CN103449519B - Dysprosium and yttrium codoped pucherite inorganic pigment and preparation method thereof - Google Patents
Dysprosium and yttrium codoped pucherite inorganic pigment and preparation method thereof Download PDFInfo
- Publication number
- CN103449519B CN103449519B CN201310343864.9A CN201310343864A CN103449519B CN 103449519 B CN103449519 B CN 103449519B CN 201310343864 A CN201310343864 A CN 201310343864A CN 103449519 B CN103449519 B CN 103449519B
- Authority
- CN
- China
- Prior art keywords
- yttrium
- dysprosium
- pucherite
- solution
- codoped
- 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.)
- Expired - Fee Related
Links
Landscapes
- Inorganic Compounds Of Heavy Metals (AREA)
- Pigments, Carbon Blacks, Or Wood Stains (AREA)
Abstract
The invention discloses a dysprosium and yttrium codoped pucherite inorganic pigment and a preparation method thereof. A general formula of the pucherite inorganic pigment is Bi1-x-yDyxYyVO4, wherein x is smaller than or equal to 0.1 and greater than or equal to 0.02; y is smaller than or equal to 0.1 and greater than or equal to 0.02; the pucherite pigment codoped with a dysprosium element and a yttrium element is prepared by using assistance of chelating agents by a microwave hydrothermal method; different chelating agents are added; slow release of metal ions in a reaction process is facilitated, so that the process of generating the pucherite pigment codoped with the dysprosium element and the yttrium element is carried out in a mitigating manner; the preparation time is shortened in preparation employing the microwave hydrothermal method. According to the pucherite pigment codoped with the dysprosium element and the yttrium element prepared by the preparation method, doping of the dysprosium element and the yttrium element contributes to improvement of the coloring property of the pucherite pigment.
Description
Technical field
The present invention relates to mineral dye preparation field, be specifically related to a kind of dysprosium, yttrium codoped pucherite mineral dye and preparation method thereof.
Background technology
Since the eighties in last century, because pucherite has the high-performance such as nontoxic, bright color, good corrosion resistance, photochemical catalysis, photocatalytic degradation and the large field of mineral dye two are widely used in.As a kind of environmentally friendly inorganic materials, in pigment art, instead of environmentally harmful pigment gradually becomes a kind of novel pigment be widely used.In nearest decades, scholars have carried out large quantifier elimination to the application of pucherite in mineral dye, such as: prepare bismuth vanadium pigments with diverse ways, its main method has: the metallo-organic chemical vapour deposition etc. of solid phase method, pickling process, hydrothermal method, photoreduction method, modification.Prepare bismuth vanadium pigments with different raw materials, the raw material mainly used has Bismuth trinitrate, ammonium meta-vanadate and sodium metavanadate.Also have and in the process preparing bismuth vanadium pigments, to add different surfaces promoting agent carry out modification, the tensio-active agent mainly used has: ethylenediamine tetraacetic acid (EDTA), PVP, cetyl trimethylammonium bromide etc.
But these can not meet the application of single pucherite in practical field far away.
Summary of the invention
The invention provides a kind of dysprosium, yttrium codoped pucherite mineral dye and preparation method thereof, utilize sequestrant to assist and use microwave-hydrothermal method to prepare the bismuth vanadium pigments of dysprosium element and yttrium co-doped, dysprosium element and yttrium doped with helping the color generation property improving bismuth vanadium pigments.
The present invention is by the following technical solutions:
A kind of dysprosium, yttrium codoped pucherite mineral dye preparation method, utilize sequestrant to assist and use microwave-hydrothermal method to prepare the bismuth vanadium pigments of dysprosium element and yttrium co-doped.
Specifically comprise the following steps:
(1), by Bi (NO
3)
35H
2o, Dy (NO
3)
36H
2o, Y (NO
3)
36H
2o and sequestrant are dissolved into the HNO of 1 ~ 4mol/L
3carry out fully stirring obtaining solution A, wherein Bi (NO in solution
3)
35H
2o, Dy (NO
3)
36H
2o, Y (NO
3)
36H
2o, HNO
3be 1:(0.02 ~ 0.1 with the mol ratio of sequestrant): (0.02 ~ 0.1): (4 ~ 16): (0.5 ~ 2); By NaVO
32H
2o to be dissolved in the NaOH solution of 1 ~ 4mol/L and to carry out fully stirring obtaining solution B, wherein NaVO
32H
2the mol ratio of O and NaOH is 1:(4 ~ 16);
(2), solution A and solution B mixed and carry out fully stirring forming suspension, wherein Bi
3+and VO
3 -mol ratio be 1:1, this suspension is the presoma of the bismuth vanadium pigments of dysprosium element and yttrium co-doped;
(3), by above-mentioned suspension be transferred in microwave hydrothermal instrument, utilize carry out microwave radiation heating; After microwave hydrothermal reacts completely, washing several times, the bismuth vanadium pigments of obtained dysprosium element and yttrium co-doped after vacuum-drying.
