Method of recovering nitric and hydrofluoric acids from pickling solutions

专利摘要:
In the pickling, etching, chemical milling etc. of steels, stainless steels, special alloys and special metals and also when dissolving these metals, metalliferous solutions of the acids used arise in the course of these processes, and these must either be disposed of by neutralisation or used in expensive processes in order to recover the acids and metals. Nitric acid or a nitric acid/hydrofluoric acid mixture are obtained or recovered according to the invention by spray-roasting the solutions at temperatures from 200 to 500 DEG C in a reactor (1) followed by absorption and condensation of the resulting gases in columns (7, 8) at temperatures from 0 to 70 DEG C. …<IMAGE>…
公开号:SU1739859A3
申请号:SU4355926
申请日:1988-06-15
公开日:1992-06-07
发明作者:Карнер Вильхельм；Криванец Хайнц；Хорн Хуанито；Вурмбауер Дитер
申请人:Машиненфабрик Андритц Аг (Фирма)；
IPC主号:

专利说明:

The invention relates to methods for the regeneration of spent pickling solutions containing salts of the metals nitric and hydrofluoric acids, which are formed, for example, during pickling and chemical milling of carbon and stainless steels and special alloys. In pickling solutions, cations of Fe, Cr, Ni, Ti, Al, Zr, Ta and other metals accumulate.
When a certain metal content is reached, which is, depending on the etched alloy, 20–20 g / l of dissolved metal,
such solutions are drained. As a rule, they are neutralized by neutralization. However, this presents a considerable environmental problem due to the large amounts of accumulated sludge and also due to pollution of wastewater with nitrates. In addition, the company has to incur considerable costs for the purchase of new acids, as well as neutralizing chemicals.
The disadvantage of these methods is that for the most part they can only be applied to one
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with
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1739859
a specific waste solution, most often to a solution of Fe, Cr, and Ni ions, a mixture of hydrofluoric and nitric acids, which accumulate, for example, when processing stainless steels.
These methods can be divided into the following groups. Distillation Method Sulfuric acid is added to the pickling solutions used and the volatile acids HNOj and HF are distilled off. Metal ions precipitate as a mixture of sulphates into the sediment, which is subjected to further processing. Along with the complex introduction of the process, several stages of evaporation, crystallization and filtration are necessary.
The disadvantage is a higher consumption of chemicals. In the case of titanium-containing solutions, this method cannot be used, since titanium sulphates crystallize very poorly. Crystallization method
The solution is evaporated in a special evaporator heated by electric current, then iron fluoride crystals are obtained by cooling, which is filtered. The filtrate forms one part of the regenerated acid, and the other part is obtained by thermally decomposing fluoride crystals in the rotary tube furnace as hydrofluoric acid
This method gives a good degree of regeneration of hydrofluoric and nitric acids, and by firing the initially accumulated FeFj t crystals, pure hydrofluoric acid can be obtained, but not pure nitric acid. During the crystallization process, not all of the cations contained in the solution are released to an equal degree, preferably iron. Due to this, with repeated use of the regenerated pickling solution, an increase in the concentration of the accompanying elements Cr, Ni may occur, which limits the use of this method,
Extraction Method
The method is carried out in several stages:
iron extraction (using diethylhexyl phosphate in paraffin);
regeneration of the extraction medium by adding
crystallization (NH4)
decomposition of (NH4) 3FeF6 at 500 ° С;
calcination product at 800
five
acid extraction (tributyl phosphate in paraffin);
neutralizing the remainder of the solution.
In addition to the complex introduction of the process, this method always has the danger of contaminating wastewater with extraction agents, as well as the danger of fire due to the use of flammable solvents. The method is clearly described only for Fe-Cr-Ni solutions, and solutions containing Ti or other metals cannot handle this way
Ion exchange method
In this case, the free acids (but not the amount bound by the metal) are sorbed by the resin exchanger, and then washed out with water. The metals accumulate in the form of a solution of metal salts, which should be neutralized. Thus, here we are not talking about the true regeneration method, but only partial extraction
five
five
0
five
0
etching acid The proportion of metal to be neutralized is as high as with a simple neutralization
Dialysis methods
Dialysis can be performed either as pure diffusion dialysis or as electrodialysis. During diffusion dialysis, by analogy with the ion exchange method, only the separation of free acid and metal salts occurs, resulting in the same problems. During electrodialysis, at first the entire solution is crystallized with potassium liquor, and the resulting neutral solution of potassium nitrate and potassium fluoride is decomposed on special membranes into acid and potassium liquor. The regeneration rates are good, but the drawbacks of the method include high energy consumption and membrane tightness.
