CN107915607A - The preparation method of polyoxymethylene dimethyl ether - Google Patents

The preparation method of polyoxymethylene dimethyl ether Download PDF

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Publication number
CN107915607A
CN107915607A CN201610881533.4A CN201610881533A CN107915607A CN 107915607 A CN107915607 A CN 107915607A CN 201610881533 A CN201610881533 A CN 201610881533A CN 107915607 A CN107915607 A CN 107915607A
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preparation
catalyst
cation exchange
exchange resin
dimethyl ether
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CN107915607B (en
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高晓晨
石竹
缪晓春
吴征
柏诗哲
朱桂莲
范弢
高焕新
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China Petroleum and Chemical Corp
Sinopec Shanghai Research Institute of Petrochemical Technology
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China Petroleum and Chemical Corp
Sinopec Shanghai Research Institute of Petrochemical Technology
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    • 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
    • C07C41/56Preparation of compounds having groups by reactions producing groups by condensation of aldehydes, paraformaldehyde, or ketones
    • 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
    • B01J31/02Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
    • B01J31/06Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing polymers
    • B01J31/08Ion-exchange resins
    • B01J31/10Ion-exchange resins sulfonated

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
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Abstract

The present invention relates to the preparation method of polyoxymethylene dimethyl ether, mainly solve the problems, such as the prior art using methanol and paraformaldehyde as reaction raw materials synthesizing polyoxymethylene dimethyl ether technique in there are catalyst activity it is low, selectivity it is low, by using the preparation method of polyoxymethylene dimethyl ether, using methanol and paraformaldehyde as raw material, raw material is contacted with polyoxymethylene dimethyl ethers catalyst, reaction generation polyoxymethylene dimethyl ether;The catalyst is the sulfonic acid polystyrene cation exchange resin of modified metal ion modification, and the sulfonic acid polystyrene cation exchange resin includes crosslinked polystyrene skeleton and sulfonic acid group;The modified metal includes the technical solution of VIII group element, available in the industrial production of polyoxymethylene dimethyl ether.

Description

The preparation method of polyoxymethylene dimethyl ether
Technical field
The present invention relates to the preparation method of polyoxymethylene dimethyl ether.
Background technology
In recent years, with the resource grid that the industrial revolution influences to go deep into increasingly and China is distinctive " more coals, less oil, have gas " Office, China's oil resource growing tension, oil supply pressure unprecedentedly increase.It is expected that 10~20 years following, China's oil supply rate Only~50%.The energy crisis that China how is solved using the coal resources of China's abundant is become as researcher urgent need solution Certainly the problem of.Therefore the attention that new oil product substitute is increasingly subject to people is developed by coal-based methanol.
Dimethyl ether is proposed as a kind of procetane earliest, yet with its own cold starting performance is poor, room temperature Lower vapour pressure is high, easily produces vapour lock make it that dimethyl ether is significantly raised as the cost of vehicle alternative fuel.Polyoxymethylene dimethyl ether, That is Polyoxymethylene dimethyl ethers (PODE), are the common names of a kind of material, its skeleton symbol can be expressed as CH3O(CH2O)nCH3, have higher octane number (>And oxygen content (42~51%) 30).When the value of n is 2~10, its thing Rationality matter, combustibility and diesel oil are very close, preferably resolve dimethyl ether and are lacked as existing for derv fuel blend component Fall into.Therefore polyoxymethylene dimethyl ether can be as new cleaning diesel component, and the additive amount in diesel oil, can up to 30% (v/v) To improve the combustion position of diesel oil within the engine, the thermal efficiency is improved, reduces particulate matter and CO in tail gasxAnd NOxRow Put.It is reported that the CH of addition 5~30%3OCH2OCH3NO can be reducedxDischarging 7~10%, PM reduces by 5~35%.By coal Ji Jia Alcohol synthesis PODE can not only substitute part diesel oil, moreover it is possible to improve the efficiency of combustion of diesel oil, reduce danger of the diesel combustion to environment Evil, has important strategic importance and good economic value.
