CN103265079A - Method for recovering molybdenum from molybdenum containing waste acid of filament wire - Google Patents
Method for recovering molybdenum from molybdenum containing waste acid of filament wire Download PDFInfo
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- CN103265079A CN103265079A CN2013102235473A CN201310223547A CN103265079A CN 103265079 A CN103265079 A CN 103265079A CN 2013102235473 A CN2013102235473 A CN 2013102235473A CN 201310223547 A CN201310223547 A CN 201310223547A CN 103265079 A CN103265079 A CN 103265079A
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Abstract
The invention relates to a method for recovering molybdenum from a molybdenum containing waste acid of a filament wire. The method comprises the following steps: 1) neutralization: slowly adding liquid ammonia into the waste acid, and adding the liquid ammonia till pH is equal to 4.8-5.5; 2) filtering: filter pressing by a filter press to generate filter cakes and a filtrate; 3) ammonia leaching: dissolving the filter cakes by ammonia water and adjusting the pH value to completely dissolve the precipitate; 4) filtering: removing small amount of insoluble impurities by filter cloth; 5) acid precipitation: adjusting a whence aging liquid by a dilute acid and precipitating ammonium tetramolybdate crystals, and performing centrifugal treatment; 6) drying: obtaining an ammonium tetramolybdate product; 7) crystallization: adding ammonia water to a mother liquor obtained in the step 5), adjusting the pH of the liquor, maintaining temperature of a crystallizing kettle and separating out ammonium heptamolybdate crystals; 8) centrifugalization: obtaining wet ammonium heptamolybdate and a centrifugal liquid; and 9) drying: obtaining an ammonium heptamolybdate product. According to the invention, all chemical components of the molybdenum containing waste acid are recycled by a general process line, and the production process is pollution-free and environmentally-friendly.
Description
Technical field
The present invention relates to the renewable field of resource, relate in particular to and a kind ofly contain the molybdenum spent acid method that reclaims molybdenum from the filament silk.
Background technology
Electricity-saving lamp is described as the new light sources of green illumination, becomes one of developing direction of 21st century energy-conserving light source.Mo in the energy-saving filament production industry mainly as tungsten (W) silk around axle, use HNO then
3And H
2SO
4Mixing acid melts away the Mo mandrel, metal M o dissolved in the strong acid solution, and the typing of W silk, Mo has become oxidation state by going back ortho states, and the Mo of oxidation state runs off in changing the silk spent acid.On the one hand, molybdenum (Mo) is a kind of rare refractory metal of preciousness, and is of many uses, expensive, but the molybdenum ore light source is limited in the world; In the process of producing filament, produce the acidic waste that contains molybdenum on the other hand, be easy to generate problem of environmental pollution.For many years, the difficult problem that is treated as puzzlement filament manufacturing enterprise of spent acid.The operational path that has worked out at present is by add NH in acid waste water
3The Mo of oxidation state is changed into ammonium molybdate and recycled, but this operational path is only reclaimed the molybdenum in the spent acid, organic efficiency is low, and does not realize the recovery of sulfuric acid and nitric acid in the spent acid.
" environmental science and technology " the 23rd the 4th phase of volume discloses the recycling of changing molybdenum in the waste water, and the Mo that changes oxidation state in the silk waste liquid is reclaimed, and the key step that generates ammonium molybdate is: after strongly-acid silk waste liquid is carried out the decon processing, feed NH in reaction container
3, carry out neutralization reaction, generate the ammonium molybdate colloid, after filtration and after taking off filter, the reactants dissolved that generates is purified, carry out crystallization again, make ammonium molybdate after the drying.Technology is by effectively controlling pH value and temperature, and the final product that generates is (NH
4)
2Mo
4O
132H
2O, the product yield is 94%.That obtain in the above-mentioned method is (NH
4)
2Mo
4O
132H
2O has the existence of a small amount of three ammonium molybdates, Ammonium Heptamolybdate and ten ammonium molybdates unavoidably in the ammonium tetramolybdate, can't accomplish effective separation of multiple ammonium molybdate; In the mother liquor of crystallization, still also comprise molybdenum in addition, so also limited the rate of recovery of molybdenum.
