CN107199013B - A kind of preparation method of magnetic bio carbon-supported nanometer iron - Google Patents

A kind of preparation method of magnetic bio carbon-supported nanometer iron Download PDF

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CN107199013B
CN107199013B CN201710485749.3A CN201710485749A CN107199013B CN 107199013 B CN107199013 B CN 107199013B CN 201710485749 A CN201710485749 A CN 201710485749A CN 107199013 B CN107199013 B CN 107199013B
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charcoal
iron
magnetic
preparation
tea polyphenols
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王向华
王新宇
吴海锁
李冰
吴剑
谢祥峰
邓林
谢飞
黄洁慧
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Jiangsu Environmental Protection Industry Technology Research Institute Co Ltd
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    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J20/00Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
    • B01J20/02Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material
    • B01J20/20Solid 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
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J20/00Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
    • B01J20/02Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material
    • B01J20/0203Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material comprising compounds of metals not provided for in B01J20/04
    • B01J20/0225Compounds of Fe, Ru, Os, Co, Rh, Ir, Ni, Pd, Pt
    • B01J20/0229Compounds of Fe
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J20/00Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
    • B01J20/28Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof characterised by their form or physical properties
    • B01J20/28002Solid 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 physical properties
    • B01J20/28009Magnetic properties
    • 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
    • C02F1/28Treatment of water, waste water, or sewage by sorption
    • C02F1/281Treatment of water, waste water, or sewage by sorption using inorganic sorbents
    • 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
    • C02F2101/22Chromium or chromium compounds, e.g. chromates

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Abstract

The invention discloses a kind of preparation method of magnetic bio carbon-supported nanometer iron, including:(1) modification biological charcoal;(2) ultrasonic immersing method load molysite;(3) Tea Polyphenols is coated;(4) liquid phase reduction prepares charcoal and carries Nanoscale Iron;(5) magnetic method sub-argument goes out magnetic bio carbon-supported nanometer iron;Wherein, the purpose for the saturation magnetization for controlling preparation-obtained magnetic bio carbon-supported nanometer iron is reached by the molar concentration of Tea Polyphenols solution in rate-determining steps (3).Preparation method provided by the invention, the magnetic bio carbon-supported nanometer iron of different magnetic can be prepared, by controlling the molar concentration of Tea Polyphenols solution so as to suitable for different wastewater treatment environment;And the magnetic bio carbon-supported nanometer iron property that the present invention prepares is stable, and reactivity is higher, can quickly remove the Cr VI in waste water, and be easy to separate with water body.

Description

A kind of preparation method of magnetic bio carbon-supported nanometer iron
Technical field
The invention belongs to Material Field, and in particular to a kind of preparation method of magnetic bio carbon-supported nanometer iron.
Background technology
Cr VI is a kind of poisonous heavy metal, and chromyl waste water is mainly derived from plating, metallurgy, mining, printing and dyeing Deng industry.For trivalent chromium, Cr VI toxicity is very big, is more than 100 times of trivalent chromium, and is easy to be absorbed by the body, Human body can be invaded by alimentary canal, respiratory tract, skin and mucous membrane and can be accumulated in human body cohesion collection, it is excessive when containing in water Cr VI when, have stronger lethal effect to aquatile, Cr VI is classified as among priority pollutant list by China. For the processing method containing hexavalent chromium wastewater, mainly including chemical reduction method, electrochemical process, absorption method, ion-exchange etc., Industrially chemical reduction method and absorption method are the more conventional methods of processing waste water containing chrome, by hexavalent chrome reduction into trivalent chromium, Handled, heavy metal precipitation is got off, to remove the chromium ion in water body by adding precipitating reagent or flocculant etc. again.But this Kind method easily produces substantial amounts of sludge, and the processing in these sludge later stages needs to solve the problems, such as with disposal and one.
In the last few years, zeroth order Nanoscale Iron is as reducing agent, removes the Cr VI in water body and receives and widely grinds both at home and abroad Study carefully.Zeroth order Nanoscale Iron has the advantages that particle diameter is small, specific surface area is big, surface-active is high, reducing power is strong, still, zeroth order nanometer Iron is due to stronger activity, it is easy to and react and inactivate with oxygen in atmosphere, and due to huge ratio Surface area, easily occur to reunite and inactivate in water body.To solve existing problem above when zeroth order Nanoscale Iron removes Cr VI, Zeroth order Nanoscale Iron-biological carbon composite using charcoal as carrier is gradually concerned by people.Using charcoal as carrier, The decentralization of metal nanoparticle can be improved, reduces the reunion of metal nanoparticle, keeps the activity of metal nanoparticle.Separately Outside, the magnetic zeroth order Nanoscale Iron-biological carbon composite prepared with reference to magnetic separation technique adds in the presence of magnetic field outside can be with The quick separating of biological adsorption agent is realized, sewage disposal efficiency is improved, is a kind of new sorbing material.Due to magnetic material Characteristic, in its reduction, after adsorbing heavy metal, heavy metal can thoroughly be separated with water body by magnetic separation technique, and And magnetic material can also be recycled, cost is reduced.
