CN1194943A - Process for synthesizing ZSM-5 molecular sieve by using NaY mother liquor - Google Patents
Process for synthesizing ZSM-5 molecular sieve by using NaY mother liquor Download PDFInfo
- Publication number
- CN1194943A CN1194943A CN97103801A CN97103801A CN1194943A CN 1194943 A CN1194943 A CN 1194943A CN 97103801 A CN97103801 A CN 97103801A CN 97103801 A CN97103801 A CN 97103801A CN 1194943 A CN1194943 A CN 1194943A
- Authority
- CN
- China
- Prior art keywords
- molecular sieve
- zsm
- silicon
- mother liquor
- synthetic
- 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.)
- Granted
Links
Images
Landscapes
- Catalysts (AREA)
- Silicates, Zeolites, And Molecular Sieves (AREA)
Abstract
A process for synthesizing molecular sieve ZSM-5 with NaY mother liquid as raw material includes such technological steps as acid deposition, spray drying to obtain Si-Al microballs, mixing them with NaOH, water and crystal seed of molecular sieve to obtain reaction mixture with mole ratio of 20-80 for SiO2-Al2O3, 0.05-0.3 for OH/SiO2 and 2-10 for H2O/SiO2, and hydrothermal crystallizing. Its advantages are low cost and high synthesis efficiency.
Description
The present invention relates to the NaY molecular sieve method that the mother liquor when synthetic synthesizes the ZSM-5 molecular sieve.
The prior art silica alumina ratio that feeds intake when synthetic NaY molecular sieve is generally 8~12, and the silica alumina ratio of product is generally 4~5.5, so just, there is greatly silicon be retained in the mother liquor and do not obtain utilizing (also containing very a spot of unreacted aluminium in the mother liquor), factory drains mother liquor as sewage, cause very big waste, and increased the sewage load of factory, cause pollution to dirty border.The research report that pair second stage employ of NaY mother liquor is also arranged in the prior art for example proposes among the DD 227416A to synthesize the X zeolite with the mother liquor of synthetic Y zeolite or mordenite; Propose among the SU 975573A NaY mother liquor is made silicon (aluminium) glue, and then synthesize the raw material of NaY zeolite with the conduct of this silicon (aluminium) glue.In general faujusite (X and Y type) and mordenite ratio are easier to synthesize, and do not see in the prior art that useful NaY mother liquor synthesizes the report of ZSM-5 zeolite.
The ZSM-5 molecular sieve from 1972 by U.S. Mobil company reported first (USP 3702886) since, in many chemical processes, obtained application, its preparation method is also being updated, synthetic by initial employing organic amine template, non-amine method finally is synthetic, and to the modification of synthetic after product etc., the Application Areas of ZSM-5 molecular sieve is constantly enlarged, how improving the single-autoclave yield rate of ZSM-5 when synthetic also is an important topic in this field.
An object of the present invention is to provide a kind of is the method that raw material synthesizes the ZSM-5 molecular sieve with the NaY mother liquor, makes refuse obtain utilizing, and reduces the synthetic cost of ZSM-5 molecular sieve.
Another object of the present invention provides the synthetic method of the ZSM-5 molecular sieve of the low water yield that feeds intake of a kind of employing, the single-autoclave yield rate when synthesizing to improve.
The synthetic method of ZSM-5 molecular sieve provided by the present invention comprises:
(1) mother liquor that will be with water glass be produced during for the synthetic NaY in silicon source regulates PH to 5~6 with mineral acid so that silicon wherein and aluminium are precipitated out with the form of alumino silica gel, filters the back making beating, the spray-dried silicon aluminium microsphere that obtains of the slurries that obtain,
(2) (1) gained silicon aluminium microsphere is mixed with NaOH and water, adds or do not add the molecular sieve crystal seed, make reaction mixture with following mole proportioning:
SiO
2/Al
2O
3=20~80
OH
-/SiO
2=0.05~0.3
H
2O/SiO
2=2~10
(3) with (2) gained reaction mixture hydrothermal crystallizing according to a conventional method.