CN 101048357A (method for preparing polyoxymethylene dimethyl ether) are described using inorganic acid, sulfonic acid, heteropoly acid, acid Property ion exchange resin, zeolite, aluminium oxide etc. are used as catalyst, are reactant synthesizing polyoxymethylene by dimethoxym ethane and metaformaldehyde The method of dimethyl ether.But using the conversion ratio and selectivity of existing catalyst all up for improving.
Cation exchange resin is shown good as solid acid catalyst in the esterification, etherification reaction in Aquo System Catalytic perfomance, but its acid strength is relatively low.Generally use prepares support type resin, makes activity by increasing acidity of catalyst It is improved.Metal-modified resin can be used, new acid site is formed on a catalyst, can't be handed over by other metal ions Change, which solves in polyoxymethylene dimethyl ether synthesis, catalyst keeps high activity in commercial Application in the case of and it is acid not The problem of being substituted by metal ion contained in raw material and inactivating.
The content of the invention
The technical problems to be solved by the invention are that the prior art synthesizes poly- first using methanol and paraformaldehyde as reaction raw materials In aldehyde dimethyl ether technique there are n=2-10 selectivity of product it is low the problem of, there is provided a kind of generation of new polyoxymethylene dimethyl ethers Method.The catalyst has the advantages that the selectivity of product of n=2-10 is high.
In order to solve the above technical problems, technical solution of the present invention is as follows:The preparation method of polyoxymethylene dimethyl ether, with methanol and Paraformaldehyde is raw material, and raw material is contacted with polyoxymethylene dimethyl ethers catalyst, reaction generation polyoxymethylene dimethyl ether;The catalyst For the sulfonic acid polystyrene cation exchange resin of modified metal ion modification, the sulfonic acid polystyrene cation exchange Resin includes crosslinked polystyrene skeleton and sulfonic acid group;The modified metal includes VIII group element.
By the element modified sulfonic acid polystyrene cation exchange resin of VIII group, significantly improve to n=2~10 The selectivity of PODE.
In above-mentioned technical proposal, preferably, the modified metal further includes Cu, Cu is with VIII group element in raising pair There is synergistic effect in terms of the selectivity of the PODE of n=2~10.Ratio between Cu and VIII group element is not particularly limited, As long as Cu and VIII group element are present in catalyst at the same time can obtain comparable synergy.
As non-restrictive, the mass ratio of Cu and VIII group element is 0.01~100, further non-within this range Limited citing such as 0.1,0.5,0.8,1,1.5,2,3,4,5,6,7,8,9,10 etc..
In above-mentioned technical proposal, the VIII group element is selected from least one of Fe, Co and Ni.
In above-mentioned technical proposal, more preferably described modified metal includes at least two and Cu in Fe, Co and Ni, this When above two VIII elements between improve to the selectivity of the PODE of n=2~10 in terms of have synergistic effect.At this time, Ni, Ratio between Co and Fe is not particularly limited, as long as at least two in Ni, Co and Fe are present in equal energy in catalyst at the same time Comparable synergy is obtained, such as, but not limited between Co and Ni, between Ni and Fe.
As non-restrictive, the mass ratio between above two VIII elements is 0.01~100, within this range into One step non-restrictive such as 0.1,0.5,0.8,1,1.5,2,3,4,5,6,7,8,9,10 etc..
As most preferred technical solution, the modified metal includes Fe, Co, Ni and Cu at the same time, at this time to n=2~10 The selectivity of PODE reach best.
In above-mentioned technical proposal, the content of modified metal is not particularly limited in catalyst, such as, but not limited to catalyst The content of middle modified metal is more than 0 and is less than or equal to 10w%.
In above-mentioned technical proposal, the full exchange capacity of the resin is preferably 3.0~6.0mmol/g.
In above-mentioned technical proposal, the resin can be gel-type or macroporous type.
