[go: up one dir, main page]

CN102604440A - White carbon black composite powder material and preparation method thereof - Google Patents

White carbon black composite powder material and preparation method thereof Download PDF

Info

Publication number
CN102604440A
CN102604440A CN2012100394377A CN201210039437A CN102604440A CN 102604440 A CN102604440 A CN 102604440A CN 2012100394377 A CN2012100394377 A CN 2012100394377A CN 201210039437 A CN201210039437 A CN 201210039437A CN 102604440 A CN102604440 A CN 102604440A
Authority
CN
China
Prior art keywords
carbon black
white carbon
composite powder
powder material
hexylcarbazole
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
CN2012100394377A
Other languages
Chinese (zh)
Other versions
CN102604440B (en
Inventor
汪徐春
张雪梅
宋常春
李小超
程年寿
王军锋
张平
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Anhui University of Science and Technology
Original Assignee
Anhui University of Science and Technology
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Anhui University of Science and Technology filed Critical Anhui University of Science and Technology
Priority to CN 201210039437 priority Critical patent/CN102604440B/en
Publication of CN102604440A publication Critical patent/CN102604440A/en
Application granted granted Critical
Publication of CN102604440B publication Critical patent/CN102604440B/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Landscapes

  • Carbon And Carbon Compounds (AREA)
  • Artificial Filaments (AREA)
  • Cosmetics (AREA)
  • Pigments, Carbon Blacks, Or Wood Stains (AREA)

Abstract

本发明涉及一种白炭黑复合粉体材料,所述的白炭黑复合粉体材料在220-400nm范围内对紫外可见光谱有较强吸收,可以做很好的紫外线吸收材料;白炭黑复合粉体材料的具有优良的光学性能,并且能够发射很纯的红色荧光,可以作为很好的荧光或红光基料。因此,对于开发具有光学功能的材料有着特殊的意义,在光电功能材料方面具有潜在应用价值。所述的白炭黑复合粉体材料的制备方法是利用己基咔唑甲醛氧化制得己基咔唑甲酸,然后将己基咔唑甲酸与活化的白炭黑合成白炭黑复合粉体材料,此制备方法简单,适合工业化生产,有很好的应用前景。

The invention relates to a white carbon black composite powder material, the white carbon black composite powder material has a strong absorption of ultraviolet-visible spectrum in the range of 220-400nm, and can be used as a good ultraviolet absorbing material; white carbon black The composite powder material has excellent optical properties and can emit very pure red fluorescence, which can be used as a good fluorescent or red light base material. Therefore, it has special significance for the development of materials with optical functions, and has potential application value in optoelectronic functional materials. The preparation method of the white carbon black composite powder material is to utilize hexylcarbazole formaldehyde to oxidize hexylcarbazole formic acid, and then synthesize the white carbon black composite powder material with hexylcarbazole formic acid and activated white carbon black. The method is simple, suitable for industrial production, and has good application prospects.

Description

白炭黑复合粉体材料及其制备方法White carbon black composite powder material and preparation method thereof

技术领域 technical field

本发明涉及一种白炭黑复合粉体材料及其制备方法。 The invention relates to a white carbon black composite powder material and a preparation method thereof.

背景技术 Background technique

白炭黑能溶于苛性碱和氢氟酸。耐高温、不燃、无味、无嗅、具有很好的电绝缘性。 Silica is soluble in caustic and hydrofluoric acid. High temperature resistance, non-combustible, tasteless, odorless, with good electrical insulation.

由于白炭黑产品的一系列优越性,使它能够广泛应用于许多领域如橡胶制品、农业化学制品、日用化工制品、胶结剂、抗结块剂、造纸填料等,此外还可用在消防剂、饲料、化妆品、消光剂、颜料、油漆等许多行业。 Due to a series of advantages of silica products, it can be widely used in many fields such as rubber products, agricultural chemicals, daily chemical products, cementing agents, anti-caking agents, paper fillers, etc., and can also be used in fire-fighting agents , feed, cosmetics, matting agents, pigments, paints and many other industries.

但是,由于白炭黑属于不吸收紫外线的物质,且白炭黑经激发波长为 350±5 nm光照射时,在400-700 nm范围内几乎不发荧光,因此,白炭黑不能作为紫外线吸收物质,也不能作为荧光或红光基料,限制了白炭黑的应用。 However, since silica is a substance that does not absorb ultraviolet rays, and when silica is irradiated by light with an excitation wavelength of 350±5 nm, it hardly fluoresces in the range of 400-700 nm. Therefore, silica cannot be used as an ultraviolet absorber. Matter, nor can it be used as a fluorescent or red light base material, which limits the application of silica.

