CN101012342A - Modified barite and preparation method thereof - Google Patents

Modified barite and preparation method thereof Download PDF

Info

Publication number
CN101012342A
CN101012342A CN 200710036979 CN200710036979A CN101012342A CN 101012342 A CN101012342 A CN 101012342A CN 200710036979 CN200710036979 CN 200710036979 CN 200710036979 A CN200710036979 A CN 200710036979A CN 101012342 A CN101012342 A CN 101012342A
Authority
CN
China
Prior art keywords
barite
modified
slurry
solution
modified barite
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
CN 200710036979
Other languages
Chinese (zh)
Other versions
CN100480339C (en
Inventor
陈焰
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.)
Foshan Onmillion Nano Materials Co. Ltd.
Original Assignee
SHANGHAI ONMILLION NANO MATERIAL CO Ltd
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 SHANGHAI ONMILLION NANO MATERIAL CO Ltd filed Critical SHANGHAI ONMILLION NANO MATERIAL CO Ltd
Priority to CNB2007100369798A priority Critical patent/CN100480339C/en
Publication of CN101012342A publication Critical patent/CN101012342A/en
Application granted granted Critical
Publication of CN100480339C publication Critical patent/CN100480339C/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Abstract

The invention discloses a modified barite and making method, which is characterized by the following: proceeding surface modifying through organic hybridization technique of titanium bundle or aluminium-titanium bundle barite; making the nanometer barite possess the same property as titanium oxide; fitting for delustring, sterilizing and masking rate-improving domain.