The preparation method of catalyst, is included in catalytic amount any one of the technical solution of one of above-mentioned technical problem Acid in the presence of, the sulfonic acid polystyrene cation exchange resin is connect with the suspension containing the modified metal-oxide Touch and carry out ion exchange.
In above-mentioned technical proposal, the acid is not particularly limited, as long as can be with being reacted containing the modified metal-oxide Obtained salt can be dissolved in solvent used in the suspension can, be such as, but not limited under this principle hydrochloric acid, nitric acid or At least one of carboxylic acid of C2~C10.
In above-mentioned technical proposal, the carboxylic acid can be hydroxyl substituted carboxylic acid, such as, but not limited to hydroxyacetic acid, lactic acid, Tartaric acid, citric acid etc..
In above-mentioned technical proposal, the carboxylic acid can be the monoacid of C2~C10, such as, but not limited to acetic acid etc..
In above-mentioned technical proposal, methanol: the mass ratio of paraformaldehyde is preferably (0.01~100): 1, more preferably 0.1~ 10, more more preferably 0.2~5.
In above-mentioned technical proposal, catalyst amount is preferably the 0.05~10% of raw material weight, more preferably raw material weight 0.1~5%.
In above-mentioned technical proposal, reaction temperature is preferably 70~200 DEG C.
In above-mentioned technical proposal, reaction pressure is preferably 0.2~6MPa.
In above-mentioned technical proposal, when the reaction time is preferably 1 to 20 small, more 4 to 12 it is small when.
In the case where the composition of catalyst of the present invention is clear, the preparation of catalyst is not particularly limited, Ke Yican Ion-exchange process commonly used in the prior art is examined to be prepared.Such as it may include following steps:By sulfonic acid sodium form polystyrene Cation exchange resin is washed with deionized water to outflow clear water, soaks 1 with 0.5~20% strong acid (such as hydrochloric acid or sulfuric acid) ~12h, soaks 1~12h with deionized water or alcohol solution dipping, is washed with deionized afterwards to pH=6, that is, obtains this hair The bright sulfonic acid polystyrene cation exchange resin.When sulfonic acid type of the present invention can also be directly obtained from commercially available channel Polystyrol cation exchange resin, rather than sulfonic acid sodium form, may be used to the preparation of catalyst of the present invention.
Catalyst using the present invention, the PODE yields of n=2~10 are good, and the selectivity of product of n=2~10 is up to 89.4%, Achieve preferable technique effect.
Heretofore described full exchange capacity is in terms of butt resin.
Below by embodiment, the present invention is further elaborated, the raw material paraformaldehyde used in embodiment and comparative example The degree of polymerization be 5, selectivity of product be by 2~10 polyoxymethylene dimethyl ether of the degree of polymerization on the basis of paraformaldehyde target production Thing calculates.
Embodiment
【Embodiment 1】
1st, the preparation of catalyst
Sulfonic acid sodium form polystyrol cation exchange resin 7320 is washed with deionized water to outflow clear water, with 4w%'s Salt acid soak four times, the 4w%'s of each 10 times equivalent to 7320 dry weight of sulfonic acid sodium form polystyrol cation exchange resin of use Hydrochloric acid, soaks 4h every time, is washed with deionized to eluate and exists without chlorion afterwards, after 60 DEG C dry, that is, obtains sulphur Acid type polystyrene cation exchange resin, its full exchange capacity are 4.10mmol/g.Take sulphur of 98 grams equivalent to butt resin Acid type polystyrene cation exchange resin is with 300ml containing the Cu (OH) that Cu is 2 grams2Aqueous suspension mixes, and adds 1 drop ice vinegar Acid, mixing, when standing 24 is small at room temperature, in vacuum drying chamber drying to constant weight, that is, is made the catalyst that Cu contents are 2w%.
2nd, the synthesis of polyoxymethylene dimethyl ether
Add 2 grams of catalyst in 300 milliliters of tank reactors, 100 grams of methanol and 100 grams of paraformaldehydes, at 130 DEG C and 4h is reacted under 0.5MPa self-generated pressures, is extracted after sample centrifuges by gas chromatographic analysis.Polyformaldehyde diformazan is included in product Ether and unreacted material benzenemethanol and paraformaldehyde, it forms distribution such as table 1.
