CN100354203C - Amino acid intercalation manganese dioxide and its preparation method - Google Patents
Amino acid intercalation manganese dioxide and its preparation method Download PDFInfo
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Abstract
The present invention relates to an amino acid inserting layer manganese bioxide composite material and a later stripping assembly preparation method thereof. The composite material has the following chemical composition: (A<+>)a(Amino<+>)bMno2. mH2o, wherein A<+> is inorganic or organic cations such as one or two kinds or all of sodium ions, hydrogen ions, tetramethyl ammonium ions; Amino is one kind of L-Lysine, L-arginine, L-histidine, etc.; a and b respectively are the numbers of A<+> and Amino<+>, and the sum of a and b is equal to 4 or smaller than 0.4; m is the number of crystallinic water and is smaller than 0.5 or larger than 0.1. In the method, manganese oxygen octahedrons form two-dimensional layer plates through common edges; Amino<+> and A<+> are positioned between layers; firstly, delta-MnO2 lamellar structures are prepaed through hydrothermal reaction; tetramethyl ammonium hydroxide is used for stripping the layers of the delta-MnO2 lamellar structures for forming electronegative layer plates; afterwards, the electronegative layer plates and amino acid cations do self assembly through static electrification for obtaining amino acid-manganese bioxide composite materials in an inserting layer structure. The composite materials have potential application value in the fields of chiral catalysis, electrochemical catalysis, electrochemical biological sensors, etc.
Description
Technical field
The present invention relates to adopt stripping layer assemble method to prepare a kind of intercalation configuration amino acid-manganese dioxide composite material, belong to composite organic-inorganic material and preparing technical field thereof.
Background technology
Based on the laminate structure precursor, utilize the intercalation package technique that the object species are introduced interlayer and construct the intercalation configuration material, can on molecular level, realize the design of material structure and cut out, give material more powerful advanced function, can be widely used in fields such as catalytic material, energy storage and transition material, sensor sensing material, be the focus of domestic and international advanced function material development.
As the laminate structure precursor, can be cationic lamellar compound, if you would take off soil, bedded zirconium phosphate, also can be the lamellar compound of anionic, as layered di-hydroxyl composite metal oxidate (hydrotalcite) etc.As the intercalation object, can be mineral ion, organic molecule, polymkeric substance and biological functionality material etc.Amino acid is the organic object of a kind of chirality, under certain pH value, can become positively charged ion or negatively charged ion, with the aminoacid insertion inorganic layered compounds, as clay, hydrotalcite, alpha zirconium phosphate etc., providing a chiral environment at interlayer, can be used for chiral catalysis and chiral separation etc., is presoma with the amino acid intercalation material, can also further carry out the intercalation assembling, other species are introduced interlayer.
At document (1) Journal of Molecular Structure, 2003,651-653: in 335, human ion exchange methods such as T.Kollar are inserted into the interlayer of polynite with six seed amino acids such as Padil, L-Beta Alanine, L-tryptophane, L-Histidine, L-methionine(Met) and L-Methionins, and the author thinks that the chiral environment that intercalation configuration provided has potential using value aspect chiral catalysis and the chiral separation.
At document (2) Catalysis Letters, 2004, among the 94:95, people such as Wen-Zhuo Li insert the alpha zirconium phosphate interlayer to L-Methionin earlier, utilize Eu again
3+With the carbonyl coordination of Methionin with Eu
3+Be incorporated in the alpha zirconium phosphate behind the Methionin intercalation, this intercalation material is to propylene oxide and CO
2Copolyreaction have catalytic activity.
At document (3) Journal of Materials Chemistry, 2003, among the 13:834, people such as Roberto Dragone have synthesized the alpha zirconium phosphate of L-Histidine intercalation earlier, the coordination that utilizes iron ion and Histidine again by ion exchange reaction respectively with Fe
2+, Fe
3+Be incorporated into interlayer, this intercalation material is to H
2O
2Oxidation Indigotindisulfonate Sodium organism has catalytic activity, and this solid catalyst can regeneration.
