CN1032951A - A kind of catalyst for reforming naphtha - Google Patents
A kind of catalyst for reforming naphtha Download PDFInfo
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- CN1032951A CN1032951A CN 87107556 CN87107556A CN1032951A CN 1032951 A CN1032951 A CN 1032951A CN 87107556 CN87107556 CN 87107556 CN 87107556 A CN87107556 A CN 87107556A CN 1032951 A CN1032951 A CN 1032951A
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- catalyzer
- heavy
- catalyst
- naphtha
- reforming
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Abstract
A kind of catalyst for reforming naphtha is to adopt single diaspore that the low-carbon alkoxy aluminium hydrolysis makes or sneak into the single diaspore of part with the additive method preparation therein, the γ-Al that obtains through moulding, roasting
2O
3Be carrier, loaded metal Pt, Re, Ti and halogen, its Pt content are 0.1～1.00 heavy %, and the Re/Pt ratio is 0.1～4.0 (weight).Owing to adopt the high γ-Al of purity
2O
3Be carrier, thereby improved activity of such catalysts, selectivity and stability.It is 40～230 ℃ virgin naphtha or the naphtha reforming that comprises explained hereafter such as coking in the refining of petroleum, cracking that catalyzer of the present invention can be used for boiling range.
Description
The invention belongs to catalyst for reforming naphtha.
Catalytic reforming is one of main machining method in the refining of petroleum industry, and it not only can provide high octane gasoline component, but also produces the aromatic hydrocarbons with valuable purposes.Particularly because the requirement of environment control limits the leading amount of motor spirit or requires not leading, make the reforming process development very fast, wherein the improvement of catalyzer is more remarkable.
The forties end United States Patent (USP) 2,479,109 and 2,479 has been introduced with noble metal platinum for No. 110 and have been replaced non-noble metal components, has invented reforming catalyst of new generation; To nineteen sixty-eight United States Patent (USP) disclosed for 3,415, No. 737 and in platinum-reforming catalyst, introduced Re, make catalyst performance, especially stability has had significant improvement; Recently, at United States Patent (USP) 4,356, in No. 081, having proposed the reforming catalyst of Re content higher (Re/Pt is 2～5), is that the reactivity worth of 1 catalyzer is better than Re/Pt.
The reforming catalyst of an excellent property not only will have the metal component of good hydrogenation-dehydrogenation functionality, and needs the carrier of proper sourness function.Can provide the carrier of acid function that amorphous silicon aluminium, molecular sieve, aluminum oxide or other inorganic oxides are arranged usually, be best with aluminum oxide.For reforming catalyst the most frequently used be γ-Al
2O
3And η-Al
2O
3The general acidity that also will improve catalyzer by introducing halogen in carrier, commonly used is fluorine and chlorine.
Because preparation method's difference of aluminum oxide, great changes have taken place for its performance, thereby also will produce bigger influence to the performance of catalyzer.In some documents, report the aluminum oxide of selecting different methods production for use and made the performance that the carrier of catalyzer improves catalyzer.United States Patent (USP) 4,178, the method that adopts in No. 268 United States Patent (USP) to introduce for 3,280, No. 041, promptly the SB aluminum oxide of Ziegler building-up reactions by-product is the preparing carriers reforming catalyst.The Germany patent has been introduced employing Al 3,508, No. 746 and greater than C
4The aluminum oxide that obtains of the higher alcohols reaction high-carbon aluminum alkoxide hydrolysis of producing be the reforming catalyst of preparing carriers, improved liquid product yield, gasoline octane rating also has raising.As a whole, platinum-rhenium reforming catalyst of the prior art compares with the reforming catalyst of other classes, and active and stability improves a lot, but selectivity is still good inadequately.
The objective of the invention is to seek γ-Al that a kind of purity is higher, crystal formation is purer
2O
3Be carrier, develop the multimetal reforming catalyst of a kind of active height and selectivity, good stability.
Characteristics of the present invention are to adopt single diaspore that the low-carbon alkoxy aluminium hydrolysis obtains or sneak into single diaspore that the part additive method is produced therein, the γ-Al that makes through moulding, high-temperature roasting
2O
3Be carrier (hereinafter to be referred as HP), loaded metal Pt, Re, Ti and halogen.
