CN103225127A - Photo-electromagnetic three-functional two-strands-paralleled nanometer fiber bundle - Google Patents
Photo-electromagnetic three-functional two-strands-paralleled nanometer fiber bundle Download PDFInfo
- Publication number
- CN103225127A CN103225127A CN2013100684942A CN201310068494A CN103225127A CN 103225127 A CN103225127 A CN 103225127A CN 2013100684942 A CN2013100684942 A CN 2013100684942A CN 201310068494 A CN201310068494 A CN 201310068494A CN 103225127 A CN103225127 A CN 103225127A
- Authority
- CN
- China
- Prior art keywords
- pvp
- phen
- nanofibers
- bursts
- functions
- 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.)
- Pending
Links
Images
Landscapes
- Artificial Filaments (AREA)
Abstract
The invention relates to a photo-electromagnetic three-functional two-strands-paralleled nanometer fiber bundle and its preparation method, and belongs to the technical field of nanomaterial preparation. The method comprises the following steps: 1, preparing a Tb(BA)3phen complex through a precipitation process; 2, preparing an Fe3O4 nanocrystal through the precipitation process; 3, preparing a spinning liquid; and 4, preparing a [Tb(BA)3phen/PVP]//[PANI/Fe3O4/PVP] photo-electromagnetic three-functional two-strands-paralleled nanometer fiber bundle, adopting a static spinning technology, and using a parallel double-spinning head. The prepared photo-electromagnetic three-functional two-strands-paralleled nanometer fiber bundle has a smooth surface and has good luminescent, conductive and magnetic functions, and the diameter and the length of a single-stranded nanofiber are 200nm and above 50mum respectively. The above nanostructured material has an important application prospect. The method is simple, is easy to implement, can realize batch production, and has a wide application prospect.
Description
Technical field
The present invention relates to the nano material preparation technical field, relate to two bursts of parallel bundles of nanofibers of a kind of photoelectromagnetic three functions and preparation method thereof specifically.
Background technology
Nanofiber is meant the filamentary material that has bidimensional to be in nanoscale on the three dimensions yardstick of material, radial dimension is a nanometer scale usually, and length is then bigger.Because the radial dimension of nanofiber is little of nanometer scale, demonstrate series of characteristics, the most outstanding is that specific area is big, thereby its surface energy and active the increase, and then produce small-size effect, surface or interfacial effect, quantum size effect, macro quanta tunnel effect etc., and therefore show a series of chemistry, physics specificity as aspects such as heat, light, sound, electricity, magnetic.In the prior art, a lot of methods that prepare nanofiber are arranged, the method for for example reeling off raw silk from cocoons, template synthetic method, split-phase method and self-assembly method etc.In addition, also has arc evaporation, laser high temperature inustion, compound pyrolysismethod.These three kinds of methods in fact all are after at high temperature making compound or simple substance evaporation, to make nanofiber or nanotube through pyrolysis or direct condensation, from essence, all belong to the compound steam sedimentation.
Two bursts of parallel bundles of nanofibers are nano-fiber materials of a kind of new structure, stick together by two strands of nanofibers and to form two bursts of parallel bundles of nanofibers, per share nanofiber has different functions, has lighting function as one fiber, another strand fiber has conduction and magnetic, this have that photoelectromagnetic is three difunctional, two bursts of parallel bundles of nanofibers of novel structure will have important application prospects in following nano structure device and medical diagnosis treatment, and the research of this respect yet there are no report.
Polyaniline PANI is because advantage such as it is easily synthetic, electrical conductivity is high and environmental stability is good has become one of focus of conducting polymer area research.People have synthesized the polyaniline PANI[J.R.Araujo of one-dimensional nano structures such as nano wire, nanometer rods, nanotube and nanofiber, C.B.Adamo and Marco-A.De Paoli, Chem.Eng.J., 2011,174,425-431; J.Huang, S.Virji, B.H.Weiller and R.B.Kaner, Chem.Eur.J.2004,10,1314 – 1319; Q.Z.Yu, M.M.Shi, M.Deng, M.Wang and H.Z.Chen, Mater.Sci.Eng.B, 2008,150,70-76].
Made from rare-earth terbium complex Tb (BA)
3Phen, Tb
3+Be terbium ion, BA is a benzoate anion, and phen is a phenanthroline, because of the electron configuration of terbium ion uniqueness becomes the light emitting ionic with special performance, Tb (BA)
3Phen has advantages such as luminous intensity height, good stability, fluorescence quantum yield height, monochromaticjty be good, is a kind of rare-earth luminescent material of extensive use.
Tri-iron tetroxide Fe
3O
4It is a kind of important and magnetic material of extensive use.People have adopted several different methods, have successfully prepared Fe as methods such as the precipitation method, sol-gel process, microemulsion method, hydro-thermal and solvent-thermal method, thermal decomposition method, method of electrostatic spinning
3O
4Nano materials such as nanocrystalline, nanometer rods, nano wire, nanometer film, hybrid structure, nuclear shell structure nano particle, the technology comparative maturity.