【Embodiment 2】
1st, the preparation of catalyst
Sulfonic acid sodium form polystyrol cation exchange resin 7320 is washed with deionized water to outflow clear water, with 4w%'s Salt acid soak four times, the 4w%'s of each 10 times equivalent to 7320 dry weight of sulfonic acid sodium form polystyrol cation exchange resin of use Hydrochloric acid, soaks 4h every time, is washed with deionized to eluate and exists without chlorion afterwards, after 60 DEG C dry, that is, obtains sulphur Acid type polystyrene cation exchange resin, its full exchange capacity are 4.10mmol/g.Take sulphur of 98 grams equivalent to butt resin Acid type polystyrene cation exchange resin, with 300ml containing the Ni (OH) that Ni is 2 grams under nitrogen protection2Aqueous suspension mixes, and adds Enter 1 drop glacial acetic acid, mix, when standing 24 is small at room temperature, in vacuum drying chamber drying to constant weight, that is, it is 2w%'s that Ni contents, which are made, Catalyst.
2nd, the synthesis of polyoxymethylene dimethyl ether
Add 2 grams of catalyst in 300 milliliters of tank reactors, 100 grams of methanol and 100 grams of paraformaldehydes, at 130 DEG C and 4h is reacted under 0.5MPa self-generated pressures, is extracted after sample centrifuges by gas chromatographic analysis.Polyformaldehyde diformazan is included in product Ether and unreacted material benzenemethanol and paraformaldehyde, it forms distribution such as table 1.
【Embodiment 3】
1st, the preparation of catalyst
Sulfonic acid sodium form polystyrol cation exchange resin 7320 is washed with deionized water to outflow clear water, with 4w%'s Salt acid soak four times, the 4w%'s of each 10 times equivalent to 7320 dry weight of sulfonic acid sodium form polystyrol cation exchange resin of use Hydrochloric acid, soaks 4h every time, is washed with deionized to eluate and exists without chlorion afterwards, after 60 DEG C dry, that is, obtains sulphur Acid type polystyrene cation exchange resin, its full exchange capacity are 4.10mmol/g.Take sulphur of 98 grams equivalent to butt resin Acid type polystyrene cation exchange resin, with 300ml containing the Co (OH) that Co is 2 grams under nitrogen protection2Aqueous suspension mixes, and adds Enter 1 drop glacial acetic acid, mix, when standing 24 is small at room temperature, in vacuum drying chamber drying to constant weight, that is, it is 2w%'s that Co contents, which are made, Catalyst.
2nd, the synthesis of polyoxymethylene dimethyl ether
Add 2 grams of catalyst in 300 milliliters of tank reactors, 100 grams of methanol and 100 grams of paraformaldehydes, at 130 DEG C and 4h is reacted under 0.5MPa self-generated pressures, is extracted after sample centrifuges by gas chromatographic analysis.Polyformaldehyde diformazan is included in product Ether and unreacted material benzenemethanol and paraformaldehyde, it forms distribution such as table 1.
【Embodiment 4】
1st, the preparation of catalyst
Sulfonic acid sodium form polystyrol cation exchange resin 7320 is washed with deionized water to outflow clear water, with 4w%'s Salt acid soak four times, the 4w%'s of each 10 times equivalent to 7320 dry weight of sulfonic acid sodium form polystyrol cation exchange resin of use Hydrochloric acid, soaks 4h every time, is washed with deionized to eluate and exists without chlorion afterwards, after 60 DEG C dry, that is, obtains sulphur Acid type polystyrene cation exchange resin, its full exchange capacity are 4.10mmol/g.Take sulphur of 98 grams equivalent to butt resin Acid type polystyrene cation exchange resin, with 300ml containing the Fe (OH) that Fe is 2 grams under nitrogen protection2Aqueous suspension mixes, and adds Enter 1 drop glacial acetic acid, mix, when standing 24 is small at room temperature, in vacuum drying chamber drying to constant weight, that is, it is 2w%'s that Fe contents, which are made, Catalyst.