Application of the magnetic separation technique in water process is more and more important, but currently, also it there are problems that, such as, Many magnetic materials have stronger saturation magnetization, and still, while its remanent magnetism or coercivity are also larger, and water body passes through magnetic After the processing of field, even if there be no externally-applied magnetic field, due to magnetic attraction between material be present so that it is easy to reunite between material, than Surface area is reduced, and it is active in itself to influence material.The small material of some saturation magnetizations, its remanent magnetism also very little, close to superparamagnetic State, in the case of no externally-applied magnetic field, will not have magnetic or magnetic smaller, compared with the Van der Waals force between material, Its size can be ignored, and what material can be stablized is dispersed in water body, its reactivity is kept, so in different water environments In, it should according to specific circumstances, handled using suitable magnetic material.
Patent CN106362690 discloses a kind of magnetic bio charcoal sorbing material and preparation method thereof, by preparing biology Charcoal, prepare ferric iron precursor liquid, solvent thermal reaction obtains magnetic bio charcoal sorbing material.Patent CN105664854 discloses one The preparation method of kind charcoal load Nanoscale Iron nickel bimetal material.At present, prior art also not publicly being capable of controlled material magnetic Property strong and weak magnetic bio charcoal sorbing material preparation method.
The content of the invention
The technical problem to be solved in the present invention is to provide a kind of preparation method of magnetic bio carbon-supported nanometer iron, this method energy The controllable of magnetic is enough realized, the magnetic bio charcoal of different magnetic can be prepared by controlling the molar concentration of Tea Polyphenols solution Nanoscale Iron is carried, so as to suitable for different wastewater treatment environment;The magnetic bio carbon-supported nanometer iron material being prepared can lead to The abundant hydroxyl in surface, carboxyl functional group are crossed, complexing occurs with heavy metal ion, by complex in material Surface.Magnetic bio carbon-supported nanometer iron material property stable in the air is high, when handling heavy metal water body, will not reunite Phenomenon, there is stronger reactivity, and can thoroughly be removed the heavy metal in water body by magnetic separation technique.
In order to solve the above technical problems, the technical solution adopted by the present invention is as follows:
A kind of preparation method of magnetic bio carbon-supported nanometer iron, including:(1) modification biological charcoal;(2) ultrasonic immersing method loads Molysite;(3) Tea Polyphenols is coated;(4) liquid phase reduction prepares charcoal and carries Nanoscale Iron;(5) magnetic method sub-argument goes out magnetic bio charcoal Carry Nanoscale Iron;Wherein, the preparation-obtained magnetic green of control is reached by the molar concentration of Tea Polyphenols solution in rate-determining steps (3) The purpose of the saturation magnetization of thing carbon-supported nanometer iron.
This method specifically includes following steps:
(1) modification of charcoal:Charcoal is taken, adds concentrated nitric acid, immersion filtering, and is rinsed to pH with water and no longer changed, Dry, obtain the charcoal of Nitric Acid Modified;
(2) load of molysite:Water-soluble trivalent ferric salt solution is prepared, adds the biology for the modification that step (1) is prepared Charcoal, ultrasonic immersing, filter, drying, then weigh the sample after drying, it is warming up to 200 under inert atmosphere or nitrogen atmosphere~ 250 DEG C, calcining, obtain the charcoal for the load molysite that theoretical duty iron is 28%~32%, wherein theoretical duty iron Calculation formula is (quality of the quality of iron ion/modification biological charcoal) × 100%;
(3) 0.002~0.008mol/L Tea Polyphenols solution is prepared, is passed through inert gas or nitrogen deoxygenation, adds step (2) The ratio between the charcoal for the load molysite being prepared, the quality of the load molysite charcoal of addition and volume of Tea Polyphenols solution are 1:40~1:50g/mL, under inert gas or nitrogen atmosphere, stirring;
(4) sodium borohydride solution is prepared, is added into step (3) resulting solution, is continued to stir, obtain biological carbon-supported nanometer Iron slurries;
(5) go out magnetic bio carbon-supported nanometer iron with magnetic method sub-argument, wash, dry;
Reach the preparation-obtained magnetic bio charcoal of control by the molar concentration of Tea Polyphenols solution in rate-determining steps (3) to carry The purpose of the saturation magnetization of Nanoscale Iron,
When the concentration of Tea Polyphenols solution is more than or equal to 0.002mol/L, less than 0.004mol/L when, the magnetic that is prepared The saturation magnetization that charcoal carries Nanoscale Iron is less than or equal to 72.9emu/g, more than 36.5emu/g;
When the concentration of Tea Polyphenols solution is more than or equal to 0.004mol/L, less than 0.006mol/L when, the magnetic that is prepared The saturation magnetization that charcoal carries Nanoscale Iron is less than or equal to 36.5emu/g, more than 26.6emu/g;
When Tea Polyphenols solution concentration be more than or equal to 0.006mol/L, less than or equal to 0.008mol/L when, be prepared The saturation magnetization of magnetic bio carbon-supported nanometer iron is less than or equal to 26.6emu/g, more than or equal to 5.2emu/g.
