Background technology
Monoxone, also known as chloroacetic acid, is a kind of important organic chemical industry's intermediate, is widely used in medicine, pesticide, dyestuff
With in multiple organic chemistry production.
At present, industrialized production method mainly has acetic acid chloridising, trichloro ethylene hydration method, chloracetyl chloride hydrolysis
Method three kinds.And trichloro ethylene hydration method and chloracetyl chloride Hydrolyze method are limited, relatively costly due to raw material sources, therefore all do not have in China
It is applied.Applying most is acetic acid chloridising.
Acetic acid chloridising is divided into again two kinds, and a kind of is the batch process with sulfur as catalyst, and this method is former with acetic acid
Material, makees catalyst with sulfur, is passed through in acetic acid by chlorine, carries out chlorination, and chlorated liquid obtains monoxone through crystallization and rejection filter and produces
Product.This method is the most commonly used, is to produce chloroacetic main method at present, and the advantage of this production method is raw material second
Acid is in liberal supply, and production technology is simple, and investment of production is few.It is disadvantageous in that production process is due to the excessive chlorine of acetic acid
Changing, cause containing dichloro, a large amount of waste liquids of trichloroacetic acid, make consumption of raw materials amount increase, monoxone yield is relatively low, purity difference, raw
Production capacity consumption height, the existence of sulfur simultaneously causes by-product HCl purity the highest, and range of application is narrow.Another kind of method is to be with acetic anhydride
The synthesis technique of catalyst, this synthesis technique mainly has intermittent chlorination method and continuous chlorination at present.Batch process is with the U.S.
Niacet intermittent chlorination technique is representative, uses Large Copacity chlorination tank, and full process automatization controls, band strong stirring, and material mixes
Closing uniformly, product monoxone purity is high.But refrigeration system power consumption is big, and power consumption is higher.Continuous chlorination is with Slovakia
VUCHT continuous chlorination technique is representative, uses tower continuous chlorination reactor, and reaction is carried out continuously, and has response speed fast, week
The advantage that phase is short.The shortcoming of this technique is that a chlorination conversion ratio is relatively low, and a large amount of unreacted acid must follow after recovery through distillation
Ring uses, and so, adds flow process and equipment, and water consumption, power consumption are the highest, but the supplies consumption of this technique is the lowest.
Patent CN 1480440A provides a kind of high temperature and high pressure method and produces chloroacetic method, though the method is pure at product
Make moderate progress on degree, yield, cost, but operating condition is still difficult to control to, there is by-product more.
Preparation process for chloroacetic acid disclosed in patent CN1382680A and CN 1180066A, is for improving product yield
And technique is improved, its technical scheme be respectively before chlorination reaction add chlorine-resisting agent and change operation condition and
Crystallization condition.But the most generally there is the problem that waste liquid can not recycle.
A kind of production of chloroacetic acid method disclosed in JP-A-7326738, including use hydrogen peroxide with reactant mixture
Chlorine monoxid acetaldehyde at a temperature of reflux temperature is almost identical, but the method by-product is many, it is difficult to separate.
Patent CN 1865217A and CN1298860A provides the method for continuous catalysis preparing monochloro-acetic acid, its technique letter
Clean, it is achieved that continuous prodution, decrease pollution, but it is low to still suffer from conversion ratio, steam consumption and the higher problem of power consumption.To sum up
Described, current production of chloroacetic acid still suffers from waste liquid can not recycle, conversion ratio low, consumption of raw materials amount is big, and energy consumption is high asks
Topic, seriously suppresses to produce.
Summary of the invention
For solving the deficiencies in the prior art, it is provided that a kind of can realization produces serialization, and can improve raw material availability, reduces
The production of chloroacetic acid equipment of energy consumption, the invention provides a kind of production of chloroacetic acid equipment, including:
Absorption tower, its top inlet connects the pipeline for supplying acetic acid and acetic anhydride, and top outlet connection has condenser system;
First chlorination reaction tower, its top inlet is connected with the bottom end outlet on absorption tower, and top outlet connection has fractionator condenser;
Second chlorination reaction tower, the bottom end outlet of its top inlet and the first chlorination reaction tower connects;
Wherein, the bottom entrance of the first chlorination reaction tower is connected, in the second chlorination reaction tower with the pipeline being used for supplying chlorine
Portion is connected with the pipeline being used for supplying chlorine.
