CN100519446C - H acid waste water by natrium chloratum addition process - Google Patents

H acid waste water by natrium chloratum addition process Download PDF

Info

Publication number
CN100519446C
CN100519446C CNB2007100516227A CN200710051622A CN100519446C CN 100519446 C CN100519446 C CN 100519446C CN B2007100516227 A CNB2007100516227 A CN B2007100516227A CN 200710051622 A CN200710051622 A CN 200710051622A CN 100519446 C CN100519446 C CN 100519446C
Authority
CN
China
Prior art keywords
acid
waste water
chlor
solid
sodium
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.)
Expired - Fee Related
Application number
CNB2007100516227A
Other languages
Chinese (zh)
Other versions
CN101041521A (en
Inventor
王国华
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.)
Individual
Original Assignee
Individual
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 Individual filed Critical Individual
Priority to CNB2007100516227A priority Critical patent/CN100519446C/en
Publication of CN101041521A publication Critical patent/CN101041521A/en
Application granted granted Critical
Publication of CN100519446C publication Critical patent/CN100519446C/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Abstract

The invention discloses a disposing method of making H acid waste water reach zero discharge, which comprises the following steps: adding common salt into waste water; distilling out of alcaine; extracting out of H acid and T acid from the remain solid; heating the solid; getting ammonii chloridum; pyrogenic oxidizing remain solid; getting anhydrous sodium sulfate.

Description

Add sodium-chlor method H Acid from Wastewater
Technical field
The present invention relates to a kind of H acid waste water that can make and reach the treatment process of zero release.
Background technology
H acid is important dyestuff intermediate, is mainly used in to produce substantive dyestuff, matching stain, reactive dyestuffs.The H acid producing waste water has very big toxicity to environment, is difficult to biological treatment, endangers quite big.
In the H acid production process,, often regulate lower pH value, make the acidity that the H acid producing waste water is has root strong building to be had severe corrosive, need a large amount of water to be diluted during discharging, extremely waste resource in order to improve the yield of H acid.
Summary of the invention
Major ingredient in the H acid waste water is: sulfuric acid, ammonium sulfate, sodium sulfate, H acid, T acid and organic impurity.
Composition according in the H acid waste water adds sodium-chlor to a certain degree, introduces an amount of chlorion, changes the Chemical Composition in the waste water.Distillation then because hydrogen ion and chlorion institute bonded hydrochloric acid volatility are higher, take the lead in distilling from waste water and, and obtains pure transparent hydrochloric acid soln.After extracting H acid and T acid, the solid that heating is remaining, ammonium ion and chlorion are combined into ammonium chloride and evaporate, and remaining solid obtains anhydrous sodium sulphate through behind the high temperature oxidation.
The mole number sum of hydrogen ion and ammonium ion equates in the mole number that adds sodium-chlor and the waste water.
The extraction liquid of H acid and T acid can be methyl alcohol, also can be alkaline organic solution, evaporate organic extract liquid after, just can get the crude product of the sour and T acid of H.
Because the restriction of fund also can save extraction step, after heat solid obtained ammonium chloride, directly high temperature oxidation obtained anhydrous sodium sulphate.
The ammonium chloride that reclaims can be used for fertilizer.
Pyritous sodium sulfate can be used for making water glass.
The temperature range of heating ammonium chloride is: 110 degrees centigrade to 500 degrees centigrade.
The temperature range of high temperature oxidation anhydrous sodium sulphate is: 500 degrees centigrade to 1000 degrees centigrade.
The entire treatment method, each step can reclaim industrial goods, realized pollution-free, zero release.
Advantageous effect
1, realized the zero release of H acid wastewater treatment, thoroughly realized pollution-free.
2, from waste water, reclaimed hydrochloric acid.
3, from waste water, reclaimed ammonium chloride.
4, H acid and T acid from waste water, have been reclaimed.
Description of drawings
Fig. 1 is the whole flow process of H acid wastewater treatment.
Realize concrete mode of the present invention
Embodiment 1: get Chu Yuan chemical plant, Shishou City, Hubei Province H acid waste water 100mL, add sodium-chlor 11 grams, make its dissolving, distillation, obtain hydrochloric acid 96mL, use the remaining solid of methyl alcohol ultrasonic extraction, obtain H acid and T acid 1 gram, solid obtained ammonium chloride 1.5 grams after 400 degree added extraction heat, obtained anhydrous sodium sulphate 7 grams behind the 950 degree high temperature oxidations.
Embodiment 2: be to get Chu Yuan chemical plant, Shishou City, Hubei Province H acid waste water 100mL equally, add sodium-chlor 11 grams, make its dissolving, distillation obtains hydrochloric acid, different is with the solid soxhlet extraction, obtains H acid 1.7 grams, illustrates that the Soxhlet cycling extraction can improve the yield of H acid and T acid.
Embodiment 3: be to get Chu Yuan chemical plant, Shishou City, Hubei Province H acid waste water 100mL equally, add sodium-chlor 11 grams, make its dissolving, distillation obtains hydrochloric acid, directly obtain ammonium chloride 1.7 grams without extraction then, obtain anhydrous sodium sulphate 7 grams behind the high temperature oxidation in 400 degree heating.Illustrate and save the yield that extraction does not influence ammonium chloride and anhydrous sodium sulphate.