Manganse Dioxide has different crystalline structure (as α, β, δ, γ etc.), has electroconductibility, has been widely used in fields such as catalysis, ion(ic)sieve and electrochemistry.δ-MnO
2Be to form two-dimentional laminate by the manganese oxygen octahedra by being total to the limit, interlayer has metallic cation and the molecular cationic lamellar compound of moisture, and wherein the metallic cation of interlayer can be come out by other cation replacements.If amino acid is introduced interlayer, the fields such as chiral catalysis, electrochemical catalysis and electrochemica biological sensor that are expected at have using value, in addition can be with amino acid intercalation manganese dioxide as precursor, by ion exchange reaction other species are introduced interlayer, make up other novel intercalation configuration materials.But because the intercropping of Manganse Dioxide laminate is firmly stronger, the intercalation of object is difficulty, and the document of amino acid intercalation manganese dioxide does not appear in the newspapers as yet.
Summary of the invention:
The objective of the invention is with cationic laminate structure δ-MnO
2Be main body, basic aminoacids is the intercalation object, and the method for assembling by the stripping layer is incorporated into MnO with basic aminoacids
2Interlayer, make up a kind of novel organic and inorganic intercalation configuration matrix material, this amino acid intercalation manganese dioxide has potential using value in fields such as chiral catalysis, electrochemical catalysis and electrochemica biological sensors, can further other species be entered interlayer with this amino acid intercalation manganese dioxide as reacting precursor in addition.
The chemical constitution general formula of intercalation configuration amino acid-manganese dioxide composite material is:
(A
+)
a(Amino
+)
bMnO
2·mH
2O，
A wherein
+For in inorganic sodium ion, hydrogen ion or the organic cation tetramethyl ammonium a kind of, two kinds or three kinds; Amino is a basic aminoacids; A, b are respectively A
+, Amino
+Quantity and a+b≤0.4; M is crystal water quantity and 0.1＜m＜0.5;
Manganese and oxygen are with covalent bonds in this matrix material, and the manganese oxygen octahedra forms two-dimentional laminate, Amino by being total to the limit
+And A
+Be positioned at interlayer.
Basic aminoacids is a kind of in L-Methionin, L-arginine, the L-Histidine.
This intercalation configuration amino acid-manganese dioxide composite material adopts the method for stripping layer assembling to be prepared.Promptly earlier prepare laminate structure δ-MnO by hydro-thermal reaction
2, utilize Tetramethylammonium hydroxide with its stripping layer again, form electronegative laminate, pass through the electrostatic interaction self-assembly with the amino acid positively charged ion then, thereby obtain intercalation configuration amino acid-manganese dioxide composite material.Concrete processing step is as follows:
A. the preparation of layered manganese oxide: press OH
-With Mn
2+Mol ratio is 3: 1～4: 1, H
2O
2With Mn
2+Mol ratio is 6: 1～8: 1, will contain 0.6～0.8mol/L NaOH and 1.0～1.5mol/L H
2O
2Mixed solution join 0.3～0.4mol/L Mn (NO fast
3)
2Solution in, vigorous stirring reaction 20～30 minutes is filtered, and filter cake is transferred in the polytetrafluoroethylcontainer container, presses OH
-With MnO
2Mol ratio is that to add concentration be the NaOH solution of 2～3mol/L to 2: 1～4: 1 and filling degree≤80%, stir in the pasty state, polytetrafluoroethylcontainer container is sealed in the water heating kettle, 150～160 ℃ of hydrothermal treatment consists 15～20 hours, water heating kettle being naturally cooled to room temperature, open the still suction filtration, is 8～9 with deionized water filter wash cake to filtrate pH value, with filter cake in 70～80 ℃ of air atmospheres dry 6～9 hours, obtain layered manganese oxide.
B. the preparation of hydrogen exchange Manganse Dioxide: according to H
+With the layered manganese oxide mol ratio be 10: 1～15: 1, it is the HNO of 1.0～1.5mol/L that the layered manganese oxide pressed powder of steps A preparation is added concentration
3In the solution, stirring at room reaction 3 days, during changed once new 1.0～1.5mol/L HNO every 24 hours
3Solution; With the mixed solution suction filtration, be 6～7 after reaction finishes,, obtain hydrogen exchange Manganse Dioxide filter cake drying 6～9 hours in 70～80 ℃ of air atmospheres with deionized water wash to filtrate pH value.
