CN111925016A - Method for treating high-arsenic waste acid by using honeycomb briquette slag - Google Patents

Method for treating high-arsenic waste acid by using honeycomb briquette slag Download PDF

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CN111925016A
CN111925016A CN202010825871.2A CN202010825871A CN111925016A CN 111925016 A CN111925016 A CN 111925016A CN 202010825871 A CN202010825871 A CN 202010825871A CN 111925016 A CN111925016 A CN 111925016A
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arsenic
honeycomb briquette
briquette slag
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waste acid
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CN111925016B (en
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祁先进
杨妮娜
王�华
段孝旭
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Kunming University of Science and Technology
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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
    • 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
    • C02F1/66Treatment of water, waste water, or sewage by neutralisation; pH adjustment
    • CCHEMISTRY; METALLURGY
    • C02TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02FTREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F1/00Treatment of water, waste water, or sewage
    • C02F1/72Treatment of water, waste water, or sewage by oxidation
    • C02F1/722Oxidation by peroxides
    • CCHEMISTRY; METALLURGY
    • C02TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02FTREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F2101/00Nature of the contaminant
    • C02F2101/10Inorganic compounds
    • C02F2101/103Arsenic compounds
    • CCHEMISTRY; METALLURGY
    • C02TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02FTREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F2101/00Nature of the contaminant
    • C02F2101/10Inorganic compounds
    • C02F2101/20Heavy metals or heavy metal compounds
    • CCHEMISTRY; METALLURGY
    • C02TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02FTREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F2305/00Use of specific compounds during water treatment
    • C02F2305/02Specific form of oxidant
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P10/00Technologies related to metal processing
    • Y02P10/20Recycling

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  • Life Sciences & Earth Sciences (AREA)
  • Hydrology & Water Resources (AREA)
  • Engineering & Computer Science (AREA)
  • Environmental & Geological Engineering (AREA)
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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Processing Of Solid Wastes (AREA)
  • Manufacture And Refinement Of Metals (AREA)

Abstract

The invention relates to a method for treating high-arsenic waste acid by using honeycomb briquette slag, belonging to the technical field of heavy metal pollution treatment. Adding a hydrogen peroxide solution into high-arsenic waste acid, and reacting for 4-5 hours at the temperature of 80-82 ℃ under a stirring condition to obtain a solution A; adding the honeycomb briquette slag powder into the solution A, carrying out oscillation reaction for 4-12 h at the temperature of 25-30 ℃, carrying out solid-liquid separation to obtain arsenic-containing solid and filtrate, drying the arsenic-containing solid, then stacking, and carrying out deep arsenic removal treatment on the filtrate. According to the invention, the honeycomb briquette slag powder is used for effectively replacing portland cement to remove arsenic in waste acid and generate a stable arsenic-containing compound, so that the diffusion and harm of arsenic in the environment are reduced, and secondary pollution is avoided.

