CN1357494A - Prepn of low temp phase barium metaborate nano powder - Google Patents
Prepn of low temp phase barium metaborate nano powder Download PDFInfo
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- CN1357494A CN1357494A CN 00135015 CN00135015A CN1357494A CN 1357494 A CN1357494 A CN 1357494A CN 00135015 CN00135015 CN 00135015 CN 00135015 A CN00135015 A CN 00135015A CN 1357494 A CN1357494 A CN 1357494A
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Abstract
Low temperature phase barium metaborate nano powder is prepared through the reactions of: Ba(OH)2.8H2O+2H3BO3+H2O2-BaB2O4.H2O2+12H2O and 2BaB2O4.H2O2-2BaB2O4+2H2O+O2. Into the liquid phase reaction system of preparing nanometer barium metaborate powder, hydrogen peroxide is added to change the reaction course of producing barium metaborate and prevent the continuous growth of product particles during preparing nanometer level beta-BaB2O4 powder. Observation with high resolution electronic microscope, the product has a size range of 40-100 nm and average size of 70 nm.
Description
The invention relates to the field of chemistry, in particular to a preparation method of nano powder, which is not searched by the inventor till now about β -BaB2O4The report about the preparation method of (low-temperature phase barium metaborate) nano powder. The nano material is a new subject which is rapidly developed in recent years, relates to the fields of multiple subjects such as chemistry, physics, materials science,biology, bionics and the like, and provides new opportunities for the cross development of the subjects. Because of its ultra-fine structure (particle size in the range of 1-100nm), nanoparticles are composed of a small number of atoms or molecules, and their particular structure gives them many unique properties. Mainly expressed in the aspects of magnetism, light absorption, heat resistance, chemical activity, catalysis, melting point and the like, which are greatly different from common materials.
Barium metaborate crystals generally have two crystal forms, the high temperature phase (α -BaB)2O4) And a low temperature phase (β -BaB)2O4) Wherein the low-temperature phase barium metaborate (β -BaB)2O4) The crystal is an excellent nonlinear optical crystal and is widely applied in the field of ultraviolet frequency doubling, and in addition, β -BaB2O4The optical fiber has frequency doubling effect, and the nonlinear optical property of the optical fiber is expected to be applied to the fields of nonlinear optical switches, functional ceramics and the like. The phase transition temperature of the high-temperature phase barium metaborate and the low-temperature phase barium metaborate is 920 +/-10 ℃. The melting points of two different crystal forms of barium metaborate are 1095 +/-5 ℃. In order to grow low-temperature phase barium metaborate crystals with high value, the crystals are grown at a temperature below the phase transition point by a molten salt method with fluxing agent added at home and abroad at present.
The invention aims to prepare nano-scale BaB2O4To reduce β -BaB204So that the melting point of the crystal is lower than or close to the phase transition point of the crystal, so that high-quality β -BaB can be rapidly grown by using a pulling method at the temperature close to the phase transition temperature of pure melt of the crystal2O4And (4) crystals. The method is a novel idea of applying nano materials to crystal growth, and is a new attempt of interpenetration of two high-tech fields of nano materials and new crystal materials.
The embodiments of the present invention are as follows:
barium hydroxide is adopted to react with boric acid and hydrogen peroxide, and the product is aged, washed, separated, dried and roasted to obtain the nano β -BaB2O4A powder having the formula:
the preparation method comprises the following specific steps:
(1) quantitative Ba (OH)2·8H2Heating and dissolving O in quantitative distilled water to obtain a solution with a concentration0.3mol/L-0.5mol/L, and filtering when the solution is hot after dissolving;
(2) quantitative determination of H3BO3Heating to dissolve in quantitative distilled water to obtain a solution with a concentration of 0.7-1.0 mol/L, cooling, adding 30% aqueous hydrogen peroxide solution, and adding H3BO3∶30％H2O2＝1mol∶250ml-500ml；
(3) Spraying (2) into the fully stirred (1), wherein the reaction temperature is 30-60 ℃, and the pH of the reaction system is 6-12, and H3BO3∶Ba(OH)·8H2O＝2∶1-1.10(mol)；
(4) Standing and aging for 30 minutes to 62 hours after the reaction is finished, thencentrifugally separating, and washing with distilled water or absolute ethyl alcohol for multiple times;
(5) drying at 100-120 deg.C under reduced pressure, and sintering at 500-600 deg.C for 0.5-3 h.