C. peeling off of layered manganese oxide: by Tetramethylammonium hydroxide and Manganse Dioxide mol ratio is 2: 1～4: 1, it is in 1.5%～2.0% the tetramethylammonium hydroxide aqueous solution that the hydrogen exchange Manganse Dioxide of step B preparation is joined massfraction, stirring reaction is 7 days under the room temperature, again with mixed solution under the rotating speed of 10000～12000 revolutions per minute centrifugal 10～15 minutes, with filter cake with deionized water repeatedly wash, centrifugation.The product that obtains is shown with XRD spectra that its laminate structure disappears to think stripped MnO 2.
The preparation of D amino acid intercalation manganese dioxide: the stripped MnO 2 filter cake of step C preparation is joined from Yu Shuizhong, being made into Manganse Dioxide content is the stripped MnO 2 colloidal sol of 0.02～0.05mol/L, it in basic aminoacids and Manganse Dioxide mol ratio 0.1～1.0 ratio, with basic aminoacids intercalation object concentration is HCl solution adjusting pH value to 7～8 of 0.1～0.2mol/L, join in the stripped MnO 2 colloidal sol, 40～50 ℃ of following stirring reactions 12～24 hours, filter, with deionized water wash 3～4 times, the amino acid of precipitation surface absorption is cleaned, then 60～70 ℃ of air dryings 12～24 hours.Wherein used basic aminoacids is any one in L-Methionin, L-arginine, the L-Histidine.
The content of sodium and manganese element in employing day island proper Tianjin ICPS-7500 type inductively coupled plasma atomic emission spectrometer mensuration product, Italy's CARLO BRBA 1106 elemental analysers are measured the content of carbon, hydrogen, nitrogen element in the product, and the PCT-1A of Beijing Optical Instrument Factory differential thermal balance is measured the water molecules content of product; Adopt day island proper Tianjin XRD-6000 type x-ray powder diffraction instrument (Cu K
αRadiation, λ=1.5406 ) the sign product structure.Analytical results shows that three kinds of basic aminoacidss such as L-Methionin, L-arginine, L-Histidine all have been inserted into the Manganse Dioxide interlayer.
Effect of the present invention and advantage are: adopt stripping layer assemble method can overcome stratiform δ-MnO
2Reactive force is big between laminate, and unfavorable factors such as intercalation difficulty successfully are inserted into the Manganse Dioxide interlayer with three kinds of basic aminoacidss such as L-Methionin, L-arginine, L-Histidines, synthesize novel amino intercalation manganese dioxide matrix material.
Description of drawings:
Fig. 1. the XRD spectra of different Manganse Dioxide intercalation products
X-coordinate-angle 2 θ, unit are ° (degree);
Ordinate zou-intensity, unit is a.u. (absolute units).
(a)-hydrogen exchange Manganse Dioxide;
(b)-the dried product of stripped MnO 2 (being the tetramethyl ammonium intercalation manganese dioxide);
(c)-L-Methionin intercalation manganese dioxide.
The infrared spectrum of Fig. 2 .L-Methionin and different Manganse Dioxide intercalation products
X-coordinate-wave number, unit is cm
-1
Ordinate zou-transmittance, unit are a.u. (absolute units).
(a)-L-Methionin;
(b)-hydrogen exchange Manganse Dioxide;
(c)-the tetramethyl ammonium intercalation manganese dioxide;
(d)-L-Methionin intercalation manganese dioxide.
The XRD spectra of the different molar ratio intercalation of Fig. 3 .L-Methionin product with Manganse Dioxide.
X-coordinate-angle 2 θ, unit are ° (degree);
Ordinate zou-intensity, unit is a.u. (absolute units).
(a)-L-Methionin and Manganse Dioxide molar ratio are 1: 1;
(b)-L-Methionin and Manganse Dioxide molar ratio are 0.5: 1;
(c)-L-Methionin and Manganse Dioxide molar ratio are 0.2: 1;
(d)-L-Methionin and Manganse Dioxide molar ratio are 0.1: 1.