发明内容 Contents of the invention

本发明所要解决的技术问题是提供一种白炭黑复合粉体材料,该白炭黑复合粉体材料能够吸收紫外线,且能够作为荧光或红光基料;本发明所要解决的另一个技术问题是提供所述白炭黑复合粉体材料的制备方法。 The technical problem to be solved by the present invention is to provide a white carbon black composite powder material, which can absorb ultraviolet rays and can be used as a fluorescent or red light base material; another technical problem to be solved by the present invention The invention provides a preparation method of the white carbon black composite powder material.

为解决上述技术问题,本发明提供了一种白炭黑复合粉体材料,其制备方法包括以下步骤: In order to solve the above-mentioned technical problems, the invention provides a kind of white carbon black composite powder material, and its preparation method comprises the following steps:

(1)将1.2±0.3 g己基咔唑甲醛和2.8±0.3 g重铬酸钾混合得混合物,加水和二氯甲烷将混合物溶解得混合液,在搅拌状态下向混合液中加入30±5 mL的水和H2SO4,水与H2SO4的体积比为1:1,然后在 80℃条件下进行加热回流 1±0.5 小时,回流液在室温下冷却,加入水20±5 mL,用二氯甲烷萃取分离、浓缩得粗品,再用10% NaOH和二氯甲烷的混合液对粗品进行重结晶,得己基咔唑甲酸; (1) Mix 1.2±0.3 g hexylcarbazole formaldehyde and 2.8±0.3 g potassium dichromate to obtain a mixture, add water and dichloromethane to dissolve the mixture to obtain a mixture, add 30±5 mL to the mixture under stirring water and H 2 SO 4 , the volume ratio of water to H 2 SO 4 is 1:1, then heat and reflux at 80°C for 1±0.5 hours, cool the reflux at room temperature, add 20±5 mL of water, Extraction, separation and concentration with dichloromethane to obtain a crude product, and then recrystallization of the crude product with a mixture of 10% NaOH and dichloromethane to obtain hexylcarbazole formic acid;

(2)将0.10±0.03g氢氧化钠和0.10±0.03 g白炭黑混合搅匀,在200±50℃条件下加热2±0.5 小时,得活化的白炭黑; (2) Mix and stir 0.10±0.03g sodium hydroxide and 0.10±0.03g white carbon black, and heat at 200±50°C for 2±0.5 hours to obtain activated white carbon black;

(3)取50±5 mL无水乙醇在80±5 ℃条件下预热3-6分钟后,将步骤(2)得到的活化的白炭黑与1.40±0.05 g己基咔唑甲酸加入到预热好的无水乙醇中搅拌均匀,保持搅拌状态加热回流48±12小时后,冷却过滤,即得白炭黑复合粉体材料粗品,再用无水乙醇洗涤三次,得白炭黑复合粉体材料。 (3) After preheating 50±5 mL of absolute ethanol at 80±5°C for 3-6 minutes, add the activated silica obtained in step (2) and 1.40±0.05 g of hexylcarbazole formic acid to the preheated Stir evenly in the heated absolute ethanol, keep the stirring state, heat and reflux for 48±12 hours, then cool and filter to obtain the crude white carbon black composite powder material, and then wash three times with absolute ethanol to obtain the white carbon black composite powder Material.

下面对本发明所述白炭黑复合粉体材料的相关特性进行分析研究。 The relevant characteristics of the white carbon black composite powder material of the present invention are analyzed and studied below.

1、紫外可见光谱吸收试验 1. Ultraviolet visible spectrum absorption test

称取一定量的己基咔唑甲醛、己基咔唑甲酸、白炭黑、白炭黑复合粉体材料,分别用无水乙醇分别配成50 mL溶液,浓度均为1.0×10-5 mol/L,然后用紫外可见分光光度计测量,研究它们的紫外可见光谱性质。 Weigh a certain amount of hexylcarbazole formaldehyde, hexylcarbazole formic acid, white carbon black, and white carbon black composite powder materials, and make 50 mL solutions with absolute ethanol respectively, with a concentration of 1.0×10 -5 mol/L , and then measured with a UV-visible spectrophotometer to study their UV-visible spectral properties.