Described sequestrant is ethylenediamine tetraacetic acid (EDTA), Trisodium Citrate, methyl ethyl diketone or several mixtures.
Suspension is transferred in microwave hydrothermal instrument in (3) by step, utilizes carry out microwave radiation heating will to 160 DEG C ~ 220 DEG C, hydro-thermal reaction 1 ~ 3h.
After in step (3), microwave hydrothermal reacts completely, with deionized water and absolute ethanol washing several times.
In step (3) after washing in vacuum drying oven dry 12h at 60 DEG C, the bismuth vanadium pigments of obtained dysprosium element and yttrium co-doped.
A kind of dysprosium, yttrium codoped pucherite mineral dye, its general formula is Bi
1-x-ydy
xy
yvO
4, wherein 0.02≤x≤0.1,0.02≤y≤0.1.
Beneficial effect of the present invention is: add different sequestrants, it act as and contributes to the slow releasing of metal ion in reaction process, thus make the process of generation dysprosium element and yttrium co-doped bismuth vanadium pigments compare the carrying out of mitigation, the bismuth vanadium pigments chemical constitution obtained is even, particle diameter is less, and within the scope of certain particle size, particle diameter is less, its opacifying power, tinting strength are stronger, from but the dominant hue of pigment and brightness improve; Microwave-hydrothermal method is used to prepare the bismuth vanadium pigments of dysprosium element and yttrium co-doped, its synthesis temperature is lower, generated time is shorter, and synthesis temperature needed for conventional solid-state method synthesis bismuth vanadium pigments is higher, generated time is longer, therefore, preparation method provided by the present invention is conducive to reducing energy consumption, reduces production cost; The product that the present invention finally obtains is the bismuth vanadium pigments of dysprosium element and yttrium co-doped, utilize dysprosium element and yttrium doped with the color generation property helping improve bismuth vanadium pigments, because the atomic structure of rare earth element uniqueness, the existence of the 4f electronic shell be not namely full of, when being subject to rayed, 4f electronic shell, to the characteristic with selective absorbing and reflection of light, due to this characteristic, can make rare earth doped beramic color have the advantage that color development is stablized, tone is pure.
Embodiment
Embodiment 1:
By 5mmol(2.4254g) Bi (NO
3)
35H
2o is dissolved into 1mol/L, the HNO of 20ml
3in solution, then add 0.1mmol(0.0457g wherein) Dy (NO
3)
36H
2o, 0.1mmol(0.0383g) Y (NO
3)
36H
2o and 2.5mmol(0.7306g) ethylenediamine tetraacetic acid (EDTA), fully stir to obtain solution A; By 5mmol(0.7898g) NaVO
32H
2o is dissolved into 1mol/L, in the NaOH solution of 20ml, fully stirs to obtain solution B; By above-mentioned A, B solution is carried out mixing and is forwarded in water heating kettle after abundant stirring, at 160 DEG C, and microwave hydrothermal 1h.Then, with deionized water and absolute ethanol washing several times, dry 12h at 60 DEG C in vacuum drying oven subsequently, obtain the bismuth vanadium pigments of dysprosium element and yttrium co-doped, its general formula is Bi
0.96dy
0.02y
0.02vO
4.
Embodiment 2:
By 5mmol(2.4254g) Bi (NO
3)
35H
2o is dissolved into 4mol/L, the HNO of 20ml
3in solution, then add 0.1mmol(0.0457g wherein) Dy (NO
3)
36H
2o, 0.1mmol(0.0383g) Y (NO
3)
36H
2o and 10mmol(2.9224g) ethylenediamine tetraacetic acid (EDTA), fully stir to obtain solution A; By 5mmol(0.7898g) NaVO
32H
2o is dissolved into 4mol/L, in the NaOH solution of 20ml, fully stirs to obtain solution B; By above-mentioned A, B solution is carried out mixing and is forwarded in water heating kettle after abundant stirring, at 220 DEG C, and microwave hydrothermal 3h.Then, with deionized water and absolute ethanol washing several times, dry 12h at 60 DEG C in vacuum drying oven subsequently, obtain the bismuth vanadium pigments of dysprosium element and yttrium co-doped, its general formula is Bi
0.96dy
0.02y
0.02vO
4.
