CN108311148A - A kind of composite catalyst SiO2The preparation method of-CuO - Google Patents

A kind of composite catalyst SiO2The preparation method of-CuO Download PDF

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Publication number
CN108311148A
CN108311148A CN201810225554.XA CN201810225554A CN108311148A CN 108311148 A CN108311148 A CN 108311148A CN 201810225554 A CN201810225554 A CN 201810225554A CN 108311148 A CN108311148 A CN 108311148A
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CN
China
Prior art keywords
parts
preparation
composite catalyst
roasted
cuo
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
CN201810225554.XA
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Chinese (zh)
Inventor
不公告发明人
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Qidong Xiangrui Construction Co Ltd
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Qidong Xiangrui Construction Co Ltd
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Filing date
Publication date
Application filed by Qidong Xiangrui Construction Co Ltd filed Critical Qidong Xiangrui Construction Co Ltd
Priority to CN201810225554.XA priority Critical patent/CN108311148A/en
Publication of CN108311148A publication Critical patent/CN108311148A/en
Withdrawn legal-status Critical Current

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Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J23/00Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • B01J23/70Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper
    • B01J23/72Copper
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
    • C10G45/00Refining of hydrocarbon oils using hydrogen or hydrogen-generating compounds
    • C10G45/02Refining of hydrocarbon oils using hydrogen or hydrogen-generating compounds to eliminate hetero atoms without changing the skeleton of the hydrocarbon involved and without cracking into lower boiling hydrocarbons; Hydrofinishing
    • C10G45/04Refining of hydrocarbon oils using hydrogen or hydrogen-generating compounds to eliminate hetero atoms without changing the skeleton of the hydrocarbon involved and without cracking into lower boiling hydrocarbons; Hydrofinishing characterised by the catalyst used
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
    • C10G2300/00Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
    • C10G2300/20Characteristics of the feedstock or the products
    • C10G2300/201Impurities
    • C10G2300/202Heteroatoms content, i.e. S, N, O, P
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
    • C10G2400/00Products obtained by processes covered by groups C10G9/00 - C10G69/14
    • C10G2400/04Diesel oil

Abstract

The invention discloses a kind of composite catalyst SiO2The preparation method of CuO, steps are as follows:Copper nitrate is dissolved in distilled water;Ethyl orthosilicate, absolute ethyl alcohol and concentrated nitric acid are uniformly mixed, above-mentioned solution is added dropwise dropwise, is stirred continuously, until forming colloidal sol, 25 35 DEG C stand 7 9h, 45 55 DEG C of 25 27h of drying, 4 5h are roasted at 485 495 DEG C, cooling to obtain the final product.This method is easy, quick, easy to operate, the composite catalyst SiO of preparation20.1CuO oxidation sweetening significant effects have huge application prospect.