Wherein, the bottom entrance on described absorption tower and the top outlet of the second chlorination reaction tower connect to dissolve the second chlorine
Change in reaction tower unreacted gas completely and realize gas-liquid mass transfer heat transfer.
Wherein, being also associated with knockout tower between described first chlorination reaction tower and fractionator condenser, described knockout tower is used for
Receive the liquid being fractionated into condenser condensation, and the liquid of condensation is back to the by the top inlet of the first chlorination reaction tower
In monochlor(in)ate reaction tower.
Wherein, described fractionator condenser is fractional distilling tube, and it exports the bottom entrance with the second chlorination reaction tower
Connect so that by the most condensed gas supply to the second chlorination reaction tower.
Wherein, described condenser system includes the first condenser, the second condenser, the 3rd condenser, for respectively to absorption
The gas of tower top end carries out degree of depth room temperature condensation, deep hypothermia condensation and the condensation of degree of depth deep cooling, the gas not simultaneously being condensed
Body is sent into as salt acid starting material and is produced hydrochloric acid section.
Wherein, described condenser system is connected with the top inlet of the first chlorination reaction tower, to be supplied by condensed liquid
To the first chlorination reaction tower.
Wherein, described first chlorination reaction tower and the second chlorination reaction tower are tower structure, and described tower structure is for filling out
Material tower or plate column.
The production of chloroacetic acid equipment that the present invention provides, can realize producing serialization, and can improve raw material availability, meanwhile,
Effectively prevent excessive chlorine and product monoxone generation side reaction, improve product yield, reduce energy consumption.
Detailed description of the invention
Further understand in order to technical scheme and beneficial effect are had, coordinate accompanying drawing to describe in detail below
Technical scheme and the beneficial effect of generation thereof.
Fig. 1 is the structural representation of the production of chloroacetic acid equipment of the present invention, as it is shown in figure 1, the invention provides a kind of chlorine
Acetic acid production equipment, including:
Absorption tower 5, its top inlet connects the pipeline 17 for supplying acetic acid and acetic anhydride, and top outlet connection has condensed system
System;
First chlorination reaction tower 1, its top inlet is connected with the bottom end outlet on absorption tower 5, is used for receiving absorption tower 5 bottom end outlet
Flow out absorbing liquid (being dissolved with chlorine and chloroacetic chloride), be also used for receiving the liquid of condensed system condensing simultaneously;
The top outlet connection of described first chlorination reaction tower 1 has fractionator condenser 4;It is also preferred that the left described first chlorination reaction tower 1
And being also associated with fractionating column 3 between fractionator condenser 4, described fractionating column 3 is used for receiving the liquid of fractionator condenser 4 condensation, and
The liquid of condensation is back in the first chlorination reaction tower 1 by the top inlet of the first chlorination reaction tower 1;
Second chlorination reaction tower 2, the bottom end outlet of its top inlet and the first chlorination reaction tower 1 connects, and therefore, the first chlorination is anti-
React the material liquids such as the monoxone generated and unreacted acetic acid in answering tower 1 to be admitted in the second chlorination reaction tower 2.
Wherein, the bottom entrance of the first chlorination reaction tower 1 is connected with the pipeline being used for supplying chlorine, the second chlorination reaction tower
The middle part of 2 is connected with the pipeline being used for supplying chlorine;When being embodied as, in the first chlorination reaction tower 1 and the second chlorination reaction tower 2
The delivery rate of chlorine is different, and in the second chlorination reaction tower 2, the delivery rate of chlorine is less than chlorine in the first chlorination reaction tower 1
Delivery rate.