Embodiment 3:
By 5mmol(2.4254g) Bi (NO
3)
35H
2o is dissolved into 1mol/L, the HNO of 20ml
3in solution, then add 0.1mmol(0.0457g wherein) Dy (NO
3)
36H
2o, 0.1mmol(0.0383g) Y (NO
3)
36H
2o and 2.5mmol(0.7353g) Trisodium Citrate, fully stir to obtain solution A; By 5mmol(0.7898g) NaVO
32H
2o is dissolved into 1mol/L, in the NaOH solution of 20ml, fully stirs to obtain solution B; By above-mentioned A, B solution is carried out mixing and is forwarded in water heating kettle after abundant stirring, at 160 DEG C, and microwave hydrothermal 1h.Then, with deionized water and absolute ethanol washing several times, dry 12h at 60 DEG C in vacuum drying oven subsequently, obtain the bismuth vanadium pigments of dysprosium element and yttrium co-doped, its general formula is Bi
0.96dy
0.02y
0.02vO
4.
Embodiment 4:
By 5mmol(2.4254g) Bi (NO
3)
35H
2o is dissolved into 4mol/L, the HNO of 20ml
3in solution, then add 0.5mmol(0.2285g wherein) Dy (NO
3)
36H
2o, 0.5mmol(0.1915g) Y (NO
3)
36H
2o and 10mmol(2.9412g) Trisodium Citrate, fully stir to obtain solution A; By 5mmol(0.7898g) NaVO
32H
2o is dissolved into 4mol/L, in the NaOH solution of 20ml, fully stirs to obtain solution B; By above-mentioned A, B solution is carried out mixing and is forwarded in water heating kettle after abundant stirring, at 220 DEG C, and microwave hydrothermal 3h.Then, with deionized water and absolute ethanol washing several times, dry 12h at 60 DEG C in vacuum drying oven subsequently, obtain the bismuth vanadium pigments of dysprosium element and yttrium co-doped, its general formula is Bi
0.8dy
0.1y
0.1vO
4.
Embodiment 5:
By 5mmol(2.4254g) Bi (NO
3)
35H
2o is dissolved into 1mol/L, the HNO of 20ml
3in solution, then add 0.5mmol(0.2285g wherein) Dy (NO
3)
36H
2o, 0.5mmol(0.1915g) Y (NO
3)
36H
2o and 2.5mmol(0.2503g) methyl ethyl diketone, fully stir to obtain solution A; By 5mmol(0.7898g) NaVO
32H
2o is dissolved into 1mol/L, in the NaOH solution of 20ml, fully stirs to obtain solution B; By above-mentioned A, B solution is carried out mixing and is forwarded in water heating kettle after abundant stirring, at 160 DEG C, and microwave hydrothermal 1h.Then, with deionized water and absolute ethanol washing several times, dry 12h at 60 DEG C in vacuum drying oven subsequently, obtain the bismuth vanadium pigments of dysprosium element and yttrium co-doped, its general formula is Bi
0.8dy
0.1y
0.1vO
4.
Embodiment 6:
By 5mmol(2.4254g) Bi (NO
3)
35H
2o is dissolved into 4mol/L, the HNO of 20ml
3in solution, then add 0.5mmol(0.2285g wherein) Dy (NO
3)
36H
2o, 0.5mmol(0.1915g) Y (NO
3)
36H
2o and 10mmol(1.0012g) methyl ethyl diketone, fully stir to obtain solution A; By 5mmol(0.7898g) NaVO
32H
2o is dissolved into 4mol/L, in the NaOH solution of 20ml, fully stirs to obtain solution B; By above-mentioned A, B solution is carried out mixing and is forwarded in water heating kettle after abundant stirring, at 220 DEG C, and microwave hydrothermal 3h.Then, with deionized water and absolute ethanol washing several times, dry 12h at 60 DEG C in vacuum drying oven subsequently, obtain the bismuth vanadium pigments of dysprosium element and yttrium co-doped, its general formula is Bi
0.8dy
0.1y
0.1vO
4.