Description

A kind of modified barite and preparation method thereof
Technical field
The present invention relates to a kind of modified barite and preparation method thereof.
Background technology
Titanium dioxide is a kind of white industrial pigment of current performance the best, is widely used in coating, plastics, papermaking, printing ink, rubber, fields such as man-made fiber and makeup.Along with the increase to the titanium dioxide demand, the imbalance between supply and demand of titanium dioxide looms large.But the research, development and production of titanium dioxide all need huge investment, force the main users of titanium dioxide to go to develop the substitute of titanium dioxide.The U.S., Germany, France, industrially developed country such as Japan just began one's study and develop the surrogate of titanium dioxide from the seventies in 20th century, and had obtained very big economic benefit.At present, the research and development of China's titanium white powder surrogate are scarcely out of swaddling-clothes, and product performance are not good, 10%-30% that generally can only the instead of titanium white powder, and its major cause is that the opacifying power of product is too low, even does not have opacifying power.
Summary of the invention
Purpose of the present invention mainly is according to deficiency of the prior art, and nano titanium oxide is coated on the matrix material on barite particle surface, improves its opacifying power, makes it to reach the application of titanium dioxide.
For realizing above purpose, the present invention is achieved through the following technical solutions:
A kind of method for preparing nano barite may further comprise the steps,
A kind of modified barite, barite particle have wrap outward, and described wrap contains titanium dioxide.
Wherein, described wrap is a titanium dioxide, and the weight content of titanium dioxide in modified barite is 5-20%.
Preferably, described wrap is Al 2O 3-TiO 2
Wherein, each composition weight content is Al in the described modified barite 2O 33%-10%; TiO 22%-15%; Surplus is a barite.
Wherein, described barite particle diameter is a nano level.
Preferably, described barite particle diameter is 30nm-500nm.
Another object of the present invention provides a kind of method for preparing modified barite, may further comprise the steps: A: barite and water are mixed and made into slurry; B: regulating the slurry pH value is 1-6, under 50-100 ℃, drips TBOT solution and sodium hydrogen carbonate solution, insulation; C: suction filtration, washing, oven dry.
Wherein, in the slurry of described steps A, water-solid ratio is 0.1: 1-0.97: 1.
Wherein, described TBOT strength of solution is 5%-20%.
Wherein, the weight content of titanium dioxide in modified barite is 5-20%.
Wherein, before step B, the slurry pH value of steps A is adjusted to 7-12, sodium aluminate solution and dilution heat of sulfuric acid are added drop-wise in the slurry of steps A gained simultaneously.
Wherein, each composition weight content of described modified barite is Al 2O 33%-10%; TiO 22%-15%; Surplus is a barite.
Wherein, described barite particle diameter is a nano level.
Preferably, described barite particle diameter is 30nm-500nm.
Described TBOT is a tetrabutyl titanate.
The present invention adopts the organic hybrid technology of titanium parcel or aluminium-titanium parcel nano barite to carry out surface modification, make the nano barite of preparing have the rerum natura same with nano titanium oxide, at aspects such as delustring, sterilization, raising hiding rares bigger application is arranged, thereby widened the Application Areas of nano barite.
Description of drawings
Fig. 1 is an embodiment 1-5 process flow sheet;
Fig. 2 is an embodiment 6-9 process flow sheet.
Embodiment
Below in conjunction with example the present invention is described further:
Example 1:
In reactor, natural barite powder 20Kg and 2Kg water are mixed and made into slurry, the pH value of slurry is adjusted to 6, gets 5KgTBOT with its solution that is made into 10%, the sodium bicarbonate of getting 1Kg again is made into 10% solution, then TBOT solution is added dropwise under 60 ℃ in the slurry in the reactor with sodium hydrogen carbonate solution, the pH value is maintained 6, adds to finish back insulation 1 hour, suction filtration then, washing, 100 ℃ of oven dry, break up then, make the modified barite of titanium dioxide parcel.
Example 2:
The natural nano ground barium sulfate 20Kg and the 5Kg water that with particle diameter are 30nm in reactor are mixed and made into slurry, the pH value of slurry is adjusted to 2, gets 2KgTBOT with its solution that is made into 5%, the sodium bicarbonate of getting 1Kg again is made into 10% solution, then TBOT solution is added dropwise under 80 ℃ in the slurry in the reactor with sodium hydrogen carbonate solution, the pH value is maintained 2, adds back insulation 1 hour, then suction filtration, washing, 100 ℃ of oven dry, break up then, make the modified barite of titanium dioxide parcel.
Example 3:
