CN106362798A - 一种用于液相工艺中生产甲缩醛的催化剂 - Google Patents

一种用于液相工艺中生产甲缩醛的催化剂 Download PDF

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CN106362798A
CN106362798A CN201610544029.5A CN201610544029A CN106362798A CN 106362798 A CN106362798 A CN 106362798A CN 201610544029 A CN201610544029 A CN 201610544029A CN 106362798 A CN106362798 A CN 106362798A
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oxygen
methanol
salt
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邓志勇
李美兰
王公应
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Chengdu Organic Chemicals Co Ltd of CAS
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    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/16Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/18Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms
    • B01J31/1805Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms the ligands containing nitrogen
    • B01J31/181Cyclic ligands, including e.g. non-condensed polycyclic ligands, comprising at least one complexing nitrogen atom as ring member, e.g. pyridine
    • B01J31/1815Cyclic ligands, including e.g. non-condensed polycyclic ligands, comprising at least one complexing nitrogen atom as ring member, e.g. pyridine with more than one complexing nitrogen atom, e.g. bipyridyl, 2-aminopyridine
    • B01J31/182Cyclic ligands, including e.g. non-condensed polycyclic ligands, comprising at least one complexing nitrogen atom as ring member, e.g. pyridine with more than one complexing nitrogen atom, e.g. bipyridyl, 2-aminopyridine comprising aliphatic or saturated rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C41/00Preparation of ethers; Preparation of compounds having groups, groups or groups
    • C07C41/48Preparation of compounds having groups
    • C07C41/50Preparation of compounds having groups by reactions producing groups
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2231/00Catalytic reactions performed with catalysts classified in B01J31/00
    • B01J2231/70Oxidation reactions, e.g. epoxidation, (di)hydroxylation, dehydrogenation and analogues
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2531/00Additional information regarding catalytic systems classified in B01J31/00
    • B01J2531/02Compositional aspects of complexes used, e.g. polynuclearity
    • B01J2531/0238Complexes comprising multidentate ligands, i.e. more than 2 ionic or coordinative bonds from the central metal to the ligand, the latter having at least two donor atoms, e.g. N, O, S, P
    • B01J2531/0241Rigid ligands, e.g. extended sp2-carbon frameworks or geminal di- or trisubstitution
    • B01J2531/0252Salen ligands or analogues, e.g. derived from ethylenediamine and salicylaldehyde
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2531/00Additional information regarding catalytic systems classified in B01J31/00
    • B01J2531/80Complexes comprising metals of Group VIII as the central metal
    • B01J2531/82Metals of the platinum group
    • B01J2531/821Ruthenium

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Inorganic Chemistry (AREA)
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Abstract

本发明涉及一种用于液相工艺中生产甲缩醛的催化剂,所使用的原料气可为氧气、空气或者其它含氧混合气体;本发明所述的Ru基催化剂可为含氮有机配体与Ru盐络合物(含氮配体与Ru盐的摩尔比为0~4),催化剂使用浓度为0.0001~0.1g/ml。一般工艺为:在高压反应釜中加入甲醇、含氧气体、催化剂,在反应温度为60~180℃、反应压力为0.5~5MPa条件下合成甲缩醛。