" environmental science guide 2007,26 " disclose and contained molybdenum silk recovering waste acid and improvement in the filament production, its processing step is: 1, add alkali neutralization: with ammoniacal liquor slowly in the injection spent acid solution, continuous injection along with ammoniacal liquor in the spent acid solution, the acidity of spent acid solution constantly reduces, temperature constantly rises, and waste liquid begin to become thickness and have precipitation to produce is mainly the mixture of molybdic acid and many ammonium molybdates.Along with the further rising of pH value, precipitation is dissolving gradually, and it is clear that solution begins to become, and the solution of this moment is mainly the mixed solution of ammonium sulfate, ammonium nitrate and ammonium molybdate.The pH value of solution value is adjusted to 7 ~ 8, carries out fine filtering, remove impurity wherein.2, acid is heavy extracts: after solution filters, when treating that it is clear state, in solution, add strong acid again, at this moment, it is muddy that solution can become, and stops to add acid when the pH value is 2 left and right sides, after static for some time, namely can produce many ammonium molybdate precipitations of white crystals shape, this throw out is based on ammonium tetramolybdate, with the mixture of a small amount of three ammonium molybdates, Ammonium Heptamolybdate, ten ammonium molybdates.Add the ammoniacal liquor neutralization in the above-mentioned method, so not only increased the treatment capacity of waste water, and improved production cost.In addition, obtain ammonium nitrate and ammonium sulfate though also disclose the waste liquid behind the distillation extraction in the method, for the heavy extraction of hypo acid again of the waste liquid after the distillation, to improve the rate of recovery.But what this method obtained is many ammonium molybdate precipitations, can't sell as commercial grades, also can't accomplish effective separation of multiple ammonium molybdate; And because treatment process limits, also can't further improve the rate of recovery of molybdenum.
For this reason, how to realize containing the classification recycling of ammonium molybdate in the molybdenum spent acid, and production technique also is not have to stain, green, to have obtained good social benefit and economic benefit, this still be the problems that needs are further studied.
Summary of the invention
In order to solve above-mentioned technical problem, the purpose of this invention is to provide and a kind ofly contain the molybdenum spent acid method that reclaims molybdenum from the filament silk, this method is converted into ammonium tetramolybdate and Ammonium Heptamolybdate classification with molybdenum and reclaims from contain the molybdenum spent acid, realize containing the secondary resourceization of molybdenum composition in the molybdenum spent acid, improved molybdenum recovery and product purity.
In order to realize above-mentioned purpose, the present invention has adopted following technical scheme:
A kind ofly contain the molybdenum spent acid method that reclaims molybdenum from the filament silk, this method comprises the steps:
1) neutralization: liquefied ammonia is slowly joined in the spent acid, and the control feed rate keeps temperature to be no more than 90 ℃; When reaching pH and be 3, precipitation appears, and continue to add liquefied ammonia and equal 4.8～5.5 to pH and stop;
2) filter: use the pressure filter press filtration, produce filter cake and filtrate;
3) ammonia soaks: with the filter cake ammonia solvent, regulate pH value to 8.0～9.0 and make all dissolvings of precipitation;
4) filter: remove a small amount of undissolved impurity with filter cloth;
5) acid is heavy: regulate to locate ageing liquid with the diluted acid of 5～20 wt%, to pH be 2.0～3.0,40～55 ℃ of temperature are settled out the ammonium tetramolybdate crystal, centrifugal treating;
6) oven dry: get the ammonium tetramolybdate product;
7) crystallization: resulting mother liquor adds the ammoniacal liquor of 10～25 wt% in the step 5), and regulator solution pH to 6.0～7.0 keep the crystallization kettle temperature at 70～80 ℃, separate out the Ammonium Heptamolybdate crystal;
8) centrifugal: as to obtain wet Ammonium Heptamolybdate and centrifugal liquid;
9) oven dry: get the Ammonium Heptamolybdate product.