Existing research is verified, as magnetic compound Fe
3O
4Perhaps dark colour electrically conductive polyaniline PANI and rare earth compounding Tb (BA)
3Phen directly mixes and can significantly reduce its illumination effect, therefore will obtain Tb (BA)
3The illumination effect that phen is good must make Tb (BA)
3Phen and Fe
3O
4Or PANI realizes effectively separating.If with Fe
3O
4Nanocrystallinely be mixed with into nanofiber with PVP with conductive polymer polyanilinc PANI, conduction PANI is continuous, has guaranteed its high conductivity, as two strands of one fibers that parallel nanofiber is intrafascicular, this strand fiber will have electric conductivity and magnetic, and with Tb (BA)
3Phen is scattered among the macromolecule PVP and is prepared into nanofiber, and as two strands of another strand fibers that parallel nanofiber is intrafascicular, this strand fiber will have luminescent properties, thereby can make Fe
3O
4Perhaps electrically conductive polyaniline PANI and Tb (BA)
3Phen has realized effective separation, so just can obtain two bursts of parallel bundles of nanofibers of well behaved photoelectromagnetic three functions.
At present, do not see by Tb (BA)
3Phen complex and polyvinylpyrrolidone PVP are compound, polyaniline PANI and Fe
3O
4Nanocrystalline and polyvinylpyrrolidone PVP are compound, construct the report of two bursts of parallel bundles of nanofibers of photoelectromagnetic three functions, i.e. two strands of parallel nanofibers formation bundles of nanofibers that sticks together side by side, and wherein one fiber is Tb (BA)
3Phen+PVP has the characteristics of luminescence, and another strand fiber is PANI+Fe
3O
4Nanocrystalline+PVP, have electric conductivity and magnetic, promptly form [Tb (BA)
3Phen/PVP] // [PANI/Fe
3O
4/ PVP] two bursts of parallel bundles of nanofibers of photoelectromagnetic three functions, // representative is parallel, i.e. the material of front [Tb (BA)
3Phen/PVP] fiber that constitutes and the material [PANI/Fe of back
3O
4/ PVP] fiber that constitutes is parallel.This kind has two bursts of parallel bundles of nanofibers of photoelectromagnetic three functions and has special structure, will have important use in following nano structure device and medical diagnosis treatment.
The patent No. technical scheme of a relevant electrospinning process (electrospinning) that has been 1975504 U.S. Patent Publication, this method is a kind of effective ways that prepare continuous, as to have macro length micro nanometer fiber, is at first proposed in 1934 by Formhals.This method is mainly used to prepare high polymer nanometer fiber, it is characterized in that making charged Polymer Solution or melt in electrostatic field, to be subjected to the traction of electrostatic force and spray by nozzle, invest the receiving screen on opposite, thereby realization wire drawing, solvent evaporation at normal temperatures then, perhaps melt is cooled to normal temperature and solidifies, and obtains micro nanometer fiber.Over nearly 10 years, occurred adopting electrospinning process to prepare the technical scheme of inorganic compound such as oxidate nano fiber at the inorfil preparing technical field, described oxide comprises TiO
2, ZrO
2, Y
2O
3, Y
2O
3: RE
3+(RE
3+=Eu
3+, Tb
3+, Er
3+, Yb
3+/ Er
3+), SnO
2, NiO, Co
3O
4, Mn
2O
3, Mn
3O
4, CuO, SiO
2, Al
2O
3, V
2O
5, ZnO, Nb
2O
5, MoO
3, CeO
2, LaMO
3(M=Fe, Cr, Mn, Co, Ni, Al), Y
3Al
5O
12, La
2Zr
2O
7Deng metal oxide and composite oxide of metal.Electrospinning process can prepare big L/D ratio micrometer fibers or nanofiber continuously.Q.Z.Yu, et al. adopt electrostatic spinning technique to prepare polyaniline PANI nanofiber [Mater.Sci.Eng.B, 2008,150,70-76]; The single spinning head of uses such as Dong Xiangting, employing electrostatic spinning technique have prepared Eu (BA)
3The difunctional composite nano fiber of phen/PANI/PVP photoelectricity [SCI, 2012,33 (8), 1657-1662]; Dong Xiangting etc. utilize electrostatic spinning technique to prepare Eu (BA)
3The difunctional two bursts of parallel bundles of nanofibers of phen/PVP//PANI/PVP photoelectricity [national inventing patent, application number: 201210407369.5]; Dong Xiangting etc. utilize electrostatic spinning technique to prepare Fe
3O
4/ PVP//Eu (BA)
3Two strands of parallel composite nano fiber bundles of phen/PVP magneto-optic double-function [national inventing patent, application number: 201110249651.0].At present, do not see and utilize electrostatic spinning technique preparation [Tb (BA)
3Phen/PVP] // [PANI/Fe
3O
4/ PVP] relevant report of two bursts of parallel bundles of nanofibers of photoelectromagnetic three functions.