Preferably, the bottom entrance on described absorption tower 5 and the top outlet of the second chlorination reaction tower 2 connect, and are used for receiving
The gas (chlorine, hydrogen chloride and chloroacetic chloride) on tower 2 top is answered in second anti-chlorination, due to from the second chlorination reaction tower 2 top
Gas temperature higher (about 90 degrees Celsius), it is in absorption tower 5, and the acetic acid being passed through with top, absorption tower 5 and acetic anhydride realize
Mass transfer and heat transfer, major part chlorine, chloroacetic chloride and partial oxidation hydrogen absorbed by liquid, and temperature of liquid improves simultaneously, makes feeding
The temperature of the first chlorination reaction tower reaches about 70 degrees Celsius.
Preferably, described condenser system includes first condenser the 6, second condenser the 7, the 3rd condenser 8, the respectively degree of depth
Room temperature, deep hypothermia and degree of depth cryogenic condenser, be used for reclaiming absorption tower 5 and discharge therein congealing into and point (include acetic acid, acyl chlorides
Deng);Wherein, not solidifying gas (predominantly hydrogen chloride) is sent into as salt acid starting material and is produced hydrochloric acid section, the liquid condensed out
(predominantly acetic acid and chloroacetic chloride) is delivered in the first chlorination reaction tower 1 together with passing through the liquid that pipeline is discharged with bottom, absorption tower 5.
Preferably, described fractionator condenser 4 is fractional distilling tube, and it exports the bottom with the second chlorination reaction tower 2
Entrance connects, for by the most condensed gas (chloroacetic chloride, chlorine and hydrogen chloride) supply to the second chlorination reaction tower 2.
Concrete, the sufficient acetic acid of unreacted, chloroacetic chloride, chlorine and hydrogen chloride etc. in the first chlorination reaction tower 1, by fractionating column 3
Entering in fractionator condenser 4, be fractionated into the partial condensation of condenser 4, liquid is back to fractionating column 3, and is fractionated into tower 3 and
Connection pipeline between the top inlet of monochlor(in)ate reaction tower 1 continues reaction in being back to the first chlorination reaction tower 1, and the coldest
Solidifying gas (predominantly chloroacetic chloride, chlorine and hydrogen chloride) is fractionated into the outlet of condenser 4 top and the second chlorination reaction tower 2
Connection pipeline between the entrance of bottom is admitted in the second chlorination reaction tower 2, with the second chlorination reaction tower 2 top inlet entrance
Liquid continues reaction, thus improves raw material availability.
Preferably, described first chlorination reaction tower 1 and the second chlorination reaction tower 2 are tower structure, described tower structure
For packed tower or plate column.
In the present invention, so-called " deep condensation ", refer to gaseous state acetic acid and gaseous state chloroacetic chloride are condensed into liquid
Condensation.
In the present invention, so-called " fractional distilling tube ", refer to the condensation condensed by boiling point not less than the gas of acetic acid
Device.
In order to be further appreciated by action principle and the beneficial effect of the production of chloroacetic acid method that the present invention provides, below will knot
Close production of chloroacetic acid equipment and the complete technological process of production of chloroacetic acid method according to the present invention is discussed in detail, incorporated by reference to referring to
Shown in Fig. 1:
(1) material liquid acetic acid and the acetic anhydride pipeline 17 through being connected with absorption tower 5 top inlet are provided in absorption tower 5, with
Time, the bottom entrance on absorption tower 5 and the top outlet connection of the second chlorination reaction tower 2, in the second chlorination reaction tower 2, unreacted is complete
Full chlorine, hydrogen chloride and chloroacetic chloride is also fed in absorption tower 5, in absorption tower 5, and acetic acid, acetic anhydride and chlorine, chlorination
Hydrogen, monoxone realize mass-and heat-transfer, and major part chlorine, chloroacetic chloride and partial oxidation hydrogen are absorbed by liquid, and liquid accepts simultaneously
The energy of gas, makes the liquid outlet temperature of bottom, absorption tower 5 reach about 70 degrees Celsius.
(2), in absorption tower 5, liquid acetic acid has dissolved most chlorine and chloroacetic chloride, major part liquid acetic acid, and liquid
These liquid together, is supplied to the first chlorination reaction tower 1 by acetic anhydride by the bottom end outlet on absorption tower 5.
