WO1996016898A1 - Procede pour la production de phosgene - Google Patents
Procede pour la production de phosgene Download PDFInfo
- Publication number
- WO1996016898A1 WO1996016898A1 PCT/JP1995/002421 JP9502421W WO9616898A1 WO 1996016898 A1 WO1996016898 A1 WO 1996016898A1 JP 9502421 W JP9502421 W JP 9502421W WO 9616898 A1 WO9616898 A1 WO 9616898A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- phosgene
- chlorine
- reaction
- carbon monoxide
- activated carbon
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B32/00—Carbon; Compounds thereof
- C01B32/80—Phosgene
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2208/00—Processes carried out in the presence of solid particles; Reactors therefor
- B01J2208/02—Processes carried out in the presence of solid particles; Reactors therefor with stationary particles
- B01J2208/023—Details
- B01J2208/024—Particulate material
- B01J2208/025—Two or more types of catalyst
Definitions
- the present invention relates to a method for producing phosgene from carbon monoxide and chlorine using activated carbon as a catalyst. More specifically, the present invention relates to a method for producing high-purity phosgene that can minimize the generation of impurities due to a rapid exothermic reaction when activated carbon is used as a catalyst in the reaction.
- Phosgene is known as an important raw material for synthetic chemistry, especially in the production of polycarbonate, and high-quality phosgene is required.
- an object of the present invention is to produce high-purity phosgene suitable for chemical reaction, particularly for production of an interfacial polycondensation method polycarbonate, and to provide a pretreatment step for activated carbon and a special cooling pipe. It is an object of the present invention to find a method that makes it possible to produce phosgene efficiently without the need for a reactor or any other special flow mode of the reaction gas. Disclosure of the invention
- the present inventor has conducted intensive studies to solve the above problems, and as a result, by adding and dispersing another inert material to the catalyst layer containing activated carbon, and diluting the activated carbon in the catalyst layer, effectively, Furthermore, they have found that high-purity phosgene can be produced more efficiently by using a specific inert material in a special shape, and completed the present invention.
- the gist of the present invention is as follows. First, in a method for producing phosgene by reacting carbon monoxide and chlorine through a catalyst layer mainly composed of activated carbon, a catalyst layer diluted with a material substantially inert to carbon monoxide and chlorine is used. Phosgene production method,
- the method for producing phosgene according to the second aspect wherein the ceramic material and / or the metal material is a molded article having a hollow spherical or tubular structure,
- the method for producing phosgene according to the first aspect wherein the material substantially inert to carbon monoxide and chlorine is 5 to 90% by volume in the catalyst layer,
- FIG. 1 is a conceptual diagram showing a phosgene production method according to the present invention
- FIG. 2 is a longitudinal sectional view of a multitubular phosgene reactor
- FIG. 3 is a reaction tube of the reactor.
- FIG. 3 is a partially cutaway view of a longitudinal section of FIG.
- reference numeral 1 is a raw material gas CO
- 2 is a raw material gas Cl 2
- 3 is a catalyst
- 4 is a diluent
- 5 is phosgene
- 6 is a phosgene reactor
- 6 a is an inlet of a phosgene reactor
- 6 b Is the outlet of the Hosgen reactor
- 6c is the reaction tube
- 6d is the cooling water passage jacket
- 6e is the cooling water inlet
- 6f is the cooling water outlet
- A is the catalyst dilution section.
- FIG. 1 is a conceptual diagram illustrating a phosgene production method according to the present invention, the raw material gas C 0 (1) and C 1 2 (2), the sera Mi catalyst (3) in which the activated carbon with a diluent (4)
- a phosgene reactor (6) filled with a charging agent mixed with a ball or a stainless steel material is introduced from an inlet (6a) of the reactor, and an outlet (6b) from the reactor (6) is supplied with a reaction product. COC 1 2 (5) is removed.
- Carbon monoxide and chlorine which are raw materials for producing phosgene according to the present invention, are required to be dry and of high purity.
- a method for producing the above-mentioned raw material carbon monoxide used in the present invention Synthetic gas, carbide furnace gas, blast furnace gas, smelting furnace gas, and the like can also be used. Purified by the above high purity requirement through an adsorption tower or cryogenic separation is supplied. Further, as a method for producing chlorine as another raw material, a method for purifying chlorine generated by electrolysis of a saline solution (eg, a diaphragm method, an ion exchange membrane method) can be applied.
