WO2011110879A1 - Method and apparatus for vaporizing liquid chlorine containing nitrogen trichloride - Google Patents
Method and apparatus for vaporizing liquid chlorine containing nitrogen trichloride Download PDFInfo
- Publication number
- WO2011110879A1 WO2011110879A1 PCT/IB2010/000467 IB2010000467W WO2011110879A1 WO 2011110879 A1 WO2011110879 A1 WO 2011110879A1 IB 2010000467 W IB2010000467 W IB 2010000467W WO 2011110879 A1 WO2011110879 A1 WO 2011110879A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- chlorine
- gas
- stream
- vaporizer
- nitrogen trichloride
- 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
- C01B7/00—Halogens; Halogen acids
- C01B7/01—Chlorine; Hydrogen chloride
- C01B7/07—Purification ; Separation
- C01B7/075—Purification ; Separation of liquid chlorine
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B21/00—Nitrogen; Compounds thereof
- C01B21/082—Compounds containing nitrogen and non-metals and optionally metals
- C01B21/083—Compounds containing nitrogen and non-metals and optionally metals containing one or more halogen atoms
- C01B21/0832—Binary compounds of nitrogen with halogens
Definitions
- the invention pertains to the processing of a stream of liquid chlorine containing nitrogen trichloride from a chlorine production process, for example a chloralkali production process.
- N-(NC1 3 ) nitrogen trichloride
- the amount formed is proportional to the amount of ammonia present in the salt fed to the process.
- Nitrogen trichloride follows the product chlorine leaving the chloralkali cell house.
- Nitrogen trichloride is an unstable compound that detonates when it reaches a critical concentration, reported to be about 13 wt%, though it is believed that nitrogen trichloride decomposes to create dangerous conditions at concentrations as low as 3 wt% .
- a critical mass of nitrogen trichloride is also required before it is considered capable of damaging equipment.
- Chlorine Institute Inc a typical chlorine vessel with a wall thickness of one-half inch can be fractured with as little as 1.5 gm/cm 2 liquid film of pure nitrogen trichloride.
- As a compound with a significantly lower vapor pressure than chlorine it can concentrate if liquid chlorine, containing nitrogen trichloride, is allowed to evaporate. Nitrogen trichloride is thought to be the cause of explosions and fatalities in chloralkali production facilities.
- Chlorine product is typically supplied as a liquid, but the end-user normally evaporates the liquid chlorine prior to use. Depending on how the chlorine is evaporated, this can lead to an increase in nitrogen trichloride concentration. A critical part of the chlorine production process is therefore to keep the nitrogen trichloride concentration low in the final chlorine product, typically only a few parts per million, to allow the end-user to safely evaporate the liquid chlorine. In the chloralkali process, nitrogen trichloride is often removed from the product chlorine through an absorption step, for example in a chlorine scrubber, prior to chlorine compression and liquefaction.
- nitrogen trichloride is absorbed into fresh, clean product chlorine and pushed down the scrubber and into a holding tank, referred to as the nitrogen trichloride decomposer, containing carbon tetrachloride or sometimes chloroform.
- the decomposer the solvent is maintained at a temperature above the boiling point of the chlorine. When the liquid chlorine contacts the warm solvent, it flashes back into the chlorine scrubber while nitrogen trichloride is absorbed by the solvent.
- Conditions in the decomposer are selected so that nitrogen trichloride slowly and safely decomposes. In time, tars and other impurities build up in the solvent, and the solvent must be periodically replaced, generating a waste stream that must be disposed of.
- Industrial chlorine vaporizers are generally non-horizontal units, such as vertical bayonet style units, or horizontal vaporizer units, such as kettle reboiler style units.
- vertical units meaning units with an angle from the horizontal from 0.1 to 90 degrees.
- These horizontal and vertical chlorine vaporizers can be of two types, namely: pool boiling vaporizers and plug-flow vaporizers.
- a pool boiling vaporizer such as a vertical bayonet or kettle reboiler style vaporizer
- liquid chlorine is evaporated out of a main body of liquid chlorine.