Description

A kind of composite catalyst SiO2The preparation method of-CuO
Technical field
The present invention relates to a kind of composite catalyst SiO2The preparation method of -0.1CuO.
Background technology
2005, sulfur content < 50mg/L in European Environment laws and regulations requirement diesel oil, 2006, U.S. environment regulation required sulphur Content < 15mg/L.2013, China proposed National V emission standard again, i.e. sulfur content is not higher than 10mg/L, and new standard is carrying Height illustrates that country increasingly payes attention to low-sulfur oil and super-low sulfur oil.Under new standard, traditional hydrodesulfurization(HDS)Technique is grasped Make condition harshness, need the operating conditions such as high temperature, high pressure, long residence time, more hydrogen and catalyst, improve HDS at This.One of non-hydrodesulfurization --- catalytic oxidation desulfurization technology is quickly grown in recent years, selection mild with oxidizing condition Property high, green the advantages that, and oxidation product can be common to aoxidize by the simple method removing such as extraction, distillation, absorption Desulphurization catalyst includes heterogeneous and homogeneous catalyst, and homogeneous catalyst includes heteropoly acid and heteropolyacid salt, formic acid/H2O2System With acetic acid/H2O2System etc.;Heterogeneous catalysis includes molecular sieve catalyst, metal oxide catalyst, heteropoly acid and heteropoly acid Salt supported catalyst etc..Most of method for preparing catalyst are complicated, commonly use active component(V、Mo、W)Higher price, cause to urge The cost of agent is higher.Cu is prepared frequently with infusion process, is used as hydrogenation catalyst as base metal.
Invention content
The purpose of the present invention is to provide a kind of composite catalyst SiO2The preparation method of -0.1CuO.
The present invention is realized by following technical solution:
A kind of composite catalyst SiO2The preparation method of -0.1CuO, includes the following steps:20-30 parts of copper nitrates are dissolved in 55-65 In part distilled water;15-25 parts of ethyl orthosilicates, 15-25 parts of absolute ethyl alcohols and 7-9 parts of concentrated nitric acids are uniformly mixed, are added dropwise dropwise Above-mentioned solution, is stirred continuously, until forming colloidal sol, 25-35 DEG C stands 7-9h, 45-55 DEG C of dry 25-27h, in 485-495 DEG C Lower roasting 4-5h, cooling to obtain the final product;Each raw material is parts by weight.
Preferably, in the preparation method, 30 DEG C of standing 8h.
Preferably, in the preparation method, 50 DEG C of dry 26h.
Preferably, in the preparation method, 4.5h is roasted at 490 DEG C.
The technology of the present invention effect:
This method is easy, quick, easy to operate, the composite catalyst SiO of preparation2- 0.1CuO oxidation sweetening significant effects have huge Big application prospect.
Specific implementation mode
The essentiality content of the present invention is specifically introduced with reference to embodiment.
Embodiment 1
A kind of composite catalyst SiO2The preparation method of -0.1CuO, includes the following steps:25 parts of copper nitrates are dissolved in 60 parts of distillations In water;20 parts of ethyl orthosilicates, 20 parts of absolute ethyl alcohols and 8 parts of concentrated nitric acids are uniformly mixed, above-mentioned solution is added dropwise dropwise, constantly stirs It mixes, until forming colloidal sol, 30 DEG C stand 8h, 50 DEG C of dry 26h, 4.5h are roasted at 490 DEG C, cooling to obtain the final product;Each raw material is Parts by weight.
Embodiment 2
A kind of composite catalyst SiO2The preparation method of -0.1CuO, includes the following steps:20 parts of copper nitrates are dissolved in 55 parts of distillations In water;15 parts of ethyl orthosilicates, 15 parts of absolute ethyl alcohols and 7 parts of concentrated nitric acids are uniformly mixed, above-mentioned solution is added dropwise dropwise, constantly stirs It mixes, until forming colloidal sol, 25 DEG C stand 7h, 45 DEG C of dry 25h, 4h are roasted at 485 DEG C, cooling to obtain the final product;Each raw material is attached most importance to Measure part.
Embodiment 3
A kind of composite catalyst SiO2The preparation method of -0.1CuO, includes the following steps:30 parts of copper nitrates are dissolved in 65 parts of distillations In water;25 parts of ethyl orthosilicates, 25 parts of absolute ethyl alcohols and 9 parts of concentrated nitric acids are uniformly mixed, above-mentioned solution is added dropwise dropwise, constantly stirs It mixes, until forming colloidal sol, 35 DEG C stand 9h, 55 DEG C of dry 27h, 5h are roasted at 495 DEG C, cooling to obtain the final product;Each raw material is attached most importance to Measure part.
This method is easy, quick, easy to operate, the composite catalyst SiO of preparation2- 0.1CuO oxidation sweetening significant effects, tool There is huge application prospect.

Claims (4)

1. a kind of composite catalyst SiO2The preparation method of -0.1CuO, it is characterised in that include the following steps:By 20-30 parts of nitric acid Copper is dissolved in 55-65 parts of distilled water;15-25 parts of ethyl orthosilicates, 15-25 parts of absolute ethyl alcohols and 7-9 parts of concentrated nitric acids are mixed equal It is even, above-mentioned solution is added dropwise dropwise, is stirred continuously, until forming colloidal sol, 25-35 DEG C stands 7-9h, 45-55 DEG C of dry 25-27h, 4-5h is roasted at 485-495 DEG C, cooling to obtain the final product;Each raw material is parts by weight.
2. preparation method according to claim 1, it is characterised in that:30 DEG C of standing 8h.
3. preparation method according to claim 1, it is characterised in that:50 DEG C of dry 26h.
4. preparation method according to claim 1, it is characterised in that:4.5h is roasted at 490 DEG C.
CN201810225554.XA 2018-03-19 2018-03-19 A kind of composite catalyst SiO2The preparation method of-CuO Withdrawn CN108311148A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201810225554.XA CN108311148A (en) 2018-03-19 2018-03-19 A kind of composite catalyst SiO2The preparation method of-CuO

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201810225554.XA CN108311148A (en) 2018-03-19 2018-03-19 A kind of composite catalyst SiO2The preparation method of-CuO

Publications (1)

Publication Number Publication Date
CN108311148A true CN108311148A (en) 2018-07-24

Family

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Family Applications (1)

Application Number Title Priority Date Filing Date
CN201810225554.XA Withdrawn CN108311148A (en) 2018-03-19 2018-03-19 A kind of composite catalyst SiO2The preparation method of-CuO

Country Status (1)

Country Link
CN (1) CN108311148A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN113244934A (en) * 2021-05-25 2021-08-13 上海华谊(集团)公司 Catalyst for producing 2,3, 6-trichloropyridine and preparation method thereof

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN113244934A (en) * 2021-05-25 2021-08-13 上海华谊(集团)公司 Catalyst for producing 2,3, 6-trichloropyridine and preparation method thereof

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Application publication date: 20180724