催化学报
催化學報
최화학보
CHINESE JOURNAL OF CATALYSIS
2013年
12期
2236-2244
,共9页
吴江浩%蒋平平%冷炎%叶媛园%秦晓洁
吳江浩%蔣平平%冷炎%葉媛園%秦曉潔
오강호%장평평%랭염%협원완%진효길
双核离子液体%多金属氧酸盐%烯烃%环氧化反应%相转移催化剂
雙覈離子液體%多金屬氧痠鹽%烯烴%環氧化反應%相轉移催化劑
쌍핵리자액체%다금속양산염%희경%배양화반응%상전이최화제
Dicationic ionic liquid%Polyoxometalate%Olefin%Epoxidation%Phase transfer catalyst
合成并表征了一类双核长链烷基咪唑阳离子修饰的过氧磷钨杂多酸盐催化剂[Dnmin]1.5PW4O24,考察了催化剂在过氧化氢为氧源的烯烃环氧化反应中的催化活性.研究表明,这类催化剂在反应过程中表现出相转移催化现象,并具有较高的催化活性和选择性.其中,双核十二烷基咪唑杂多酸盐催化剂[D12min]1.5PW4O24的活性最佳,其环己烯转化率和环氧环己烷选择性分别达到97.7%和96.3%.催化剂在经过简单离心分离后可重复使用,重复使用4次后环己烯转化率和环氧环己烷选择性仍可分别达到72.4%和97.2%.催化剂[D12min]1.5PW4O24在其它几种烯烃的环氧化反应中均表现出相转移催化特性,且具有较高的催化活性.
閤成併錶徵瞭一類雙覈長鏈烷基咪唑暘離子脩飾的過氧燐鎢雜多痠鹽催化劑[Dnmin]1.5PW4O24,攷察瞭催化劑在過氧化氫為氧源的烯烴環氧化反應中的催化活性.研究錶明,這類催化劑在反應過程中錶現齣相轉移催化現象,併具有較高的催化活性和選擇性.其中,雙覈十二烷基咪唑雜多痠鹽催化劑[D12min]1.5PW4O24的活性最佳,其環己烯轉化率和環氧環己烷選擇性分彆達到97.7%和96.3%.催化劑在經過簡單離心分離後可重複使用,重複使用4次後環己烯轉化率和環氧環己烷選擇性仍可分彆達到72.4%和97.2%.催化劑[D12min]1.5PW4O24在其它幾種烯烴的環氧化反應中均錶現齣相轉移催化特性,且具有較高的催化活性.
합성병표정료일류쌍핵장련완기미서양리자수식적과양린오잡다산염최화제[Dnmin]1.5PW4O24,고찰료최화제재과양화경위양원적희경배양화반응중적최화활성.연구표명,저류최화제재반응과정중표현출상전이최화현상,병구유교고적최화활성화선택성.기중,쌍핵십이완기미서잡다산염최화제[D12min]1.5PW4O24적활성최가,기배기희전화솔화배양배기완선택성분별체도97.7%화96.3%.최화제재경과간단리심분리후가중복사용,중복사용4차후배기희전화솔화배양배기완선택성잉가분별체도72.4%화97.2%.최화제[D12min]1.5PW4O24재기타궤충희경적배양화반응중균표현출상전이최화특성,차구유교고적최화활성.
Peroxopolyoxotungsten-based hybrid catalysts modified by dicationic long-chain alkyl imidazolium cations have been synthesized and characterized. The catalytic activity of the catalysts was meas-ured for the epoxidation of olefins with H2O2. These catalysts proved to be high catalytic activity phase transfer catalysts. In particular, for the catalyst [D12min]1.5PW4O24 modified by the dodecyl dicationic imidazolium cation, the conversion of cyclohexene and selectivity for epoxycyclohexane were 97.7%and 96.3%, respectively. After the reaction, the catalyst could be recovered simply by filtration and reused four times. The conversion of cyclohexene and selectivity for epoxycyclohex-ane were still 72.4%and 97.2%, respectively, after recycling the catalyst four times. In addition, this phase transfer catalyst can be applied to the epoxidation of a wide range of olefins.