In step (3), the molar concentration of Tea Polyphenols solution is different, and magnetic strength that its final obtained material has is not yet Together.Its relatively high magnetism when the molar concentration of Tea Polyphenols solution is 0.002mol/L, magnetic is weaker when concentration is 0.008mol/L.
It should be noted that the molecular weight Mr=281.36 of Tea Polyphenols of the present invention.
In step (1), the mass ratio of charcoal and concentrated nitric acid is 1:10~1:70.
In step (1), charcoal is weighed, adds concentrated nitric acid, after soaking 12h, centrifugal filtration, and with deionized water rinsing extremely PH no longer changes (pH value is about 5-6), 70 DEG C of dryings, obtains the charcoal of Nitric Acid Modified.
In step (2), the theoretical duty iron of the charcoal for the load molysite being prepared is 30%.
In step (2), water-soluble trivalent ferric salt FeCl3、FeCl3·6H2O、Fe2(SO4)3In one or more, it is excellent Elect FeCl as3;Drying temperature is 60~105 DEG C, preferably 70 DEG C.Indifferent gas is the one or more in helium, neon, argon, krypton, xenon, It is preferred that argon gas.
In step (2), water-soluble trivalent ferric salt solution is prepared, adds the charcoal for the modification that step (1) is prepared, so Ultrasonic immersing 8h afterwards, filter, 70 DEG C of drying, then weigh the sample after drying in quartz boat, quartz boat is placed in tube furnace, Under argon atmosphere, 200 DEG C are risen to 5 DEG C/min heating rate, calcines 3h, obtain loading the charcoal of molysite.
In step (3), the ratio between the quality of the load molysite charcoal of addition and the volume of Tea Polyphenols solution are 1:45g/mL. Indifferent gas is the one or more in helium, neon, argon, krypton, xenon.
In step (4), the molar concentration of sodium borohydride solution is 0.005~0.014mol/L, preferably 0.007mol/L; The volume ratio of Tea Polyphenols solution of the sodium borohydride solution of preparation with being prepared in step (3) is 1:6~1:10.Feed way can be with It is by constant pressure funnel dropwise addition or other conventional feed way.
In step (5), go out magnetic bio carbon-supported nanometer iron with magnetic method sub-argument, with distillation water washing three times, vacuum drying It can obtain charcoal and carry nano-iron material.Described magnetic method can be that magnet is placed in into container lower end, static a period of time Afterwards, supernatant liquid is discharged.
The magnetic bio carbon-supported nanometer iron that above-mentioned preparation method is prepared is within protection scope of the present invention.
Above-mentioned magnetic bio carbon-supported nanometer iron applying in protection scope of the present invention in the Cr VI in removing water body Within.
The magnetic bio carbon-supported nanometer iron 1g that the present invention is prepared, can apply to hexavalent chromium concentration is below 60mg/L 100mL waste water, the Cr VI in the waste water can be removed after 2d completely.
Beneficial effect:
(1) preparation method provided by the invention according to the power of required magnetic, can prepare the magnetic green of different magnetic Thing carbon-supported nanometer iron, so as to suitable for different wastewater treatment environment.
(2) the magnetic bio carbon-supported nanometer iron that the present invention prepares, property is stable, and spontaneous combustion will not occur in atmosphere, and Nanoscale Iron good dispersion, reactivity is higher, can quickly remove the Cr VI in waste water.
(3) the magnetic bio carbon-supported nanometer iron that the present invention prepares, is respectively provided with magnetic, passes through Magneto separate skill afterwards before the reaction Art, it is easy to separate with water body so that the separation of the material becomes simple possible.
Brief description of the drawings
Fig. 1 is the Technology Roadmap that synthesizing magnetic charcoal carries Nanoscale Iron;
Fig. 2 is that (SEM, left figure resolution ratio 100nm, right figure resolution ratio are 1 μ to magnetic bio carbon-supported nanometer iron scanning electron microscope (SEM) photograph m);
Fig. 3 is charcoal, modification biological charcoal, magnetic bio carbon-supported nanometer iron Fourier infrared spectrum figure (FTIR);
Fig. 4 is charcoal, modification biological charcoal, magnetic bio carbon-supported nanometer iron X-ray diffractogram (XRD);
Fig. 5 is the magnetic bio carbon-supported nanometer iron UV-Vis scans figure (UV-VIS) of different Tea Polyphenols cladding concentration;
Fig. 6 is the hysteresis curve (M-H) of the magnetic bio carbon-supported nanometer iron of different Tea Polyphenols cladding concentration;
Fig. 7 is the graph of a relation between Tea Polyphenols cladding concentration and saturation magnetization;
Fig. 8 is removal effect figure of the different Tea Polyphenols cladding concentration for Cr VI;
Fig. 9 is the graph of a relation between hexavalent chromium removal rate after hexavalent chromium solution initial concentration and 2d, 5d, 10d.
Embodiment
According to following embodiments, the present invention may be better understood.It is however, as it will be easily appreciated by one skilled in the art that real Apply the content described by example and be merely to illustrate the present invention, without should be also without limitation on sheet described in detail in claims Invention.
In addition to being defined, technical term used has universal with those skilled in the art of the invention in following examples The identical meanings of understanding.Test reagent used, is routine biochemistry reagent unless otherwise specified in following examples;It is described Experimental method, it is conventional method unless otherwise specified.
