物理化学学报
物理化學學報
물이화학학보
ACTA PHYSICO-CHIMICA SINICA
2014年
12期
2315-2322
,共8页
王沾祺%周志明%张锐%李莉%程振民
王霑祺%週誌明%張銳%李莉%程振民
왕첨기%주지명%장예%리리%정진민
Pd-Cu/γ-Al2O3%选择性加氢%苯乙炔%苯乙烯%结构-性能关系
Pd-Cu/γ-Al2O3%選擇性加氫%苯乙炔%苯乙烯%結構-性能關繫
Pd-Cu/γ-Al2O3%선택성가경%분을결%분을희%결구-성능관계
Pd-Cu/γ-Al2O3%Selective hydrogenation%Phenylacetylene%Styrene%Structure-performance relationship
为了提高苯乙炔加氢反应中的苯乙烯选择性,本文采用“胶体-等体积浸渍”两步法制备了Pd-Cu/γ-Al2O3双金属催化剂.利用高分辨率透射电镜(HRTEM)、X射线光电子能谱(XPS)、CO脉冲化学吸附、N2物理吸附、电感耦合等离子体原子发射光谱(ICP-AES)等技术表征了Pd-Cu/γ-Al2O3的结构性质,考察了Cu/Pd摩尔比、Pd负载量以及金属引入顺序对Pd-Cu/γ-Al2O3催化苯乙炔选择性加氢性能的影响.结果表明,与Pd/γ-Al2O3单金属催化剂相比, Pd-Cu/γ-Al2O3的苯乙烯选择性大幅度提高,尤其是当Pd负载量为0.3%(w),且Cu/Pd摩尔比为0.6时, Pd-Cu/γ-Al2O3表现出优异的加氢选择性;在0.1 MPa和40°C下,当苯乙炔转化率为90%时,双金属催化剂的苯乙烯选择性可达95%;当转化率达到99%以上时,苯乙烯选择性仍保持在82%左右.分析表明, Pd-Cu/γ-Al2O3中形成了Pd-Cu合金,但是两种金属间不存在电子转移, Cu对Pd的几何效应才是导致Pd-Cu/γ-Al2O3苯乙烯选择性增加的主要原因.
為瞭提高苯乙炔加氫反應中的苯乙烯選擇性,本文採用“膠體-等體積浸漬”兩步法製備瞭Pd-Cu/γ-Al2O3雙金屬催化劑.利用高分辨率透射電鏡(HRTEM)、X射線光電子能譜(XPS)、CO脈遲化學吸附、N2物理吸附、電感耦閤等離子體原子髮射光譜(ICP-AES)等技術錶徵瞭Pd-Cu/γ-Al2O3的結構性質,攷察瞭Cu/Pd摩爾比、Pd負載量以及金屬引入順序對Pd-Cu/γ-Al2O3催化苯乙炔選擇性加氫性能的影響.結果錶明,與Pd/γ-Al2O3單金屬催化劑相比, Pd-Cu/γ-Al2O3的苯乙烯選擇性大幅度提高,尤其是噹Pd負載量為0.3%(w),且Cu/Pd摩爾比為0.6時, Pd-Cu/γ-Al2O3錶現齣優異的加氫選擇性;在0.1 MPa和40°C下,噹苯乙炔轉化率為90%時,雙金屬催化劑的苯乙烯選擇性可達95%;噹轉化率達到99%以上時,苯乙烯選擇性仍保持在82%左右.分析錶明, Pd-Cu/γ-Al2O3中形成瞭Pd-Cu閤金,但是兩種金屬間不存在電子轉移, Cu對Pd的幾何效應纔是導緻Pd-Cu/γ-Al2O3苯乙烯選擇性增加的主要原因.
위료제고분을결가경반응중적분을희선택성,본문채용“효체-등체적침지”량보법제비료Pd-Cu/γ-Al2O3쌍금속최화제.이용고분변솔투사전경(HRTEM)、X사선광전자능보(XPS)、CO맥충화학흡부、N2물리흡부、전감우합등리자체원자발사광보(ICP-AES)등기술표정료Pd-Cu/γ-Al2O3적결구성질,고찰료Cu/Pd마이비、Pd부재량이급금속인입순서대Pd-Cu/γ-Al2O3최화분을결선택성가경성능적영향.결과표명,여Pd/γ-Al2O3단금속최화제상비, Pd-Cu/γ-Al2O3적분을희선택성대폭도제고,우기시당Pd부재량위0.3%(w),차Cu/Pd마이비위0.6시, Pd-Cu/γ-Al2O3표현출우이적가경선택성;재0.1 MPa화40°C하,당분을결전화솔위90%시,쌍금속최화제적분을희선택성가체95%;당전화솔체도99%이상시,분을희선택성잉보지재82%좌우.분석표명, Pd-Cu/γ-Al2O3중형성료Pd-Cu합금,단시량충금속간불존재전자전이, Cu대Pd적궤하효응재시도치Pd-Cu/γ-Al2O3분을희선택성증가적주요원인.
A two-step method combining col oid synthesis and incipient wetness impregnation was developed for the preparation of bimetal ic Pd-Cu/γ-Al2O3 catalysts, with the aim of increasing the selectivity to styrene in the selective hydrogenation of phenylacetylene. The structural properties of the catalysts were characterized using high-resolution transmission electron microscopy (HRTEM), X-ray photoelectron spectroscopy (XPS), CO-pulse chemisorption, N2 physisorption, and inductively coupled plasma atomic emission spectrometry (ICP-AES). The effects of changing the Cu/Pd molar ratio, the Pd loading, and the order in which the Pd and Cu were introduced into the catalysts on the catalytic activity and selectivity were investigated. The results showed that Pd-Cu/γ-Al2O3 exhibited much higher selectivity toward styrene than Pd/γ-Al2O3. In particular, Pd-Cu/γ-Al2O3 with a Pd loading of 0.3%(w) and a Cu/Pd molar ratio of 0.6 displayed excel ent performance at 40 °C under 0.1 MPa H2, with a high selectivity of 95%at a conversion of 90%, and a selectivity of approximately 82%, even at conversions of higher than 99%. The increased selectivity of Pd-Cu/γ-Al2O3 was ascribed mainly to the geometrical effects of the Pd-Cu bimetal ic al oys, rather than the electronic effects, since no electron transfer occurred between Pd and Cu.