CN1403382A - Method of treating phenol-containing effluent and recovering resource in 2-methyl-4-chlorophenoxyacetic acid producing process - Google Patents

Method of treating phenol-containing effluent and recovering resource in 2-methyl-4-chlorophenoxyacetic acid producing process Download PDF

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CN1403382A
CN1403382A CN02138466.5A CN02138466A CN1403382A CN 1403382 A CN1403382 A CN 1403382A CN 02138466 A CN02138466 A CN 02138466A CN 1403382 A CN1403382 A CN 1403382A
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tower
desorption
production processes
macroporous adsorbent
improvement
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CN1176026C (en
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张全兴
李洁莹
邱宇平
陆朝阳
潘丙才
叶必华
苏庆
朱兆连
金小元
陈金龙
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Nanjing University
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Nanjing University
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Abstract

The present invention is the method of treating phenol-containing effluent and recovering resource in 2-methyl-4-chlorophenoxyacetic acid (MCPA) as one farm herbicide. The steps includes: filtering of the effluent, macroporous resin adsorption in adsorbing tower and biochemical treatment of the adsorbed water before discharge; desorbing regeneration of adsorbed macroporous resin with orthocresol as desorption agent; and pH regulation and separation of the desorption agent liquid to obtain orthocresol, which is returned to production, water phase, which is returned to waste water treatment, and low concentration desorption liquid, which is reused. The said process can result in phenol concentration in the effluent below 5 mg/L, phenol eliminating rate higher than 99% and phenol recovering rate greater than 80%.

