CN112156754A - Preparation method of waste sponge foam carbon-based composite adsorption material and application of waste sponge foam carbon-based composite adsorption material in adsorption removal of chromium in wastewater - Google Patents
Preparation method of waste sponge foam carbon-based composite adsorption material and application of waste sponge foam carbon-based composite adsorption material in adsorption removal of chromium in wastewater Download PDFInfo
- Publication number
- CN112156754A CN112156754A CN202011048024.6A CN202011048024A CN112156754A CN 112156754 A CN112156754 A CN 112156754A CN 202011048024 A CN202011048024 A CN 202011048024A CN 112156754 A CN112156754 A CN 112156754A
- Authority
- CN
- China
- Prior art keywords
- carbon
- waste sponge
- based composite
- moo
- mgo
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
Images
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
- B01J20/02—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material
- B01J20/04—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material comprising compounds of alkali metals, alkaline earth metals or magnesium
- B01J20/041—Oxides or hydroxides
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
- B01J20/02—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material
- B01J20/06—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material comprising oxides or hydroxides of metals not provided for in group B01J20/04
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
- B01J20/02—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material
- B01J20/20—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material comprising free carbon; comprising carbon obtained by carbonising processes
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
- B01J20/28—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof characterised by their form or physical properties
- B01J20/28014—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof characterised by their form or physical properties characterised by their form
- B01J20/28042—Shaped bodies; Monolithic structures
- B01J20/28045—Honeycomb or cellular structures; Solid foams or sponges
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/28—Treatment of water, waste water, or sewage by sorption
- C02F1/281—Treatment of water, waste water, or sewage by sorption using inorganic sorbents
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/28—Treatment of water, waste water, or sewage by sorption
- C02F1/283—Treatment of water, waste water, or sewage by sorption using coal, charred products, or inorganic mixtures containing them
-
- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2101/00—Nature of the contaminant
- C02F2101/10—Inorganic compounds
- C02F2101/20—Heavy metals or heavy metal compounds
- C02F2101/22—Chromium or chromium compounds, e.g. chromates
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Analytical Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Inorganic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Hydrology & Water Resources (AREA)
- Engineering & Computer Science (AREA)
- Environmental & Geological Engineering (AREA)
- Water Supply & Treatment (AREA)
- Water Treatment By Sorption (AREA)
- Solid-Sorbent Or Filter-Aiding Compositions (AREA)
Abstract
A preparation method of a waste sponge carbon-based composite adsorption material and application of the waste sponge carbon-based composite adsorption material in adsorption removal of chromium in wastewater relate to the technical field of waste sponge foam treatment and chromium-containing wastewater treatment. The invention uses waste sponge/foam carbon base as main carrier material toZnO-MoO with certain content and composition3MgO is used as filler to prepare the multielement composite adsorption material with excellent performance. And the adsorption performance is tested, and the modified waste sponge carbon-based adsorption material C-ZnO-MoO with excellent performance is screened out3MgO, and experiments prove that the modified waste sponge foam carbon-based adsorption material can be used for treating chromium-containing wastewater.
Description
Technical Field
The invention relates to the technical field of waste sponge foam treatment and chromium-containing wastewater treatment, in particular to a preparation method of a waste sponge foam carbon-based composite adsorption material and application of the adsorption material in adsorption removal of chromium in wastewater.
