JP3303341B2 - Method for producing beta zeolite - Google Patents

Method for producing beta zeolite

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Publication number
JP3303341B2
JP3303341B2 JP20353592A JP20353592A JP3303341B2 JP 3303341 B2 JP3303341 B2 JP 3303341B2 JP 20353592 A JP20353592 A JP 20353592A JP 20353592 A JP20353592 A JP 20353592A JP 3303341 B2 JP3303341 B2 JP 3303341B2
Authority
JP
Japan
Prior art keywords
slurry
beta zeolite
acid
zeolite
added
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.)
Expired - Fee Related
Application number
JP20353592A
Other languages
Japanese (ja)
Other versions
JPH0648725A (en
Inventor
正之 大竹
賢治 森
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.)
Mitsubishi Chemical Corp
Original Assignee
Mitsubishi Chemical Corp
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Mitsubishi Chemical Corp filed Critical Mitsubishi Chemical Corp
Priority to JP20353592A priority Critical patent/JP3303341B2/en
Publication of JPH0648725A publication Critical patent/JPH0648725A/en
Application granted granted Critical
Publication of JP3303341B2 publication Critical patent/JP3303341B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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  • Silicates, Zeolites, And Molecular Sieves (AREA)

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【産業上の利用分野】本発明は吸着剤や有機化合物の異
性化、トランスアルキル化、不均化、水和、エステル
化、分解等の反応の触媒として有用なベータ型ゼオライ
トの製造方法に関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a process for producing a beta zeolite useful as a catalyst for reactions such as isomerization, transalkylation, disproportionation, hydration, esterification, and decomposition of adsorbents and organic compounds. It is.

【0002】[0002]

【従来の技術】ベータ型ゼオライトは公知である。この
ものはシリカ源、アルミナ源、アルカリ源、テトラエチ
ルアンモニウムカチオンなどのテンプレート剤及び水を
含有する混合物を密閉容器中に入れ、加熱して自己発生
圧下に反応させる水熱合成により製造される。この合成
法に関してはU.S.P.3,308,069に記載さ
れている。また、最近ではP.A.Jacobs他、A
ppl.Catal.,31,P35(1987)や、
EP187,522等にも合成法が記載されている。さ
らにこのものの結晶構造については、J.B.Higg
ins他 Zeolites,,P446(198
8)およびChem.&Eng.News,1988、
6/20号P23に記載されている。
BACKGROUND OF THE INVENTION Beta zeolites are known. This is produced by a hydrothermal synthesis in which a mixture containing a template agent such as a silica source, an alumina source, an alkali source, a tetraethylammonium cation and water is placed in a closed vessel, and heated to react under self-generated pressure. Regarding this synthesis method, see U.S. Pat. S. P. 3,308,069. Recently, P.I. A. Jacobs et al., A
ppl. Catal. , 31 ,, P35 (1987),
A synthesis method is also described in EP187, 522 and the like. Further, the crystal structure of this is described in J. Am. B. Higg
ins et al. Zeolites, 8 , P446 (198
8) and Chem. & Eng. News, 1988,
6/20, p. 23.

【0003】[0003]

【発明が解決しようとする課題】このベータ型ゼオライ
トを製造する際の問題点の一つは、水熱合成により生成
したベータ型ゼオライトを含むスラリーの濾過性が極め
て悪いことである。これはベータ型ゼオライトの粒子径
が0.1μm以下と極めて小さいことに加えて、スラリ
ー中にポリ珪酸塩成分が存在することによるものと推定
される。一般にゼオライトは荷電粒子なので、これを含
むスラリーに高分子凝集剤を添加して凝集させることが
できる。しかし、水熱合成により生成するベータ型ゼオ
ライトを含むスラリーは強アルカリ性であり、通常のア
ニオン系またはカチオン系の高分子凝集剤を添加しても
凝集が生じない。
One of the problems in producing the beta zeolite is that the slurry containing beta zeolite produced by hydrothermal synthesis has extremely poor filterability. This is presumed to be due to the fact that the beta zeolite has a very small particle size of 0.1 μm or less, and the presence of a polysilicate component in the slurry. In general, zeolite is a charged particle, and thus a slurry containing the zeolite can be aggregated by adding a polymer flocculant. However, the slurry containing beta-type zeolite produced by hydrothermal synthesis is strongly alkaline, and does not aggregate even when a general anionic or cationic polymer flocculant is added.

