Nothing Special   »   [go: up one dir, main page]

CN105869822A - Preparation method of p-MaFe2O4 and p-NiFe2O4 binary magnetic mixed ionic magnetic fluid - Google Patents

Preparation method of p-MaFe2O4 and p-NiFe2O4 binary magnetic mixed ionic magnetic fluid Download PDF

Info

Publication number
CN105869822A
CN105869822A CN201610336717.2A CN201610336717A CN105869822A CN 105869822 A CN105869822 A CN 105869822A CN 201610336717 A CN201610336717 A CN 201610336717A CN 105869822 A CN105869822 A CN 105869822A
Authority
CN
China
Prior art keywords
magnetic
solution
mgfe
nife
preparation
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.)
Pending
Application number
CN201610336717.2A
Other languages
Chinese (zh)
Inventor
靳汇奇
谢宇
黄彦
杨少凡
李诗琪
张亚萍
贺艳香
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Nanchang Hangkong University
Original Assignee
Nanchang Hangkong University
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Nanchang Hangkong University filed Critical Nanchang Hangkong University
Priority to CN201610336717.2A priority Critical patent/CN105869822A/en
Publication of CN105869822A publication Critical patent/CN105869822A/en
Pending legal-status Critical Current

Links

Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01FMAGNETS; INDUCTANCES; TRANSFORMERS; SELECTION OF MATERIALS FOR THEIR MAGNETIC PROPERTIES
    • H01F1/00Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties
    • H01F1/44Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of magnetic liquids, e.g. ferrofluids
    • H01F1/445Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of magnetic liquids, e.g. ferrofluids the magnetic component being a compound, e.g. Fe3O4

Landscapes

  • Engineering & Computer Science (AREA)
  • Power Engineering (AREA)
  • Lubricants (AREA)
  • Soft Magnetic Materials (AREA)

Abstract

The invention discloses a preparation method of a p-MaFe2O4 and p-NiFe2O4 binary magnetic mixed ionic magnetic fluid. The p-MaFe2O4 and p-NiFe2O4 binary magnetic mixed ionic magnetic fluid is prepared from three parts, namely p-MaFe2O4 magnetic particles, p-NiFe2O4 magnetic particles and base fluid. The preparation method comprises the following steps: respectively compounding the p-MaFe2O4 magnetic particles and the p-NiFe2O4 magnetic particles through a chemical coprecipitation method; then respectively mixing the p-MaFe2O4 magnetic particles and the p-NiFe2O4 magnetic particles with hydrochloric acid and the base fluid according to a certain proportion, and forming two kinds of unit ionic magnetic fluids of p-MaFe2O4 and p-NiFe2O4 in the same volume fraction; finally mixing the two kinds of magnetic fluids according to a volume ratio of 1:1, and thus forming the p-MaFe2O4 and p-NiFe2O4 binary magnetic mixed ionic magnetic fluid. The preparation method of the p-MaFe2O4 and p-NiFe2O4 binary magnetic mixed ionic magnetic fluid, disclosed by the invention, has the advantages that raw materials are commonly used, the operation is simple, the obtained magnetic fluid is high in stability, uniform in particle diameter and good in dispersibility, and the like. The p-MaFe2O4 and p-NiFe2O4 binary magnetic mixed ionic magnetic fluid is prepared through the preparation method, an embedding action of a surfactant does not exist, and the reaction is more flexible under a magnetic field.

