A multitube reactor, wherein tubes having smaller tolerance between a nominal size and actual sizes are used as reaction tubes to stably perform a high yield reaction for a long period, a catalyst is filled into the reaction tubes so that the catalyst layer peak temperature portions of the reaction
A multitube reactor, wherein tubes having smaller tolerance between a nominal size and actual sizes are used as reaction tubes to stably perform a high yield reaction for a long period, a catalyst is filled into the reaction tubes so that the catalyst layer peak temperature portions of the reaction tubes are not overlapped with the connection sites thereof with baffles to effectively prevent hot spots from occurring and stably perform a reaction for a long period without the clogging of the reaction tubes, a heat medium and raw material gas are allowed to flow in the direction of a countercurrent and a specified type of catalyst is filled into the reaction tubes so that activity is increased from the inlet of the raw material gas to the outlet thereof to prevent the autooxidation of products so as to prevent equipment from being damaged due to the reaction, and, at the time of starting, gas with a temperature of 100 to 400째 C. is led to the outside of the reaction tubes to increase the temperature of the reaction tubes and, a heat medium, which is solid at the room temperature, is heated to circulate to the outside of the reaction tubes to efficiently start up the reactor without affecting the activity of the catalyst.
대표청구항▼
The invention claimed is: 1. A vapor phase catalytic oxidation method comprising: providing a multitube reactor comprising a plurality of reaction tubes having a catalyst packed therein, and a shell equipped with the reaction tubes inside and into which a heat medium flowing outside the reaction tu
The invention claimed is: 1. A vapor phase catalytic oxidation method comprising: providing a multitube reactor comprising a plurality of reaction tubes having a catalyst packed therein, and a shell equipped with the reaction tubes inside and into which a heat medium flowing outside the reaction tubes is introduced, wherein the reaction tubes are selected from tubes having same nominal outside diameter and same nominal wall-thickness, an outside diameter tolerance of 짹0.62%, and a wall-thickness tolerance of +19% to-0%, which further comprises baffles connected to the reaction tubes through connecting sites for changing a flow path of a heat medium introduced into the shell; circulating the heat medium through the outside of the reaction tubes; and feeding a reaction raw material gas inside the reaction tubes packed with a catalyst to obtain reaction product gas; wherein the method comprises setting catalyst packing specifications in the reaction tubes so that catalyst layer peak temperature sites of the reaction tubes are not located at the connecting sites between the baffles and the reaction tubes. 2. A vapor phase catalytic oxidation method comprising: providing a multitube reactor comprising a plurality of reaction tubes having a catalyst packed therein, and a shell equipped with the reaction tubes inside and into which a heat medium flowing outside the reaction tubes is introduced, wherein the reaction tubes are selected from tubes having same nominal outside diameter and same nominal wall-thickness, an outside diameter tolerance of 짹0.56%, and a wall-thickness tolerance of +17% to-0%, which further comprises baffles connected to the reaction tubes through connecting sites for changing a flow path of a heat medium introduced into the shell; circulating the heat medium through the outside of the reaction tubes; and feeding a reaction raw material gas inside the reaction tubes packed with a catalyst to obtain reaction product gas; wherein the method comprises setting catalyst packing specifications in the reaction tubes so that catalyst layer peak temperature sites of the reaction tubes are not located at the connecting sites between the baffles and the reaction tubes. 3. The vapor phase catalytic oxidation method according to claim 1, wherein the method comprises: packing the reaction tubes with a Mo--Bi catalyst and/or Sb--Mo catalyst so that an activity increases from a process gas inlet to a process gas outlet of the reaction tubes; allowing the heat medium and the process gas to flow in a countercurrent; and oxidizing propylene, propane, or isobutylene, and/or (meth)acrolein through vapor phase catalytic oxidation with a molecular oxygen-containing gas. 4. The vapor phase catalytic oxidation method according to claim 2, wherein the method comprises: packing the reaction tubes with a Mo--Bi catalyst and/or Sb--Mo catalyst so that an activity increases from a process gas inlet to a process gas outlet of the reaction tubes; allowing the heat medium and the process gas to flow in a countercurrent; and oxidizing propylene, propane, or isobutylene, and/or (meth)acrolein through vapor phase catalytic oxidation with a molecular oxygen-containing gas. 5. The vapor phase catalytic oxidation method according to claim 1, wherein the method comprises: heating the reaction tubes through introduction of a gas having temperature of 100 to 400째 C. outside the reaction tubes; and circulating the heat medium which is solid at normal temperature outside the heated reaction tubes to start up the multitube reactor. 