催化学报
催化學報
최화학보
CHINESE JOURNAL OF CATALYSIS
2009年
10期
1041-1048
,共8页
范闽光%李斌%张飞跃%方金龙%李望良%邢建民%刘自力
範閩光%李斌%張飛躍%方金龍%李望良%邢建民%劉自力
범민광%리빈%장비약%방금룡%리망량%형건민%류자력
HY分子筛%铜%镧%吸附剂%修饰%二苯并噻吩%吸附脱硫
HY分子篩%銅%鑭%吸附劑%脩飾%二苯併噻吩%吸附脫硫
HY분자사%동%란%흡부제%수식%이분병새분%흡부탈류
HY zeolite%copper%lanthanum%adsorbent%modification%dibenzothiophene%adsorption desulfurization
在氮气气氛下采用等体积浸渍法制备了载Cu的HY和LaHY分子筛.用x射线衍射(XRD)、N2吸附、氨程序升温脱附和X射线光电子能谱对分子筛进行了表征.通过多晶XRD确定了Cu~(2+)离子在Y型分子筛笼内的结构与分布,并测定了分子筛在含二苯并噻吩(DBT)的模拟柴油中的吸附脱硫性能.结果表明,前驱体CuCl_2中的大部分Cu物种与HY和LaHY分子筛进行了离子交换.对于La~(3+)改性的CuHY分子筛(CuLaHY),进入分子筛超笼中的Cu~(2+)离子与骨架氧和水分子配位,牢固地定位于Y型分子筛超笼的SⅡ及SⅢ位;对于CuHY分子筛,超笼中的Cu~(2+)离子只接近于SⅡ及SⅢ位.极少部分CuCl分子高度分散在分子筛笼内,没有定位.处于超笼中SⅡ及SⅢ位的Cu~(2+)离子对模拟柴油中的DBT分子具有吸附作用,是吸附脱硫的活性中心.CuLaHY分子筛的吸附脱硫性能优于CuHY分子筛.当模拟柴油中含有萘时,萘与DBT分子会产生竞争吸附.
在氮氣氣氛下採用等體積浸漬法製備瞭載Cu的HY和LaHY分子篩.用x射線衍射(XRD)、N2吸附、氨程序升溫脫附和X射線光電子能譜對分子篩進行瞭錶徵.通過多晶XRD確定瞭Cu~(2+)離子在Y型分子篩籠內的結構與分佈,併測定瞭分子篩在含二苯併噻吩(DBT)的模擬柴油中的吸附脫硫性能.結果錶明,前驅體CuCl_2中的大部分Cu物種與HY和LaHY分子篩進行瞭離子交換.對于La~(3+)改性的CuHY分子篩(CuLaHY),進入分子篩超籠中的Cu~(2+)離子與骨架氧和水分子配位,牢固地定位于Y型分子篩超籠的SⅡ及SⅢ位;對于CuHY分子篩,超籠中的Cu~(2+)離子隻接近于SⅡ及SⅢ位.極少部分CuCl分子高度分散在分子篩籠內,沒有定位.處于超籠中SⅡ及SⅢ位的Cu~(2+)離子對模擬柴油中的DBT分子具有吸附作用,是吸附脫硫的活性中心.CuLaHY分子篩的吸附脫硫性能優于CuHY分子篩.噹模擬柴油中含有萘時,萘與DBT分子會產生競爭吸附.
재담기기분하채용등체적침지법제비료재Cu적HY화LaHY분자사.용x사선연사(XRD)、N2흡부、안정서승온탈부화X사선광전자능보대분자사진행료표정.통과다정XRD학정료Cu~(2+)리자재Y형분자사롱내적결구여분포,병측정료분자사재함이분병새분(DBT)적모의시유중적흡부탈류성능.결과표명,전구체CuCl_2중적대부분Cu물충여HY화LaHY분자사진행료리자교환.대우La~(3+)개성적CuHY분자사(CuLaHY),진입분자사초롱중적Cu~(2+)리자여골가양화수분자배위,뢰고지정위우Y형분자사초롱적SⅡ급SⅢ위;대우CuHY분자사,초롱중적Cu~(2+)리자지접근우SⅡ급SⅢ위.겁소부분CuCl분자고도분산재분자사롱내,몰유정위.처우초롱중SⅡ급SⅢ위적Cu~(2+)리자대모의시유중적DBT분자구유흡부작용,시흡부탈류적활성중심.CuLaHY분자사적흡부탈류성능우우CuHY분자사.당모의시유중함유내시,내여DBT분자회산생경쟁흡부.
The Cu-loaded CuHY and CuLaHY zeolites were prepared by an incipient wetness method under nitrogen gas atmosphere. The samples were characterized by X-ray diffraction (XRD), N_2 adsorption, NH_3 temperature-programmed desorption, and X-ray photoelectron spectroscopy. The crystalline structure and the distribution of Cu~(2+) cations in the cages of Y zeolite were determined by XRD. The adsorption desulfurization performance of the zeolites was investigated for model diesel containing dibenzothiophene (DBT). The results showed that most of Cu species from the precursor CuCl_2 was ion-exchanged with the HY and LaHY zeolites. For the La3+-modified CuHY zeolite (CuLaHY), the Cu~(2+) cations entering the supercages of the zeolite coordinated with both skeleton-oxygen atoms and water molecules, and thus being firmly situated at the sites Sn and Snr in the supercages. For the CuHY zeolite, however, Cu~(2+) cations entering the supercages were only near the sites Sn and Sm in the supercages. A very small percentage of CuCl molecules was highly scattered in the cages of the Y zeolite, with no definite position. The Cu~(2+) cations at the sites Sn and Snr in the supercages adsorbed DBT molecules in the model diesel were the centers of adsorption desulfurization. The desulfurization capacity of the CuLaHY zeolite was better as compared with the CuHY zeolite. However, naphthalene molecules will result in competitive adsorption with DBT molecules if there are naphthalene molecules in the model diesel.