- Euro Chlor recommends that the concentration of nitrogen trichloride in liquid chlorine in "reboilers" be maintained below 1000 ppm to avoid excessive concentration. There is a balance between the tendency to concentrate and the tendency for nitrogen trichloride to decompose which is complex and not completely
- chlorine flows the length of the unit through three distinct regime zones.
- liquid chlorine is heated to its boiling point.
- chlorine is evaporated and in the third zone the resulting chlorine gas is superheated.
- nitrogen trichloride can concentrate dangerously.
- reflux of liquid from the boiling zone to the preheat zone can also cause concentration.
- three flow regimes are commonly encountered. The first flow regime occurs at the beginning of boiling when little vapor has yet formed and a "churn" flow regime develops. In the churn flow regime, vapor and liquid randomly mix and back-mix.
- the invention provides a method of vaporizing liquid chlorine containing nitrogen trichloride in a plug-flow vaporizer oriented non- horizontally and having an upward flow direction.
- the method comprises receiving a stream comprising liquid chlorine containing nitrogen trichloride, introducing a gas into the liquid stream upstream of a boiling zone of the vaporizer to induce a flow regime in the liquid stream that prevents or minimizes any mass accumulation of nitrogen trichloride in the boiling zone, and vaporizing the liquid stream to produce a stream comprising chlorine gas and nitrogen trichloride gas.
- the method includes processing the vaporized stream by destroying the nitrogen trichloride therein, to produce a stream comprising chlorine gas with nitrogen gas formed by decomposition of the nitrogen trichloride.
- the stream comprising chlorine gas with nitrogen gas may be recycled to the chlorine train of a chlorine production process.
- the invention also provides an apparatus for carrying out the methods of the invention.
- the apparatus comprises a plug-flow chlorine vaporizer oriented non-horizontally and having an upward flow direction.
- the apparatus has an inlet for receiving a stream of liquid chlorine containing nitrogen trichloride into the vaporizer. There is a boiling zone in the vaporizer downstream of the liquid inlet.
- the apparatus has a gas inlet upstream of the boiling zone for introducing a gas into the liquid stream, the gas being, for example, air, nitrogen or chlorine gas.
- the invention accordingly provides a method and apparatus to safely evaporate a liquid chlorine stream rich in mtrogen trichloride.
- the chlorine vaporization process presents an effective mean of avoiding a churn flow regime within the boiling zone of an upward plug-flow chlorine vaporizer, and therefore providing the means to safely vaporize liquid chlorine containing a high concentration of nitrogen trichloride, e.g. greater than 50 ppm. Because of the vertical position of the vaporizer, accidental flooding of the vaporizer does not lead to pool boiling, avoiding the potential for nitrogen trichloride concentration.
- the process includes the introduction of gas (vapor), at any point upstream of the boiling zone of a chlorine vaporizer, in sufficient quantity to force the feed liquid chlorine into any flow regime not leading to significant back-mixing or pool boiling within the boiling zone of the vaporizer.
- the plug-flow vaporizer can be oriented at any angle from 0.1 ° to 90 ° from the horizontal position.
- the gas introduced into the liquid stream can be any suitable gas or vapor, for example but not limited to air, nitrogen, chlorine gas, hydrogen, helium and oxygen, and mixtures thereof.
- the liquid chlorine feed to the vaporizer is forced into an appropriate flow regime before it reaches the boiling zone of the vaporizer, hence allowing the safe vaporization of liquid chlorine.
- Figure 1 is a schematic diagram of a first embodiment of the process of the invention.
- Figure 2 is a schematic diagram of the chlorine vaporizer.
- Figure 3 is a schematic diagram of a second embodiment of the process, in which nitrogen trichloride is destroyed using a superheater.
- Figure 4 is a schematic diagram of a third embodiment of the process, in which nitrogen trichloride is destroyed using a catalytic bed.
- a vertical upward plug-flow vaporizer 20 receives a stream of liquid chlorine containing nitrogen trichloride (stream 22) from the chlorine production train 24 of a chloralkali plant.
