CN100510171C - Preparation method of carbon coated TiO* core-shell composite nanometer powder - Google Patents
Preparation method of carbon coated TiO* core-shell composite nanometer powder Download PDFInfo
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- CN100510171C CN100510171C CNB2007100507482A CN200710050748A CN100510171C CN 100510171 C CN100510171 C CN 100510171C CN B2007100507482 A CNB2007100507482 A CN B2007100507482A CN 200710050748 A CN200710050748 A CN 200710050748A CN 100510171 C CN100510171 C CN 100510171C
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Abstract
The invention discloses a preparation method of a carbon-coated nanometer TiO2 core-shell composite powder (expressed as TiO2 @C). The low-cost amorphous hydrated titanium dioxide is used as the titanium oxide source, and the long-chain liquid alkane mixture (C11-C12) is used as the carbon source. The carbon coats an organic carbon chain by flowing back original positions, and then is heat-treated at a certain temperature under vacuum conditions to manufacture the nanometer TiO2 composite powder. The invention has the advantages that the carbon source and the titanium oxide source are cheap, the carbon source can be used repeatedly, the carbon coating amount can be controlled and adjusted, the technical operation is simple and is liable to industrialization, and so on.
Description
Technical field
The invention belongs to nano core-shell composite powder material preparation field, the organic carbon source that can recycle repeatedly that relates to a kind of cheapness coats preparation bag carbon by liquid phase and covers nano-TiO
2The method of nucleocapsid composite granule.
Background technology
Design and controlledly construct the research field that becomes more and more important that the composite nano-powder material with nucleocapsid structure is Materials science forward position recent years.Constructing the favor why this class material of novel capabilitiesization be subjected to the investigator is because they have the character of many uniquenesses, for example: the operability of monodispersity, nucleocapsid, stability, Modulatory character, self-assembly and relate to the ability of light, electricity, magnetic, catalysis, chemistry and biological respinse.Therefore can be regulated and control many character of composite nano materials to a great extent by rational contrived experiment condition.That the core-shell nano material mainly comprises is inorganic-several types such as organic and inorganic-inorganic, organic-organic and organic and inorganic.The present invention has related generally to a kind of nano-TiO that wraps carbon
2The nucleocapsid composite powder material (can be expressed as TiO
2Preparation method @C).
At present, preparation TiO
2The main method of @C composite nano-powder has:
Gaseous alkanes cracking bag carbon method: this method is the common method of preparation bag carbon nano core-shell composite powder material, and still, this method can not realize nano-TiO
2Particle wraps carbon under monodisperse status, prepared TiO
2The @C particle is bigger than normal, equipment requirements is high, power consumption is big, product purity is lower etc., has therefore also just limited this method in industrial application.
Arc discharge method: impel hydrocarbons decompose by arc-over, prepare the nano core-shell composite powder material thereby unbodied carbon laydown is coated on powder surface.This method has been owing to adopted arc-over that thermal source is provided, thus the higher while of equipment cost because the higher by product that more easily produces of transient temperature, gained nano core-shell composite granule is often impure.This method can not realize nano-TiO equally
2Particle wraps carbon under monodisperse status.
Sol-gel method: this method generally adopts the organism of the alkoxide of titanium and other a kind of rich carbon as raw material.Therefore the defective of this method is apparent, and at first the alkoxide price of titanium is more expensive relatively, and very easily hydrolysis under the environment of humidity; Secondly, other the bag carbon method of comparing, this method technology is comparatively complicated; At last, the difficult control of the content of the decolorizing carbon that the organism in the gel produces when thermolysis is easy to carbon quantity not sufficient or enrichment.
Organic polymer coats cracking process: this method adopts the mechanically mixing mode, at first allows macromolecular material be coated on the nano-powder material, heat-treats then, and making the organism thermolysis is inorganic carbon film, thereby prepares the composite nano-powder material of bag carbon.The greatest drawback of this method is that technology is prone to the inorganic carbon enrichment than complexity, can not realize nano-TiO simultaneously
2Particle wraps carbon under monodisperse status, because high molecular mechanically mixing process is difficult to evenly.