As further improvement, between step 4) and step 5), increase the ageing operation, the ageing operation was descended static 5～30 hours for maintaining the temperature at 60～70 ℃.
As preferably, the rare nitric acid of the rare employing of the diluted acid of described step 5) or dilute sulphuric acid.
As further improvement, increase step 10), step 10) is with from step 2) and/or the liquid of step 8) enter anionite-exchange resin and carry out ion-exchange, molybdate is exchanged on the anionite-exchange resin; With ammoniacal liquor anionite-exchange resin is carried out desorb then, obtain containing the stripping liquid of ammonium molybdate, stripping liquid is added in the molybdenum spent acid of step 1) as the raw material that reclaims.
As preferably, the anionite-exchange resin described in the described step 10) adopts macroporous anion exchange resin, and the basic group of macroporous anion exchange resin is selected from one or more in primary amine groups, secondary amine and the tertiary amine groups.
As preferred again, the framework types of the macroporous anion exchange resin described in the described step 10) is selected from one or more in polystyrene and the acrylic acid series.
As preferably, the concentration of ammoniacal liquor is 20～25 wt% in the described step 10).
As preferably, anionite-exchange resin soaked 1 hour with the 1wt% salpeter solution in the described step 10) process (1), in the exchange column of then it being packed into, added speed control and made filtrate and anionite-exchange resin 15～25min duration of contact.
As preferably, the anionite-exchange resin effluent liquid receives with a test tube by every 5mL in the described step 10) process (1), utilize the spectrophotometric analysis method to monitor molybdenum content in each test tube, when the content of molybdenum from blank level when beginning to increase, show that this moment, anion-exchange column reached capacity to exchange and the absorption of molybdate, stop the adding of anion-exchange column top and contain the molybdenum pressing filtering liquid, with described ammoniacal liquor anion-exchange column is carried out drip washing then, the content of molybdenum is lower than till 1 wt% in leacheate.
As preferably, described anion-exchange column is regenerated exchange column with 30 wt% strong aquas, 1wt% salpeter solution successively.
The present invention is owing to adopted above-mentioned technical scheme, the molybdenum that will contain in the molybdenum spent acid is converted into ammonium tetramolybdate and Ammonium Heptamolybdate classification recovery, realize containing the secondary resourceization of molybdenum composition in the molybdenum spent acid, obtained the more good Ammonium Heptamolybdate of product quality, improved molybdenum recovery and product purity.Further, the present invention contains the recovery that the molybdenum tail washings carries out molybdenum by ion exchange resin to many places, makes the total yield of molybdenum reach 99% because molybdenum is scarce resource, such production technique not only efficient recovery the molybdenum resource, and produce good economic benefit.Overall craft route of the present invention has realized containing the recycling of the whole chemical ingredientss of molybdenum spent acid, and production technique also is not have to stain, green.
Description of drawings
Fig. 1 is process flow sheet of the present invention.
Embodiment
Below in conjunction with accompanying drawing the specific embodiment of the present invention is made a detailed explanation.
