CN106477769A - A kind of processing method of nitrobenzene compounds waste water - Google Patents

A kind of processing method of nitrobenzene compounds waste water Download PDF

Info

Publication number
CN106477769A
CN106477769A CN201610948625.XA CN201610948625A CN106477769A CN 106477769 A CN106477769 A CN 106477769A CN 201610948625 A CN201610948625 A CN 201610948625A CN 106477769 A CN106477769 A CN 106477769A
Authority
CN
China
Prior art keywords
waste water
reaction
processing method
nitrobenzene compounds
filtrate
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
CN201610948625.XA
Other languages
Chinese (zh)
Inventor
贾军芳
陈磊
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Zhejiang Qicai Eco Technology Co Ltd
Original Assignee
Zhejiang Qicai Eco Technology Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Zhejiang Qicai Eco Technology Co Ltd filed Critical Zhejiang Qicai Eco Technology Co Ltd
Priority to CN201610948625.XA priority Critical patent/CN106477769A/en
Publication of CN106477769A publication Critical patent/CN106477769A/en
Pending legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C02TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02FTREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F9/00Multistage treatment of water, waste water or sewage
    • CCHEMISTRY; METALLURGY
    • C02TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02FTREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F1/00Treatment of water, waste water, or sewage
    • C02F1/001Processes for the treatment of water whereby the filtration technique is of importance
    • CCHEMISTRY; METALLURGY
    • C02TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02FTREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F1/00Treatment of water, waste water, or sewage
    • C02F1/52Treatment of water, waste water, or sewage by flocculation or precipitation of suspended impurities
    • C02F1/5236Treatment of water, waste water, or sewage by flocculation or precipitation of suspended impurities using inorganic agents
    • CCHEMISTRY; METALLURGY
    • C02TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02FTREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F1/00Treatment of water, waste water, or sewage
    • C02F1/58Treatment of water, waste water, or sewage by removing specified dissolved compounds
    • CCHEMISTRY; METALLURGY
    • C02TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02FTREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F1/00Treatment of water, waste water, or sewage
    • C02F1/66Treatment of water, waste water, or sewage by neutralisation; pH adjustment
    • CCHEMISTRY; METALLURGY
    • C02TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02FTREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F1/00Treatment of water, waste water, or sewage
    • C02F1/70Treatment of water, waste water, or sewage by reduction
    • CCHEMISTRY; METALLURGY
    • C02TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02FTREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F1/00Treatment of water, waste water, or sewage
    • C02F1/72Treatment of water, waste water, or sewage by oxidation
    • C02F1/722Oxidation by peroxides
    • CCHEMISTRY; METALLURGY
    • C02TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02FTREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F1/00Treatment of water, waste water, or sewage
    • C02F1/72Treatment of water, waste water, or sewage by oxidation
    • C02F1/725Treatment of water, waste water, or sewage by oxidation by catalytic oxidation
    • CCHEMISTRY; METALLURGY
    • C02TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02FTREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F2101/00Nature of the contaminant
    • C02F2101/30Organic compounds
    • C02F2101/38Organic compounds containing nitrogen
    • CCHEMISTRY; METALLURGY
    • C02TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02FTREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F2305/00Use of specific compounds during water treatment
    • C02F2305/02Specific form of oxidant
    • C02F2305/026Fenton's reagent

Abstract

The invention discloses a kind of nitrobenzene compounds produce the processing method of waste water, including:(1) sodium sulfide reducing:Waste water is adjusted to alkalescence, adds akali sulphide, stirring reaction 30~60min at 80~100 DEG C, obtain reduction reaction liquid;(2) formaldehyde condensation:Reduction reaction liquid is adjusted to acidity, mixes with formalin at 70~80 DEG C and carry out condensation reaction, filter to get filtrate, in filtrate, COD clearance reaches 50~55%;(3) advanced oxidation reaction:Filtrate is carried out advanced oxidation reaction, obtains oxidation liquid;(4) discharge after will be post-treated for oxidation liquid, described post processing is at least one in flocculation reaction, absorption, air supporting and filtration.After the disposal methods of the present invention, the COD < 350mg/L of nitrobenzene compounds waste water, total organic carbon TOC < 150mg/L, COD clearance reaches more than 97%, TOC clearance reaches more than 97%, the total removal rate of Organic substance reaches 98%, reaches the discharge standard of national regulation.