Background
Chromium pollution mainly comes from industrial waste water, waste gas and waste residues of chromium ore and metal smelting, electroplating, leather making and the like. Chromium is a heavy metal with high toxicity, trivalent chromium is easy to form oxide or hydroxide precipitate, the toxicity is relatively weak, and hexavalent chromium is generally considered to be 100 times more toxic than trivalent chromium. Chromium and its compounds are blacklisted as water environment priority pollutants in china due to its high toxicity. Chromium entering the human body is accumulated in human tissues and is slowly metabolized and removed. After entering blood, chromium is mainly combined with globulin, albumin and r-globulin in blood plasma. Hexavalent chromium can also permeate erythrocyte membranes, and 50% of hexavalent chromium can enter cells within 15 minutes and is combined with hemoglobin after entering the erythrocytes. Chromium metabolites are mainly excreted from the kidneys and a small amount is excreted via the feces. Hexavalent chromium is mainly chronic toxic to humans, and it can invade the human body through the digestive tract, respiratory tract, skin and mucous membrane, accumulating in the body mainly in the liver, kidney and endocrine glands. The air entering through the respiratory tract is easily accumulated in the lungs. Hexavalent chromium has a strong oxidizing effect, so chronic poisoning gradually progresses to irrecoverable drugs from local lesions. When invading into human body through respiratory tract, it starts to invade upper respiratory tract, causing rhinitis, pharyngitis, laryngitis and bronchitis.
Excessive intake of chromium can cause poisoning. Chromium poisoning is mainly caused by the occasional inhalation of a limited amount of chromic acid or chromate, causing extensive pathologies in the kidneys, liver, nervous system and blood, leading to death. There are also cases of poisoning caused by sodium chromate absorbed by the burned wound. Prolonged occupational exposure, air pollution or exposure to chromium dust can cause skin irritation and ulceration, inflammation, necrosis of the nasal cavity and even lung cancer. When orally taken, it can cause gastrointestinal tract injury, circulatory disturbance and renal failure. The treatment method is characterized in that the turtle mixture is used for treatment after the turtle is separated from contact, and the chromium excretion amount is increased due to high sugar intake. Chromium has three compounds with valences of 2, 3 and 6. The main cause of poisoning is 6-valent chromium which has strong oxidizing property and is easy to penetrate into a biological membrane to play a role; the 2-valent and 3-valent chromium is combined with protein on the surface layer of skin to form stable complex without causing biological effect.
In recent years, with the rapid development of economy and science and technology, a carbon-based material is a non-pollution and environment-friendly adsorbent material. The composite adsorption material loaded with the adsorption modifier has rich porous structure, ultrahigh specific surface area and rich surface functional groups, and is widely applied to the fields of adsorption separation, sewage treatment, gas purification and the like. Because the unique three-dimensional structure is widely concerned at present, the composite material has a unique framework structure, a higher surface area, directional pore channel distribution and higher chemical stability. The synthesis methods of common modified composite adsorbing materials comprise a carbonization method, a physical-chemical activation method, a catalytic activation method, an organogel carbonization method, a self-assembly method, a template method and the like, and the composite adsorbing materials prepared by the methods have different adsorption properties and good and uneven product quality.
Disclosure of Invention
The invention aims to solve the technical problem of providing a preparation method of a waste sponge foam carbon-based composite adsorption material and application of the waste sponge foam carbon-based composite adsorption material in adsorption removal of chromium in wastewater so as to prepare an adsorption material capable of being used for treating chromium-containing wastewater.
In order to achieve the purpose, the technical scheme adopted by the invention is as follows: a process for preparing the composite adsorptive material of foam carbon based on waste sponge includes dissolving Zn, Mg and Mo salts in water, adding diluted nitric acid, mixing, adding foam carbon of waste sponge, mixing, and ultrasonic reactionHydrothermal dipping for reaction to prepare the waste sponge foam carbon-based composite adsorption material C-ZnO-MoO3-MgO。
As an optimal technical scheme of the preparation method of the waste sponge foam carbon-based composite adsorption material, the preparation method comprises the following specific steps:
1) weighing zinc nitrate, magnesium oxide and ammonium molybdate, adding the zinc nitrate, the magnesium oxide and the ammonium molybdate into a beaker, dissolving the zinc nitrate, the magnesium oxide and the ammonium molybdate by using distilled water and dilute nitric acid, then adding the waste sponge carbon foam, adding ammonia water to adjust the pH value of the solution to 6-12, and fully stirring;
2) placing the mixture into an ultrasonic reactor, placing a beaker into hydrothermal impregnation, and reacting for 30min at 85 ℃, wherein the ultrasonic starting power is 1200W;
3) after the reaction is finished, drying the obtained product at 120 ℃ to obtain the waste sponge carbon-based composite adsorbing material C-ZnO-MoO3-MgO。
As a further preferable technical scheme of the preparation method of the waste sponge carbon-based composite adsorption material, the preparation method of the waste sponge carbon foam comprises the following steps: and (2) placing the waste sponge and the waste foamed plastic in inert gas for high-temperature carbonization, then cleaning and drying, and finally activating and forming pores in the inert atmosphere to obtain the waste sponge foamed carbon material.