Embodiment:
Embodiment 1:
200mL is contained 0.6mol/L NaOH and 1.5mol/L H
2O
2Mixed solution be added to 100mL fast and contain 0.4mol/L Mn (NO
3)
2Solution in, vigorous stirring reaction 30 minutes is filtered, and filter cake is transferred in the 100mL tetrafluoroethylene cup, adding 40mL concentration is the NaOH solution of 2mol/L, stirs in the pasty state, the tetrafluoroethylene cup is sealed in the water heating kettle, 160 ℃ of hydrothermal treatment consists 15 hours.Treating that water heating kettle naturally cools to room temperature, open the still suction filtration, is 8 with deionized water filter wash cake to filtrate pH value.With filter cake in 70 ℃ of air atmospheres dry 9 hours, obtain layered manganese oxide.
Take by weighing 2.5g layered manganese oxide pressed powder and join the HNO that 300mL concentration is 1.0mol/L
3In the solution, once new 1.0mol/L HNO was changed in stirring at room reaction 3 days therebetween every 24 hours
3Solution.With the mixed solution suction filtration, be 6 with deionized water wash to filtrate pH value, with filter cake in 70 ℃ of air atmospheres dry 9 hours, obtain hydrogen exchange Manganse Dioxide.
Measure the 12mL massfraction and be 25% Tetramethylammonium hydroxide, be dissolved in the 200mL deionized water, take by weighing the hydrogen exchange Manganse Dioxide of 1.4g and be dispersed in the above-mentioned tetramethylammonium hydroxide aqueous solution, stirring reaction is 7 days under the room temperature.With mixed solution under the rotating speed of 12000 revolutions per minute centrifugal 10 minutes, go from four washings of moisture, centrifugation with 400mL.XRD spectra shows that laminate structure disappears and can think and obtained stripped MnO 2.
Get stripped MnO 2 and join in the deionized water, being made into Manganse Dioxide content is the stripped MnO 2 colloidal sol 100mL of 0.05mol/L; Other takes by weighing 0.73g L-Methionin and is dissolved in the 50mL deionized water, regulates pH value to 8 with the hydrochloric acid soln of 0.1mol/L, presses L-Methionin and MnO
2Mol ratio be 1: 1 above-mentioned two kinds of solution are mixed, 40 ℃ of stirring reactions 24 hours filter, with deionized water wash 3～4 times, the L-Methionin of precipitation surface absorption is cleaned up, 70 ℃ of air dryings 12 hours, obtain L-Methionin intercalation manganese dioxide product then.
The content of sodium and manganese element in employing day island proper Tianjin ICPS-7500 type inductively coupled plasma atomic emission spectrometer mensuration product, Italy's CARLO BRBA 1106 elemental analysers are measured the content of carbon, hydrogen, nitrogen element in the product, the PCT-1A of Beijing Optical Instrument Factory differential thermal balance is measured the water in products molecule content, determines that the chemical constitution of L-Methionin intercalation manganese dioxide product is: Na
0.044H
0.012(C
4H
12N)
0.060(C
6H
15N
2O
2)
0.170MnO
20.32H
2O.L-Methionin intercalation manganese dioxide product is carried out X-ray powder diffraction characterize, the results are shown in Figure 1, product has reasonable laminate structure, d as shown in Figure 1
001Be 1.23nm, the interlamellar spacing expansion than hydrogen exchange Manganse Dioxide and tetramethyl ammonium intercalation manganese dioxide illustrates that L-Methionin successfully is inserted into the Manganse Dioxide interlayer.L-Methionin intercalation manganese dioxide product is carried out IR characterize, the results are shown in Figure 2, L-Methionin can come out Tetramethylammonium hydroxide ion-exchange by ion exchange reaction as seen from Figure 2.
Embodiment 2:
200mL is contained 0.8mol/L NaOH and 1.2mol/L H
2O
2Mixed solution be added to 100mL fast and contain 0.4mol/L Mn (NO
3)
2Solution in, vigorous stirring reaction 20 minutes is filtered, and filter cake is transferred in the 100mL tetrafluoroethylene cup, adding 50mL concentration is the NaOH solution of 3mol/L, stirs in the pasty state, the tetrafluoroethylene cup is sealed in the water heating kettle, 150 ℃ of hydrothermal treatment consists 20 hours.Treating that water heating kettle naturally cools to room temperature, open the still suction filtration, is 9 with deionized water filter wash cake to filtrate pH value.With filter cake in 80 ℃ of air atmospheres dry 6 hours, obtain layered manganese oxide.
