CN107715924A - 一种mto催化剂载体的制备方法 - Google Patents

一种mto催化剂载体的制备方法 Download PDF

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CN107715924A
CN107715924A CN201711275649.4A CN201711275649A CN107715924A CN 107715924 A CN107715924 A CN 107715924A CN 201711275649 A CN201711275649 A CN 201711275649A CN 107715924 A CN107715924 A CN 107715924A
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Abstract

本发明的目的是提供一种MTO催化剂载体的制备方法。具体步骤如下:制备纳米改性复合粉体,取铝源、磷源、水、ZSM‑5原粉和纳米改性复合粉体,搅拌混匀后依次加入模板剂、氢氟酸制得分子筛合成凝胶,将分子筛合成凝胶经晶化处理后,回收晶化产物即得ZSM‑5/AlPO4‑34复合分子筛。以该分子筛作为MTO催化剂载体。本发明制备ZSM‑5/AlPO4‑34复合分子筛的方法简单,晶化时间较短,适于大规模生产应用,其经济效益显著。采用本发明方法制得的ZSM‑5/AlPO4‑34复合分子筛应用于MTO反应中能够显著提高反应的选择性和催化效率。

Description

一种MTO催化剂载体的制备方法
技术领域
本发明涉及一种制备MTO催化剂载体的方法,属于化工合成技术领域。
背景技术
MTO(Methanol To Olefin)是指由甲醇制取低碳烯烃(乙烯和丙烯)的化工工艺技术,为烯烃生产寻找了一条新的原料路线。不用石油而以甲醇为原料生产烯烃,不仅可使烯烃价格摆脱石油产品的影响,还能减少我国对石油资源的过度依赖。
MTO技术的关键是高性能催化剂的研制,早期对于MTO催化剂的研究主要以ZSM-5等中孔分子筛为主,ZSM-5的中大孔结构使其具有低碳少、寿命长等优点,但是由于其酸性太强,同时又具有烯烃收率低副产物多等缺点。1984年,UCC公司发明了SAPO-34分子筛用于MTO反应,其较小的孔径和较大的比表面积加快了MTO反应速率并且提高了反应的选择性,但是具有积碳高、易失活和寿命短等缺点。
鉴于甲醇制烯烃反应中的应用,需要制备一种ZSM-5/磷酸铝复合分子筛,与ZSM-5相比,ZSM-5/磷酸铝复合分子筛表现出了良好的协同作用和优良的催化性能。
发明内容
为了解决上述技术问题,本发明的目的是提供一种制备MTO催化剂载体的方法,具体步骤如下:
(1)取粒径均为40-50nm的二氧化硅、二氧化钛和氧化银的混合粉体加入容器中,其中二氧化硅、二氧化钛和氧化银的质量比为2.8:2:1.6,而后加入聚乙烯醇和水的混合溶液,室温下搅拌分散60分钟,而后加入硅烷偶联剂KH550和酸,其中KH550与酸的摩尔比为1:1,70℃搅拌反应5h,而后降温至室温,过滤,得到纳米改性复合粉体;
(2)将铝源、磷源加入水中搅拌待溶解完全,再加入ZSM-5原粉和步骤(1)得到的纳米改性复合粉体继续搅拌,并加入模板剂、氢氟酸,待搅拌3~5小时后制得纳米改性分子筛合成凝胶;
(3)将步骤(2)的分子筛合成凝胶在150~190℃下晶化12~24小时后冷却至室温,过滤,洗涤、在60-80℃下干燥,再在350~580℃下焙烧4~8小时即得纳米改性复合分子筛;
(4)将步骤(3)中制得的纳米改性复合分子筛做为载体用于MTO催化剂。
所述铝源、磷源、模板剂、氢氟酸和水的摩尔比为铝源:磷源:模板剂: 氢氟酸:水=1:(1.0~1.5):(0.5~2):(0.1~0.2):(50~300);
所述的模板剂为吗啉、哌啶或吡啶。
所述的铝源为拟薄水铝石、异丙醇铝、氢氧化铝、氧化铝中的一种或两种任意比例的混合物。
所述的磷源为正磷酸。
步骤(1)中的酸选自盐酸、硝酸、甲酸、乙酸中的一种或几种。
步骤(3)中合成凝胶在160~180℃水热晶化18小时,干燥温度为60~80℃。
所述ZSM-5原粉的质量占分子筛合成凝胶总量的约1/10~1/5。
本发明的有益效果:
本发明制备纳米改性ZSM-5/AlPO4-34复合分子筛的方法简单,晶化时间较短,适于大规模生产应用,其经济效益显著。分子筛中还采用了特定配比的改性纳米复合粉体,经过表面改性的上述纳米复合粉体可有效改善分子筛的附着性、强度、韧性和耐高温性。ZSM-5/AlPO4-34复合分子筛特定组成中各组分的相互协同,在应用于MTO反应中能够显著提高反应的选择性和催化效率。
具体实施方式
实施例1
本实施例中纳米改性ZSM-5/AlPO4-34复合分子筛的制备方法具体包括以下步骤:
(1)取粒径均为40-50nm的二氧化硅、二氧化钛和氧化银的混合粉体加入容器中,其中二氧化硅、二氧化钛和氧化银的质量比为2.8:2:1.6,而后加入聚乙烯醇和水的混合溶液,室温下搅拌分散60分钟,而后加入硅烷偶联剂KH550和酸,其中KH550与酸的摩尔比为1:1,70℃搅拌反应5h,而后降温至室温,过滤,得到纳米改性复合粉体;
(2)按照摩尔比为(异丙醇铝+氧化铝):正磷酸:(哌啶+吡啶):氢氟酸:去离子水=1:1.0:0.5:0.1:50取各组分,将异丙醇铝和氧化铝石分别添加入到去离子水中搅拌6小时,待溶解完全后加入正磷酸搅拌3小时,再加入硅铝比为50的ZSM-5原粉和步骤(1)得到的纳米改性复合粉体继续搅拌,并加入哌啶和吡啶,以及氢氟酸,ZSM-5原粉的质量占分子筛合成凝胶总量的1/5,待搅拌3小时制得分子筛合成凝胶;
(3)将步骤(2)中分子筛合成凝胶移至带聚四氟乙烯内衬的不锈钢晶化釜中,在150℃下晶化24小时后冷却至室温,抽滤,洗涤至中性后在80℃下干燥6小时,再在580℃下焙烧4小时即得ZSM-5/AlPO4-34复合分子筛;
(4)将步骤(3)中制得的纳米改性复合分子筛做为载体用于MTO催化剂。
实施例2
本实施例中纳米改性ZSM-5/AlPO4-34复合分子筛的制备方法具体包括以下步骤:
(1)取粒径均为40-50nm的二氧化硅、二氧化钛和氧化银的混合粉体加入容器中,其中二氧化硅、二氧化钛和氧化银的质量比为2.8:2:1.6,而后加入聚乙烯醇和水的混合溶液,室温下搅拌分散60分钟,而后加入硅烷偶联剂KH550和酸,其中KH550与酸的摩尔比为1:1,70℃搅拌反应5h,而后降温至室温,过滤,得到纳米改性复合粉体;
(2)按照摩尔比为(氢氧化铝+拟薄水铝石):正磷酸:(吗啉+吡啶):氢氟酸:去离子水=1: 1.2: 1: 0.15:200取各组分,将氢氧化铝和拟薄水铝石分别添加入到去离子水中搅拌8小时,待溶解完全后加入正磷酸搅拌3小时,再加入硅铝比为50的ZSM-5原粉和步骤(1)得到的纳米改性复合粉体继续搅拌,并加入吗啉和吡啶,以及氢氟酸,ZSM-5原粉的质量占分子筛合成凝胶总量的1/7,待搅拌4小时制得分子筛合成凝胶;
(3)将步骤(2)中分子筛合成凝胶移至带聚四氟乙烯内衬的不锈钢晶化釜中,在在180℃下晶化18小时,然后冷却至室温,抽滤,洗涤至中性后在70℃下干燥8小时,再在450℃下焙烧6小时即得ZSM-5/AlPO4-34复合分子筛;
(4)将步骤(3)中制得的纳米改性复合分子筛做为载体用于MTO催化剂。
实施例3
本实施例中纳米改性ZSM-5/AlPO4-34复合分子筛的制备方法具体包括以下步骤:
(1)取粒径均为40-50nm的二氧化硅、二氧化钛和氧化银的混合粉体加入容器中,其中二氧化硅、二氧化钛和氧化银的质量比为2.8:2:1.6,而后加入聚乙烯醇和水的混合溶液,室温下搅拌分散60分钟,而后加入硅烷偶联剂KH550和酸,其中KH550与酸的摩尔比为1:1,70℃搅拌反应5h,而后降温至室温,过滤,得到纳米改性复合粉体;
(2)按照摩尔比为(异丙醇铝+拟薄水铝石):正磷酸:(哌啶+吡啶):氢氟酸:去离子水=1: 1.5: 2: 0.2:300取各组分,将异丙醇铝和拟薄水铝石分别添加入到去离子水中搅拌8小时,待溶解完全后加入正磷酸搅拌3小时,再加入硅铝比为50的ZSM-5原粉和步骤(1)得到的纳米改性复合粉体继续搅拌,并加入哌啶和吡啶,以及氢氟酸,ZSM-5原粉的质量占分子筛合成凝胶总量的1/5,待搅拌5小时制得分子筛合成凝胶;
(3)将步骤(2)中分子筛合成凝胶移至带聚四氟乙烯内衬的不锈钢晶化釜中,在在190℃下晶化12小时,然后冷却至室温,抽滤,洗涤至中性后在60℃下干燥10小时,再在350℃下焙烧8小时即得ZSM-5/AlPO4-34复合分子筛;
(4)将步骤(3)中制得的纳米改性复合分子筛做为载体用于MTO催化剂。