The present invention is described in detail with reference to embodiment.
The preparation of embodiment 1, magnetic bio carbon-supported nanometer iron
A kind of preparation method of magnetic bio carbon-supported nanometer iron, comprises the following steps (as shown in Figure 1):
(1) modification of charcoal:2g charcoal is weighed in conical flask, adds 100mL concentrated nitric acid, after soaking 12h, Centrifugal filtration, and no longer change (pH value is about 5-6) with deionized water rinsing to pH, 70 DEG C are dried overnight, you can obtain nitric acid Modified charcoal.
(2) load of molysite:Prepare Fe3+Ion molar concentration is 0.108mol/L ferric chloride solution, takes 50mL in burning In cup, and the modification biological charcoal being prepared is added in 1g above-mentioned (1), then ultrasonic immersing 8h, filtered, 70 DEG C dried At night, the sample after a certain amount of drying is then weighed in quartz boat, quartz boat is placed in tube furnace, under argon atmosphere, with 5 DEG C/min heating rate rises to 200 DEG C, 3h is calcined, obtains loading the charcoal of molysite.
(3) compound concentration is 0.002mol/L Tea Polyphenols (Mr=281.36) solution 45mL, is passed through nitrogen deoxygenation 40min, it is placed in three-necked flask, centre insertion agitating paddle, the load molysite that then addition 1g above-mentioned (2) are prepared Charcoal, under nitrogen atmosphere, 30min is stirred with 1000r/min.
(4) 0.007mol/L sodium borohydride solution 5mL is prepared, (3) resulting solution is then added dropwise to by constant pressure funnel In, after being added dropwise to complete, continue to stir 30min with 1000r/min speed, you can obtain the slurries that charcoal carries Nanoscale Iron.
(5) gone out with magnetic method (magnet being placed in into there-necked flask lower end, after static a period of time, supernatant liquid is discharged) sub-argument The magnetic bio carbon-supported nanometer iron, with distillation water washing three times, vacuum drying can obtain magnetic bio carbon-supported nanometer iron.
Experimental result:
(1) Fig. 2 is scanning electron microscope (SEM) photograph (SEM, the left figure resolution for the magnetic bio carbon-supported nanometer iron prepared in embodiment 1 Rate 100nm, right figure resolution ratio are 1 μm).It can be seen that charcoal has an abundant pore structure, thus its have compared with Strong adsorption capacity, Nanoscale Iron are supported on charcoal, and its size is in 70nm or so, therefore the magnetic green that the present invention is prepared Thing carbon-supported nanometer iron has great specific surface area and reactivity.
(2) Fig. 3 is charcoal, modification biological charcoal, magnetic bio carbon-supported nanometer iron Fourier infrared spectrum figure.Can from figure To find out, modification biological charcoal is compared with the infrared figure of charcoal:In 3600cm-1There is stronger sharp peak at left and right, this is freely Hydroxyl O-H stretching vibration absworption peak;In 1720cm-1There is the weak peak of C=O stretching vibrations at left and right, in 1320cm-1At left and right There are C-O stretching vibration absworption peaks, after Nitric Acid Modified, biological carbon surface has the hydrophilic radicals such as carboxy hydroxy.Magnetic green The infrared spectrum of thing carbon-supported nanometer iron is compared with Nitric Acid Modified charcoal:In 550cm-1, strong peak disappears, and may be iron and charcoal The result of surface functional group interaction, also there are some new peaks to occur, in 3000cm-1At left and right, there is the C-H on phenyl ring to stretch Vibration, 1600~1450cm-1C=C skeletal vibrations, and 880~680cm-1There is more peak at place, is C-H out-of-plane bending vibrations, Therefore phenyl ring being present, this is the functional group in Tea Polyphenols, illustrates that Tea Polyphenols has successfully been coated to the surface of charcoal.
(3) Fig. 4 is charcoal, modification biological charcoal, magnetic bio carbon-supported nanometer iron X-ray diffractogram (XRD).Can from figure To find out, unmodified charcoal is similar with modified charcoal image, there is the wide diffraction maximum diffused at 23 ° or so, this It is the diffraction maximum of charcoal, and shows that charcoal is not crystal.The magnetic bio carbon-supported nanometer iron material of synthesis is at 44.75 ° There is obvious diffraction maximum, corresponding to body-centred cubic α-Fe 110 diffraction, while also exist at 65.16 ° body-centred cubic α- Fe 200 diffraction, it is known that, final obtained material is mutually present with the thing of α-Fe simple substance.
(4) Fig. 6 is that different Tea Polyphenols coat removal effect figure of the concentration for Cr VI.Wherein prepared by embodiment 1 The charcoal of 0.002mol/L Tea Polyphenols cladding carries Nanoscale Iron can be by concentration in 20mg/L hexavalent chromium solution after 1h Cr VI remove completely.
