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CN111518282B - Visible-light-catalyzed degradation of organic dyes with cadmium hydroxypyrazolecarboxylate coordination polymers and their preparation and application - Google Patents

Visible-light-catalyzed degradation of organic dyes with cadmium hydroxypyrazolecarboxylate coordination polymers and their preparation and application Download PDF

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CN111518282B
CN111518282B CN202010586419.5A CN202010586419A CN111518282B CN 111518282 B CN111518282 B CN 111518282B CN 202010586419 A CN202010586419 A CN 202010586419A CN 111518282 B CN111518282 B CN 111518282B
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杨廷海
林陈兰
王淑凡
王欣
陈超越
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Nantong Longrun Chemical Co ltd
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Abstract

The invention discloses a hydroxypyrazole cadmium carboxylate coordination polymer for visible light catalytic degradation of organic dye and preparation and application thereof, wherein the chemical expression of the cadmium coordination polymer is [ Cd (hpCH) (H)2O)(DMF)]nIn the formula of hpCH3Is 5-hydroxypyrazole-3-carboxylic acid, each asymmetric unit of which contains 1 metal Cd2+Ionic, 1 deprotonated organic ligand (hpCH)2‑) 1 coordinated water molecule and 1 coordinated DMF molecule, Cd2+Ions are connected through a 5-hydroxypyrazole-3-carboxylic acid ligand to form a two-dimensional layered structure. The synthesis method of the cadmium coordination polymer is simple and has high yield; the material has stable dye photocatalytic degradation performance at normal temperature, can efficiently carry out photocatalytic degradation on Methylene Blue (MB) azo dye, and has high repeated utilization rate; meanwhile, the polymer has stable structure, is insoluble in water and common organic solvents, and can avoid the problem of secondary pollution.