Description

Method for treating high-arsenic waste acid by using honeycomb briquette slag
Technical Field
The invention relates to a method for treating high-arsenic waste acid by using honeycomb briquette slag, belonging to the technical field of heavy metal pollution treatment.
Background
Arsenic can form high-toxicity compounds, can be absorbed by human bodies from respiratory tracts, skins and digestive tracts, can cause neurasthenia syndrome, polyneuropathy, skin mucosa pathological changes and the like, and inorganic compounds of arsenic can cause lung cancer and skin cancer. After arsenic-containing wastewater is treated, most harmful substances such as arsenic are transferred into sludge, so that the method has important practical significance for safe treatment and disposal research of the arsenic-containing sludge.
At present, various methods such as wet treatment, pyrogenic treatment, solidification treatment and the like are used for treating arsenic-containing sludge. The wet treatment has low energy consumption, low pollution and high efficiency, but the operation steps are complicated; the pyrogenic process has simple treatment process and stable production, but has high efficiency, but can generate secondary pollution. The most commonly used method for arsenic-containing sludge is solidification. The portland cement method is often adopted in the curing method, but the method has higher cost and is not beneficial to large-scale use of enterprises.
Disclosure of Invention
Aiming at the problems in the prior art, the invention provides a method for treating high-arsenic waste acid by using honeycomb briquette slag, which effectively replaces portland cement with honeycomb briquette slag powder to remove arsenic in the waste acid and generate a stable arsenic-containing compound, thereby reducing the diffusion and harm of arsenic in the environment and avoiding secondary pollution.
A method for treating high-arsenic waste acid by using honeycomb briquette slag comprises the following specific steps:
(1) adding a hydrogen peroxide solution into high-arsenic waste acid, and reacting for 4-5 hours at the temperature of 80-82 ℃ under a stirring condition to obtain a solution A;
(2) adding honeycomb briquette slag powder into the solution A obtained in the step (1), adjusting the pH value of a system to be not higher than 5.0 by using a hydrogen peroxide solution, carrying out oscillation reaction for 4-12 h at the temperature of 25-30 ℃, carrying out solid-liquid separation to obtain arsenic-containing solid and filtrate, drying the arsenic-containing solid, then stacking the arsenic-containing solid, and carrying out deep arsenic removal treatment on the filtrate.
The concentration of the hydrogen peroxide solution in the step (1) is 30%, the volume ratio of the hydrogen peroxide solution to the high-arsenic contaminated acid is 1: 4-6, and the concentration of arsenic in the high-arsenic contaminated acid is 3000.0-7000.0 mg/L.
The particle size of the honeycomb briquette slag powder in the step (2) is 200-300 meshes, and the solid-to-liquid ratio g: mL of the honeycomb briquette slag powder to the solution A is (12-24): 100.
The principle of treating high-arsenic waste acid by honeycomb briquette slag comprises the following steps: in the process of adding the oxidized waste acid into the honeycomb briquette slag powder, Ca and Si in the honeycomb briquette slag powder are subjected to arsenic precipitation reaction, and precipitates contain SiO2With CaSO4.2H2Oho with beeOther alkali metal elements in the honeycomb briquette slag powder form complex precipitates, so that the precipitates have compact structures and high crystallinity, arsenic ions are locked in the complex precipitates, the migration capacity and leaching toxicity of arsenic are reduced, and the effect of stabilizing harmful pollutants is achieved.
The invention has the beneficial effects that:
(1) according to the invention, the honeycomb briquette slag powder is used for effectively replacing portland cement to realize removal of arsenic in waste acid and generation of a stable arsenic-containing compound, so that the diffusion and harm of arsenic in the environment are reduced, secondary pollution is avoided, and the purpose of treating waste by waste is realized;
(2) the honeycomb briquette slag of the invention has high content of alkaline compounds and contains SiO2With CaSO4.2H2The precipitate of O and other alkali metal elements in the honeycomb briquette slag powder form a complex precipitate, so that the precipitate has a compact structure, arsenic ions are locked in the complex precipitate, and the stability of an arsenic-containing compound is enhanced.
Detailed Description
The present invention will be described in further detail with reference to specific embodiments, but the scope of the present invention is not limited to the description.
Example 1: the waste acid is from a certain smelting plant in southwest of China, the waste water obtained by washing water in the acid making link by using flue gas is strong in acidity, metal elements, nonmetal elements and heavy metal elements in the flue gas in the washing process are accumulated continuously and enter the waste acid, the waste acid contains various metal elements such As Cu, Zn, Al and the like, the nonmetal elements such As Cl, F, S, C and the like, the heavy metal elements such As As, Pb, Cd and the like, arsenic is the heavy metal element with the highest content in the waste acid, the content of the elements in the waste acid is shown in table 1 through ICP element detection, the components of honeycomb briquette slag powder are shown in table 2, and the most content of the honeycomb briquette slag is SiO2And 16.09% Fe2O3And 14.96% CaO;