Description

A kind of processing method of nitrobenzene compounds waste water
Technical field
The present invention relates to field of waste water treatment, more particularly, to a kind of processing method of nitrobenzene compounds waste water.
Background technology
Nitrobenzene compounds waste component is complicated, and toxicity is big, and colourity is high, and COD is high, and biodegradation difficulty is big, to ecology Environment has larger harm.
The Chinese patent literature of Publication No. CN1626257 discloses a kind of organic dirt of wet oxidation process treatment of Nitrobenzene class The method of dye thing, in autoclave, in liquid-phase system, under high-temperature and high-pressure conditions, with oxygen or air as oxidant, Add cooxidation material, oxidation removal organic pollution;Cooxidation material and the mass concentration ratio of processed organic pollution For 0.1~20, reaction temperature is 130~325 DEG C, and pressure is 0.5~20MPa, and wherein partial pressure of oxygen is 0.2~10MPa.The method Range is narrow, is relatively suitable for the Nitrobenzol that electron-donating group replaces, and the clearance ratio of Nitrobenzene in Wastewater class material Relatively low.
The Chinese patent literature of Publication No. CN1679983 discloses a kind of catalytic wet conjugated oxidation degrading nitrobenzene class The method of pollutant, in the autoclave filling nitrobenzene class pollutant waste liquid, adds cooxidation material and catalyst, altogether Oxidation material is 0.1~20 with the mass concentration ratio of processed organic pollution, with oxygen or air as oxidant, reaction temperature Spend for 100~250 DEG C, reaction pressure is 0.5Mpa~10Mpa, wherein partial pressure of oxygen is 0.2Mpa~5Mpa.The method reacts bar Part requirement is higher, and the clearance ratio of Nitrobenzol is relatively low, and very big to the clearance difference of each nitrobenzene derivative.
Fast red KD base, is the higher developer of fastness in azoic dyes, is mainly used in the dyeing of cotton, synthetic cotton, flaxen fiber And stamp, it is also synthetic organic pigment C.I. pigment red 31,32,146,147,150,176,261 and C.I. pigment violet 43 etc. Important intermediate.Multiple benzene ring structures are contained in the molecular structure of these organic pigments, compared with general azo organic pigment, Because its molecular weight is big, sun-proof, the fastness ability such as heat-resisting are good, are the focuses of domestic technique exploitation, are also walking on international market Pretty kind.
At present, this intermediate of fast red KD base is domestic many productions, and the process route being adopted is:With ortho-nitrophenyl first Ether be raw material, through chloromethylation, hydrolysis, oxidation, chloride, condensation, reduction and be obtained.
Contain substantial amounts of nitrobenzene compounds in the production waste water of fast red KD base, wastewater contaminated by nitro-benzene compounds becomes Divide complexity, toxicity is big, colourity is high, COD is high, biodegradation difficulty greatly, has larger harm to ecological environment.
Content of the invention
The invention provides a kind of processing method of nitrobenzene compounds waste water, the method is simple to operate, total in waste water Organic removal rate is higher.
A kind of processing method of nitrobenzene compounds waste water, including:
(1) sodium sulfide reducing:Waste water is adjusted to alkalescence, adds akali sulphide, at 80~100 DEG C stirring reaction 30~ 60min, obtains reduction reaction liquid;
(2) formaldehyde condensation:Reduction reaction liquid is adjusted to acidity, mixes with formalin at 70~80 DEG C and be condensed Reaction, filters to get filtrate, in filtrate, COD clearance reaches 50~55%;
(3) advanced oxidation reaction:Filtrate is carried out advanced oxidation reaction, obtains oxidation liquid;
(4) discharge after will be post-treated for oxidation liquid, described post processing is flocculation reaction, absorption, air supporting and filtration In at least one.
Nitrobenzene compounds species is more, complicated component, and common processing method is difficult to always effectively remove in this waste water Organic substance.
Nitrobenzene compounds are reduced to relatively degradable benzene initially with akali sulphide by the processing method of the present invention Aminated compoundss, part amino benzenes compounds again with formaldehyde condensation, the condensation product water solublity of generation is poor, is removed by filtration, In filtrate, the Organic substance of residual is removed by advanced oxidation depth degradation, finally post-treated, and water outlet can reach waste water straightly discharging will Ask.