Description

A kind of p-MgFe2O4And p-NiFe2O4Binary magnetic hybrid ionic type magnetic liquid Preparation method
Technical field
The invention belongs to liquid magnetic field of material technology, be specifically related to p-MgFe2O4And p-NiFe2O4Binary magnetic mixes Close the preparation method of ionic ferrofluid.
Background technology
At present the preparation method of magnetic liquid has polishing, anion-exchange resin method, hydrogen reduction method, thermal decomposition method, true Empty evaporation, electricity method, chemical coprecipitation etc..Polishing is to be pulverized by magnetic-particle by the method for mechanical lapping, then warp Filtering or be centrifuged and obtain magnetic liquid, this method milling time is long, high cost.Anion-exchange resin method be with iron content with The aqueous solution of ferrous salt, processes with anion-exchange resin method and can produce the stable magnetic γ-Fe2O3 hydrosol.The oxygen made Change iron particle averagely at 3~12 nm.Thermal decomposition method can obtain nano level magnetic liquid, but power consumption is bigger.Vacuum vapor deposition method The magnetic fluid magnetic particle good dispersion of preparation, particle is little, uniform particle, but equipment and operation complexity.Electricity method be to pass through Electrolysis makes Fe2+Separate out with the form of iron monomer, thus form magnetic liquid, but the kind of preparation is single.Chemical coprecipitation is After metal ion each in magnetic nanoparticle is stoichiometrically mixed, with NaOH regulation pH value of solution by each precipitation by metallic ion Getting off, period to be stirred continuously, then by separating, cleaning, except water, dry and grinding, prepares nano magnetic particle, and this method prepares Magnetic particle epigranular, granularity is little, good dispersion, and the equipment of needs is simple, and preparation method is fairly simple.
Relative to surfactant type magnetic liquid, the preparation of ion magnetic magnetic liquid is simpler, cost is lower, pollution Less, and there is physically better performance.
Summary of the invention
It is an object of the invention to provide a kind of p-MgFe2O4And p-NiFe2O4Binary magnetic hybrid ionic type magnetic liquid The preparation method of body, it is characterised in that:
(1) p-MgFe2O4、p-NiFe2O4The preparation method of magnetic particle is as follows:
By HCl solution and the 1.23mol/LMg (NO of 1mol/L3)2Solution is (molten by HCl after mixing for 1:25 by volume Liquid pours Mg (NO into3)2Solution is in order to prevent from working as FeCl3With Mg (NO3)2There is complex reaction), add 2.41mol/L's FeCl3Solution, adds 4mol/L NaOH solution afterwards and (will be stirred, to allow solution during these solution mixes Mix), wherein control Fe3+、Mg2+、OH-Mol ratio be 2:1:8;By above-mentioned mixed solution in the stirring of 2500r/min Under speed, heating is until boiling, naturally cools to room temperature after 1min under room temperature;Product after cooling filters, and uses HNO3 Solution washs and is centrifuged again being precipitated, and repeats this process until joining the Fe (NO of boiling after being precipitated as neutrality3)3 In solution, naturally cool to room temperature after keeping boiling 30min under the mixing speed of 2500r/min, then filter, gained Filter cake acetone be dehydrated, 60 DEG C of drying boxes are dried 24h, more ground process, obtain p-MgFe2O4Magnetic particle;
By HCl solution and the 1.00moi/L Ni (NO of 1mol/L3)2Solution is (molten by HCl after mixing for 1:25 by volume Liquid pours Ni (NO into3)2Solution is in order to prevent from working as FeCl3With Ni (NO3)2There is complex reaction), add 2.03mol/L's FeCl3Solution, adds 4mol/L NaOH solution afterwards and (will be stirred, to allow solution during these solution mixes Mix), wherein control Fe3+、Ni2+、OH-Mol ratio be 2:1:8;By above-mentioned mixed solution in the stirring of 2500r/min Under speed, heating is until boiling, naturally cools to room temperature after 1min under room temperature;Product after cooling filters, and uses HNO3 Solution washs and is centrifuged again being precipitated, and repeats this process until joining the Fe (NO of boiling after being precipitated as neutrality3)3 In solution, naturally cool to room temperature after keeping boiling 30min under the mixing speed of 2500r/min, then filter, gained Filter cake be dehydrated with acetone after, 60 DEG C of drying boxes are dried 24h, more ground process, obtain p-NiFe2O4Magnetic particle;
(2) p-MgFe2O4、p-NiFe2O4The preparation of unit ionic ferrofluid:
By p-MgFe2O4After magnetic particle, the HCl of 1mol/L and solvent mix for 1:3.3:20.7 by volume, obtain p-MgFe2O4Unit ionic ferrofluid;
By p-NiFe2O4After magnetic particle, the HCl of 1mol/L and solvent mix for 1:2.85:21.15 by volume, To p-NiFe2O4Unit ionic ferrofluid;
(3) p-MgFe2O4-p-NiFe2O4The preparation of binary weak magnetic hybrid ionic type magnetic liquid: by p-MgFe2O4Unit from Subtype magnetic liquid and p-NiFe2O4Unit ionic ferrofluid shakes up according to the mixing of volume ratio 1:1, prepares p-MgFe2O4- p-NiFe2O4Binary weak magnetic hybrid ionic type magnetic liquid.