Obtaining the waste sponge foam carbon-based composite adsorbing material C-ZnO-MoO3-C, ZnO and MoO in MgO3And the doping molar ratio of MgO is 7: 1-2: 1-2: 1 to 2. Further preferably, the waste sponge foam carbon-based composite adsorbing material C-ZnO-MoO is obtained3-C, ZnO and MoO in MgO3And the doping molar ratio of MgO is 7: 1: 2: 2.
the invention also provides application of the waste sponge foam carbon-based composite adsorption material prepared by the method in adsorption removal of chromium in wastewater.
Compared with the prior art, the invention has the beneficial effects that:
the invention takes waste sponge/foam carbon base as a main carrier material and ZnO-MoO with certain content and composition3MgO is used as filler of the adsorbing material to prepare the multi-element composite adsorbing material with excellent performance. Characterization of hands using instrumentsThe section XRD and SEM characterize the structure of the ZnO-MoO material, and the adsorption performance is tested to screen out ZnO-MoO with excellent performance3MgO modified waste sponge carbon-based adsorption material. Experiments show that the prepared ZnO-MoO3The MgO (1: 2: 2) modified waste sponge carbon-based adsorption material has the best adsorption effect, and the adsorption amount reaches 231 mg/g. The prepared target product reaches the expected target of experimental design, and the ZnO-MoO is proved3The MgO modified waste sponge carbon-based adsorption material can be used for treating chromium-containing wastewater. In addition, the enriched chromium can be used in the fields of electroplating, tanning, printing and dyeing, medicine, fuel, catalysts, oxidants, matches, metal corrosion inhibitors and the like.
Drawings
The following provides further details of the preparation method of the waste sponge foam carbon-based composite adsorption material and the application of the waste sponge foam carbon-based composite adsorption material in adsorption removal of chromium in wastewater, with reference to the examples and the accompanying drawings.
FIG. 1 is an XRD pattern of each series of composite adsorbents prepared in examples 1 to 7.
Fig. 2 is SEM images of low, medium, and high magnification in order of the composite adsorbent prepared in example 1.
FIG. 3 is a graph showing percentage of adsorbed residual chromium ions in each series of composite adsorbent materials prepared in examples 1 to 9.
FIG. 4 is a graph showing the adsorption amount of each series of composite adsorbents prepared in examples 1 to 7.
Detailed Description
Example 1
In the implementation, the prepared waste sponge carbon-based composite adsorbing material C-ZnO-MoO3in-MgO, C, ZnO, MoO3And the doping molar ratio of MgO is 7: 1: 2: 2. the preparation method comprises the following steps:
1) and placing the waste sponge and the waste foamed plastic in inert gas for high-temperature carbonization, then cleaning and drying, and finally activating and forming pores in inert atmosphere to obtain the waste sponge foamed carbon material.
2) Weighing zinc nitrate, magnesium oxide and ammonium molybdate, adding the zinc nitrate, the magnesium oxide and the ammonium molybdate into a beaker, dissolving the zinc nitrate, the magnesium oxide and the ammonium molybdate by using distilled water and dilute nitric acid, then adding the waste sponge carbon foam, adding ammonia water to adjust the pH value of the solution to 10, and fully stirring.