Claims (3)

1.一种MTO催化剂载体的制备方法,其特征在于:具体步骤如下:
(1)取粒径均约为40-50nm的二氧化硅、二氧化钛和氧化银的混合粉体加入容器中,其中二氧化硅、二氧化钛和氧化银的质量比为2.8:2:1.6,而后加入聚乙烯醇和水的混合溶液,室温下搅拌分散60分钟,而后加入硅烷偶联剂KH550和酸,其中硅烷偶联剂KH550与酸的摩尔比为1:1,70℃搅拌反应5h,而后降温至室温,过滤,得到纳米改性复合粉体;
(2)将铝源、磷源加入水中搅拌待溶解完全,再加入ZSM-5原粉和步骤(1)得到的纳米改性复合粉体继续搅拌,并加入模板剂、氢氟酸,待搅拌3~5小时后制得纳米改性分子筛合成凝胶;
(3)将步骤(2)的分子筛合成凝胶在约160~180℃下晶化18小时后冷却至室温,过滤,洗涤、在70℃下干燥,再在350~580℃下焙烧4~8小时即得纳米改性复合分子筛;
(4)将步骤(3)中制得的纳米改性复合分子筛做为载体用于MTO催化剂;
所述铝源、磷源、模板剂、氢氟酸和水的摩尔比为铝源:磷源:模板剂: 氢氟酸:水=1:(1.0~1.5):(0.5~2):(0.1~0.2):(50~300);
所述的模板剂为吗啉、哌啶或吡啶;
所述的铝源为拟薄水铝石、异丙醇铝、氢氧化铝、氧化铝中的一种或两种任意比例的混合物;
步骤(1)中的酸选自盐酸、硝酸、甲酸、乙酸中的一种或几种。
2.根据权利要求1所述的方法,其特征在于:所述的磷源为正磷酸。
3.根据权利要求1所述的方法,其特征在于:所述ZSM-5原粉的质量占分子筛合成凝胶总量的1/10~1/5。
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