When utilizing electrostatic spinning technique to prepare nano material, the structure of the composition of the kind of raw material, the molecular weight of high polymer templates, spinning solution, spinning process parameter and spinning head all has material impact to the pattern and the size of final products.The present invention adopts electrostatic spinning technique, and spinning head cuts the double-spinneret arranged side by side that the identical syringe needle of flat diameter is close together and forms by two 8#, with Tb (BA)
3The mixed liquor of phen complex, PVP and DMF is a kind of spinning solution, with Fe
3O
4Nanocrystalline, aniline, camphorsulfonic acid, PVP, DMF and ammonium persulfate mix, and treat to constitute another kind of spinning solution after aniline polymerization becomes polyaniline, and the viscosity of control spinning solution is most important, under the process conditions of the best, obtains [the Tb (BA) of novel structure
3Phen/PVP] // [PANI/Fe
3O
4/ PVP] two bursts of parallel bundles of nanofibers of photoelectromagnetic three functions.
Summary of the invention
Various in background technology prepare in the method for nanofiber, the shortcoming of the method for reeling off raw silk from cocoons be solution viscosity is required too harsh; The shortcoming of template synthetic method is to prepare the continuous fibers that the root root separates; Split-phase method and self-assembly method production efficiency are all lower; And the compound steam sedimentation is owing to the demand to high temperature, so process conditions are difficult to control.And the nanofiber major diameter of above-mentioned several method preparation is than little.Employing electrostatic spinning technique in the background technology has prepared metal oxide nano fiber, composite oxide of metal nanofiber, polyaniline PANI nanofiber, Eu (BA)
3The difunctional composite nano fiber of phen/PANI/PVP photoelectricity, Eu (BA)
3Difunctional two bursts of parallel bundles of nanofibers of phen/PVP//PANI/PVP photoelectricity and Fe
3O
4/ PVP//Eu (BA)
3Two strands of parallel composite nano fiber bundles of phen/PVP magneto-optic double-function, but the character of employed raw material, template agent, solvent and final objective product is different with the present invention.The present invention adopts electrostatic spinning technique, uses double-spinneret arranged side by side to prepare the [Tb (BA) of novel structure
3Phen/PVP] // [PANI/Fe
3O
4/ PVP] two bursts of parallel bundles of nanofibers of photoelectromagnetic three functions, one is Tb (BA)
3The phen/PVP luminous nano fibre, another strand is PANI/Fe
3O
4/ PVP conduction and magnetic Nano fiber, two strands of nanofibers stick together and form two bursts of parallel bundles of nanofibers, two bursts of parallel bundles of nanofibers of photoelectromagnetic three functions that the present invention is prepared have increased a kind of nano-fiber material with photoelectromagnetic three functions of new construction new property for the nanofiber field.
The present invention is achieved in that and at first adopts the precipitation method to prepare Tb (BA)
3Phen complex and Fe
3O
4Nanocrystalline, with Tb (BA)
3The mixed liquor of phen complex, PVP and DMF is a kind of spinning solution, with Fe
3O
4Nanocrystalline, aniline, camphorsulfonic acid, PVP, DMF and ammonium persulfate mix, and treat to constitute another kind of spinning solution after aniline polymerization becomes polyaniline, and the viscosity of control spinning solution is most important.Adopt double-spinneret arranged side by side, application electrostatic spinning technique to carry out electrostatic spinning, under the process conditions of the best, obtain [Tb (BA)
3Phen/PVP] // [PANI/Fe
3O
4/ PVP] two bursts of parallel bundles of nanofibers of photoelectromagnetic three functions.The steps include:
(1) precipitation method prepare Tb (BA)
3The phen complex
With 1.8693g Tb
4O
7Be dissolved in the 10ml concentrated hydrochloric acid, evaporation is removed excessive concentrated hydrochloric acid and is obtained TbCl
3Solid adds the 10ml absolute ethyl alcohol and obtains TbCl
3Ethanolic solution is dissolved in 1.8320g benzoic acid HBA and 0.9910g Phen Phen in the 100ml absolute ethyl alcohol, and water-bath is heated to 50~60 ° of C, drips TbCl
3Ethanolic solution drips dense NH
3H
2It is 6~6.5 that O regulates pH, and meeting constantly produces white precipitate in the dropping process, stirs and makes it to react 3h, after the centrifugation of gained sediment, washs 3 times with ethanol and deionized water respectively, in the dry 12h of 60 ° of C, obtains Tb (BA)