(3) simultaneously, unabsorbed gases (predominantly hydrogen chloride, containing a small amount of acetic acid, chloroacetic chloride, trace chlorine),
Sequentially enter first condenser the 6, second condenser the 7, the 3rd condenser 8, lower the temperature further so that it is in can congeal into point condensation (bag
Include acetic acid, chloroacetic chloride, chlorine etc.) reclaim, and by pipeline, together with the liquid of the bottom end outlet on absorption tower 5 in step (2) by
Supply to the first chlorination reaction tower 1.The raw material of synthesis of chloroacetic acid has not only been reclaimed in cooling condensation, makes to send hydrochloric acid to produce car simultaneously
Between hydrogen chloride gas be purified.
(4) first chlorination reaction towers 1 receive the liquid acetic acid (being dissolved with chlorine and chloroacetic chloride) through absorption tower 5 supply and second
Anhydride, and a small amount of liquid acetic acid of first condenser the 6, second condenser the 7, the 3rd condenser 8 supply and chloroacetic chloride, and its end
End entrance is separately externally connected with the pipeline of supply chlorine, and chlorine, chloroacetic chloride, acetic acid and acetic anhydride are anti-in the first chlorination reaction tower 1
Should.
The product monoxone generated in (5) first chlorination reaction towers 1 and the acetic acid of liquid and acetic anhydride are by the first chlorine
The connection pipeline of the top inlet changing reaction tower 1 bottom end outlet and the second chlorination reaction tower 2 is provided to the second chlorination reaction
In tower 2 (now, at the first chlorination reaction tower 1 bottom end outlet, the percentage ratio of product is about 50-60%).
Unreacted chlorine completely, chloroacetic chloride, hydrogen chloride and vaporized acetic acid warp in (6) first chlorination reaction towers 1
Fractionating column 3 is admitted to fractionator condenser 4 partial condensation, and liquid refluxes, and gas (predominantly chlorine, chloroacetic chloride and hydrogen chloride) leads to
Cross the pipeline being connected with the second chlorination reaction tower 2 bottom entrance to be admitted in the second chlorination reaction tower 2.
(7) second chlorination reaction tower 2 top inlet have received the product chloroethene of the first chlorination reaction tower 1 bottom end outlet conveying
Sour and unreacted acetic acid and acetic anhydride, middle part have received the chlorine of chlorine supply line supply, and bottom entrance have received the
Unreacted chlorine completely, chloroacetic chloride and hydrogen chloride in first chlorination reaction tower 1 of two condenser 4 supplies, these materials exist
Reacting further in second chlorination reaction tower 2, in the second chlorination reaction tower 2, top acetic acid is many, middle part chlorine is many, acetic acid also
Many;Bottom monoxone and chloroacetic chloride are many, but chlorine is few;Therefore can reduce side reaction and occur by high degree, it is to avoid existing skill
In art acetic acid and chlorine reaction complete after, chlorine and product chloroacetate reaction and produce the defect of impurity, from the second chlorination reaction tower 2
In the product collected at the bottom of tower, chloroacetic percentage ratio is about 70-80%.
Below, beneficial effects of the present invention it is discussed in detail by introducing specific embodiment:
Example 1
In the bottom of the first chlorination reaction tower 1 with 3.6m3/ h speed is passed through chlorine, at the middle part of the second chlorination reaction tower 2 with
3.6m3/ h speed is passed through chlorine, and absorption tower 5 is passed through acetic acid (containing 7% acetic anhydride) with 30L/h speed, to unreacted chlorine,
Hydrogen chloride, chloroacetic chloride absorb, with 31L/h speed bottom the second chlorination reaction tower 2, and extraction material, after testing chloroacetic acid
Content 54.3%, dichloroacetic acid content 0.75%, in terms of chlorine, conversion ratio is 98%.