Description

The improvement and its recovery method as resource of phenolic wastewater in 2 first, the 4 chlorine production processes
One, technical field
The present invention relates to the improvement and its recovery method as resource of phenolic wastewater in a kind of pesticide herbicide production process, specifically, be the improvement and its recovery method as resource of the phenolic wastewater that produces in weedicide 2-methyl-4-chlorophenoxyacetic acid (being called for short 2 first, 4 chlorine or the MCPA) production process.
Two, background technology
2 first, 4 chlorine are hormone-type selective herbicides behind a kind of bud.Domestic main employing at present is traditional with the ortho-cresol be raw material through condensation, acidifying, chlorating synthetic route, produce one ton of 2 first 4 chlorine and discharge 15 tons of strongly acid wastewaters, COD approximately CrUp to 20000~30000mg/L, wherein phenol content 1500~3000mg/L also contains the sodium-chlor about 10% in addition.
Before the present invention finishes, the existing domestic and foreign literature of recent two decades is retrieved, do not find about the improvement of phenolic wastewater and the report of resource recycling in 2 first, the 4 chlorine production processes.
Three, summary of the invention
1, goal of the invention
The improvement and its recovery method as resource that the purpose of this invention is to provide phenolic wastewater in a kind of 2 first, 4 chlorine production processes, utilize the inventive method can from this waste water, remove and separate, reclaim the organic raw material ortho-cresol that runs off therein, realize the combination of waste water treatment and resource recycling.
2, technical scheme
The improvement and the resource recycling method of phenolic wastewater in a kind of 2 first, 4 chlorine production processes, key step is as follows:
A) the strongly-acid phenolic wastewater that gives off in 2 first, the 4 chlorine production processes after filtration, is the condition of 0.5~5BV/h (BV be resin bed volume) under at 0~40 ℃ with flow with filtrate, by being filled with the adsorption tower of macroporous adsorbent resin, absorption effluent realizes qualified discharge through biochemical treatment again;
B) will adsorb the macroporous adsorbent resin desorption and regeneration of ortho-cresol with desorbing agent;
C) high concentration desorption liquid that gets off of desorption returns the organic raw material ortho-cresol of separating out to production process after regulating pH and being 0.5~1.5, and water returns the waste water treatment flow process and adsorbs again, and light concentration desorption liquid is used to prepare next batch desorbing agent recycled.
Described desorbing agent is the NaOH aqueous solution.The NaOH concentration of aqueous solution is 1~3mol/L, and desorption temperature is 40~80 ℃, and the flow of desorbing agent is 0.2~3.5BV/h.
Described macroporous adsorbent resin can be home-made NDA-99, NDA-88, NDA-150, CHA-101, CHA-111, NKA, H-103 etc. have the superhigh cross-linking macroporous adsorbent resin of high-specific surface area, or U.S. Amberlite XAD-2, XAD-4, XAD-7, XAD-8 series polymeric adsorbent, or Japanese Diaion HP series macroporous adsorbent resin.Preferred superhigh cross-linking macroporous adsorbent resin NDA-99.
The improvement of phenolic wastewater and resource recycling method can adopt double-column in series absorption in the present invention's 2 first 4 chlorine production processes, the operation scheme of single tower desorption, I, II, three adsorption towers of III promptly are set, earlier with I, II tower series connection following current absorption, the I tower is as first post, the II tower is as stern post, after the absorption of I tower is saturated, switch to II, III tower series connection following current absorption, the II tower is as first post, and the III tower is as stern post, the I tower carries out the following current desorption and regeneration simultaneously, so cyclical operation, thus guarantee the operation continuously all the time of whole device, increase work efficiency.
3, beneficial effect
The present invention compared with prior art, its remarkable advantage is: can to make phenol content be that the strongly acid wastewater of 1500~3000mg/L is through after the above-mentioned processing for the improvement of phenolic wastewater and resource recycling method in 2 first, the 4 chlorine production processes of the present invention, the water outlet water white transparency, phenol content is reduced to below the 5mg/L, phenol clearance>99%, the phenol rate of recovery>80%, but and water outlet qualified discharge after biochemical treatment.
Four, embodiment
Below further specify the present invention by specific embodiment:
Embodiment 1