6. The vapor phase catalytic oxidation method according to claim 2, wherein the method comprises: heating the reaction tubes through introduction of a gas having temperature of 100 to 400째 C. outside the reaction tubes; and circulating the heat medium which is solid at normal temperature outside the heated reaction tubes to start up the multitube reactor. 7. A vapor phase catalytic oxidation method comprising: using a fixed bed multitube heat-exchanger type reactor having a plurality of reaction tubes and baffles connected to the reaction tubes through connecting sites for changing a flow path of a heat medium flowing outside the reaction tubes; circulating the heat medium through the outside of the reaction tubes; feeding a reaction raw material gas inside the reaction tubes packed with a catalyst to obtain a reaction product gas, wherein the method comprises setting catalyst packing specifications in the reaction tubes so that catalyst layer peak temperature sites of the reaction tubes are not located at the connecting sites between the baffles and the reaction tubes. 8. The vapor phase catalytic oxidation method according to claim 7, wherein layers having different catalyst packing specifications are provided with at least two or more in one reaction tube. 9. The vapor phase catalytic oxidation method according to claim 7, wherein items for setting the catalyst packing specifications comprise a type of the catalyst, an amount of the catalyst, a form of the catalyst, a method for diluting the catalyst, and lengths of reaction zones. 10. The vapor phase catalytic oxidation method according to claim 7, wherein the method comprises oxidizing propane, propylene, and/or isobutylene with molecular oxygen through the vapor phase catalytic oxidation method to produce (meth)acrylic acid. 11. A vapor phase catalytic oxidation method comprises: using a multitube reactor which comprises: a cylindrical shell having a raw material feed port and a product discharging port; a plurality of ring-shaped tubes arranged on an outer periphery of the cylindrical shell for introducing or discharging a heat medium into or from the cylindrical shell; a circulating device connecting the plurality of the ring-shaped tubes one another; a plurality of reaction tubes restrained by a plurality of tube plates of the reactor and comprising a catalyst; and a plurality of baffles provided in a longitudinal direction of the reactor and for changing a direction of the heat medium introduced into the cylindrical shell; oxidizing propylene, propane, or isobutylene, and/or (meth)acrolein through vapor phase catalytic oxidation with a molecular oxygen-containing gas to obtain (meth)acrolein and/or (meth)acrylic acid,; wherein the method comprises, packing a Mo--Bi catalyst and/or Sb--MO catalyst in the reaction tubes so that anactivity increases from a process gas inlet to a process gas outlet of the reaction tubes; and allowing the heat medium and the process gas to flow in a countercurrent. 12. The vapor phase catalytic oxidation method according to claim 11, wherein the Mo--Bi catalyst is represented by the following general formula (I) and the Sb--Mo catalyst is represented by the following general formula (II): description="In-line Formulae" end="lead"MoaWbBicFedAcB fCgDhEiOj (I)description="In-line Formulae" end="tail" (wherein, Mo represents molybdenum; W represents tungsten; Bi represents bismuth; Fe represents iron; A represents at least one type of element chosen from nickel and cobalt; B represents at least one type of element selected from the group consisting of sodium, potassium, rubidium, cesium, and thallium; C represents at least one type of element selected from alkaline earth metals; D represents at least one type of element selected from the group consisting of phosphorus, tellurium, antimony, tin, cerium, lead, niobium, manganese, arsenic, boron, and zinc; E represents at least one type of element selected from the group consisting of silicon, aluminum, titanium, and zirconium; O represents oxygen; a, b, c, d, e, f, g, h, i, and j represent atomic ratios of Mo, W, Bi, Fe, A, B, C, D, E, and O respectively; and if a=12, 0≦b≦10, 0kMOl(V/Nb)mXnYp SiqOr (II)description="In-line Formulae" end="tail" (wherein, Sb represents antimony; Mo represents molybdenum; V represents vanadium; Nb represents niobium; X represents at least one type of element selected from the group consisting of iron (Fe), cobalt (Co), nickel (Ni), and bismuth (Bi); Y represents at least one type of element chosen from copper (Cu) and tungsten (W); Si represents silicon; O represents oxygen; (V/Nb) represents V and/or Nb; k, l, m, n, p, q, and r represent atomic ratios of Sb, Mo, (V/Nb), X, Y, Si, and O respectively; and 1≦k≦100, 1≦l≦100, 0.1≦m≦50, 1≦n≦100, 0.1≦p≦50, 1≦q≦100; and r is a value determined from oxidation states of the respective elements).
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