The product β -BaB is obtained after the steps2O4The powder has a particle size in the range of 40-100nm and an average particle size of 70 nm.
The wet chemical method for synthesizing barium metaborate must be implemented in strong alkaline medium, and in the course of reaction a large quantity of OH is adsorbed on the surface of product granules-OH in the reaction process and the subsequent drying and sintering processes-Dehydration is extremely likely to occur ( ) So that oxygen bridge connection is generated among particles to grow up, and the phenomenon that crystal water is carried in the product for preparing the metaborate is very common. These crystal waters are very likely to cause the particles to cross-link and grow during the subsequent sintering process, and thus the nanoparticles cannot be prepared. The invention provides that hydrogen peroxide is added into a reaction system, and the reaction system has two functions: firstly, the reaction process of generating barium metaborate is changed, secondly, the product synthesized by the reaction can not be coagulated to generate large-particle sediment due to the dispersion and support of hydrogen peroxide, and only a gel state can be generated.
The product prepared by the method is confirmed to be β -BaB by X-ray powder diffraction analysis2O4The particle size range of the product is 40nm-100nm, the average particle size is 70nm and the product is similar to a sphere through the observation of a high-resolution electron microscope.
The first embodiment is as follows:
(1) taking Ba (OH)2·8H2Heating and dissolving 15.8g of O in 150ml of distilled water, and filtering while the solution is hot;
(2) taking analytically pure H3BO36.2g of the aqueous solution was dissolved in 120ml of distilled water under heating, and after cooling, 20ml of a 30% aqueous solution of hydrogen peroxide was added;
(3) spraying the (2) into the fully stirred (1), and reacting at the temperature of 36 ℃, wherein the final PH of the reaction system is 6;
(4) after aging for 2h, the mixture was centrifuged, washed 3 times with absolute ethanol, dried under vacuum (120 ℃) for 4h, and then sintered in a muffle furnace at 500 ℃ for 1 h.
As a result, β -BaB was measured by a high resolution electron microscope2O4The average particle size of (2) was 100 nm.
Example two:
(1) weighing Ba (OH)2·8H2Heating and dissolving 33.4g of O in 300ml of distilled water, and filtering while the solution is hot;
(2) weighing analytically pure H3BO312.4g of the aqueous solution was dissolved in 300ml of distilled water under heating, and after cooling, 50ml of a 30% aqueous solution of hydrogen peroxide was added;
(3) spraying the (2) into the fully stirred (1), and reacting at the temperature of 36 ℃, wherein the final PH of the reaction system is 6;
(4) after the reaction is finished, aging for 0.5h, performing centrifugal separation, and washing for 3 times by using distilled water;
(5) drying at 120 deg.C for 4 hr, sintering in muffle furnace at500 deg.C for 1 hr, and taking out.
As a result: the average particle diameter of the particles is observed to be 70nm when the particle diameter is 40nm-100nm by a high-resolution electron microscope.
Example three:
(1) weighing Ba (OH)2·8H2Heating and dissolving 33.4g of O in 300ml of distilled water, and filtering while the solution is hot;
(2) weighing analytically pure H3BO312.4g of the aqueous solution was dissolved in 300ml of distilled water under heating, and after cooling, 50ml of a 30% aqueous solution of hydrogen peroxide was added;
(3) spraying the (2) into the fully stirred (1), and reacting at 60 ℃ until the final pH of the reaction system is 6;
(4) after the reaction is finished, aging for 0.5h, performing centrifugal separation, washing for 2 times by using water, then washing for 2 times by using absolute ethyl alcohol, and then adding 250ml of n-butyl alcohol for azeotropic distillation;
(5) vacuum drying at 120 deg.C, and sintering at 500 deg.C for 1 hr.