3) Placing the mixture into an ultrasonic reactor, placing a beaker into a hydrothermal dipping reactor, and reacting for 30min at 85 ℃ with the ultrasonic starting power of 1200W.
4) After the reaction is finished, drying the obtained product at 120 ℃ to obtain the waste sponge carbon-based composite adsorbing material C-ZnO-MoO3-MgO(7:1:2:2)。
Example 2
In this example, the prepared waste sponge carbon-based composite adsorbing material C-ZnO-MoO3in-MgO, C, ZnO, MoO3And the doping molar ratio of MgO is 7: 1: 1: 1, the preparation method is the same as that of example 1, and the waste sponge foam carbon-based composite adsorbing material C-ZnO-MoO is obtained3-MgO(7:1:1:1)。
Example 3
In this example, the prepared waste sponge carbon-based composite adsorbing material C-ZnO-MoO3in-MgO, C, ZnO, MoO3And the doping molar ratio of MgO is 7: 1: 1: 2, the preparation method is the same as that of the example 1, and the waste sponge foam carbon-based composite adsorbing material C-ZnO-MoO is obtained3-MgO(7:1:1:2)。
Example 4
In this example, the prepared waste sponge carbon-based composite adsorbing material C-ZnO-MoO3in-MgO, C, ZnO, MoO3And the doping molar ratio of MgO is 7: 1: 2: 1, the preparation method is the same as that of example 1, and the waste sponge foam carbon-based composite adsorbing material C-ZnO-MoO is obtained3-MgO(7:1:2:1)。
Example 5
In this example, the prepared waste sponge carbon-based composite adsorbing material C-ZnO-MoO3in-MgO, C, ZnO, MoO3And the doping molar ratio of MgO is 7: 2: 1: 1, the preparation method is the same as that of example 1, and the waste sponge foam carbon-based composite adsorbing material C-ZnO-MoO is obtained3-MgO(7:2:1:1)。
Example 6
In this example, the prepared waste sponge carbon-based composite adsorbing material C-ZnO-MoO3in-MgO, C, ZnO, MoO3And the doping molar ratio of MgO is 7: 2: 1: 2, the preparation method is the same as that of the example 1, and the waste sponge foam carbon-based composite adsorbing material C-ZnO-MoO is obtained3-MgO(7:2:1:2)。
Example 7
In this example, the prepared waste sponge carbon-based composite adsorbing material C-ZnO-MoO3in-MgO, C, ZnO, MoO3And the doping molar ratio of MgO is 7: 2: 2: 1, the preparation method is the same as that of example 1, and the waste sponge foam carbon-based composite adsorbing material C-ZnO-MoO is obtained3-MgO(7:2:2:1)。
Example 8
In this example, zinc nitrate and magnesium oxide were not added, and the prepared waste sponge carbon-based composite adsorption material C-MoO3C, MoO3Is 7: 1, the other preparation methods are the same as example 1, and the waste sponge foam carbon-based composite adsorption material C-MoO is obtained3(7:1)。
Example 9
In this embodiment, ammonium molybdate and magnesium oxide are not added, and in the prepared waste sponge carbon-based composite adsorbing material C-ZnO, the doping molar ratio of C, ZnO is 7: and 2, obtaining the waste sponge foam carbon-based composite adsorbing material C-ZnO (7: 2) by the same preparation method as the example 1.
FIG. 1 is an XRD pattern of each series of composite adsorbents prepared in examples 1 to 7. As can be seen from FIG. 1, the diffraction intensity peak and C-ZnO-MoO of the sample3MgO basically corresponds to MgO. The XRD diffraction pattern has obvious MgO, ZnO and MoO3The diffraction peaks are relatively sharp, which shows that the synthesized composite adsorbent is in phase with the experimental design target waste sponge carbon-based composite adsorption material C-ZnO-MoO3MgO inosculation.
