydrotalcite precursor, which is denoted as LDHs. urea means urea, the same below.
[0039] Step B: Take 3.5g of LDHs precursor powder, add 150mL of cyclohexane, and then sonicate for 10 minutes, then transfer to a clean 250mL three-neck flask. Weigh 0.175g of KH-570 (Sinopharm Chemical Reagent Co., Ltd.) and dissolve it in 2mL o...
Embodiment 2
[0047] This embodiment discloses a method for preparing a surface polymerization modified hydrotalcite material, comprising the following steps:
[0048] Step A: Accurately weigh 0.01mol (2.5641g) of Mg(NO 3 ) 2 ·6H 2 O, 0.005mol (1.8756g) of Al(NO 3 ) 3 9H 2 O and 0.05mol (3g) of CO(NH 2 ) 2 , dissolved in 80mL deionized water. Using the urea method, the solution was transferred to a polytetrafluoroethylene lining, placed in an oven, and crystallized at 130 ° C for 24 hours. The product was centrifuged to separate the filter cake and used to remove CO 2 The filtrate was washed with deionized water until the pH of the filtrate was 7, and dried for 12 hours. The obtained hydrotalcite precursor was recorded as LDHs.
[0049] Step B: Take 3.5g of LDHs precursor powder, add 150mL of cyclohexane, and then sonicate for 10 minutes, then transfer to a clean 250mL three-neck flask. Weigh 0.175g of KH-570 and dissolve it in 2mL of cyclohexane, sonicate for 5 minutes to obtain ...
PUM
Login to View More Abstract
Description
Claims
Application Information
Login to View More 