TABLE 1 contaminated acid composition (mg. L)-1)
Figure BDA0002636183100000021
TABLE 2 composition of Honeycomb briquet slag
Figure BDA0002636183100000022
A method for treating high-arsenic waste acid by using honeycomb briquette slag comprises the following specific steps:
(1) adding a hydrogen peroxide solution into high-arsenic contaminated acid, and reacting for 4 hours at the temperature of 80 ℃ and the stirring speed of 180r/min to obtain a solution A; wherein the concentration of the hydrogen peroxide solution is 30%, and the volume ratio of the hydrogen peroxide solution to the high-arsenic contaminated acid is 1: 4-6;
(2) adding honeycomb briquette slag powder into 50mL of the solution A obtained in the step (1), detecting the pH value of a system to be 3.47, oscillating the system in a constant-temperature oscillator at the temperature of 25 ℃ for 12h at an oscillation speed of 180r/min, carrying out solid-liquid separation to obtain arsenic-containing solid and filtrate, carrying out deep arsenic removal treatment on the filtrate, diluting the filtrate, measuring the concentration of residual arsenic by using ICP (inductively coupled plasma), drying the arsenic-containing solid at the temperature of 60 ℃ for 12h, and carrying out SEM (scanning electron microscope) and EDS (electronic discharge spectroscopy) analysis; the particle size of the honeycomb briquette slag powder is 200-300 meshes, and the adding amount of the honeycomb briquette slag powder is 2g, 4g, 6g, 8g, 10g and 12g in sequence;
TABLE 3 arsenic content and arsenic removal rate of the remaining solution under different honeycomb briquette slag powder usage
Figure BDA0002636183100000031
As can be seen from Table 3, the arsenic content in the solution decreases with the increase of the amount of the added honeycomb briquette slag, the arsenic removal rate gradually increases, the rising trend of the arsenic removal rate gradually decreases with the increase of the amount of the added honeycomb briquette slag, particularly, the arsenic content of the residual solution and the arsenic removal rate do not change greatly when the amount of the added honeycomb briquette slag is between 10g and 12g, the arsenic content of the residual solution is 118.2mg/L when the amount of the added honeycomb briquette slag is 10g, the arsenic removal rate of the residual solution reaches 97.05% (the arsenic content of the raw solution is 4g/L), and the arsenic content of the residual solution is 109mg/L and the arsenic removal rate reaches 97.28% when the amount of the added honeycomb briquette slag is 12 g.
The dry arsenic-containing solid was subjected to a leaching toxicity test, the toxicity test results are shown in table 4,
TABLE 4 Leaching toxicity analysis
Figure BDA0002636183100000032
As can be seen from Table 4, the arsenic content of the leachate of the obtained precipitates is very high when the addition amount of the honeycomb briquette slag is 2g and 4g, and both can not meet the national stacking standard, but when the addition amount of the honeycomb briquette slag exceeds 6g, the arsenic content in the steel slag is high, only a small amount of arsenide is stably fixed in the steel slag to be leached into the solution again, the leaching toxicity of the obtained arsenic-containing solid is less than 5.0mg/L, and the arsenic-containing solid can be directly stacked.
Example 2: the high arsenic contaminated acid and the honeycomb briquette slag in the embodiment are the same as those in embodiment 1;
a method for treating high-arsenic waste acid by using honeycomb briquette slag comprises the following specific steps:
(1) adding a hydrogen peroxide solution into high-arsenic contaminated acid, and reacting for 4.5 hours at the temperature of 81 ℃ and the stirring speed of 180r/min to obtain a solution A; wherein the concentration of the hydrogen peroxide solution is 30 percent, and the volume ratio of the hydrogen peroxide solution to the high-arsenic contaminated acid is 1: 5;
(2) adding honeycomb briquette slag powder into 50mL of the solution A obtained in the step (1), detecting the pH value of a system to be 2.33, carrying out oscillation reaction in a constant-temperature oscillator at the temperature of 28 ℃ at an oscillation speed of 180r/min, carrying out solid-liquid separation to obtain arsenic-containing solid and filtrate, carrying out deep arsenic removal treatment on the filtrate, diluting the filtrate, measuring the concentration of residual arsenic by using ICP (inductively coupled plasma), drying the arsenic-containing solid at the temperature of 60 ℃ for 12 hours, and carrying out SEM (scanning electron microscope) and EDS (electronic discharge spectroscopy) analysis; the particle size of the honeycomb briquette slag powder is 200-300 meshes, and the vibration reaction time is 1h, 2h, 4h, 6h, 9h and 12h in sequence;
TABLE 5 arsenic content and arsenic removal rate of the remaining solution at different reaction times
Figure BDA0002636183100000041