上述四种物质的紫外光谱图对比结果见附图1。 See accompanying drawing 1 for the comparison result of the ultraviolet spectrograms of the above four substances.

附图1中的横坐标为波长(nm)、纵坐标为吸光度(相对强度);其中的醛为己基咔唑甲醛、酸为己基咔唑甲酸、复合材料为本发明所述的白炭黑复合粉体材料。 The abscissa in accompanying drawing 1 is wavelength (nm), and ordinate is absorbance (relative intensity); Wherein aldehyde is hexylcarbazole formaldehyde, acid is hexylcarbazole formic acid, composite material is white carbon black composite of the present invention Powder material.

从附图1可以看出: It can be seen from Figure 1 that:

白炭黑对紫外可见光谱几乎不吸收; Silica hardly absorbs the ultraviolet-visible spectrum;

己基咔唑甲醛和己基咔唑甲酸在 220-350 nm有吸收,在235±2 nm、275±2 nm、290±2 nm和345±2 nm处有吸收峰; Hexylcarbazole formaldehyde and hexylcarbazole formic acid have absorption at 220-350 nm, with absorption peaks at 235±2 nm, 275±2 nm, 290±2 nm and 345±2 nm;

白炭黑复合粉体材料在 220-400 nm均有较强吸收,相对于己基咔唑甲酸向长波方向移动,在 235±2 nm的吸收峰红移至 242±2 nm处;白炭黑复合粉体材料在275±2 nm、290±2 nm和345±2 nm处相对于己基咔唑甲酸也发生了红移,大约红移5-10 nm。 The silica composite powder material has a strong absorption at 220-400 nm, which shifts to the long-wave direction relative to hexylcarbazole formic acid, and the absorption peak at 235±2 nm red shifts to 242±2 nm; The powder material also has a red shift at 275±2 nm, 290±2 nm and 345±2 nm relative to hexylcarbazole formic acid, about 5-10 nm in red shift.

由于白炭黑的纳米效应与己基咔唑甲酸的配位效应,使得白炭黑复合粉体材料的前沿分子轨道之间的能级差降低,电子受激发跃迁时需要的能量降低,因而复合粉体材料的紫外吸收相对于己基咔唑甲酸发生了红移。 Due to the nano effect of silica and the coordination effect of hexylcarbazole carboxylic acid, the energy level difference between the front molecular orbitals of the silica composite powder material is reduced, and the energy required for the excited transition of electrons is reduced, so the composite powder The UV absorption of the material is red-shifted relative to hexylcarbazole carboxylic acid.

紫外可见光谱吸收试验表明:利用本发明所述的白炭黑复合粉体材料的制备方法,将原本不吸收紫外线的白炭黑变成了可吸收紫外线的有机无机复合粉体材料。 The ultraviolet-visible spectrum absorption test shows that: by using the preparation method of the white carbon black composite powder material of the present invention, the white carbon black that does not absorb ultraviolet rays is transformed into an organic-inorganic composite powder material that can absorb ultraviolet rays.

2、白炭黑、己基咔唑甲酸和白炭黑复合粉体材料的荧光测试结果 2. Fluorescence test results of white carbon black, hexylcarbazole formic acid and white carbon black composite powder materials

己基咔唑甲酸和白炭黑复合粉体材料的荧光测试结果分别见附图2和附图3。 The fluorescence test results of hexylcarbazole carboxylic acid and white carbon black composite powder materials are shown in Figure 2 and Figure 3 respectively.

附图2和附图3中的横坐标为波长(nm)、纵坐标为荧光强度(相对强度);附图2中的咔唑甲酸1为己基咔唑甲酸,附图3中的复合材料EM1为本发明所述的白炭黑复合粉体材料。 The abscissa in accompanying drawings 2 and 3 is the wavelength (nm), and the ordinate is the fluorescence intensity (relative intensity); the carbazole formic acid 1 in the accompanying drawing 2 is hexylcarbazole formic acid, and the composite material EM1 in the accompanying drawing 3 It is the white carbon black composite powder material described in the present invention.