The dosage of formaldehyde in formaldehyde condensation processes, should be controlled, effectively can remove amino benzenes compounds, make in filtrate COD clearance reaches 50~55%, and filtrate water outlet after follow-up advanced oxidation afterwards requires up to waste water straightly discharging.
Described akali sulphide is one of sodium sulfide, sodium disulfide, sodium polysulphide and NaHS, preferably, institute The akali sulphide stated is sodium sulfide.The reduction non-selectivity to nitro on phenyl ring for the sodium sulfide, can by multiple nitrobenzene compounds also Originally it was corresponding amino benzenes compounds.
Preferably, on the basis of the quality of waste water, the addition of akali sulphide is 5~10%;It is further preferred that sulfuration The addition of alkali is 7~8%.
According to the content of the useless Organic substance in water of nitrobenzene compounds, slightly excessive addition akali sulphide, make Nitrobenzene in Wastewater Class compound is easier to be reduced, and reduces more abundant.
Akali sulphide can add in solid form, preferably, akali sulphide adds as a solution.
During sodium sulfide reducing, the pH value impact reduction effect of reduction system, preferably, in step (1), reduction The pH value of reaction is 7~8.
Nitrobenzene compounds in waste water generate the amino benzenes compounds of relatively easy degraded through reduction, by with formaldehyde Condensation generates the poor condensation substance of water solublity, separates out, be removed by filtration from waste water.
Preferably, in step (2), the pH value of condensation reaction is 2~3.
Control the addition of formaldehyde, the COD clearance in filtrate can be made after filtering to reach 50~55%.Can pass through afterwards The Organic substance of follow-up advanced oxidation reaction fully degraded wherein residual.
Preferably, on the basis of the quality of reduction reaction liquid, the addition of formaldehyde is 3~5%.Formaldehyde is controlled to be to add When entering amount, effectively can remove amino benzenes compounds, make COD clearance in filtrate reach 50~55%.
In step (3), advanced oxidation reaction can be Fenton's reaction, ozone oxidation, wet-type peroxide catalysis oxidation, wet Formula ClO 2 catalyzed oxidation or wet type sodium hypochlorite catalysis oxidation.
Wherein, Fenton's reaction is with H2O2It is Fenton reagent with ferrous salt, H2O2In Fe2+Catalytic action under produce hydroxyl from By base, it has strong oxidizing property, can aoxidize some difficult degradations and virose material;Fenton reagent energy when processing organic wastewater Produce ferric hydroxide colloid, equally can play flocculation.
Preferably, advanced oxidation reacts for Fenton's reaction:At 40~50 DEG C, add ferrous salt, H in filtrate2O2, Reaction 0.5~5h.
Preferably, on the basis of the quality of filtrate, the addition of ferrous salt is 0.2~0.5%, H2O2Addition be 6 ~8%.
Preferably, in step (4), described post processing is flocculation reaction:The pH value of oxidation liquid is adjusted to 8~ 9, stirring reaction 20~40min, add flocculant, stand 3~5min, filter.
The pH value of oxidation liquid is adjusted to after 8~9, wherein iron ion can generate ferric hydroxide colloid, absorption is useless The particle suspensions of residual and Organic substance in water, are gone further by filtering the Organic substance making residual in oxidation liquid Remove.
Described nitrobenzene compounds waste water is derived from the production process of dyestuff intermediate fast red KD base.
Compared with prior art, beneficial effects of the present invention are:
After the disposal methods of the present invention, the COD < 350mg/L, total organic carbon TOC of nitrobenzene compounds waste water < 150mg/L, COD clearance reaches more than 97%, TOC clearance and reaches more than 97%, and the total removal rate of Organic substance reaches 98%, reaches Discharge standard to national regulation.
The present invention is combined by sodium sulfide reducing-formaldehyde condensation-advanced oxidation-flocculation reaction.Akali sulphide is by Nitrobenzol Class compound is reduced to relatively degradable amino benzenes compounds, amino benzenes compounds again with formaldehyde condensation, the condensation of generation Product water solublity is poor, is removed by filtration, and in filtrate, the Organic substance Fenton's reaction depth degradation of residual removes, and eventually passes flocculation Filter, water outlet can reach waste water straightly discharging requirement;Between each step of the present invention, mutual synergism, indispensable, and operates Order can not overturn, otherwise it is impossible to obtain the treatment effect of the present invention.
