CN103007957A - Method for preparing modified hollow glass beads with magnetism and photocatalytic activity - Google Patents
Method for preparing modified hollow glass beads with magnetism and photocatalytic activity Download PDFInfo
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- CN103007957A CN103007957A CN201210474638XA CN201210474638A CN103007957A CN 103007957 A CN103007957 A CN 103007957A CN 201210474638X A CN201210474638X A CN 201210474638XA CN 201210474638 A CN201210474638 A CN 201210474638A CN 103007957 A CN103007957 A CN 103007957A
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- hollow glass
- glass micropearl
- deionized water
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- 239000011521 glass Substances 0.000 title claims abstract description 107
- 238000000034 method Methods 0.000 title claims abstract description 58
- 230000001699 photocatalysis Effects 0.000 title claims abstract description 33
- 239000011324 bead Substances 0.000 title abstract description 10
- 230000005389 magnetism Effects 0.000 title abstract 3
- 238000001027 hydrothermal synthesis Methods 0.000 claims abstract description 13
- 230000004048 modification Effects 0.000 claims abstract description 11
- 238000012986 modification Methods 0.000 claims abstract description 11
- FOIXSVOLVBLSDH-UHFFFAOYSA-N Silver ion Chemical compound [Ag+] FOIXSVOLVBLSDH-UHFFFAOYSA-N 0.000 claims abstract description 5
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 58
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 50
- 239000008367 deionised water Substances 0.000 claims description 44
- 238000006243 chemical reaction Methods 0.000 claims description 42
- 229910021641 deionized water Inorganic materials 0.000 claims description 41
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 41
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 39
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 34
- 229910052742 iron Inorganic materials 0.000 claims description 33
- VCJMYUPGQJHHFU-UHFFFAOYSA-N iron(3+);trinitrate Chemical compound [Fe+3].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O VCJMYUPGQJHHFU-UHFFFAOYSA-N 0.000 claims description 30
- 239000004408 titanium dioxide Substances 0.000 claims description 26
- 239000000243 solution Substances 0.000 claims description 25
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 21
- 238000003756 stirring Methods 0.000 claims description 21
- 238000005238 degreasing Methods 0.000 claims description 18
- 239000012530 fluid Substances 0.000 claims description 18
- 230000008569 process Effects 0.000 claims description 17
- 239000011790 ferrous sulphate Substances 0.000 claims description 15
- 235000003891 ferrous sulphate Nutrition 0.000 claims description 15
- 238000001914 filtration Methods 0.000 claims description 15
- BAUYGSIQEAFULO-UHFFFAOYSA-L iron(2+) sulfate (anhydrous) Chemical compound [Fe+2].[O-]S([O-])(=O)=O BAUYGSIQEAFULO-UHFFFAOYSA-L 0.000 claims description 15
- 229910000359 iron(II) sulfate Inorganic materials 0.000 claims description 15
- 238000001291 vacuum drying Methods 0.000 claims description 15
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 14
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 claims description 12
- 238000007789 sealing Methods 0.000 claims description 12
- CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Substances [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims description 12
- 238000005303 weighing Methods 0.000 claims description 12
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 11
- 239000004202 carbamide Substances 0.000 claims description 11
- DCKVFVYPWDKYDN-UHFFFAOYSA-L oxygen(2-);titanium(4+);sulfate Chemical compound [O-2].[Ti+4].[O-]S([O-])(=O)=O DCKVFVYPWDKYDN-UHFFFAOYSA-L 0.000 claims description 11
- 229910000348 titanium sulfate Inorganic materials 0.000 claims description 11
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 claims description 10
- 239000008103 glucose Substances 0.000 claims description 10
- 239000002202 Polyethylene glycol Substances 0.000 claims description 9
- 230000008859 change Effects 0.000 claims description 9
- 239000011259 mixed solution Substances 0.000 claims description 9
- 229920001223 polyethylene glycol Polymers 0.000 claims description 9
- 230000004044 response Effects 0.000 claims description 9
- 238000005406 washing Methods 0.000 claims description 9
- 229910052757 nitrogen Inorganic materials 0.000 claims description 7
- 229920000036 polyvinylpyrrolidone Polymers 0.000 claims description 7
- 239000001267 polyvinylpyrrolidone Substances 0.000 claims description 7
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 claims description 7
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 6
- 239000004115 Sodium Silicate Substances 0.000 claims description 6
- 238000013019 agitation Methods 0.000 claims description 6
- 238000012545 processing Methods 0.000 claims description 6
- 229910000029 sodium carbonate Inorganic materials 0.000 claims description 6
- 235000019795 sodium metasilicate Nutrition 0.000 claims description 6
