CN110981066A - Ammonium molybdate-containing wastewater recovery treatment process method - Google Patents

Ammonium molybdate-containing wastewater recovery treatment process method Download PDF

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Publication number
CN110981066A
CN110981066A CN201911334064.4A CN201911334064A CN110981066A CN 110981066 A CN110981066 A CN 110981066A CN 201911334064 A CN201911334064 A CN 201911334064A CN 110981066 A CN110981066 A CN 110981066A
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wastewater
ammonium molybdate
enters
condensed water
evaporator
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赖祖明
赖兴
赖永发
韩博平
葛玉翠
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Shenzhen Yuanyu Environmental Protection Technology Co ltd
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Shenzhen Yuanyu Environmental Protection Technology Co ltd
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    • 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
    • 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
    • C02F1/02Treatment of water, waste water, or sewage by heating
    • C02F1/04Treatment of water, waste water, or sewage by heating by distillation or evaporation
    • C02F1/08Thin film evaporation
    • 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
    • C02F1/20Treatment of water, waste water, or sewage by degassing, i.e. liberation of dissolved gases
    • 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
    • C02F2001/007Processes including a sedimentation step

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  • Life Sciences & Earth Sciences (AREA)
  • Hydrology & Water Resources (AREA)
  • Engineering & Computer Science (AREA)
  • Environmental & Geological Engineering (AREA)
  • Water Supply & Treatment (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Removal Of Specific Substances (AREA)
  • Heat Treatment Of Water, Waste Water Or Sewage (AREA)

Abstract

The invention discloses a process method for recycling waste water containing ammonium molybdate, which comprises the following steps: a. ammonium molybdate wastewater pretreatment: b. ammonium molybdate wastewater deamination procedure: c. and (3) an ammonium molybdate wastewater evaporation process: and (4) the wastewater after full reaction enters a solid-liquid separator II, and the precipitate generated by the reaction is removed by using a gravity settling method. The clarified ammonium molybdate wastewater after gravity settling separation enters a reaction barrel, is lifted by a first-effect forced evaporator and enters a vacuum crystallizer, is crystallized in the vacuum crystallizer, and is then lifted to a thickener, a centrifuge, a dryer and a packaging machine in sequence to prepare finished nitrate; raw steam firstly enters a heating chamber of the first-effect forced circulation evaporator to be heated, then condensed water returns to a boiler room after heat exchange, secondary steam generated by the first-effect forced circulation evaporator is sent to the heating chamber of the second-effect forced circulation evaporator to be used as a heat source to heat the heating chamber, then the condensed water enters a raw condensed water tank, condensed water after condensation is decomposed enters a condensed water tank, and water in the condensed water tank is conveyed back to the ammonium molybdate production process for recycling or other purposes after heat exchange.