The preparation of embodiment 2, magnetic bio carbon-supported nanometer iron
A kind of preparation method of magnetic bio carbon-supported nanometer iron, comprises the following steps:
(1) modification of charcoal:2g charcoal is weighed in conical flask, adds 20mL concentrated nitric acid, after soaking 12h, Centrifugal filtration, and no longer change (pH value is about 5-6) with deionized water rinsing to pH, 70 DEG C are dried overnight, you can obtain nitric acid Modified charcoal.
(2) load of molysite:Prepare Fe3+Ion molar concentration is 0.101mol/L Fe2(SO4)3Solution, take 50mL in In beaker, and the modification biological charcoal being prepared is added in 1g above-mentioned (1), then ultrasonic immersing 8h, filtered, 70 DEG C dried At night, the sample after a certain amount of drying is then weighed in quartz boat, quartz boat is placed in tube furnace, under argon atmosphere, with 5 DEG C/min heating rate rises to 250 DEG C, 3h is calcined, obtains loading the charcoal of molysite.
(3) compound concentration is 0.002mol/L Tea Polyphenols (Mr=281.36) solution 50mL, is passed through nitrogen deoxygenation 20min, it is placed in three-necked flask, centre insertion agitating paddle, the load molysite that then addition 1g above-mentioned (2) are prepared Charcoal, under nitrogen atmosphere, 30min is stirred with 1000r/min.
(4) 0.014mol/L sodium borohydride solution 5mL is prepared, (3) resulting solution is then added dropwise to by constant pressure funnel In, after being added dropwise to complete, continue to stir 30min with 1000r/min speed, you can obtain the slurries that charcoal carries Nanoscale Iron.
(5) the magnetic bio carbon-supported nanometer iron is gone out with magnetic method sub-argument, with distillation water washing three times, vacuum drying can obtain To magnetic bio carbon-supported nanometer iron.
The 2h clearances of the Cr VI for the magnetic bio carbon-supported nanometer iron being prepared are 100%.
The preparation of embodiment 3, magnetic bio carbon-supported nanometer iron
A kind of preparation method of magnetic bio carbon-supported nanometer iron, comprises the following steps:
(1) modification of charcoal:2g charcoal is weighed in conical flask, adds 140mL concentrated nitric acid, after soaking 12h, Centrifugal filtration, and no longer change (pH value is about 5-6) with deionized water rinsing to pH, 70 DEG C are dried overnight, you can obtain nitric acid Modified charcoal.
(2) load of molysite:Prepare Fe3+Ion molar concentration is 0.115mol/L FeCl3·6H2O solution, takes 50mL In beaker, and the modification biological charcoal being prepared is added in 1g above-mentioned (1), then ultrasonic immersing 8h, filtered, 70 DEG C of drying Overnight, the sample after a certain amount of drying is then weighed in quartz boat, quartz boat is placed in tube furnace, under argon atmosphere, with 5 DEG C/min heating rate rises to 200 DEG C, 3h is calcined, obtains loading the charcoal of molysite.
(3) compound concentration is 0.002mol/L Tea Polyphenols (Mr=281.36) solution 40mL, is passed through nitrogen deoxygenation 40min, it is placed in three-necked flask, centre insertion agitating paddle, the load molysite that then addition 1g above-mentioned (2) are prepared Charcoal, under nitrogen atmosphere, 30min is stirred with 1000r/min.
(4) 0.005mol/L sodium borohydride solution 5mL is prepared, (3) resulting solution is then added dropwise to by constant pressure funnel In, after being added dropwise to complete, continue to stir 30min with 1000r/min speed, you can obtain the slurries that charcoal carries Nanoscale Iron.
(5) the magnetic bio carbon-supported nanometer iron is gone out with magnetic method sub-argument, with distillation water washing three times, vacuum drying can obtain To magnetic bio carbon-supported nanometer iron.
The 2h clearances of the Cr VI for the magnetic bio carbon-supported nanometer iron being prepared are 100%.
Embodiment 4, choice of parameters experiment
According to the preparation method of embodiment 1, change important two preparation parameter in preparation process:Calcining heat and tea The cladding concentration of polyphenol, calcining heat is prepared respectively as 150 DEG C, 200 DEG C, 250 DEG C, 300 DEG C, 500 DEG C, 600 DEG C, and tea is more Phenol cladding concentration is respectively 0mol/L, 0.002mol/L, 0.004mol/L, 0.006mol/L, 0.008mol/L, 0.01mol/L, 0.012mol/L magnetic bio carbon-supported nanometer iron, and pass through the iron load capacity of magnetic bio carbon-supported nanometer iron and 100mL 20mg/L hexavalent chromium removals are tested to select optimal parameter.
The assay method of iron load capacity is:It is 1 that concentrated nitric acid, which is configured, with concentrated sulfuric acid volume ratio:3 nitration mixture, as digestion solution, 80ml is taken in digestion tube;0.1g magnetic bio carbon-supported nanometer iron is weighed, adds in digestion tube, is cleared up at a temperature of 150 DEG C Clarified to solution, then with atomic absorption spectrophotometry, measure the content of the iron in digestion solution.Experimental result is shown in Table 1, its In, the Nanoscale Iron load capacity described in the present embodiment refers to Nanoscale Iron actual negative carrying capacity, is (quality/magnetic of zeroth order Nanoscale Iron Charcoal carries Nanoscale Iron gross mass) × 100%.