【0004】[0004]

【課題を解決するための手段】本発明によれば、水熱合
成により生成したベータ型ゼオライトを含むスラリーに
酸を添加してスラリーのpHを4〜8.5に調整したの
ち常法に従って濾過することにより、容易にスラリーか
らゼオライトを分離・回収することができる。この際、
スラリーに更にアニオン系高分子凝集剤を添加すると、
濾過は更に容易となる。本発明について更に詳細に説明
すると、本発明においてはベータ型ゼオライトの合成反
応自体は常法に従って行なうことができる。シリカ源と
してはシリカゾル、シリカゲル、アイロジル、沈降シリ
カ、珪酸エチルその他の珪酸エステル等が用いられる。
アルミナ源としては、アルミン酸ナトリウム、アルミン
酸カリウムなどのアルミン酸塩が好ましいが、硝酸アル
ミニウム、硫酸アルミニウム、酢酸アルミニウムその他
のアルミニウムの鉱酸塩や有機酸塩、さらには水和アル
ミナ等も用いることができる。アルカリ源としては水酸
化アルカリ、特に水酸化ナトリウムが一般的である。テ
ンプレート剤としてはテトラエチルアンモニウム(TE
A)の塩またはハイドロオキサイドを用いるのが一般的
であるが、テトラエチルホスホニウムカチオンを用いる
こともできる。これらの原料は一般に次のようなモル組
成となるように配合される。
According to the present invention, an acid is added to a slurry containing beta-type zeolite produced by hydrothermal synthesis to adjust the pH of the slurry to 4-8.5, followed by filtration according to a conventional method. By doing so, zeolite can be easily separated and recovered from the slurry. On this occasion,
When further adding an anionic polymer flocculant to the slurry,
Filtration becomes easier. The present invention will be described in more detail. In the present invention, the beta zeolite synthesis reaction itself can be carried out according to a conventional method. Examples of the silica source include silica sol, silica gel, irisole, precipitated silica, ethyl silicate, and other silicate esters.
As the alumina source, aluminates such as sodium aluminate and potassium aluminate are preferable, but aluminum nitrate, aluminum sulfate, aluminum acetate and other aluminum mineral and organic acid salts, and also hydrated alumina and the like may be used. Can be. Alkali hydroxide, particularly sodium hydroxide, is generally used as the alkali source. Tetraethylammonium (TE
The salt or hydroxide of A) is generally used, but a tetraethylphosphonium cation can also be used. These raw materials are generally blended so as to have the following molar composition.

【0005】 SiO2 /Al2 3 =10〜200 Na2 O/(TEA)2O=0.0〜0.2 (TEA)2O/SiO2 =0.05〜0.5 H2 O/(TEA)2O=40〜150[0005] SiO 2 / Al 2 O 3 = 10 to 200 Na 2 O / (TEA) 2 O = 0.0 to 0.2 (TEA) 2 O / SiO 2 = 0.05 to 0.5 H 2 O / (TEA) 2 O = 40-150

【0006】これらの原料をよく混合して反応容器に仕
込み、密閉して60〜200℃、好ましくは100〜1
80℃に加熱して自己発生圧下に反応を行なわせる。反
応に要する時間は一般に数時間〜数百時間であり、低温
で反応させるほど長時間を要する。従って通常は110
〜180℃で反応を行なうのが最も好ましい。ゼオライ
トの合成反応が完了したら反応器を冷却し、次いでスラ
リーに酸を添加してpHを4〜8.5に調整する。取扱
いを容易にするため、酸を添加するに先立ち水を加えて
スラリーを希釈しておくのが好ましい。酸としては硫酸
や塩酸が好ましいが、所望ならば硝酸や炭酸などの他の
無機酸、更には有機酸を用いることもできる。この中和
によりゲル状物が生成するが、これはスラリー中に存在
していたポリ珪酸塩成分に由来するものと考えられる。
そしてこのものは微細なベータ型ゼオライトのバインダ
ー様の作用を呈し、濾過性さらには取扱性の改善に寄与
しているものと推定される。本発明では上記により中和
したスラリーを濾過するに先立ち、これにポリアクリル
アマイドの部分加水分解物のようなアニオン系の高分子
凝集剤を添加すると更に濾過性が改善される。
[0006] These raw materials are mixed well, charged into a reaction vessel, and sealed, and the temperature is 60 to 200 ° C, preferably 100 to 1 ° C.
The reaction is carried out under self-generated pressure by heating to 80 ° C. The time required for the reaction is generally from several hours to several hundred hours, and the longer the reaction, the lower the temperature. Therefore usually 110
Most preferably, the reaction is carried out at -180 ° C. Upon completion of the zeolite synthesis reaction, the reactor is cooled and then the pH is adjusted to 4-8.5 by adding acid to the slurry. To facilitate handling, it is preferable to dilute the slurry by adding water before adding the acid. As the acid, sulfuric acid or hydrochloric acid is preferred, but if desired, other inorganic acids such as nitric acid or carbonic acid, and furthermore, organic acids can be used. This neutralization produces a gel-like substance, which is considered to be derived from the polysilicate component existing in the slurry.
It is presumed that this exhibits a binder-like action of fine beta zeolite, and contributes to improvement in filterability and further in handling. In the present invention, prior to filtering the neutralized slurry as described above, adding an anionic polymer flocculant such as a partial hydrolyzate of polyacrylamide to the slurry further improves the filterability.