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 claims description 6
- 229910052911 sodium silicate Inorganic materials 0.000 claims description 6
- TWPYJTOUBHEHFW-UHFFFAOYSA-J titanium(4+) urea disulfate Chemical compound NC(=O)N.[Ti+4].S(=O)(=O)([O-])[O-].S(=O)(=O)([O-])[O-] TWPYJTOUBHEHFW-UHFFFAOYSA-J 0.000 claims description 6
- 238000010792 warming Methods 0.000 claims description 6
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 claims description 4
- 238000009413 insulation Methods 0.000 claims description 4
- 235000019441 ethanol Nutrition 0.000 claims description 3
- 238000005253 cladding Methods 0.000 claims description 2
- 239000002105 nanoparticle Substances 0.000 abstract description 9
- SOQBVABWOPYFQZ-UHFFFAOYSA-N oxygen(2-);titanium(4+) Chemical compound [O-2].[O-2].[Ti+4] SOQBVABWOPYFQZ-UHFFFAOYSA-N 0.000 abstract description 9
- 230000008901 benefit Effects 0.000 abstract description 4
- SZVJSHCCFOBDDC-UHFFFAOYSA-N ferrosoferric oxide Chemical compound O=[Fe]O[Fe]O[Fe]=O SZVJSHCCFOBDDC-UHFFFAOYSA-N 0.000 abstract description 4
- 239000002994 raw material Substances 0.000 abstract description 4
- 239000011248 coating agent Substances 0.000 abstract description 3
- 238000000576 coating method Methods 0.000 abstract description 3
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 22
- 239000002245 particle Substances 0.000 description 17
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 12
- 239000004810 polytetrafluoroethylene Substances 0.000 description 12
- 239000013078 crystal Substances 0.000 description 9
- -1 iron ion Chemical class 0.000 description 8
- STZCRXQWRGQSJD-GEEYTBSJSA-M methyl orange Chemical compound [Na+].C1=CC(N(C)C)=CC=C1\N=N\C1=CC=C(S([O-])(=O)=O)C=C1 STZCRXQWRGQSJD-GEEYTBSJSA-M 0.000 description 8
- 229940012189 methyl orange Drugs 0.000 description 8
- 239000000463 material Substances 0.000 description 7
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 6
- 238000002425 crystallisation Methods 0.000 description 6
- 230000008025 crystallization Effects 0.000 description 6
- SQGYOTSLMSWVJD-UHFFFAOYSA-N silver(1+) nitrate Chemical compound [Ag+].[O-]N(=O)=O SQGYOTSLMSWVJD-UHFFFAOYSA-N 0.000 description 6
- 239000010936 titanium Substances 0.000 description 6
- 229910052719 titanium Inorganic materials 0.000 description 6
- 239000001048 orange dye Substances 0.000 description 5
- 230000035484 reaction time Effects 0.000 description 5
- STZCRXQWRGQSJD-UHFFFAOYSA-M sodium;4-[[4-(dimethylamino)phenyl]diazenyl]benzenesulfonate Chemical compound [Na+].C1=CC(N(C)C)=CC=C1N=NC1=CC=C(S([O-])(=O)=O)C=C1 STZCRXQWRGQSJD-UHFFFAOYSA-M 0.000 description 5
- 238000005054 agglomeration Methods 0.000 description 4
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- 238000013033 photocatalytic degradation reaction Methods 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 4
- VTLYFUHAOXGGBS-UHFFFAOYSA-N Fe3+ Chemical compound [Fe+3] VTLYFUHAOXGGBS-UHFFFAOYSA-N 0.000 description 3
- 238000003556 assay Methods 0.000 description 3
- 239000003153 chemical reaction reagent Substances 0.000 description 3
- 239000000975 dye Substances 0.000 description 3
- 230000005415 magnetization Effects 0.000 description 3
- 230000001376 precipitating effect Effects 0.000 description 3
- 229910001961 silver nitrate Inorganic materials 0.000 description 3
- 229910001220 stainless steel Inorganic materials 0.000 description 3
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- 238000005516 engineering process Methods 0.000 description 2
- 229910001447 ferric ion Inorganic materials 0.000 description 2
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- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
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Abstract
The invention discloses a method for preparing modified hollow glass beads with magnetism and photocatalytic activity, which comprises the following process steps of: I, firstly coating a magnetic nano ferroferric oxide film on a hollow glass bead by using a hydrothermal method; II, then coating an anatase-type nano titanium dioxide film on the magnetic nano ferroferric oxide film of the hollow glass bead; and III, finally carrying out silver ion modification on the hollow glass bead coated with the magnetic nano ferroferric oxide film and the anatase-type nano titanium dioxide film. A hollow glass bead modified by using the method disclosed by the invention has magnetism and photocatalytic activity, the binding strength of nanoparticles and hollow glass beads is better, and raw materials are saved; and the method has the advantages of simplicity and convenience in operation, and the like.
Description
Technical field
The invention belongs to functional technical field of inorganic nonmetallic materials, relate to a kind of method of modifying of hollow glass micropearl, specifically a kind of employing hydro-thermal method is to the first coated magnetic nano ferriferrous oxide film in hollow glass micropearl surface, the clad nano titanium deoxid film carries out the method for modifying that Nano Silver is modified at last again.