The conventional spraying drying condition that is adopted when said spraying drying is according to the preparation cracking catalyst in the step in the method provided by the invention (1) is carried out, and wherein the solid content of said slurries is advisable with 10~45 heavy %.
Said molecular sieve crystal seed can be one or more in faujusite (X type or y-type zeolite), A type zeolite, β zeolite and the ZSM-5 zeolite in the step in the method provided by the invention (2), the usage quantity of crystal seed is 0~8 heavy % of said silicon aluminium microsphere weight, the SiO in the crystal seed
2And Al
2O
3Count in total composition of reaction mixture.
Aluminium adjustment in the method provided by the invention in useful molecules sieve crystal seed feeds intake the silica alumina ratio, also can by in the NaY mother liquor, add aluminium salt then set by step (1) make the silicon aluminium microsphere adjustment silica alumina ratio that feeds intake, perhaps adding aluminium salt or the aluminate adjustment silica alumina ratio that feeds intake in step (2).
The condition of said crystallization generally is 120~220 ℃ of following crystallization 6 hours to 8 days in the said method of the present invention, preferably 140~200 ℃ of following crystallization 8 hours to 6 days.
The synthetic method of ZSM-5 molecular sieve provided by the present invention can make the NaY mother liquor be utilized effectively, the synthetic cost of ZSM-5 molecular sieve is reduced, silicon source and part aluminium source when being synthetic owing to employing solid silicon aluminium glue simultaneously, reaction mixture only is divided into glue at the surface element of silicon aluminium microsphere, the nucleation crystallization of molecular sieve takes place on the surface of silicon aluminium microsphere first, progressively be deep into the center, show as the surface and concentrate effect, therefore the water yield that feeds intake of synthetic system just can significantly reduce, prior art feeds intake water silicon ratio greater than 10 when adopting water glass to synthesize the ZSM-5 molecular sieve for the silicon source, generally greater than 20, and the water silicon ratio that feeds intake in the inventive method is 2~10, owing to the reduction of the water yield that feeds intake, also improved the combined coefficient of reactor unit volume greatly.
Fig. 1 is X-ray diffraction (XRD) the crystalline phase figure of embodiment 2 gained samples.
The following examples will the present invention is described further.
In each embodiment, relative crystallinity be with product and standard specimen separately the ratio of the peak height sum of five diffraction peaks (be commonly called as Five Fingers Peak) of 2 θ angles between 22.5~25.0 of X-ray diffraction (XRD) represent, standard specimen herein (degree of crystallinity is decided to be 100%) is the ZSM-5 of industrial goods (Qilu Petrochemical company Zhou village catalyst plant is produced, and the industrial trade mark is ZRP-1); The BET surface-area of sample adopts the GB/T5816-1995 standard method to measure; SiO in the silicon aluminium microsphere
2And Al
2O
3Content is measured with RIPP134-90 standard method (see " petrochemical complex analytical procedure ", Yang Cuiding etc. write, Science Press, nineteen ninety publication).
Embodiment 1
The present embodiment explanation is with the silicon aluminium microsphere of NaY mother liquor preparation as the raw material of synthetic ZSM-5 molecular sieve.
With NaY mother liquor (taking from Chang Ling oil-refining chemical factory molecular sieve workshop of Catalyst Factory) is dilute sulphuric acid adjusting PH to 5~6 of 40 heavy % with concentration, silicon in the mother liquor and aluminium are precipitated out with the form of alumino silica gel, after the filtration, filter cake is added the water making beating make the slurries that solid content is 25 heavy %, to obtain silicon aluminium microsphere after this slurries spraying drying, wherein the particle diameter more than 80% is 40~80 μ m, again with the microballoon after this spraying with 3% ammoniumsulphate soln pulping and washing to Na
2The heavy % in O<1, it is synthetic with the ZSM-5 that is used for the back to obtain the silicon aluminium microsphere product after the drying, its SiO of analysis revealed
2Content is 94 heavy %, Al
2O
3Content is 2.7 heavy %, and the BET surface-area is 501m
2/ g.