The result is that the particle size range of the particles is 40nm-100nm, β -BaB through the observation of a high-resolution electron microscope2O4Has an average particle diameter of 70 nm.
Claims (5)
1. A process for preparing low-temp phase barium metaborate nanoparticles includes such steps as reaction of barium hydroxide with boric acid and hydrogen peroxide, ageing, washing, separating, baking and calcining to obtain β -BaB nanoparticles2O4A powder having the formula:
the preparation method comprises the following specific steps:
(1) quantitative Ba (OH)2·8H2Heating and dissolving O in quantitative distilled water to prepare a solution with the concentration of 0.3-0.5 mol/L, and filtering the solution while the solution is hot;
(2) quantitative determination of H3BO3Heating to dissolve in quantitative distilled water to obtain a solution with a concentration of 0.7-1.0 mol/L, cooling, adding 30% aqueous hydrogen peroxide solution, and adding H3BO3∶30％H2O2＝1mol∶250ml-500ml；
(3) Spraying (2) into the fully stirred (1), reacting at 30-60 deg.C and pH 6-12, and reacting with hydrogen3BO3∶Ba(OH)·8H2O＝2∶1-1.10(mol)；
(4) Standing and aging for 0.5-62 h after the reaction is finished, then performing centrifugal separation, and washing with distilled water or absolute ethyl alcohol for multiple times;
(5) drying at 100-120 ℃ under reduced pressure, and sintering at 500-600 ℃ for 0.5-3 h.
2. The method for preparing low-temperature phase barium metaborate nanopowder according to claim 1, wherein hydrogen peroxide is added to the reaction system.
3. The method for preparing low-temperature phase barium metaborate nanopowder according to claim 1, wherein the reaction system has a pH of 6-12.
4. The method for preparing low-temperature phase barium metaborate nanopowder according to claim 1, wherein the aging time is 0.5h-10 h.
5. The method for preparing low-temperature phase barium metaborate nanopowder according to claim 1, which is characterized in that the sintering is carried out for 0.5h-2h in the air at 500 ℃ -550 ℃.
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| CNB001350153A CN1183035C (en) | 2000-12-07 | 2000-12-07 | Prepn of low temp phase barium metaborate nano powder |
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Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN100429147C (en) * | 2004-03-16 | 2008-10-29 | 中国科学院福建物质结构研究所 | Preparation method of low temperature phase barium metaborate nano powder |
| CN101913619A (en) * | 2010-09-29 | 2010-12-15 | 河北大学 | Preparation method of barium metaborate nano-powder |
| CN108557836A (en) * | 2018-04-28 | 2018-09-21 | 陕西师范大学 | A kind of BaB8O11(OH)4Flame retardant nano-materials and preparation method thereof |
| CN109112626A (en) * | 2018-10-25 | 2019-01-01 | 莱芜职业技术学院 | Non-linear optical crystal material β-BaB2O4Growing method |
-
2000
- 2000-12-07 CN CNB001350153A patent/CN1183035C/en not_active Expired - Fee Related
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN100429147C (en) * | 2004-03-16 | 2008-10-29 | 中国科学院福建物质结构研究所 | Preparation method of low temperature phase barium metaborate nano powder |
| CN101913619A (en) * | 2010-09-29 | 2010-12-15 | 河北大学 | Preparation method of barium metaborate nano-powder |
| CN101913619B (en) * | 2010-09-29 | 2012-09-05 | 河北大学 | Preparation method of barium metaborate nano-powder |
| CN108557836A (en) * | 2018-04-28 | 2018-09-21 | 陕西师范大学 | A kind of BaB8O11(OH)4Flame retardant nano-materials and preparation method thereof |
| CN109112626A (en) * | 2018-10-25 | 2019-01-01 | 莱芜职业技术学院 | Non-linear optical crystal material β-BaB2O4Growing method |
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| CN1183035C (en) | 2005-01-05 |
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