Background technology
The magnetic iron ore tri-iron tetroxide is a kind of important spinels Ferrite Material, have many characteristics such as light, electricity, sound, heat and magnetic that are different from conventional material, it is one of soft magnetic material that is most widely used, be commonly used for recording materials, pigment, magnetic fluid material, catalyst, magnetic macromolecular microsphere and electronic material etc. also have good application prospect at biological technical field and medical domain.Anatase titanium dioxide is because having the characteristics such as shielding ultraviolet rays, photocatalysis and automatically cleaning, and is widely used in the fields such as solar cell, cosmetics, functional fibre, coating and fine ceramics.Nano Silver is nano level argent simple substance; grain size is generally about 25nm; has broad spectrum antibacterial; the tens of kinds of pathogenic microorganisms such as Escherichia coli, gonococcus and chlamydia trachomatis there are strong inhibition and killing action; nontoxic; drug resistance be can not produce, environmental protection, the fields such as weaving dress ornament, fruit freshness preserving and food hygiene can be applicable to.At present, preparation nano ferriferrous oxide, titanium dioxide granule method mainly contain chemical precipitation method, sol-gel process, microwave irradiation and hydro-thermal reaction method etc., and the method for preparing Nano Silver mainly contains chemical reduction method, photoreduction met hod, electrochemical process and electroless plating method etc.Adopt hydro-thermal method to prepare the nano ferriferrous oxide particle and have significant advantage, the one, relatively high temperature is conducive to the raising of product magnetic property; The 2nd, in closed container, produce relatively high pressure and avoided component volatilization, improved product purity.Under the hydrothermal condition, by conditions such as control reaction temperature, acid-base value and raw material proportionings, can access the product of different crystal structure, composition, pattern and particle size, uniform particles, favorable dispersibility need not high-temperature roasting, and process is polluted little, simple to operate, easily realize the advantages such as suitability for industrialized production.Hollow glass micropearl is the small hollow glass spheroid of a kind of size, having the advantages such as light weight, low heat conduction, resistance to compression, high dispersive, sound insulation, electrical insulating property and Heat stability is good, is the novel light material of a kind of of many uses, the excellent performance that gets up of development in recent years.Utilize the characteristics of hollow glass micropearl light weight, hollow, it is carried out surface modification treatment, can access and have property the new material of (as inhaling ripple, reflective and catalysis etc.).But the hollow glass micropearl of existing method of modifying does not have magnetic and photocatalytic activity, exists the relatively poor problem of nano particle and hollow glass micropearl binding strength.
Summary of the invention
The hollow glass micropearl that technical problem to be solved by this invention is to propose after a kind of modification has magnetic and photocatalytic activity, nano particle and hollow glass micropearl binding strength are better, conservation of raw material, preparation easy and simple to handle have the method for the active Filled With Hollow Bead of magnetic photocatalytic.
For solving the problems of the technologies described above, a kind of method with the active Filled With Hollow Bead of magnetic photocatalytic for preparing of the present invention comprises following processing step: I. adopt first hydro-thermal method to hollow glass micropearl coated magnetic nano ferriferrous oxide film; II. again at the magnetic Nano ferriferrous oxide film outer cladding anatase-type nanometer titanium dioxide film of hollow glass micropearl; III. at last the hollow glass micropearl that has coated magnetic Nano ferriferrous oxide film and anatase-type nanometer titanium dioxide film is carried out the silver ion modification.
Above-mentioned a kind of method with the active hollow glass micropearl of magnetic photocatalytic for preparing before adopting hydro-thermal method to hollow glass micropearl coated magnetic nano ferriferrous oxide film, is carried out preliminary treatment to hollow glass micropearl first.
Above-mentioned a kind of method with the active hollow glass micropearl of magnetic photocatalytic for preparing is describedly carried out pretreated technical process to hollow glass micropearl and is comprised and deoiling and two programs of alligatoring.
Above-mentioned a kind of method with the active hollow glass micropearl of magnetic photocatalytic for preparing, the technical process of the described program of deoiling is as follows: weighing sodium hydroxide, sodium carbonate and sodium metasilicate are dissolved in the deionized water, obtain degreasing fluid, described NaOH, sodium carbonate and the sodium metasilicate quality-volumetric concentration in described degreasing fluid is respectively 40g/L, 10g/L and 5g/L; Described degreasing fluid is heated to 80~100 ℃; Take by weighing hollow glass micropearl 5~10g, add in the described degreasing fluid of 1L, adopt the mechanical agitation method that cenosphere is fully disperseed in degreasing fluid, filtration behind reaction 40~60min, washing.
Above-mentioned a kind of method with the active hollow glass micropearl of magnetic photocatalytic for preparing, the technical process of described alligatoring program is as follows: with the upper step obtain deoil after hollow glass micropearl be immersed in the hydrofluoric acid solution of mass concentration 1~3%, volume 1L, under 40~60 ℃ of conditions, react 1~2h, wash respectively dry 1~2h under 80 ℃ of conditions after the filtration with acetone, absolute ethyl alcohol and deionized water.
Above-mentioned a kind of method with the active hollow glass micropearl of magnetic photocatalytic for preparing, the technical process of described step I is as follows: be 0.05~0.15mol/L according to total concentration of iron, ferrous sulfate and ferric nitrate mass ratio are Fe
2+: Fe
3+=1:2~3:2 takes by weighing ferrous sulfate and ferric nitrate, obtain ferrous iron and ferric mixed solution with deionized water dissolving, adding mass concentration is the NaOH of 15~30g/L, mass concentration is the ethylene glycol of 20~40g/L, mass concentration is the polyvinylpyrrolidone of 10~20g/L, add ethanol solution according to volume ratio 4:1~1:4, add hollow glass micropearl, change over to subsequently to the high pressure reaction cylinder, under 120~160 ℃ of conditions, 4~8h is processed in insulation, filters out cenosphere after question response is finished after the sealing, wash respectively vacuum drying 1~2h under 60 ℃ of conditions with absolute ethyl alcohol and deionized water.