Take by weighing 2.5g layered manganese oxide pressed powder and join the HNO that 280mL concentration is 1.5mol/L
3In the solution, once new 1.5mol/L HNO was changed in stirring at room reaction 3 days therebetween every 24 hours
3Solution.With the mixed solution suction filtration, be 7 with deionized water wash to filtrate pH value, with filter cake in 80 ℃ of air atmospheres dry 6 hours, obtain hydrogen exchange Manganse Dioxide.
Measure the 18mL massfraction and be 25% Tetramethylammonium hydroxide, be dissolved in the 200mL deionized water, take by weighing the hydrogen exchange Manganse Dioxide of 1.1g and be dispersed in the above-mentioned tetramethylammonium hydroxide aqueous solution, stirring reaction is 7 days under the room temperature.With mixed solution under the rotating speed of 10000 revolutions per minute centrifugal 15 minutes, with four washings of 400mL deionization moisture, centrifugation, XRD spectra showed that laminate structure disappears and can think and obtained stripped MnO 2.
Get stripped MnO 2 and join in the deionized water, being made into Manganse Dioxide content is the stripped MnO 2 colloidal sol 100mL of 0.04mol/L; Other takes by weighing 0.29g L-Methionin and is dissolved in the 50mL deionized water, is the hydrochloric acid soln adjusting pH value to 7 of 0.1mol/L with concentration, presses L-Methionin and MnO
2Mol ratio be 0.5: 1 two kinds of solution are mixed, 50 ℃ of stirring reactions 12 hours filter, and with deionized water wash 3～4 times, the L-Methionin of precipitation surface absorption are cleaned up, then 60 ℃ of air dryings 24 hours.
The method of employing embodiment 1 is analyzed product, obtains its chemical constitution and is: Na
0.048H
0.011(C
4H
12N)
0.069(C
6H
15N
2O
2)
0.090MnO
20.27H
2O, X-ray powder diffraction analytical results see Fig. 3 (b), d
001Be 1.17nm, illustrate that L-Methionin successfully is inserted into the Manganse Dioxide interlayer.
Embodiment 3:
Manganse Dioxide stripping layer method is with embodiment 1.
Get stripped MnO 2 and join in the deionized water, being made into Manganse Dioxide content is the stripped MnO 2 colloidal sol 100mL of 0.04mol/L; Other takes by weighing 0.12g L-Methionin and is dissolved in the 50mL deionized water, is the hydrochloric acid soln adjusting pH value to 8 of 0.1mol/L with concentration, presses L-Methionin and MnO
2Mol ratio be 0.2: 1 two kinds of solution are mixed, 40 ℃ of stirring reactions 24 hours filter, and with deionized water wash 3～4 times, the L-Methionin of precipitation surface absorption are cleaned up, then 70 ℃ of air dryings 12 hours.
The method of employing embodiment 1 is analyzed product, obtains its chemical constitution and is: Na
0.043H
0.067(C
4H
12N)
0.070(C
6H
15N
2O
2)
0.050MnO
20.38H
2O, X-ray powder diffraction analytical results see Fig. 3 (c), d
001Be 0.89nm, illustrate that L-Methionin successfully is inserted into the Manganse Dioxide interlayer.
Embodiment 4:
Manganse Dioxide stripping layer method is with embodiment 2.
Get stripped MnO 2 and join in the deionized water, being made into Manganse Dioxide content is the stripped MnO 2 colloidal sol 200mL of 0.02mol/L; Other takes by weighing 0.06g L-Methionin and is dissolved in the 50mL deionized water, is the hydrochloric acid soln adjusting pH value to 8 of 0.1mol/L with concentration, presses L-Methionin and MnO
2Mol ratio be 0.1: 1 two kinds of solution are mixed, 40 ℃ of stirring reactions 24 hours filter, and with deionized water wash 3～4 times, the L-Methionin of precipitation surface absorption are cleaned up, then 70 ℃ of air dryings 12 hours.
The method of employing embodiment 1 is analyzed product, obtains its chemical constitution and is: Na
0.046H
0.081(C
4H
12N)
0.068(C
6H
15N
2O
2)
0.042MnO
20.31H
2O, X-ray powder diffraction analytical results see Fig. 3 (d), d
001Be 0.81nm, illustrate that L-Methionin successfully is inserted into the Manganse Dioxide interlayer.