【0007】上記のような中和、さらには凝集剤の添加
により、スラリーの濾過性は著るしく改善されるので、
濾過は常用の各種の濾過機を用いて容易に行なうことが
でき、更には濾過後の水洗も容易である。
[0007] By the above-described neutralization and further addition of a flocculant, the filterability of the slurry is remarkably improved.
Filtration can be easily carried out using various conventional filter machines, and further, washing with water after filtration is easy.

【0008】[0008]

【発明の効果】本発明によれば水熱合成により生成した
ベータ型ゼオライトを含むスラリーから、ベータ型ゼオ
ライトを容易に分離・回収することができる。
According to the present invention, beta zeolite can be easily separated and recovered from a slurry containing beta zeolite produced by hydrothermal synthesis.

【0009】[0009]

【実施例】【Example】

(実施例1)アルミン酸ナトリウム水溶液(住友化学社
製品。NA−170,Al2 3 含有量18.15%)
18.72g,テトラエチルアンモニウムハイドロオキ
サイドの40%水溶液129.60gおよび水90.6
8gを混合して均一な溶液とした。これにテトラエチル
オルトシリケート208.3gを添加して撹拌したとこ
ろ徐々に発熱して白濁した。2時間後、これをロータリ
ーエバポレーターで60〜70℃に加熱してエタノール
の大部分を留出させた。水で全量を380gに希釈した
のちオートクレーブに入れ、100℃に加熱して200
時間反応させた。
(Example 1) aqueous solution of sodium aluminate (Sumitomo Chemical's products .NA-170, Al 2 O 3 content of 18.15%)
18.72 g, 129.60 g of a 40% aqueous solution of tetraethylammonium hydroxide and 90.6 water
8 g were mixed to form a uniform solution. 208.3 g of tetraethylorthosilicate was added to the mixture, and the mixture was stirred and gradually heated to cloudy. After 2 hours, this was heated to 60-70 ° C. on a rotary evaporator to distill most of the ethanol. After diluting the total amount to 380 g with water, the mixture was placed in an autoclave and heated to 100 ° C.
Allowed to react for hours.

【0010】オートクレーブ内容物は乳白色のスラリー
であり、静置しても沈降性を示さなかった。スラリーの
一部を室温で風乾し、X線回折を行なったところ、X線
チャートはベータ型ゼオライトのものと完全に一致し
た。スラリーは濾紙を用いた常法の濾過では殆んど濾過
できなかったので、水で20倍に希釈したのち1規定硫
酸でpH7.5に中和したところゲル状物質が生成し
た。次いでこれにポリアクリルアマイドの部分加水分解
物であるアニオン系高分子凝集剤[三菱化成社製品、ダ
イアクリヤー(登録商標)MA−3000H]の0.1
%水溶液を凝集剤として3ppmとなるように添加し
た。スラリーは無色透明の上澄と沈澱とに分離した。常
法により濾過し、濾滓を水洗・乾燥した。X線回折を行
なったところ、そのX線チャートはベータ型ゼオライト
のものと完全に一致した。
The contents of the autoclave were milky white slurries and did not show sedimentation when allowed to stand. When a part of the slurry was air-dried at room temperature and subjected to X-ray diffraction, the X-ray chart completely coincided with that of the beta zeolite. Since the slurry could hardly be filtered by a conventional filtration method using filter paper, the slurry was diluted 20 times with water and then neutralized to pH 7.5 with 1 N sulfuric acid to produce a gel substance. Next, 0.1 part of an anionic polymer flocculant [Diaclear (registered trademark) MA-3000H], which is a partial hydrolyzate of polyacrylamide, was added thereto.
% Aqueous solution was added as a coagulant so as to be 3 ppm. The slurry separated into a clear and colorless supernatant and a precipitate. The mixture was filtered by a conventional method, and the cake was washed with water and dried. When X-ray diffraction was performed, the X-ray chart was completely consistent with that of the beta zeolite.