Description

一种用于液相工艺中生产甲缩醛的催化剂
技术领域
本发明涉及一种甲醇与含氧气体在液相工艺条件下,一步氧化生成甲缩醛的催化剂,属于化工领域。
背景技术
甲缩醛(Methylal),化学名称为二甲氧基甲烷(Dimethoxymethane,DMM),因具有低毒、低沸点、良好的溶解性以及与水相溶性,是一种优良的环保型溶剂,也是重要的化工中间体。甲缩醛具有高含氧量,其氧的质量分数为42.1%,且无C-C键,是一种高潜力的油品添加剂。在柴油中添加质量分数为5%~10%的甲缩醛,可有效改善发动机内的燃烧性能,降低排放尾气中HC和CO的含量,减少环境污染。甲缩醛还是一种高值的甲醇下游产品,因此开发甲缩醛产业不仅有利于缓解甲醇产能过剩,同时对环境保护具有重要意义。
目前工业上用来生产甲缩醛的方法是甲醇与甲醛缩合法,包括两步:第一步是甲醇在银或者铁钼催化剂作用下生成甲醛;第二步是甲醇与甲醛再在酸催化剂作用下生成甲缩醛。该工艺是现今甲缩醛生产的主要工艺,已比较成熟,但存在反应温度高,催化剂活性较低及设备腐蚀严重等问题,并且工艺流程复杂,导致生产成本居高不下。因此从经济性和环境保护角度出发,国内外研究者对甲醇一步氧化法制甲缩醛越来越感兴趣。
针对甲醇一步氧化制甲缩醛催化剂的研究,多数集中在气相连续工艺中,并在此工艺条件下开发了多种催化剂体系。研究者们考察了载体负载的Re基催化剂在催化甲醇一步氧化甲缩醛反应上的性能差异。相对而言Re/TiO2、Re/γ-Fe2O3催化剂比较具有优势,性能较好,但甲缩醛的收率并不高,不足以制备出高纯度的甲缩醛产品(Yuan Y Z,Liu H C,Imoto H,et al.Performance and characterization of a new crystalline SbRe2O6catalyst for selective oxidation of methanol to methylal[J].Journal ofCatalysis,2000.195(1):51-61.Nikonova O A,Capron M,Fang G,et al.Novel approachto rhenium oxide catalysts for selective oxidation of methanol to DMM[J].Journal of Catalysis,2011.279(2):310-318.)。近年来针对V基催化剂的研究比较多,研究者们***的考察了其负载在不同结构TiO2载体上的催化性能差异,取得了较好结果。虽然V廉价易得,但有较大毒性,不利于环境保护(Zhao H,Bennici S,Shen J,etal.Calorimetric study of the acidic character of V2O5-TiO2/SO4 2-catalysts usedin methanol oxidation to dimethoxymethane[J].Journal of Thermal Analysis andCalorimetry,2010.99(3):843-847.Guo H Q,Li D B,Chen C B,et al.One-StepOxidation of Methanol to Dimethoxymethane on V2O5/CeO2 Catalyst[J].ChineseJournal of Catalysis,2012.33(5):813-818.)。也有将杂多酸经SiO2负载作为该反应的催化剂,且用V改性后具有较高的甲缩醛选择性(Zhang Q D,Tan Y S,Yang C H,etal.MnCl2modified H4SiW12O40/SiO2 catalysts for catalytic oxidation of dimethyether to dimethoxymethane[J].Journal of Molecular Catalysis a-Chemical,2007.263(1-2):149-155.)。
而用在液相间歇工艺条件下,甲醇与氧气一步合成制甲缩醛反应的催化剂,目前报道的只有一种铜含氮配体催化剂(刘鹏,邓志勇,杨先贵,等.CuCl/肟配合物催化甲醇液相一步氧化生成二甲氧基甲烷[J].天然气化工:Cl化学与化工.2013,(06):16-19),该催化剂对甲缩醛的选择性较高,但催化剂寿命差。
发明内容
本发明使用Ru基催化剂,将甲醇与含氧气体在液相工艺条件下一步氧化合成甲缩醛。所使用的Ru基催化剂为Ru盐与含氮有机配合物,或者仅为Ru盐;其中含氮配体可为具有以下骨架的双齿、多齿含氮化合物:如1,2-环己二酮二肟、乙二肟、丁二酮肟等化合物及其它们的衍生物;Ru盐可为其卤化物、硫酸盐、硝酸盐等化合物。
本发明一般反应条件为:催化剂中的含氮配体与Ru盐的摩尔比为0~4,催化剂用量0.0001~0.1g/ml,温度60℃~180℃,压力0.5MPa~5.0MPa。
本发明中所使用的催化剂极具有工业应用前景。
具体实施例
下面通过具体实施例对本发明做进一步阐述。
[实施例1]在100ml高反反应釜中加入甲醇20ml(15.8g),水合三氯化钌0.1g,1,2-环己二酮二肟0.0171g;用O2置换反应釜内空气后,再充入2.0MPa的O2;釜内压力稳定后,开始搅拌(500r/min)并升温,反应温度110℃,反应时间40min。使用气相色谱内标法对反应产物进行分析,结果列于表1中。
[实施例2~4]改变1,2-环己二酮二肟的使用量,其它条件与[实施例1]相同,产物分析结果列于表1中。
[实施例5]在100ml高反反应釜中加入甲醇20ml(15.8g),水合三氯化钌0.1g;用O2置换反应釜内空气后,再充入2.0MPa的O2;釜内压力稳定后,开始搅拌(500r/min)并升温,反应温度110℃,反应时间40min。使用气相色谱内标法对反应产物进行分析,结果列于表1中。
[实施例6~7]改变水合三氯化钌的使用量,其它条件与[实施例5]相同,产物分析结果列于表1中。
[实施例8~9]改变通入反应釜内的O2压力,其它条件与[实施例5]相同,产物分析结果列于表1中。
[实施例10~11]改变反应温度,压力为3MPa,其它条件与[实施例5]相同,产物分析结果列于表1中。
表1 各实施例产物分析结果

Claims (6)

1.一种在液相工艺条件下,甲醇与氧气直接一步合成甲缩醛的Ru基催化剂。
2.根据权利要求1所述,其特征在于所使用的原料气可为氧气、空气以及其他含氧混合气体。
3.根据权利要求1所述的Ru基催化剂,其特征在于Ru盐与含氮配体直接混合或者预先络合作为催化剂使用;其中Ru盐可为其卤化物、硫酸盐、硝酸盐等化合物,含氮配体为具有以下骨架的双齿、多齿含氮化合物:如1,2-环己二酮二肟、乙二肟、丁二酮二肟等。
4.根据权利要求1所述的Ru基催化剂,其特征在于使用的含氮配体与Ru盐的摩尔比为0~4。
5.根据权利要求1所述的Ru基催化剂,其特征在于催化剂使用浓度为0.0001~0.1g/ml。
6.根据权利要求1所述的Ru基催化剂,其特征在于反应温度为60~180℃、反应压力为0.5~5MPa。
CN201610544029.5A 2015-07-24 2016-07-12 一种用于液相工艺中生产甲缩醛的催化剂 Pending CN106362798A (zh)

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Cited By (1)

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN107413386A (zh) * 2017-08-21 2017-12-01 中国科学院成都有机化学有限公司 一种甲醇液相一步氧化合成甲缩醛的催化剂及其制备方法和使用方法
CN107413386B (zh) * 2017-08-21 2020-11-24 中国科学院成都有机化学有限公司 一种甲醇液相一步氧化合成甲缩醛的催化剂及其制备方法和使用方法

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