荧光测试结果表明: Fluorescent test results showed:

白炭黑经激发波长为 350±5 nm光照射时,在400-700 nm范围内几乎不发荧光(无附图表示); When white carbon black is irradiated by light with an excitation wavelength of 350±5 nm, it hardly fluoresces in the range of 400-700 nm (not shown in the figure);

己基咔唑甲酸经激发波长为 350±5 nm光照射时,在400-600 nm范围内发较强的荧光; When hexylcarbazole carboxylic acid is irradiated by light with an excitation wavelength of 350±5 nm, it emits strong fluorescence in the range of 400-600 nm;

白炭黑复合粉体材料经激发波长为 350±5 nm光照射时,在400-580 nm范围内有较强的荧光,而且在695±2 nm处有一个较强的红色荧光峰,这主要是白炭黑的纳米效应、配位效应和硅羟基作用等,使得白炭黑复合粉体材料的前沿分子轨道之间的能级差有部分降低,部分高能π电子回迁时需要的能量降低,因而白炭黑复合粉体材料相对于己基咔唑甲酸在长波方向695±2 nm处多出一个明显的红色荧光峰。 When the white carbon black composite powder material is irradiated by light with an excitation wavelength of 350±5 nm, it has strong fluorescence in the range of 400-580 nm, and there is a strong red fluorescence peak at 695±2 nm, which is mainly It is the nano-effect, coordination effect and silanol effect of silica, which partially reduces the energy level difference between the front molecular orbitals of the silica composite powder material, and reduces the energy required for some high-energy π electrons to move back. Therefore, Compared with hexylcarbazole formic acid, silica composite powder has an obvious red fluorescence peak at 695±2 nm in the long-wave direction.

荧光测试表明此白炭黑复合粉体材料具有优良的光学性能,并且在346±5 nm的激光激发下能够发射很纯的红色荧光(685-710 nm范围),本发明所述的白炭黑复合粉体材料可以作为很好的发荧光或红光基料。 Fluorescence test shows that this white carbon black composite powder material has excellent optical properties, and can emit very pure red fluorescence (685-710 nm range) under the laser excitation of 346 ± 5 nm, white carbon black of the present invention Composite powder material can be used as a good fluorescent or red light base material.

综上所述,本发明所述的白炭黑复合粉体材料在 220-400 nm 范围内对紫外可见光谱有较强吸收,相对于己基咔唑甲酸来说向长波方向移动,可以做很好的紫外线吸收材料;白炭黑复合粉体材料具有优良的光学性能,并且能够发射很纯的红色荧光,可以作为很好的荧光或红光基料。因此,对于开发具有光学功能的材料有着特殊的意义,在光电功能材料方面具有潜在应用价值。 In summary, the white carbon black composite powder material of the present invention has a strong absorption in the ultraviolet-visible spectrum in the range of 220-400 nm, and it can move to the long-wave direction compared with hexylcarbazole formic acid, which can be done very well. Ultraviolet absorbing material; white carbon black composite powder material has excellent optical properties, and can emit very pure red fluorescence, which can be used as a good fluorescent or red light base material. Therefore, it has special significance for the development of materials with optical functions, and has potential application value in optoelectronic functional materials.

本发明所述的白炭黑复合粉体材料的制备方法是利用己基咔唑甲醛氧化制得己基咔唑甲酸,然后将己基咔唑甲酸与活化的白炭黑合成白炭黑复合粉体材料,此制备方法简单,适合工业化生产,有很好的应用前景。 The preparation method of the white carbon black composite powder material of the present invention is to utilize hexylcarbazole formaldehyde oxidation to obtain hexylcarbazole formic acid, then synthesize white carbon black composite powder material with hexylcarbazole formic acid and activated white carbon black, The preparation method is simple, suitable for industrial production, and has good application prospects.

附图说明 Description of drawings

图1:四种物质的紫外可见光谱吸收试验结果。 Figure 1: The results of UV-Vis absorption tests of four substances.

图2:激发波长为350 nm的己基咔唑甲酸的荧光光谱。 Figure 2: Fluorescence spectrum of hexylcarbazole formic acid with an excitation wavelength of 350 nm.

图3:激发波长为346 nm的白炭黑复合粉体材料的荧光光谱。 Figure 3: The fluorescence spectrum of the silica composite powder material with an excitation wavelength of 346 nm.