Above-mentioned a kind of method with the active hollow glass micropearl of magnetic photocatalytic for preparing, the technical process of described step II is as follows: the titanium sulfate of 18~20g is dissolved in the deionized water of temperature 60 C, volume 400mL, then add the urea of 8~12g and the polyethylene glycol of 3~8g, and constantly stir; Hollow glass micropearl after the processing of step I is joined in the titanium sulfate urea mixed solution, mechanical agitation 5~10min, then replenish the deionized water of 200~400ml, and in solution, pass into nitrogen 10~20min, then change over to immediately in the reaction cylinder of volume 1L, sealing is placed in the homogeneous reactor, is warming up to 110~150 ℃, isothermal reaction 2~5h with the speed of 1~2 ℃/min; Question response filters after finishing, with absolute ethyl alcohol and washed with de-ionized water, 60 ℃ of vacuum drying 1~2h.
Above-mentioned a kind of method with the active hollow glass micropearl of magnetic photocatalytic for preparing, the technical process of described step III is as follows: the hollow glass micropearl after the step II is processed adds volume 1L to, mass concentration is in the liquor argenti nitratis ophthalmicus of 1~4g/L, fully stir 5~10min, then slowly add volume 200mL, mass concentration is the glucose solution of 4~10g/L, and constantly stir, under 20~40 ℃ of conditions, react 10~30min, wash with absolute ethyl alcohol and deionized water respectively after the filtration, vacuum drying 30~50min under 80 conditions, namely finish at the first coated magnetic nano ferriferrous oxide in hollow glass micropearl surface, coat again anatase-type nanometer titanium dioxide, carry out at last the modified film that Nano Silver is modified.
The present invention is owing to adopted technique scheme, adopt hydro-thermal method at preparation magnetic Nano ferriferrous oxide particles, and when the anatase-type nanometer titanium dioxide particle, directly coat one deck magnetic Nano ferriferrous oxide film and titanium deoxid film on the hollow glass micropearl surface, give hollow glass micropearl magnetic property and photocatalytic activity, by control reaction temperature and time, the technological parameters such as the consumption of predecessor, precipitating reagent and surfactant, optimized modified technique, the method is saved raw material, and is easy and simple to handle.Intersperse decorated nanometer silver on the nano-titanium dioxide film surface on this basis, to strengthen the ability of photocatalysis degradation organic contaminant.Test result shows, the hollow glass micropearl that has coated behind magnetic Nano tri-iron tetroxide, titanium dioxide and the Nano Silver modification has good magnetic and high photocatalytic activity, can satisfy actual needs.
The specific embodiment
A kind of method with the active hollow glass micropearl of magnetic photocatalytic for preparing of the present invention adopts first hydro-thermal method to hollow glass micropearl coated magnetic nano ferriferrous oxide film, coats the anatase-type nanometer titanium dioxide film again, carries out at last the silver ion modification.It can directly coat the hollow glass micropearl surface when adopting hydro-thermal method to prepare magnetic Nano tri-iron tetroxide, anatase-type nanometer titanium dioxide crystal, carries out at last Nano Silver and modifies, and specifically implements according to following steps:
Step 1: hollow glass micropearl preliminary treatment:
A. deoil.Weighing sodium hydroxide, sodium carbonate and sodium metasilicate are dissolved in the deionized water, obtain degreasing fluid, and NaOH, sodium carbonate and the sodium metasilicate quality-volumetric concentration in degreasing fluid is respectively 40g/L, 10g/L and 5g/L; Degreasing fluid is heated to 80~100 ℃; Take by weighing hollow glass micropearl 5~10g, add in the described degreasing fluid of 1L, adopt the mechanical agitation method that cenosphere is fully disperseed in degreasing fluid, filtration behind reaction 40~60min, washing.
B. alligatoring.With the upper step obtain deoil after hollow glass micropearl be immersed in the hydrofluoric acid solution of mass concentration 1~3%, volume 1L, under 40~60 ℃ of conditions, react 1~2h, wash respectively dry 1~2h under 80 ℃ of conditions after the filtration with acetone, absolute ethyl alcohol and deionized water.
Step 2: hollow glass micropearl coated magnetic nano ferriferrous oxide film.Be 0.05~0.15mol/L according to total concentration of iron, ferrous sulfate and ferric nitrate mass ratio are Fe
2+: Fe
3+=1:2~3:2 takes by weighing ferrous sulfate and ferric nitrate, obtain ferrous iron and ferric mixed solution with deionized water dissolving, adding mass concentration is the NaOH of 15~30g/L, mass concentration is the ethylene glycol of 20~40g/L, mass concentration is the polyvinylpyrrolidone of 10~20g/L, add ethanol solution according to volume ratio 4:1~1:4, add the hollow glass micropearl after step 1 is processed, change over to subsequently to the high pressure reaction cylinder, under 120~160 ℃ of conditions, 4~8h is processed in insulation, filters out cenosphere after question response is finished after the sealing, wash respectively vacuum drying 1~2h under 60 ℃ of conditions with absolute ethyl alcohol and deionized water.The present invention is by the total concentration of iron of control, ferrous sulfate and ferric nitrate mass ratio, the selection of precipitating reagent and emulsifying agent and consumption, reaction temperature, in the reaction time, so that it is even, fine and close to be coated on the ferriferrous oxide film on hollow glass micropearl surface, particle diameter is nanoscale, good with the hollow glass micropearl binding strength, have certain magnetic.Because total concentration of iron, ferrous sulfate and ferric nitrate mass ratio, emulsifier, the factors such as reaction temperature and time all affect magnetic, purity, crystallization degree, pattern and the particle size of tri-iron tetroxide.When total concentration of iron during at 0.05~0.15mol/L, the hollow glass micropearl surface can coat certain thickness magnetic Nano ferriferrous oxide film, particle generation