Fig. 2 is SEM images of low, medium, and high magnification in order of the composite adsorbent prepared in example 1. As can be seen from FIG. 2, example 1 obtained a spent sponge carbon-based composite adsorbent C-ZnO-MoO having a mixed structure of a spherical shape and a rod shape3MgO, the channel structure is obvious, the microstructure of the composite material presents multi-level and multi-scale, and the size range is 400nm-Between 3 um.
FIG. 3 shows the influence of a series of waste sponge carbon-based composite adsorbent materials composed of different composite proportions on the removal rate of chromium-containing sewage solution under the sunlight condition. Wherein the dosage of the sample material is 30mg, the adsorption time is 70min, the volume of the chromium-containing sewage solution is 100mL, and the initial concentration is 80 mg/L. As can be seen from FIG. 3, the waste sponge carbon-based composite adsorbing material C-ZnO-MoO prepared in example 13The adsorption effect of MgO (7: 1: 2: 2) is the best, the removal rate reaches 99.5%, and the adsorption removal effect of all series products with different compositions is the better along with the time.
FIG. 4 is a curve of adsorption capacity, removal time and substance composition of a series of waste sponge carbon-based composite materials with different compositions on a chromium (3-valent chromium and 6-valent chromium) containing solution under a sunlight condition. Wherein the dosage of the sample material is 60mg, the adsorption time is 140min, and the volume of the chromium-containing (3-valent chromium and 6-valent chromium) solution is 500 mL. As can be seen from FIG. 4, the waste sponge carbon-based composite adsorbing material C-ZnO-MoO prepared in example 13The best adsorption effect of MgO (7: 1: 2: 2), the adsorption amount reaches 231mg/g, and the adsorption removal effect of all series products with different compositions is better along with the prolonging of time, and the adsorption amount basically reaches stability along with the increasing of time after the adsorption time reaches 60 minutes, which shows that the adsorption process is mainly completed within 60 minutes, and the adsorption effect is good.
Experiments show that the prepared target product achieves the expected target of experimental design, and the prepared waste sponge foam carbon-based composite adsorption material C-ZnO-MoO is proved3the-MgO can be used for the environmental treatment of industrial sewage and wastewater containing chromium heavy metal solution.
The foregoing is merely exemplary and illustrative of the principles of the present invention and various modifications, additions and substitutions of the specific embodiments described herein may be made by those skilled in the art without departing from the principles of the present invention or exceeding the scope of the claims set forth herein.
Claims (6)
1. Abandonment sponge bubbleThe preparation method of the foam carbon-based composite adsorption material is characterized by firstly dissolving zinc salt, magnesium salt and molybdenum salt in water, adding a proper amount of dilute nitric acid, uniformly mixing, then adding the waste sponge foam carbon, uniformly mixing, and then carrying out hydrothermal impregnation reaction in an ultrasonic reactor to prepare the waste sponge foam carbon-based composite adsorption material C-ZnO-MoO3-MgO。
2. The preparation method according to claim 1, comprising the following steps:
1) weighing zinc nitrate, magnesium oxide and ammonium molybdate, adding the zinc nitrate, the magnesium oxide and the ammonium molybdate into a beaker, dissolving the zinc nitrate, the magnesium oxide and the ammonium molybdate by using distilled water and dilute nitric acid, then adding the waste sponge carbon foam, adding ammonia water to adjust the pH value of the solution to 6-12, and fully stirring;
2) placing the mixture into an ultrasonic reactor, placing a beaker into hydrothermal impregnation, and reacting for 30min at 85 ℃, wherein the ultrasonic starting power is 1200W;
3) after the reaction is finished, drying the obtained product at 120 ℃ to obtain the waste sponge carbon-based composite adsorbing material C-ZnO-MoO3-MgO。
3. The method of manufacturing as claimed in claim 1 or 2, wherein the method of manufacturing the waste sponge carbon foam is: and (2) placing the waste sponge and the waste foamed plastic in inert gas for high-temperature carbonization, then cleaning and drying, and finally activating and forming pores in the inert atmosphere to obtain the waste sponge foamed carbon material.