Description

Ammonium molybdate-containing wastewater recovery treatment process method
Technical Field
The invention relates to the technical field of industrial sewage treatment, in particular to a process method for recovering and treating waste water containing ammonium molybdate.
Background
Along with the increasing attention of the country to the environmental protection business, the relevant standards of environmental protection are more and more strict, the wastewater generated in the ammonium molybdate production industry is discharged after being simply treated, and the treated ammonium molybdate wastewater can not meet the discharge standards of the country and the industry, the wastewater contains heavy metal impurities, alkaline earth metal impurities and a large amount of ammonium nitrate besides molybdenum, and is difficult to treat for a long time, valuable metals are lost after being discharged, and the heavy metals and ammonia nitrogen compounds pollute the environment, so that the comprehensive treatment of the industrial wastewater in the ammonium molybdate production is necessary, the excessive ammonia nitrogen ions in the ammonium molybdate wastewater is a practical problem facing a plurality of domestic ammonium molybdate production enterprises, and a perfect treatment method and a facility are not available in China for a long time, and a certain recyclable product also exists in the ammonium molybdate wastewater, how to treat the wastewater to reach the standard and discharge and not bring secondary pollutants is a main problem to be solved for wastewater treatment Therefore, a process which can meet the standard discharge after sewage treatment, cannot generate new pollution and can realize resource recycling needs to be designed through the analysis of the source of sewage generation.
Disclosure of Invention
In order to solve the problems in the existing ammonium molybdate production wastewater treatment, the invention provides a process for recovering and treating ammonium molybdate-containing wastewater, which does not produce secondary pollution wastewater in the whole treatment process, and extracts the products of ammonia water, sodium nitrate salt and pure evaporation condensate water from the wastewater by the process, thereby realizing zero discharge of sewage and recycling wastewater.
The technical scheme adopted by the invention for solving the technical problem is that the process method for recycling the wastewater containing ammonium molybdate comprises the following steps:
a. ammonium molybdate wastewater pretreatment: lifting the wastewater from a wastewater pool to a reaction barrel I, adding a reagent I into the reaction barrel I, removing impurity anions except main anions in the wastewater, feeding the fully reacted wastewater into a solid-liquid separator I, removing precipitates generated by the reaction by using a gravity settling method, feeding clarified wastewater subjected to gravity settling separation into a reaction barrel II, adding a reagent II into the reaction barrel II, removing impurity cations except main cations in the wastewater, feeding the fully reacted wastewater into a solid-liquid separator II, removing precipitates generated by the reaction by using a gravity settling method, feeding the clarified wastewater subjected to gravity settling separation into a reaction barrel III, adding a reagent III into the reaction barrel III, further removing impurity cations except main cations dissolved in a trace amount in the wastewater, feeding the fully reacted wastewater into a solid-liquid separator III, removing the precipitates generated by the reaction by using a gravity settling method, the clarified wastewater after gravity settling separation is lifted by a pump to enter a precision filter, and trace solid impurities contained in the wastewater are further removed; the medicament I is barium nitrate, the medicament II is sodium carbonate or sodium hydroxide, and the medicament III is sodium sulfide;
b. ammonium molybdate wastewater deamination procedure: after the pretreatment procedure, the wastewater enters a deamination wastewater pool, liquid alkali is added into the deamination wastewater pool to adjust the pH of the wastewater to 11-12, the wastewater is lifted to exchange heat with the effluent of a tower kettle, then enters a deamination tower, passes through the deamination tower and then the effluent of the tower kettle is sent to an evaporation procedure, and ammonia-containing steam at the tower top is condensed and absorbed by a condenser and an ammonia water preparation pry block to prepare ammonia water;