In recent years, fire is measured to such an extent that document shows, people studys always and using new organic carbon source bag carbon to reduce the cost, and prepares the nano combined nucleocapsid powder body material that the even and thickness of carbon film thickness makes things convenient for controlled bag carbon.Koc, people such as Rasit (Journal of materials science 34 (1999) 3083-3093) are with TiO
2Powder is a raw material, by thermolysis propylene (C
3H
6) the inorganic C of simple substance is deposited on TiO
2On the powder, prepare the nano-TiO that wraps carbon
2Composite powder material.Limin Shi, people (Powder Technology 169 (2006) 71-76) such as Hongsheng Zhao join the Si powder in the spirituous solution of resol and obtain the composite granule that organism coats by mixing, thermal treatment under certain condition forms the matrix material that inorganic carbon coats then, and further thermal treatment is translated into the SiC powder body material of submicron.
In the present invention, we are the titanium source with the unbodied hydrated titanium dioxide of cheapness, and the liquid alkane of long-chain is as carbon source, and the method by liquid-phase reflux and subsequent heat treatment is through making the nano-TiO that coats carbon film
2The nucleocapsid composite powder material.
Summary of the invention
The present invention is by refluxing under the long-time certain temperature, progressively the liquid alkane carbochain is embedded into single dispersion, network-like hydration TiO
2Go in the skeleton, again under vacuum condition and certain temperature thermal treatment to make organic carbochain thermolysis be that unbodied inorganic carbon and original position are coated on TiO
2Thereby powder surface is prepared the nano level TiO that is coated with carbon film
2Compound nucleocapsid powder (TiO
2@C).
A kind of organic carbon source can recycle repeatedly, is coated with the nano level TiO of carbon film
2Compound nucleocapsid powder (TiO
2Preparation method @C).Its feature comprises following concrete process:
(1) gets the raw materials ready: the volume ratio of dehydrated alcohol and liquid alkane mixture 4: 1～6: 1, every 500ml liquid alkane mixture (C
11-C
16) with 25～100g hydrated titanium dioxide.
(2) reflux: the formed suspension of dehydrated alcohol and hydrated titanium dioxide is at 40～100 ℃ of 1～10h that reflux down; Then with the paraffins mixture (C of liquid state
11-C
16) mix with precipitation powder with gained behind the alcohol reflux, and refluxed 12～72 hours down at 100～250 ℃, filter, obtain throw out; The alkane filtrate of filtering gained is through water collection (removal ethanol), anhydrous CaCl
2After dry (dewatering), recycle.
(3) charging: pack into the precursor powder in high alumina porcelain boat or the container and compress, it is airtight to put into the tubular type atmosphere furnace;
(4) high-temperature heat treatment: the reaction chamber of tube furnace is extracted into-0.09～-0.1MPa vacuum tightness, close vacuum pump then.Heat temperature raising to 600～1000 ℃, insulation 1～4h.Then, reaction chamber naturally cools to room temperature.
(5) sampling: take out sample in the porcelain boat from the alundum tube reaction chamber, obtain nano-TiO
2The @C powder,
The purpose that the present invention at first uses ethanol to reflux is from net catenate hydration TiO with free water
2In remove clean, simultaneously also with hydration TiO
2The hydroxyl on surface carries out esterification; Secondly the powder after refluxing in ethanol refluxes in the liquid alkane mixture again, purpose be for allow carbochain all or part of be embedded into amorphous hydrated TiO
2Network-like skeleton in go; To filter the gained throw out at last heat-treats, allow the cracking of organic carbochain original position that inorganic carbon is provided, because the particle growth that inorganic carbon coats the nucleocapsid powder has the effect of significant inhibition particle diameter, therefore be easy to obtain the TiO 2 particles that the inorganic carbon of nano-scale particle coats, thereby prepare the nano-TiO of original position bag carbon
2Compound nucleocapsid powder.
The present invention compared with prior art has following advantage and beneficial effect:
1. adopt new carbon source and new bag carbon mode, this makes the precursor particle be monodisperse status, and grain fineness number is little, specific surface area is huge and have porousness, the reactive behavior height of precursor, it is higher that organic carbon changes the number turnover of inorganic carbon into, thereby the productive rate of the finished product is higher.Since the iris action of carbon, the nano-TiO that the present invention prepares
2@C crystal grain and particulate size little (all less than 20nm) with the difference of thermal treatment temp, both can make anatase crystal type TiO
2@C also can make rutile TiO
2The @C nano particle.
2. precursor powder carbon content (organic carbon) is controlled, and the carbon amount of inorganicization of organic carbon transformation is controlled in the precursor powder, be difficult for to produce the enrichment or the deficiency of decolorizing carbon, and this makes the nano-TiO that present method prepares
2@C powder carbon amount is adjustable, controlled and purity is higher.
The carbon content that reflux temperature when preparing by adjusting precursor and time can be controlled the precursor powder; Thermal treatment process by control precursor powder can realize the control to inorganicization of organic carbon transformation amount.