4. The preparation method according to claim 2, wherein the waste sponge foam carbon-based composite adsorbing material C-ZnO-MoO is obtained3-C, ZnO and MoO in MgO3And the doping molar ratio of MgO is 7: 1-2: 1-2: 1 to 2.
5. The preparation method according to claim 4, wherein the waste sponge foam carbon-based composite adsorbing material C-ZnO-MoO is obtained3-C, ZnO and MoO in MgO3And the doping molar ratio of MgO is 7: 1: 2: 2.
6. the application of the waste sponge foam carbon-based composite adsorption material prepared by the method of any one of claims 1 to 5 in adsorption removal of chromium in wastewater.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202011048024.6A CN112156754B (en) | 2020-09-29 | 2020-09-29 | Preparation method of waste sponge foam carbon-based composite adsorption material and application of waste sponge foam carbon-based composite adsorption material in adsorption removal of chromium in wastewater |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202011048024.6A CN112156754B (en) | 2020-09-29 | 2020-09-29 | Preparation method of waste sponge foam carbon-based composite adsorption material and application of waste sponge foam carbon-based composite adsorption material in adsorption removal of chromium in wastewater |
Publications (2)
Publication Number | Publication Date |
---|---|
CN112156754A true CN112156754A (en) | 2021-01-01 |
CN112156754B CN112156754B (en) | 2022-10-18 |
Family
ID=73860634
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN202011048024.6A Active CN112156754B (en) | 2020-09-29 | 2020-09-29 | Preparation method of waste sponge foam carbon-based composite adsorption material and application of waste sponge foam carbon-based composite adsorption material in adsorption removal of chromium in wastewater |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN112156754B (en) |
Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0037537A1 (en) * | 1980-04-03 | 1981-10-14 | Fraunhofer-Gesellschaft Zur Förderung Der Angewandten Forschung E.V. | Process for the manufacture of highly specific active char |
US5000858A (en) * | 1989-07-17 | 1991-03-19 | Coltec Industries Inc. | Method for removing hexavalent chromium from water |
CN103754869A (en) * | 2014-01-02 | 2014-04-30 | 上海大学 | Method for preparing high-quality active carbon by adopting waste polyurethane foamed plastic |
CN107398252A (en) * | 2017-08-25 | 2017-11-28 | 内江师范学院 | The method for preparing the compound sorbing material of MgO/ charcoals using lemon dregs and magnesium slag one-step method |
CN110898809A (en) * | 2019-12-20 | 2020-03-24 | 北京化工大学 | Mechanochemical preparation method of alkyne carbon-transition metal oxide composite material and application thereof in heavy metal ion adsorption |
CN111097384A (en) * | 2019-12-16 | 2020-05-05 | 合肥学院 | C-Bi2O3-CuO-ZnO adsorption material and preparation method and application thereof |
CN111530420A (en) * | 2020-05-13 | 2020-08-14 | 合肥学院 | Preparation method of porous carbon-based composite adsorbing material for agricultural and forestry waste |
CN111530422A (en) * | 2020-05-14 | 2020-08-14 | 合肥学院 | Method for preparing modified carbon composite adsorbent by using carbon-containing high-molecular industrial wastes |
-
2020
- 2020-09-29 CN CN202011048024.6A patent/CN112156754B/en active Active
Patent Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0037537A1 (en) * | 1980-04-03 | 1981-10-14 | Fraunhofer-Gesellschaft Zur Förderung Der Angewandten Forschung E.V. | Process for the manufacture of highly specific active char |
US5000858A (en) * | 1989-07-17 | 1991-03-19 | Coltec Industries Inc. | Method for removing hexavalent chromium from water |
CN103754869A (en) * | 2014-01-02 | 2014-04-30 | 上海大学 | Method for preparing high-quality active carbon by adopting waste polyurethane foamed plastic |
CN107398252A (en) * | 2017-08-25 | 2017-11-28 | 内江师范学院 | The method for preparing the compound sorbing material of MgO/ charcoals using lemon dregs and magnesium slag one-step method |