γ-Al
2O
3Preparation process: according to the method that No. 85100218, Chinese patent is introduced, promptly use C
1～C
4Single diaspore that low-carbon alkoxy aluminium and water content generate less than 20% low-carbon alcohol generation hydrolysis reaction, drip ball forming through extrusion molding or oil-ammonia post, 60～80 ℃ of dryings 4～12 hours, 120～130 ℃ of dryings 6～24 hours, in the presence of dry air (gas agent volume ratio is 400～700) then, through 450～700 ℃, best 550～650 ℃ of roastings can obtain γ-Al
2O
3The single diaspore that also can sneak into 30～70% usefulness additive methods such as productions such as the high temperature precipitator method, Ziegler building-up reactions by-product alumina method in above-mentioned single diaspore is a raw material, takes above-mentioned same operation steps and condition to prepare γ-Al
2O
3
Catalyst preparation process: stoichiometric metal-salt (to the platinum constituent element, is preferably Platinic chloride, chlorine platinum ammonium; The rhenium constituent element is preferably perrhenic acid, rhenium carbonyl), hydrochloric acid and deionized water mixing solutions, at room temperature flood γ-Al
2O
3Carrier, the volume ratio of carrier and solution are 1.0～2.0, preferably 1.0～1.5, and soak time is 6～24 hours; Then after filtration, dry i.e. 60～80 ℃ of dryings of two-stage 6～12 hours, 110～130 ℃ of dryings 12～24 hours; (gas agent volume ratio is 700～1200) activates 2～12 hours down in 450～550 ℃ in dry air, then in 400～500 ℃ of following hydrogen reductase 12～12 hour (gas agent volume ratio 400～1000).
Also can adopt branch to soak method, but must after super-dry, roasting, soak another component again after a kind of component on every dipping.Also can adopt common coprecipitation method.For the titanium constituent element, can adopt pickling process, also can when the preparation carrier, adopt glue method introducing altogether, so that the glue method is best altogether, used salt is titanium chloride, Titanium Nitrate preferably.
Another constituent element of catalyzer of the present invention is the halogen that comprises fluorine, chlorine, and is best with chlorine.It can be introduced in catalyst preparation process, also can in the catalyzer use, introduce, preferably mode be the form of or Organohalogen compounds inorganic with hydrochloric acid or other when dipping and the metal constituent element together introduce.
Catalyzer of the present invention is formed (with the butt aluminum oxide is benchmark, heavy %): Pt 0.10～1.00, and best 0.10～0.60; Re 0.10～3.00, and best 0.10～2.00; Ti 0.00～0.15, and best 0.01～0.15; Cl 0.5～3.0, and best 0.8～2.0.Re/Pt is that 0.1～4.0(is heavy), it is heavy to be preferably 1.00～3.00().
The molding mode of catalyzer of the present invention can be with the common methods such as ball forming, spin granulation, extrusion molding, compression molding of dripping, to drip ball forming and extrinsion pressing for well.Catalyst shape can be bar shaped (comprising abnormity such as cylindrical, trilobal, quatrefoil), spherical, sheet shape or particulate state, with spherical and bar shaped for well.
Catalyzer of the present invention is the same with other platinum-rhenium reforming catalysts, must pass through prevulcanized before use.Prevulcanized can be by (the gas agent is than 400～1000) injection H in hydrogen or nitrogen gas stream
2The mode of S or other organic or inorganic sulfide is carried out, and the sulphur content on the catalyzer is 0.01～2.00 heavy %, is preferably 0.04～0.15 heavy %.
Catalyzer of the present invention can be used for boiling range and is 40～230 ℃ and (presses the GB255 methods analyst, as follows) virgin naphtha or comprise that the boiling range of explained hereafter such as coking in the refining of petroleum, cracking is the reformation of 40～230 ℃ petroleum naphtha, be specially adapted to the reformation of virgin naphtha.
The present invention is because the HP that has used or partly used crystalline phase purity height, pore size distribution to concentrate is carrier, therefore the multimetal reforming catalyst that makes has following advantage: active high, under identical reaction conditions, the peace and quiet octane value of gasoline research method (RONC) is high approximately 1.0～2.0 units of Pt-Re catalyzer of carrier than with the SB aluminum oxide; Selectivity is good, when aromaticity content is identical in liquid product, and liquid product yield high 1.0～5.0 heavy %; Good stability, long service life.
Further describe feature of the present invention with example below.