3Phen;
(2) precipitation method prepare Fe
3O
4Nanocrystalline
With 5.4060g FeCl
36H
2O, 2.7800g FeSO
47H
2O, 4.04g NH
4NO
3With the 1.9g molecular weight be that 20000 polyethylene glycol is dissolved in the 100mL deionized water, be heated to 50 ° of C and feed argon gas 30min, slow then dropping ammonia to the pH value of solution is 11, continue logical argon gas 20min and obtain black suspension, after this turbid liquid magnetic separation, wash successively three times with absolute ethyl alcohol and deionized water, product is placed the dry 12h of vacuum drying chamber of 60 ° of C, obtain the Fe that diameter is 8-10nm
3O
4Nanocrystalline;
(3) preparation spinning solution
High polymer templates adopts polyvinylpyrrolidone PVP in the spinning solution, and molecular weight is 90000, with 0.225g Tb (BA)
3Phen and 1.5g PVP join among the 11g DMF, and magnetic agitation 12h obtains spinning solution I, with 0.75g Fe
3O
4Nanocrystalline being scattered among the 7g DMF behind the ultrasonic dispersion 15min, adds 0.75g aniline, 0.9336g camphorsulfonic acid and 1.5g PVP, behind the magnetic agitation 2h, be positioned in 0 ° of C refrigerator and leave standstill 1h, the 1.84g ammonium persulfate is scattered among the DMF of 4g, be positioned in 0 ° of C refrigerator and leave standstill 1h, ammonium persulfate solution is added drop-wise in the aniline solution, behind the magnetic agitation 10min, is positioned over 0 ° of C refrigerator internal reaction 24h, make aniline polymerization become polyaniline PANI, obtain spinning solution II;
(4) preparation [Tb (BA)
3Phen/PVP] // [PANI/Fe
3O
4/ PVP] two bursts of parallel bundles of nanofibers of photoelectromagnetic three functions
Spinning head cuts the double-spinneret arranged side by side that the flat identical syringe needle of diameter is close together and forms by two, two syringe needles are for cutting the 8# stainless steel syringe needle after putting down, external diameter is 0.8mm, internal diameter is 0.49mm, two spinning solutions that prepare are joined respectively in two syringe tubes, adopt electrostatic spinning technique, use perpendicular spray mode, shower nozzle is vertical with horizontal plane, and applying voltage is 16kV, and shower nozzle is 15cm to the curing distance of receiving screen wire netting, 15 ° of C~20 ° C of indoor temperature, relative humidity is 40%~50%, along with the volatilization of solvent, just can collect ganoid [Tb (BA) on as the wire netting of negative pole
3Phen/PVP] // [PANI/Fe
3O
4/ PVP] two bursts of parallel bundles of nanofibers of photoelectromagnetic three functions, the diameter of sub-thread nanofiber is 200nm, length is greater than 50 μ m.
Prepared [Tb (BA) in said process
3Phen/PVP] // [PANI/Fe
3O
4/ PVP] two strands of parallel nanofibers of photoelectromagnetic three functions are intrafascicular, and the diameter of sub-thread nanofiber is 200nm, and length under the ultraviolet excitation of 273nm, is launched the bright green glow that main peak is positioned at 544nm greater than 50 μ m, and its electrical conductivity is 8.953 * 10
-4S/cm, saturation magnetization is 11.42emu/g, has good luminous, electric conductivity and magnetic three functions, has realized goal of the invention.
Description of drawings
Fig. 1 is Fe
3O
4Nanocrystalline TEM photo;
Fig. 2 is Fe
3O
4Nanocrystalline XRD spectra;
Fig. 3 is [Tb (BA)
3Phen/PVP] // [PANI/Fe
3O
4/ PVP] XRD spectra of two bursts of parallel bundles of nanofibers of photoelectromagnetic three functions;
Fig. 4 is [Tb (BA)
3Phen/PVP] // [PANI/Fe
3O
4/ PVP] the SEM photo of two bursts of parallel bundles of nanofibers of photoelectromagnetic three functions;
Fig. 5 is [Tb (BA)
3Phen/PVP] // [PANI/Fe
3O
4/ PVP] the TEM photo of two bursts of parallel bundles of nanofibers of photoelectromagnetic three functions, this figure double as Figure of abstract;
Fig. 6 is [Tb (BA)
3Phen/PVP] // [PANI/Fe
3O
4/ PVP] the EDS spectrogram of two bursts of parallel bundles of nanofibers of photoelectromagnetic three functions;
Fig. 7 is [Tb (BA)
3Phen/PVP] // [PANI/Fe
3O
4/ PVP] the exciting light spectrogram of two bursts of parallel bundles of nanofibers of photoelectromagnetic three functions;
Fig. 8 is [Tb (BA)
3Phen/PVP] // [PANI/Fe
3O
4/ PVP] the emission spectrum figure of two bursts of parallel bundles of nanofibers of photoelectromagnetic three functions;
Fig. 9 is [Tb (BA)
3Phen/PVP] // [PANI/Fe
3O
4/ PVP] the hysteresis curve figure of two bursts of parallel bundles of nanofibers of photoelectromagnetic three functions.