Table 1
From result, important two preparation parameters change and material overall performance can be had a certain impact, When calcining heat is too low (200 DEG C of <), its Nanoscale Iron load capacity can be very low, when its reason is that calcining heat is too low, iron ion Can not firmly it be bonded with the functional group on charcoal, when later stage liquid phase prepares magnetic bio carbon-supported nanometer iron, largely Iron ion meeting dissolution, causes certain loss so that its load capacity is relatively low.When temperature is too high (250 DEG C of >), in inert atmosphere Under, charcoal can serve as reducing agent, cause the loss of charcoal, and be possible to collapse the hole in charcoal, under load factor Drop.Therefore 200 DEG C~250 DEG C are the optimum temperatures calcined in preparation process.
Tea Polyphenols concentration influences little on Nanoscale Iron load capacity, and has large effect to the clearance of Cr VI, when not having When having cladding Tea Polyphenols, its clearance is relatively low, and is less than the clearance of blank charcoal, and reason is that Nanoscale Iron activity is too strong, With oxygen reaction in air before being tested, aoxidized, activity is too low when causing to react, and the Nanoscale Iron loaded occupies The pore structure of charcoal, causes charcoal specific surface area to decline, and adsorption capacity also accordingly reduces.And when cladding concentration is excessive When, due to Existential Space steric effect, there is resistance in Cr VI and Nanoscale Iron or charcoal haptoreaction, and electron transmission also can be by Resistance, cause to remove the reduction of Cr VI ability.Therefore can be prepared when Tea Polyphenols concentration is 0.002mol/L~0.008mol/L Preferable magnetic bio carbon-supported nanometer iron.
Test example 1, Tea Polyphenols concentration influence experiment
It is respectively 0.002mol/L, 0.004mol/L, 0.006mol/L to change Tea Polyphenols concentration according to embodiment 1, 0.008mol/L, the magnetic bio carbon-supported nanometer iron of different magnetic is prepared, and with deionized water and 0.002mol/L Tea Polyphenols Solution is control, carries out ultraviolet sedimentation experiment, comprises the following steps that:
It is respectively 0.002mol/L, 0.004mol/L, 0.006mol/L to change Tea Polyphenols concentration according to embodiment 1, 0.008mol/L, prepare the magnetic bio carbon-supported nanometer iron of different magnetic.
Take 0.5g to be dissolved in 50mL glass centrifuge tube respectively, cover plug, 10min is had children outside the state plan after shaken well, then will Centrifuge tube is placed on magnet 10 seconds, is pipetted upper solution 0.5mL with liquid-transfering gun, is added in 50mL colorimetric cylinders, add water to quarter Spend at line, shake up, be subsequently poured into the cuvette that light path is 1cm, scan 190nm-800nm ultraviolet-visible absorption situation, Using wavelength as abscissa, absorbance is ordinate, mapping.Simultaneously using deionized water and 0.002mol/L Tea Polyphenols solution as Control.
Experimental result:
Fig. 5 is the ultravioletvisible absorption figure of different Tea Polyphenols concentration cladding.As shown in Figure 5, obtained magnetic bio charcoal carries Nanoscale Iron supernatant has absorption at 206nm and 295nm or so place, and Tea Polyphenols only has obvious absorption at 206nm, therefore can With the characteristic absorption wavelength using 295nm or so as the magnetic bio carbon-supported nanometer iron material.As shown in Figure 5, it is dense with coating The increase of degree, its absorbance also increase, and positive correlation is presented in absorbance and the concentration of the material, so cladding concentration is bigger, its The more not free settling under magnetic fields.Therefore Tea Polyphenols is selected to control the magnetic size of the material of preparation as covering.
Test example 2, the magnetic bio carbon-supported nanometer ferromagnetism size of various concentrations Tea Polyphenols cladding compare
It is respectively 0mol/L, 0.001mol/L, 0.002mol/L, 0.003mol/ to change Tea Polyphenols concentration according to embodiment 1 L, 0.004mol/L, 0.005mol/L, 0.006mol/L, 0.007mol/L, 0.008mol/L, 0.009mol/L, 0.01mol/ L, the charcoal for preparing different magnetic carry Nanoscale Iron.By obtained solid material with SQUID VSM magnetometers to the magnetic prepared Charcoal carries Nanoscale Iron and applies AC magnetic field, obtains the M-H hysteresis curves (see Fig. 6) of magnetic bio carbon-supported nanometer iron, and analyzes The magnetic size of each magnetic bio carbon-supported nanometer iron.The remanent magnetization (Mr) and saturation magnetization (Ms) of each material It is shown in Table 2.The relation that Tea Polyphenols is coated between concentration and saturation magnetization is shown in Fig. 7.
Table 2
It can be obtained by hysteresis curve and its obtained remanent magnetization and saturation magnetization data analysis, when low concentration Tea Polyphenols to charcoal carry Nanoscale Iron coat when, its saturation magnetization is higher, and remanent magnetization is also larger, have compared with Good ferromagnetism.When the concentration rise of Tea Polyphenols, its saturation magnetization and remanent magnetization all reduce, the magnetic of material Die down.Therefore, the magnetic size of the magnetic bio carbon-supported nanometer iron can be regulated and controled by the concentration of Tea Polyphenols.