Embodiment 5:
Manganse Dioxide stripping layer method is with embodiment 1.
Get stripped MnO 2 and join in the deionized water, being made into Manganse Dioxide content is the stripped MnO 2 colloidal sol 200mL of 0.02mol/L; Other takes by weighing 0.70g L-arginine and is dissolved in the 50mL deionized water, is the hydrochloric acid soln adjusting pH value to 8 of 0.1mol/L with concentration, presses L-arginine and MnO
2Mol ratio be 1: 1 two kinds of solution are mixed, 40 ℃ of stirring reactions 24 hours filter, and with deionized water wash 3～4 times, the L-arginine of precipitation surface absorption are cleaned up, then 70 ℃ of air dryings 12 hours.
The method of employing embodiment 1 is analyzed product, obtains its chemical constitution and is: Na
0.046H
0.012(C
4H
12N)
0.066(C
6H
15N
4O
2)
0.160MnO
20.27H
2O, the X-ray powder diffraction analytical results shows d
001Be 1.26nm, illustrate that the L-arginine successfully is inserted into the Manganse Dioxide interlayer.
Embodiment 6:
Manganse Dioxide stripping layer method is with embodiment 2.
Get stripped MnO 2 and join in the deionized water, being made into Manganse Dioxide content is the stripped MnO 2 colloidal sol 100mL of 0.05mol/L; Other takes by weighing 0.78g L-Histidine and is dissolved in the 50mL deionized water, is the hydrochloric acid soln adjusting pH value to 7 of 0.1mol/L with concentration, presses L-Histidine and MnO
2Mol ratio be 1: 1 two kinds of solution are mixed, 50 ℃ of stirring reactions 12 hours filter, and with deionized water wash 3～4 times, the L-Histidine of precipitation surface absorption are cleaned up, then 70 ℃ of air dryings 12 hours.
The method of employing embodiment 1 is analyzed product, obtains its chemical constitution and is: Na
0.045H
0.010(C
4H
12N)
0.068(C
6H
10N
3O
2)
0.150MnO
20.27H
2O, the X-ray powder diffraction analytical results shows d
001Be 1.45nm, illustrate that the L-Histidine successfully is inserted into the Manganse Dioxide interlayer.
Claims (2)
1. amino acid intercalation manganese dioxide, its chemical constitution general formula is:
(A
+)
a(Amino
+)
bMnO
2·mH
2O，
A wherein
+Be sodium ion, hydrogen ion and three kinds of ionic combinations of tetramethyl ammonium; Amino is a kind of in L-Methionin, L-arginine, the L-Histidine; A, b are respectively A
+, Amino
+Quantity and a+b≤0.4; M is crystal water quantity and 0.1＜m＜0.5;
Manganese and oxygen are with covalent bonds in this matrix material, and the manganese oxygen octahedra forms two-dimentional laminate, Amino by being total to the limit
+And A
+Be positioned at interlayer.