Embodiment 2
With 53.37 gram NaOH (chemical pure, the commercial reagent) is dissolved in the 1100 gram water, (Zhengzhou Aluminium Plant produces to wherein adding 30.0 gram NaA type molecular sieves then, burning residual solid content is 78.8 heavy %) as crystal seed, (burning residual solid content is 82.7 heavy % to add 650 gram embodiment, 1 gained silicon aluminium microsphere again, down together), after stirring the gained mixture is transferred in 2 liters the autoclave, stirred crystallization 18 hours down in 180 ℃, product is taken out in the cooling back, after filtration, after washing and the drying, the XRD crystalline phase figure of products obtained therefrom as shown in Figure 1, be indicated as the ZSM-5 structure, its relative crystallinity is 98%, and the BET surface-area is 321m
2/ g.
Embodiment 3
1.07 gram NaOH are dissolved in the 20.0 gram water, and (American I ntercat company commerical prod burns residual solid content 80.5 heavy %, SiO to wherein adding 0.5 gram ZSM-5 molecular sieve
2/ Al
2O
3=450) and 18.0 gram embodiment 1 gained silicon aluminium microspheres, pack into after stirring in the stainless steel cauldron in 140 ℃ of static crystallization 5 days, product is taken out in the cooling back, after filtration, obtain the ZSM-5 zeolite product after washing and the drying, figure is identical with Fig. 1 for its XRD crystalline phase, and relative crystallinity is 95%.
Embodiment 4
1.4 gram NaOH are dissolved in the 17 gram water, and (Chang Ling oil-refining chemical factory catalyst plant is produced, and burning residual solid content is 82.0 heavy %, SiO to wherein adding 0.5 gram NaY molecular sieve
2/ Al
2O
3=5.0) and 18.0 gram embodiment 1 gained silicon aluminium microspheres, pack into after stirring in the stainless steel cauldron in 180 ℃ of static crystallization 16 hours down, product is taken out in the cooling back, after filtration, obtain the ZSM-5 zeolite product after washing and the drying, figure is identical with Fig. 1 for its XRD crystalline phase, and relative crystallinity is 96%.
Embodiment 5
1.72 gram NaOH are dissolved in the 30 gram water, to wherein adding 1.2 gram NaA type molecular sieves (with embodiment 2) and 18.0 gram embodiment, 1 gained silicon aluminium microsphere, pack into after stirring in the stainless steel cauldron in 180 ℃ of static crystallization 18 hours down, product is taken out in the cooling back, after filtration, obtain the ZSM-5 zeolite product after washing and the drying, figure is identical with Fig. 1 for its XRD crystalline phase, and relative crystallinity is 98%.
Embodiment 6
0.70 gram NaOH is dissolved in the 20 gram water, and (Fushun No.3 Petroleum Factory produces, and burning residual solid content is 81.5 heavy %, SiO to wherein adding 0.38 gram beta-molecular sieve
2/ Al
2O
3=30) and 18.0 the gram embodiment 1 in the gained silicon aluminium microsphere, pack into after stirring in the stainless steel cauldron in 160 ℃ of static crystallization 36 hours down, product is taken out in the cooling back, after filtration, obtain the ZSM-5 zeolite product after washing and the drying, figure is identical with Fig. 1 for its XRD crystalline phase, and relative crystallinity is 90%.
Embodiment 7
According to the same terms preparation of embodiment 5, different is not add any molecular sieve crystal seed, and the XRD crystalline phase figure of products therefrom is identical with Fig. 1, and relative crystallinity is 90%.
Claims (3)
1. the synthetic method of a ZSM-5 molecular sieve is characterized in that this method comprises:
(1) mother liquor that will be with water glass be produced during for the synthetic NaY in silicon source regulates PH to 5~6 with mineral acid so that silicon wherein and aluminium are precipitated out with the form of alumino silica gel, filters the back making beating, the spray-dried silicon aluminium microsphere that obtains of the slurries that obtain,
(2) the molecular sieve crystal seed with (1) gained silicon aluminium microsphere and NaOH, water and 0~8 heavy % (with respect to the consumption of silicon aluminium microsphere) mixes, and makes the reaction mixture with following mole proportioning:
SiO
2/Al
2O
3=20~80
OH
-/SiO
2=0.05~0.3
H
2O/SiO
2=2~10
(3) with (2) gained reaction mixture hydrothermal crystallizing according to a conventional method.