10mL (about 7.5 gram) NDA-99 superhigh cross-linking macroporous adsorbent resin packed in the glass adsorption column of strap clamp cover, and (φ 12 * 160mm).(20~25 ℃) pass through resin bed with the flow of 40mL/h after filtering with the light yellow strongly-acid phenolic wastewater (pH=0.86) that emits in 2 first, the 4 chlorine production processes under the room temperature, and wastewater treatment capacity is that 220mL/ criticizes.Raw wastewater phenol content is 2333mg/L, and absorption effluent water white transparency, phenol content are 2.88mg/L, phenol clearance>99%.
Use the NaOH aqueous solution of 20mL2mol/L, the NaOH aqueous solution and the 20mL tap water flow with 15mL/h under 60 ± 5 ℃ temperature of 10mL1mol/L to carry out desorption by resin bed, phenol desorption rate>99% successively.Just begun effusive 10mL desorption liquid and be red-brown, be high concentration desorption liquid, phenol content is 38574mg/L.Hydrochloric acid soln with 37% transfers to 1.05 with its pH, separates out the scarlet oil reservoir, it can be returned production process through separating, the water after the acid adjustment with carry out adsorption treatment again after waste water mixes.The back is effusive to be light concentration desorption liquid (about 40mL), is used to prepare the next batch desorbing agent.
Embodiment 2
100mL (about 75 gram) NDA-99 resin packed in the glass adsorption column of strap clamp cover, and (φ 32 * 360mm).(25~30 ℃) pass through resin bed with the flow of 350mL/h after filtering with the light yellow strongly-acid phenolic wastewater (pH=1.02) that emits in 2 first, the 4 chlorine production processes under the room temperature, and wastewater treatment capacity is that 2250mL/ criticizes.Raw wastewater phenol content is 2387mg/L, and absorption effluent water white transparency, phenol content are 3.23mg/L, phenol clearance>99%.
Use the NaOH aqueous solution of 200mL2mol/L, the NaOH aqueous solution and the 200mL tap water flow with 100mL/h under 60 ± 5 ℃ temperature of 100mL1mol/L to carry out desorption by resin bed, phenol desorption rate>99% successively.Just begun effusive 100mL desorption liquid and be red-brown, be high concentration desorption liquid, phenol content is 42358mg/L.Hydrochloric acid soln with 37% transfers to 0.54 with its pH, separates out the scarlet oil reservoir, and the weight that obtains the crude product ortho-cresol through separation is about 3.3g, it can be returned production process, water with carry out adsorption treatment again after waste water mixes.The back is effusive to be light concentration desorption liquid (about 400mL), is used to prepare the next batch desorbing agent.
Embodiment 3
A) absorbing process
(φ 600 * 3500mm), every tower filling 600 kilograms of resins of NDA-99 (about 800L) to select 3 identical adsorption towers of specification for use.Under room temperature (25~30 ℃), with the light yellow strongly-acid phenolic wastewater (phenol content 2431mg/L) that gives off in 2 first, the 4 chlorine production processes, squeeze into adsorption tower with pump after filtering, the method for I, II tower double-column in series following current absorption is adopted in absorption, and absorption flow is 3.2m 3/ h, every batch processed amount is controlled at 20m 3Waste water after treatment, water outlet phenol content is reduced to 3.16mg/L, but after biochemical treatment qualified discharge.
B) desorption and regeneration
With the first post I tower of absorption NaOH aqueous solution desorption.The concrete operations step is as follows: earlier raffinate in the I tower is drained, and inject adsorption tower with the hot water adverse current, make it be preheated to 60 ℃.Use 1.6m then successively 3The 2mol/L NaOH aqueous solution, 0.8m 3The 1mol/L NaOH aqueous solution and 1.6m 3Tap water is with 0.8m 3The flow of/h carries out the following current desorption.Preceding 0.8m 3Desorption liquid phenol content be 48976mg/L, transfer pH to 0.51 with 37% hydrochloric acid soln, the ortho-cresol crude product weight of separating out through separation is about 28.3kg, and it is returned production process, water after the acid adjustment and waste water carry out adsorption treatment after mixing again; The desorption liquid of back 3.2m3 is put into storage tank, is used to prepare the next batch desorption liquid.
I tower after desorption finishes will be as the stern post of the 3rd batch of waste water adsorption operations (when handling second batch of waste water, post headed by the II tower, the III tower is a stern post).
Embodiment 4
Change the NDA-99 resin among the embodiment 1 into NDA-88, NDA-150, H-103, CHA-111, CHA-101, other has the macroporous adsorbent resin of high-specific surface area NKA etc., or AmberliteXAD-2, XAD-4, XAD-7, XAD-8 series polymeric adsorbent, or Diaion HP series macroporous adsorbent resin etc., handle this waste water under the identical operations condition, the result shows that they have in various degree decline to absorption, the desorption performance of phenol.