具体实施方式 Detailed ways

实施例1: Example 1:

白炭黑复合粉体材料,其制备方法包括以下步骤: White carbon black composite powder material, its preparation method comprises the following steps:

(1)将1.2 g己基咔唑甲醛和2.8 g重铬酸钾混合得混合物,加水和二氯甲烷将混合物溶解得混合液,在搅拌状态下向混合液中加入30 mL的水和H2SO4,水与H2SO4的体积比为1:1,然后在 80℃条件下进行加热回流60分钟,回流液在室温下冷却,加入水20 mL,用二氯甲烷萃取分离、浓缩得粗品,再用10% NaOH和二氯甲烷的混合液对粗品进行重结晶,得己基咔唑甲酸; (1) Mix 1.2 g of hexylcarbazole formaldehyde and 2.8 g of potassium dichromate to obtain a mixture, add water and dichloromethane to dissolve the mixture to obtain a mixture, add 30 mL of water and H 2 SO to the mixture under stirring 4. The volume ratio of water and H 2 SO 4 is 1:1, and then heated and refluxed at 80°C for 60 minutes, the reflux solution is cooled at room temperature, 20 mL of water is added, extracted and separated with dichloromethane, and concentrated to obtain a crude product , then recrystallize the crude product with a mixed solution of 10% NaOH and dichloromethane to obtain hexylcarbazole formic acid;

(2)将0.1 g氢氧化钠和0.1 g白炭黑混合搅匀,在200℃条件下加热120分钟,得活化的白炭黑; (2) Mix and stir 0.1 g sodium hydroxide and 0.1 g white carbon black, and heat at 200°C for 120 minutes to obtain activated white carbon black;

(3)将50 mL无水乙醇在80 ℃条件下预热5分钟后,将步骤(2)得到的活化的白炭黑与1.40 g己基咔唑甲酸加入到预热好的无水乙醇中搅拌均匀,保持搅拌状态加热回流48小时后,冷却过滤,即得白炭黑复合粉体材料粗品,用无水乙醇洗涤三次,得本发明所述的白炭黑复合粉体材料。 (3) After preheating 50 mL of absolute ethanol at 80 °C for 5 minutes, add the activated silica obtained in step (2) and 1.40 g of hexylcarbazole formic acid into the preheated absolute ethanol and stir After heating and refluxing for 48 hours in a stirring state, cool and filter to obtain the crude white carbon black composite powder material, wash with absolute ethanol three times, and obtain the white carbon black composite powder material of the present invention.

实施例2: Example 2:

白炭黑复合粉体材料,其制备方法包括以下步骤: White carbon black composite powder material, its preparation method comprises the following steps:

(1)将0.9 g己基咔唑甲醛和2.5 g重铬酸钾混合得混合物,加水和二氯甲烷将混合物溶解得混合液,在搅拌状态下向混合液中加入25 mL的水和H2SO4,水与H2SO4的体积比为1:1,然后在 80℃条件下进行加热回流30分钟,回流液在室温下冷却,加入水15 mL,用二氯甲烷萃取分离、浓缩得粗品,再用10% NaOH和二氯甲烷的混合液对粗品进行重结晶,得己基咔唑甲酸; (1) Mix 0.9 g hexylcarbazole formaldehyde and 2.5 g potassium dichromate to obtain a mixture, add water and dichloromethane to dissolve the mixture to obtain a mixture, add 25 mL of water and H 2 SO to the mixture under stirring 4. The volume ratio of water to H 2 SO 4 is 1:1, and then heated and refluxed at 80°C for 30 minutes, the reflux solution is cooled at room temperature, 15 mL of water is added, extracted and separated with dichloromethane, and concentrated to obtain a crude product , then recrystallize the crude product with a mixed solution of 10% NaOH and dichloromethane to obtain hexylcarbazole formic acid;

(2)将0.07 g氢氧化钠和0.07 g白炭黑混合搅匀,在150℃条件下加热150分钟,得活化的白炭黑; (2) Mix and stir 0.07 g sodium hydroxide and 0.07 g white carbon black, and heat at 150°C for 150 minutes to obtain activated white carbon black;

(3)将45 mL无水乙醇在75℃条件下预热3分钟后,将步骤(2)得到的活化的白炭黑与1.35 g己基咔唑甲酸加入到预热好的无水乙醇中搅拌均匀,保持搅拌状态加热回流48小时后,冷却过滤,即得白炭黑复合粉体材料粗品,用无水乙醇洗涤三次,得本发明所述的白炭黑复合粉体材料。 (3) After preheating 45 mL of absolute ethanol at 75°C for 3 minutes, add the activated silica obtained in step (2) and 1.35 g of hexylcarbazole formic acid into the preheated absolute ethanol and stir After heating and refluxing for 48 hours in a stirring state, cool and filter to obtain the crude white carbon black composite powder material, wash with absolute ethanol three times, and obtain the white carbon black composite powder material of the present invention.