- the production train 24 includes a chloralkali cell house 10 in which chlorine gas is produced by the electrolysis of brine.
- a chlorine scrubber 11 receives a stream 12 of gas chlorine from the cell house and receives a liquid chlorine stream 13.
- Other unit operations usually present between the
- chloralkali cell house 10 and the chlorine scrubber 11 are not shown in the drawings.
- a gas chlorine stream 14 from the scrubber is fed to a compressor 15 and is thereafter liquified.
- liquid chlorine, rich in nitrogen trichloride From the bottom of the chlorine scrubber 11, liquid chlorine, rich in nitrogen trichloride
- stream 16 is fed to a holding tank 17, from which a stream 22 is routed to the vaporizer 20.
- the liquid chlorine, rich in nitrogen trichloride may be fed directly from the scrubber 11 to the vaporizer 20 (stream 16A) without using any holding tank.
- the stream 22 typically has 50 ppm or more of nitrogen trichloride.
- the vaporizer 20 is illustrated in Figure 2. It is oriented substantially vertically, but it may be oriented at any angle from the horizontal in the range of 0.1 to 90°; that is, the vaporizer is non- horizontal, sloping upward and has an upward flow direction.
- the vaporizer 20 has a body 26 and is heated by a stream 28 of heating medium flowing through a heating jacket 30.
- the vaporizer 20 has a heating zone 32 at the inlet end 34, in which the liquid stream is heated, and a boiling zone 36 downstream of the heating zone, in which the liquid chlorine is evaporated.
- a stream 40 of chlorine gas and nitrogen trichloride gas exits the
- a gas such as air, nitrogen or chlorine gas, or mixtures thereof, from a gas source 42 is introduced into the stream 22 of liquid chlorine and nitrogen trichloride upstream of the boiling zone 36 of the vaporizer.
- the gas stream 44 may be introduced into the liquid stream 22 before entry into the vaporizer, or it may be introduced directly into the heating zone 32 of the vaporizer, as indicated by optional streams 44A and 44B shown in Figure 2.
- the gas stream 44 is fed at a flow rate sufficient to force the feed liquid chlorine into a flow regime within the vaporizer 20 that does not permit significant back-mixing or pool boiling within the boiling zone 36 of the vaporizer.
- flow regimes are annular and mist flow regimes.
- the flow rate of the gas stream 44 may be in the range of 0.01 to 10 kg of gas per kg of liquid chlorine, alternatively 0.01 to 1 kg, alternatively 0.02 to 0.15 kg of gas per kg of liquid chlorine. The effect is to keep the nitrogen trichloride from
- a stream 40 comprising chlorine gas with nitrogen trichloride gas and the gas fed into the liquid stream is sent for further processing at step 46.
- the stream 40 may be routed to a hydrochloric acid plant, in which chlorine is reacted with hydrogen to make hydrochloric acid.
- the gas stream 40 may be absorbed in a hypochlorite system. Another option is to destroy the nitrogen trichloride and recycle the stream 40 to the chlorine production train, as explained below.
- the gas mixture produced in the vaporizer 20 is routed to one or more unit operations for the destruction of nitrogen trichloride.
- the gas leaving the nitrogen trichloride destruction step i.e. chlorine gas and nitrogen gas, is recycled back to the chlorine train of the chloralkali process.
- the invention thus avoids the generation of a waste stream or the addition of other chemicals or solvents to deal with the nitrogen trichloride.
- the step of destroying the nitrogen trichloride can be carried out in various ways.
- the gas mixture evaporated in the vaporizer may be introduced into a superheater, which may be part of the vaporizer unit.
- the vaporizer 20 includes a superheater zone 37 downstream of the boiling zone 36.
- the operating conditions in the superheater are selected so as to achieve substantially complete destruction of nitrogen trichloride.
