首页|叔丁基过氧化氢催化分解制备丙酮及催化剂失活原因

叔丁基过氧化氢催化分解制备丙酮及催化剂失活原因

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以催化异丁烷和氧气为原料生成的叔丁基过氧化氢(TBHP)分解来制备丙酮.对制备丙酮的最优反应条件、催化体系、催化剂稳定性、循环利用性以及催化剂失活的原因进行了考察.结果表明,催化剂的酸性对反应的活性有明显的影响,β分子筛具有最优的催化性能(TBHP转化率为 100%),且主要产物丙酮的选择性为49%;在28 h的反应周期内,丙酮的选择性明显下降(降低21%),说明催化剂的稳定性较差,但多次(5次)再生活性仍可恢复.通过不同产物预处理催化剂,确定了丙酮的进一步反应是催化剂失活的主要原因;使用无水乙醇稀释TBHP后反应28 h的稳定性明显提高,并且催化剂的反应性能及重复利用性并未受到影响.
Acetone synthesis from catalytic decomposition of tert-butyl hydroperoxide and analysis on catalyst deactivation
Acetone was prepared from catalytic decomposition of tert-butyl hydrogen peroxide(TBHP),which was synthesized from isobutane and oxygen.The optimum reaction conditions,catalytic system,catalyst stability,recycling and the reason of catalyst deactivation in acetone synthesis were investigated.The results indicated that the acid property of catalysts had significant influence on reaction activity.β zeolite exhibited the best catalytic activity with TBHP conversion rate of 100%and the acetone selectivity of 49%.Within 28 h of the reaction cycle,the selectivity of acetone decreased significantly(decreased by 21%),indicating poor stability of the catalyst,but the multiple regeneration(5 times)activity could still be recovered.Catalyst pretreatment with different reaction products indicated that further reaction of acetone was the main reason for catalyst deactivation.After diluting TBHP with anhydrous ethanol,the stability of the reaction for 28 h was greatly improved,while the reaction performance and reusability of the catalyst were not affected.

tert-butyl hydroperoxidecatalytic decompositionβ zeolite catalystssynthesis of acetonestabilityacetone polymerizationreusability

李宁、袁孟真、徐家乐、李修仪、王国玮、祝晓琳、李春义

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中国石油大学 国家重质油重点实验室,山东 青岛 266580

叔丁基过氧化氢 催化分解 β分子筛催化剂 丙酮制备 稳定性 丙酮聚合 重复利用性

国家自然科学基金项目山东省重点研发计划项目

221783902018GGX107011

2024

精细化工
大连化工研究院设计院 中国化工学会精细化工专业委员会 辽宁省化工研究院

精细化工

CSTPCD北大核心
影响因子:0.557
ISSN:1003-5214
年,卷(期):2024.41(8)
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