The specific embodiment
The terbium oxide Tb that the present invention is selected
4O
7Purity be 99.99%, polyvinylpyrrolidone PVP, molecular weight 90000, N, dinethylformamide DMF, aniline, camphorsulfonic acid, ammonium persulfate, hydrochloric acid, benzoic acid HBA, phenanthroline phen, Iron(III) chloride hexahydrate, green vitriol, ammonium nitrate, molecular weight are 20000 polyethylene glycol, argon gas, absolute ethyl alcohol, NH
3H
2O is commercially available analysis net product, the self-control of deionized water laboratory; Used glass apparatus and equipment are instrument and equipments commonly used in the laboratory.
Embodiment: with 1.8693g Tb
4O
7Be dissolved in the 10ml concentrated hydrochloric acid, evaporation is removed excessive concentrated hydrochloric acid and is obtained TbCl
3Solid adds the 10ml absolute ethyl alcohol and obtains TbCl
3Ethanolic solution is dissolved in 1.8320g benzoic acid HBA and 0.9910g Phen Phen in the 100ml absolute ethyl alcohol, and water-bath is heated to 50~60 ° of C, drips TbCl
3Ethanolic solution drips dense NH
3H
2It is 6~6.5 that O regulates pH, and meeting constantly produces white precipitate in the dropping process, stirs and makes it to react 3h, after the centrifugation of gained sediment, washs 3 times with ethanol and deionized water respectively, in the dry 12h of 60 ° of C, obtains Tb (BA)
3Phen; With 5.4060g FeCl
36H
2O, 2.7800g FeSO
47H
2O, 4.04g NH
4NO
3With the 1.9g molecular weight be that 20000 polyethylene glycol is dissolved in the 100mL deionized water, be heated to 50 ° of C and feed argon gas 30min, slow then dropping ammonia to the pH value of solution is 11, continue logical argon gas 20min and obtain black suspension, after this turbid liquid magnetic separation, wash successively three times with absolute ethyl alcohol and deionized water, product is placed the dry 12h of vacuum drying chamber of 60 ° of C, obtain the Fe that diameter is 8-10nm
3O
4Nanocrystalline, see shown in Figure 1; Prepared Fe
3O
4Nanocrystalline have good crystallinity, the d value of its diffraction maximum and relative intensity and a Fe
3O
4The listed d value of PDF standard card (74-0748) consistent with relative intensity, belong to cubic system, see shown in Figure 2; High polymer templates adopts polyvinylpyrrolidone PVP in the spinning solution, and molecular weight is 90000, with 0.225g Tb (BA)
3Phen and 1.5g PVP join among the 11g DMF, and magnetic agitation 12h obtains spinning solution I, with 0.75g Fe
3O
4Nanocrystalline being scattered among the 7g DMF behind the ultrasonic dispersion 15min, adds 0.75g aniline, 0.9336g camphorsulfonic acid and 1.5g PVP, behind the magnetic agitation 2h, be positioned in 0 ° of C refrigerator and leave standstill 1h, the 1.84g ammonium persulfate is scattered among the DMF of 4g, be positioned in 0 ° of C refrigerator and leave standstill 1h, ammonium persulfate solution is added drop-wise in the aniline solution, behind the magnetic agitation 10min, is positioned over 0 ° of C refrigerator internal reaction 24h, make aniline polymerization become polyaniline PANI, obtain spinning solution II; Spinning head cuts the double-spinneret arranged side by side that the flat identical syringe needle of diameter is close together and forms by two, two syringe needles are for cutting the 8# stainless steel syringe needle after putting down, external diameter is 0.8mm, internal diameter is 0.49mm, two spinning solutions that prepare are joined respectively in two syringe tubes, adopt electrostatic spinning technique, use perpendicular spray mode, shower nozzle is vertical with horizontal plane, and applying voltage is 16kV, and shower nozzle is 15cm to the curing distance of receiving screen wire netting, 15 ° of C~20 ° C of indoor temperature, relative humidity is 40%~50%, along with the volatilization of solvent, just can collect ganoid [Tb (BA) on as the wire netting of negative pole
3Phen/PVP] // [PANI/Fe
3O
4/ PVP] two bursts of parallel bundles of nanofibers of photoelectromagnetic three functions, using Hall effect Department of Survey its electrical conductivity of unified test is 8.953 * 10
-4S/cm.Prepared [Tb (BA)
3Phen/PVP] // [PANI/Fe
3O
4/ PVP] two bursts of parallel bundles of nanofibers of photoelectromagnetic three functions have tangible Fe
3O
4Diffraction maximum, show two gangs of intrafascicular Fe of containing of parallel nanofiber of prepared photoelectromagnetic three functions
3O
4Nanocrystalline, see shown in Figure 3; Prepared [Tb (BA)
3Phen/PVP] // [PANI/Fe
3O