Claims (6)

1, the improvement and the resource recycling method of phenolic wastewater in a kind of 2 first, 4 chlorine production processes is characterized in that this method may further comprise the steps:
A) the strongly-acid phenolic wastewater that gives off in 2 first, the 4 chlorine production processes is the condition of 0.5~5BV/h under at 0~40 ℃ with flow with filtrate after filtration, and by being filled with the adsorption tower of macroporous adsorbent resin, absorption effluent gets final product qualified discharge through biochemical treatment again;
B) will adsorb the macroporous adsorbent resin desorption and regeneration of ortho-cresol with desorbing agent;
C) high concentration desorption liquid that gets off of desorption returns the organic raw material ortho-cresol of separating out to production process after regulating pH to 0.5~1.5, and water is got back to the waste water treatment flow process and adsorbed again, and light concentration desorption liquid is used to prepare next batch desorbing agent recycled.
2, the improvement of phenolic wastewater and the method for resource recycling in 2 first, the 4 chlorine production processes according to claim 1 is characterized in that described desorbing agent is the NaOH aqueous solution.
3, the improvement of phenolic wastewater and the method for resource recycling in 2 first, the 4 chlorine production processes according to claim 1 and 2, when it is characterized in that using the NaOH aqueous solution as desorbing agent, the NaOH concentration of aqueous solution is 1~3mol/L, desorption temperature is 40~80 ℃, and the flow of desorbing agent is 0.2~3.5BV/h.
4, the improvement of phenolic wastewater and the method for resource recycling in 2 first, the 4 chlorine production processes according to claim 1 is characterized in that described macroporous adsorbent resin, can be home-made NDA-99, NDA-88, NDA-150, CHA-101, CHA-111, NKA, H-103 etc. have the superhigh cross-linking macroporous adsorbent resin of high-specific surface area, or U.S. Amberlite XAD-2, XAD-4, XAD-7, XAD-8 series polymeric adsorbent, or Japanese Diaion HP series macroporous adsorbent resin.
5, according to the improvement of phenolic wastewater and the method for resource recycling in claim 1 or 4 described 2 first, the 4 chlorine production processes, it is characterized in that the preferred superhigh cross-linking macroporous adsorbent resin of described macroporous adsorbent resin NDA-99.
6, the improvement and the resource recycling method of phenolic wastewater in 2 first, the 4 chlorine production processes according to claim 1 is characterized in that adopting double-column in series absorption, single tower desorption operation scheme, I, II, three adsorption towers of III promptly are set, with I, II tower series connection following current absorption, the I tower is as first post earlier, and the II tower is as stern post, after the absorption of I tower is saturated, switch to II, III tower series connection following current absorption, the II tower is as first post, and the III tower is as stern post, the I tower carries out the following current desorption simultaneously, so cyclical operation.
CNB021384665A 2002-10-21 2002-10-21 Method of treating phenol-containing effluent and recovering resource in 2-methyl-4-chlorophenoxyacetic acid producing process Expired - Fee Related CN1176026C (en)

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Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101973660A (en) * 2010-09-21 2011-02-16 浙江大学 Recycling and pretreatment methods of raw materials containing benzene thiazole alcohol pesticide industrial wastewater
CN102381806A (en) * 2011-08-11 2012-03-21 南京师范大学 Method for treating nonylphenol polyoxyethylene ether industrial wastewater
CN102674607A (en) * 2012-05-03 2012-09-19 江苏健谷化工有限公司 Method for treating acid wastewater of 2-methyl-4-chlorophenoxyacetic acid through extraction, neutralization and distillation integration
CN104844416A (en) * 2015-03-26 2015-08-19 南京师范大学 Method for multistage extracting and absorpting dichloromethane and monochloroacetone in MCPa synthetic tail gas
CN111995185A (en) * 2020-08-20 2020-11-27 京博农化科技有限公司 Treatment method of deep-color high-concentration and high-toxicity mixed pesticide industrial wastewater

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101973660A (en) * 2010-09-21 2011-02-16 浙江大学 Recycling and pretreatment methods of raw materials containing benzene thiazole alcohol pesticide industrial wastewater
CN102381806A (en) * 2011-08-11 2012-03-21 南京师范大学 Method for treating nonylphenol polyoxyethylene ether industrial wastewater
CN102674607A (en) * 2012-05-03 2012-09-19 江苏健谷化工有限公司 Method for treating acid wastewater of 2-methyl-4-chlorophenoxyacetic acid through extraction, neutralization and distillation integration
CN104844416A (en) * 2015-03-26 2015-08-19 南京师范大学 Method for multistage extracting and absorpting dichloromethane and monochloroacetone in MCPa synthetic tail gas
CN111995185A (en) * 2020-08-20 2020-11-27 京博农化科技有限公司 Treatment method of deep-color high-concentration and high-toxicity mixed pesticide industrial wastewater

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