Specific embodiment
Certain nitrobenzene compounds waste water is in brown color, and pH is 6.2, COD is 11560mg/L, and TOC (total organic carbon) is 5214mg/L.
Embodiment 1
(1) sodium sulfide reducing:It is 7.6 with the pH that liquid caustic soda adjusts waste water, add the sodium sulfide solution that mass fraction is 30%, On the basis of the quality of waste water, the addition of sodium sulfide is 8%, is placed in 90 DEG C of stirred in water bath reaction 50min;
(2) formaldehyde condensation:It is 2 with the pH of dilute sulfuric acid regulating step (1) water outlet, add formaldehyde to be condensed, with waste water On the basis of quality, the addition of formaldehyde is 5%, is placed in 80 DEG C of stirred in water bath reaction 40min, filters;
The COD of filtrate is 5630mg/L, and TOC is 2586mg/L, and the clearance of COD and TOC is respectively 51.3% He 50.4%;
(3) Fenton's reaction:FeSO is added in the water outlet of step (2)4·7H2O, is placed in 50 DEG C of water-bath, then uses pump H is inputted in waste water2O2, react 3h;
On the basis of the quality of waste water, FeSO4·7H2The addition of O is 0.4%, H2O2Addition be 8%;
(4) flocculation reaction:Adding liquid caustic soda to adjust its pH in the water outlet of step (3) is 8, stirring reaction 30min, Ran Houjia Enter the PAM solution that the mass fraction that mass percent is 0.05% is 0.2%, stand 3min, filter;
The COD of water outlet is 320mg/L, and TOC is 120mg/L, and the total removal rate of Organic substance is 97.7%.
Embodiment 2
(1) sodium sulfide reducing:It is 7.2 with the pH that liquid caustic soda adjusts waste water, add the sodium sulfide solution that mass fraction is 30%, On the basis of the quality of waste water, the addition of sodium sulfide is 8%, is placed in 100 DEG C of stirred in water bath reaction 30min;
(2) formaldehyde condensation:It is 3 with the pH of dilute sulfuric acid regulating step (1) water outlet, add formaldehyde to be condensed, with waste water On the basis of quality, the addition of formaldehyde is 4%, is placed in 80 DEG C of stirred in water bath reaction 30min, filters;
The COD of filtrate is 5438mg/L, and TOC is 2398mg/L, and the clearance of COD and TOC is respectively 53% and 54%;
(3) Fenton's reaction:FeSO is added in the water outlet of step (2)4·7H2O, is placed in 40 DEG C of water-bath, then uses pump H is inputted in waste water2O2, react 2h;
On the basis of the quality of waste water, FeSO4·7H2The addition of O is 0.5%, H2O2Addition be 6%;
(4) flocculation reaction:Adding liquid caustic soda to adjust its pH in the water outlet of step (3) is 9, stirring reaction 40min, Ran Houjia Enter the PAM solution that the mass fraction that mass percent is 0.15% is 0.2%, stand 5min, filter;
The COD of water outlet is 280mg/L, and TOC is 98mg/L, and the total removal rate of Organic substance is 98.1%.
Embodiment 3
(1) sodium sulfide reducing:It is 7.6 with the pH that liquid caustic soda adjusts waste water, add the sodium sulfide solution that mass fraction is 30%, On the basis of the quality of waste water, the addition of sodium sulfide is 7%, is placed in 90 DEG C of stirred in water bath reaction 40min;
(2) formaldehyde condensation:It is 2 with the pH of dilute sulfuric acid regulating step (1) water outlet, add formaldehyde to be condensed, with waste water On the basis of quality, the addition of formaldehyde is 5%, is placed in 70 DEG C of stirred in water bath reaction 40min, filters;
The COD of filtrate is 5582mg/L, and TOC is 2432mg/L, and the clearance of COD and TOC is respectively 51.7% He 53.3%;
(3) Fenton's reaction:FeSO is added in the water outlet of phase step (2)4·7H2O, is placed in 45 DEG C of water-bath, then uses pump H is inputted in waste water2O2, react 2.5h;
On the basis of the quality of waste water, FeSO4·7H2The addition of O is 0.3%, H2O2Addition be 7%;
(4) flocculation reaction:Adding liquid caustic soda to adjust its pH in the water outlet of step (3) is 8.5, stirring reaction 30min, then Add the PAM solution that the mass fraction that mass percent is 0.2% is 0.2%, stand 3min, filter;
The COD of water outlet is 298mg/L, and TOC is 106mg/L, and the total removal rate of Organic substance is 98%.
Comparative example 1
Compared with Example 2, only execution step (3) and step (4).
The COD of water outlet is 6382mg/L, and TOC is 2843mg/L, and the total removal rate of Organic substance is 53%.
Comparative example 2
Compared with Example 2, the order of each step execution is step (3)-step (1)-step (2)-step (4).
The COD of water outlet is 849mg/L, and TOC is 546mg/L, and the total removal rate of Organic substance is 83%.
Comparative example 3