Embodiment 7:
By 5mmol(2.4254g) Bi (NO
3)
35H
2o is dissolved into 2.5mol/L, the HNO of 20ml
3in solution, then add 0.4mmol(0.1828g wherein) Dy (NO
3)
36H
2o, 0.4mmol(0.1532) Y (NO
3)
36H
2o, 8mmol(0.80096g) methyl ethyl diketone and ethylenediamine tetraacetic acid (EDTA), fully stir to obtain solution A; By 5mmol(0.7898g) NaVO
32H
2o is dissolved into 2.5mol/L, in the NaOH solution of 20ml, fully stirs to obtain solution B; By above-mentioned A, B solution is carried out mixing and is forwarded in water heating kettle after abundant stirring, at 180 DEG C, and microwave hydrothermal 2.5h.Then, with deionized water and absolute ethanol washing several times, dry 12h at 60 DEG C in vacuum drying oven subsequently, obtain the bismuth vanadium pigments of dysprosium element and yttrium co-doped, its general formula is Bi
0.84dy
0.08y
0.08vO
4.
Embodiment 8:
By 5mmol(2.4254g) Bi (NO
3)
35H
2o is dissolved into 3mol/L, the HNO of 20ml
3in solution, then add 0.3mmol(0.1371g wherein) Dy (NO
3)
36H
2o, 0.3mmol(0.1149g) Y (NO
3)
36H
2o, 9mmol(0.90108g) the mixture of ethylenediamine tetraacetic acid (EDTA), methyl ethyl diketone and Trisodium Citrate, fully stir to obtain solution A; By 5mmol(0.7898g) NaVO
32H
2o is dissolved into 3mol/L, in the NaOH solution of 20ml, fully stirs to obtain solution B; By above-mentioned A, B solution is carried out mixing and is forwarded in water heating kettle after abundant stirring, at 200 DEG C, and microwave hydrothermal 3h.Then, with deionized water and absolute ethanol washing several times, dry 12h at 60 DEG C in vacuum drying oven subsequently, obtain the bismuth vanadium pigments of dysprosium element and yttrium co-doped, its general formula is Bi
0.88dy
0.06y
0.06vO
4.
Therefore, in the present invention, with the addition of different sequestrants, effectively can control speed of reaction, make the carrying out of the process gentleness of generation bismuth vanadium pigments; Secondly, the present invention improves the color generation property of bismuth vanadium pigments by the co-doped of dysprosium element and yttrium; Finally, the present invention uses the microwave-hydrothermal method that effectively can shorten preparation time to carry out the preparation of bismuth vanadium pigments.
Claims (5)
1. dysprosium, a yttrium codoped pucherite mineral dye preparation method, is characterized in that: utilize sequestrant to assist and use microwave-hydrothermal method to prepare the bismuth vanadium pigments of dysprosium element and yttrium co-doped;
Specifically comprise the following steps:
(1), by Bi (NO
3)
35H
2o, Dy (NO
3)
36H
2o, Y (NO
3)
36H
2o and sequestrant are dissolved into the HNO of 1 ~ 4mol/L
3carry out fully stirring obtaining solution A, wherein Bi (NO in solution
3)
35H
2o, Dy (NO
3)
36H
2o, Y (NO
3)
36H
2o, HNO
3be 1:(0.02 ~ 0.1 with the mol ratio of sequestrant): (0.02 ~ 0.1): (4 ~ 16): (0.5 ~ 2); By NaVO
32H
2o to be dissolved in the NaOH solution of 1 ~ 4mol/L and to carry out fully stirring obtaining solution B, wherein NaVO
32H
2the mol ratio of O and NaOH is 1:(4 ~ 16); Described sequestrant is ethylenediamine tetraacetic acid (EDTA), Trisodium Citrate, methyl ethyl diketone or several mixtures;
(2), solution A and solution B mixed and carry out fully stirring forming suspension, wherein Bi
3+and VO
3 -mol ratio be 1:1, this suspension is the presoma of the bismuth vanadium pigments of dysprosium element and yttrium co-doped;
(3), by above-mentioned suspension be transferred in microwave hydrothermal instrument, utilize carry out microwave radiation heating; After microwave hydrothermal reacts completely, washing several times, the bismuth vanadium pigments of obtained dysprosium element and yttrium co-doped after vacuum-drying.
2. dysprosium according to claim 1, yttrium codoped pucherite mineral dye preparation method, it is characterized in that: suspension is transferred in microwave hydrothermal instrument in step (3), utilize carry out microwave radiation heating will to 160 DEG C ~ 220 DEG C, hydro-thermal reaction 1 ~ 3h.
3. dysprosium according to claim 1, yttrium codoped pucherite mineral dye preparation method, is characterized in that: after in step (3), microwave hydrothermal reacts completely, with deionized water and absolute ethanol washing several times.
4. dysprosium according to claim 2, yttrium codoped pucherite mineral dye preparation method, it is characterized in that: in step (3) after washing in vacuum drying oven dry 12h at 60 DEG C, the bismuth vanadium pigments of obtained dysprosium element and yttrium co-doped.