Embodiment 1
As shown in Figure 1 a kind of contains the molybdenum spent acid method that reclaims molybdenum from the filament silk, and this method comprises the steps:
1) neutralization: liquefied ammonia is slowly joined in the spent acid, and along with the continuous adding of liquefied ammonia in the spent acid solution, spent acid solution acidity constantly reduces, and temperature constantly rises, and the control feed rate keeps temperature to be no more than 90 ℃; When reaching pH and be 3, precipitation appears, and continue to add liquefied ammonia and equal 5 to pH and stop;
2) filter: use the pressure filter press filtration, produce filter cake and filtrate;
3) ammonia soaks: with the filter cake ammonia solvent, regulate pH value to 8～9 and make all dissolvings of precipitation;
4) filter: remove a small amount of undissolved impurity with filter cloth;
5) ageing: maintain the temperature at 60～70 ℃ and descended static 24 hours;
6) acid is heavy: regulate to locate ageing liquid with 10% rare nitric acid, to pH be 2～3,40～5 ℃ of temperature are settled out the ammonium tetramolybdate crystal;
7) oven dry: get the ammonium tetramolybdate product, ammonium tetramolybdate accounts for and reclaims about 20% of molybdenum salt;
8) crystallization: resulting mother liquor adds 15% ammoniacal liquor in the step 6), and regulator solution pH to 6.0～7.0 keep the crystallization kettle temperature at 70～80 ℃, separate out the Ammonium Heptamolybdate crystal;
9) centrifugal: as to obtain wet Ammonium Heptamolybdate and centrifugal liquid;
10) oven dry: get the Ammonium Heptamolybdate product, account for and reclaim about 80% of molybdenum salt; To the Ammonium Heptamolybdate product, the impurity chemical constitution that obtains the Ammonium Heptamolybdate product by the inductivity coupled plasma mass spectrometry analytical procedure is:
| Element | Content (mg/kg) |
| Mg | 0.55 |
| Cr | 0.48 |
| Fe | 4.69 |
| Ni | 0.43 |
The Mg of sample, Cr, Fe, the content of Ni is very low, is far superior to like product;
11) ion-exchange/ammonia desorb:
Process (1):: will be from step 2) and the liquid of step 9) enter macroporous anion exchange resin and carry out ion-exchange, molybdenum acid ion is exchanged on the macroporous anion exchange resin, play the effect of the molybdenum acid ion in the recovering liquid;
Process (2): with ammoniacal liquor macroporous anion exchange resin is carried out desorb, obtain containing the stripping liquid of ammonium molybdate, stripping liquid is added in the molybdenum spent acid of step 1) as the raw material that reclaims, and realizes that total molybdenum recovery reaches 99%; Process (1) and process (2) hocket;
12) evaporative crystallization: the liquid that ion-exchange is got off is squeezed into and is carried out evaporative crystallization in the 2nd effect evaporator, must contain ammonium sulfate and the ammonium nitrate mixture of micro-ammonium molybdate, as containing molybdenum chemical fertilizer product.The composition of chemical fertilizer product: ammonium sulfate 50～58%, nitric acid 42～50%, ammonium molybdate 0.02～0.06%.Above-mentioned technical process can realize that the total yield of ammonium sulfate and ammonium nitrate reaches 99%.The highly purified distilled water of condensation water system is used for this enterprises pure water and uses, and also can be used as product and sells.
Embodiment 2
On the basis of embodiment 1, step 2) molybdenum of pressing filtering liquid reclaims, and containing the molybdenum pH value of filtrate is 4.0～5.0.
Select for use Xi'an Lanxiao Sci-Tech Co., Ltd., Tianjin Nankai Hecheng S﹠T Co., Ltd., Zhejiang to win honour for macropore polystyrene weak base anion-exchange resin that resin company or Shanghai Jin Yang resin scientific ﹠ technical corporation produce.Soaked above-mentioned anionite-exchange resin 1 hour with 1% salpeter solution, then it is packed in the F40 ' 450mm exchange column, add above-described embodiment 1 step 2 from the exchange column top) pressing filtering liquid, add speed control and make filtrate and ion exchange resin about 20min duration of contact.The exchange column effluent liquid is received with a test tube by every 5mL, utilize the spectrophotometric analysis method to monitor molybdenum content in each test tube, when the content of molybdenum from blank level when beginning to increase, show that this moment, ion exchange column reached capacity to exchange and the absorption of molybdate, stop the exchange column top and add and contain the molybdenum pressing filtering liquid.Ammoniacal liquor with 20～25% carries out drip washing to exchange column, and the content of molybdenum is lower than till 1% in leacheate, and leacheate contains molybdenum acid ammonia, with its with contain the molybdenum spent acid and mix and recycle.With 30% strong aqua, 1% salpeter solution exchange column is regenerated successively.Can realize 90% rate of recovery to molybdenum in the pressing filtering liquid with this method.