Certain nitrobenzene compounds waste water be in brown color, pH be 6.2, COD=11560mg/L, TOC (total organic carbon)= 5214mg/L.
(1) Fenton's reaction:It is 3.5 with the pH of dilute sulfuric acid regulating step waste water, add mass percent to be 0.4% FeSO4·7H2O, is placed in 60 DEG C of water-bath, then inputs H in waste water with pump2O2, total coreaction 2h, H2O2Total addition For 8%.
(2) flocculation reaction:The pH that liquid caustic soda adjusts waste water is added to be 8 in the water outlet of step (1), stirring reaction 30min, so Add the PAM that the mass fraction that mass percent is 0.15% is 0.2% afterwards, be slowly stirred 2min, then stand 3min, mistake Filter.
(3) vulcanize sodium reduction:Sodium sulfide (the matter of sodium sulfide that mass percent is 8% is added in the water outlet of step (2) Amount fraction is 30%), it is placed in 90 DEG C of stirred in water bath reaction 50min
(4) formaldehyde condensation:It is 2 with the pH that dilute sulfuric acid adjusts the waste water processing through step (1), addition mass percent is 5% formalin, is placed in 80 DEG C of stirred in water bath reaction 40min, filters, the COD=3420mg/L of filtrate, TOC (always have Machine carbon)=1658mg/L
Comparative example 4
Certain nitrobenzene compounds waste water be in brown color, pH be 6.2, COD=11560mg/L, TOC (total organic carbon)= 5214mg/L.
(1) vulcanize sodium reduction:It is 7.6 with the pH that liquid caustic soda adjusts waste water, add the sodium sulfide (sulfur that mass percent is 8% The mass fraction changing sodium is 30%), it is placed in 90 DEG C of stirred in water bath reaction 50min
(2) formaldehyde condensation:It is 2 with the pH that dilute sulfuric acid adjusts the waste water processing through step (1), addition mass percent is 5% formalin, is placed in 80 DEG C of stirred in water bath reaction 40min, filters, the COD=5630mg/L of filtrate, TOC (always have Machine carbon)=2586mg/L
(3) flocculation reaction:The pH that liquid caustic soda adjusts waste water is added to be 8 in the water outlet of step (2), stirring reaction 30min, so Add the PAM that the mass fraction that mass percent is 0.15% is 0.2% afterwards, be slowly stirred 2min, then stand 3min, mistake Filter, the COD=4563mg/L of water outlet, TOC (total organic carbon)=2230mg/L.
Compared with Example 2, lack step (3).
Comparative example 5
Certain nitrobenzene compounds waste water be in brown color, pH be 6.2, COD=11560mg/L, TOC (total organic carbon)= 5214mg/L.
(1) vulcanize sodium reduction:It is 7.6 with the pH that liquid caustic soda adjusts waste water, add the sodium sulfide (sulfur that mass percent is 8% The mass fraction changing sodium is 30%), it is placed in 90 DEG C of stirred in water bath reaction 50min
(2) Fenton's reaction:The pH adjusting the waste water of the process through step (1) with dilute sulfuric acid is 3.5, adds mass percent FeSO for 0.4%4·7H2O, is placed in 50 DEG C of water-bath, then inputs H in waste water with pump2O2, total coreaction 2h, H2O2 Total addition be 8%.
(3) flocculation reaction:The pH that liquid caustic soda adjusts waste water is added to be 8 in the water outlet of step (2), stirring reaction 30min, so Add the PAM that the mass fraction that mass percent is 0.15% is 0.2% afterwards, be slowly stirred 2min, then stand 3min, mistake Filter, the COD=5982mg/L of water outlet, TOC (total organic carbon)=2738mg/L.
By the contrast between embodiment 2, comparative example 1,2,3,4,5 it is found that mutually assisting between step (1)~(4) Same-action, four is indispensable, and four execution sequences can not overturn, and is otherwise unable to reach the treatment effect of the present invention.
Comparative example 6
By adjusting the addition of formaldehyde, in the filtrate that rate-determining steps (2) produce, COD clearance is 30%, other operations With embodiment 2.
The COD of water outlet is 1183mg/L, and TOC is 558mg/L, and the total removal rate of Organic substance is 78%.
By the contrast between embodiment 2 and comparative example 6 it is found that after step (1) and step (2), waste water should be made Middle nitrobenzene Organic substance is effectively removed, and that is, COD clearance reaches more than 50%, then through advanced oxidation reaction and after locate Reason, processes the requirement that water outlet can be only achieved waste water straightly discharging.
Embodiment described above technical scheme and beneficial effect have been described in detail it should be understood that The foregoing is only the specific embodiment of the present invention, be not limited to the present invention, all done in the spirit of the present invention Any modification, supplement and equivalent etc., should be included within the scope of the present invention.