For the complete regeneration of the hydrochloric acid used to pickle carbon steels, the method of drying aerosols is used. In this case, the used pickling solution is injected into the reactor, where it comes into contact with the hot gases produced by the burner delivered to the reactor. solution decomposition:
2ГеС1а + 2Н2р + 1/202 Ft CV4HCl
The metal content of the solution falls out - in the form of metal oxide, and
five
The gaseous HC1 and - formed are absorbed into hydrochloric acid. In order to achieve the decomposition described, a temperature of 500 to 1000 ° C, as a rule, should be ensured in the reactor.
This method and similar methods have so far been used only for the regeneration of hydrochloric acid. The use of this method for the regeneration of other acids (for example, hydrofluoric acid or nitric acid) at the indicated temperatures is impossible because of the decomposition of nitric acid into No. difficult to absorb with. In addition, at these temperatures there is a danger of corrosion problems ...
The purpose of the invention is to simplify the process, to obtain a metal-containing precipitate in the form of a dry powder and to reduce equipment corrosion.
A method for separating nitric acid or a mixture of nitric and hydrofluoric acids from spent pickling solutions containing the metal salts of these acids is as follows.
The spent solution is spray dried at 200 - 500 ° C, with the acid vapors separated from the metal containing precipitate as a dry powder. Preferably, drying is carried out at 300-400 ° C. Spraying at a temperature of less than 200 ° C is not economically feasible. At temperatures above 500 ° C, equipment corrosion increases and nitric acid decomposition occurs.
Then pairs of acids are absorbed and / or condensed with an aqueous absorption solution at 0 - 70 ° C. The absorption and / or condensation of acid vapors can be carried out in two stages: at the first stage at 20–70 ° C, and at the second stage at 0–40 ° C., The aqueous absorption solution may contain an oxidizing agent, for example, hydrogen peroxide „
In a very advantageous manner, the gases produced during the spray-drying process can be used to preheat the initial solution.
In contrast to the known methods developed for the regeneration of hydrofluoric acid and nitric acid, using the proposed method, solutions of any composition can be processed, i.e. solutions that contain any comp
0
five
biations of cations (Fe, Cr, Ni, Ti, Zr, A1 and others), as well as solutions that contain either only hydrofluoric, or only nitric, or a combination of these acids
The metals from the solution are precipitated in the form of dry metal oxides or metal salts, which can be reused as such.
or processed into products of even greater value (powdered metal), or buried in a waste repository,
5 During thermal decomposition in the reactor, the following chemical and physical transformations occur: water evaporation
Н20 (ж) Н20 (g), (1) 0 evaporation of nitric acid НЖ) 3 (ж) НЫ05 (g) (2) evaporation of hydrofluoric acid
HF (g) NK (g) (3) decomposition of HNO-j
2HN03 (r) NOa (g) + NO (g) + HgO (g) + +02 (g), (4)
decomposition HN03
4HN03 (r) 3N02 (r) + NO r) + + 2HZ0 (r) + 1.502 (r) (4a) decomposition of K02
2NOZ (r) 2NO (g) +02 (g), (5) fluoride decomposition
MeF (g) + K20 (g) MeO (TV) + 2 GN (g),
(6) nitrate decomposition
Me (MO) 2 + H O (g) MeO (TV) + 2NS3 (g),
(7)
Reactions (6) and (7) should be evaluated only as an example of a divalent cation. For other metals, and also when charged or oxygen-containing complexes arise, the reaction equations look different.
The metal oxides formed according to reactions (6) and (7) are mostly collected on the bottom of the reactor and continuously removed therefrom by means of a removal device. In part, they are removed with the flow of outgoing gases and then removed by means of dust collectors. gaseous products are supplied to the absorption and condensation device. In case the solution contains only HF as an acid component or, for example, a mixture of HF and HC1, then the absorption and condensation device can consist of only one column. If the solution contains HNO $,
0
five
0
S
O
five
then at least two columns should be used. The columns are loaded with circulating absorption solution, which is cooled in heat exchangers to a certain temperature. By choosing the temperature of absorption or condensation, the concentration of the resulting acid can be affected,
Figure 1 shows a block diagram of a device for the regeneration of an acid; in figure 2. the same, using the heat of vapor obtained in the spray drying process; FIGS. 3–5 are graphs of the concentration of acids in the sorption and / or condensation columns as a function of temperature in the first column along the vapor path, when the temperature in the second column along the vapor column is 20 ° C lower than in the first column
