Sulfonic acid-containing polymeric materials as amine sorbents
A technology of polymer materials and polymer compositions, applied in cation exchange materials, chemical/physical processes, organic cation exchangers, etc., can solve problems such as reducing the adsorption capacity of activated carbon
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Embodiment 24
[0113] Embodiment 24 is the polymeric material of embodiment 23, wherein the polyvinylaromatic monomer is divinylbenzene, trivinylbenzene, divinylbenzene substituted with one or more alkyl groups Benzene, or trivinylbenzene substituted with one or more alkyl groups.
[0114] Embodiment 25 is the polymeric material of any one of embodiments 18 to 24, wherein the polymerizable composition further optionally comprises up to 25% by weight of a monovinylaromatic monomer or is replaced by one or more Alkyl group substituted monovinyl aromatic monomers, wherein the weight % is based on the total weight of monomers in the polymerizable composition.
[0115] Embodiment 26 is the polymeric material of embodiment 25, wherein the polymerizable composition comprises 1% to 99% by weight of the monomer of formula (I), 0% to 25% by weight of monovinyl Aromatic monomers and 1 wt. % to 99 wt. % polyvinylaromatic monomers, wherein the wt. % is based on the total weight of monomers in the polyme...
Embodiment
[0126] Table 1: List of materials
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[0129] Gas adsorption analysis
[0130] Using the Rapid Surface Area and Porosity Analyzer (ASAP2020) system from Micromeritics Instrument Corporation (Norcross, GA), Micromeritics Instrument Corporation (Norcross, GA), USA, the porosity experiments and gas Adsorption experiment. Typical methods used to characterize porosity within example materials are described below. Take 50 to 300 mg of material into a half-inch diameter sample tube produced by Micromeritics, place the sample tube on the analytical port of ASPA 2020, and place the sample tube under ultra-high vacuum (3 to 7 μm Hg) at 150 °C for 2 hours to remove residual solvent and other adsorbates. When the relative pressure (p / p°) is less than 0.1, select low pressure dosing (low pressure dosing) mode (5cm 3 / g), and the argon adsorption isotherm at 77°K was obtained using a pressure plot of linearly spaced pressure points at relative pressures (p / p°) r...
preparation example 1
[0139] Preparation Example 1 : Synthesis of 3,3,3',3'-tetramethyl-1,1'-spirobisindane-6,6'-divinyl (SBI-DV)
[0140] The monomer 3,3,3',3'-tetramethyl-1,1'-spirobisindane-6,6'-diethylene (SBI-DV) was prepared by first preparing 3,3,3',3' -tetramethyl-1,1'-spirobisindane-6,6'-diol (SBI-diol). The SBI-diol is then converted to perfluoromethane-1-sulfonic acid 6'-(perfluoromethane-1-sulfonyloxy)-3,3,3',3'-tetramethyl-1,1'- Spirobisindan-6-yl ester (SBI-bistriflate), which is further converted to SBI-DV.
[0141] Synthesis of 3,3,3',3'-tetramethyl-1,1'-spirobisindane-6,6'-diol (SBI-diol)
[0142] 1000.69 g (4.38 moles) of 4,4'-isopropylidenediphenol (BPA) was melted in a 5.0 L round bottom flask. Once all the BPA had melted, 50.51 grams (0.526 moles) of methanesulfonic acid was slowly added. The temperature of the reaction mixture was maintained between 135°C and 150°C, and the reaction mixture was stirred under nitrogen atmosphere for 3 hours. After 3 hours, while still ...
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