材料导报
材料導報
재료도보
MATERIALS REVIEW
2015年
16期
22-26
,共5页
田永胜%王光辉%赵磊%邱江华%曾丹林
田永勝%王光輝%趙磊%邱江華%曾丹林
전영성%왕광휘%조뢰%구강화%증단림
聚乙二醇%PEG-HPMo/SiO2%氧化脱硫%苯并噻吩
聚乙二醇%PEG-HPMo/SiO2%氧化脫硫%苯併噻吩
취을이순%PEG-HPMo/SiO2%양화탈류%분병새분
PEG%PEG-HPMo/SiO2%oxidative desulfurization%benzothiophene
分别以聚乙二醇(PEG6000)及正硅酸乙酯(TEOS)为模板剂和硅源,采用沉淀法制备了 SiO2负载型磷钼酸(HPMo)催化剂 PEG-HPMo/SiO2,对催化剂进行了 FT-IR、XRD、FE-SEM 等表征。采用 NLDFT 平衡模型对吸附-脱附等温数据进行处理,计算了催化剂的孔径分布及比表面积。研究结果表明:催化剂 PEG-HPMo/SiO2含有HPMo 的 Keggin 结构且具有较高的脱硫活性。当催化剂用量0.06 g、H 2 O2用量0.04 mL、反应温度70℃、反应时间35 min 时,10 mL 模型油中的苯并噻吩(BT)基本被完全脱除;催化剂重复使用6次后,催化剂的催化活性没有明显降低。
分彆以聚乙二醇(PEG6000)及正硅痠乙酯(TEOS)為模闆劑和硅源,採用沉澱法製備瞭 SiO2負載型燐鉬痠(HPMo)催化劑 PEG-HPMo/SiO2,對催化劑進行瞭 FT-IR、XRD、FE-SEM 等錶徵。採用 NLDFT 平衡模型對吸附-脫附等溫數據進行處理,計算瞭催化劑的孔徑分佈及比錶麵積。研究結果錶明:催化劑 PEG-HPMo/SiO2含有HPMo 的 Keggin 結構且具有較高的脫硫活性。噹催化劑用量0.06 g、H 2 O2用量0.04 mL、反應溫度70℃、反應時間35 min 時,10 mL 模型油中的苯併噻吩(BT)基本被完全脫除;催化劑重複使用6次後,催化劑的催化活性沒有明顯降低。
분별이취을이순(PEG6000)급정규산을지(TEOS)위모판제화규원,채용침정법제비료 SiO2부재형린목산(HPMo)최화제 PEG-HPMo/SiO2,대최화제진행료 FT-IR、XRD、FE-SEM 등표정。채용 NLDFT 평형모형대흡부-탈부등온수거진행처리,계산료최화제적공경분포급비표면적。연구결과표명:최화제 PEG-HPMo/SiO2함유HPMo 적 Keggin 결구차구유교고적탈류활성。당최화제용량0.06 g、H 2 O2용량0.04 mL、반응온도70℃、반응시간35 min 시,10 mL 모형유중적분병새분(BT)기본피완전탈제;최화제중복사용6차후,최화제적최화활성몰유명현강저。
PEG-HPMo/SiO2 catalysts were prepared through precipitation method using PEG6000 as template and tetraethyl orthosilicate (TEOS)as silica source.The catalysts were characterized by FT-IR,XRD and FE-SEM. Pore size distribution and specific surface area of catalysts were calculated through the NLDFT equilibrium model by using adsorption-desorption isotherm datas.Results showed that PEG-HPMo/SiO2 contained the Keggin structure as catalytic activity in HPMo.BT in 10 mL model oil can be totally removed under the conditions of catalyst 0.06 g, H 2 O2 0.04 mL,reaction temperature 70 ℃ and reaction time 35 min.The catalytic activity of PEG-HPMo/SiO2 is not significantly reduced after the catalysts was reused for 6 times.