天然气化工
天然氣化工
천연기화공
NATURAL GAS CHEMICAL INDUSTRY
2015年
1期
1-5
,共5页
范素兵%申达%吕俊敏%张建利%赵天生
範素兵%申達%呂俊敏%張建利%趙天生
범소병%신체%려준민%장건리%조천생
多级孔ZSM-5%催化剂%甲醇制丙烯(MTP)%十六烷基三甲基溴化铵(CTAB)
多級孔ZSM-5%催化劑%甲醇製丙烯(MTP)%十六烷基三甲基溴化銨(CTAB)
다급공ZSM-5%최화제%갑순제병희(MTP)%십륙완기삼갑기추화안(CTAB)
hierarchical ZSM-5%catalyst%methanol to propylene (MTP)%cetyltrimethylammonium bromide (CTAB)
以十六烷基三甲基溴化铵(CTAB)为介孔导向剂水热晶化法合成了介孔孔容可控的多级孔ZSM-5分子筛,并考察了其多级孔性质及表面酸性质对甲醇制丙烯(MTP)反应产物分布的影响。结果表明:CTAB的添加基本没有影响晶体的结晶度及比表面积,但明显减小了晶粒大小;介孔孔容增大,改善了分子扩散能力,抑制了氢转移二次反应,有利于丙烯及低碳烯烃(C2=~C4=)总选择性的提高;而表面酸量增加却促进了氢转移二次反应,引起丙烯及低碳烯烃的选择性降低、烷烃及C5+高碳组分选择性增加,不利于低碳烯烃的生成。
以十六烷基三甲基溴化銨(CTAB)為介孔導嚮劑水熱晶化法閤成瞭介孔孔容可控的多級孔ZSM-5分子篩,併攷察瞭其多級孔性質及錶麵痠性質對甲醇製丙烯(MTP)反應產物分佈的影響。結果錶明:CTAB的添加基本沒有影響晶體的結晶度及比錶麵積,但明顯減小瞭晶粒大小;介孔孔容增大,改善瞭分子擴散能力,抑製瞭氫轉移二次反應,有利于丙烯及低碳烯烴(C2=~C4=)總選擇性的提高;而錶麵痠量增加卻促進瞭氫轉移二次反應,引起丙烯及低碳烯烴的選擇性降低、烷烴及C5+高碳組分選擇性增加,不利于低碳烯烴的生成。
이십륙완기삼갑기추화안(CTAB)위개공도향제수열정화법합성료개공공용가공적다급공ZSM-5분자사,병고찰료기다급공성질급표면산성질대갑순제병희(MTP)반응산물분포적영향。결과표명:CTAB적첨가기본몰유영향정체적결정도급비표면적,단명현감소료정립대소;개공공용증대,개선료분자확산능력,억제료경전이이차반응,유리우병희급저탄희경(C2=~C4=)총선택성적제고;이표면산량증가각촉진료경전이이차반응,인기병희급저탄희경적선택성강저、완경급C5+고탄조분선택성증가,불리우저탄희경적생성。
The hierarchical ZSM-5 zeolites with controllable mesopore volumes were synthesized using surfactant cetyltrimethylammonium bromide (CTAB) as mesoporous structure directing agent by the soft-template hydrothermal crystallization method, and the effects of their hierarchy and acidity on the product distribution in the reaction of methanol to propylene (MTP) were investigated. Results showed that the introduction of CTAB didn’t affect the crystallinity and specific surface area of the zeolites, but reduced the crystal size. The increased mesopore volumes enhanced the molecule diffusion and inhibited the secondary reaction of hydrogen transfer, which improved propylene selectivity and total light olefin selectivity of ethylene, propylene and butene. However, the increased acid amount promoted the hydrogen transfer reaction, resulting in decrease of the selectivities of propylene and total light olefins, and increase of the selectivities of alkanes and C5+hydrocarbons, which were unfavorable for the formation of olefins.