As can be seen from table 5, the arsenic content of the remaining solution gradually decreased with the increase of the reaction time, the arsenic removal rate gradually increased, and when the reaction time was less than 9 hours, the increase amplitude was large, the curve was shaken straight, and when the reaction time was greater than 9 hours, the curve increased more smoothly, because the honeycomb briquette slag mainly achieved the purpose of removing arsenic by adsorption in a short time, and as the time increased, the generation of ferric arsenate by chemical reaction was more stable, the removal rate curve was relatively gentle; when the reaction time is 12 hours, the arsenic content of the residual solution is 118.2mg/L, and the arsenic removal rate reaches 97.04%;
toxicity leaching experiments were carried out on arsenic-containing precipitates under different oscillation reaction time conditions, and the experimental results are shown in Table 6
TABLE 6 Leaching toxicity analysis
Figure BDA0002636183100000042
As can be seen from Table 6, when the reaction time is less than 2 hours, the arsenic-containing precipitates can not meet the national stacking standard, are all larger than 5.0mg/L, and can not be directly stacked in the environment, but when the reaction time exceeds 4 hours, the arsenic content in the precipitates is all lower than 5.0mg/L, and can be directly stacked in the environment; arsenic is attached to the surface of honeycomb briquette slag in a short time, although arsenic removal effect is achieved, arsenic-containing precipitate is unstable, the toxic leaching cannot reach the standard, more stable ferric arsenate is generated through chemical reaction along with the increase of reaction time, and the toxic leaching is gradually reduced.
Example 3: the high arsenic contaminated acid and the honeycomb briquette slag in the embodiment are the same as those in embodiment 1;
a method for treating high-arsenic waste acid by using honeycomb briquette slag comprises the following specific steps:
(1) adding a hydrogen peroxide solution into high-arsenic contaminated acid, and reacting for 5 hours at the temperature of 82 ℃ and the stirring speed of 180r/min to obtain a solution A; wherein the concentration of the hydrogen peroxide solution is 30 percent, and the volume ratio of the hydrogen peroxide solution to the high-arsenic contaminated acid is 1: 6;
(2) adding honeycomb briquette slag powder into 50mL of solution A obtained in the step (1), adjusting the pH value of a system to be 0.98, 3, 5, 7, 9 and 12 in sequence by adopting a hydrogen peroxide solution, carrying out oscillation reaction for 4 hours in a constant-temperature oscillator at the temperature of 30 ℃ at an oscillation speed of 180r/min, carrying out solid-liquid separation to obtain an arsenic-containing solid and a filtrate, carrying out deep arsenic removal treatment on the filtrate, measuring the residual arsenic concentration by using ICP (inductively coupled plasma) after the filtrate is diluted, drying the arsenic-containing solid at the temperature of 60 ℃ for 12 hours, and carrying out SEM (scanning electron microscope) and EDS (electronic discharge spectroscopy) analysis; wherein the particle size of the honeycomb briquette slag powder is 200-300 meshes;
TABLE 7 arsenic content and arsenic removal rate of residual solution under different initial pH values of oscillation reaction
Figure BDA0002636183100000051
As can be seen from Table 7, the arsenic content of the remaining solution containing arsenic in the remaining solution gradually decreased with increasing pH, the arsenic removal rate gradually increased, the fluctuation range of the arsenic removal rate with different initial pH was large, and when the initial pH was higher than 3, the hydrogen ion concentration in the solution was too low, and Fe2O3The reaction with the waste acid is less, and the dissolved part of iron ions can not react with arsenic ions under the condition that the pH value is higher than 3, the arsenic removal effect is best when the pH value is 12, the arsenic removal rate reaches 99.72%, and the arsenic content of the residual solution is 146.6 mg/L; but when the pH value is 0.98-5, the arsenic removal rate also reaches 92-95%;
toxicity leaching experiments were carried out on the filter residue under different initial pH values of the shaking reaction, and the experimental results are shown in Table 8
TABLE 8 Leaching toxicity analysis
Figure BDA0002636183100000052
As shown in Table 8, Fe was found to be present at a pH of 0.98 to 32O3Can be dissolved in the solution and reacts with arsenic ions in the solution to generate arsenate, and when the pH value is less than 5, the arsenic content of the obtained arsenic-containing slag is equal to or higher than that of the arsenic-containing slag<5.0mg/L, can be directly stacked,when the pH value is more than 5, the arsenic content in the slag does not meet the national stacking standard and can not be directly stacked in the environment, so the initial pH value of the oscillation reaction is less than 5; therefore, in the process of adding the oxidized waste acid into the honeycomb briquette slag powder, Ca and Si in the honeycomb briquette slag powder are subjected to arsenic precipitation reaction, and precipitates contain SiO2With CaSO4.2H2O and other alkali metal elements in the honeycomb briquette slag powder form a complex precipitate, so that the precipitate has a compact structure and high crystallinity, arsenic ions are locked in the complex precipitate, the arsenic migration capacity and leaching toxicity are reduced, and the effect of stabilizing harmful pollutants is achieved.