- the average operating temperature of the superheater may be in the range of 30° to 300° C, the operating pressure in the range of 0.5 to 100 bar, and the residence time in the range of 0.5 seconds to 5 minutes. Alternatively, the average operating temperature may be in the range of 35° to 250° C, the operating pressure in the range of atmospheric pressure to 90 bar, and the residence time in the range of 1 second to 3 minutes.
- the gas stream 52 leaving the superheater comprising chlorine gas and nitrogen gas, is recycled back to the chlorine production train 24 of the chloralkali process.
- the gas evaporated in the vaporizer 20 can be routed to a catalytic bed 54 in which the nitrogen trichloride is destroyed.
- the catalytic bed may contain, for example, Monel (trademark) as a catalyst to destroy nitrogen trichloride.
- the catalytic bed may be operated at temperatures in the range of minus 40 to 300° C, pressures in the range of 0.5 to 100 bar, and a residence time in the range of 0.1 seconds to 5 minutes.
- the gas stream 52 leaving the catalytic bed, comprising chlorine gas and nitrogen gas is recycled back to the chlorine production train 24 or can be routed to other unit operations.
- the process may use both a superheater and a catalytic bed to destroy the nitrogen trichloride.
- the catalytic bed may be within a superheater zone of the vaporizer, rather than being a separate unit.
- the gas leaving the nitrogen trichloride destruction step e.g. the superheater or catalytic bed, may be routed to a
- temperature conditioning step 56 before being recycled back to the chlorine train (stream 60), as shown in Figures 3 and 4. This reduces the temperature of the gas stream leaving the nitrogen trichloride destruction step, which may be at a temperature of about 80° to 120° C, to a lower temperature for introduction into the chlorine train, which may be at a temperature of about minus 35° C.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Treating Waste Gases (AREA)
- Vaporization, Distillation, Condensation, Sublimation, And Cold Traps (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Gas Separation By Absorption (AREA)
Abstract
Description
Claims
Priority Applications (10)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
BRPI1014230A BRPI1014230A2 (en) | 2010-03-06 | 2010-03-06 | method for vaporizing liquid chlorine, and apparatus for vaporizing liquid chlorine containing nitrogen trichloride |
ES10711932.3T ES2558328T3 (en) | 2010-03-06 | 2010-03-06 | Method and apparatus for vaporization of liquid chlorine containing nitrogen trichloride |
PCT/IB2010/000467 WO2011110879A1 (en) | 2010-03-06 | 2010-03-06 | Method and apparatus for vaporizing liquid chlorine containing nitrogen trichloride |
JP2012555500A JP5795602B2 (en) | 2010-03-06 | 2010-03-06 | Method and apparatus for vaporizing liquid chlorine containing nitrogen trichloride |
CN201080018797.8A CN102414119B (en) | 2010-03-06 | 2010-03-06 | Method and apparatus for vaporizing liquid chlorine containing nitrogen trichloride |
US13/262,151 US10377629B2 (en) | 2010-03-06 | 2010-03-06 | Method and apparatus for vaporizing liquid chlorine containing nitrogen trichloride |
CA2758368A CA2758368C (en) | 2010-03-06 | 2010-03-06 | Method and apparatus for vaporizing liquid chlorine containing nitrogen trichloride |
HUE10711932A HUE027488T2 (en) | 2010-03-06 | 2010-03-06 | Method and apparatus for vaporizing liquid chlorine containing nitrogen trichloride |
KR20127002770A KR20120136344A (en) | 2010-03-06 | 2010-03-06 | Method and apparatus for vaporizing liquid chlorine containing nitrogen trichloride |