The device contains a reactor 1, into which the solution to be treated containing metal cations and acid anions is fed through a metering pump 2 through heating 3. Heats up the reactor 1 with, for example, an acetylene-oxygen burner located next to the bottom of the reactor 4. At the bottom of the reactor, a device 5 is provided for the continuous removal of the resulting solids. Hot gases are removed from the reactor head 1 to the dust separator 6, in which the remaining solids are released. After that, the flowing gases enter the absorption and condensation device, for example, which are connected in series with the first 7 and second 8 columns. Absorbent liquid (water) flows from the bottom of each column with the "- power of pumps 9 and 10 and again supplies - with the head of each of the columns 7 and 8 after passing through the heat exchange - peaks 11 and 12. Heat exchangers 11 and 12 are cooled, for example, water. Finally, the gases leaving the second column 8 pass through two successive scrubbers 13 and 14, and then are sucked off with the help of a fan 15.
In the device (Fig. 2), the solution to be processed is subjected to roar in the heat exchanger 16 by means of hot water coming out of the reactor 1, due to which energy can be saved
five
0
five
0
0
five
0
five
0
By choosing the temperature of sorption and condensation, the concentration of lots in columns 7 and 8 can be influenced. At (rig 3, 4 it is shown what the variational possibilities are, for example, if the temperature in column 8 (second along the gas flow) is constant maintained at 20 ° C less than in column 7 (first along the gas), and in column 7 itself will vary within 40 -
Such operating conditions are possible under which a mixture of hydrofluoric and nitric acids is accumulated in column 7 and nitric acid is formed in column 8 with very low HFt content. This is of particular importance in connection with the surface treatment of metals. Some pickling processes should be carried out using a mixture of hydrofluoric and nitric acids, and others using pure nitric acid.
Fig. 5 shows the relationship between the circulating volume of the circulating solution and the temperature.
Hydrofluoric acid accumulating for the most part is contained in the effluent of column 7 (95%). to a much lesser extent - in the waste device of the column 8 (4%), and in an insignificant amount - in de (the content of fluoride in the dry residue - 0.2 g - 0.02%).
It is advisable to generate nitric acid by means of the absorption of nit "- pink gas. In this case, initially, only a part of the mixture is converted into nitric acid by means of the following: —nitrogen dioxide:
 (g) + H20 (1) 2HM03 (g) + MO (g)
(eight)
Nitrogen monoxide, contained in gas mixture 5, leaving the reactor, as well as resulting from the absorption reaction 8, must be oxidized by the following reaction to ensure further absorption: oxidation
2NO (g) + 0g (g) 2Sha (g). (9)
Gases formed in the reactor during the decomposition of waste solutions; have a ratio of N02 / -N0, which makes it possible to regenerate about 33% of the initially used nitric acid in column 7 (the first along the gas flow). This corresponds to the degree of oxidation of the starting material, equal to 50%, according to the decomposition reaction / 4 /.
Using an oxidation tower located between column 7 and column 8 (not shown), which is used to increase the processing time of the regenerated substances, a high degree of oxidation N0 is achieved, and 40% of nitric acid is absorbed in column 8; for example, hydrogen peroxide, it is also possible to increase the yield of nitric acid H202 can be introduced into column 7 or into column 8 or into a separate scrubber. A combination of these options is possible.,
The reaction of N0 with the oxidizing agent proceeds as follows:
10. NO + HgO NOZ + HZ0.
Example 1. A thief that accumulates during the etching of stainless steel, or nitric and hydrofluoric acids, is regenerated. Into reactor 1, a total of 16.36 l of a solution having the following composition, g / l (318.0 NM) is introduced in 5.5 hours 3, 35.8 HF, 36.3 Fe, 19.8 Cg, 25.2 Ni. The solution is supplied by means of pump 2 dispenser through nozzle 3. The reactor is heated with the power of an acetylene-oxygen burner 4 located near the bottom of the reactor. At the same time, the temperature above the reel plane is 39.0 - 47 ° C, and in the outgoing gases 140 - 10 ° C. The installation is connected to the fan 14, the suction volume being 12.5 me / h. The flue gases are first passed through a dust collector 5, and then through columns 7 and 8 filled with packed rings (such as palls) - Columns 7 and 8 are loaded with absorption solution using circulation pumps 9 and 10. The temperature of the circulating solution is maintained at a certain level using heat exchangers 11 and 12, the temperature is 50 ° C in the column
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7 and 22 C in column 8. The absorption solution is water at the beginning of the test, and as the test proceeds, the proportion of acids in the solution increases. Ultimately, the gas is directed through two more successively scrubber units 13 and 14,
During the course of the test, samples are withdrawn from columns 7 and 8 and scrubbers 13, 14 and analyzed for HNO, HF.

