专利摘要:
Water is fed together with formamide in vapor form in the production of isocyanates by silver-catalyzed oxidative dehydrogenation of formamides.
公开号:SU1586510A3
申请号:SU874202326
申请日:1987-04-10
公开日:1990-08-15
发明作者:Нотт Малликарюна Рао Веллюр
申请人:Е.И.Дюпон Де Немур Энд Компани (Фирма);
IPC主号:
专利说明:

This invention relates to methods for quenching aliphatic isocyanates, more specifically methyl isocyanate.
The purpose of the invention is to simplify the process of obtaining the desired product.
In accordance with the method, water in the form of vapor is added to the formamide reagent prior to contact of the formamide with oxygen. Water can be added to the reactant stream just prior to its introduction. Into the reactor, where oxidative dehydrogenation occurs.
Immediately after contacting the catalyst and forming the isocyanate, the reaction mixture containing water, unreacted formamide and a low boiling isocyanate can be introduced into the apparatus
partial condensation, where water and unreacted formamide can be condensed and separated from the reactor effluent stream and then recycled to the reactor. The resulting isocyanate can be dried by contact with molecules of the sieve sieve, for example, zeolite A3, before further purification and / or condensation, or being sent to subsequent processing steps.
The absolute pressure in the method does not play a decisive role; As a rule, the reaction pressures vary from 100 to 1000 kPa. However, preferably the reaction pressure is about 1 atm / 100 kPao
SP
00 O)
sd

s
Example 1. 17.8 ml / h of monomethylformamide (MMF) is continuously evaporated and preheated to 240 ° C. It is then mixed with 505 ml / min of nitrogen and 145 ml / min of air or oxygen (enough to convert 53.5% MMF) and sent to the reactor. The reactor is a quarter-wave tube with an internal diamatre of 10 mm, containing 8.0 g of full-silver opaque, forming a layer about 2.5 cm deep. The thermocouple for measuring the temperature of the catalytic pas layer of the reactor containing the catalyst is in the reaction tube to a temperature sufficient to initiate the reaction between the IMF and oxygen.
After initiating the reaction, the supply of energy to the heater is brought to a level that compensates for the Tg; the loss of energy into the environment, the conditions
so create adiabati Average temperature
The scientific research institute MIC exit at this higher conversion is equal to 91.4%.
Examples 4-9. Reproduce timer 2 except that the flow rate of nitrogen is reduced to 404 ml / min. Oxygen is sufficient to convert 62% MMF. Under these conditions, the supply of raw materials conducted several experiments.
The results are presented in table. one.
l
T a b l and c a 1
35
40
reactors in this experiment are equal to 25 554 ° С “The reaction product is analyzed by gas chromatography. A very small amount of unreacted oxygen is released from the reactor. The average yield of methyl isodianate (MIC) is 0 92.8%.
The product contains non-reactive monomethylformamide, water, carbon dioxide and methyl isogan. This product is placed in a partial condensate to condense water and non-reactive monomethylformamide. The gas leaving the condenser contains residual water, carbon dioxide and methyl isocyanate. It is dried using a molecular sieve column to remove residual water, and the isocyanate is separated from carbon dioxide using a standard distillation technique.
Example 2. Reproduce fitting
1 except that a mixture and water with a molar ratio are used. O, 5. Since the flow rate of the fluid is constant, there is enough oxygen for the conversion of 62% MMF. The average reactor temperature is
and the average yield of MIC. with a higher conversion is 92.3%.
EXAMPLE 3. Reproduced Example
2 except that the molar ratio of MMF to water is 1.0. Oxygen is sufficient to convert approximately 70% MS. The average reactor temperature is, and