EP10711932.3A EP2401226B1 (en) | 2010-03-06 | 2010-03-06 | Method and apparatus for vaporizing liquid chlorine containing nitrogen trichloride |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PCT/IB2010/000467 WO2011110879A1 (en) | 2010-03-06 | 2010-03-06 | Method and apparatus for vaporizing liquid chlorine containing nitrogen trichloride |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2011110879A1 true WO2011110879A1 (en) | 2011-09-15 |
Family
ID=42670519
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/IB2010/000467 WO2011110879A1 (en) | 2010-03-06 | 2010-03-06 | Method and apparatus for vaporizing liquid chlorine containing nitrogen trichloride |
Country Status (10)
Country | Link |
---|---|
US (1) | US10377629B2 (en) |
EP (1) | EP2401226B1 (en) |
JP (1) | JP5795602B2 (en) |
KR (1) | KR20120136344A (en) |
CN (1) | CN102414119B (en) |
BR (1) | BRPI1014230A2 (en) |
CA (1) | CA2758368C (en) |
ES (1) | ES2558328T3 (en) |
HU (1) | HUE027488T2 (en) |
WO (1) | WO2011110879A1 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2016523695A (en) * | 2013-05-22 | 2016-08-12 | コベストロ、ドイチュラント、アクチエンゲゼルシャフトCovestro Deutschland Ag | Purification method of raw material gas by fractionation |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2013009835A1 (en) * | 2011-07-11 | 2013-01-17 | Andrew Llc | Method and apparatuses for managing a distributed antenna system |
JP6563484B2 (en) * | 2014-08-14 | 2019-08-21 | コベストロ、ドイチュラント、アクチエンゲゼルシャフトCovestro Deutschland Ag | Apparatus and method for evaporating liquids containing potentially explosive impurities |
KR102181570B1 (en) | 2016-06-02 | 2020-11-20 | 한국전기연구원 | Durability is improved metal/2-D nanomaterials/polymer hybrid conductive film and a manufacturing method thereof |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2692818A (en) * | 1950-07-18 | 1954-10-26 | Allied Chem & Dye Corp | Removing nitrogen trichloride from chlorine |
US3568409A (en) | 1969-06-04 | 1971-03-09 | Dow Chemical Co | Hydrochloric acid treatment for chlorine |
US4230673A (en) * | 1979-02-05 | 1980-10-28 | Basf Wyandotte Corporation | Apparatus for removing nitrogen trichloride from chlorine gas |
US5639422A (en) * | 1996-08-02 | 1997-06-17 | Occidental Chemical Corporation | Reducing corrosion of carbon steel reboilers |
CN101407314A (en) * | 2008-09-27 | 2009-04-15 | 山东鲁西化工股份有限公司 | Continuous production process for vaporizing chlorine |
CN101446381A (en) | 2007-11-27 | 2009-06-03 | 贵阳铝镁设计研究院 | Method for storing and gasifying liquefied chlorine gas and complete equipments thereof |
Family Cites Families (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2199797A (en) * | 1937-09-13 | 1940-05-07 | Dow Chemical Co | Purification of chlorine |
JPS5244316B2 (en) * | 1973-04-14 | 1977-11-07 | ||
US4138296A (en) * | 1977-06-03 | 1979-02-06 | Basf Wyandotte Corporation | Method for removing nitrogen trichloride from chlorine gas |
DE2917974A1 (en) * | 1979-05-04 | 1980-11-13 | Hoechst Ag | METHOD FOR PRODUCING LIQUID CHLORINE |
JPS62175575A (en) * | 1985-10-14 | 1987-08-01 | 関東電化工業株式会社 | Method of treating chlorine gas |
JPS63271083A (en) | 1987-04-28 | 1988-11-08 | 株式会社神戸製鋼所 | Condenser |
JPH028683A (en) * | 1988-02-16 | 1990-01-12 | Mitsui Toatsu Chem Inc | Method for separating and recovering chlorine |
US5437711A (en) * | 1993-12-16 | 1995-08-01 | Occidental Chemical Corporation | Method of purifying chlorine-containing gases |
JP3246705B2 (en) * | 1995-03-09 | 2002-01-15 | 株式会社トクヤマ | How to supply chlorine gas |