Example 1
This example is that the single diaspore with the production of low-carbon alkoxy aluminium method for hydrolysis prepares γ-Al
2O
3
Take by weighing a certain amount of single diaspore wet cake and mix, Gu the add-on of deionized water makes liquid/(weight) than being 3.0: 1 with a certain amount of deionized water.Simultaneously, titanium content as requested adds stoichiometric TiCl hydrochloric acid soln.This mixture at room temperature stirred 1 hour, make its pulp, add stoichiometric analytical pure nitric acid then and carry out acidifying, the final add-on of nitric acid is 7.5 milliliters of nitric acid/single diaspore of 100 grams, after the acidifying 2 hours, with the acidifying slurries after colloidal mill once grinds, become to drip ball forming in the goalpost at an oily ammonia, the wet bulb of moulding continues to solidify 1 hour, filters then, with water purification washing 3 times, 60 ℃ of dryings 10 hours, 120 ℃ of dryings 20 hours, dried bead promptly obtains containing γ-Al of Ti 580 ℃ of blowing air roastings 4 hours
2O
3, its performance sees Table the HP-2 ball in 1.
With wet cake exsiccant dry glue powder or slurries spray dried rubber powder is γ-Al that feedstock production contains Ti
2O
3The method of bead is identical with aforesaid method, and its performance sees Table HP-3 ball and the HP-4 ball in 1 respectively.
Prepare strip γ-Al with single diaspore dry glue powder
2O
3Method: with dry glue powder, deionized water, analytical pure HNO
3Mix Hou Hun Pinch, its amount is: deionized water: dry glue powder is 0.8: 1(is heavy), nitric acid: dry glue powder is 4, and: 100(is heavy), extruded moulding then, γ-Al that drying, roasting (dry, roasting condition with the preparation spheroid carrier time identical) must strips again
2O
3, its performance sees Table the HP-1 bar in 1.
Example 2
This case introduction is sneaked into the method that Zieg-ler building-up reactions by-product list diaspore prepares support of the catalyst in single diaspore of producing with the low-carbon alkoxy aluminium hydrolysis method.
In the single diaspore wet cake produced with the low-carbon alkoxy aluminium hydrolysis method or dry glue powder, sneak into Ziegler building-up reactions by-product list diaspore, wherein single diaspore of low-carbon alkoxy aluminium hydrolysis method production accounts for 50 heavy %, all the other are Ziegler building-up reactions by-product list diaspore, other preparation methods are identical with the preparation method of HP-1 bar carrier in the example 1, make carrier HP-5.
Example 3
This case introduction is sneaked into by AlCl in single diaspore of producing with the low-carbon alkoxy aluminium hydrolysis method
3, NH
4Single diaspore that OH produces through the high temperature precipitator method prepares γ-Al
2O
3Method:
In the single diaspore wet cake produced with the low-carbon alkoxy aluminium hydrolysis method or dry glue powder, sneak into a certain proportion of by AlCl
3, NH
4Single diaspore that OH produces through the high temperature precipitator method, other preparation methods are identical with the preparation method of HP-1 bar in the example 1.Make carrier HP-6, HP-7, wherein single diaspore of producing with the low-carbon alkoxy aluminium hydrolysis method among the HP-6 accounts for 30 heavy %, and single diaspore that the precipitator method are produced accounts for 70 heavy %.Single diaspore of producing with the low-carbon alkoxy aluminium hydrolysis method among the HP-7 accounts for 70 heavy %, and single diaspore that the precipitator method are produced accounts for 30 heavy %.
Example 4
This case introduction is the method for preparing carriers catalyzer with HP.
To pour at room temperature that (stoichiometry is all with Al in the mixing solutions by Platinic chloride, perrhenic acid and the hydrochloric acid of chemical constitution preparation by HP-1 strip carrier 100 grams of example 1 preparation into
2O
3Be benchmark), contain Pt 0.22 heavy % in the mixing solutions, Re 0.44 heavy %, Cl 1.6 heavy % are Gu liquid/(body) is 1.2.Flood 24 hours after-filtration, moist catalysis 60 ℃, 120 ℃ dry 6 and 12 hours down respectively, 500 ℃ of activation 4 hours down in air then at 500 ℃ of logical hydrogen reducings 4 hours down, are injected H again again in hydrogen stream
2Till S sulfuration, hydrogen sulfide add to beds and penetrate, promptly get catalyst A-1.
A-2, A-3 support of the catalyst and the same A-1 of preparation method, different is Pt, Re content difference.