agglomeration is less, can not deposit too many nano particle in the solution simultaneously, is combined with hollow glass micropearl firmly; When less than 0.05mol/L, iron ion can not form continuous film very little in the solution, affects magnetic property; When greater than 0.15mol/L, iron concentration is excessive easily to cause waste, and the magnetic Nano ferriferrous oxide film of hollow glass micropearl surface adhesion is too thick, and attachment fastness is bad, and nano particle comes off easily in the use procedure.When ferrous sulfate and ferric nitrate mass ratio during at 1:2~3:2, the hollow glass micropearl surface can coat certain thickness film, and nano particle is combined with hollow glass micropearl firmly; When less than 1:2, the ferric ion consumption is too large, prepares to contain the more impurity of ferric iron, and magnetic property is very weak; When greater than 3:2, the ferric ion consumption is prepared and is contained the more impurity of ferrous iron very little, and magnetic property is also very weak.When precipitating reagent sodium hydroxide concentration during at 15~30g/L, can guarantee that chemical reaction normally carries out, tri-iron tetroxide crystal well-grown during less than 15g/L or greater than 30g/L, all can not impel tri-iron tetroxide synthetic smoothly.When the polyvinylpyrrolidone consumption at 10~20g/L, the ethylene glycol consumption can reduce the agglomeration of nano ferriferrous oxide when 20~40g/L, strengthen the dispersiveness of particle.Surpassing above-mentioned scope consumption nano ferriferrous oxide agglomeration obviously increases the weight of.When absolute ethyl alcohol and deionized water volume ratio are 4:1~1:4, can guarantee that the tri-iron tetroxide particle diameter that generates is less, surpass this scope, particle diameter increases.Crystallization degree, crystal morphology and the size of reaction temperature and reaction time major effect tri-iron tetroxide.When reaction temperature during at 120~160 ℃, the magnetite nano tri-iron tetroxide that can generate, when being lower than 120 ℃, the tri-iron tetroxide of generation does not have magnetic, when being higher than 160 ℃, wastes energy, and the instrument security reduces.When the reaction time is controlled at 4~8h, can be at hollow glass micropearl Surface Creation magnetic Nano ferriferrous oxide film; When being lower than 4h, nano ferriferrous oxide and hollow glass micropearl binding strength are relatively poor, also affect the crystallization degree of magnetic Nano tri-iron tetroxide, and magnetic property is bad; When greater than 8h, obvious reunion can occur in the magnetic Nano ferriferrous oxide particles of generation, and granularity obviously increases, and rough surface is uneven, and particle comes off easily.
Step 3: hollow glass micropearl coats the anatase-type nanometer titanium dioxide film.The titanium sulfate of 18~20g is dissolved in the deionized water of temperature 60 C, volume 400mL, then adds the urea of 8~12g and the polyethylene glycol of 3~8g, and constantly stir; Hollow glass micropearl after step 2 processing is joined in the titanium sulfate urea mixed solution, mechanical agitation 5~10min, then replenish the deionized water of 200~400ml, and in solution, pass into nitrogen 10~20min, then change over to immediately in the reaction cylinder of volume 1L, sealing is placed in the homogeneous reactor, is warming up to 110~150 ℃, isothermal reaction 2~5h with the speed of 1~2 ℃/min; Question response filters after finishing, with absolute ethyl alcohol and washed with de-ionized water, 60 ℃ of vacuum drying 1~2h.The present invention adopts hydro-thermal method in the preparation nano titanium dioxide crystal, directly at hollow glass micropearl surface clad nano titanium deoxid film.The usage ratio of titanium sulfate, urea and deionized water, the surfactant polyethylene consumption, reaction temperature and time etc. all affects crystalline phase, crystallization degree, pattern and the crystallite dimension of nano titanium oxide.When titanium sulfate and urea quality than for 2.5:1~1.5:1 the time, can generate anatase-type nanometer titanium dioxide, hollow glass micropearl surface clad nano film is comparatively complete; When titanium sulfate and amount of urea ratio were higher than 2.5:1, residual titanium sulfate was many; When titanium sulfate and amount of urea compared less than 1.5:1, urea can cause waste.When polyethylene glycol consumption during at 5~10g/L, can effectively control the speed of growth of nano titanium dioxide crystal, particle can not produce agglomeration, and crystal formation is intact, is combined with hollow glass micropearl firmly; When polyethylene glycol consumption during less than 5g/L, nanoparticle agglomerates is comparatively obvious; When polyethylene glycol consumption during greater than 10g/L, can affect the normal growth of nano titanium dioxide crystal.Pass into nitrogen and get rid of unnecessary courteously, can protect the magnetic of nano ferriferrous oxide in thermal and hydric environment, can not lose or descend.The vessel filling amount can generate the anatase-type nanometer titanium dioxide particle 60~80% the time; When less than 60% the time, the reaction cylinder internal pressure is on the low side, can affect the generation of nano titanium oxide; When the generation that is unfavorable for equally nano titanium oxide greater than 80% time, reaction cylinder is dangerous.When hydrothermal temperature is controlled at 110~150 ℃, can generate the anatase-type nanometer titanium dioxide particle; When being lower than 110 ℃, the anatase nano titanium dioxide crystal form of generation is imperfect; When being higher than 150 ℃, reaction cylinder security meeting is affected, and the titanium dioxide nanoparticle of generation easily produces reunion.The hydro-thermal reaction time is controlled in 2~5h scope, can be at hollow glass micropearl Surface Creation anatase-type nanometer titanium dioxide film; When less than 2h, can affect the crystallization degree of nano titanium oxide; When greater than 5h, secondary crystallization can occur in the titanium dioxide nanoparticle of generation, and binding strength descends.