JP3495267B2 (en) | 1998-11-13 | 2004-02-09 | 株式会社神戸製鋼所 | Refrigeration equipment for gas liquefaction and re-vaporization |
US6758277B2 (en) * | 2000-01-24 | 2004-07-06 | Shell Oil Company | System and method for fluid flow optimization |
JP2002316804A (en) | 2001-04-19 | 2002-10-31 | Sumitomo Chem Co Ltd | Method for refining chlorine |
WO2005044725A1 (en) * | 2003-11-05 | 2005-05-19 | Toagosei Co., Ltd. | Method for producing high purity liquid chlorine |
JP4308810B2 (en) | 2004-10-18 | 2009-08-05 | 株式会社カネカ | Method for producing chlorine gas, sodium hypochlorite aqueous solution and liquid chlorine |
US8048203B2 (en) | 2005-10-14 | 2011-11-01 | Kaneka Corporation | Method of producing chlorine gas, aqueous sodium hypochlorite solution and liquid chlorine |
DE102007013964A1 (en) * | 2007-03-23 | 2008-09-25 | Bayer Materialscience Ag | Process for removing and recycling condensable components from chlorine-containing gas streams |
CN101343040B (en) * | 2008-08-22 | 2010-04-07 | 山东聊城中盛蓝瑞化工有限公司 | Liquefied chlorine flash evaporation purification preparation technique |
JP5439779B2 (en) * | 2008-09-24 | 2014-03-12 | 東ソー株式会社 | Method for producing high pressure and high purity chlorine gas |
TWI432815B (en) | 2009-12-15 | 2014-04-01 | Lite On Technology Corp | Lens module |
-
2010
- 2010-03-06 KR KR20127002770A patent/KR20120136344A/en not_active Application Discontinuation
- 2010-03-06 HU HUE10711932A patent/HUE027488T2/en unknown
- 2010-03-06 EP EP10711932.3A patent/EP2401226B1/en active Active
- 2010-03-06 WO PCT/IB2010/000467 patent/WO2011110879A1/en active Application Filing
- 2010-03-06 US US13/262,151 patent/US10377629B2/en active Active
- 2010-03-06 BR BRPI1014230A patent/BRPI1014230A2/en not_active Application Discontinuation
- 2010-03-06 JP JP2012555500A patent/JP5795602B2/en not_active Expired - Fee Related
- 2010-03-06 CA CA2758368A patent/CA2758368C/en active Active
- 2010-03-06 CN CN201080018797.8A patent/CN102414119B/en not_active Expired - Fee Related
- 2010-03-06 ES ES10711932.3T patent/ES2558328T3/en active Active
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2692818A (en) * | 1950-07-18 | 1954-10-26 | Allied Chem & Dye Corp | Removing nitrogen trichloride from chlorine |
US3568409A (en) | 1969-06-04 | 1971-03-09 | Dow Chemical Co | Hydrochloric acid treatment for chlorine |
US4230673A (en) * | 1979-02-05 | 1980-10-28 | Basf Wyandotte Corporation | Apparatus for removing nitrogen trichloride from chlorine gas |
US5639422A (en) * | 1996-08-02 | 1997-06-17 | Occidental Chemical Corporation | Reducing corrosion of carbon steel reboilers |
CN101446381A (en) | 2007-11-27 | 2009-06-03 | 贵阳铝镁设计研究院 | Method for storing and gasifying liquefied chlorine gas and complete equipments thereof |
CN101407314A (en) * | 2008-09-27 | 2009-04-15 | 山东鲁西化工股份有限公司 | Continuous production process for vaporizing chlorine |
Non-Patent Citations (4)
Title |
---|
"Database WPI Section PQ", accession no. 009-K40537 |
DATABASE WPI Section Ch Week 200936, Derwent World Patents Index; Class E36, AN 2009-H74378, XP002599825, (SHAN-N) SHANDONG LUXI CHEM ENG CO LTD * |
DATABASE WPI Section PQ Week 200941, Derwent World Patents Index; Class Q69, AN 2009-K40537, XP002599824 * |
GUSTIN ET AL: "Safety of chlorine production and chlorination processes", CHEMICAL HEALTH AND SAFETY, AMERICAN CHEMICAL SOCIETY, WASHINGTON, DC, US LNKD- DOI:10.1016/J.CHS.2004.08.002, vol. 12, no. 1, 1 January 2005 (2005-01-01), pages 5 - 16, XP025311177, ISSN: 1074-9098, [retrieved on 20050101] * |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2016523695A (en) * | 2013-05-22 | 2016-08-12 | コベストロ、ドイチュラント、アクチエンゲゼルシャフトCovestro Deutschland Ag | Purification method of raw material gas by fractionation |