2nd, the synthesis of polyoxymethylene dimethyl ether
Add 2 grams of catalyst in 300 milliliters of tank reactors, 100 grams of methanol and 100 grams of paraformaldehydes, at 130 DEG C and 4h is reacted under 0.5MPa self-generated pressures, is extracted after sample centrifuges by gas chromatographic analysis.Polyformaldehyde diformazan is included in product Ether and unreacted material benzenemethanol and paraformaldehyde, it forms distribution such as table 1.
【Embodiment 5】
1st, the preparation of catalyst
Sulfonic acid sodium form polystyrol cation exchange resin 7320 is washed with deionized water to outflow clear water, with 4w%'s Salt acid soak four times, the 4w%'s of each 10 times equivalent to 7320 dry weight of sulfonic acid sodium form polystyrol cation exchange resin of use Hydrochloric acid, soaks 4h every time, is washed with deionized to eluate and exists without chlorion afterwards, after 60 DEG C dry, that is, obtains sulphur Acid type polystyrene cation exchange resin, its full exchange capacity are 4.10mmol/g.Take sulphur of 98 grams equivalent to butt resin Acid type polystyrene cation exchange resin, the Cu (OH) that it is 1 gram containing Cu with 300ml that nitrogen protection is lower and Ni is 1 gram2And Ni (OH)2Mix aqueous suspension mixing, add 1 drop glacial acetic acid, mixing, at room temperature stand 24 it is small when, vacuum drying chamber dry to Constant weight, that is, it is the catalyst that 1w% and Ni contents are 1w% that Cu contents, which are made,.
2nd, the synthesis of polyoxymethylene dimethyl ether
Add 2 grams of catalyst in 300 milliliters of tank reactors, 100 grams of methanol and 100 grams of paraformaldehydes, at 130 DEG C and 4h is reacted under 0.5MPa self-generated pressures, is extracted after sample centrifuges by gas chromatographic analysis.Polyformaldehyde diformazan is included in product Ether and unreacted material benzenemethanol and paraformaldehyde, it forms distribution such as table 1.
【Embodiment 6】
1st, the preparation of catalyst
Sulfonic acid sodium form polystyrol cation exchange resin 7320 is washed with deionized water to outflow clear water, with 4w%'s Salt acid soak four times, the 4w%'s of each 10 times equivalent to 7320 dry weight of sulfonic acid sodium form polystyrol cation exchange resin of use Hydrochloric acid, soaks 4h every time, is washed with deionized to eluate and exists without chlorion afterwards, after 60 DEG C dry, that is, obtains sulphur Acid type polystyrene cation exchange resin, its full exchange capacity are 4.10mmol/g.Take sulphur of 98 grams equivalent to butt resin Acid type polystyrene cation exchange resin, the Cu (OH) that it is 1 gram containing Cu with 300ml that nitrogen protection is lower and Co is 1 gram2And Co (OH)2Mix aqueous suspension mixing, add 1 drop glacial acetic acid, mixing, at room temperature stand 24 it is small when, vacuum drying chamber dry to Constant weight, that is, it is the catalyst that 1w% and Co contents are 1w% that Cu contents, which are made,.
2nd, the synthesis of polyoxymethylene dimethyl ether
Add 2 grams of catalyst in 300 milliliters of tank reactors, 100 grams of methanol and 100 grams of paraformaldehydes, at 130 DEG C and 4h is reacted under 0.5MPa self-generated pressures, is extracted after sample centrifuges by gas chromatographic analysis.Polyformaldehyde diformazan is included in product Ether and unreacted material benzenemethanol and paraformaldehyde, it forms distribution such as table 1.