Claims (10)

1. a kind of processing method of nitrobenzene compounds waste water is it is characterised in that include:
(1) sodium sulfide reducing:Waste water is adjusted to alkalescence, adds akali sulphide, stirring reaction 30~60min at 80~100 DEG C, Obtain reduction reaction liquid;
(2) formaldehyde condensation:Reduction reaction liquid is adjusted to acidity, mixes with formalin at 70~80 DEG C and carry out condensation instead Should, filter to get filtrate, in filtrate, COD clearance reaches 50~55%;
(3) advanced oxidation reaction:Filtrate is carried out advanced oxidation reaction, obtains oxidation liquid;
(4) discharge after will be post-treated for oxidation liquid, described post processing is in flocculation reaction, absorption, air supporting and filtration At least one.
2. the processing method of nitrobenzene compounds waste water according to claim 1 is it is characterised in that in step (1), go back The pH value of former reaction is 7~8.
3. the processing method of nitrobenzene compounds waste water according to claim 1 is it is characterised in that in step (1), with On the basis of the quality of waste water, the addition of akali sulphide is 5~10%.
4. the processing method of nitrobenzene compounds waste water according to claim 1 is it is characterised in that institute in step (1) The akali sulphide stated is sodium sulfide, sodium disulfide, sodium polysulphide, at least one in NaHS.
5. the processing method of nitrobenzene compounds waste water according to claim 1 is it is characterised in that in step (2), contract The pH value closing reaction is 2~3.
6. the processing method of nitrobenzene compounds waste water according to claim 1 is it is characterised in that with reduction reaction liquid Quality on the basis of, the addition of formaldehyde is 3~5%.
7. the processing method of nitrobenzene compounds waste water according to claim 1 is it is characterised in that in step (3), high Level oxidation reaction is Fenton's reaction:At 40~50 DEG C, add ferrous salt, H in filtrate2O2, react 0.5~5h.
8. the processing method of nitrobenzene compounds waste water according to claim 6 is it is characterised in that quality with filtrate On the basis of, the addition of ferrous salt is 0.2~0.5%, H2O2Addition be 6~8%.
9. the processing method of nitrobenzene compounds waste water according to claim 1 is it is characterised in that in step (4), institute The post processing stated is flocculation reaction:The pH value of oxidation liquid is adjusted to 8~9, stirring reaction 20~40min, addition helps solidifying Agent, stands 3~5min, filters.
10. the processing method of nitrobenzene compounds waste water according to claim 1 is it is characterised in that described nitro Benzene-like compounds waste water is derived from the production process of dyestuff intermediate fast red KD base.
CN201610948625.XA 2016-10-26 2016-10-26 A kind of processing method of nitrobenzene compounds waste water Pending CN106477769A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201610948625.XA CN106477769A (en) 2016-10-26 2016-10-26 A kind of processing method of nitrobenzene compounds waste water