3. technology of the present invention is simple, is easy to realize industrialization.
Do not need strict dosage relation between this preparation method raw material, so technological operation is simple; Preparation simultaneously, Equipment for Heating Processing is simple, and alkane filtrate reclaiming clean reclaim equiment is simple, is convenient to the industrialization operation.
4. titanium source of using among the present invention and organic carbon source cheapness and organic carbon source can recycle repeatedly.
The liquid alkane mixture carbon chain lengths that the present invention uses is about 11-16 C atom, and after paraffins mixture refluxed, the alkane filtrate of filtering gained can be changed the liquid alkane mixture that can be recycled into.
Specific embodiments
Example one
(1) gets the raw materials ready: liquid alkane mixture (C
11-C
16) 1000ml, dehydrated alcohol 5000ml, hydrated titanium dioxide 100g.
(2) reflux: the dehydrated alcohol of 100g hydrated titanium dioxide and 1000ml refluxed one hour down at 70 ℃, filtered then; Gained precipitates with the dehydrated alcohol of fresh 1000ml and mixes, and refluxes one hour down at 70 ℃ once more, and above reflux course repeats 5 times; To filter the throw out and the 1000ml liquid alkane mixture (C of gained then
11-C
16) at first refluxed 2 hours down at 120 ℃, then powder is filtered out, extract ethanol in the alkane filtrate repeatedly with distilled water, next in filtrate, add an amount of anhydrous CaCl
2The water that removal left behind, obtain reusable paraffins mixture, regenerated liquid alkane mixture is mixed with the powder that filters out again 150 ℃ of following backflows 4 hours, the paraffins mixture that obtains recycling with above-mentioned same method, next successively at 180 ℃, respectively refluxed under 210 ℃ 3 hours, and filtered out powder at last, and with liquid alkane mixture repetitive scrubbing 5 times.
(3) charging: put into the precursor powder in the high alumina porcelain boat and compress, place the tubular type atmosphere furnace airtight.
(4) high-temperature heat treatment: the reaction chamber of tube furnace is extracted into-0.09～-0.1MPa vacuum tightness, close vacuum pump then.Heat temperature raising to 600 ℃, insulation 4h, reaction chamber naturally cools to room temperature.
(5) sampling: take out sample in the porcelain boat from the tube furnace reaction chamber, obtain nano-TiO
2The @C powder, the evaluation of powder sees Table one.
Example two
(1) gets the raw materials ready: liquid alkane mixture (C
11-C
16) 1000ml, dehydrated alcohol 5000ml, hydrated titanium dioxide 200g.
(2) reflux: the dehydrated alcohol of 200g hydrated titanium dioxide and 1000ml refluxed one hour down at 85 ℃, filtered then; Gained precipitates with the dehydrated alcohol of fresh 1000ml and mixes, and refluxes one hour down at 85 ℃ once more, and above reflux course repeats 5 times; To filter the throw out and the 1000ml liquid alkane mixture (C of gained then
11-C
16) at first refluxed 8 hours down at 120 ℃, then powder is filtered out, extract ethanol in the alkane filtrate repeatedly with distilled water, next in filtrate, add an amount of anhydrous CaCl
2The water that removal left behind, obtain reusable paraffins mixture, regenerated liquid alkane mixture is mixed with the powder that filters out again 150 ℃ of following backflows 8 hours, the paraffins mixture that obtains recycling with above-mentioned same method, next successively at 180 ℃, respectively refluxed under 210 ℃ 6 hours, and filtered out powder at last, and with liquid alkane mixture washing repeatedly 5 times.
(3) charging: put into the precursor powder in the high alumina porcelain boat and compress, place the tubular type atmosphere furnace airtight.
(4) high-temperature heat treatment: the reaction chamber of tube furnace is extracted into-0.09～-0.1MPa vacuum tightness, close vacuum pump then.Heat temperature raising to 700 ℃, insulation 2h, reaction chamber naturally cools to room temperature.
(5) sampling: take out sample in the porcelain boat from the tube furnace reaction chamber, obtain nano-TiO
2The @C powder, the evaluation of powder sees Table one.
Example three:
(1) gets the raw materials ready: liquid alkane mixture (C
11-C
16) 1000ml, dehydrated alcohol 5000ml, hydrated titanium dioxide 50g.