2. according to the synthetic method of claim 1, wherein said molecular sieve crystal seed is one or more in faujusite, A type zeolite, β zeolite and the ZSM-5 zeolite.
3. according to the synthetic method of claim 1, wherein said crystallization condition is that temperature is 120~220 ℃, and the time is 6 hours to 8 days.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN97103801A CN1057067C (en) | 1997-03-31 | 1997-03-31 | Process for synthesizing ZSM-5 molecular sieve by using NaY mother liquor |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN97103801A CN1057067C (en) | 1997-03-31 | 1997-03-31 | Process for synthesizing ZSM-5 molecular sieve by using NaY mother liquor |
Publications (2)
Publication Number | Publication Date |
---|---|
CN1194943A true CN1194943A (en) | 1998-10-07 |
CN1057067C CN1057067C (en) | 2000-10-04 |
Family
ID=5166886
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN97103801A Expired - Lifetime CN1057067C (en) | 1997-03-31 | 1997-03-31 | Process for synthesizing ZSM-5 molecular sieve by using NaY mother liquor |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN1057067C (en) |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1100005C (en) * | 2000-06-28 | 2003-01-29 | 中国科学院山西煤炭化学研究所 | Method for quickly synthesizing small crystal grain ZSM-5 molecular sieve by using guide agent method |
CN1307102C (en) * | 2004-06-29 | 2007-03-28 | 中国石油化工股份有限公司 | Process for preparing ZSM-5 molecular sieve |
CN1325377C (en) * | 2004-11-24 | 2007-07-11 | 山东铝业股份有限公司 | Method for producing 4A molecular sieve by using waste liquid of NaY molecular sieve production |
CN100429149C (en) * | 2004-11-26 | 2008-10-29 | 中国石油天然气股份有限公司 | Production for synthesizing high-content NaY molecular sieve from kaolin atomized microball |
CN102372284A (en) * | 2010-08-23 | 2012-03-14 | 中国石油化工股份有限公司 | Method for preparing small crystal grain ZSM-5 zeolite |
CN102757069A (en) * | 2011-04-29 | 2012-10-31 | 山东齐鲁华信高科有限公司 | Method for reusing mother liquor generated in ZSM (zeolite socony mobil)-5 molecular sieve preparation |
CN110194467A (en) * | 2019-07-04 | 2019-09-03 | 青岛惠城环保科技股份有限公司 | A method of 13X molecular sieve is prepared by NaY mother liquor |
CN110342533A (en) * | 2018-04-02 | 2019-10-18 | 国家能源投资集团有限责任公司 | Molecular sieve and its preparation method and application |
CN112694099A (en) * | 2019-10-21 | 2021-04-23 | 中国石油化工股份有限公司 | ZSM-5 molecular sieve and synthetic method thereof |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6908603B2 (en) | 2003-06-02 | 2005-06-21 | Engelhard Corporation | In-situ ZSM-5 synthesis |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3702886A (en) * | 1969-10-10 | 1972-11-14 | Mobil Oil Corp | Crystalline zeolite zsm-5 and method of preparing the same |
US4061724A (en) * | 1975-09-22 | 1977-12-06 | Union Carbide Corporation | Crystalline silica |
US4526879A (en) * | 1978-11-13 | 1985-07-02 | Mobil Oil Corporation | Synthesis of zeolite ZSM-5 |
-
1997
- 1997-03-31 CN CN97103801A patent/CN1057067C/en not_active Expired - Lifetime
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1100005C (en) * | 2000-06-28 | 2003-01-29 | 中国科学院山西煤炭化学研究所 | Method for quickly synthesizing small crystal grain ZSM-5 molecular sieve by using guide agent method |
CN1307102C (en) * | 2004-06-29 | 2007-03-28 | 中国石油化工股份有限公司 | Process for preparing ZSM-5 molecular sieve |
CN1325377C (en) * | 2004-11-24 | 2007-07-11 | 山东铝业股份有限公司 | Method for producing 4A molecular sieve by using waste liquid of NaY molecular sieve production |