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201610948625.XA CN106477769A (en) 2016-10-26 2016-10-26 A kind of processing method of nitrobenzene compounds waste water

Publications (1)

Publication Number Publication Date
CN106477769A true CN106477769A (en) 2017-03-08

Family

ID=58271682

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201610948625.XA Pending CN106477769A (en) 2016-10-26 2016-10-26 A kind of processing method of nitrobenzene compounds waste water

Country Status (1)

Country Link
CN (1) CN106477769A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108793552A (en) * 2018-06-07 2018-11-13 浙江奇彩环境科技股份有限公司 A kind of processing method of nigrosine production waste water

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6379562B1 (en) * 2001-03-21 2002-04-30 Atr Products And Chemicals, Inc. Treatment of water containing organic wastes with aromatic amine nitrate salts
CN101402503A (en) * 2008-10-23 2009-04-08 浙江龙盛化工研究有限公司 Treatment method for wastewater from dinitrobenzene production with benzene mixed acid nitrification
CN104045142A (en) * 2014-07-08 2014-09-17 北京师范大学 Method for treating m-dinitrobenzene wastewater through catalytic reduction
CN104445711A (en) * 2014-10-29 2015-03-25 绍兴奇彩化工有限公司 Treatment method for aniline wastewater

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6379562B1 (en) * 2001-03-21 2002-04-30 Atr Products And Chemicals, Inc. Treatment of water containing organic wastes with aromatic amine nitrate salts
CN101402503A (en) * 2008-10-23 2009-04-08 浙江龙盛化工研究有限公司 Treatment method for wastewater from dinitrobenzene production with benzene mixed acid nitrification
CN104045142A (en) * 2014-07-08 2014-09-17 北京师范大学 Method for treating m-dinitrobenzene wastewater through catalytic reduction
CN104445711A (en) * 2014-10-29 2015-03-25 绍兴奇彩化工有限公司 Treatment method for aniline wastewater

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108793552A (en) * 2018-06-07 2018-11-13 浙江奇彩环境科技股份有限公司 A kind of processing method of nigrosine production waste water

Similar Documents

Publication Publication Date Title
Wang et al. Textile dyeing wastewater treatment
Abo-Farha Comparative study of oxidation of some azo dyes by different advanced oxidation processes: Fenton, Fenton-like, photo-Fenton and photo-Fenton-like
Buscio et al. Sustainable dyeing of denim using indigo dye recovered with polyvinylidene difluoride ultrafiltration membranes
CN100457654C (en) Printing-dyeing waste water treatment process
CN101412571B (en) Technique for reclaiming waste water of azoic dye production
CN101139338B (en) Preparation of 2,2'-disulfo-dibenzopyrene by oxygen process based on 2-mercaptan benzothiazole ammonia salt
CN102942281B (en) Treatment method of high-concentration mixing organic acid waste water
CN110902747B (en) Method for recovering bromine from bromine-containing wastewater generated in production of bromoaniline
CN103819024B (en) Pretreatment method for fluorenone production wastewater
CN105130062A (en) Anthraquinone wastewater treatment method
Shah Bioremediation of azo dye
CN105692952A (en) Treatment method of textile wastewater
CN106477769A (en) A kind of processing method of nitrobenzene compounds waste water
CN104628195A (en) Method for purifying aromatic amine wastewater
CN104445551A (en) Silk dyeing process wastewater treatment agent and preparation method thereof
CN107857444A (en) A kind of environment protection method for handling dyeing waste water
CN108455757A (en) A kind of processing method of amino benzene analog waste water
CN104926033A (en) Efficient treatment method for printing and dyeing wastewater
CN105254067B (en) The resource utilization method of advanced treatment of wastewater Fenton process sludge
CN105084436B (en) A kind of application of the recycle-water that efficient decolorizing of printing waste water obtains in printcloth washing process
Uzal Effluent treatment in denim and jeans manufacture
CN105753204A (en) Method for treating textile biologically-dysoxidizable wastewater
CN103771562B (en) A kind of nitro-chlorobenzene hot wastewater advanced treatment and reuse method
Ramesh et al. Removal of colour and chemical oxygen demand from textile effluent by Fenton oxidation method
CN105692859A (en) Strong oxidant and application thereof

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
RJ01 Rejection of invention patent application after publication
RJ01 Rejection of invention patent application after publication

Application publication date: 20170308