The A-4 support of the catalyst is the HP-2 ball, the same basically A-1 of method for preparing catalyst, and the hydrochloric acid consumption was 2.2 heavy % when different was the A-4 catalyst soakage.
A-5, A-6, A-7 support of the catalyst are HP-5 bar, HP-6 bar, HP-7 bar, the same A-1 of method for preparing catalyst.The catalyzer composition sees Table 3.
Example 5～7
This example is the composition and the performance of correlated catalyzer and carrier.
γ-the Al of different methods preparation
2O
3Physical and chemical performance see Table 2.The composition of comparative catalyst B, C, D sees Table 3.The used carrier of catalyst B is the γ-Al of Ziegler building-up reactions by-product
2O
3Be SB aluminum oxide (performance sees Table SB-ball in 2), method for preparing catalyst is identical with example 4; γ-Al that the aluminium colloidal sol that catalyzer C adopts oil three factories of China PetroChemical Corporation to produce makes through forming oil column
2O
3(industrial trade mark GM, performance sees Table GM-ball in 2), method for preparing catalyst and example 4 are together; Catalyzer D is industrial platinum-rhenium catalyst (industrial trade mark CB-6) that Changling Refining Plant of Chinese General Petrochemical Industrial Cooperation produces, and is to be carrier with SB.
Example 8
This example is activity of such catalysts of the present invention and evaluation experimental optionally, and compares with other catalyzer.
The performance of evaluate catalysts A-1, B, C, D on the device of 100 milliliters of band hydrogen gas circulating systems.Raw materials used is 60～140 ℃ of virgin naphthas of big Khanh Hoa North China crude oil mixing, and its character sees Table 4.Appreciation condition: 480～520 ℃ of temperature of reaction, pressure 14.7 * 10
5Pa, hydrogen-oil ratio are the 1200(body), during air speed 2.0
-1Evaluation result sees Table 5.By result in the table as can be seen, catalyst A of the present invention is compared with comparative catalyst B, C, D, high 1～2.3 unit of liquid product research octane number (RON) (RON), and under the identical situation of aromaticity content, liquid product yield high 1.0～5.0 heavy %.
Example 9
This example is the stability test of catalyzer, and compares with other catalyzer.
Estimate used device, stock oil is identical with example 8.Appreciation condition: 540 ℃ of temperature of reaction, pressure 6.9 * 10
5Pa, hydrogen-oil ratio 800(body), during air speed 3.0
-1Evaluation result sees Table 6.The result shows that the stability of catalyzer of the present invention is better than B, C, D catalyzer.
Example 10
On the pressurization microreactor apparatus is raw material with normal heptane, the comparative evaluation catalyst A of the present invention-1 and catalyzer D, the results are shown in Table 7.The hull productive rate of liquid product yield, toluene and benzene of sole Fu Learn-about-1 of result all is higher than D.
Example 11
This example is the contrast experiment of catalyst A of the present invention-3 and catalyzer D, and condition the results are shown in Table 8 with example 10.Table 8 is the result show, the activity of catalyst A-1, selectivity all are better than D.
Example 12
This example contains the contrast experiment of Ti catalyst A-4 and catalyzer D for the present invention, and appreciation condition the results are shown in Table 9 with example 10.The result shows that the A-4 catalyzer is lower than the catalyzer D except that the productive rate of initial reaction stage benzene and toluene, and the reaction result under other conditions all is better than catalyzer D.
Example 13
This example is the contrast experiment of catalyst A of the present invention-5 and catalyzer D, and appreciation condition the results are shown in Table 10 with example 10.The result shows, A-5 catalyst reaction initial stage benzene and toluene productivity ratio catalyzer D high about 1.4 heavy %, and liquid is received low about 2 heavy %, and in the reaction later stage, liquid product yield is suitable, benzene and toluene productivity ratio catalyzer D high nearly 5 heavy %.
Example 14
This example is the contrast experiment of catalyst A of the present invention-6 with catalyzer D, and experiment condition the results are shown in Table 11 with example 10.Table 11 is the result show, A-6 catalyzer benzene and toluene yield are lower than the D catalyzer slightly, but liquid yield high nearly 2 heavy %.