2. the preparation method of an amino acid intercalation manganese dioxide, concrete processing step is as follows:
A. the preparation of layered manganese oxide: press OH
-With Mn
2+Mol ratio is 3: 1～4: 1, H
2O
2With Mn
2+Mol ratio is 6: 1～8: 1, will contain 0.6～0.8mol/L NaOH and 1.0～1.5mol/L H
2O
2Mixed solution join 0.3～0.4mol/L Mn (NO fast
3)
2Solution in, vigorous stirring reaction 20～30 minutes is filtered, and filter cake is transferred in the polytetrafluoroethylcontainer container, presses OH
-With MnO
2Mol ratio is that to add concentration be the NaOH solution of 2～3mol/L to 2: 1～4: 1 and filling degree≤80%, stir in the pasty state, polytetrafluoroethylcontainer container is sealed in the water heating kettle, 150～160 ℃ of hydrothermal treatment consists 15～20 hours, water heating kettle being naturally cooled to room temperature, open the still suction filtration, is 8～9 with deionized water filter wash cake to filtrate pH value, with filter cake in 70～80 ℃ of air atmospheres dry 6～9 hours, obtain layered manganese oxide;
B. the preparation of hydrogen exchange Manganse Dioxide: according to H
+With the layered manganese oxide mol ratio be 10: 1～15: 1, it is the HNO of 1.0～1.5mol/L that the layered manganese oxide pressed powder of steps A preparation is added concentration
3In the solution, stirring at room reaction 3 days, during changed once new 1.0～1.5mol/L HNO every 24 hours
3Solution; With the mixed solution suction filtration, be 6～7 after reaction finishes,, obtain hydrogen exchange Manganse Dioxide filter cake drying 6～9 hours in 70～80 ℃ of air atmospheres with deionized water wash to filtrate pH value;
C. peeling off of layered manganese oxide: by Tetramethylammonium hydroxide and Manganse Dioxide mol ratio is 2: 1～4: 1, it is in 1.5%～2.0% the tetramethylammonium hydroxide aqueous solution that the hydrogen exchange Manganse Dioxide of step B preparation is joined massfraction, stirring reaction is 7 days under the room temperature, again with mixed solution under the rotating speed of 10000～12000 revolutions per minute centrifugal 10～15 minutes, with filter cake with deionized water repeatedly wash, centrifugation, obtain stripped MnO 2;
D. the preparation of amino acid intercalation manganese dioxide: the stripped MnO 2 of step C preparation is joined in the deionized water, being made into Manganse Dioxide content is the stripped MnO 2 colloidal sol of 0.02～0.05mol/L, it in basic aminoacids and Manganse Dioxide mol ratio 0.1～1.0 ratio, with amino acid intercalation object concentration is HCl solution adjusting pH value to 7～8 of 0.1～0.2mol/L, join in the stripped MnO 2 colloidal sol, 40～50 ℃ of following stirring reactions 12～24 hours, filter, with deionized water wash 3～4 times, the amino acid of precipitation surface absorption is cleaned, then 60～70 ℃ of air dryings 12～24 hours; Described amino acid is any one in L-Methionin, L-arginine, the L-Histidine.
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| CN102306554B (en) * | 2011-07-06 | 2013-07-24 | 北京化工大学 | Polyphenylene sulfide intercalated manganese dioxide and preparation method thereof as well as application of using polyphenylene sulfide intercalated manganese dioxide as electrode material |
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| CN103065806B (en) * | 2013-01-31 | 2015-07-22 | 武汉理工大学 | Sodion-embedded manganese dioxide nanometer sheet electrode as well as preparation method and application of electrode |
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| CN113788499B (en) * | 2021-09-22 | 2022-05-24 | 江南大学 | Chiral manganese oxide nano particle and preparation method and application thereof |
| CN115318277A (en) * | 2022-08-16 | 2022-11-11 | 中国计量大学 | Ion exchange stripping manganese dioxide method for formaldehyde degradation catalyst |
| CN115594223A (en) * | 2022-10-25 | 2023-01-13 | 广东邦普循环科技有限公司（Cn） | Modified lithium ion sieve, manganese dioxide adsorbent, preparation method and application of manganese dioxide adsorbent, and method for extracting lithium from salt lake |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6214493B1 (en) * | 1996-01-15 | 2001-04-10 | The University Court Of The University Of St. Andrews | Manganese oxide based material for an electrochemical cell |
| CN1654541A (en) * | 2005-01-27 | 2005-08-17 | 同济大学 | Process for in-situ polymerization preparation of poly-lactic acid/montmorillonite nano composite materials |
-
2005
- 2005-12-19 CN CNB2005101347180A patent/CN100354203C/en not_active Expired - Fee Related
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6214493B1 (en) * | 1996-01-15 | 2001-04-10 | The University Court Of The University Of St. Andrews | Manganese oxide based material for an electrochemical cell |
| CN1654541A (en) * | 2005-01-27 | 2005-08-17 | 同济大学 | Process for in-situ polymerization preparation of poly-lactic acid/montmorillonite nano composite materials |
Non-Patent Citations (2)
| Title |
|---|
| Eu3+ and lysine co-intercalated α-zirconium phosphate andits catalytic activity for copolymerization of propylene oxideand CO2.Wen.Zhuo Li,et al.Catalysis Letters,Vol.94 No.1.2. 2004 * |
| Intercalating amino acid guests into montmorillonite host T.Kollar,et al.Journal of Molecular Structure,No.651.653. 2003 * |
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