- the activated carbon used as a catalyst in the present invention it is not necessary to use a special one, but typical ones can be classified and exemplified as follows. (1) From the aspect of form: powdered activated carbon, granulated (pellet, tablet, etc.) activated carbon.
- the diluent for the catalyst layer in the present invention is to reduce the concentration of the catalyst component in the catalyst layer to reduce the heat generated by the reaction. To prevent concentration
- the diluent must be a material that is inert to carbon monoxide and chlorine as a raw material. If the diluent itself is reactive with carbon monoxide or chlorine, it is difficult to achieve the object of the present invention. Further, even if the catalyst has a positive or negative catalytic activity in the reaction between carbon monoxide and chlorine, the effect of the present invention cannot be obtained as described above. Further, the diluent used in the present invention needs to be inert in the impurity contained therein as well.
- the diluent for the activated carbon-containing catalyst layer used in the present invention the following can be classified and exemplified.
- Ceramic A material made from alumina, zirconia, magnesium oxide, chromium oxide, silicon carbide, zinc sulfide, etc.
- Metals In addition to precious metals as simple substances, alloys such as stainless steel, hastelloy, and inconel.
- Metals generally have better thermal conductivity than ceramics and are therefore suitable for lowering the heat generation temperature.
- Raschig ring For example, Raschig ring, Lessing ring, Terralet, Boring, etc.
- Diameter and length are each about 0.1 to 10 mm.
- the molar ratio between the two materials is usually equimolar or it is preferred to use a slight excess of carbon monoxide.
- the dilution of the catalyst layer (activated carbon) in the present invention is most preferably performed over the entire area of the catalyst layer.
- an exothermic reaction such as in the case of the production of phosgene by the reaction of carbon monoxide and chlorine is performed in a tubular reactor. It is known that there is a sharp rise in temperature in the first half of the reactor (for example, since the Chemical Engineering Society, “Chemical Equipment Design Guide” (1991)) It is necessary to dilute the catalyst layer at least in the first half or in the feed gas introduction part, and this dilution can avoid an undesired increase in the reaction temperature.
- the dilution ratio of the catalyst layer according to the present invention is preferably 5 to 90% by volume, more preferably 5 to 80% by volume of a diluent. Less than 5% by volume for dilution The effect of lowering the reaction temperature cannot be obtained, and if it exceeds 90% by volume, uniform dilution is difficult. If the dilution ratio is in a more preferable range than the above, the above effects are further improved.
- a multitubular tubular reactor is preferable.
- Fig. 2 is a longitudinal sectional view of a horizontal multitubular tube reactor.
- the phosgene reactor (6) has a large number of built-in reaction tubes (6c) at the center in the longitudinal direction, and the inlet of the phosgene reactor (6a) is installed.
- Side and outlet (6b) side Side and outlet (6b) side.
- the gap between the reaction tubes constitutes a cooling water passage (6d), and cooling water introduced from the cooling water inlet (6e) passes through this jacket and is discharged from the cooling water outlet (6f). Is done.
- the cooling water is used to remove a large amount of heat generated in each reaction tube quickly, and makes the reaction between carbon monoxide and chlorine using activated carbon as a catalyst as efficient as possible.
- Each reaction tube (6c) is filled with a mixture of a catalyst (3) containing activated carbon as a main component and a diluent (4), and a raw material gas C introduced from an inlet (6a) of a phosgene reactor. 0 (1), C 1 is passed through 2 (2), reacted in the reaction tube, the generated phosgene (5) Ru is discharged from the outlet of the phosgene reactor (6b) o
- C 1 2 (2) pre-merging is not a raw material in Fig. 2 C 0 (1)
- the raw material C 0 (1) and C 1 2 (2) is the reaction tube It is sufficient if they are supplied at a predetermined molar ratio to the phosgene reactor.
- the mode of introduction into the phosgene reactor There is no particular limitation on the mode of introduction into the phosgene reactor. The effect of the present invention is not particularly influenced by the mode of introduction.
- each reaction tube is not particularly limited, but is preferably about 3 to 200 mm in order to uniformly fill the catalyst and the diluent.