The natural nano ground barium sulfate 20Kg and the 10Kg water that with particle diameter are 200nm in reactor are mixed and made into slurry, the pH value of slurry is adjusted to 4, get 3KgTBOT it is made into 15% solution, the sodium bicarbonate of getting 0.8Kg again is made into 10% solution, then TBOT solution is added dropwise under 90 ℃ in the slurry in the reactor with sodium hydrogen carbonate solution, the pH value is maintained 4, add back insulation 1 hour, suction filtration then, washing, 100 ℃ of oven dry, break up then, make the modified barite of titanium dioxide parcel.
Example 4:
The natural nano ground barium sulfate 20Kg and the 19Kg water that with particle diameter are 400nm in reactor are mixed and made into slurry, the pH value of slurry is adjusted to 5, get 4KgTBOT it is made into 20% solution, the sodium bicarbonate of getting 0.8Kg again is made into 10% solution, then TBOT solution is added dropwise under 95 ℃ in the slurry in the reactor with sodium hydrogen carbonate solution, the pH value is maintained 5, add back insulation 1 hour, suction filtration then, washing, 100 ℃ of oven dry, break up then, make the modified barite of titanium dioxide parcel.
Example 5:
The natural nano ground barium sulfate 20Kg and the 8Kg water that with particle diameter are 500nm in reactor are mixed and made into slurry, the pH value of slurry is adjusted to 5, get 2.5KgTBOT it is made into 20% solution, the sodium bicarbonate of getting 0.8Kg again is made into 10% solution, then TBOT solution is added dropwise under 70 ℃ in the slurry in the reactor with sodium hydrogen carbonate solution, the pH value is maintained 5, add back insulation 1 hour, suction filtration then, washing, 100 ℃ of oven dry, break up then, make the modified barite of titanium dioxide parcel.
Example 6
The natural barite powder 19Kg and the 5Kg water that in reactor with particle diameter are are mixed and made into slurry, the pH value of slurry is adjusted to 10, get sodium metaaluminate 0.7Kg and be made into 8% solution, preparation dilute sulphuric acid concentration is 5%, is added drop-wise to sodium aluminate solution and dilute sulphuric acid in the slurry simultaneously 80 ℃ of high-speed stirring; The pH value of slurry is adjusted to 2, gets 0.4KgTBOT with its solution that is made into 5%, the sodium bicarbonate of getting 1Kg again is made into 10% solution, then TBOT solution is added dropwise under 60 ℃ in the slurry in the reactor with sodium hydrogen carbonate solution,, dripping off in 1 hour, the pH value is maintained 2, add back insulation 1 hour, suction filtration is washed, 100 ℃ of oven dry then, break up then, make Al 2O 3-TiO 2The modified barite of parcel.
Example 7
The natural nano ground barium sulfate 15Kg and the 5Kg water that with particle diameter are 100nm in reactor are mixed and made into slurry, the pH value of slurry is adjusted to 7, get sodium metaaluminate 2Kg and be made into 8% solution, preparation dilute sulphuric acid concentration is 10%, drips simultaneously under 80 ℃ of high-speed stirring; The pH value of slurry is adjusted to 2, gets 3KgTBOT with its solution that is made into 15%, the sodium bicarbonate of getting 1Kg again is made into 10% solution, then TBOT solution is added dropwise under 80 ℃ in the slurry in the reactor with sodium hydrogen carbonate solution,, dripping off in 1 hour, the pH value is maintained 4, add back insulation 1 hour, suction filtration is washed, 100 ℃ of oven dry then, break up then, make modified barite.
Example 8
The natural nano ground barium sulfate 17Kg and the 5Kg water that with particle diameter are 300nm in reactor are mixed and made into slurry, the pH value of slurry is adjusted to 9, get sodium metaaluminate 1Kg and be made into 8% solution, preparation dilute sulphuric acid concentration is 10%, is added drop-wise to sodium aluminate solution and dilute sulphuric acid in the slurry simultaneously 80 ℃ of high-speed stirring; The pH value of slurry is adjusted to 4, get 2KgTBOT with its solution that is made into 18%, the sodium bicarbonate of getting 2Kg again is made into 10% solution, then TBOT solution is added dropwise under 85 ℃ in the slurry in the reactor with sodium hydrogen carbonate solution, drip off in 1 hour, the pH value is maintained 5, adds back insulation 1 hour, then suction filtration, washing, 100 ℃ of oven dry, break up then, make Al 2O 3-TiO 2The modified barite of parcel.
Example 9
The natural nano ground barium sulfate 19Kg and the 5Kg water that with particle diameter are 400nm in reactor are mixed and made into slurry, the pH value of slurry is adjusted to 12, get sodium metaaluminate 1.6Kg and be made into 8% solution, preparation dilute sulphuric acid concentration is 1%, is added drop-wise to sodium aluminate solution and dilute sulphuric acid in the slurry simultaneously 80 ℃ of high-speed stirring; The pH value of slurry is adjusted to 2, gets 0.4KgTBOT with its solution that is made into 5%, the sodium bicarbonate of getting 1Kg again is made into 10% solution, then TBOT solution is added dropwise under 70 ℃ in the slurry in the reactor with sodium hydrogen carbonate solution,, dripping off in 1 hour, the pH value is maintained 6, add back insulation 1 hour, suction filtration is washed, 100 ℃ of oven dry then, break up then, make Al 2O 3-TiO 2The modified barite of parcel.
The foregoing description only is used for that the present invention will be described, does not constitute the restriction to the claim scope, and other alternative means that it may occur to persons skilled in the art that are all in claim scope of the present invention.