Claims (6)
1, a kind of catalyst for reforming naphtha that contains metal Pt, Re, Ti and halogen, it is characterized in that adopting single diaspore that the low-carbon alkoxy aluminium method for hydrolysis obtains or sneaking into single diaspore that 30～70% usefulness additive methods obtain therein is raw material, through moulding, 450～700 ℃ of γ-Al that following roasting makes
2O
3Be carrier, loaded metal Pt, Re, Ti and halogen Cl, its composition (with the butt aluminum oxide is benchmark, heavy %):
Pt 0.10～1.00
Re 0.10～3.00
Ti 0.00～0.15
Cl 0.50～3.00
All the other are γ-Al
2O
3
2,, it is characterized in that best composition the (heavy %): Pt 0.10～0.60, Re 0.10～2.00, Ti 0.01～0.15, Cl 0.8～2.0 according to the described catalyzer of claim 1.
3,, it is characterized in that catalyzer Re/Pt ratio is that 0.1～4.0(is heavy according to claim 1 or 2 described catalyzer), it is heavy to be preferably 1.00～3.00().
4, according to the described catalyzer of claim 1, it is characterized in that single diaspore before the moulding can be slurries after spray-dried dry glue powder or the dry glue powder after the wet cake spraying drying, also available wet cake is directly made raw material, and is best with the latter.
5,, it is characterized in that preferably 550～650 ℃ of single diaspore maturing temperatures after the moulding according to claim 1 or 4 described catalyzer.
6, according to claim 1 or 2 described catalyzer, it is characterized in that it is that 40～230 ℃ of virgin naphthas or the boiling range that comprises coking in the refining of petroleum, cracking explained hereafter are 40～230 ℃ naphtha reforming that this catalyzer can be used for boiling range, is specially adapted to virgin naphtha and reforms.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN 87107556 CN1015636B (en) | 1987-11-04 | 1987-11-04 | Naphtha reforming catalyst |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN 87107556 CN1015636B (en) | 1987-11-04 | 1987-11-04 | Naphtha reforming catalyst |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1032951A true CN1032951A (en) | 1989-05-17 |
| CN1015636B CN1015636B (en) | 1992-02-26 |
Family
ID=4816135
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN 87107556 Expired CN1015636B (en) | 1987-11-04 | 1987-11-04 | Naphtha reforming catalyst |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN1015636B (en) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1039818C (en) * | 1995-10-06 | 1998-09-16 | 中国石油化工总公司石油化工科学研究院 | Multiple-metal reforming catalyst |
| CN1044377C (en) * | 1996-03-21 | 1999-07-28 | 中国石油化工总公司 | Preparation of reforming platinum-rhenium catalyst |
| CN1047326C (en) * | 1995-06-14 | 1999-12-15 | 中国石油化工总公司石油化工科学研究院 | Platinum-rhenium reforming catalyst |
| CN101293208B (en) * | 2007-04-28 | 2010-10-20 | 中国石油化工股份有限公司 | Reforming catalyst and preparation method thereof |
| CN105385470A (en) * | 2014-09-05 | 2016-03-09 | 北京安耐吉能源工程技术有限公司 | Catalytic reforming method |
| CN105435821A (en) * | 2014-09-05 | 2016-03-30 | 北京安耐吉能源工程技术有限公司 | Three-metal reforming catalyst, preparation method and application |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN100344373C (en) * | 2004-08-31 | 2007-10-24 | 中国石油化工股份有限公司 | Multi-metal reforming catalyst and preparing method |
-
1987
- 1987-11-04 CN CN 87107556 patent/CN1015636B/en not_active Expired
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1047326C (en) * | 1995-06-14 | 1999-12-15 | 中国石油化工总公司石油化工科学研究院 | Platinum-rhenium reforming catalyst |
| CN1039818C (en) * | 1995-10-06 | 1998-09-16 | 中国石油化工总公司石油化工科学研究院 | Multiple-metal reforming catalyst |
| CN1044377C (en) * | 1996-03-21 | 1999-07-28 | 中国石油化工总公司 | Preparation of reforming platinum-rhenium catalyst |
| CN101293208B (en) * | 2007-04-28 | 2010-10-20 | 中国石油化工股份有限公司 | Reforming catalyst and preparation method thereof |
| CN105385470A (en) * | 2014-09-05 | 2016-03-09 | 北京安耐吉能源工程技术有限公司 | Catalytic reforming method |
| CN105435821A (en) * | 2014-09-05 | 2016-03-30 | 北京安耐吉能源工程技术有限公司 | Three-metal reforming catalyst, preparation method and application |
Also Published As
| Publication number | Publication date |
|---|---|
| CN1015636B (en) | 1992-02-26 |
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