石油化工高等学校学报
石油化工高等學校學報
석유화공고등학교학보
JOURNAL OF PETROCHEMICAL UNIVERSITIES
2014年
2期
26-31,64
,共7页
范跃超%董世伟%秦玉才%于文宇%张磊%王红%宋丽娟
範躍超%董世偉%秦玉纔%于文宇%張磊%王紅%宋麗娟
범약초%동세위%진옥재%우문우%장뢰%왕홍%송려연
CeY分子筛%吸附脱硫%加氢脱硫油%表面酸性%催化反应
CeY分子篩%吸附脫硫%加氫脫硫油%錶麵痠性%催化反應
CeY분자사%흡부탈류%가경탈류유%표면산성%최화반응
CeY zeolite%Adsorptive desulfurization%Hydrodesulfurized fuels%Surface acidity%Catalytic reaction
用固相离子交换和液相离子交换法制备了 CeY分子筛,利用 X射线衍射(XRD)、N2物理吸附脱附、电感耦合等离子原子发射光谱仪(ICP)等方法表征了吸附剂的物理性质,借助 NH3-TPD及吡啶-原位傅里叶变换红外(Py-FTIR)技术考察了吸附剂表面的酸度分布及酸类型。采用固定床动态吸附实验和色谱-硫化学发光检测(GC-SCD)偶联技术系统考查了改性 Y分子筛对加氢脱硫燃料油的吸附脱硫性能。结果表明,4种 Y分子筛对加氢脱硫油脱硫能力大小顺序为 S-CeY>L-CeY>NaY>HY。表面酸性的差异显著地影响分子筛的吸附脱硫性能,两种方法制备的CeY分子筛表面酸性与 NaY原粉差异较大,分子筛表面B酸中心是噻吩发生催化反应的活性中心。
用固相離子交換和液相離子交換法製備瞭 CeY分子篩,利用 X射線衍射(XRD)、N2物理吸附脫附、電感耦閤等離子原子髮射光譜儀(ICP)等方法錶徵瞭吸附劑的物理性質,藉助 NH3-TPD及吡啶-原位傅裏葉變換紅外(Py-FTIR)技術攷察瞭吸附劑錶麵的痠度分佈及痠類型。採用固定床動態吸附實驗和色譜-硫化學髮光檢測(GC-SCD)偶聯技術繫統攷查瞭改性 Y分子篩對加氫脫硫燃料油的吸附脫硫性能。結果錶明,4種 Y分子篩對加氫脫硫油脫硫能力大小順序為 S-CeY>L-CeY>NaY>HY。錶麵痠性的差異顯著地影響分子篩的吸附脫硫性能,兩種方法製備的CeY分子篩錶麵痠性與 NaY原粉差異較大,分子篩錶麵B痠中心是噻吩髮生催化反應的活性中心。
용고상리자교환화액상리자교환법제비료 CeY분자사,이용 X사선연사(XRD)、N2물리흡부탈부、전감우합등리자원자발사광보의(ICP)등방법표정료흡부제적물이성질,차조 NH3-TPD급필정-원위부리협변환홍외(Py-FTIR)기술고찰료흡부제표면적산도분포급산류형。채용고정상동태흡부실험화색보-류화학발광검측(GC-SCD)우련기술계통고사료개성 Y분자사대가경탈류연료유적흡부탈류성능。결과표명,4충 Y분자사대가경탈류유탈류능력대소순서위 S-CeY>L-CeY>NaY>HY。표면산성적차이현저지영향분자사적흡부탈류성능,량충방법제비적CeY분자사표면산성여 NaY원분차이교대,분자사표면B산중심시새분발생최화반응적활성중심。
CeY zeolites were prepared by liquid phase ion exchange (LPIE)and solid state ion exchange (SSIE).The adsorbents were characterized by means of XRD,N2 physisorption,ICP and the total surface acidity of the adsorbents was monitored by NH3-TPD and in situ FTIR spectroscopy using pyridine as a probe.Properties of selective adsorptive desulfurization of HDS gasolines on the adsorbents have been investigated in this paper by using a fixed-bed adsorber and a GC-SCD technique.The adsorption capacity was found to follow the order of S-CeY>L-CeY>NaY>HY.After LPIE and SSIE, and CeY zeolites had different surface acidity from NaY and HY,which greatly affected the adsorption desulfurization process. Additionally,Br?nsted (B)acid sites was thought toresult in catalytic reaction of thiophene.