to
20
25
73985910
Experience with the help of the Dräger tubes is determined by the composition of the waste gases at N0 and HF. Based on the results of the analyzes and the known volume of individual devices, one can make a balance of volumes. Formed in the reactor 1 and the dust collector 6, the oxides are collected, weighed and analyzed.
Measurements carried out at the end of the experiment show that the nitric acid obtained is distributed as follows: 33.0% in column 7 or in the column transfer device 7; 43.2% 15 in column 8 or in the overflow device of column 8; 7.2% in scrubber 13; 3.0% in scrubber 14; 11.5% in exhaust gases; 0% in oxide; 97.9% is the amount.
HF is distributed as follows: 86% in column 7 or column bypass device 7; 9.6% in column 8 or in column bypass 8; 1.9% in scrubber 13; 0% in scrubber 14; 0% in waste gas; 1.3% in oxide; 98.8% “is the amount.
Deviations of amounts from 100% are the results of errors in the analysis.
Example 2 A solution resulting from pickling steel was nitrated with ammonium nitrate and ammonium nitrate was regenerated. The experiment was carried out with the same solution as in Example 1, but with the addition of ammonium nitrate in the amount of 15 g / l. The measurements carried out show that the additive does not lead to an increase in the nitration concentration in the regenerated acid. In the latter, it does not detect 1 s ammonium. This suggests that ammonium nitrate is completely decomposed by one of the following reactions:
NH4NG3 N20 + 2K20; (11a)
NH4.N03 Ni + 2H20 + 1/20. (116)
Thus, ammonium nitrate can be destroyed by the proposed method.
EXAMPLE 3 A thief that accumulates during the etching of pure titanium with nitric and hydrofluoric acids is regenerated. The test was carried out analogously to example 1. For 9 hours, 12.29 liters of a solution containing, g / l: 32.0 Ti were passed; 132.4 HN03; 34.8 HF; 5.0 H2SO ..
The temperature is 390 ° C in actor 1; 4 ° C in column 7 and column 8 "
thirty
35
40
45
50
55
35 ° C in
eleven
The analysis performed shows the following distribution of HM03: 33.0% in column 7 or in bypass devices of column 7; 41.4% in column 8 or in column bypass 8; 7.0% in scubber 13; 3.0% in agriculture 14; 14.5% in exhaust gases; 0% in oxide; V8.9% cyMMav
i
HF is distributed as follows: CB, L% in column 7 or in the column inlet 7; 2.9% in the column Y or in the discharge port of column 8; 0% in scubber 13; 0% in scubber 14; 0% to waste; 0% in oxyl; 101.5% amount t
 is distributed as follows: 58.0% in column 7 or in the "- start-up device of column 7; 42.0% in oxide; 100.0% - the amount
II p and me 4 The experiment was carried out with the same solution as in the ZS example.
17
The difference is that hydrogen peroxide is added to column 8. The leases show an increased yield of nitric acid in this column and a decrease in the fraction of NQy in the exhaust gases.
The analysis performed shows the following distribution: 33.2% in the 7th of the 7th section in the bypass device - “ve columns 7; 46.5% in column 8 or in the overflow device of column G; 8.4% in Skuboer 13%; 3.0% in stocking 14; 9.5% in waste gases; 0% in oxide; 100.4% is the amount.
 added to N0 (according to reaction 10) in a stoichiometric proportion, with N0 contained in the exhaust gases being taken as 100%.
Example 5: The solution (composition), the composition of which is given in Example 1, is regenerated (composition). A 20.5 l of solution is introduced into the reactor during spraying for 6 hours.
The temperature above the plane of the reamer is 470 ° 500 ° C, in the ambient gas 240 ° C. Exhaust gases are removed from the entire installation with blower 14, and their amount is 15 me / h.
The temperature in column 7 is 70 ° C and in the column 8 is 40 ° C.
1 The RR is distributed as follows: 15.5% in column 7 or in column bypass 7;