c. and (3) an ammonium molybdate wastewater evaporation process: after the deamination process, the wastewater enters an evaporation water tank, the pH value of the wastewater is adjusted to be below 7, then the wastewater is lifted to exchange heat with secondary effect condensed water, then the wastewater exchanges heat with primary effect condensed water and enters an MVR falling film evaporator, the wastewater from the MVR falling film evaporator is lifted to enter a secondary effect forced evaporator, the wastewater from the secondary effect forced evaporator is lifted to enter a primary effect forced evaporator, the wastewater from the primary effect forced evaporator is lifted to enter a vacuum crystallizer, the wastewater is crystallized in the vacuum crystallizer, and then the wastewater is lifted to a thickener, a centrifugal machine, a drying machine and a packaging machine in sequence to prepare finished nitrate; raw steam firstly enters a heating chamber of a first-effect forced circulation evaporator to be heated, then condensed water returns to a boiler room after heat exchange, secondary steam generated by a first-effect forced circulation evaporation chamber is sent to a heating chamber of a second-effect forced circulation evaporator to be used as a heat source to heat the heating chamber, then the condensed water enters a raw condensed water tank, the secondary steam generated by the evaporation chamber of the second-effect forced circulation evaporator is condensed and vacuumized, the condensed water enters a condensed water tank, the secondary steam generated by an evaporation chamber of an MVR falling-film evaporator enters an MVR compressor to be used as the heat source of the MVR heating chamber after being compressed and heated, the condensed water enters the condensed water tank, and water in the condensed water tank is conveyed back to an ammonium molybdate production process for recycling or other purposes after heat exchange.
Further, the precision filter in the step a is a precision filter with a filtration precision of 0.5 micron or less.
Further, the cation content of the effluent after the ammonium molybdate wastewater deamination procedure treatment in the step a is as follows: mo is less than or equal to 0.5 mg/L; cu is less than or equal to 0.5 mg/L; fe is less than or equal to 0.1 mg/L; ca is less than or equal to 0.1 mg/L.
And further, the content of ammonia nitrogen in the tower kettle effluent of the deamination tower in the ammonium molybdate wastewater deamination procedure in the step b is less than or equal to 10 mg/L.
The invention has the beneficial effects that: the ammonium molybdate wastewater is effectively recycled by an optimized process, impurities, anions and cations in the wastewater can be effectively removed by the graded precipitation treatment adopted in the pretreatment process, and the content of the impurities, anions and cations in the treated wastewater can reach the discharge standard of inorganic chemical industry pollutants. The ammonia nitrogen content can be reduced to be below 10mg/L by the ammonia removal process adopted in the ammonia removal process, 5-25% concentration ammonia water can be prepared, the MVR falling film evaporation and counter-current double-effect forced circulation evaporation process is adopted in the evaporation process, fresh steam consumption is greatly saved, finished nitrate and purer condensed water are prepared, the problem of sewage discharge is solved by treating ammonium molybdate wastewater through the processes, water resources are saved, energy recycling is realized, and zero sewage discharge is realized.
Drawings
FIG. 1 is a process flow diagram of the present invention.
Detailed Description
A process method for recycling and treating waste water containing ammonium molybdate comprises the following steps:
a. ammonium molybdate wastewater pretreatment: the wastewater is lifted to a reaction barrel I from a wastewater pool by a pump, and a medicament I (barium nitrate) is added into the reaction barrel I to remove impurity anions except main anions in the ammonium molybdate wastewater by utilizing the chemical precipitation reaction principle. And (3) the wastewater after full reaction enters a solid-liquid separator I, and the precipitate generated by the reaction is removed by using a gravity settling method. And (3) feeding the clarified ammonium molybdate wastewater subjected to gravity settling separation into a reaction barrel II, and adding a medicament II (sodium carbonate or sodium hydroxide) into the reaction barrel II to remove impurity cations except main cations in the ammonium molybdate wastewater by using the chemical precipitation reaction principle. And (4) the wastewater after full reaction enters a solid-liquid separator II, and the precipitate generated by the reaction is removed by using a gravity settling method. And (3) feeding the clarified ammonium molybdate wastewater subjected to gravity settling separation into a reaction barrel III, and adding a medicament III (sodium sulfide) into the reaction barrel III to further remove trace dissolved impurity cations except main cations in the ammonium molybdate wastewater by utilizing the chemical precipitation reaction principle. And (3) the wastewater after full reaction enters a solid-liquid separator III, and the precipitate generated by the reaction is removed by using a gravity settling method. The clarified ammonium molybdate wastewater after gravity settling separation is lifted by a pump to enter a precision filter (the filtration precision is below 0.5 micron), and trace solid impurities contained in the ammonium molybdate wastewater are further removed. Through detection, the cation content of the effluent is as follows: mo is less than or equal to 0.5 mg/L; cu is less than or equal to 0.5 mg/L; fe is less than or equal to 0.1 mg/L; ca is less than or equal to 0.1 mg/L.