Step 4: the hollow glass micropearl Nano Silver is modified.Add the hollow glass micropearl after step 3 processing to volume 1L, mass concentration is in the liquor argenti nitratis ophthalmicus of 1~4g/L, fully stir 5~10min, then slowly add volume 200mL, mass concentration is the glucose solution of 4~10g/L, and constantly stir, under 20~40 ℃ of conditions, react 10~30min, wash with absolute ethyl alcohol and deionized water respectively after the filtration, vacuum drying 30~50min under 80 conditions, namely finish at the first coated magnetic nano ferriferrous oxide in hollow glass micropearl surface, coat again anatase-type nanometer titanium dioxide, carry out at last the modified film that Nano Silver is modified.The present invention uses the liquor argenti nitratis ophthalmicus of low concentration to soak hollow glass micropearl, and glucose is as reducing agent reduced nano silver ion.When the silver nitrate consumption is 1~4g/L, the glucose consumption is 4~10g/L, during volume ratio 5:1, can intersperse nano-silver ionic on the nano-titanium dioxide film surface; When the silver nitrate consumption less than 1g/L, the glucose consumption is during less than 4g/L, the nano-silver ionic time of interspersing is very long and few; When the silver nitrate consumption greater than 4g/L, the glucose consumption is during greater than 10g/L, the Nano Silver of generation is too many again, and nano-titanium dioxide film is hidden fully.When reaction temperature at 20~40 ℃, during reaction time 10~30min, the Nano Silver of interspersing is relatively evenly, particle diameter is less, photocatalytic activity is high.
Embodiment 1
Get hollow glass micropearl 5g, add in the 1L degreasing fluid, filtering, washing behind the reaction 40min under 80 ℃ of conditions of temperature.Hollow glass micropearl after deoiling is immersed in the hydrofluoric acid solution of 1L, mass concentration 1%, under 40 ℃ of conditions, reacts 1h, filter, wash 80 ℃ of dry 1h.Take by weighing a certain amount of ferrous sulfate and ferric nitrate, use deionized water dissolving, controlling total concentration of iron is 0.05mol/L, ferrous sulfate and ferric nitrate mass ratio are 1:2, add the NaOH of 15g/L, the ethylene glycol of 20g/L, the polyvinylpyrrolidone of 10g/L, 1:4 adds absolute ethyl alcohol by volume again, adds until completely dissolved the hollow glass micropearl after the alligatoring, moving into immediately polytetrafluoroethylene (PTFE) is in the stainless steel reaction cylinder of substrate, insert after the sealing in the homogeneous reactor, under 120 ℃ of conditions, process 8h, filter out cenosphere after question response is finished, wash respectively vacuum drying 1h under 60 ℃ of conditions with absolute ethyl alcohol and deionized water.The 18g titanium sulfate is dissolved in 60 ℃, the deionized water of 400mL, add the urea of 8g and the polyethylene glycol of 3g, fully stir, the hollow glass micropearl of coated ferriferrous oxide is joined in the titanium sulfate urea mixed solution, stir 5min, add the deionized water of 200ml, in solution, pass into nitrogen 10min, change over to immediately in the reaction cylinder that is lined with polytetrafluoroethylene (PTFE) in the 1L, sealing is placed in the homogeneous reactor, is warming up to 110 ℃ with the speed of 1 ℃/min, isothermal reaction 5h, reaction is filtered after finishing, with absolute ethyl alcohol and deionized water washing, 60 ℃ of vacuum drying 1h.The hollow glass micropearl of clad nano tri-iron tetroxide, titanium deoxid film is added in the liquor argenti nitratis ophthalmicus of 1L, mass concentration 1g/L, stir 5min, slowly add the glucose solution of 200mL, mass concentration 4g/L, stirring reaction 10min under 20 ℃ of conditions, wash 80 dry 30min with absolute ethyl alcohol and deionized water respectively after the filtration.