Embodiment 3
On the basis of embodiment 1, step 2) molybdenum of pressing filtering liquid reclaims, and containing the molybdenum pH value of filtrate is 4.0～5.0.
Macroporous acrylic that resin company or Shanghai Jin Yang resin scientific ﹠ technical corporation produce is weak base anion-exchange resin to select for use Xi'an Lanxiao Sci-Tech Co., Ltd., Tianjin Nankai Hecheng S﹠T Co., Ltd., Zhejiang to win honour for.Soaked above-mentioned anionite-exchange resin 1 hour with 1% salpeter solution, in the F40 ' 450mm exchange column of then it being packed into, add above-mentioned operational path 1 pressing filtering liquid from the exchange column top, add speed control and make filtrate and ion exchange resin about 20min duration of contact.The exchange column effluent liquid is received with a test tube by every 5mL, utilize the spectrophotometric analysis method to monitor molybdenum content in each test tube, when the content of molybdenum from blank level when beginning to increase, show that this moment, ion exchange column reached capacity to exchange and the absorption of molybdate, stop the exchange column top and add and contain the molybdenum pressing filtering liquid.Ammoniacal liquor with 20～25% carries out drip washing to exchange column, and the content of molybdenum is lower than till 1% in leacheate, and leacheate contains molybdenum acid ammonia, with its with contain the molybdenum spent acid and mix and recycle.With 30% strong aqua, 1% salpeter solution exchange column is regenerated successively.Can realize 95% rate of recovery to molybdenum in the pressing filtering liquid with this method.
Embodiment 4
On the basis of embodiment 1, the recovery of molybdenum mixed solution in the step 9) centrifugate, containing the molybdenum pH value of filtrate is 6.9～7.2.
Macroporous acrylic that resin company or Shanghai Jin Yang resin scientific ﹠ technical corporation produce is weak base anion-exchange resin to select for use Xi'an Lanxiao Sci-Tech Co., Ltd., Tianjin Nankai Hecheng S﹠T Co., Ltd., Zhejiang to win honour for.Soaked above-mentioned anionite-exchange resin 1 hour with 1% salpeter solution, then it is packed in the F40 ' 450mm exchange column, add above-described embodiment 1 step 9) centrifugate mixed solution from the exchange column top, add speed control and make filtrate and ion exchange resin about 20min duration of contact.The exchange column effluent liquid is received with a test tube by every 5mL, utilize the spectrophotometric analysis method to monitor molybdenum content in each test tube, when the content of molybdenum from blank level when beginning to increase, show that this moment, ion exchange column reached capacity to exchange and the absorption of molybdate, stop the exchange column top and add and contain the molybdenum pressing filtering liquid.Ammoniacal liquor with 20-25% carries out drip washing to exchange column, and the content of molybdenum is lower than till 1% in leacheate, and leacheate contains molybdenum acid ammonia, with its with contain the molybdenum spent acid and mix and recycle.With 30% strong aqua, 1% salpeter solution exchange column is regenerated successively.Can realize 94% rate of recovery to molybdenum in the centrifugate with this method.
Adopt above-described embodiment 2 and 4 or the combination of embodiment 3 and 4, can whole production technology reach 99% to the rate of recovery that contains molybdenum in the molybdenum spent acid.