Also Published As
Publication number | Publication date |
---|---|
CN102414119B (en) | 2015-02-11 |
KR20120136344A (en) | 2012-12-18 |
EP2401226B1 (en) | 2015-11-25 |
JP2013521210A (en) | 2013-06-10 |
CA2758368A1 (en) | 2011-09-15 |
ES2558328T3 (en) | 2016-02-03 |
HUE027488T2 (en) | 2016-11-28 |
CA2758368C (en) | 2016-05-24 |
JP5795602B2 (en) | 2015-10-14 |
EP2401226A1 (en) | 2012-01-04 |
US10377629B2 (en) | 2019-08-13 |
US20120017848A1 (en) | 2012-01-26 |
CN102414119A (en) | 2012-04-11 |
BRPI1014230A2 (en) | 2016-04-12 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP5303453B2 (en) | Improved method for purifying anhydrous hydrogen chloride gas | |
RU2537584C2 (en) | Methods and constructions of reactor for obtaining phosphorus pentafluoride | |
CA2758368C (en) | Method and apparatus for vaporizing liquid chlorine containing nitrogen trichloride | |
BR112019010088B1 (en) | A PROCESS FOR THE INTEGRATED PRODUCTION OF UREA AND UREA-AMMONIUM NITRATE | |
EP2544992B1 (en) | Method of processing liquid chlorine containing nitrogen trichloride | |
JP3658692B2 (en) | Removal of acid and salt contaminants | |
JP3246705B2 (en) | How to supply chlorine gas | |
JP3649572B2 (en) | PCB decomposition method and PCB decomposition apparatus | |
JP6250794B2 (en) | Purification method of raw material gas by fractionation | |
EP4185552A1 (en) | High pressure desorption of hydrogen chloride gas | |
SA111320736B1 (en) | Method and Apparatus for Vaporizing Liquid Chlorine Containing Nitrogen Trichloride | |
US20090142248A1 (en) | Method For Purifying Nitrogen Trifluoride | |
US3071452A (en) | Safe handling of acetylene under pressure | |
JP2004002142A (en) | Method of manufacturing hydrogen chloride gas which hardly contains hydrogen bromide and hydrogen chloride aqueous solution which hardly contains hydrogen bromide | |
US4658012A (en) | Process for purifying chlorinated aliphatic polymers | |
CN107076528B (en) | Device and method for evaporating a liquid selected from chlorine, dinitrotoluene and ethers | |
JP2006016380A (en) | Method for producing highly chlorinated methanes | |
CN116457333A (en) | Method for concentrating dilute sulfuric acid | |
JPS589803A (en) | Preparation of hydrogen chloride | |
JP2001026402A (en) | Recovery of hydrogen chloride | |
KR20020062399A (en) | Recycling method and device for wasted-carbon tetrachloride |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
WWE | Wipo information: entry into national phase |
Ref document number: 201080018797.8 Country of ref document: CN |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2010711932 Country of ref document: EP |
|
WWE | Wipo information: entry into national phase |
Ref document number: 13262151 Country of ref document: US |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2012555500 Country of ref document: JP |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2758368 Country of ref document: CA |
|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 10711932 Country of ref document: EP Kind code of ref document: A1 |
|
ENP | Entry into the national phase |
Ref document number: 20127002770 Country of ref document: KR Kind code of ref document: A |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
REG | Reference to national code |
Ref country code: BR Ref legal event code: B01A Ref document number: PI1014230 Country of ref document: BR |
|
ENP | Entry into the national phase |
Ref document number: PI1014230 Country of ref document: BR Kind code of ref document: A2 Effective date: 20111013 |