Claims (3)

1. A method for treating high-arsenic waste acid by using honeycomb briquette slag is characterized by comprising the following specific steps:
(1) adding a hydrogen peroxide solution into high-arsenic waste acid, and reacting for 4-5 hours at the temperature of 80-82 ℃ under a stirring condition to obtain a solution A;
(2) adding honeycomb briquette slag powder into the solution A obtained in the step (1), adjusting the pH value of a system to be not higher than 5.0 by using a hydrogen peroxide solution, carrying out oscillation reaction for 4-12 h at the temperature of 25-30 ℃, carrying out solid-liquid separation to obtain arsenic-containing solid and filtrate, drying the arsenic-containing solid, then stacking the arsenic-containing solid, and carrying out deep arsenic removal treatment on the filtrate.
2. The method for treating high-arsenic waste acid by using honeycomb briquette slag as claimed in claim 1, which is characterized in that: the concentration of the hydrogen peroxide solution in the step (1) is 30%, the volume ratio of the hydrogen peroxide solution to the high-arsenic contaminated acid is 1: 4-6, and the concentration of arsenic in the high-arsenic contaminated acid is 3000.0-7000.0 mg/L.
3. The method for treating high-arsenic waste acid by using honeycomb briquette slag as claimed in claim 1, which is characterized in that: the particle size of the honeycomb briquette slag powder in the step (2) is 200-300 meshes, and the solid-to-liquid ratio g/mL of the honeycomb briquette slag powder to the solution A is (12-24): 100.
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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN113060791A (en) * 2021-04-01 2021-07-02 昆明理工大学 Method for treating high-arsenic waste acid by using modified coal slag adsorbent
CN113548755A (en) * 2021-08-18 2021-10-26 昆明理工大学 Method for purifying arsenic-containing wastewater

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EA200970643A1 (en) * 2006-12-28 2009-12-30 МОЛИКОРП МИНЕРАЛЗ, ЭлЭлСи METHOD AND INSTALLATION FOR REMOVAL OF A BRAZE FROM CONTAINING BABY MATERIAL
CN108947021A (en) * 2018-08-29 2018-12-07 昆明理工大学 A kind of method of iron-based oxide Solid state fermentation waste acid
CN109078962A (en) * 2018-08-30 2018-12-25 西北矿冶研究院 Combined treatment method of arsenic-containing acidic wastewater, red mud and carbide slag
CN110746168A (en) * 2019-09-23 2020-02-04 昆明理工大学 Method for solidifying arsenic-containing sludge by steel slag and silica fume cementing material
CN111003775A (en) * 2019-12-09 2020-04-14 昆明理工大学 Method for treating arsenic in waste acid by copper slag and carbide slag

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EA200970643A1 (en) * 2006-12-28 2009-12-30 МОЛИКОРП МИНЕРАЛЗ, ЭлЭлСи METHOD AND INSTALLATION FOR REMOVAL OF A BRAZE FROM CONTAINING BABY MATERIAL
CN108947021A (en) * 2018-08-29 2018-12-07 昆明理工大学 A kind of method of iron-based oxide Solid state fermentation waste acid
CN109078962A (en) * 2018-08-30 2018-12-25 西北矿冶研究院 Combined treatment method of arsenic-containing acidic wastewater, red mud and carbide slag
CN110746168A (en) * 2019-09-23 2020-02-04 昆明理工大学 Method for solidifying arsenic-containing sludge by steel slag and silica fume cementing material
CN111003775A (en) * 2019-12-09 2020-04-14 昆明理工大学 Method for treating arsenic in waste acid by copper slag and carbide slag

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN113060791A (en) * 2021-04-01 2021-07-02 昆明理工大学 Method for treating high-arsenic waste acid by using modified coal slag adsorbent
CN113548755A (en) * 2021-08-18 2021-10-26 昆明理工大学 Method for purifying arsenic-containing wastewater

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