Claims (1)

1, the present invention relates to a kind of H acid waste water that can make and reach the treatment process of zero release, it is characterized in that comprising the steps:
1) add sodium-chlor in waste water, change the waste water component, the mole number sum of hydrogen ion and ammonium ion equates in the mole number that adds sodium-chlor and the waste water;
2) waste water that will add behind the sodium-chlor distills, and steams hydrochloric acid wherein;
3) go out H acid and T acid in the remaining solid with methanol extraction;
4) solid after the reheat extraction obtains ammonium chloride;
5) the remaining solid of oxidation obtains anhydrous sodium sulphate under 500 ℃ to 1000 ℃ temperature.
CNB2007100516227A 2007-03-07 2007-03-07 H acid waste water by natrium chloratum addition process Expired - Fee Related CN100519446C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CNB2007100516227A CN100519446C (en) 2007-03-07 2007-03-07 H acid waste water by natrium chloratum addition process

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CNB2007100516227A CN100519446C (en) 2007-03-07 2007-03-07 H acid waste water by natrium chloratum addition process

Publications (2)

Publication Number Publication Date
CN101041521A CN101041521A (en) 2007-09-26
CN100519446C true CN100519446C (en) 2009-07-29

Family

ID=38807347

Family Applications (1)

Application Number Title Priority Date Filing Date
CNB2007100516227A Expired - Fee Related CN100519446C (en) 2007-03-07 2007-03-07 H acid waste water by natrium chloratum addition process

Country Status (1)

Country Link
CN (1) CN100519446C (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101066824B (en) * 2007-06-14 2010-10-27 南开大学 Process of treating and reusing effluent from 1-amino-8-naphthol-3, 6-disulfonic acid production
CN102775808B (en) * 2012-08-23 2013-08-21 楚源高新科技集团股份有限公司 Process for recycling ammonium sulfate and synthesizing acidic dye by T-acid mother liquor wastewater
CN113087249B (en) * 2019-12-23 2022-04-22 南京延长反应技术研究院有限公司 System and method for treating wastewater in H acid production

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
络合萃取法处理高浓度H酸废水. 金晓红,王云祥,孙向东.江苏环境科技,第14卷第2期. 2001
络合萃取法处理高浓度H酸废水. 金晓红,王云祥,孙向东.江苏环境科技,第14卷第2期. 2001 *

Also Published As

Publication number Publication date
CN101041521A (en) 2007-09-26

Similar Documents

Publication Publication Date Title
CN101381298B (en) Method for preparing conjugate linolic acid using idesia polycarpa maxim. var. vestita diels oil
CN102603000B (en) Process for preparing high-purity vanadium pentoxide by adopting ammonium metavanadate as raw material
CN102229548B (en) Method for producing thioglycollic acid
CN104086362A (en) Method for recycling organic solvents of wastewater generated in synthesis of hydrazine hydrate by ketazine method
US11773073B2 (en) Method for synthesizing myricetin
CN108439438A (en) The method that nickel cobalt mn sulphate and lithium carbonate are prepared by waste and old ternary battery material
CN100519446C (en) H acid waste water by natrium chloratum addition process
CN108910849B (en) Method for circularly extracting phosphorus from sludge ash
CN105085411A (en) Preparation method of 6-hydroxy-2,3,5-triamidopyrimidine sulfate
CN104817480B (en) Reuse of Bunte salt in sodium hydrosulfite waste residue
CN103664527B (en) A kind of method of clean preparation 2,4-bis-chloro-α-chloromethylbenzene methyl alcohol
CN110627754B (en) Method for preparing 2-oxo-2-furyl acetic acid by using continuous flow microchannel reactor
CN102603514B (en) Process for preparing sodium gluconate from crop straws
CN101920994A (en) Method for preparing vanadyl sulfate
CN101429129A (en) Method for extracting admantadine
CN100376551C (en) Semicarbazone synthesis method
CN103435016A (en) Method for extracting selenium from acid mud
CN102659572B (en) Preparation method of dehydroabietic acid
CN101898974B (en) Method for producing ethylene glycol-bis (2-aminoethyl ether) tetraacetic acid (EGTA)
CN102268303B (en) Method for preparing biological diesel oil by using sludge from municipal wastewater treatment plant
CN109437145B (en) Method for extracting plant conduits from biomass materials in large batch
CN107298641A (en) The preparation method of gossypol and the preparation method of gossypol acetate
CN105295061A (en) Temperature-sensitive polymer containing heavy metal chelate group and preparation method and application of temperature-sensitive polymer
CN103360213B (en) Chloropropanediol purifying apparatus and production method thereof
CN101851157B (en) Method for preparing and purifying hydroxyacetic acid by using hydroxyacetonitrile as raw material

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant
C17 Cessation of patent right
CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20090729

Termination date: 20110307