Claims (14)

1. a modified barite is characterized in that, barite particle has wrap outward, and described wrap contains titanium dioxide.
2. modified barite according to claim 1 is characterized in that, described wrap is a titanium dioxide, and the weight content of titanium dioxide in modified barite is 5-20%.
3. modified barite according to claim 1 is characterized in that, described wrap is Al 2O 3-TiO 2
4. modified barite according to claim 3 is characterized in that, each composition weight content is Al in the described modified barite 2O 33%-10%; TiO 22%-15%; Surplus is a barite.
5. according to the described modified barite of the arbitrary claim of claim 1-4, it is characterized in that described barite particle diameter is a nano level.
6. modified barite according to claim 5 is characterized in that, described barite particle diameter is 30nm-500nm.
7. prepare the method for the described modified barite of claim 1, it is characterized in that, may further comprise the steps: A: barite and water are mixed and made into slurry; B: regulating the slurry pH value is 1-6, under 50-100 ℃, drips TBOT solution and sodium hydrogen carbonate solution, insulation; C: suction filtration, washing, oven dry.
8. the method for preparing modified barite according to claim 7 is characterized in that, in the slurry of described steps A, water-solid ratio is 0.1: 1-0.97: 1.
9. the method for preparing modified barite according to claim 7 is characterized in that, described TBOT strength of solution is 5%-20%.
10. the method for preparing modified barite according to claim 7 is characterized in that, the weight content of titanium dioxide in modified barite is 5-20%.
11. according to the described method for preparing modified barite of the arbitrary claim of claim 7-10, it is characterized in that, before step B, the slurry pH value of steps A is adjusted to 7-12, again sodium aluminate solution and dilution heat of sulfuric acid are added drop-wise in the slurry of steps A gained simultaneously.
12. the method for preparing modified barite according to claim 11 is characterized in that, each composition weight content of described modified barite is Al 2O 33%-10%; TiO 22%-15%; Surplus is a barite.
13., it is characterized in that described barite particle diameter is a nano level according to the described method for preparing modified barite of the arbitrary claim of claim 7-12.
14. the method for preparing modified barite according to claim 13 is characterized in that, described barite particle diameter is 30nm-500nm.
CNB2007100369798A 2007-01-30 2007-01-30 Modified barite and preparation method thereof Expired - Fee Related CN100480339C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CNB2007100369798A CN100480339C (en) 2007-01-30 2007-01-30 Modified barite and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CNB2007100369798A CN100480339C (en) 2007-01-30 2007-01-30 Modified barite and preparation method thereof

Publications (2)

Publication Number Publication Date
CN101012342A true CN101012342A (en) 2007-08-08
CN100480339C CN100480339C (en) 2009-04-22

Family

ID=38700075

Family Applications (1)

Application Number Title Priority Date Filing Date
CNB2007100369798A Expired - Fee Related CN100480339C (en) 2007-01-30 2007-01-30 Modified barite and preparation method thereof

Country Status (1)

Country Link
CN (1) CN100480339C (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102428155A (en) * 2009-03-23 2012-04-25 哈利伯顿能源服务公司 High performance drilling fluids with submicron-size particles as the weighting agent
CN101250336B (en) * 2008-04-10 2012-07-11 佛山安亿纳米材料有限公司 Barium sulfate based polybasic composite white pigments and method for preparing same
CN104371673A (en) * 2013-08-12 2015-02-25 中国石油化工股份有限公司 Weighting agent for high density drilling fluid, manufacturing method thereof, and drilling liquid containing same
CN104745153A (en) * 2013-12-31 2015-07-01 中国石油天然气集团公司 Barite micro-powder for drilling fluid and preparation method of concentrated liquor of barite micro-powder
CN108752013A (en) * 2018-06-19 2018-11-06 南方科技大学 A kind of modified ceramic material and its modification method for preparing and ceramic slurry
CN113234255A (en) * 2021-05-07 2021-08-10 江苏群鑫粉体科技股份有限公司 Ultraviolet screening agent and preparation method and application thereof