In the pretreatment step, the main cations: NH4 in ammonium salt+And free ammonia and sodium ions, the major anions: nitrate ion NO3 -(ii) a Adding barium nitrate to generate barium sulfate precipitate and barium molybdate precipitate, adding sodium carbonate to generate calcium carbonate, magnesium hydroxide, iron carbonate, copper carbonate and other precipitates, adding sodium sulfide to sulfurize to further remove trace amount of dissolved Cu in waste water+And (3) cationic ions, the adding amount of the medicament: added according to 1.2 times of the molar mass of the ions to be removed in the wastewater.
b. Ammonium molybdate wastewater deamination procedure: after the pretreatment procedure, the wastewater enters a deamination wastewater pool, liquid alkali is added into the deamination wastewater pool for pH adjustment, after the pH of the ammonium molybdate wastewater is adjusted to about 12, the ammonium molybdate wastewater is lifted by a pump, exchanges heat with tower kettle outlet water, enters a deamination tower, passes through the deamination tower, and then the content of ammonia nitrogen in tower kettle outlet water is less than or equal to 10 mg/L; the tower top ammonia-containing steam is condensed and absorbed by a condenser and an ammonia water preparation skid block to prepare ammonia water, ammonia water with different concentrations can be prepared by controlling the temperature and the water adding amount, and the mass concentration range of the ammonia water is 5-25%. And adjusting to prepare the corresponding ammonia water concentration according to the ammonia water concentration required by the front-end process of ammonium molybdate production.
c. And (3) an ammonium molybdate wastewater evaporation process: after the deamination process, the wastewater enters an evaporation water tank, the pH of the wastewater is adjusted to below 7, then the wastewater is lifted by a pump to exchange heat with two-effect condensed water, then the wastewater exchanges heat with one-effect condensed water and enters an MVR falling film evaporator, the wastewater evaporated and concentrated by the MVR falling film evaporator is lifted by the pump to enter a two-effect forced circulation evaporator, the wastewater evaporated and concentrated by the two-effect forced circulation evaporator is lifted by the pump to enter a one-effect forced circulation evaporator, the wastewater evaporated and concentrated by the one-effect forced circulation evaporator is lifted by the pump to enter a vacuum crystallizer, the wastewater is crystallized in the vacuum crystallizer, and then the wastewater is lifted by the pump to a thickener, a centrifuge, a dryer and a packaging machine in sequence to prepare finished nitrate; raw steam (fresh steam) firstly enters a first-effect forced circulation heating chamber to be heated, then condensed water returns to a boiler room after heat exchange, secondary steam generated by a first-effect forced circulation evaporation chamber is sent to a heating chamber of a second-effect forced circulation evaporator to be used as a heat source to heat the heating chamber, then the condensed water enters a raw condensed water tank, the secondary steam generated by the evaporation chamber of the second-effect forced circulation evaporator is condensed and vacuumized, the condensed water enters a condensed water tank, the secondary steam generated by an evaporation chamber of an MVR falling-film evaporator enters an MVR compressor to be used as the heat source of the MVR heating chamber after being compressed and heated, the condensed water enters the condensed water tank, and water in the condensed water tank is conveyed back to an ammonium molybdate production process for recycling or other purposes after heat exchange.
The first-effect forced evaporator and the second-effect forced evaporator described in the above description or the accompanying drawings are all forced circulation evaporators, each forced circulation evaporator includes a heating chamber and a separation chamber (also called as an evaporation chamber), after entering the separation chamber, the material enters a forced circulation pump through the separation chamber, after being lifted by the forced circulation pump, the material enters the heating chamber, after being heated in the heating chamber, the material is changed into a boiling gas-liquid two-phase state, the material in the gas-liquid two-phase state after being heated in the heating chamber enters the separation chamber for gas-liquid separation, then the liquid phase enters the forced circulation pump again to repeat the above steps in sequence, and after the concentration reaches a certain degree, the material is lifted by a material transfer pump and discharged to a.
Although the present invention has been described in detail with reference to specific embodiments, it will be understood by those skilled in the art that various changes may be made and equivalents may be substituted without departing from the spirit and scope of the invention as defined in the appended claims.