- the length depends on the inner diameter of the reaction tube, the flow rate of the raw material gas, the cooling efficiency, and the like, and cannot be specified.
- the number of reaction tubes is variable according to i of the phosgene to be produced, and is not particularly limited.
- a vertical reactor is more preferably used than a horizontal reactor because of the work of filling the inside with a catalyst and the like.
- FIG. 2 is a partially cutaway view of a vertical cross section of the reaction tube of FIG. 1, which is a diagram schematically showing a dispersedly charged state of a catalyst (3) and a diluent (4) charged in the reaction tube. 1) and (2) are supplied from the upper inlet, but the catalyst is diluted mainly at the part where the temperature is expected to increase at the inlet of the reactor (A in Fig. 3). It indicates the range of dilution and can be called the catalyst dilution section).
- This catalyst diluting section is effective in one stage, but two-stage dilution or more may be carried out depending on the size of the reaction tube.
- thermocouples were attached at intervals of 5 cm from the raw material gas inlet side of the reaction tube, so that the maximum temperature of the reactor could be measured.
- the reaction tube became a double tube, forming a jacket, and flowing hot water at about 75 to remove the heat of reaction.
- the results were evaluated based on the maximum temperature at a predetermined position from the inlet of the reaction tube, the reaction rate of the reacted gas measured by gas chromatography, and the content of impurities in phosgene.
- Phosgene was produced under the same conditions as in Example 1 except that the type of activated carbon in the catalyst layer and the length of the packed catalyst were changed.
- Example 1 the inside of the reaction tube was directly charged with the activated carbon of the catalyst without dilution.
- the reaction temperature is considerably lowered by diluting the catalyst layer mainly composed of activated carbon, particularly the catalyst layer on the raw material gas inlet side, with the diluent, and the content of impurities in the generated phosgene is reduced.
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Catalysts (AREA)
- Linear Motors (AREA)
Description
Claims
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP95937202A EP0796819B1 (en) | 1994-12-01 | 1995-11-28 | Process for producing phosgene |
BR9509842A BR9509842A (pt) | 1994-12-01 | 1995-11-28 | Processo para produção de fosgênio |
DE69515693T DE69515693T2 (de) | 1994-12-01 | 1995-11-28 | Verfahren zur herstellung von phosgen |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6/298686 | 1994-12-01 | ||
JP06298686A JP3124455B2 (ja) | 1994-12-01 | 1994-12-01 | ホスゲンの製造方法 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1996016898A1 true WO1996016898A1 (fr) | 1996-06-06 |
Family
ID=17862976
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP1995/002421 WO1996016898A1 (fr) | 1994-12-01 | 1995-11-28 | Procede pour la production de phosgene |
Country Status (7)
Country | Link |
---|---|
EP (1) | EP0796819B1 (ja) |
JP (1) | JP3124455B2 (ja) |
KR (1) | KR100365081B1 (ja) |
BR (1) | BR9509842A (ja) |
DE (1) | DE69515693T2 (ja) |
TW (1) | TW366327B (ja) |
WO (1) | WO1996016898A1 (ja) |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE102007020444A1 (de) | 2007-04-27 | 2008-11-06 | Bayer Materialscience Ag | Verfahren zur Oxidation eines Chlorwasserstoffenthaltenden Gasgemisches |