实施例3: Example 3:

白炭黑复合粉体材料,其制备方法包括以下步骤: White carbon black composite powder material, its preparation method comprises the following steps:

(1)将1.5 g己基咔唑甲醛和3.1 g重铬酸钾混合得混合物,加水和二氯甲烷将混合物溶解得混合液,在搅拌状态下向混合液中加入35 mL的水和H2SO4,水与H2SO4的体积比为1:1,然后在 80℃条件下进行加热回流90分钟,回流液在室温下冷却,加入水25 mL,用二氯甲烷萃取分离、浓缩得粗品,再用10% NaOH和二氯甲烷的混合液对粗品进行重结晶,得己基咔唑甲酸; (1) Mix 1.5 g of hexylcarbazole formaldehyde and 3.1 g of potassium dichromate to obtain a mixture, add water and dichloromethane to dissolve the mixture to obtain a mixture, add 35 mL of water and H 2 SO to the mixture under stirring 4. The volume ratio of water to H 2 SO 4 is 1:1, and then heated and refluxed at 80°C for 90 minutes, the reflux solution is cooled at room temperature, 25 mL of water is added, extracted and separated with dichloromethane, and concentrated to obtain a crude product , then recrystallize the crude product with a mixed solution of 10% NaOH and dichloromethane to obtain hexylcarbazole formic acid;

(2)将0.13 g氢氧化钠和0.13g白炭黑混合搅匀,在250℃条件下加热90分钟,得活化的白炭黑; (2) Mix and stir 0.13 g sodium hydroxide and 0.13 g white carbon black, and heat at 250°C for 90 minutes to obtain activated white carbon black;

(3)将55 mL无水乙醇在85 ℃条件下预热6分钟后,将步骤(2)得到的活化的白炭黑与1.45 g己基咔唑甲酸加入到预热好的无水乙醇中搅拌均匀,保持搅拌状态加热回流60小时后,冷却过滤,即得白炭黑复合粉体材料粗品,用无水乙醇洗涤三次,得本发明所述的白炭黑复合粉体材料。 (3) After preheating 55 mL of absolute ethanol at 85 °C for 6 minutes, add the activated silica obtained in step (2) and 1.45 g of hexylcarbazole formic acid into the preheated absolute ethanol and stir Evenly, keep the stirring state, heat and reflux for 60 hours, cool and filter to obtain the crude white carbon black composite powder material, wash with absolute ethanol three times, and obtain the white carbon black composite powder material of the present invention.

Claims (2)