4/ PVP] smooth surface of two bursts of parallel bundles of nanofibers of photoelectromagnetic three functions, be two bursts of parallel bundles of nanofibers structures, length is seen shown in Figure 4 greater than 50 μ m; Prepared [Tb (BA)
3Phen/PVP] // [PANI/Fe
3O
4/ PVP] two strands of parallel nanofibers of photoelectromagnetic three functions are intrafascicular, and the diameter of sub-thread nanofiber is 200nm, wherein is dispersed with Fe in one nanofiber
3O
4Nanocrystalline, see shown in Figure 5; Prepared [Tb (BA)
3Phen/PVP] // [PANI/Fe
3O
4/ PVP] two bursts of parallel bundles of nanofibers of photoelectromagnetic three functions are made up of C, N, O, Tb and Fe element, and S derives from initiator ammonium persulfate, and the Au conductive layer of surface plating was seen shown in Figure 6 when Au derived from the SEM sample preparation; When the monitoring wavelength is 544nm, [Tb (BA)
3Phen/PVP] // [PANI/Fe
3O
4/ PVP] the excitation spectrum highest peak of two bursts of parallel bundles of nanofibers of photoelectromagnetic three functions is positioned at the 273nm place, belongs to the π → π of part
*Transition is seen shown in Figure 7; Under the ultraviolet excitation of 273nm, [Tb (BA)
3Phen/PVP] // [PANI/Fe
3O
4/ PVP] two bursts of parallel bundles of nanofibers of photoelectromagnetic three functions launch the bright green glow that main peak is positioned at 544nm, and it is corresponding to Tb
3+Ion
5D
4→
5F
5Transition is seen shown in Figure 8; [Tb (BA)
3Phen/PVP] // [PANI/Fe
3O
4/ PVP] two bursts of parallel bundles of nanofibers of photoelectromagnetic three functions have stronger magnetic, and its hysteresis curve is seen shown in Figure 9, and saturation magnetization is 11.42emu/g.
Certainly; the present invention also can have other various embodiments; under the situation that does not deviate from spirit of the present invention and essence thereof; those of ordinary skill in the art work as can make various corresponding changes and distortion according to the present invention, but these corresponding changes and distortion all should belong to the protection domain of the appended claim of the present invention.
Claims (2)
1. two bursts of parallel bundles of nanofibers of photoelectromagnetic three functions, it is characterized in that nano-fiber material presents two bursts of parallel bundles of nanofibers structures, have luminous, conduction and three kinds of functions of magnetic, the diameter of two strands of intrafascicular sub-thread nanofibers of parallel nanofiber is 200nm, and length is greater than 50 μ m.
2. the preparation method of two bursts of parallel bundles of nanofibers of photoelectromagnetic three functions as claimed in claim 1, it is characterized in that, adopt electrostatic spinning technique, use double-spinneret arranged side by side, high polymer templates is the polyvinylpyrrolidone PVP of molecular weight 90000, N, dinethylformamide DMF are solvent, and the preparation product is [Tb (BA)
3Phen/PVP] // [PANI/Fe
3O
4/ PVP] two bursts of parallel bundles of nanofibers of photoelectromagnetic three functions, the steps include:
(1) precipitation method prepare Tb (BA)
3The phen complex
With 1.8693g Tb
4O
7Be dissolved in the 10ml concentrated hydrochloric acid, evaporation is removed excessive concentrated hydrochloric acid and is obtained TbCl
3Solid adds the 10ml absolute ethyl alcohol and obtains TbCl
3Ethanolic solution is dissolved in 1.8320g benzoic acid HBA and 0.9910g Phen Phen in the 100ml absolute ethyl alcohol, and water-bath is heated to 50~60 ° of C, drips TbCl
3Ethanolic solution drips dense NH
3H
2It is 6~6.5 that O regulates pH, and meeting constantly produces white precipitate in the dropping process, stirs and makes it to react 3h, after the centrifugation of gained sediment, washs 3 times with ethanol and deionized water respectively, in the dry 12h of 60 ° of C, obtains Tb (BA)
3Phen;
(2) precipitation method prepare Fe
3O
4Nanocrystalline
With 5.4060g FeCl
36H
2O, 2.7800g FeSO
47H
2O, 4.04g NH
4NO
3With the 1.9g molecular weight be that 20000 polyethylene glycol is dissolved in the 100ml deionized water, be heated to 50 ° of C and feed argon gas 30min, slow then dropping ammonia to the pH value of solution is 11, continue logical argon gas 20min and obtain black suspension, after this turbid liquid magnetic separation, wash successively three times with absolute ethyl alcohol and deionized water, product is placed the dry 12h of vacuum drying chamber of 60 ° of C, obtain the Fe that diameter is 8-10nm
3O
4Nanocrystalline;
(3) preparation spinning solution
With 0.225g Tb (BA)