【Embodiment 7】
1st, the preparation of catalyst
Sulfonic acid sodium form polystyrol cation exchange resin 7320 is washed with deionized water to outflow clear water, with 4w%'s Salt acid soak four times, the 4w%'s of each 10 times equivalent to 7320 dry weight of sulfonic acid sodium form polystyrol cation exchange resin of use Hydrochloric acid, soaks 4h every time, is washed with deionized to eluate and exists without chlorion afterwards, after 60 DEG C dry, that is, obtains sulphur Acid type polystyrene cation exchange resin, its full exchange capacity are 4.10mmol/g.Take sulphur of 98 grams equivalent to butt resin Acid type polystyrene cation exchange resin, the Cu (OH) that it is 1 gram containing Cu with 300ml that nitrogen protection is lower and Fe is 1 gram2And Fe (OH)2Mix aqueous suspension mixing, add 1 drop glacial acetic acid, mixing, at room temperature stand 24 it is small when, vacuum drying chamber dry to Constant weight, that is, it is the catalyst that 1w% and Fe contents are 1w% that Cu contents, which are made,.
2nd, the synthesis of polyoxymethylene dimethyl ether
Add 2 grams of catalyst in 300 milliliters of tank reactors, 100 grams of methanol and 100 grams of paraformaldehydes, at 130 DEG C and 4h is reacted under 0.5MPa self-generated pressures, is extracted after sample centrifuges by gas chromatographic analysis.Polyformaldehyde diformazan is included in product Ether and unreacted material benzenemethanol and paraformaldehyde, it forms distribution such as table 1.
【Embodiment 8】
1st, the preparation of catalyst
Sulfonic acid sodium form polystyrol cation exchange resin 7320 is washed with deionized water to outflow clear water, with 4w%'s Salt acid soak four times, the 4w%'s of each 10 times equivalent to 7320 dry weight of sulfonic acid sodium form polystyrol cation exchange resin of use Hydrochloric acid, soaks 4h every time, is washed with deionized to eluate and exists without chlorion afterwards, after 60 DEG C dry, that is, obtains sulphur Acid type polystyrene cation exchange resin, its full exchange capacity are 4.10mmol/g.Take sulphur of 98 grams equivalent to butt resin Acid type polystyrene cation exchange resin, nitrogen protection is down 1 gram containing Cu with 300ml, Co is 0.5 gram and Ni is 0.5 gram Cu(OH)2、Co(OH)2With Ni (OH)2Mixing aqueous suspension mixing, adds 1 drop glacial acetic acid, mixes, when standing 24 is small at room temperature, In vacuum drying chamber drying to constant weight, that is, it is that 1w%, Co content are that 0.5w% and Ni contents are urging for 0.5w% that Cu contents, which are made, Agent.
2nd, the synthesis of polyoxymethylene dimethyl ether
Add 2 grams of catalyst in 300 milliliters of tank reactors, 100 grams of methanol and 100 grams of paraformaldehydes, at 130 DEG C and 4h is reacted under 0.5MPa self-generated pressures, is extracted after sample centrifuges by gas chromatographic analysis.Polyformaldehyde diformazan is included in product Ether and unreacted material benzenemethanol and paraformaldehyde, it forms distribution such as table 1.
【Embodiment 9】
1st, the preparation of catalyst
Sulfonic acid sodium form polystyrol cation exchange resin 7320 is washed with deionized water to outflow clear water, with 4w%'s Salt acid soak four times, the 4w%'s of each 10 times equivalent to 7320 dry weight of sulfonic acid sodium form polystyrol cation exchange resin of use Hydrochloric acid, soaks 4h every time, is washed with deionized to eluate and exists without chlorion afterwards, after 60 DEG C dry, that is, obtains sulphur Acid type polystyrene cation exchange resin, its full exchange capacity are 4.10mmol/g.Take sulphur of 98 grams equivalent to butt resin Acid type polystyrene cation exchange resin, nitrogen protection is down 1 gram containing Cu with 300ml, Co is 0.5 gram and Fe is 0.5 gram Cu(OH)2、Co(OH)2With Fe (OH)2Mixing aqueous suspension mixing, adds 1 drop glacial acetic acid, mixes, when standing 24 is small at room temperature, In vacuum drying chamber drying to constant weight, that is, it is that 1w%, Co content are that 0.5w% and Fe contents are urging for 0.5w% that Cu contents, which are made, Agent.