(2) reflux: the dehydrated alcohol of 50g hydrated titanium dioxide and 1000ml refluxed one hour down at 60 ℃, filtered then; Gained precipitates with the dehydrated alcohol of fresh 1000ml and mixes, and refluxes one hour down at 60 ℃ once more, and above reflux course repeats 5 times; To filter the throw out and the 1000ml liquid alkane mixture (C of gained then
11-C
16) at first refluxed 8 hours down at 120 ℃, then powder is filtered out, extract alcohol in the alkane filtrate repeatedly with distilled water, next in filtrate, add an amount of anhydrous CaCl
2The water that removal left behind, obtain reusable paraffins mixture, regenerated liquid alkane mixture is mixed with the powder that filters out again 150 ℃ of following backflows 8 hours, the paraffins mixture that obtains recycling with above-mentioned same method, next successively at 180 ℃, respectively refluxed under 210 ℃ 8 hours, and filtered out powder at last, and with liquid alkane mixture washing repeatedly 5 times.
(3) charging: put into the precursor powder in the high alumina porcelain boat and compress, place the tubular type atmosphere furnace airtight.
(4) high-temperature heat treatment: the reaction chamber of tube furnace is extracted into-0.09～-0.1MPa vacuum tightness, close vacuum pump then.Heat temperature raising to 800 ℃, insulation 1h, reaction chamber naturally cools to room temperature.
(5) sampling: take out sample in the porcelain boat from the tube furnace reaction chamber, obtain nano-TiO
2The @C powder, the evaluation of powder sees Table one.
Example four:
(1) gets the raw materials ready: liquid alkane mixture (C
11-C
16) 1000ml, dehydrated alcohol 5000ml, hydrated titanium dioxide 100g.
(2) reflux: the dehydrated alcohol of 100g hydrated titanium dioxide and 1000ml refluxed one hour down at 90 ℃, filtered then; Gained precipitates with the dehydrated alcohol of fresh 1000ml and mixes, and refluxes one hour down at 90 ℃ once more, and above reflux course repeats 5 times; To filter the throw out and the 1000ml liquid alkane mixture (C of gained then
11-C
16) at first refluxed 8 hours down at 120 ℃, then powder is filtered out, extract alcohol in the alkane filtrate repeatedly with distilled water, next in filtrate, add an amount of anhydrous CaCl
2The water that removal left behind, obtain reusable paraffins mixture, regenerated liquid alkane mixture is mixed with the powder that filters out again 150 ℃ of following backflows 8 hours, the paraffins mixture that obtains recycling with above-mentioned same method, next successively at 180 ℃, respectively refluxed under 210 ℃ 8 hours, and filtered out powder at last, and with liquid alkane mixture washing repeatedly 5 times.
(3) charging: put into the precursor powder in the high alumina porcelain boat and compress, place the tubular type atmosphere furnace airtight.
(4) high-temperature heat treatment: the reaction chamber of tube furnace is extracted into-0.09～-0.1MPa vacuum tightness, close vacuum pump then.Heat temperature raising to 900 ℃, insulation 1h, reaction chamber naturally cools to room temperature.
(5) sampling: take out sample in the porcelain boat from the tube furnace reaction chamber, obtain nano-TiO
2The @C powder, the evaluation of powder sees Table one.
Example five:
(1) gets the raw materials ready: liquid alkane mixture (C
11-C
16) 1000ml, dehydrated alcohol 5000ml, hydrated titanium dioxide 150g.
(2) reflux: the dehydrated alcohol of 150g hydrated titanium dioxide and 1000ml refluxed one hour down at 70 ℃, filtered then; Gained precipitates with the dehydrated alcohol of fresh 1000ml and mixes, and refluxes one hour down at 70 ℃ once more, and above reflux course repeats 5 times; To filter the throw out and the 1000ml liquid alkane mixture (C of gained then
11-C
16) at first refluxed 8 hours down at 120 ℃, then powder is filtered out, extract alcohol in the alkane filtrate repeatedly with distilled water, next in filtrate, add an amount of anhydrous CaCl
2The water that removal left behind, obtain reusable paraffins mixture, regenerated liquid alkane mixture is mixed with the powder that filters out again 150 ℃ of following backflows 10 hours, the paraffins mixture that obtains recycling with above-mentioned same method, next successively at 180 ℃, respectively refluxed under 210 ℃ 12 hours, and filtered out powder at last, and with liquid alkane mixture washing repeatedly 5 times.
(3) charging: put into the precursor powder in the high alumina porcelain boat and compress, place the tubular type atmosphere furnace airtight.
(4) high-temperature heat treatment: the reaction chamber of tube furnace is extracted into-0.09～-0.1MPa vacuum tightness, close vacuum pump then.Heat temperature raising to 900 ℃, insulation 1h, reaction chamber naturally cools to room temperature.