【0011】(実施例2)アルミン酸ナトリウム水溶液
9.36g、水酸化ナトリウム0.95g、水酸化カリ
ウム2.38gを、10%のテトラエチルアンモニウム
ハイドロオキサイド水溶液736.3gに溶解した。こ
れに粉末状のシリカゲル63.0gを添加し、テフロン
内筒を含むオートクレーブに装入した。135℃に加熱
して24時間反応させた。生成したスラリーの外観は実
施例1のものに近似しており、濾過性は極めて悪かっ
た。このものの一部を採取してX線回折を行なったとこ
ろ、そのX線チャートはベータ型ゼオライトのものと一
致した。
(Example 2) 9.36 g of an aqueous solution of sodium aluminate, 0.95 g of sodium hydroxide and 2.38 g of potassium hydroxide were dissolved in 736.3 g of a 10% aqueous solution of tetraethylammonium hydroxide. 63.0 g of powdered silica gel was added thereto, and the mixture was charged into an autoclave including a Teflon inner cylinder. The mixture was heated to 135 ° C. and reacted for 24 hours. The appearance of the resulting slurry was similar to that of Example 1, and the filterability was extremely poor. When a part of this product was sampled and subjected to X-ray diffraction, the X-ray chart coincided with that of beta zeolite.

【0012】このスラリーを実施例1と全く同様にして
水で希釈したのち硫酸でpH7.5まで中和し、さらに
アニオン系高分子凝集剤を添加した。スラリーは上澄と
沈澱に分離し、常法により容易に濾過することができ
た。
This slurry was diluted with water in the same manner as in Example 1, neutralized to pH 7.5 with sulfuric acid, and further added with an anionic polymer flocculant. The slurry was separated into a supernatant and a precipitate, and could be easily filtered by a conventional method.

───────────────────────────────────────────────────── フロントページの続き (58)調査した分野(Int.Cl.7,DB名) C01B 39/00 - 39/54 B01J 29/00 B01J 20/16 CA(STN) JICSTファイル(JOIS) WPI/L──────────────────────────────────────────────────続 き Continued on the front page (58) Field surveyed (Int. Cl. 7 , DB name) C01B 39/00-39/54 B01J 29/00 B01J 20/16 CA (STN) JICST file (JOIS) WPI / L

Claims (3)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】 シリカ源、アルミナ源、アルカリ源、テ
ンプレート剤及び水を含有する混合物を密閉容器中で加
熱してベータ型ゼオライトを含むスラリーを生成させ、
次いでこれに酸を加えてスラリーのpHを4〜8.5に
調整したのち濾過することを特徴とするベータ型ゼオラ
イトの製造方法。
Claims 1. A mixture containing a silica source, an alumina source, an alkali source, a template agent and water is heated in a closed vessel to form a slurry containing beta zeolite.
Then, an acid is added to the slurry to adjust the pH of the slurry to 4-8.5, followed by filtration.
【請求項2】 ベータ型ゼオライトを含むスラリーに酸
とアニオン系高分子凝集剤を加えてスラリーのpHを4
〜8.5に調整したのち濾過することを特徴とする請求
項1記載の方法。
2. An acid and an anionic polymer coagulant are added to a slurry containing beta-type zeolite to adjust the pH of the slurry to 4.
2. The method according to claim 1, wherein the filtration is carried out after adjusting to -8.5.
【請求項3】 アニオン系高分子凝集剤がポリアクリル
アミドの部分加水分解物であることを特徴とする請求項
2記載の方法。
3. The method according to claim 2, wherein the anionic polymer flocculant is a partial hydrolyzate of polyacrylamide.
JP20353592A 1992-07-30 1992-07-30 Method for producing beta zeolite Expired - Fee Related JP3303341B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP20353592A JP3303341B2 (en) 1992-07-30 1992-07-30 Method for producing beta zeolite

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP20353592A JP3303341B2 (en) 1992-07-30 1992-07-30 Method for producing beta zeolite

Publications (2)

Publication Number Publication Date
JPH0648725A JPH0648725A (en) 1994-02-22
JP3303341B2 true JP3303341B2 (en) 2002-07-22

Family

ID=16475763

Family Applications (1)

Application Number Title Priority Date Filing Date
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Country Status (1)

Country Link
JP (1) JP3303341B2 (en)

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Publication number Priority date Publication date Assignee Title
US7253331B2 (en) 2004-05-12 2007-08-07 Exxonmobil Chemical Patents Inc. Molecular sieve catalyst composition, its making and use in conversion processes
US7732537B2 (en) 2008-01-29 2010-06-08 Exxonmobil Chemical Patents Inc. Methods addressing aging in flocculated molecular sieve catalysts for hydrocarbon conversion processes

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