2nd, the synthesis of polyoxymethylene dimethyl ether
Add 2 grams of catalyst in 300 milliliters of tank reactors, 100 grams of methanol and 100 grams of paraformaldehydes, at 130 DEG C and 4h is reacted under 0.5MPa self-generated pressures, is extracted after sample centrifuges by gas chromatographic analysis.Polyformaldehyde diformazan is included in product Ether and unreacted material benzenemethanol and paraformaldehyde, it forms distribution such as table 1.
【Embodiment 10】
1st, the preparation of catalyst
Sulfonic acid sodium form polystyrol cation exchange resin 7320 is washed with deionized water to outflow clear water, with 4w%'s Salt acid soak four times, the 4w%'s of each 10 times equivalent to 7320 dry weight of sulfonic acid sodium form polystyrol cation exchange resin of use Hydrochloric acid, soaks 4h every time, is washed with deionized to eluate and exists without chlorion afterwards, after 60 DEG C dry, that is, obtains sulphur Acid type polystyrene cation exchange resin, its full exchange capacity are 4.10mmol/g.Take sulphur of 98 grams equivalent to butt resin Acid type polystyrene cation exchange resin, nitrogen protection is down 1 gram containing Cu with 300ml, Ni is 0.5 gram and Fe is 0.5 gram Cu(OH)2、Ni(OH)2With Fe (OH)2Mixing aqueous suspension mixing, adds 1 drop glacial acetic acid, mixes, when standing 24 is small at room temperature, In vacuum drying chamber drying to constant weight, that is, it is that 1w%, Ni content are that 0.5w% and Fe contents are urging for 0.5w% that Cu contents, which are made, Agent.
2nd, the synthesis of polyoxymethylene dimethyl ether
Add 2 grams of catalyst in 300 milliliters of tank reactors, 100 grams of methanol and 100 grams of paraformaldehydes, at 130 DEG C and 4h is reacted under 0.5MPa self-generated pressures, is extracted after sample centrifuges by gas chromatographic analysis.Polyformaldehyde diformazan is included in product Ether and unreacted material benzenemethanol and paraformaldehyde, it forms distribution such as table 1.
【Embodiment 11】
1st, the preparation of catalyst
Sulfonic acid sodium form polystyrol cation exchange resin 7320 is washed with deionized water to outflow clear water, with 4w%'s Salt acid soak four times, the 4w%'s of each 10 times equivalent to 7320 dry weight of sulfonic acid sodium form polystyrol cation exchange resin of use Hydrochloric acid, soaks 4h every time, is washed with deionized to eluate and exists without chlorion afterwards, after 60 DEG C dry, that is, obtains sulphur Acid type polystyrene cation exchange resin, its full exchange capacity are 4.10mmol/g.Take sulphur of 98 grams equivalent to butt resin Acid type polystyrene cation exchange resin, nitrogen protection is lower and 300ml containing Cu is 1 gram, Co is 0.4 gram, Ni is 0.3 gram and Fe For 0.3 gram of Cu (OH)2、Co(OH)2、Ni(OH)2With Fe (OH)2Aqueous suspension mixing is mixed, 1 drop glacial acetic acid is added, mixes, When standing 24 is small at room temperature, in vacuum drying chamber drying to constant weight, that is, it is that 1w%, Co content are 0.4w%, Ni that Cu contents, which are made, Content is the catalyst that 0.3w% and Fe contents are 0.3w%.
2nd, the synthesis of polyoxymethylene dimethyl ether
Add 2 grams of catalyst in 300 milliliters of tank reactors, 100 grams of methanol and 100 grams of paraformaldehydes, at 130 DEG C and 4h is reacted under 0.5MPa self-generated pressures, is extracted after sample centrifuges by gas chromatographic analysis.Polyformaldehyde diformazan is included in product Ether and unreacted material benzenemethanol and paraformaldehyde, it forms distribution such as table 1.