P-MgFe of the present invention2O4Unit ionic ferrofluid, p-NiFe2O4Unit ionic ferrofluid Volume fraction φVBeing 2%, Q value is 0.12.
P-MgFe in step of the present invention (2)2O4Control as 1:0.36, p-with the molar concentration rate of 1mol/L HCl NiFe2O4Control as 1:0.36 with the molar concentration rate of 1mol/L HCl.
The invention have the advantage that this preparation method has the magnetic liquid stability that raw material is conventional, simple to operate, obtained High, uniform particle diameter, the advantage such as good dispersion.Prepared by this method is ionic ferrofluid, does not has the embedding of surfactant to make With, under magnetic field, react sensitiveer.p-MgFe2O4And p-NiFe2O4Magnetic is relatively weak and difference is less, reduce two kinds micro- Impact between Li.
Detailed description of the invention
Below by embodiment, the invention will be further described.
Embodiment one
p-MgFe2O4、p-NiFe2O4The preparation of magnetic particle
By HCl solution and the 1.23mol/LMg (NO of 1mol/L3)2Solution is (molten by HCl after mixing for 1:25 by volume Liquid pours Mg (NO into3)2Solution is in order to prevent from working as FeCl3With Mg (NO3)2There is complex reaction), add 2.41mol/L's FeCl3Solution, adds 4mol/L NaOH solution afterwards and (will be stirred, to allow solution during these solution mixes Mix), wherein control Fe3+、Mg2+、OH-Mol ratio be 2:1:8;By above-mentioned mixed solution in the stirring of 2500r/min Under speed, heating is until boiling, naturally cools to room temperature after 1min under room temperature;Product after cooling filters, and uses HNO3 Solution washs and is centrifuged again being precipitated, and repeats this process until joining the Fe (NO of boiling after being precipitated as neutrality3)3 In solution, naturally cool to room temperature after keeping boiling 30min under the mixing speed of 2500r/min, then filter, gained Filter cake acetone be dehydrated, 60 DEG C of drying boxes are dried 24h, more ground process, obtain p-MgFe2O4Magnetic particle;
By HCl solution and the 1.00moi/L Ni (NO of 1mol/L3)2Solution is (molten by HCl after mixing for 1:25 by volume Liquid pours Ni (NO into3)2Solution is in order to prevent from working as FeCl3With Ni (NO3)2There is complex reaction), add 2.03mol/L's FeCl3Solution, adds 4mol/L NaOH solution afterwards and (will be stirred, to allow solution during these solution mixes Mix), wherein control Fe3+、Ni2+、OH-Mol ratio be 2:1:8;By above-mentioned mixed solution in the stirring of 2500r/min Under speed, heating is until boiling, naturally cools to room temperature after 1min under room temperature;Product after cooling filters, and uses HNO3 Solution washs and is centrifuged again being precipitated, and repeats this process until joining the Fe (NO of boiling after being precipitated as neutrality3)3 In solution, naturally cool to room temperature after keeping boiling 30min under the mixing speed of 2500r/min, then filter, gained Filter cake be dehydrated with acetone after, 60 DEG C of drying boxes are dried 24h, more ground process, obtain p-NiFe2O4Magnetic particle;
p-MgFe2O4、p-NiFe2O4The preparation of unit ionic ferrofluid
Precise 3.644g p-MgFe2O4The HCl of magnetic particle and 6.6ml 1mol/L pours 50ml volumetric flask deionization into Water constant volume, configures three bottles of identical p-MgFe2O4Unit magnetic liquid, hand 30min.In like manner precise 3.695g p- NiFe2O4Magnetic particle pour into the HCl of 5.7ml 1mol/L 50ml volumetric flask spend deionized water constant volume configure three bottles identical p-NiFe2O4Unit magnetic liquid, hand 30min.Then being diluted by deionized water, respectively obtaining volume fraction is 0.4%, the unit ionic ferrofluid of 0.8%, 1.2%, 1.6%.
p-MgFe2O4-p-NiFe2O4The preparation of binary weak magnetic hybrid ionic type magnetic liquid
Respectively by unit p-MgFe identical for volume fraction2O4Magnetic liquid and unit p-NiFe2O4Magnetic liquid equal-volume mixes Close, obtain the p-MgFe of different volumes mark2O4And p-NiFe2O4Binary magnetic hybrid ionic type magnetic liquid.
Embodiment two
p-MgFe2O4、p-NiFe2O4The preparation of magnetic particle
By HCl solution and the 1.23mol/LMg (NO of 1mol/L3)2Solution is (molten by HCl after mixing for 1:25 by volume Liquid pours Mg (NO into3)2Solution is in order to prevent from working as FeCl3With Mg (NO3)2There is complex reaction), add 2.41mol/L's FeCl3Solution, adds 4mol/L NaOH solution afterwards and (will be stirred, to allow solution during these solution mixes Mix), wherein control Fe3+、Mg2+、OH-Mol ratio be 2:1:8;By above-mentioned mixed solution in the stirring of 2500r/min Under speed, heating is until boiling, naturally cools to room temperature after 1min under room temperature;Product after cooling filters, and uses HNO3 Solution washs and is centrifuged again being precipitated, and repeats this process until joining the Fe (NO of boiling after being precipitated as neutrality3)3 In solution, naturally cool to room temperature after keeping boiling 30min under the mixing speed of 2500r/min, then filter, gained Filter cake acetone be dehydrated, 60 DEG C of drying boxes are dried 24h, more ground process, obtain p-MgFe2O4Magnetic particle;