3Phen and 1.5g PVP join among the 11g DMF, and magnetic agitation 12h obtains spinning solution I, with 0.75g Fe
3O
4Nanocrystalline being scattered among the 7g DMF behind the ultrasonic dispersion 15min, adds 0.75g aniline, 0.9336g camphorsulfonic acid and 1.5g PVP, behind the magnetic agitation 2h, be positioned in 0 ° of C refrigerator and leave standstill 1h, the 1.84g ammonium persulfate is scattered among the DMF of 4g, be positioned in 0 ° of C refrigerator and leave standstill 1h, ammonium persulfate solution is added drop-wise in the aniline solution, behind the magnetic agitation 10min, is positioned over 0 ° of C refrigerator internal reaction 24h, make aniline polymerization become polyaniline PANI, obtain spinning solution II;
(4) preparation [Tb (BA)
3Phen/PVP] // [PANI/Fe
3O
4/ PVP] two bursts of parallel bundles of nanofibers of photoelectromagnetic three functions
Spinning head cuts the double-spinneret arranged side by side that the flat identical syringe needle of diameter is close together and forms by two, two syringe needles are for cutting the 8# stainless steel syringe needle after putting down, external diameter is 0.8mm, internal diameter is 0.49mm, two spinning solutions that prepare are joined respectively in two syringe tubes, adopt electrostatic spinning technique, use perpendicular spray mode, shower nozzle is vertical with horizontal plane, and applying voltage is 16kV, and shower nozzle is 15cm to the curing distance of receiving screen wire netting, indoor temperature is 15 ° of C~20 ° C, relative humidity is 40%~50%, along with the volatilization of solvent, just can collect ganoid [Tb (BA) on as the wire netting of negative pole
3Phen/PVP] // [PANI/Fe
3O
4/ PVP] two bursts of parallel bundles of nanofibers of photoelectromagnetic three functions, the diameter of sub-thread nanofiber is 200nm, and length under the ultraviolet excitation of 273nm, is launched the bright green glow that main peak is positioned at 544nm greater than 50 μ m, and its electrical conductivity is 8.953 * 10
-4S/cm, saturation magnetization is 11.42emu/g, that these two bursts of parallel bundles of nanofibers have is luminous, conduction and magnetic three functions.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN2013100684942A CN103225127A (en) | 2013-03-05 | 2013-03-05 | Photo-electromagnetic three-functional two-strands-paralleled nanometer fiber bundle |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN2013100684942A CN103225127A (en) | 2013-03-05 | 2013-03-05 | Photo-electromagnetic three-functional two-strands-paralleled nanometer fiber bundle |
Publications (1)
Publication Number | Publication Date |
---|---|
CN103225127A true CN103225127A (en) | 2013-07-31 |
Family
ID=48835759
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN2013100684942A Pending CN103225127A (en) | 2013-03-05 | 2013-03-05 | Photo-electromagnetic three-functional two-strands-paralleled nanometer fiber bundle |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN103225127A (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104342851A (en) * | 2014-09-30 | 2015-02-11 | 东华大学 | A method for preparing CaSi2O2N2: ce, tb/Eu multilayer multicolor fluorescent fiber film |
CN104532394A (en) * | 2014-12-18 | 2015-04-22 | 长春理工大学 | Janus nano-belt array with three functions of anisotropy, conductivity and magneto-optic and preparation method thereof |
CN104532393A (en) * | 2014-12-18 | 2015-04-22 | 长春理工大学 | Tricolor flag type nano-belt array with three functions of anisotropy, conductivity and magneto-optic and preparation method thereof |
CN104538121A (en) * | 2014-11-27 | 2015-04-22 | 长春理工大学 | Photo-electro-magnetic three-function banded coaxial nano cable array and preparation method thereof |
CN106283397A (en) * | 2016-08-30 | 2017-01-04 | 长春理工大学 | Green emitting electromagnetism three function two-layer composite nano-fiber membrane and preparation method thereof |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102433610A (en) * | 2011-08-29 | 2012-05-02 | 长春理工大学 | Method for preparing magneto-optical difunctional two parallel strand composite nanofiber bundle |
CN102504805A (en) * | 2011-10-10 | 2012-06-20 | 长春理工大学 | Magneto-optic dual-function composite nanobelt and its preparation method |
CN102943317A (en) * | 2012-10-24 | 2013-02-27 | 长春理工大学 | Method for constructing photoelectricity double function two-stranded parallel nanometer fiber bundle |
-
2013
- 2013-03-05 CN CN2013100684942A patent/CN103225127A/en active Pending
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102433610A (en) * | 2011-08-29 | 2012-05-02 | 长春理工大学 | Method for preparing magneto-optical difunctional two parallel strand composite nanofiber bundle |