US7612234B2 (en) | 2006-05-23 | 2009-11-03 | Bayer Materialscience Ag | Processes for separating carbon monoxide from a hydrogen chloride-containing gas |
EP2272890A1 (de) | 2009-07-07 | 2011-01-12 | Bayer MaterialScience AG | Verfahren zur Herstellung von Polycarbonat |
CN105408249A (zh) * | 2013-07-26 | 2016-03-16 | 沙特基础全球技术有限公司 | 用于生产高纯光气的方法和装置 |
EP3498752A1 (de) | 2017-12-18 | 2019-06-19 | Covestro Deutschland AG | Verfahren zur herstellung eines polycarbonats unter verwendung eines organischen lösungsmittels auf der grundlage von chlorkohlenwasserstoffen |
WO2019121248A1 (de) | 2017-12-18 | 2019-06-27 | Covestro Deutschland Ag | Verfahren zur herstellung eines polycarbonats unter verwendung eines organischen lösungsmittels auf der grundlage von chlorkohlenwasserstoffen |
WO2021023690A1 (en) | 2019-08-08 | 2021-02-11 | Covestro Intellectual Property Gmbh & Co. Kg | Process for the preparation of a polycarbonate |
EP3985047A1 (de) | 2020-10-13 | 2022-04-20 | Covestro Deutschland AG | Verfahren zur herstellung eines polycarbonats nach dem phasengrenzflächenverfahren unter lösungsmittelaustausch |
EP4083106A1 (de) | 2021-04-30 | 2022-11-02 | Covestro Deutschland AG | Verfahren zur herstellung von polycarbonat mit verbesserter nachhaltigkeit |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE19848668A1 (de) | 1998-10-22 | 2000-04-27 | Bayer Ag | Tetrachlorkohlenstoffarmes Phosgen |
JP4504552B2 (ja) * | 2000-12-01 | 2010-07-14 | 旭化成ケミカルズ株式会社 | 触媒性能評価装置 |
CN101356213B (zh) * | 2006-01-17 | 2011-12-28 | 帝人化成株式会社 | 聚碳酸酯低聚物的连续制造方法 |
DE102007057462A1 (de) * | 2007-11-29 | 2009-06-10 | Bayer Materialscience Ag | Verfahren zur Herstellung von Phosgen mit reduzierter CO-Emission |
JP5222089B2 (ja) * | 2008-10-23 | 2013-06-26 | 帝人化成株式会社 | ホスゲンの製造方法 |
FR2965490B1 (fr) | 2010-09-30 | 2013-01-11 | Aet Group | Dispositif et procede pour la phosgenation en continu |
JP6045825B2 (ja) | 2012-07-05 | 2016-12-14 | 出光興産株式会社 | ポリカーボネート−ポリオルガノシロキサン共重合体及びその連続的な製造方法 |
CN105408250B (zh) | 2013-07-26 | 2018-08-07 | 沙特基础全球技术有限公司 | 用于生产高纯光气的方法和装置 |
JP6316446B2 (ja) | 2014-02-04 | 2018-04-25 | サビック グローバル テクノロジーズ ベスローテン フェンノートシャップ | カーボネートの製造方法 |
JP6286057B2 (ja) * | 2014-02-04 | 2018-02-28 | サビック グローバル テクノロジーズ ベスローテン フェンノートシャップ | カーボネートを生成する方法 |
Citations (8)
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JPS4518703B1 (ja) * | 1966-02-07 | 1970-06-26 | ||
JPS5253768A (en) * | 1975-10-29 | 1977-04-30 | Toshiba Mach Co Ltd | Structure of packing |
JPS52100365A (en) * | 1976-02-20 | 1977-08-23 | Ricoh Co Ltd | Decomposition of ammonia gas |
JPS5514044B1 (ja) * | 1970-12-26 | 1980-04-14 | ||
JPS61161133A (ja) * | 1985-01-08 | 1986-07-21 | Mitsubishi Heavy Ind Ltd | 吸熱反応装置 |
JPS621736U (ja) * | 1985-06-21 | 1987-01-08 | ||
JPS6358696U (ja) * | 1986-10-02 | 1988-04-19 | ||
JPH0629129B2 (ja) * | 1988-06-25 | 1994-04-20 | 出光石油化学株式会社 | ホスゲンの製造方法 |
-
1994
- 1994-12-01 JP JP06298686A patent/JP3124455B2/ja not_active Expired - Lifetime
-
1995
- 1995-11-28 KR KR1019970703639A patent/KR100365081B1/ko active
- 1995-11-28 EP EP95937202A patent/EP0796819B1/en not_active Expired - Lifetime
- 1995-11-28 BR BR9509842A patent/BR9509842A/pt not_active IP Right Cessation
- 1995-11-28 WO PCT/JP1995/002421 patent/WO1996016898A1/ja active IP Right Grant
- 1995-11-28 DE DE69515693T patent/DE69515693T2/de not_active Expired - Lifetime
- 1995-12-23 TW TW840113829A patent/TW366327B/zh not_active IP Right Cessation