Claims (10)
1. one kind contains the molybdenum spent acid method that reclaims molybdenum from the filament silk, it is characterized in that this method comprises the steps:
1) neutralization: liquefied ammonia is slowly joined in the spent acid, and the control feed rate keeps temperature to be no more than 90 ℃; When reaching pH and be 3, precipitation appears, and continue to add liquefied ammonia and equal 4.8 ~ 5.5 to pH and stop;
2) filter: use the pressure filter press filtration, produce filter cake and filtrate;
3) ammonia soaks: with the filter cake ammonia solvent, regulate pH value to 8.0～9.0 and make all dissolvings of precipitation;
4) filter: remove a small amount of undissolved impurity with filter cloth;
5) acid is heavy: regulate to locate ageing liquid with the diluted acid of 5 ~ 20 wt%, to pH be 2.0～3.0,40 ~ 55 ℃ of temperature are settled out the ammonium tetramolybdate crystal, centrifugal treating;
6) oven dry: get the ammonium tetramolybdate product;
7) crystallization: resulting mother liquor adds the ammoniacal liquor of 10 ~ 25 wt% in the step 5), and regulator solution pH to 6.0～7.0 keep the crystallization kettle temperature at 70～80 ℃, separate out the Ammonium Heptamolybdate crystal;
8) centrifugal: as to obtain wet Ammonium Heptamolybdate and centrifugal liquid;
9) oven dry: get the Ammonium Heptamolybdate product.
2. according to claim 1ly a kind ofly contain the molybdenum spent acid method that reclaims molybdenum from the filament silk, it is characterized in that: increase the ageing operation between step 4) and step 5), the ageing operation is for maintaining the temperature at 60～70 ℃ times static 5 ~ 30 hours.
3. according to claim 1ly a kind ofly contain the molybdenum spent acid method that reclaims molybdenum from the filament silk, it is characterized in that: the rare nitric acid of the rare employing of the diluted acid of step 5) or dilute sulphuric acid.
4. describedly a kind ofly contain the molybdenum spent acid method that reclaims molybdenum from the filament silk according to claim 1 or 2 or 3, it is characterized in that: increase step 10), step 10) is with from step 2) and/or the liquid of step 8) enter anionite-exchange resin and carry out ion-exchange, molybdate is exchanged on the anionite-exchange resin; With ammoniacal liquor anionite-exchange resin is carried out desorb then, obtain containing the stripping liquid of ammonium molybdate, stripping liquid is added in the molybdenum spent acid of step 1) as the raw material that reclaims.
5. according to claim 4ly a kind ofly contain the molybdenum spent acid method that reclaims molybdenum from the filament silk, it is characterized in that: anionite-exchange resin described in the step 10) adopts macroporous anion exchange resin, the basic group of macroporous anion exchange resin one or more in primary amine groups, secondary amine and tertiary amine groups.
6. according to claim 5ly a kind ofly contain the molybdenum spent acid method that reclaims molybdenum from the filament silk, it is characterized in that: the framework types of the macroporous anion exchange resin described in the step 10) is selected from one or more in polystyrene and the acrylic acid series.
7. according to claim 4ly a kind ofly contain the molybdenum spent acid method that reclaims molybdenum from the filament silk, it is characterized in that: the concentration of ammoniacal liquor is 20 ~ 25 wt% in the step 10).
8. according to claim 4ly a kind ofly contain the molybdenum spent acid method that reclaims molybdenum from the filament silk, it is characterized in that: anionite-exchange resin soaked 1 hour with 1 wt% salpeter solution in the step 10), then it is packed in the exchange column, add speed control and make filtrate and anionite-exchange resin 15 ~ 25min duration of contact.
9. according to claim 4ly a kind ofly contain the molybdenum spent acid method that reclaims molybdenum from the filament silk, it is characterized in that: the anionite-exchange resin effluent liquid receives with a test tube by every 5mL in the step 10), utilize the spectrophotometric analysis method to monitor molybdenum content in each test tube, when the content of molybdenum from blank level when beginning to increase, show that this moment, anion-exchange column reached capacity to exchange and the absorption of molybdate, stop the adding of anion-exchange column top and contain the molybdenum pressing filtering liquid, with described ammoniacal liquor anion-exchange column is carried out drip washing then, the content of molybdenum is lower than till 1 wt% in leacheate.
10. according to claim 9ly a kind ofly contain the molybdenum spent acid method that reclaims molybdenum from the filament silk, it is characterized in that: anion-exchange column is regenerated exchange column with 30wt% strong aqua, 1wt% salpeter solution successively.
