IP Library Granted Patent US 7,217,836
Granted Patent B2
US 7,217,836 · App. 10/479,228 · Granted May 15, 2007

Process for producing (meth)acrolein and/or (meth)acrylic acid

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Quick Facts
Patent No.
US 7,217,836
App. No.
10/479,228
Granted
May 15, 2007
Kind
B2
Abstract

A method for producing (meth)acrolein and/or (meth)acrylic acid by subjecting isobutylene and the like or propylene to a vapor-phase catalytic oxidation with molecular oxygen in the presence of a solid oxidation catalyst in a tubular type of fixed bed reactor, wherein a temperature of a hot-spot zone is sufficiently controlled and (meth)acrolein and (meth)acrylic acid are produced with a high yield. A method for producing (meth)acrolein and/or (meth)acrylic acid by passing a raw material gas comprising isobutylene and the like or propylene and oxygen through a catalyst layer in a tubular type of fixed bed reactor which is filled with a solid oxidation catalyst, which includes passing a gas containing isobutylene and the like or propylene in a concentration lower than that of the raw material gas, and oxygen through the catalyst layer for a period of one hour or more prior to passing the raw material gas through the catalyst layer.

Claims (18)

1. A method for producing methacrolein and/or methacrylic acid by passing a raw material gas comprising isobutylene and/or tertiary butanol and oxygen through a catalyst layer in a tubular type of fixed bed reactor which is filled with a solid oxidation catalyst, which comprises passing a gas comprising isobutylene and/or tertiary butanol in a concentration lower than that of said raw material gas, and oxygen through said catalyst layer for a period of one hour or more prior to passing said raw material gas through said catalyst layer.

2. A method for producing methacrolein and/or methacrylic acid, which comprises:

filling a tubular type of fixed bed reactor with a solid oxidation catalyst;

elevating a temperature of the resultant catalyst layer to a range of 250° C. to 400° C. while passing a gas including oxygen, nitrogen, water vapor and 0 to 0.5% by volume of isobutylene and/or tertiary butanol through said catalyst layer;

passing a gas including 1 to 3.8% by volume of isobutylene and/or tertiary butanol, 7 to 16% by volume of oxygen and 5 to 50% by volume of water vapor through said catalyst layer at a temperature of 250° C. to 400° C. for a period of one hour or more; and thereafter

passing a raw material gas including 4 to 9% by volume of isobutylene and/or tertiary butanol, 7 to 16% by volume of oxygen and 5 to 50% by volume of water vapor through said catalyst layer at a temperature of 250° C. to 400° C.

3. The method for producing methacrolein and/or methacrylic acid according to claim 1 or 2 , wherein said solid oxidation catalyst is a compound oxide represented by the following formula (1):

Mo a Bi b Fe c A d X e Y f Z g O h   (1)

wherein Mo, Bi, Fe and O represent molybdenum, bismuth, iron and oxygen, respectively; A represents nickel and/or cobalt; X represents at least one element selected from the group consisting of magnesium, zinc, chromium, manganese, tin and lead; Y represents at least one element selected from the group consisting of phosphorus, boron, sulfur, tellurium, silicon, germanium, cerium, niobium, titanium, zirconium, tungsten and antimony; Z represents at least one element selected from the group consisting of potassium, sodium, rubidium, cesium and thallium; and each of a, b, c, d, e, f, g and h represents an atomic ratio of each element, wherein 0.1≦b≦5, 0.1≦c≦5, 1≦d≦12, 0≦e≦10, 0≦f≦10 and 0.01≦g≦3 when a=12, and h means an atomic ratio of oxygen necessary to satisfy the atomic valence of each of said elements.

4. A method for producing acrolein and/or acrylic acid by passing a raw material gas comprising propylene and oxygen through a catalyst layer in a tubular type of fixed bed reactor which is filled with a solid oxidation catalyst, which comprises passing a gas comprising propylene in a concentration lower than that of said raw material gas, and oxygen through said catalyst layer for a period of one hour or more prior to passing said raw material gas through said catalyst layer.

5. A method for producing acrolein and/or acrylic acid, which comprises:

filling a tubular type of fixed bed reactor with a solid oxidation catalyst;

elevating a temperature of the resultant catalyst layer to a range of 250° C. to 400° C. while passing a gas including oxygen, nitrogen, water vapor and 0 to 0.5% by volume of propylene through said catalyst layer;

passing a gas including 1 to 3.8% by volume of propylene, 7 to 16% by volume of oxygen and 5 to 50% by volume of water vapor through said catalyst layer at a temperature of 250° C. to 400° C. for a period of one hour or more; and thereafter

passing a raw material gas including 4 to 9% by volume of propylene, 7 to 16% by volume of oxygen and 5 to 50% by volume of water vapor through said catalyst layer at a temperature of 250° C. to 400° C.

6. The method for producing acrolein and/or acrylic acid according to claim 4 or 5 , wherein said solid oxidation catalyst is a compound oxide represented by the following formula (2):

Mo a′ Bi b′ Fe c′ A′ d′ X′ e′ Y′ f′ Z′ g′ Si h′ O i   (2)

wherein Mo, Bi, Fe, Si and O represent molybdenum, bismuth, iron, silicon and oxygen, respectively; A′ represents nickel and/or cobalt; X′ represents at least one element selected from the group consisting of magnesium, zinc, chromium, manganese, tin, strontium, barium, copper, silver and lead; Y′ represents at least one element selected from the group consisting of phosphorus, boron, sulfur, tellurium, aluminum, gallium, germanium, indium, lanthanum, cerium, niobium, tantalum, titanium, zirconium, tungsten and antimony; Z′ represents at least one element selected from the group consisting of potassium, sodium, rubidium, cesium and thallium; each of a′, b′, c′, d′, e′, f′, g′, h′ and i represents an atomic ratio of each element, wherein 0.01≦b′≦5, 0.01≦c′≦5, 1≦d′≦12, 0≦e′≦10, 0≦f′≦10, 0.001≦g′≦3 and 0≦h′≦20 when a′=12, and i means an atomic ratio of oxygen necessary to satisfy the atomic valence of each of said elements.

Assignments (2)
CHANGE OF NAME Recorded Sep 5, 2017
From: MITSUBISHI RAYON CO., LTD.
To: MITSUBISHI CHEMICAL CORPORATION
Reel/Frame 043750/0834 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 20, 2004
From: WATANABE, SEIGO; OH-KITA, MOTOMU; SATO, TOSHIHIRO
To: MITSUBISHI RAYON CO., LTD.
Reel/Frame 015240/0739 →