By HCl solution and the 1.00moi/L Ni (NO of 1mol/L3)2Solution is (molten by HCl after mixing for 1:25 by volume Liquid pours Ni (NO into3)2Solution is in order to prevent from working as FeCl3With Ni (NO3)2There is complex reaction), add 2.03mol/L's FeCl3Solution, adds 4mol/L NaOH solution afterwards and (will be stirred, to allow solution during these solution mixes Mix), wherein control Fe3+、Ni2+、OH-Mol ratio be 2:1:8;By above-mentioned mixed solution in the stirring of 2500r/min Under speed, heating is until boiling, naturally cools to room temperature after 1min under room temperature;Product after cooling filters, and uses HNO3 Solution washs and is centrifuged again being precipitated, and repeats this process until joining the Fe (NO of boiling after being precipitated as neutrality3)3 In solution, naturally cool to room temperature after keeping boiling 30min under the mixing speed of 2500r/min, then filter, gained Filter cake be dehydrated with acetone after, 60 DEG C of drying boxes are dried 24h, more ground process, obtain p-NiFe2O4Magnetic particle;
p-MgFe2O4、p-NiFe2O4The preparation of unit ionic ferrofluid
Precise 3.644g p-MgFe2O4The HCl of magnetic particle and 6.6ml 1mol/L pours 50ml volumetric flask polymethyl benzene into Constant volume, configures three bottles of identical p-MgFe2O4Unit magnetic liquid, hand 30min.In like manner precise 3.695g p- NiFe2O4Magnetic particle is poured 50ml volumetric flask into and is spent polymethyl benzene constant volume three bottles of identical p-of configuration with the HCl of 5.7ml 1mol/L NiFe2O4Unit magnetic liquid, hand 30min.Then be diluted with polymethyl benzene, respectively obtain volume fraction be 0.4%, 0.8%, the unit ionic ferrofluid of 1.2%, 1.6%.
p-MgFe2O4-p-NiFe2O4The preparation of binary weak magnetic hybrid ionic type magnetic liquid
Respectively by unit p-MgFe identical for volume fraction2O4Magnetic liquid and unit p-NiFe2O4Magnetic liquid equal-volume mixes Close, obtain the p-MgFe of different volumes mark2O4And p-NiFe2O4Binary magnetic hybrid ionic type magnetic liquid.
Embodiment three
p-MgFe2O4、p-NiFe2O4The preparation of magnetic particle
By HCl solution and the 1.23mol/LMg (NO of 1mol/L3)2Solution is (molten by HCl after mixing for 1:25 by volume Liquid pours Mg (NO into3)2Solution is in order to prevent from working as FeCl3With Mg (NO3)2There is complex reaction), add 2.41mol/L's FeCl3Solution, adds 4mol/L NaOH solution afterwards and (will be stirred, to allow solution during these solution mixes Mix), wherein control Fe3+、Mg2+、OH-Mol ratio be 2:1:8;By above-mentioned mixed solution in the stirring of 2500r/min Under speed, heating is until boiling, naturally cools to room temperature after 1min under room temperature;Product after cooling filters, and uses HNO3 Solution washs and is centrifuged again being precipitated, and repeats this process until joining the Fe (NO of boiling after being precipitated as neutrality3)3 In solution, naturally cool to room temperature after keeping boiling 30min under the mixing speed of 2500r/min, then filter, gained Filter cake acetone be dehydrated, 60 DEG C of drying boxes are dried 24h, more ground process, obtain p-MgFe2O4Magnetic particle;
By HCl solution and the 1.00moi/L Ni (NO of 1mol/L3)2Solution is (molten by HCl after mixing for 1:25 by volume Liquid pours Ni (NO into3)2Solution is in order to prevent from working as FeCl3With Ni (NO3)2There is complex reaction), add 2.03mol/L's FeCl3Solution, adds 4mol/L NaOH solution afterwards and (will be stirred, to allow solution during these solution mixes Mix), wherein control Fe3+、Ni2+、OH-Mol ratio be 2:1:8;By above-mentioned mixed solution in the stirring of 2500r/min Under speed, heating is until boiling, naturally cools to room temperature after 1min under room temperature;Product after cooling filters, and uses HNO3 Solution washs and is centrifuged again being precipitated, and repeats this process until joining the Fe (NO of boiling after being precipitated as neutrality3)3 In solution, naturally cool to room temperature after keeping boiling 30min under the mixing speed of 2500r/min, then filter, gained Filter cake be dehydrated with acetone after, 60 DEG C of drying boxes are dried 24h, more ground process, obtain p-NiFe2O4Magnetic particle;
p-MgFe2O4、p-NiFe2O4The preparation of unit ionic ferrofluid
Precise 3.644g p-MgFe2O4It is fixed that the HCl of magnetic particle and 6.6ml 1mol/L pours 50ml volumetric flask kerosene into Hold, configure three bottles of identical p-MgFe2O4Unit magnetic liquid, hand 30min.In like manner precise 3.695g p-NiFe2O4 Magnetic particle is poured 50ml volumetric flask into and is spent kerosene constant volume three bottles of identical p-NiFe of configuration with the HCl of 5.7ml 1mol/L2O4Single Unit's magnetic liquid, hand 30min.Then be diluted with kerosene, respectively obtain volume fraction be 0.4%, 0.8%, 1.2%, The unit ionic ferrofluid of 1.6%.