CN111097384A (en) * | 2019-12-16 | 2020-05-05 | 合肥学院 | C-Bi2O3-CuO-ZnO adsorption material and preparation method and application thereof |
CN110898809A (en) * | 2019-12-20 | 2020-03-24 | 北京化工大学 | Mechanochemical preparation method of alkyne carbon-transition metal oxide composite material and application thereof in heavy metal ion adsorption |
CN111530420A (en) * | 2020-05-13 | 2020-08-14 | 合肥学院 | Preparation method of porous carbon-based composite adsorbing material for agricultural and forestry waste |
CN111530422A (en) * | 2020-05-14 | 2020-08-14 | 合肥学院 | Method for preparing modified carbon composite adsorbent by using carbon-containing high-molecular industrial wastes |
Also Published As
Publication number | Publication date |
---|---|
CN112156754B (en) | 2022-10-18 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Huang et al. | Heavy metal ion removal of wastewater by zeolite-imidazolate frameworks | |
CN111203180B (en) | Magnetic biochar composite adsorbent and preparation method and application thereof | |
CN110102260A (en) | A kind of iron and manganese oxides-charcoal composite material and preparation method and application | |
CN111111612B (en) | Preparation and use method of magnetic porous biochar for removing chromium in water | |
WO2014161705A1 (en) | Activated carbon with a special finishing, production and use thereof | |
CN106902742A (en) | A kind of porous activated carbon supported magnesium oxide composite and its preparation method and application | |
CN102784624A (en) | Preparation method and use of carbon coated magnetic adsorption material | |
CN107349932B (en) | Method for preparing nickel-based catalyst by adsorbing nickel-plating wastewater by using activated carbon | |
Nian et al. | Preparation of a pure ZIF-67 membrane by self-conversion of cobalt carbonate hydroxide nanowires for H 2 separation | |
CN110683540A (en) | Nitrogen-rich hierarchical pore biomass charcoal and application thereof | |
CN111001390A (en) | Composite metal organic adsorption material and preparation method thereof | |
CN111151221A (en) | Macroporous biochar-based hybrid material for ultra-fast removal of heavy metals in water body and preparation method and application thereof | |
CN112316903A (en) | One-step solvothermal preparation method and application of carbon fiber @ MAL hydrotalcite composite film | |
CN102500167B (en) | Core-shell structure composite filter material for water treatment and preparation method thereof | |
CN111013543B (en) | Porous CuBTC ligand assembly synthesis method | |
CN112156754B (en) | Preparation method of waste sponge foam carbon-based composite adsorption material and application of waste sponge foam carbon-based composite adsorption material in adsorption removal of chromium in wastewater | |
Sheng et al. | Rationally designed calcium carbonate multifunctional trap for contaminants adsorption | |
CN113000052B (en) | Wet oxidation catalyst and preparation method and application thereof | |
WO2024198490A1 (en) | Multivalent manganese oxide filler and preparation method therefor and use thereof | |
CN110773200A (en) | Preparation method of biochar-supported iron sulfide Fenton catalyst | |
CN114713260B (en) | N, S Co-doped Co/CoO/Co 9 S 8 Nano catalyst @ NSOC, preparation method and application thereof | |
CN112755953B (en) | Adsorbent for removing nitrogen oxides in fluid, preparation method and application | |
CN110563094B (en) | Application of sulfonated carbon cloth electrode | |
CN109796002B (en) | Synthesis method of metal modified sulfonic mesoporous carbon material | |
Zhang et al. | Carbon-supported Ni and MoO 2 nanoparticles with Fe 3 O 4 cores as a protein adsorbent |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
PB01 | Publication | ||
SE01 | Entry into force of request for substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
GR01 | Patent grant | ||
GR01 | Patent grant |