JP2008285416A5 - - Google Patents

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JP2008285416A5
JP2008285416A5 JP2007129039A JP2007129039A JP2008285416A5 JP 2008285416 A5 JP2008285416 A5 JP 2008285416A5 JP 2007129039 A JP2007129039 A JP 2007129039A JP 2007129039 A JP2007129039 A JP 2007129039A JP 2008285416 A5 JP2008285416 A5 JP 2008285416A5
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producing methacrolein
catalyst
group
element selected
sulfur
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JP2007129039A
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JP5301110B2 (en
JP2008285416A (en
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Description

また、本発明のメタクロレインの製造方法では、原料ガス中の硫黄化合物の濃度は、該原料ガス中の第三級ブタノールとイソブチレンとの合計質量に対し、硫黄原子として0.1〜5000質量ppmとなるようにすることが望ましい。
また、本発明のメタクロレインの製造方法では、硫黄化合物としてメルカプタン類を含む原料ガスを使用することが望ましい。
Further, in the method for producing methacrolein of the present invention, the concentration of the sulfur compound in the raw material gas is 0.1 to 5,000 mass ppm as a sulfur atom with respect to the total mass of the tertiary butanol and isobutylene in the raw material gas. It is desirable that
In the method for producing methacrolein of the present invention, it is desirable to use a raw material gas containing mercaptans as a sulfur compound.

Claims (4)

触媒の存在下、第三級ブタノール及び/又はイソブチレンを分子状酸素により気相接触酸化するメタクロレインの製造方法において、硫黄化合物を含む原料ガスを使用することを特徴とする、メタクロレインの製造方法。   A method for producing methacrolein, characterized in that a raw material gas containing a sulfur compound is used in a method for producing methacrolein in which gas phase catalytic oxidation of tertiary butanol and / or isobutylene with molecular oxygen is carried out in the presence of a catalyst. . 前記原料ガス中の第三級ブタノールとイソブチレンとの合計質量に対し、硫黄原子として0.1〜5000質量ppmとなるように、硫黄化合物が原料ガス中に含まれていることを特徴とする、請求項1に記載のメタクロレインの製造方法。   The sulfur compound is contained in the source gas so that the total mass of tertiary butanol and isobutylene in the source gas is 0.1 to 5000 ppm by mass as a sulfur atom, The method for producing methacrolein according to claim 1. 前記硫黄化合物として、メルカプタン類を含む原料ガスを使用することを特徴とする、請求項1又は2のいずれかに記載のメタクロレインの製造方法。The method for producing methacrolein according to claim 1, wherein a raw material gas containing a mercaptan is used as the sulfur compound. 触媒として、下記組成式(1)のものを使用することを特徴とする、請求項1〜3のいずれかに記載のメタクロレインの製造方法。
MoBiFeSi (1)
ここで、Mo、Bi、Fe、Si及びOは、それぞれモリブデン、ビスマス、鉄、ケイ素および酸素を示し、Mはコバルト及びニッケルからなる群より選ばれた少なくとも1種の元素を示し、Xはクロム、鉛、マンガン、カルシウム、マグネシウム、ニオブ、銀、バリウム、スズ、タンタル及び亜鉛からなる群より選ばれた少なくとも1種の元素を示し、Yはリン、ホウ素、硫黄、セレン、テルル、セリウム、タングステン、アンチモン及びチタンからなる群より選ばれた少なくとも1種の元素を示し、Zはリチウム、ナトリウム、カリウム、ルビジウム、セシウム及びタリウムからなる群より選ばれた少なくとも1種の元素を示す。
a、b、c、d、e、f、g、h及びiは、各元素の原子比率を表し、a=12のとき、b=0.01〜3、c=0.01〜5、d=1〜12、e=0〜8、f=0〜5、g=0.001〜2、h=0〜20であり、iは前記各成分の原子価を満足するのに必要な酸素原子比率である。
The method for producing methacrolein according to any one of claims 1 to 3, wherein a catalyst having the following composition formula (1) is used as a catalyst.
Mo a Bi b Fe c M d X e Y f Z g Si h O i (1)
Here, Mo, Bi, Fe, Si and O represent molybdenum, bismuth, iron, silicon and oxygen, M represents at least one element selected from the group consisting of cobalt and nickel, and X represents chromium. Represents at least one element selected from the group consisting of lead, manganese, calcium, magnesium, niobium, silver, barium, tin, tantalum and zinc, and Y represents phosphorus, boron, sulfur, selenium, tellurium, cerium, tungsten , Z represents at least one element selected from the group consisting of lithium, sodium, potassium, rubidium, cesium and thallium.
a, b, c, d, e, f, g, h, and i represent the atomic ratio of each element. When a = 12, b = 0.01-3, c = 0.01-5, d = 1 to 12, e = 0 to 8, f = 0 to 5, g = 0.001 to 2, h = 0 to 20, and i is an oxygen atom necessary for satisfying the valence of each component. It is a ratio.
JP2007129039A 2007-05-15 2007-05-15 Method for producing methacrolein Active JP5301110B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2007129039A JP5301110B2 (en) 2007-05-15 2007-05-15 Method for producing methacrolein

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2007129039A JP5301110B2 (en) 2007-05-15 2007-05-15 Method for producing methacrolein

Publications (3)

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JP2008285416A JP2008285416A (en) 2008-11-27
JP2008285416A5 true JP2008285416A5 (en) 2010-06-17
JP5301110B2 JP5301110B2 (en) 2013-09-25

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JP2007129039A Active JP5301110B2 (en) 2007-05-15 2007-05-15 Method for producing methacrolein

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Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS54157522A (en) * 1978-05-31 1979-12-12 Nippon Kayaku Co Ltd Preparation of methacrolein and methacrylic acid
JPH0681749B2 (en) * 1985-04-30 1994-10-19 三菱化成株式会社 Method for producing maleic anhydride
DE4113423A1 (en) * 1991-04-25 1992-10-29 Roehm Gmbh OXIDATION CATALYST IMPLEMENTED WITH MACROPORES
JP3342794B2 (en) * 1994-12-21 2002-11-11 三菱レイヨン株式会社 Method for producing supported catalyst for synthesis of methacrolein and methacrylic acid
JP3347246B2 (en) * 1995-10-30 2002-11-20 三菱レイヨン株式会社 Method for producing catalyst for the synthesis of unsaturated aldehydes and unsaturated carboxylic acids
US6258992B1 (en) * 1999-09-17 2001-07-10 Saudi Basic Industries Corporation Gas phase catalytic oxidation of hydrocarbons to carboxylic acids and dehydrogenated products
JP4179780B2 (en) * 2001-12-28 2008-11-12 三菱レイヨン株式会社 Method for producing catalyst for synthesizing unsaturated aldehyde and unsaturated carboxylic acid, catalyst produced by this method, and method for synthesizing unsaturated aldehyde and unsaturated carboxylic acid using this catalyst
CN100592932C (en) * 2002-02-19 2010-03-03 三菱丽阳株式会社 Catalyst for production of unsaturated aldehyde and unsaturated carboxylic acid and process for producing the same
JP4678765B2 (en) * 2005-05-09 2011-04-27 三菱レイヨン株式会社 A method for producing a metal oxide catalyst, and a method for producing an unsaturated aldehyde and an unsaturated carboxylic acid.

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