As shown in Figure 7:
When the concentration of Tea Polyphenols solution is more than or equal to 0.002mol/L, less than 0.004mol/L when, the magnetic that is prepared The saturation magnetization that charcoal carries Nanoscale Iron is less than or equal to 72.9emu/g, more than 36.5emu/g, suitable for not passing through magnetic Handling process processing does not have magnetic waste water.
When the concentration of Tea Polyphenols solution is more than or equal to 0.004mol/L, less than 0.006mol/L when, the magnetic that is prepared The saturation magnetization that charcoal carries Nanoscale Iron is less than or equal to 36.5emu/g, more than 26.6emu/g, and work is handled suitable for weak magnetic Skill has faint magnetic water body;
When Tea Polyphenols solution concentration be more than or equal to 0.006mol/L, less than or equal to 0.008mol/L when, be prepared The saturation magnetization of magnetic bio carbon-supported nanometer iron is less than or equal to 26.6emu/g, more than or equal to 5.2emu/g, suitable for have compared with The water body of strong magnetic treatment technique or relatively high magnetism.
Test example 3, the experiment of water body hexavalent chromium removal
It is respectively 0mol/L, 0.001mol/L, 0.002mol/L, 0.003mol/ to change Tea Polyphenols concentration according to embodiment 1 L, 0.004mol/L, 0.005mol/L, 0.006mol/L, 0.007mol/L, 0.008mol/L, 0.009mol/L, 0.01mol/ L, the charcoal for preparing different magnetic carry Nanoscale Iron, and using modification biological charcoal as blank, it is real to carry out hexavalent chromium removal in water body Test, comprise the following steps that:
It is respectively 0mol/L, 0.001mol/L, 0.002mol/L, 0.003mol/ to change Tea Polyphenols concentration according to embodiment 1 L, 0.004mol/L, 0.005mol/L, 0.006mol/L, 0.007mol/L, 0.008mol/L, 0.009mol/L, 0.01mol/ L, the charcoal for preparing different magnetic carry Nanoscale Iron.
A certain amount of potassium bichromate is weighed, prepares 20mg/L hexavalent chromium solution, adjusts pH to 6.Take 100mL 20mg/L Cr VI as reaction solution add reaction bulb in.And the 1g materials are taken, it is added in reaction bulb, is put into vibration case, with 180r/min, 25 DEG C of vibrations, is sampled in 5min, 10min, 20min, 30min, 45min, 60min, 90min, 120min respectively, Filter membrane, measure the Cr (VI) of supernatant concentration.
Experimental result:
Fig. 8 is removal effect figure of the different Tea Polyphenols cladding concentration for Cr VI.It can be seen that cladding The material of 0.002mol/L Tea Polyphenols solution can all remove Cr VI in 2h, with the increase of cladding concentration, remove Efficiency also slightly reduces.Different Tea Polyphenols coat clearance of Cr VI of the concentration for 20mg/L in 2h and are shown in Table 3.
Table 3
From data in table 3, magnetic bio carbon-supported nanometer iron prepared by embodiment 1 can be whole by Cr VI in 1h Removing, the Cr VI in the degraded water body that it can be rapidly and efficiently, in 1h and 2h, its clearance is more or less the same the charcoal of blank, Illustrate charcoal already close to adsorption equilibrium.The material of Tea Polyphenols is not coated, its clearance is minimum, and reason one is due to not have The cladding of Tea Polyphenols, Nanoscale Iron property are not sufficiently stable, have been oxidized before the test, and reactivity reduces;Second, Nanoscale Iron occupies The pore structure of charcoal, causes the reduction of its specific surface area, and adsorption capacity is deteriorated.The magnetic bio of remaining Tea Polyphenols concentration cladding Carbon-supported nanometer iron, there is part lifting to the removal effect of Cr VI, particularly when cladding concentration is 0.002-0.008mol/L When, its 1h clearance can reach more than 85%, 2h clearances more than 90%.Therefore the material can be quick, efficiently Remove the Cr VI in water body.
Its partial results and pseudo-first-order dynamics and pseudo-second order kinetic equation are fitted,
Pseudo-first-order kinetics equation:DC/dt=-kC,
Pseudo-second order kinetic equation:
Its reactive kinetics parameters fitting result is shown in Table 4.
Table 4
As can be seen from Table 4, the reaction is not high to first _ order kinetics equation degree of fitting, and it is low to coat Tea Polyphenols concentration Its one-level Kinetics Rate Constants By Using highest of charcoal.The reaction is higher for second-order kinetic equation degree of fitting, illustrates reaction point For two stages of fast response and long response time, the material for coating Tea Polyphenols, it starts based on quick adsorption, and the later stage is main For the reaction of iron and Cr VI.When cladding concentration is low, its removal rate is higher, and its main cause is probably the sky due to Tea Polyphenols Between steric hindrance hinder the quick adsorption of charcoal, and also cause contact of the Cr VI with Nanoscale Iron by certain limit System.But the presence of Tea Polyphenols make it that the property of Nanoscale Iron is relatively stable, not easy in inactivation, therefore in practical application, can root The concentration of Tea Polyphenols is prepared according to concrete condition.