Claims (5)

1. A process method for recycling and treating waste water containing ammonium molybdate is characterized by comprising the following steps: the method comprises the following steps:
a. ammonium molybdate wastewater pretreatment: lifting the wastewater from a wastewater pool to a reaction barrel I, adding a reagent I into the reaction barrel I, removing impurity anions except main anions in the wastewater, feeding the fully reacted wastewater into a solid-liquid separator I, removing precipitates generated by the reaction by using a gravity settling method, feeding clarified wastewater subjected to gravity settling separation into a reaction barrel II, adding a reagent II into the reaction barrel II, removing impurity cations except main cations in the wastewater, feeding the fully reacted wastewater into a solid-liquid separator II, removing precipitates generated by the reaction by using a gravity settling method, feeding the clarified wastewater subjected to gravity settling separation into a reaction barrel III, adding a reagent III into the reaction barrel III, further removing impurity cations except main cations dissolved in a trace amount in the wastewater, feeding the fully reacted wastewater into a solid-liquid separator III, removing the precipitates generated by the reaction by using a gravity settling method, the clarified wastewater after gravity settling separation is lifted by a pump to enter a precision filter, and trace solid impurities contained in the wastewater are further removed; the medicament I is barium nitrate, the medicament II is sodium carbonate or sodium hydroxide, and the medicament III is sodium sulfide;
b. ammonium molybdate wastewater deamination procedure: after the pretreatment procedure, the wastewater enters a deamination wastewater pool, liquid alkali is added into the deamination wastewater pool to adjust the pH of the wastewater to 11-12, the wastewater is lifted to exchange heat with the effluent of a tower kettle, then enters a deamination tower, passes through the deamination tower and then the effluent of the tower kettle is sent to an evaporation procedure, and ammonia-containing steam at the tower top is condensed and absorbed by a condenser and an ammonia water preparation pry block to prepare ammonia water;
c. and (3) an ammonium molybdate wastewater evaporation process: after the deamination process, the wastewater enters an evaporation water tank, the pH of the wastewater is firstly adjusted to be below 7, then the wastewater is lifted to exchange heat with secondary effect condensed water, then the wastewater exchanges heat with primary effect condensed water and enters an MVR falling film evaporator, the wastewater of the MVR falling film evaporator is lifted to enter a secondary effect forced evaporator, the wastewater of the secondary effect forced evaporator is lifted to enter a primary effect forced evaporator, the wastewater of the primary effect forced evaporator is lifted to enter a vacuum crystallizer, the wastewater is crystallized in the vacuum crystallizer, and then the wastewater is lifted to a thickener, a centrifugal machine, a drying machine and a packaging machine in sequence to prepare finished nitrate; raw steam firstly enters a heating chamber of a first-effect forced evaporator to be heated, then condensed water returns to a boiler room after heat exchange, secondary steam generated by a separation chamber of the first-effect forced evaporator is sent to a heating chamber of a second-effect forced circulation evaporator to be used as a heat source to heat the first-effect forced circulation evaporator, then the condensed water enters a raw condensed water tank, the secondary steam generated by the separation chamber of the second-effect forced evaporator is condensed and vacuumized, the condensed water enters a condensed water tank, the secondary steam generated by a separation chamber of an MVR falling-film evaporator enters an MVR compressor to be used as the heat source of the MVR heating chamber after being compressed and heated, the condensed water enters the condensed water tank, and water in the condensed water tank is conveyed back to an ammonium molybdate production process for recycling or other purposes.
2. The process method for recycling and treating the wastewater containing ammonium molybdate according to claim 1, which is characterized in that: the precision filter in the step a is a precision filter with the filtering precision of less than 0.5 micron.
3. The process method for recycling and treating the wastewater containing ammonium molybdate according to claim 1, which is characterized in that: the cation content of the effluent after the ammonium molybdate wastewater deamination procedure treatment in the step a is as follows: mo is less than or equal to 0.5 mg/L; cu is less than or equal to 0.5 mg/L; fe is less than or equal to 0.1 mg/L; ca is less than or equal to 0.1 mg/L.
4. The process method for recycling and treating the wastewater containing ammonium molybdate according to claim 1, which is characterized in that: and c, in the step b, the ammonia nitrogen content of the water discharged from the tower bottom of the deamination tower in the deamination procedure of the ammonium molybdate wastewater is less than or equal to 10 mg/L.
5. The resource recycling treatment process method for ammonium molybdate wastewater as claimed in claim 1, which is characterized in that: and c, the concentration of the prepared ammonia water in the ammonium molybdate wastewater deamination procedure in the step b can be adjusted within the range of 5-25%.
CN201911334064.4A 2019-12-23 2019-12-23 Ammonium molybdate-containing wastewater recovery treatment process method Pending CN110981066A (en)

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN115124177A (en) * 2022-06-23 2022-09-30 清远佳致新材料研究院有限公司 Device and method for improving anhydrous sodium sulphate quality and realizing zero emission
CN117902760A (en) * 2023-12-27 2024-04-19 辽宁北方环境保护有限公司 A wastewater treatment process in the production of ammonium molybdate in the molybdenum smelting industry

