发明名称 Synthesis of ZSM-58 crystals with improved diffusivity for use in gas separations
摘要 Methods are provided for synthesizing ZSM-58 crystals with an improved morphology and/or an improved size distribution. By controlling the conditions during synthesis of the ZSM-58 crystals, crystals of a useful size with a narrow size distribution can be generated. Steaming the H-form DDR framework type crystals at a temperature from 426±° C. to 1100±° C. for a time period from about 30 minutes to about 48 hours can attain one or more of the following properties: a CH4 diffusivity of no more than 95% of the CH4 diffusivity of the unsteamed H-form DDR framework type crystals; an N2 BET surface area from 85% to 110% of the surface area of unsteamed H-form DDR framework type crystals; and an equilibrium CO2 sorption capacity from 80% to 105% of the equilibrium CO2 sorption capacity of unsteamed H-form DDR framework type crystals.
申请公布号 US9573116(B2) 申请公布日期 2017.02.21
申请号 US201414573177 申请日期 2014.12.17
申请人 EXXONMOBIL RESEARCH AND ENGINEERING COMPANY 发明人 Johnson Ivy D.;Beutel Tilman W.;Ravikovitch Peter I.;Deckman Harry W.;Johnson Jack W.;Beeckman Jean W.;Fassbender Natalie A.;Hrycenko Nadya A;Smiley Randolph J.
分类号 C01B39/02;B01J20/30;C01B39/04;B01J20/18;B01J20/282;B01D53/02;C01B37/02;C01B39/48 主分类号 C01B39/02
代理机构 代理人 Weisberg David M.
主权项 1. A method for synthesizing a DDR framework type zeolite, comprising: forming a reaction mixture capable of forming crystalline DDR framework type material, the mixture comprising water, a silicon oxide, an alkali or alkaline earth hydroxide, and a methyltropinium salt structure directing agent, the mixture having a ratio of silicon oxide to hydroxide of about 0.01 to about 1.0, a ratio of silicon oxide to alkali and alkaline earth metal of about 0.01 to about 2.0, a ratio of silicon oxide to structure directing agent of about 0.01 to about 2.0, and at least about 0.05 wt % of seeds relative to the weight of the mixture; recovering DDR framework type crystals from the reaction mixture; converting the recovered DDR framework type crystals to their H-form, wherein the H-form DDR framework type crystals have an N2 BET surface area and a methane diffusivity; and steaming the H-form DDR framework type crystals at a temperature from 426° C. to 1100° C. for a time period from about 30 minutes to about 48 hours, so as to attain one or more of the following properties: a CH4 diffusivity of no more than 95% of the CH4 diffusivity of otherwise identical but unsteamed H-form DDR framework type crystals;an N2 BET surface area from 85% to 110% of the N2 BET surface area of otherwise identical but unsteamed H-form DDR framework type crystals;following a pre-treatment at about 100° C., an equilibrium CO2 sorption capacity from 80% to 105% of the equilibrium CO2 sorption capacity of otherwise identical pre-treated but unsteamed H-form DDR framework type crystals; andfollowing a pre-treatment at about 400° C., an equilibrium CO2 sorption capacity from 80% to 105% of the equilibrium CO2 sorption capacity of otherwise identical pre-treated but unsteamed H-form DDR framework type crystals.
地址 Annandale NJ US