Test example 4, the experiment of water body hexavalent chromium removal
Compound concentration is 20mg/L, 40mg/L, 60mg/L, 80mg/L, 100mg/L hexavalent chromium solution, adjusts pH to 6, The above-mentioned solution of 100mL is taken to add in reaction bulb respectively, and the magnetic bio carbon-supported nanometer for respectively taking 1g to be prepared according to embodiment 1 Iron is separately added into above-mentioned reaction bulb, and reaction bulb is put into vibration case, with 180r/min, 25 DEG C of vibrations, respectively at vibration 2 My god, 5 days, after 10 days, take supernatant, the content of Cr VI in supernatant is measured with diphenyl carbazide spectrophotometry, and is counted Calculate clearance of the magnetic bio carbon-supported nanometer iron to Cr VI in water body.Experimental result is shown in Table 5, hexavalent chromium solution initial concentration And the relation after 2d, 5d, 10d between hexavalent chromium removal rate is shown in Fig. 9.
Table 5
The magnetic bio carbon-supported nanometer iron that the 1g present invention is prepared it can be seen from experimental result table 5, Fig. 9, Ke Yiying For the 100mL waste water that hexavalent chromium concentration is below 60mg/L, the Cr VI in the waste water can be removed after 2d completely.

Claims (8)

1. a kind of preparation method of magnetic bio carbon-supported nanometer iron, it is characterised in that comprise the following steps:
(1) modification of charcoal:Charcoal is taken, adds concentrated nitric acid, immersion filtering, and is rinsed to pH with water and no longer changed, is dried, Obtain the charcoal of Nitric Acid Modified;
(2) load of molysite:Water-soluble trivalent ferric salt solution is prepared, adds the charcoal for the modification that step (1) is prepared, is surpassed Sound impregnates, and filters, and drying, then weighs the sample after drying, 200~250 DEG C are warming up under inert atmosphere or nitrogen atmosphere, Calcining, obtains the charcoal for the load molysite that theoretical duty iron is 28%~32%, and the wherein calculating of theoretical duty iron is public Formula is (quality of the quality of iron ion/modification biological charcoal) × 100%;
(3) 0.002~0.008mol/L Tea Polyphenols solution is prepared, is passed through inert gas or nitrogen deoxygenation, step (2) is added and prepares The charcoal of obtained load molysite, the ratio between the quality of the load molysite charcoal of addition and the volume of Tea Polyphenols solution are 1:40 ~1:50g/mL, under inert gas or nitrogen atmosphere, stirring;
(4) sodium borohydride solution is prepared, adds into step (3) resulting solution, continues to stir, charcoal is obtained and carries nano-iron slurry Liquid;The molar concentration of the sodium borohydride solution is 0.005~0.014mol/L;The sodium borohydride solution of preparation and step (3) The volume ratio of the Tea Polyphenols solution of middle preparation is 1:6~1:10;
(5) go out magnetic bio carbon-supported nanometer iron with magnetic method sub-argument, wash, dry;
The preparation-obtained magnetic bio carbon-supported nanometer of control is reached by the molar concentration of Tea Polyphenols solution in rate-determining steps (3) The purpose of the saturation magnetization of iron,
When the concentration of Tea Polyphenols solution is more than or equal to 0.002mol/L, less than 0.004mol/L when, the magnetic bio that is prepared The saturation magnetization of carbon-supported nanometer iron is less than or equal to 72.9emu/g, more than 36.5emu/g;
When the concentration of Tea Polyphenols solution is more than or equal to 0.004mol/L, less than 0.006mol/L when, the magnetic bio that is prepared The saturation magnetization of carbon-supported nanometer iron is less than or equal to 36.5emu/g, more than 26.6emu/g;
When the concentration of Tea Polyphenols solution is more than or equal to 0.006mol/L, less than or equal to 0.008mol/L when, the magnetic that is prepared The saturation magnetization that charcoal carries Nanoscale Iron is less than or equal to 26.6emu/g, more than or equal to 5.2emu/g.
2. preparation method according to claim 1, it is characterised in that in step (1), the mass ratio of charcoal and concentrated nitric acid For 1:10~1:70.
3. preparation method according to claim 1, it is characterised in that in step (2), water-soluble trivalent ferric salt FeCl3、 FeCl3·6H2O、Fe2(SO4)3In one or more.
4. the preparation method stated according to claim 3, it is characterised in that in step (2), water-soluble trivalent ferric salt FeCl3
5. preparation method according to claim 1, it is characterised in that in step (2), the inert gas is argon gas.
6. preparation method according to claim 1, it is characterised in that in step (3), the load molysite charcoal of addition The ratio between quality and the volume of Tea Polyphenols solution are 1:45g/mL.
7. the magnetic bio carbon-supported nanometer iron that the preparation method described in claim 1~6 any one is prepared.
8. application of the magnetic bio carbon-supported nanometer iron in the Cr VI in removing water body described in claim 7.
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