Sampling: take out sample in the porcelain boat from the tube furnace reaction chamber, obtain nano-TiO
2The @C powder, the evaluation of powder sees Table one.
Precursor powder and TiO in each example of table one
2The evaluation of @C product
Claims (3)
1, the nano level TiO that a kind of carbon coats
2The preparation method of nucleocapsid composite granule is characterized in that comprising following process:
(1) gets the raw materials ready: the volume ratio 4:1～6:1 of dehydrated alcohol and liquid alkane mixture, every 500ml liquid alkane mixture is with 25～100g hydrated titanium dioxide, wherein the carbon chain lengths of liquid alkane mixture is between 11 carbon atoms and 16 carbon atoms, 180～250 ℃ of boiling points;
(2) reflux: the formed suspension of dehydrated alcohol and hydrated titanium dioxide refluxed 1～10 hour down at 40～100 ℃, then the precipitation powder of liquid alkane mixture with the back gained that refluxes with dehydrated alcohol mixed, and under 100～250 ℃, refluxed 12～72 hours, filter, obtain black precursor powder, filter the paraffins mixture filtrate of gained and after the water collection, remove dehydrated alcohol, use anhydrous CaCl again
2After drying dewaters, recycle;
(3) charging: pack into black precursor powder in the high alumina porcelain boat and compress, it is airtight to put into tube furnace;
(4) high-temperature heat treatment: the reaction chamber of tube furnace is extracted into-0.09～-0.1MPa vacuum tightness, close vacuum then, heat temperature raising to 600～1000 ℃ are incubated 1～4 hour, and then, reaction chamber naturally cools to room temperature;
(5) sampling: take out sample in the porcelain boat from the tube furnace reaction chamber, obtain the nano level TiO that carbon coats
2The nucleocapsid composite granule.
2, by the nano level TiO of the described a kind of carbon coating of claim 1
2The preparation method of nucleocapsid composite granule is characterized in that carbon source is provided by the liquid alkane mixture, and the titanium source is provided by hydrated titanium dioxide, realizes that by liquid-phase reflux bag carbon mixes.
3, by the nano level TiO of the described a kind of carbon coating of claim 1
2The preparation method of nucleocapsid composite granule is characterized in that black precursor powder grain-size 4-9nm, and specific surface is bigger, 300～400m
2/ g, and have the cellular structure of non-material self, total pore volume: 0.5～1cm
3/ g, mean pore size: 10～15nm.
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Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101773821B (en) * | 2010-02-03 | 2012-03-07 | 湘潭大学 | TiO2 @ graphitized carbon nuclear shell compound photocatalyst with high visible light catalytic activity and preparation method thereof |
| CN101869829B (en) * | 2010-07-20 | 2012-02-22 | 黑龙江大学 | Preparation method of carbon-titanium dioxide chromatography stationary phase with shell-core structure and application |
| CN102172501B (en) * | 2011-03-14 | 2013-07-03 | 广东工业大学 | Preparation method of carbon-coated silicon carbide nano powder with nuclear shell structure |
| CN102343239B (en) * | 2011-05-20 | 2013-05-29 | 四川大学 | Oxidized graphene or graphene/inorganic particle core/shell material and preparation method thereof |
| CN102274756B (en) * | 2011-06-10 | 2014-06-25 | 华东理工大学 | Processing method for enhancing visible light absorption and photooxidation and photoreduction ability of metallic oxide |
| CN102990075A (en) * | 2012-11-05 | 2013-03-27 | 四川大学 | Method for preparing carbon-coated iron nano particles |
| CN105833858B (en) * | 2016-04-28 | 2018-04-17 | 北京科技大学 | A kind of preparation method of two dimension carbon film coated sea urchin shape composite titania material |
| CN106563433B (en) * | 2016-11-15 | 2019-02-26 | 电子科技大学 | A kind of carbon-coated TiO2Material and preparation method thereof |
| CN107313246B (en) * | 2017-06-21 | 2020-02-21 | 浙江理工大学 | Ultraviolet aging resistant modification method for polyester fiber |
| CN108155353B (en) * | 2017-11-20 | 2020-11-03 | 中南大学 | Graphitized carbon coated electrode material, preparation method thereof and application of graphitized carbon coated electrode material as energy storage device electrode material |
| CN110744052A (en) * | 2018-07-23 | 2020-02-04 | 哈尔滨工业大学 | Preparation method of graphene-like or graphene metal composite powder |
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