【Embodiment 12】
1st, the preparation of catalyst
Sulfonic acid sodium form polystyrol cation exchange resin 7320 is washed with deionized water to outflow clear water, with 4w%'s Salt acid soak four times, the 4w%'s of each 10 times equivalent to 7320 dry weight of sulfonic acid sodium form polystyrol cation exchange resin of use Hydrochloric acid, soaks 4h every time, is washed with deionized to eluate and exists without chlorion afterwards, after 60 DEG C dry, that is, obtains sulphur Acid type polystyrene cation exchange resin, its full exchange capacity are 4.10mmol/g.Take sulphur of 98 grams equivalent to butt resin Acid type polystyrene cation exchange resin, nitrogen protection is lower and 300ml containing Cu is 1 gram, Co is 0.4 gram, Ni is 0.3 gram and Fe For 0.3 gram of Cu (OH)2、Co(OH)2、Ni(OH)2With Fe (OH)2Aqueous suspension mixing is mixed, 1 drop glacial acetic acid is added, mixes, When standing 24 is small at room temperature, in vacuum drying chamber drying to constant weight, that is, it is that 1w%, Co content are 0.4w%, Ni that Cu contents, which are made, Content is the catalyst that 0.3w% and Fe contents are 0.3w%.
2nd, the synthesis of polyoxymethylene dimethyl ether
Add 2 grams of catalyst in 300 milliliters of tank reactors, 100 grams of methanol and 100 grams of paraformaldehydes, at 90 DEG C and 4h is reacted under 0.6MPa self-generated pressures, is extracted after sample centrifuges by gas chromatographic analysis.Polyformaldehyde diformazan is included in product Ether and unreacted material benzenemethanol and paraformaldehyde, it forms distribution such as table 1.
【Comparative example 1】
For embodiment 1 in proportion, the catalyst used is differed only in for the drying sulfonic acid type described in embodiment 1 to gather 2 grams of styrene cation exchange resin, other process conditions are same as Example 1, the results are shown in Table 1.
Table 1
N is the degree of polymerization, product CH3O(CH2O)nCH3

Claims (10)

1. the preparation method of polyoxymethylene dimethyl ether, using methanol and paraformaldehyde as raw material, raw material is catalyzed with polyoxymethylene dimethyl ethers Agent contacts, reaction generation polyoxymethylene dimethyl ether;It is characterized in that the catalyst is the sulfonic acid type polyphenyl of modified metal ion modification Ethene cation exchange resin, the sulfonic acid polystyrene cation exchange resin include crosslinked polystyrene skeleton and sulfonic acid Group;The modified metal includes VIII group element.
2. preparation method according to claim 1, it is characterized in that VIII group element in Fe, Co and Ni at least one Kind.
3. preparation method according to claim 1, it is characterized in that the content of modified metal is more than 0 and is less than in catalyst Equal to 10w%.
4. preparation method according to claim 1, it is characterized in that the full exchange capacity of the resin is 3.0~6.0mmol/ g。
5. preparation method according to claim 1, it is characterized in that the resin is gel-type or macroporous type.
6. preparation method according to claim 1, it is characterized in that methanol: the mass ratio of paraformaldehyde is (0.01~100): 1。
7. preparation method according to claim 1, it is characterized in that catalyst amount is the 0.05~10% of raw material weight.
8. preparation method according to claim 1, it is characterized in that reaction temperature is 70~200 DEG C.
9. preparation method according to claim 1, it is characterized in that reaction pressure is 0.2~6MPa.
10. preparation method according to claim 1, it is characterized in that when the reaction time is 1 to 20 small.
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CN104549502A (en) * 2013-10-28 2015-04-29 中国石油化工股份有限公司 Catalyst for synthesis of polyoxymethylene dimethyl ether and application of catalyst
CN106582835A (en) * 2015-10-16 2017-04-26 中国石油化工股份有限公司 Polyformaldehyde dimethyl ether synthesis catalyst

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