Citations (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2009017389A2 (en) * 2007-08-01 2009-02-05 Malaysian Palm Oil Board Method for extracting crude palm oil
CN102020389A (en) * 2010-11-19 2011-04-20 杭州蓝然环境技术有限公司 Process for recycling ammonium chloride waste water
CN102407029A (en) * 2011-10-17 2012-04-11 宜兴市格兰特干燥浓缩设备有限公司 Evaporated crystallization device
CN102838180A (en) * 2012-08-16 2012-12-26 广州新普利节能环保科技有限公司 Rare metal wastewater zero discharge process
CN105152435A (en) * 2015-07-06 2015-12-16 江苏德邦工程有限公司 Zero discharge industrial wastewater treatment method
CN205258214U (en) * 2014-12-05 2016-05-25 浙江龙盛集团股份有限公司 Phenyl amines midbody waste water's processing apparatus
CN106007133A (en) * 2016-05-27 2016-10-12 苏州乔发环保科技股份有限公司 Desulfurization wastewater concentration, evaporation, crystallization and salt separation process
CN106517626A (en) * 2016-11-30 2017-03-22 江苏迈安德节能蒸发设备有限公司 Sodium sulfate wastewater treatment process
CN206121196U (en) * 2016-09-09 2017-04-26 深圳市源禹环保科技有限公司 Pneumatic forced circulation triple -effect evaporator
CN207632536U (en) * 2017-09-07 2018-07-20 北京赛科康仑环保科技有限公司 A kind of recycling treatment system of high ammonia nitrogen and high salt waste water
CN110127761A (en) * 2019-06-24 2019-08-16 安庆市月铜钼业有限公司 A kind of ammonium molybdate method for crystallising

Patent Citations (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2009017389A2 (en) * 2007-08-01 2009-02-05 Malaysian Palm Oil Board Method for extracting crude palm oil
CN102020389A (en) * 2010-11-19 2011-04-20 杭州蓝然环境技术有限公司 Process for recycling ammonium chloride waste water
CN102407029A (en) * 2011-10-17 2012-04-11 宜兴市格兰特干燥浓缩设备有限公司 Evaporated crystallization device
CN102838180A (en) * 2012-08-16 2012-12-26 广州新普利节能环保科技有限公司 Rare metal wastewater zero discharge process
CN205258214U (en) * 2014-12-05 2016-05-25 浙江龙盛集团股份有限公司 Phenyl amines midbody waste water's processing apparatus
CN105152435A (en) * 2015-07-06 2015-12-16 江苏德邦工程有限公司 Zero discharge industrial wastewater treatment method
CN106007133A (en) * 2016-05-27 2016-10-12 苏州乔发环保科技股份有限公司 Desulfurization wastewater concentration, evaporation, crystallization and salt separation process
CN206121196U (en) * 2016-09-09 2017-04-26 深圳市源禹环保科技有限公司 Pneumatic forced circulation triple -effect evaporator
CN106517626A (en) * 2016-11-30 2017-03-22 江苏迈安德节能蒸发设备有限公司 Sodium sulfate wastewater treatment process
CN207632536U (en) * 2017-09-07 2018-07-20 北京赛科康仑环保科技有限公司 A kind of recycling treatment system of high ammonia nitrogen and high salt waste water
CN110127761A (en) * 2019-06-24 2019-08-16 安庆市月铜钼业有限公司 A kind of ammonium molybdate method for crystallising

Non-Patent Citations (6)

* Cited by examiner, † Cited by third party
Title
吕炳南等: "《污水好氧处理新工艺》", 31 October 2007, 哈尔滨工业大学出版社 *
孔庆颐等: "工业废水处理的几种装置", 《环境技术》 *
李云飞等: "《食品工程原理》", 31 August 2018, 中国农业大学出版社 *
李崇: "一种钼酸铵废水的环保低成本处理方式研究", 《环境保护与循环经济》 *
王凯波等: "机械蒸汽压缩技术在脱硫废水处理中的应用", 《山西电力》 *
郭焕雄: "混联法种分母液蒸发", 《轻金属》 *

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN115124177A (en) * 2022-06-23 2022-09-30 清远佳致新材料研究院有限公司 Device and method for improving anhydrous sodium sulphate quality and realizing zero emission
CN117902760A (en) * 2023-12-27 2024-04-19 辽宁北方环境保护有限公司 A wastewater treatment process in the production of ammonium molybdate in the molybdenum smelting industry

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