The photo-catalytic degradation of methyl-orange dyestuff is the result show, the methyl orange solution of mass concentration 10mg/L, volume 500mL, add the hollow glass micropearl that 0.5g clad nano tri-iron tetroxide, titanium dioxide and Nano Silver are modified, through 100W ultraviolet lamp 1h irradiation, the methyl orange dye photocatalytic activity is 93.5%.The saturation magnetization that records the hollow glass micropearl of clad nano tri-iron tetroxide, titanium dioxide and Nano Silver modification is 12emu/g.Photo-catalytic degradation of methyl-orange dye activity assay method is as follows: the hollow glass micropearl behind 0.5g clad nano tri-iron tetroxide, titanium dioxide and the Nano Silver modification is put into the methyl orange solution of volume 500mL, mass concentration 10mg/L, and lucifuge leaves standstill behind the 2h with the absorbance of 720S type spectrophotometric determination solution at the 464nm place
A 0 , then methyl orange solution is placed under the ultraviolet lamp of power 100W, dominant wavelength 254nm and carries out irradiation, liquid level is apart from ultraviolet lamp 15cm, behind the irradiation 1h with the absorbance of 720S type spectrophotometric determination solution at the 464nm place
A 1 , by formula (1) calculates the methyl orange dye photocatalytic activity
D
Embodiment 2
Get hollow glass micropearl 10g, add in the 1L degreasing fluid, filtering, washing behind the reaction 60min under 100 ℃ of conditions of temperature.Hollow glass micropearl after deoiling is immersed in the hydrofluoric acid solution of 1L, mass concentration 3%, under 60 ℃ of conditions, reacts 2h, filter, wash 80 ℃ of dry 2h.Take by weighing a certain amount of ferrous sulfate and ferric nitrate, use deionized water dissolving, controlling total concentration of iron is 0.15mol/L, ferrous sulfate and ferric nitrate mass ratio are 3:2, add the NaOH of 30g/L, the ethylene glycol of 40g/L, the polyvinylpyrrolidone of 20g/L, 4:1 adds absolute ethyl alcohol by volume again, adds until completely dissolved the hollow glass micropearl after the alligatoring, moving into immediately polytetrafluoroethylene (PTFE) is in the stainless steel reaction cylinder of substrate, insert after the sealing in the homogeneous reactor, under 160 ℃ of conditions, process 4h, filter out cenosphere after question response is finished, wash respectively vacuum drying 2h under 60 ℃ of conditions with absolute ethyl alcohol and deionized water.The 20g titanium sulfate is dissolved in 60 ℃, in the deionized water of 400mL, add the urea of 12g and the polyethylene glycol of 8g, fully stir, the hollow glass micropearl of coated ferriferrous oxide is joined in the titanium sulfate urea mixed solution, stir 10min, add the deionized water of 400ml, in solution, pass into nitrogen 20min, change over to immediately in the reaction cylinder that is lined with polytetrafluoroethylene (PTFE) in the 1L, sealing is placed in the homogeneous reactor, is warming up to 150 ℃ with the speed of 2 ℃/min, isothermal reaction 2h, reaction is filtered after finishing, with absolute ethyl alcohol and deionized water washing, 60 ℃ of vacuum drying 2h.The hollow glass micropearl of clad nano tri-iron tetroxide, titanium deoxid film is added in the liquor argenti nitratis ophthalmicus of 1L, mass concentration 4g/L, stir 10min, slowly add the glucose solution of 200mL, mass concentration 10g/L, stirring reaction 30min under 40 ℃ of conditions, wash 80 dry 50min with absolute ethyl alcohol and deionized water respectively after the filtration.
Photo-catalytic degradation of methyl-orange dyestuff result shows (assay method is the same), the methyl orange solution of mass concentration 10mg/L, volume 500mL, add the hollow glass micropearl that 0.5g clad nano tri-iron tetroxide, titanium dioxide and Nano Silver are modified, through 100W ultraviolet lamp 1h irradiation, the methyl orange dye photocatalytic activity is 99.6%.The saturation magnetization that records the hollow glass micropearl of clad nano tri-iron tetroxide, titanium dioxide and Nano Silver modification is 38emu/g.
Embodiment 3
Get hollow glass micropearl 7g, add in the 1L degreasing fluid, filtering, washing behind the reaction 50min under 90 ℃ of conditions of temperature.Hollow glass micropearl after deoiling is immersed in the hydrofluoric acid solution of 1L, mass concentration 2%, under 50 ℃ of conditions, reacts 1.5h, filter, wash 80 ℃ of dry 1.5h.Take by weighing a certain amount of ferrous sulfate and ferric nitrate, use deionized water dissolving, controlling total concentration of iron is 0.1mol/L, ferrous sulfate and ferric nitrate mass ratio are 2:3, add the NaOH of 20g/L, the ethylene glycol of 30g/L, the polyvinylpyrrolidone of 15g/L, 2:1 adds absolute ethyl alcohol by volume again, adds until completely dissolved the hollow glass micropearl after the alligatoring, moving into immediately polytetrafluoroethylene (PTFE) is in the stainless steel reaction cylinder of substrate, insert after the sealing in the homogeneous reactor, under 140 ℃ of conditions, process 6h, filter out cenosphere after question response is finished, wash respectively vacuum drying 1h under 60 ℃ of conditions with absolute ethyl alcohol and deionized water.The 19g titanium sulfate is dissolved in 60 ℃, in the deionized water of 400mL, add the urea of 10g and the polyethylene glycol of 5g, fully stir, the hollow glass micropearl of coated ferriferrous oxide is joined in the titanium sulfate urea mixed solution, stir 8min, add the deionized water of 300ml, in solution, pass into nitrogen 15min, change over to immediately in the reaction cylinder that is lined with polytetrafluoroethylene (PTFE) in the 1L, sealing is placed in the homogeneous reactor, is warming up to 140 ℃ with the speed of 2 ℃/min, isothermal reaction 3h, reaction is filtered after finishing, with absolute ethyl alcohol and deionized water washing, 60 ℃ of vacuum drying 1.5h.The hollow glass micropearl of clad nano tri-iron tetroxide, titanium deoxid film is added in the liquor argenti nitratis ophthalmicus of 1L, mass concentration 2g/L, stir 8min, slowly add the glucose solution of 200mL, mass concentration 7g/L, stirring reaction 20min under 30 ℃ of conditions, wash 80 dry 40min with absolute ethyl alcohol and deionized water respectively after the filtration.