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101250336B (en) * 2008-04-10 2012-07-11 佛山安亿纳米材料有限公司 Barium sulfate based polybasic composite white pigments and method for preparing same
CN102428155A (en) * 2009-03-23 2012-04-25 哈利伯顿能源服务公司 High performance drilling fluids with submicron-size particles as the weighting agent
CN102428155B (en) * 2009-03-23 2014-04-23 哈利伯顿能源服务公司 High performance drilling fluids with submicron-size particles as the weighting agent
CN104371673A (en) * 2013-08-12 2015-02-25 中国石油化工股份有限公司 Weighting agent for high density drilling fluid, manufacturing method thereof, and drilling liquid containing same
CN104745153A (en) * 2013-12-31 2015-07-01 中国石油天然气集团公司 Barite micro-powder for drilling fluid and preparation method of concentrated liquor of barite micro-powder
CN108752013A (en) * 2018-06-19 2018-11-06 南方科技大学 A kind of modified ceramic material and its modification method for preparing and ceramic slurry
CN113234255A (en) * 2021-05-07 2021-08-10 江苏群鑫粉体科技股份有限公司 Ultraviolet screening agent and preparation method and application thereof
CN113234255B (en) * 2021-05-07 2022-12-02 江苏群鑫粉体科技股份有限公司 Ultraviolet screening agent and preparation method and application thereof

Also Published As

Publication number Publication date
CN100480339C (en) 2009-04-22

Similar Documents

Publication Publication Date Title
CN100480339C (en) Modified barite and preparation method thereof
CN101613537B (en) Method for preparing nano silicon dioxide coated by nano titanium dioxide
CN101343424B (en) Pearlescent pigment and preparation thereof
CN105568663B (en) A kind of natural weaving antibacterial finishing agent and preparation method thereof
CN101654862B (en) Preparation method of waterborne nano slurry
CN101235223A (en) High water dispersity titanium dioxide and coating method thereof
CN103613957A (en) Preparation method of novel zirconium-aluminum-coated titanium dioxide
CN106587126B (en) A kind of calcium carbonate nano wire and preparation method thereof
CN104387808A (en) Preparation method of jointly-coated titanium dioxide powder
CN101245198A (en) Coated titanium dioxide and manufacture method thereof
CN109370344A (en) Zeolite negative ion paint
CN103556275B (en) A kind of far infrared bamboo-carbon viscose fibre and preparation method thereof
CN100475916C (en) Composite white pigment and preparing method thereof
CN102086310B (en) Preparation method of weather-resistance environmental-friendly synthetic mica pearlescent pigment
CN103540171B (en) Preparation method of single-coating cobalt titanate green/mica pearlescent composite pigment
CN103897577A (en) Glass paint and preparation method thereof
CN114318948B (en) Antibacterial impregnated paper and preparation method and application thereof
CN108547172A (en) A kind of paper grade (stock) low solubility calcium sulfate, its production method and its application
CN104312209B (en) A kind of glass flake based pearlescent pigments and preparation method thereof
CN113733693B (en) Preparation method of stock solution coloring chlorine-bleaching-resistant surgical gown fabric
CN110283479B (en) Super-white composite sericite and preparation method thereof
CN104559390A (en) Synthetic latex paint powder
CN109281202A (en) A kind of nanocomposite and preparation method thereof for ramie cotton fabric
CN108517712A (en) A kind of paper grade (stock) micro nanometer fiber mill base and the preparation method and application thereof
CN108716042A (en) A kind of preparation method of functionality heavy twist color spot silk

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
ASS Succession or assignment of patent right

Owner name: FUSHAN ANYI NANO MATERIALS CO., LTD.

Free format text: FORMER OWNER: SHANGHAI ANYI NANO MATERIAL CO., LTD.

Effective date: 20090605

C41 Transfer of patent application or patent right or utility model
TR01 Transfer of patent right

Effective date of registration: 20090605

Address after: Shop No. 53-3, A District, grand pond garden, science and Technology Industrial Zone, Sanshui center, Guangdong, Foshan five, China

Patentee after: Foshan Onmillion Nano Materials Co. Ltd.

Address before: Block B, building 3, No. 395 West Court, Zhabei, Shanghai

Patentee before: Shanghai Onmillion Nano Material Co., Ltd.

C17 Cessation of patent right
CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20090422

Termination date: 20140130