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Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103663561A (en) * | 2012-09-10 | 2014-03-26 | 中国石油化工股份有限公司 | Recycling method of molybdenum in filament-melting waste acid |
| CN105838882A (en) * | 2016-06-21 | 2016-08-10 | 昆明冶金研究院 | Separation and recovery process for molybdenum and nickel in nickel-molybdenum associated ore oxygen pressure acid leaching liquid |
| CN112744864A (en) * | 2020-12-30 | 2021-05-04 | 成都虹波钼业有限责任公司 | Production process of 5N-grade high-purity molybdenum trioxide |
| CN113801997A (en) * | 2020-06-12 | 2021-12-17 | 杭州临安慧尔钼业科技有限公司 | Method for recycling ammonium molybdate and molybdenum precipitation agent from low-molybdenum raffinate molybdenum |
| CN113800565A (en) * | 2020-06-11 | 2021-12-17 | 杭州临安慧尔钼业科技有限公司 | Method for preparing high-purity ammonium heptamolybdate by photooxidation conversion of filament-melting molybdenum-containing waste acid |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3963823A (en) * | 1975-02-25 | 1976-06-15 | Westinghouse Electric Corporation | Molybdenum recovery from spent acid solution |
| CN102259927A (en) * | 2011-06-27 | 2011-11-30 | 西部鑫兴金属材料有限公司 | Method for preparing high-purity ammonium tetramolybdate |
-
2013
- 2013-06-05 CN CN201310223547.3A patent/CN103265079B/en active Active
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3963823A (en) * | 1975-02-25 | 1976-06-15 | Westinghouse Electric Corporation | Molybdenum recovery from spent acid solution |
| CN102259927A (en) * | 2011-06-27 | 2011-11-30 | 西部鑫兴金属材料有限公司 | Method for preparing high-purity ammonium tetramolybdate |
Non-Patent Citations (4)
| Title |
|---|
| 刘先德: "化丝废酸的无废利用", 《中国照明电器》 * |
| 向铁根等: "《钼冶金》", 31 December 2009, 中南大学出版社 * |
| 杨世珖等: "《近代化学实验》", 31 August 2010, 石油工业出版社 * |
| 金瑜等: "化丝废水中钼的回收利用", 《环境科技》 * |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103663561A (en) * | 2012-09-10 | 2014-03-26 | 中国石油化工股份有限公司 | Recycling method of molybdenum in filament-melting waste acid |
| CN105838882A (en) * | 2016-06-21 | 2016-08-10 | 昆明冶金研究院 | Separation and recovery process for molybdenum and nickel in nickel-molybdenum associated ore oxygen pressure acid leaching liquid |
| CN113800565A (en) * | 2020-06-11 | 2021-12-17 | 杭州临安慧尔钼业科技有限公司 | Method for preparing high-purity ammonium heptamolybdate by photooxidation conversion of filament-melting molybdenum-containing waste acid |
| CN113801997A (en) * | 2020-06-12 | 2021-12-17 | 杭州临安慧尔钼业科技有限公司 | Method for recycling ammonium molybdate and molybdenum precipitation agent from low-molybdenum raffinate molybdenum |
| CN112744864A (en) * | 2020-12-30 | 2021-05-04 | 成都虹波钼业有限责任公司 | Production process of 5N-grade high-purity molybdenum trioxide |
| CN112744864B (en) * | 2020-12-30 | 2022-03-29 | 成都虹波钼业有限责任公司 | Production process of 5N-grade high-purity molybdenum trioxide |
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Denomination of invention: A Method for Recovering Molybdenum from Molybdenum Containing Waste Acid in Filament Production Effective date of registration: 20230427 Granted publication date: 20150812 Pledgee: Zhejiang Lin'an CITIC Rural Bank Co.,Ltd. Pledgor: Hangzhou Lin'an Huier Molybdenum Industry Science & Technology Co.,Ltd. Registration number: Y2023330000810 |