Photo-catalytic degradation of methyl-orange dyestuff result shows (assay method is the same), the methyl orange solution of mass concentration 10mg/L, volume 500mL, add the hollow glass micropearl that 0.5g clad nano tri-iron tetroxide, titanium dioxide and Nano Silver are modified, through 100W ultraviolet lamp 1h irradiation, the methyl orange dye photocatalytic activity is 95.8%.The saturation magnetization that records the hollow glass micropearl of clad nano tri-iron tetroxide, titanium dioxide and Nano Silver modification is 26emu/g.
Claims (8)
1. one kind prepares the method with the active hollow glass micropearl of magnetic photocatalytic, it is characterized in that it comprises following processing step: I. and adopt first hydro-thermal method to hollow glass micropearl coated magnetic nano ferriferrous oxide film; II. again at the magnetic Nano ferriferrous oxide film outer cladding anatase-type nanometer titanium dioxide film of hollow glass micropearl; III. at last the hollow glass micropearl that has coated magnetic Nano ferriferrous oxide film and anatase-type nanometer titanium dioxide film is carried out the silver ion modification.
2. a kind of method with the active hollow glass micropearl of magnetic photocatalytic for preparing as claimed in claim 1 is characterized in that, before adopting hydro-thermal method to hollow glass micropearl coated magnetic nano ferriferrous oxide film, first hollow glass micropearl is carried out preliminary treatment.
3. a kind of method with the active hollow glass micropearl of magnetic photocatalytic for preparing as claimed in claim 2 is characterized in that, describedly hollow glass micropearl is carried out pretreated technical process comprises and deoiling and two programs of alligatoring.
4. a kind of method with the active hollow glass micropearl of magnetic photocatalytic for preparing as claimed in claim 3, it is characterized in that, the technical process of the described program of deoiling is as follows: weighing sodium hydroxide, sodium carbonate and sodium metasilicate are dissolved in the deionized water, obtain degreasing fluid, described NaOH, sodium carbonate and the sodium metasilicate quality-volumetric concentration in described degreasing fluid is respectively 40g/L, 10g/L and 5g/L; Described degreasing fluid is heated to 80~100 ℃; Take by weighing hollow glass micropearl 5~10g, add in the described degreasing fluid of 1L, adopt the mechanical agitation method that cenosphere is fully disperseed in degreasing fluid, filtration behind reaction 40~60min, washing.
5. such as claim 3 or 4 described a kind of methods with the active hollow glass micropearl of magnetic photocatalytic that prepare, it is characterized in that, the technical process of described alligatoring program is as follows: with the upper step obtain deoil after hollow glass micropearl be immersed in the hydrofluoric acid solution of mass concentration 1~3%, volume 1L, under 40~60 ℃ of conditions, react 1~2h, wash respectively dry 1~2h under 80 ℃ of conditions after the filtration with acetone, absolute ethyl alcohol and deionized water.
6. such as claim 1,2 or 3 described a kind of methods with the active hollow glass micropearl of magnetic photocatalytic that prepare, it is characterized in that, the technical process of described step I is as follows: be 0.05~0.15mol/L according to total concentration of iron, ferrous sulfate and ferric nitrate mass ratio are Fe
2+: Fe
3+=1:2~3:2 takes by weighing ferrous sulfate and ferric nitrate, obtain ferrous iron and ferric mixed solution with deionized water dissolving, adding mass concentration is the NaOH of 15~30g/L, mass concentration is the ethylene glycol of 20~40g/L, mass concentration is the polyvinylpyrrolidone of 10~20g/L, add ethanol solution according to volume ratio 4:1~1:4, add hollow glass micropearl, change over to subsequently to the high pressure reaction cylinder, under 120~160 ℃ of conditions, 4~8h is processed in insulation, filters out cenosphere after question response is finished after the sealing, wash respectively vacuum drying 1~2h under 60 ℃ of conditions with absolute ethyl alcohol and deionized water.
7. such as claim 1,2 or 3 described a kind of methods with the active hollow glass micropearl of magnetic photocatalytic that prepare, it is characterized in that, the technical process of described step II is as follows: the titanium sulfate of 18~20g is dissolved in the deionized water of temperature 60 C, volume 400mL, then add the urea of 8~12g and the polyethylene glycol of 3~8g, and constantly stir; Hollow glass micropearl after the processing of step I is joined in the titanium sulfate urea mixed solution, mechanical agitation 5~10min, then replenish the deionized water of 200~400ml, and in solution, pass into nitrogen 10~20min, then change over to immediately in the reaction cylinder of volume 1L, sealing is placed in the homogeneous reactor, is warming up to 110~150 ℃, isothermal reaction 2~5h with the speed of 1~2 ℃/min; Question response filters after finishing, with absolute ethyl alcohol and washed with de-ionized water, 60 ℃ of vacuum drying 1~2h.
8. such as claim 1,2 or 3 described a kind of methods with the active hollow glass micropearl of magnetic photocatalytic that prepare, it is characterized in that, the technical process of described step III is as follows: the hollow glass micropearl after the step II is processed adds volume 1L to, mass concentration is in the liquor argenti nitratis ophthalmicus of 1~4g/L, fully stir 5~10min, then slowly add volume 200mL, mass concentration is the glucose solution of 4~10g/L, and constantly stir, under 20~40 ℃ of conditions, react 10~30min, wash with absolute ethyl alcohol and deionized water respectively after the filtration, vacuum drying 30~50min under 80 conditions, namely finish at the first coated magnetic nano ferriferrous oxide in hollow glass micropearl surface, coat again anatase-type nanometer titanium dioxide, carry out at last the modified film that Nano Silver is modified.
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