p-MgFe2O4-p-NiFe2O4The preparation of binary weak magnetic hybrid ionic type magnetic liquid
Respectively by unit p-MgFe identical for volume fraction2O4Magnetic liquid and unit p-NiFe2O4Magnetic liquid equal-volume mixes Close, obtain the p-MgFe of different volumes mark2O4And p-NiFe2O4Binary magnetic hybrid ionic type magnetic liquid.
Embodiment four
p-MgFe2O4、p-NiFe2O4The preparation of magnetic particle
By HCl solution and the 1.23mol/LMg (NO of 1mol/L3)2Solution is (molten by HCl after mixing for 1:25 by volume Liquid pours Mg (NO into3)2Solution is in order to prevent from working as FeCl3With Mg (NO3)2There is complex reaction), add 2.41mol/L's FeCl3Solution, adds 4mol/L NaOH solution afterwards and (will be stirred, to allow solution during these solution mixes Mix), wherein control Fe3+、Mg2+、OH-Mol ratio be 2:1:8;By above-mentioned mixed solution in the stirring of 2500r/min Under speed, heating is until boiling, naturally cools to room temperature after 1min under room temperature;Product after cooling filters, and uses HNO3 Solution washs and is centrifuged again being precipitated, and repeats this process until joining the Fe (NO of boiling after being precipitated as neutrality3)3 In solution, naturally cool to room temperature after keeping boiling 30min under the mixing speed of 2500r/min, then filter, gained Filter cake acetone be dehydrated, 60 DEG C of drying boxes are dried 24h, more ground process, obtain p-MgFe2O4Magnetic particle;
By HCl solution and the 1.00moi/L Ni (NO of 1mol/L3)2Solution is (molten by HCl after mixing for 1:25 by volume Liquid pours Ni (NO into3)2Solution is in order to prevent from working as FeCl3With Ni (NO3)2There is complex reaction), add 2.03mol/L's FeCl3Solution, adds 4mol/L NaOH solution afterwards and (will be stirred, to allow solution during these solution mixes Mix), wherein control Fe3+、Ni2+、OH-Mol ratio be 2:1:8;By above-mentioned mixed solution in the stirring of 2500r/min Under speed, heating is until boiling, naturally cools to room temperature after 1min under room temperature;Product after cooling filters, and uses HNO3 Solution washs and is centrifuged again being precipitated, and repeats this process until joining the Fe (NO of boiling after being precipitated as neutrality3)3 In solution, naturally cool to room temperature after keeping boiling 30min under the mixing speed of 2500r/min, then filter, gained Filter cake be dehydrated with acetone after, 60 DEG C of drying boxes are dried 24h, more ground process, obtain p-NiFe2O4Magnetic particle;
p-MgFe2O4、p-NiFe2O4The preparation of unit ionic ferrofluid
Precise 3.644g p-MgFe2O4It is fixed that the HCl of magnetic particle and 6.6ml 1mol/L pours 50ml volumetric flask silicone oil into Hold, configure three bottles of identical p-MgFe2O4Unit magnetic liquid, hand 30min.In like manner precise 3.695g p-NiFe2O4 Magnetic particle is poured 50ml volumetric flask into and is spent silicone oil constant volume three bottles of identical p-NiFe of configuration with the HCl of 5.7ml 1mol/L2O4Single Unit's magnetic liquid, hand 30min.Then be diluted with silicone oil, respectively obtain volume fraction be 0.4%, 0.8%, 1.2%, The unit ionic ferrofluid of 1.6%.
p-MgFe2O4-p-NiFe2O4The preparation of binary weak magnetic hybrid ionic type magnetic liquid
Respectively by unit p-MgFe identical for volume fraction2O4Magnetic liquid and unit p-NiFe2O4Magnetic liquid equal-volume mixes Close, obtain the p-MgFe of different volumes mark2O4And p-NiFe2O4Binary magnetic hybrid ionic type magnetic liquid.
Embodiment five
p-MgFe2O4、p-NiFe2O4The preparation of magnetic particle
By HCl solution and the 1.23mol/LMg (NO of 1mol/L3)2Solution is (molten by HCl after mixing for 1:25 by volume Liquid pours Mg (NO into3)2Solution is in order to prevent from working as FeCl3With Mg (NO3)2There is complex reaction), add 2.41mol/L's FeCl3Solution, adds 4mol/L NaOH solution afterwards and (will be stirred, to allow solution during these solution mixes Mix), wherein control Fe3+、Mg2+、OH-Mol ratio be 2:1:8;By above-mentioned mixed solution in the stirring of 2500r/min Under speed, heating is until boiling, naturally cools to room temperature after 1min under room temperature;Product after cooling filters, and uses HNO3 Solution washs and is centrifuged again being precipitated, and repeats this process until joining the Fe (NO of boiling after being precipitated as neutrality3)3 In solution, naturally cool to room temperature after keeping boiling 30min under the mixing speed of 2500r/min, then filter, gained Filter cake acetone be dehydrated, 60 DEG C of drying boxes are dried 24h, more ground process, obtain p-MgFe2O4Magnetic particle;