CN100429149C (en) * | 2004-11-26 | 2008-10-29 | 中国石油天然气股份有限公司 | Production for synthesizing high-content NaY molecular sieve from kaolin atomized microball |
CN102372284A (en) * | 2010-08-23 | 2012-03-14 | 中国石油化工股份有限公司 | Method for preparing small crystal grain ZSM-5 zeolite |
CN102372284B (en) * | 2010-08-23 | 2013-01-09 | 中国石油化工股份有限公司 | Method for preparing small crystal grain ZSM-5 zeolite |
CN102757069A (en) * | 2011-04-29 | 2012-10-31 | 山东齐鲁华信高科有限公司 | Method for reusing mother liquor generated in ZSM (zeolite socony mobil)-5 molecular sieve preparation |
CN110342533A (en) * | 2018-04-02 | 2019-10-18 | 国家能源投资集团有限责任公司 | Molecular sieve and its preparation method and application |
CN110194467A (en) * | 2019-07-04 | 2019-09-03 | 青岛惠城环保科技股份有限公司 | A method of 13X molecular sieve is prepared by NaY mother liquor |
CN112694099A (en) * | 2019-10-21 | 2021-04-23 | 中国石油化工股份有限公司 | ZSM-5 molecular sieve and synthetic method thereof |
Also Published As
Publication number | Publication date |
---|---|
CN1057067C (en) | 2000-10-04 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN1107644C (en) | Process for preparing molecular sieve (MCM-22) with special crystal structure | |
CN1057067C (en) | Process for synthesizing ZSM-5 molecular sieve by using NaY mother liquor | |
CN1699173A (en) | Synthesis method of fine grain ZSM-5 zeolite molecular sieve with high silicon aluminium ratio | |
CN1107645C (en) | Process for synthesizing molecular sieve (MCM-22) with special crystal structure | |
CN1107646C (en) | Preparation of A-type zeolite | |
CN1048697C (en) | Method for synthesis of beta-zeolite | |
CN1187462A (en) | Process for synthesizing ZSM-5 molecular sieve | |
CN1035668C (en) | Method No.1 for synthesizing beta zealite | |
CN1267345C (en) | Preparation method of NaY molecular sieve | |
CN1031791C (en) | Preparation of high-silicon Y-shaped molecular sieve | |
CN1247457C (en) | Synthetic method for ZSM-5 zeolite | |
CN1051055C (en) | Method for synthesis of beta-zeolite | |
CN1171789C (en) | X zeolite preparation | |
CN1088406C (en) | Synthetic method for high silicon ZSM-5 zeolite | |
CN1781600A (en) | Method for preparing composite material containing Y-type molecular sieve | |
CN1099788A (en) | Cracking catalyst of rich producing olefines | |
CN1111085C (en) | Molecular sieve containing heteroatoms and its synthesis | |
CN1272246C (en) | Synthesis method of NaY molecular sieve | |
CN1074389C (en) | Process for synthesizing fine-grain octahedra zeolite | |
CN1299857A (en) | Petroleum hydrocarbon cracking catalyst and its preparation | |
CN1030286C (en) | Preparation of ZSM-5 zeolite/silica-gel composite catalyst material | |
CN1111087C (en) | Molecular sieve containing zinc and its synthesis | |
CN1083399C (en) | Synthesis of high-silicon mordenite | |
CN1102535C (en) | Preparation method of molecular sieve | |
CN1111137C (en) | Process for synthesizing Y-type molecular sieve from stellerite |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
C14 | Grant of patent or utility model | ||
GR01 | Patent grant | ||
CX01 | Expiry of patent term | ||
CX01 | Expiry of patent term |
Granted publication date: 20001004 |
|
DD01 | Delivery of document by public notice | ||
DD01 | Delivery of document by public notice |
Addressee: China Petrochemical Corporation Document name: Notification of Expiration of Patent Right Duration |