5., as dysprosium, a yttrium codoped pucherite mineral dye that claim 1-4 preparation method obtains, it is characterized in that: its general formula is Bi
1-x-ydy
xy
yvO
4, wherein 0.02≤x≤0.1,0.02≤y≤0.1.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201310343864.9A CN103449519B (en) | 2013-08-08 | 2013-08-08 | Dysprosium and yttrium codoped pucherite inorganic pigment and preparation method thereof |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201310343864.9A CN103449519B (en) | 2013-08-08 | 2013-08-08 | Dysprosium and yttrium codoped pucherite inorganic pigment and preparation method thereof |
Publications (2)
Publication Number | Publication Date |
---|---|
CN103449519A CN103449519A (en) | 2013-12-18 |
CN103449519B true CN103449519B (en) | 2015-01-28 |
Family
ID=49732422
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201310343864.9A Expired - Fee Related CN103449519B (en) | 2013-08-08 | 2013-08-08 | Dysprosium and yttrium codoped pucherite inorganic pigment and preparation method thereof |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN103449519B (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN105838111B (en) * | 2016-05-25 | 2018-02-23 | 赣州有色冶金研究所 | Pearlescent pigment with heat discoloration effect and preparation method thereof and system |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102641732B (en) * | 2012-04-17 | 2014-05-07 | 淮阴师范学院 | Multi-morphology rare earth doped BiVO4 composite photocatalyst and preparation method thereof |
-
2013
- 2013-08-08 CN CN201310343864.9A patent/CN103449519B/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
CN103449519A (en) | 2013-12-18 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN104437587B (en) | A kind of phosphoric acid bismuthino composite photocatalyst material and preparation method thereof | |
CN103420417B (en) | Lanthanum-cerium co-doping bismuth vanadate inorganic pigment and preparation method thereof | |
CN103449518B (en) | Lanthanum, yttrium and cerium co-doped bismuth vanadate inorganic pigment and preparation method thereof | |
CN104031647B (en) | A kind of preparation method of round pie europium doping vanadic acid lanthanum red fluorescence powder | |
CN103204490B (en) | Preparation method of iron trioxide/carbon yolk-eggshell nano-composite structure | |
CN105036178B (en) | A kind of preparation method of modified nano zinc oxide | |
CN102191060B (en) | Vanadate phosphor and preparation method thereof | |
CN103894216B (en) | A kind of preparation method of magnetic Nano silver oxide/titanic oxide composite photochemical catalyst material | |
CN103421353B (en) | Dysprosium and praseodymium co-doped bismuth vanadate inorganic pigment and preparation method thereof | |
CN104475139B (en) | Co-doped bismuth phosphate-base composite photocatalytic material and preparation method thereof | |
CN102698749B (en) | Ruthenium ammonia synthesis catalyst taking ruthenium ammonia complex as precursor | |
CN103449519B (en) | Dysprosium and yttrium codoped pucherite inorganic pigment and preparation method thereof | |
CN106978170A (en) | A kind of preparation method of water-solubility fluorescent carbon quantum dot | |
CN103666447B (en) | For the two conversion of solar cell core-shell structured nanomaterials and preparation method thereof | |
CN103420688B (en) | Lanthanum-yttrium co-doping bismuth vanadate inorganic pigment and preparation method thereof | |
CN107399763A (en) | A kind of ultrasonic microwave combines the method for preparing sodium dichromate | |
CN104383911B (en) | A kind of banded Bi17V3O33/Bi1.7V8O16Photochemical catalyst and its preparation method and application | |
CN102513543A (en) | Microwave heating reduction technology for preparing superfine silver powder | |
CN105238404A (en) | Mesoporous core-shell phosphor and liquid phase preparation method thereof | |
CN107827155A (en) | A kind of nanometer V2O5Preparation method | |
CN104588025B (en) | A kind of self assembly near-spherical Sm2o3the preparation method of/CuO nano-complex | |
CN107899560A (en) | The preparation method of graphene titanium dioxide composite photocatalyst | |
CN103508492A (en) | Method for rapidly preparing NdWO4(OH) nanopowder | |
CN105080544A (en) | Method for synthesizing cuprous oxide-carbon nanotube compound through laser liquid phase ablation | |
CN103302303B (en) | Method for preparing copper-nickel solid solution powder by microwaves |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
C14 | Grant of patent or utility model | ||
GR01 | Patent grant | ||
CF01 | Termination of patent right due to non-payment of annual fee | ||
CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20150128 Termination date: 20210808 |