Patent Citations (8)
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JPS4518703B1 (ja) * | 1966-02-07 | 1970-06-26 | ||
JPS5514044B1 (ja) * | 1970-12-26 | 1980-04-14 | ||
JPS5253768A (en) * | 1975-10-29 | 1977-04-30 | Toshiba Mach Co Ltd | Structure of packing |
JPS52100365A (en) * | 1976-02-20 | 1977-08-23 | Ricoh Co Ltd | Decomposition of ammonia gas |
JPS61161133A (ja) * | 1985-01-08 | 1986-07-21 | Mitsubishi Heavy Ind Ltd | 吸熱反応装置 |
JPS621736U (ja) * | 1985-06-21 | 1987-01-08 | ||
JPS6358696U (ja) * | 1986-10-02 | 1988-04-19 | ||
JPH0629129B2 (ja) * | 1988-06-25 | 1994-04-20 | 出光石油化学株式会社 | ホスゲンの製造方法 |
Non-Patent Citations (1)
Title |
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See also references of EP0796819A4 * |
Cited By (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7612234B2 (en) | 2006-05-23 | 2009-11-03 | Bayer Materialscience Ag | Processes for separating carbon monoxide from a hydrogen chloride-containing gas |
DE102007020444A1 (de) | 2007-04-27 | 2008-11-06 | Bayer Materialscience Ag | Verfahren zur Oxidation eines Chlorwasserstoffenthaltenden Gasgemisches |
EP1992592A2 (de) | 2007-04-27 | 2008-11-19 | Bayer MaterialScience AG | Verfahren zur Oxidation eines Chlorwasserstoff enthaltenden Gasgemisches |
EP2272890A1 (de) | 2009-07-07 | 2011-01-12 | Bayer MaterialScience AG | Verfahren zur Herstellung von Polycarbonat |
DE102009032020A1 (de) | 2009-07-07 | 2011-01-13 | Bayer Materialscience Ag | Verfahren zur Herstellung von Polycarbonat |
US8173762B2 (en) | 2009-07-07 | 2012-05-08 | Bayer Materialscience Ag | Process for the preparation of polycarbonate |
CN105408249A (zh) * | 2013-07-26 | 2016-03-16 | 沙特基础全球技术有限公司 | 用于生产高纯光气的方法和装置 |
EP3498752A1 (de) | 2017-12-18 | 2019-06-19 | Covestro Deutschland AG | Verfahren zur herstellung eines polycarbonats unter verwendung eines organischen lösungsmittels auf der grundlage von chlorkohlenwasserstoffen |
WO2019121240A1 (de) | 2017-12-18 | 2019-06-27 | Covestro Deutschland Ag | Verfahren zur herstellung eines polycarbonats unter verwendung eines organischen lösungsmittels auf der grundlage von chlorkohlenwasserstoffen |
WO2019121248A1 (de) | 2017-12-18 | 2019-06-27 | Covestro Deutschland Ag | Verfahren zur herstellung eines polycarbonats unter verwendung eines organischen lösungsmittels auf der grundlage von chlorkohlenwasserstoffen |
WO2021023690A1 (en) | 2019-08-08 | 2021-02-11 | Covestro Intellectual Property Gmbh & Co. Kg | Process for the preparation of a polycarbonate |
EP3985047A1 (de) | 2020-10-13 | 2022-04-20 | Covestro Deutschland AG | Verfahren zur herstellung eines polycarbonats nach dem phasengrenzflächenverfahren unter lösungsmittelaustausch |
EP4083106A1 (de) | 2021-04-30 | 2022-11-02 | Covestro Deutschland AG | Verfahren zur herstellung von polycarbonat mit verbesserter nachhaltigkeit |
WO2022229245A1 (de) | 2021-04-30 | 2022-11-03 | Covestro Deutschland Ag | Verfahren zur herstellung von polycarbonat mit verbesserter nachhaltigkeit |
Also Published As
Publication number | Publication date |
---|---|
KR987000231A (en) | 1998-03-30 |
DE69515693T2 (de) | 2000-07-27 |
TW366327B (en) | 1999-08-11 |
JPH08157206A (ja) | 1996-06-18 |
EP0796819B1 (en) | 2000-03-15 |
DE69515693D1 (de) | 2000-04-20 |
EP0796819A1 (en) | 1997-09-24 |
JP3124455B2 (ja) | 2001-01-15 |
KR100365081B1 (ko) | 2003-02-19 |
EP0796819A4 (ja) | 1997-09-24 |
BR9509842A (pt) | 1997-12-23 |
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