PRI me R s 10-16. Reproduce Examples 4-9, except that the molar ratio of water to MMF is 1.0. Oxygen is sufficient to convert approximately 70%.
The results are presented in table. 2 „
 table 2
Examples 17-22. Examples 17-22 are carried out essentially as described for Ete, except that the air flow rate varies between 145-186 ml / min, achieving an MMF conversion of 70-90%. The flow rate of nitrogen also varies. The fluid supply is 17.8 mp / h with a molar ratio of water to MMF in a 1: 1 mixture.
The results are presented in table. 3
When water is added, although the yield of the product remains relatively constant, the percent conversion of monomethylformamide increases. In addition, the nitrogen tOK can be reduced, and there is no negative impact on the process. Thus, water can replace nitrogen as the heat source in the reaction. This provides a more efficient release of methyl isocyanate, since water is easily condensed, observes - with less need for handling inert substances, and methyl isozymeTable 3
the anat is more concentrated in the product stream.
权利要求:
Claims (1)
[1]
Invention Formula
Method for producing methyl isocyanates by exposure to gaseous monemetcl-formamide with oxygen-containing gas
under a nitrogen atmosphere at 541-632 ° C in the presence of a silver catalyst, characterized in that, in order to simplify the process, monomethylforne-IMVD with water is used in the form of vapor at a low ratio of 1: 0.5-1.
类似技术:
公开号 | 公开日 | 专利标题
SU1586510A3|1990-08-15|Method of producing methyl isocyanates
US5414193A|1995-05-09|Removal of organic volatiles from polymer solutions and dispersions
US6008375A|1999-12-28|Process for manufacturing 2-pyrrolidone or N-alkylpyrrolidones
US4171316A|1979-10-16|Preparation of maleic anhydride using a crystalline vanadium|bis| catalyst
KR100481566B1|2005-05-16|Improved acrylonitrile rec0very process
EP0255948B1|1992-03-18|Process for producing isobutylene
ES8106878A1|1981-10-01|Process for the separation of water from mixtures with vinyl acetate and acetic acid.
US2736695A|1956-02-28|Process for preparing trichloroacetyl chloride
ES375942A1|1972-04-16|Continuous process for the preparation of maleic anhydride from an aqueous solution of maleic acid by distillation
US2792430A|1957-05-14|Production of phenolic compounds
US1889945A|1932-12-06|Production of monocarboxylic acids
GB2065650A|1981-07-01|Mehtod for dehydration of unsaturated aldehyde-containing gas
SU428601A3|1974-05-15|METHOD OF OBTAINING INDOL
US3518281A|1970-06-30|Production of 2,3-dihydropyran
JPH01242547A|1989-09-27|Method for absorbing methacrolein
SU891583A1|1981-12-23|Method of utilizing waste water
US3328428A|1967-06-27|Purification of pyromellitic dianhydride
JPH0532605A|1993-02-09|Method for purifying acetonitrile
GB827435A|1960-02-03|Substituted halogenated bicyclo heptenes and a process for preparing the same
KR20120059251A|2012-06-08|Continuous Preparation Method for Furfural from Xylose
US4668832A|1987-05-26|Dehydration of halogenated, unsaturated alcohols to form halogenated, conjugated dienes
RU2083559C1|1997-07-10|Process for preparing 1-cyano-2-iminocyclopentane
SU910581A1|1982-03-07|Process for producing propionic aldehyde
SU363688A1|1972-12-25|METHOD OF OBTAINING FORMALDEHYDE
GB1466444A|1977-03-09|Manufacture of formaldehyde
同族专利:
公开号 | 公开日
EP0242203A1|1987-10-21|
BR8701796A|1988-01-26|
PT84689B|1989-11-30|
PT84689A|1987-05-01|
DE3764995D1|1990-10-25|
JPS62255463A|1987-11-07|
EP0242203B1|1990-09-19|
IL82204D0|1987-10-30|
US4683329A|1987-07-28|
AT56700T|1990-10-15|
KR870009986A|1987-11-30|
IN167822B|1990-12-29|
引用文献:
公开号 | 申请日 | 公开日 | 申请人 | 专利标题

US3960914A|1975-05-06|1976-06-01|Sun Ventures, Inc.|Conversion of formamides to isocyanates|
US4207251A|1977-08-02|1980-06-10|Akzona Incorporated|Catalytic oxidation of formamides to form isocyanates|
DE3229323A1|1982-08-06|1984-02-09|Basf Ag, 6700 Ludwigshafen|METHOD FOR PRODUCING ALIPHATIC ISOCYANATES BY OXIDATIVE DEHYDRATION OF FORMAMIDS|
US4537726A|1984-11-09|1985-08-27|E. I. Du Pont De Nemours And Company|Multi-stage process with adiabatic reactors for the preparation of isocyanates|US4795830A|1986-09-02|1989-01-03|E. I. Du Pont De Nemours And Company|Use of water to inhibit decomposition of monoalkylformamides|
US5162575A|1991-04-01|1992-11-10|Olin Corporation|Preparation of isocyanates using a silver salt promoted rearrangement|
US5155267A|1991-10-24|1992-10-13|Arco Chemical Technology, L.P.|Synthesis of isocyanate precursors from primary formamides|
US8316660B2|2005-11-16|2012-11-27|Technologies Holdings Corp.|Defrost bypass dehumidifier|
US10227568B2|2011-03-22|2019-03-12|Nanofiber Solutions, Llc|Fiber scaffolds for use in esophageal prostheses|
WO2013078051A1|2011-11-21|2013-05-30|Johnson Jed K|Fiber scaffolds for use in tracheal prostheses|
US9884027B2|2012-01-12|2018-02-06|Nanofiber Solutions, Inc.|Nanofiber scaffolds for biological structures|
US10953097B2|2015-11-02|2021-03-23|Nanofiber Solutions. Llc|Electrospun fibers having contrast agents and methods of making the same|
WO2018144858A1|2017-02-02|2018-08-09|Nanofiber Solutions, Inc.|Methods of improving bone-soft tissue healing using electrospun fibers|
法律状态:
优先权:
申请号 | 申请日 | 专利标题
US06/852,707|US4683329A|1986-04-16|1986-04-16|Beneficial use of water in catalytic conversion of formamides to isocyanates|
[返回顶部]