By HCl solution and the 1.00moi/L Ni (NO of 1mol/L3)2Solution is (molten by HCl after mixing for 1:25 by volume Liquid pours Ni (NO into3)2Solution is in order to prevent from working as FeCl3With Ni (NO3)2There is complex reaction), add 2.03mol/L's FeCl3Solution, adds 4mol/L NaOH solution afterwards and (will be stirred, to allow solution during these solution mixes Mix), wherein control Fe3+、Ni2+、OH-Mol ratio be 2:1:8;By above-mentioned mixed solution in the stirring of 2500r/min Under speed, heating is until boiling, naturally cools to room temperature after 1min under room temperature;Product after cooling filters, and uses HNO3 Solution washs and is centrifuged again being precipitated, and repeats this process until joining the Fe (NO of boiling after being precipitated as neutrality3)3 In solution, naturally cool to room temperature after keeping boiling 30min under the mixing speed of 2500r/min, then filter, gained Filter cake be dehydrated with acetone after, 60 DEG C of drying boxes are dried 24h, more ground process, obtain p-NiFe2O4Magnetic particle;
p-MgFe2O4、p-NiFe2O4The preparation of unit ionic ferrofluid
Precise 3.644g p-MgFe2O4The HCl of magnetic particle and 6.6ml 1mol/L pours 50ml volumetric flask polyethylene into Alcohol constant volume, configures three bottles of identical p-MgFe2O4Unit magnetic liquid, hand 30min.In like manner precise 3.695g p- NiFe2O4Magnetic particle pour into the HCl of 5.7ml 1mol/L 50ml volumetric flask spend polyvinyl alcohol constant volume configure three bottles identical p-NiFe2O4Unit magnetic liquid, hand 30min.Then being diluted with polyvinyl alcohol, respectively obtaining volume fraction is 0.4%, the unit ionic ferrofluid of 0.8%, 1.2%, 1.6%.
p-MgFe2O4-p-NiFe2O4The preparation of binary weak magnetic hybrid ionic type magnetic liquid
Respectively by unit p-MgFe identical for volume fraction2O4Magnetic liquid and unit p-NiFe2O4Magnetic liquid equal-volume mixes Close, obtain the p-MgFe of different volumes mark2O4And p-NiFe2O4Binary magnetic hybrid ionic type magnetic liquid.
Embodiment six
p-MgFe2O4、p-NiFe2O4The preparation of magnetic particle
By HCl solution and the 1.23mol/LMg (NO of 1mol/L3)2Solution is (molten by HCl after mixing for 1:25 by volume Liquid pours Mg (NO into3)2Solution is in order to prevent from working as FeCl3With Mg (NO3)2There is complex reaction), add 2.41mol/L's FeCl3Solution, adds 4mol/L NaOH solution afterwards and (will be stirred, to allow solution during these solution mixes Mix), wherein control Fe3+、Mg2+、OH-Mol ratio be 2:1:8;By above-mentioned mixed solution in the stirring of 2500r/min Under speed, heating is until boiling, naturally cools to room temperature after 1min under room temperature;Product after cooling filters, and uses HNO3 Solution washs and is centrifuged again being precipitated, and repeats this process until joining the Fe (NO of boiling after being precipitated as neutrality3)3 In solution, naturally cool to room temperature after keeping boiling 30min under the mixing speed of 2500r/min, then filter, gained Filter cake acetone be dehydrated, 60 DEG C of drying boxes are dried 24h, more ground process, obtain p-MgFe2O4Magnetic particle;
By HCl solution and the 1.00moi/L Ni (NO of 1mol/L3)2Solution is (molten by HCl after mixing for 1:25 by volume Liquid pours Ni (NO into3)2Solution is in order to prevent from working as FeCl3With Ni (NO3)2There is complex reaction), add 2.03mol/L's FeCl3Solution, adds 4mol/L NaOH solution afterwards and (will be stirred, to allow solution during these solution mixes Mix), wherein control Fe3+、Ni2+、OH-Mol ratio be 2:1:8;By above-mentioned mixed solution in the stirring of 2500r/min Under speed, heating is until boiling, naturally cools to room temperature after 1min under room temperature;Product after cooling filters, and uses HNO3 Solution washs and is centrifuged again being precipitated, and repeats this process until joining the Fe (NO of boiling after being precipitated as neutrality3)3 In solution, naturally cool to room temperature after keeping boiling 30min under the mixing speed of 2500r/min, then filter, gained Filter cake be dehydrated with acetone after, 60 DEG C of drying boxes are dried 24h, more ground process, obtain p-NiFe2O4Magnetic particle;
p-MgFe2O4、p-NiFe2O4The preparation of unit ionic ferrofluid
Precise 3.644g p-MgFe2O4The HCl of magnetic particle and 6.6ml 1mol/L pours 50ml volumetric flask fluorine carbonization into Compound constant volume, configures three bottles of identical p-MgFe2O4Unit magnetic liquid, hand 30min.In like manner precise 3.695g p- NiFe2O4Magnetic particle pour into the HCl of 5.7ml 1mol/L 50ml volumetric flask spend fluorocarbons constant volume configure three bottles identical P-NiFe2O4Unit magnetic liquid, hand 30min.Then being diluted with fluorocarbons, respectively obtaining volume fraction is 0.4%, the unit ionic ferrofluid of 0.8%, 1.2%, 1.6%.
p-MgFe2O4-p-NiFe2O4The preparation of binary weak magnetic hybrid ionic type magnetic liquid
Respectively by unit p-MgFe identical for volume fraction2O4Magnetic liquid and unit p-NiFe2O4Magnetic liquid equal-volume mixes Close, obtain the p-MgFe of different volumes mark2O4And p-NiFe2O4Binary magnetic hybrid ionic type magnetic liquid.