 ,
ten
15
20
73985912
68.4% in column 8 or in column overflow device C; 5.2%, in the scrub - Bere 13; 2.2% in scrubber 14; 10.5% in exhaust gas; 0% in oxide; 101.8% is the amount.
HF is distributed as follows: 93.4% in column 7 or in the column discharge device 7; 4.5% in column 8 or in column bypass 8; 1.0% in scrub Bere 13; 0% in scrubber 14; 0% in waste gas; 0.3% in oxide; 99.2% of the amount.
The invention allows a relatively simple method to extract acids from spent pickling solutions of complex composition, while simultaneously obtaining a metal-containing precipitate as a dry powder.

权利要求:
Claims (5)
[1]
1. Method of separating nitric and hydrofluoric acids from spent pickling solutions containing salts
25 metals of these acids, including the separation of acid vapors from the metal-containing sediment and the subsequent absorption and / or condensation of acid vapors, due to
In order to simplify the process and obtain a metal-containing precipitate as a dry powder, the separation of acid vapors from the metal-containing precipitate is carried out in one stage by spray drying the spent pickling solutions at 200 f 500 ° C, and the sorption and / or condensation of lot vapors is conducted at 0 - 70 ° C.
[2]
2. Method pop. 1, differing in kg and so that, in order to reduce equipment corrosion, spray drying is preferably carried out at 300 g - 400 ° C
[3]
3. Method according to paragraphs. 1 and 2, about tl and "40
45
50
55
This is because the absorption and / or condensation is carried out in two stages, and in the first stage - at 20 - 70VC, and in the second stage at O - 40 ° C.
[4]
4. The method according to claims 1 to 3, about aphids, and so that an oxidizing agent is added to the aqueous absorption solution.
[5]
5. The method according to claim 4, about tl and h a kg u and so that hydrogen peroxide is used as the oxide.
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法律状态:
2005-05-10| REG| Reference to a code of a succession state|Ref country code: RU Ref legal event code: MM4A Effective date: 20030616 |

优先权:

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申请号 | 申请日 | 专利标题

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AT0153487A|AT395312B|1987-06-16|1987-06-16|METHOD FOR RECOVERY OR RECOVERY OF ACID FROM METAL SOLUTIONS OF THIS ACID|

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