CN102504805A (en) * | 2011-10-10 | 2012-06-20 | 长春理工大学 | Magneto-optic dual-function composite nanobelt and its preparation method |
CN102943317A (en) * | 2012-10-24 | 2013-02-27 | 长春理工大学 | Method for constructing photoelectricity double function two-stranded parallel nanometer fiber bundle |
Non-Patent Citations (1)
Title |
---|
王莹熇等: "静电纺丝技术制备Tb_BA_3phen/PANI/PVP光电双功能复合纳米纤维", 《化学学报》, no. 14, 28 July 2012 (2012-07-28), pages 1576 - 1582 * |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104342851A (en) * | 2014-09-30 | 2015-02-11 | 东华大学 | A method for preparing CaSi2O2N2: ce, tb/Eu multilayer multicolor fluorescent fiber film |
CN104538121A (en) * | 2014-11-27 | 2015-04-22 | 长春理工大学 | Photo-electro-magnetic three-function banded coaxial nano cable array and preparation method thereof |
CN104532394A (en) * | 2014-12-18 | 2015-04-22 | 长春理工大学 | Janus nano-belt array with three functions of anisotropy, conductivity and magneto-optic and preparation method thereof |
CN104532393A (en) * | 2014-12-18 | 2015-04-22 | 长春理工大学 | Tricolor flag type nano-belt array with three functions of anisotropy, conductivity and magneto-optic and preparation method thereof |
CN106283397A (en) * | 2016-08-30 | 2017-01-04 | 长春理工大学 | Green emitting electromagnetism three function two-layer composite nano-fiber membrane and preparation method thereof |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN102433610A (en) | Method for preparing magneto-optical difunctional two parallel strand composite nanofiber bundle | |
CN101786596B (en) | Polycrystalline nano-fiber with europium ion doped with lanthanum aluminate and preparation method thereof | |
CN104532393B (en) | Anisotropic conductive magneto-optic three function trichroism flag form nano-band array and preparation method thereof | |
CN102031586B (en) | Method for preparing europium-doped yttrium fluoride nano fiber/polymer composite nano fiber | |
CN104532394B (en) | Anisotropic conductive magneto-optic three function Janus nano-band array and preparation method thereof | |
CN102592716B (en) | Magnetic and optical dual-function coaxial nano cable and preparation method thereof | |
CN103225127A (en) | Photo-electromagnetic three-functional two-strands-paralleled nanometer fiber bundle | |
CN103225129A (en) | Photo-electromagnetic three-functional three-strands-paralleled nanometer fiber bundle and its preparation method | |
CN102041583A (en) | Method for preparing europium and fluorine-doped yttrium oxide nanofibres | |
CN102943317A (en) | Method for constructing photoelectricity double function two-stranded parallel nanometer fiber bundle | |
CN102965762A (en) | Method for preparing Er-Yb co-blended yttrium fluoride up-conversion luminescence hollow nanofibers | |
CN104538121B (en) | Photo-electro-magnetic three-function banded coaxial nano cable array and preparation method thereof | |
CN102504805B (en) | Magneto-optic dual-function composite nanobelt and its preparation method | |
CN103225120A (en) | Magneto-optical bifunctional double-strand parallel nanoribbon bundle and preparation method thereof | |
CN103225128A (en) | Photo-electromagnetic three-functional two-strands-paralleled nanometer fiber bundle and its preparation method | |
CN102392322A (en) | Method for preparing europium-doped sulfur oxide gadolinium light-emitting nanometer fiber | |
CN102660802B (en) | Preparation method for erbium and ytterbium double-doped up-conversion luminescence nano-fiber | |
CN107881593B (en) | Double-anisotropic conductive green fluorescent Janus structure film and preparation method thereof | |
CN103225121A (en) | Magnetic up-conversion luminescence dual-functional coaxial composite nanofiber and preparation method thereof | |
CN102392319B (en) | Preparation method of europium-doped LaOBr nanofiber | |
CN102817113B (en) | Preparation method of terbium-doped octafluoro yttrium barium green luminescent nano-fiber | |
CN102817108B (en) | Preparation method for terbium doped yttrium trifluoride green luminescence hollow nano-fibers | |
CN102605465A (en) | Method for preparing europium-doped LaAlO3 red luminescence hollow nanometer fiber | |
CN102817114A (en) | Method for preparing europium-doped octafluoro yttrium barium red luminescent nano-fiber | |
CN102443880A (en) | Preparation method for europium-doped yttrium oxysulfide red luminous nano fiber |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
C02 | Deemed withdrawal of patent application after publication (patent law 2001) | ||
WD01 | Invention patent application deemed withdrawn after publication |
Application publication date: 20130731 |