1.白炭黑复合粉体材料的制备方法,包括以下步骤: 1. The preparation method of white carbon black composite powder material, comprises the following steps: (1)将1.2±0.3 g己基咔唑甲醛和2.8±0.3 g重铬酸钾混合得混合物,加水和二氯甲烷将混合物溶解得混合液,在搅拌状态下向混合液中加入30±5 mL的水和H2SO4,水与H2SO4的体积比为1:1,然后在 80℃条件下进行加热回流 1±0.5 小时,回流液在室温下冷却,加入水20±5 mL,用二氯甲烷萃取分离、浓缩得粗品,再用10% NaOH和二氯甲烷的混合液对粗品进行重结晶,得己基咔唑甲酸; (1) Mix 1.2±0.3 g hexylcarbazole formaldehyde and 2.8±0.3 g potassium dichromate to obtain a mixture, add water and dichloromethane to dissolve the mixture to obtain a mixture, add 30±5 mL to the mixture under stirring water and H 2 SO 4 , the volume ratio of water to H 2 SO 4 is 1:1, then heat and reflux at 80°C for 1±0.5 hours, cool the reflux at room temperature, add 20±5 mL of water, Extraction, separation and concentration with dichloromethane to obtain a crude product, and then recrystallization of the crude product with a mixture of 10% NaOH and dichloromethane to obtain hexylcarbazole formic acid; (2)将0.10±0.03g氢氧化钠和0.10±0.03 g白炭黑混合搅匀,在200±50℃条件下加热2±0.5 小时,得活化的白炭黑; (2) Mix and stir 0.10±0.03g sodium hydroxide and 0.10±0.03g white carbon black, and heat at 200±50°C for 2±0.5 hours to obtain activated white carbon black; (3)取50±5 mL无水乙醇在80±5 ℃条件下预热3-6分钟后,将步骤(2)得到的活化的白炭黑与1.40±0.05 g己基咔唑甲酸加入到预热好的无水乙醇中搅拌均匀,保持搅拌状态加热回流48±12小时后,冷却过滤,即得白炭黑复合粉体材料粗品,再用无水乙醇洗涤三次,得白炭黑复合粉体材料。 (3) After preheating 50±5 mL of absolute ethanol at 80±5°C for 3-6 minutes, add the activated silica obtained in step (2) and 1.40±0.05 g of hexylcarbazole formic acid to the preheated Stir evenly in the heated absolute ethanol, keep the stirring state, heat and reflux for 48±12 hours, then cool and filter to obtain the crude white carbon black composite powder material, and then wash three times with absolute ethanol to obtain the white carbon black composite powder Material. 2.根据权利要求1所述的白炭黑复合粉体材料的制备方法制得的白炭黑复合粉体材料。 2. the white carbon black composite powder material that the preparation method of white carbon black composite powder material according to claim 1 makes.
CN 201210039437 2012-02-21 2012-02-21 White carbon black composite powder material and preparation method thereof Expired - Fee Related CN102604440B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN 201210039437 CN102604440B (en) 2012-02-21 2012-02-21 White carbon black composite powder material and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN 201210039437 CN102604440B (en) 2012-02-21 2012-02-21 White carbon black composite powder material and preparation method thereof

Publications (2)

Publication Number Publication Date
CN102604440A true CN102604440A (en) 2012-07-25
CN102604440B CN102604440B (en) 2013-12-18

Family

ID=46522236

Family Applications (1)

Application Number Title Priority Date Filing Date
CN 201210039437 Expired - Fee Related CN102604440B (en) 2012-02-21 2012-02-21 White carbon black composite powder material and preparation method thereof

Country Status (1)

Country Link
CN (1) CN102604440B (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106118595A (en) * 2016-07-06 2016-11-16 安徽科技学院 A kind of method that quartz sand mine tailing prepares uv absorption powder body material
CN113755033A (en) * 2021-08-14 2021-12-07 南通双华纳米新材料有限公司 High-temperature treatment device for processing red carbon black and high-temperature treatment method thereof

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6351468A (en) * 1986-08-20 1988-03-04 Dainichi Color & Chem Mfg Co Ltd Pigment composition
US4756993A (en) * 1986-01-27 1988-07-12 Fuji Photo Film Co., Ltd. Electrophotographic photoreceptor with light scattering layer or light absorbing layer on support backside
JPH03131617A (en) * 1989-10-17 1991-06-05 Nippon Jiyouriyuu Kogyo Kk Condensate of carbazolesulfonic acid or its salt and formaldehyde and production thereof
US5139688A (en) * 1990-08-06 1992-08-18 Texaco, Inc. Dispersant and antioxidant additive and lubricating oil composition containing same
CN101544805A (en) * 2009-04-24 2009-09-30 苏州大学 Method for preparing noble metal/polymer nanometer hybrid particles

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3131617B2 (en) * 1998-06-29 2001-02-05 日本リフト株式会社 lift device

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4756993A (en) * 1986-01-27 1988-07-12 Fuji Photo Film Co., Ltd. Electrophotographic photoreceptor with light scattering layer or light absorbing layer on support backside
JPS6351468A (en) * 1986-08-20 1988-03-04 Dainichi Color & Chem Mfg Co Ltd Pigment composition
JPH03131617A (en) * 1989-10-17 1991-06-05 Nippon Jiyouriyuu Kogyo Kk Condensate of carbazolesulfonic acid or its salt and formaldehyde and production thereof
US5139688A (en) * 1990-08-06 1992-08-18 Texaco, Inc. Dispersant and antioxidant additive and lubricating oil composition containing same
CN101544805A (en) * 2009-04-24 2009-09-30 苏州大学 Method for preparing noble metal/polymer nanometer hybrid particles

Non-Patent Citations (4)

