CN108097217B - 一种含双氨官能团微孔硅吸附剂的制备方法和应用 - Google Patents

一种含双氨官能团微孔硅吸附剂的制备方法和应用 Download PDF

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CN108097217B
CN108097217B CN201711438712.1A CN201711438712A CN108097217B CN 108097217 B CN108097217 B CN 108097217B CN 201711438712 A CN201711438712 A CN 201711438712A CN 108097217 B CN108097217 B CN 108097217B
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徐荣
黄劲荣
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Changzhou University
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Abstract

本发明属于吸附剂材料制备领域,特别涉及一种含双氨官能团微孔硅吸附剂的制备方法和应用。将3‑(2‑氨基乙基氨基)丙基‑三乙氧基硅烷充分分散于异丙醇中,并向其中滴加硝酸水溶液,搅拌充分后转移至水浴条件下继续搅拌反应;将得到的反应体系过滤,滤饼经洗涤并干燥,得到含双氨官能团微孔硅吸附剂,用于对酸性气体(如二氧化碳)的吸附。

Description

一种含双氨官能团微孔硅吸附剂的制备方法和应用
技术领域
本发明属于吸附剂材料制备领域,特别涉及一种含双氨官能团微孔硅吸附剂的制备方法和应用。
背景技术
化石燃料燃烧导致的温室效应已经严重威胁人类的生存环境,而CO2气体则是温室效应的主要来源,当前以及今后几十年内,人类活动所需的能源仍主要来源于化石燃料,因此必须控制燃料燃烧过程中所排放的CO2
目前,使用现有的吸附材料对CO2进行吸附处理时,往往会表现出吸附速率较慢、吸附量不高等问题。
发明内容
本发明提供了一种含双氨官能团微孔硅吸附剂的制备方法和应用,
本专利所制备的是一种微孔吸附材料,与常用的介孔吸附材料相比,微孔材料具有比表面积大的优点,但微孔孔径小(~1nm,与CO2分子动力学直径在同一个数量级),因此现有技术中,微孔结构的吸附剂不适用于动力学直径较大的CO2这类分子的吸附,这是因为CO2分子由于无规则的热运动在微孔吸附剂孔道入口处无法自由地进入,吸附阻力较大,吸附性能达不到实际应用的要求,
而本专利通过在微孔硅吸附材料上负载双氨基团,诱导CO2分子方向明确地进入孔道内,使CO2吸附具有导向性,大大缩短了其进入孔道内的行程以及时间,这是本领域内不容易想到的,虽然氨官能团和CO2分子具有较强化学结合作用,但想不到负载氨基还可使CO2分子的吸附具有导向性,减少了气体进入孔道的难度,解决了“一般微孔吸附剂虽然比表面积大,但较大的气体分子不容易进入其微孔”这一重要问题。在宏观上提高了吸附速率和吸附量,实现微孔硅材料在CO2气体吸附上的实际应用。
本专利利用溶胶-凝胶法,通过3-(2-氨基乙基氨基)丙基-三乙氧基硅烷或3-(2-氨基乙基氨基)丙基-三甲氧基硅烷水解聚合,制备出含双氨官能团微孔硅吸附剂PTES-bis(NH2),
具体操作为:
(1)将3-(2-氨基乙基氨基)丙基-三乙氧基硅烷或3-(2-氨基乙基氨基)丙基-三甲氧基硅烷充分分散于异丙醇IPA中,并向其中滴加硝酸水溶液,搅拌充分后转移至水浴条件下继续搅拌反应,
向3-(2-氨基乙基氨基)丙基-三乙氧基硅烷或3-(2-氨基乙基氨基)丙基-三甲氧基硅烷分散液(分散液中,硅源的质量分数为5%)中滴加硝酸水溶液时,控制n[3-(2-氨基乙基氨基)丙基-三乙氧基硅烷]或n[3-(2-氨基乙基氨基)丙基-三甲氧基硅烷]:n(H2O):n(HNO3)=1:120:0.2,
水浴条件下搅拌反应的温度为60℃,反应时间为6h;
(2)将步骤(1)得到的反应体系过滤,滤饼经洗涤并干燥,得到含双氨官能团微孔硅吸附剂,
干燥为,80~100℃下真空干燥8~10h。
附图说明
图1为本专利实施例1中制备的含双氨官能团微孔硅吸附剂对CO2的吸附等温线。
图2为本专利实施例1中制备的含双氨官能团微孔硅吸附剂的溶胶粒径分布图,可见溶胶仅具有1到10纳米的粒径。
图3为本专利实施例1中制备的含双氨官能团微孔硅吸附剂的孔径分布图,可见孔径分布在0~2纳米之间,可以明确判断是微孔结构。
图4为本专利实施例1中制备的含双氨官能团微孔硅吸附剂对N2的吸附等温线。
图5为本专利实施例1中制备的含双氨官能团微孔硅吸附剂和实施例2中制备的硅基介孔吸附材料SBA-15对CO2的吸附动力学曲线的对比,其中,吸附实验的条件为:25℃、1atm、二氧化碳气体流量100mL/min,
从附图5中可见,采用实施例1制备的吸附剂对二氧化碳的吸附能力达到~2毫摩尔/克,而根据本领域公知,该吸附条件下,如果二氧化碳仅仅是被吸附在外表面而没有进入吸附剂孔道中的话,吸附量会比这个值小2~3个数量级,因此只有进入微孔孔道内,利用微孔材料大的比表面积才能达到这个吸附量。
具体实施方式
实施例1
(1)将2.65g的3-(2-氨基乙基氨基)丙基-三乙氧基硅烷充分分散于66mL异丙醇中,并向其中滴加硝酸水溶液,控制n[3-(2-氨基乙基氨基)丙基-三乙氧基硅烷]:n(H2O):n(HNO3)=1:120:0.2,搅拌10min后转移至60℃的水浴条件下继续搅拌反应6h;
(2)将步骤(1)得到的反应体系过滤,滤饼经洗涤并于80℃下真空干燥10h,得到含双氨官能团微孔硅吸附剂PTES-bis(NH2)。
将实施例1制备的含双氨官能团微孔硅吸附剂PTES-bis(NH2)对二氧化碳气体进行吸附。
实施例2
(1)将2.5g模板剂P123(EO20PO70EO20)和15.0g盐酸溶于75mL蒸馏水中,并将混合物倒入125mL玻璃瓶中,在30℃下用磁棒搅拌2h,
(2)继续向步骤(1)得到的混合体系中加入5.2g正硅酸乙酯(TEOS),30℃下搅拌20h后,在100℃下老化静置24h,
(3)用56mL乙醇和4mL盐酸的混合溶液洗涤步骤(2)得到的体系,并用吸盘过滤,最终得到介孔硅吸附剂SBA-15。
将实施例2制备的介孔硅吸附剂SBA-15对二氧化碳气体进行吸附。