Claims (3)

1. a p-MgFe2O4And p-NiFe2O4The preparation method of binary magnetic hybrid ionic type magnetic liquid, it is characterised in that Method step is as follows:
p-MgFe2O4、p-NiFe2O4The preparation of magnetic particle:
By HCl solution and the 1.23mol/LMg (NO of 1mol/L3)2After solution mixes for 1:25 by volume, add 2.41mol/L FeCl3Solution, adds 4mol/L NaOH solution afterwards, wherein controls Fe3+、Mg2+、OH-Mol ratio be 2: 1:8;Above-mentioned mixed solution being heated until seething with excitement under the mixing speed of 2500r/min, naturally cooling under room temperature after 1min Room temperature;Product after cooling filters, and uses HNO3Solution washs and is centrifuged again being precipitated, and repeats this process Until joining the Fe (NO of boiling after being precipitated as neutrality3)3In solution, under the mixing speed of 2500r/min, keep boiling Naturally cooling to room temperature after 30min, then filter, the filter cake acetone of gained is dehydrated, dry in 60 DEG C of drying boxes Dry 24h, more ground process, obtain p-MgFe2O4Magnetic particle;
By HCl solution and the 1.00moi/L Ni (NO of 1mol/L3)2After solution mixes for 1:25 by volume, add 2.03mol/L FeCl3Solution, adds 4mol/L NaOH solution afterwards, wherein controls Fe3+、Ni2+、OH-Mol ratio be 2: 1:8;Above-mentioned mixed solution being heated until seething with excitement under the mixing speed of 2500r/min, naturally cooling under room temperature after 1min Room temperature;Product after cooling filters, and washs with HNO3 solution and is centrifuged again being precipitated, repeats this process Until joining the Fe (NO of boiling after being precipitated as neutrality3)3In solution, under the mixing speed of 2500r/min, keep boiling Naturally cool to room temperature after 30min, then filter, after the filter cake of gained is dehydrated with acetone, be dried in 60 DEG C of drying boxes 24h, more ground process, obtain p-NiFe2O4Magnetic particle;
p-MgFe2O4、p-NiFe2O4The preparation of unit ionic ferrofluid:
By p-MgFe2O4After magnetic particle, the HCl of 1mol/L and base fluid mix for 1:3.3:20.7 by volume, obtain p- MgFe2O4Unit ionic ferrofluid;
By p-NiFe2O4After magnetic particle, the HCl of 1mol/L and base fluid mix for 1:2.85:21.15 by volume, obtain p-NiFe2O4Unit ionic ferrofluid;
p-MgFe2O4-p-NiFe2O4The preparation of binary weak magnetic hybrid ionic type magnetic liquid:
By p-MgFe2O4Unit ionic ferrofluid and p-NiFe2O4Unit ionic ferrofluid mixes according to volume ratio 1:1 Shake up, prepare p-MgFe2O4-p-NiFe2O4Binary weak magnetic hybrid ionic type magnetic liquid.
A kind of p-MgFe the most according to claim 12O4And p-NiFe2O4Binary magnetic hybrid ionic type magnetic liquid Preparation method, it is characterised in that: described p-MgFe2O4Unit ionic ferrofluid, p-NiFe2O4Unit ionic magnetic Volume fraction φ of liquidVBeing 2%, Q value is 0.12.
A kind of p-MgFe the most according to claim 12O4And p-NiFe2O4Binary magnetic hybrid ionic type magnetic liquid Preparation method, rises and is characterised by: p-MgFe in described step (2)2O4Control to be 1 with the molar concentration rate of 1mol/L HCl: 0.36, p-NiFe2O4Control as 1:0.36 with the molar concentration rate of 1mol/L HCl.
CN201610336717.2A 2016-05-20 2016-05-20 Preparation method of p-MaFe2O4 and p-NiFe2O4 binary magnetic mixed ionic magnetic fluid Pending CN105869822A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201610336717.2A CN105869822A (en) 2016-05-20 2016-05-20 Preparation method of p-MaFe2O4 and p-NiFe2O4 binary magnetic mixed ionic magnetic fluid