* Cited by examiner, † Cited by third party
Title
《Journal of Non-Crystalline Solids》 20040923 Raffaella Raschella,et al. Silica-based photorefractive sol-gel films for holography 428-432 第345-346卷, *
RAFFAELLA RASCHELLA,ET AL.: "Silica-based photorefractive sol–gel films for holography", 《JOURNAL OF NON-CRYSTALLINE SOLIDS》, vol. 345346, 23 September 2004 (2004-09-23), pages 428 - 432 *
安利民等: "PVK/ SiO2 纳米粒子复合体系能量传递的研究", 《发光学报》, vol. 23, no. 6, 30 December 2002 (2002-12-30), pages 590 - 594 *
黄远明等: "SiO2 薄膜中咔唑的发光特性", 《光子学报》, vol. 36, no. 4, 15 April 2007 (2007-04-15), pages 719 - 721 *

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106118595A (en) * 2016-07-06 2016-11-16 安徽科技学院 A kind of method that quartz sand mine tailing prepares uv absorption powder body material
CN113755033A (en) * 2021-08-14 2021-12-07 南通双华纳米新材料有限公司 High-temperature treatment device for processing red carbon black and high-temperature treatment method thereof

Also Published As

Publication number Publication date
CN102604440B (en) 2013-12-18

Similar Documents

Publication Publication Date Title
Xu et al. Rational synthesis of solid‐state ultraviolet B emitting carbon dots via acetic acid‐promoted fractions of sp3 bonding strategy
Yuan et al. Highly efficient carbon dots with reversibly switchable green–red emissions for trichromatic white light-emitting diodes
Schneider et al. Molecular fluorescence in citric acid-based carbon dots
Khatun et al. A thirty-fold photoluminescence enhancement induced by secondary ligands in monolayer protected silver clusters
Yuan et al. Multicolor fluorescent graphene quantum dots colorimetrically responsive to all-pH and a wide temperature range
Han et al. Facilely prepared blue-green light sensitive curcuminoids with excellent bleaching properties as high performance photosensitizers in cationic and free radical photopolymerization
Wang et al. Aggregation-induced emission enhancement (AIEE)-active tetraphenylethene (TPE)-based chemosensor for CN−
Zhang et al. Panchromatic photoinitiators for radical, cationic and thiol-ene polymerization reactions: A search in the diketopyrrolopyrrole or indigo dye series
Zhu et al. Modulation of the photoluminescence in carbon dots through surface modification: from mechanism to white light-emitting diodes
Zhang et al. Transparent and Hazy Eu x Tb1–x-Nanopaper with Color-Tuning, Photo-Switching, and White Light-Emitting Properties for Anti-counterfeiting and Light-Softened WLEDs
Göl et al. Novel zinc (II) phthalocyanine conjugates bearing different numbers of BODIPY and iodine groups as substituents on the periphery
Gan et al. Manganese Ion‐Sensitized Near‐Infrared Light in Cs2NaBi1− xErxCl6 Lead‐Free Double Perovskite
Fang et al. A hybrid materials approach for fabricating efficient WLEDs based on di‐ureasils doped with carbon dots and a europium complex
He et al. Insights into fluorophores of dual-emissive carbon dots derived by naphthalenediol solvothermal synthesis
Wang et al. Preparation of ethanediamine-doped carbon quantum dots and their applications in white LEDs and fluorescent TLC plate
CN102604440B (en) White carbon black composite powder material and preparation method thereof
CN113429963A (en) Continuous color-changing fluorescent anti-counterfeiting material and preparation method and application thereof
Dubey et al. Halide perovskite nanocrystals and lanthanide complex-based bi-luminescent security ink for multilevel static-dynamic anticounterfeiting
Fresnadillo et al. Reference photosensitizers for the production of singlet oxygen
CN103359774B (en) Preparation method of castor-oil-coated zinc oxide nano particle
Li et al. Preparation and photochromic properties of phosphomolybdic acid/rare earth strontium aluminate luminous fiber
CN107200721A (en) The long wavelength light initiator and preparation method of furan ring structure
Liuye et al. Construction of a photo-controlled fluorescent switching with diarylethene modified carbon dots
Wang et al. Supramolecular polymers based on host-guest interactions for the construction of artificial light-harvesting systems
Hara et al. A unique photofunction of YVO4: Bi3+, Eu3+ nanophosphor: Photoluminescent indication for photochemical decomposition of polyurethane

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant
CF01 Termination of patent right due to non-payment of annual fee
CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20131218

Termination date: 20160221