Claims (1)

1.一种含双氨官能团微孔硅吸附剂的应用,其特征在于:采用含双氨官能团微孔硅吸附剂对二氧化碳进行吸附;所述含双氨官能团微孔硅吸附剂的制备方法为,利用溶胶-凝胶法,通过3-(2-氨基乙基氨基)丙基-三乙氧基硅烷或3-(2-氨基乙基氨基)丙基-三甲氧基硅烷水解聚合,制备出含双氨官能团微孔硅吸附剂;
所述方法的具体步骤为,
(1)将3-(2-氨基乙基氨基)丙基-三乙氧基硅烷或3-(2-氨基乙基氨基)丙基-三甲氧基硅烷充分分散于异丙醇中,并向其中滴加硝酸水溶液,搅拌充分后转移至水浴条件下继续搅拌反应;
滴加硝酸的水溶液时,控制n [3-(2-氨基乙基氨基)丙基-三乙氧基硅烷]或n[3-(2-氨基乙基氨基)丙基-三甲氧基硅 烷]:n(H2O):n(HNO3)=1:120:0.2;
水浴温度为60℃,水浴条件下继续搅拌反应时间为6h;
(2)将步骤(1)得到的反应体系过滤,滤饼经洗涤并干燥,得到含双氨官能团微孔硅吸附剂;
干燥为80~100℃下真空干燥8~10h。
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