Example 2
In the bottom of the first chlorination reaction tower 1 with 7.2m3/ h speed is passed through chlorine, at the middle part of the second chlorination reaction tower 2 with
3.6m3/ h speed is passed through chlorine, and absorption tower 5 is passed through acetic acid (containing 7% acetic anhydride) with 30L/h speed, to unreacted chlorine,
Hydrogen chloride, chloroacetic chloride absorb, with 31L/h speed bottom the second chlorination reaction tower 2, and extraction material, after testing chloroacetic acid
Content 74.4%, dichloroacetic acid content 1.2%, in terms of chlorine, conversion ratio is 98%.
Example 3
In the bottom of the first chlorination reaction tower 1 with 10.8m3/ h speed is passed through chlorine, at the middle part of the second chlorination reaction tower 2 with
3.6m3/ h speed is passed through chlorine, and absorption tower 5 is passed through acetic acid (containing 7% acetic anhydride) with 30L/h speed, to unreacted chlorine,
Hydrogen chloride, chloroacetic chloride absorb, and react 2 tower bottoms with 32L/h speed, extraction material, after testing chloroacetic acid content 90.4%
, dichloroacetic acid content 1.7%, conversion ratio is 98.3%.
Example 4
In the bottom of the first chlorination reaction tower 1 with 14.4m3/ h speed is passed through chlorine, at the middle part of the second chlorination reaction tower 2 with
3.6m3/ h speed is passed through chlorine, and absorption tower 5 is passed through acetic acid (containing 7% acetic anhydride) with 35L/h speed, to unreacted chlorine,
Hydrogen chloride, chloroacetic chloride absorb, with 38L/h speed bottom the second chlorination reaction tower 2, and extraction material, after testing chloroacetic acid
Content 94.2%, dichloroacetic acid content 1.7%, conversion ratio is 97%.
Example 5
In the bottom of the first chlorination reaction tower 1 with 10.8m3/ h speed is passed through chlorine, at the middle part of the second chlorination reaction tower 2 with
7.2m3/ h speed is passed through chlorine, and absorption tower 5 is passed through acetic acid (containing 7% acetic anhydride) with 35L/h speed, to unreacted chlorine,
Hydrogen chloride, chloroacetic chloride absorb, with 38L/h speed bottom the second chlorination reaction tower 2, and extraction material, after testing chloroacetic acid
Content 95.2%, dichloroacetic acid content 1.7%, conversion ratio is 97%.
Example 6
In the bottom of the first chlorination reaction tower 1 with 10.8m3/ h speed is passed through chlorine, at the middle part of the second chlorination reaction tower 2 with
10.8m3/ h speed is passed through chlorine, and absorption tower 5 is passed through acetic acid with 45L/h speed, to unreacted chlorine, hydrogen chloride, acetyl
Chlorine absorbs, with 48L/h speed bottom the second chlorination reaction tower 2, and extraction material, after testing chloroacetic acid content 90.2%,
Dichloroacetic acid content 1.8%, conversion ratio is 97%.
Example 7
In the bottom of the first chlorination reaction tower 1 with 10.8m3/ h speed is passed through chlorine, at the middle part of the second chlorination reaction tower 2 with
10.8m3/ h speed is passed through chlorine, and absorption tower 5 is passed through acetic acid (containing 7% acetic anhydride) with 40L/h speed, to unreacted chlorine,
Hydrogen chloride, chloroacetic chloride absorb, with 42L/h speed bottom the second chlorination reaction tower 2, and extraction material, after testing chloroacetic acid
Content 97.5%, dichloroacetic acid content 1.2%, conversion ratio is 96%.
To sum up, the production of chloroacetic acid equipment that the present invention provides, can realize producing serialization, and raw material availability can be improved,
Meanwhile, effectively prevent excessive chlorine and product monoxone generation side reaction, improve product yield, reduce energy consumption.
Although the present invention has utilized above-mentioned preferred embodiment to illustrate, so it is not limited to the protection model of the present invention
Enclosing, any those skilled in the art are within without departing from the spirit and scope of the present invention, and relative above-described embodiment carries out various change
Dynamic and amendment still belongs to the scope that the present invention is protected, and therefore protection scope of the present invention is with being as the criterion that claims are defined.