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201610336717.2A CN105869822A (en) 2016-05-20 2016-05-20 Preparation method of p-MaFe2O4 and p-NiFe2O4 binary magnetic mixed ionic magnetic fluid

Publications (1)

Publication Number Publication Date
CN105869822A true CN105869822A (en) 2016-08-17

Family

ID=56634478

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201610336717.2A Pending CN105869822A (en) 2016-05-20 2016-05-20 Preparation method of p-MaFe2O4 and p-NiFe2O4 binary magnetic mixed ionic magnetic fluid

Country Status (1)

Country Link
CN (1) CN105869822A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111270205A (en) * 2020-02-18 2020-06-12 哈尔滨工业大学 Preparation method of spinel phase p-type nickel ferrite semiconductor oxide film

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7122502B1 (en) * 2001-06-20 2006-10-17 Sandia Corporation Inorganic ion sorbents
CN104934185A (en) * 2015-07-14 2015-09-23 南昌航空大学 Binary weak magnetic mixed ionic type magnetic liquid preparation method

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7122502B1 (en) * 2001-06-20 2006-10-17 Sandia Corporation Inorganic ion sorbents
CN104934185A (en) * 2015-07-14 2015-09-23 南昌航空大学 Binary weak magnetic mixed ionic type magnetic liquid preparation method

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111270205A (en) * 2020-02-18 2020-06-12 哈尔滨工业大学 Preparation method of spinel phase p-type nickel ferrite semiconductor oxide film

Similar Documents

Publication Publication Date Title
CN107428544A (en) Silica-based composite particles dispersion liquid, its manufacture method and the polishing slurry for including silica-based composite particles dispersion liquid
Wang et al. Size-controlled synthesis of water-dispersible superparamagnetic Fe 3 O 4 nanoclusters and their magnetic responsiveness
WO1995004700A1 (en) Metal oxide powder and process for producing the same
CN108483474B (en) Preparation method of nanoscale spherical alumina
CN108083316B (en) Preparation method of nano rare earth oxide powder
Yang et al. Gram-scale synthesis of superparamagnetic Fe 3 O 4 nanocrystal clusters with long-term charge stability for highly stable magnetically responsive photonic crystals
JP2010155931A (en) Core-shell-type ceria-polymer hybrid nanoparticle and producing method of dispersion liquid thereof
Xia et al. Facile synthesis of inorganic nanoparticles by a precipitation method in molten ε-caprolactam solvent
KR20130142852A (en) Method for preparing silver cluster of micro-size consisting of agglomerate nano-silver particle
CN108862362A (en) A kind of preparation method of micron order cerium oxide powder
CN104934185B (en) A kind of preparation method of binary weak magnetic hybrid ionic type magnetic liquid
CN108975378A (en) A kind of dysprosia raw powder's production technology
EP2799185B1 (en) Method for separating polishing material and regenerated polishing material
Treadwell et al. Impact of oleylamine: oleic acid ratio on the morphology of yttria nanomaterials
CN105469920B (en) A kind of hypergravity preparation method of the magnetic Nano material of cysteine modified
CN105869822A (en) Preparation method of p-MaFe2O4 and p-NiFe2O4 binary magnetic mixed ionic magnetic fluid
CN109437317A (en) A kind of flower-shaped BiFeO of hydro-thermal method preparation3Powder and preparation method thereof
Park et al. Synthesis of hierarchical copper oxide composites prepared via electrical explosion of the wire in liquids method
Anzlovar et al. Sub micrometer and nano-ZnO as filler in PMMA materials
Zou et al. Fabricating BaZrO 3 hollow microspheres by a simple reflux method
CN109867310B (en) In-situ preparation of SmCo5/Sm2Co17Method for preparing biphase composite magnetic nano particles with core-shell structure
JP2018172227A (en) ε IRON OXIDE POWDER WITH PART OF IRON SITES SUBSTITUTED WITH METAL ELEMENT OTHER THAN IRON, METHOD OF PRODUCING THE SAME, AND PASTE
CN102730740B (en) Method for preparing cubic crystal system cerium oxide nanocrystal
US10106433B2 (en) Metal oxide nanoparticle material
Tsai et al. Formation mechanisms of colloidal silica via sodium silicate

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
WD01 Invention patent application deemed withdrawn after publication
WD01 Invention patent application deemed withdrawn after publication

Application publication date: 20160817