Description

Hydroxypyrazole cadmium carboxylate coordination polymer for visible light catalytic degradation of organic dye and preparation and application thereof
Technical Field
The invention relates to the technical field of photocatalytic materials, in particular to a hydroxypyrazole cadmium carboxylate coordination polymer for degrading organic dye under catalysis of visible light, and preparation and application thereof.
Background
The discharge of large amounts of factory waste water causes serious environmental problems, and the waste water produced in many industrial processes often contains toxic organic compounds, and is therefore not suitable for direct biological treatment. Taking organic dyes as an example, there are over 10 million commercial dyes on the market, with annual yields of over 70 million tons. These organic dyes are chemically stable, are not easily degraded in water, and are potentially harmful to the ecological environment. Therefore, in order to better protect the global environment where we rely on to live, it is necessary to research and develop materials capable of efficiently degrading organic dyes in wastewater to put into the wastewater degradation field.
Photocatalysis is a degradation method based on in-situ generation of transition substances with strong reactivity, and has the advantages of good environmental operation conditions, low cost, high efficiency and the like compared with other traditional physical and chemical methods.
To date, a range of semiconductor photocatalysts such as metal oxides, chalcogenides and other metal salts and composites thereof have been found to be useful for dye degradation. Wherein, TiO2The composite material has the advantages of biological inertia, chemical inertia, no toxicity, low cost, strong ultraviolet oxidation resistance and the like, so that the composite material is widely concerned in recent years. However, TiO2Energy band gap (E)g3.2eV) and the response to ultraviolet light does not exceed 4%, limiting the absorption of visible light and thus affecting its practical application. Another type of semiconductor metal sulfide, e.g. CdS, In2S3、Sb2S3And CoS, etc., are also considered promising catalysts due to their high ability to respond to visible light, coupled with appropriate valence and conduction band positions. However, since sulfide ions are relatively easily dissolved in light, secondary pollution of heavy metal ions is caused. Therefore, the development of new efficient photocatalysts remains a great challenge.
The coordination polymer as a novel multifunctional material has the advantages of adjustability and designability, and the structure of the coordination polymer can be controlled by selecting different organic connecting agents, metal centers/metal clusters and reaction conditions. Therefore, the method has attracted wide attention in the fields of adsorption, catalysis, photoelectric devices, gas storage and separation and the like. Due to the abundant metal nodes and organic bridging agents and the controllability of synthesis, the coordination polymer with adjustable light absorption property is easy to construct, thereby providing an ideal photocatalytic material for the degradation of organic pollutants. Based on the cadmium coordination polymer, the cadmium coordination polymer based on the novel structure of the 5-hydroxypyrazole-3-carboxylic acid is designed, so that the organic dye can be efficiently degraded in a photocatalytic manner.
Disclosure of Invention
The invention aims to solve the problems in the prior art, and provides a cadmium coordination polymer based on a novel structure of 5-hydroxypyrazole-3-carboxylic acid, which has a simple synthesis process and can efficiently degrade organic dyes in a photocatalytic manner.
In order to achieve the technical purpose, the invention is realized by the following technical scheme: the invention provides a hydroxypyrazole cadmium carboxylate coordination polymer for visible light catalytic degradation of organic dye, wherein the chemical expression of the cadmium coordination polymer is [ Cd (hpCH) (H)2O)(DMF)]nIn the formula of hpCH3Is 5-hydroxypyrazole-3-carboxylic acid, each asymmetric unit of which contains 1 metal Cd2+Ionic, 1 deprotonated organic ligand (hpCH)2-) 1 coordinated water molecule and 1 coordinated DMF molecule, Cd2+Ions are connected through a 5-hydroxypyrazole-3-carboxylic acid ligand to form a two-dimensional layered structure, and the molecular structure of the two-dimensional layered structure is as follows:
Figure BDA0002554826890000021
further, the coordination polymer belongs to monoclinic system, P21/c space group, and the unit cell parameters are as follows:
Figure BDA0002554826890000022
α=90°,β=92.916(2)°,γ=90°,
Figure BDA0002554826890000023
the preparation method of the hydroxypyrazole cadmium carboxylate coordination polymer for degrading organic dye by visible light catalysis comprises the following steps: dissolving 5-hydroxypyrazole-3-carboxylic acid in a mixed solution of distilled water and DMF, dissolving cadmium nitrate in distilled water, uniformly mixing the two solutions, carrying out heating reaction in a closed oven, and naturally cooling to room temperature after the reaction is finished to obtain the hydroxypyrazole cadmium carboxylate coordination polymer for degrading the organic dye by visible light catalysis.
Furthermore, the molar ratio of the 5-hydroxypyrazole-3-carboxylic acid to the cadmium nitrate is 1: 1.5-1: 2, and the volume ratio of the distilled water to the DMF is 2: 1-3: 1.
Further, the temperature of the oven is 80-100 ℃, and the heating reaction time is 1-2 days.
The cadmium coordination polymer can be used for efficiently degrading Methylene Blue (MB) azo dye through photocatalysis, has high cycle stability, and can be recycled.
The invention has the beneficial effects that:
the synthesis method of the hydroxypyrazole cadmium carboxylate coordination polymer for degrading the organic dye by visible light catalysis is simple, convenient and fast to operate and high in preparation efficiency;
the obtained cadmium coordination polymer has stable structure, is insoluble in water and common organic solvents, and can avoid the problem of secondary pollution;
the cadmium coordination polymer disclosed by the invention has excellent performance, organic dyes, especially Methylene Blue (MB) azo dyes, can be efficiently degraded in a photocatalytic manner at normal temperature, and the photocatalytic degradation rate can even reach 96.7% under the irradiation of visible light.
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FIG. 1 is a crystal structure diagram of a cadmium hydroxypyrazole carboxylate coordination polymer for visible light photocatalytic degradation of organic dyes;
FIG. 2 is a graph of the ultraviolet absorption spectrum of a cadmium hydroxypyrazole carboxylate coordination polymer for photocatalytic degradation of methylene blue by visible light;
FIG. 3 is a graph of the rate of change of methylene blue concentration upon photocatalytic degradation of methylene blue by a cadmium hydroxypyrazole carboxylate coordination polymer of a visible photocatalytic degradation organic dye;
FIG. 4 is a graph of the rate of change of cyclic concentration of cadmium hydroxypyrazole carboxylate coordination polymer photocatalytically degrading methylene blue 5 times with visible photocatalytic degradation of organic dyes;
FIG. 5 is a PXRD pattern of photocatalytic degradation of methylene blue by a cadmium hydroxypyrazole carboxylate coordination polymer of visible photocatalytic degradation of organic dyes.
Detailed Description
The following examples further illustrate the present invention but are not to be construed as limiting the invention. Modifications and substitutions to methods, procedures, or conditions of the invention may be made without departing from the spirit of the invention.
Example 1: preparation of hydroxypyrazole cadmium carboxylate coordination polymer for visible light catalytic degradation of organic dye
Weighing 5-hydroxypyrazole-3-carboxylic acid (0.05mmol, 0.0064g) and dissolving in a mixed solution of 1.6mL of DMF and 2mL of distilled water to prepare a ligand solution, weighing cadmium nitrate (0.1mmol, 0.0308g) and dissolving in 1mL of distilled water, adding the cadmium nitrate solution into the ligand solution, uniformly mixing to obtain a transparent colorless solution, reacting in an oven at 90 ℃ for 2 days, cooling to room temperature to obtain a light yellow blocky crystal, and obtaining the yield: 54.7 percent. And (3) performing infrared characterization on the product, wherein the specific result is as follows: IR (KBr, cm)-1):3252(m),2360(w),1665(s),1580(s),1446(s),1359(m),1263(w),1149(m),1014(m),846(w),752(m),648(m),570(w)。
Example 2: preparation of hydroxypyrazole cadmium carboxylate coordination polymer for visible light catalytic degradation of organic dye
Weighing 5-hydroxypyrazole-3-carboxylic acid (0.05mmol, 0.0064g) and dissolving in a mixed solution of 1mL of DMF and 2mL of distilled water to prepare a ligand solution, weighing cadmium nitrate (0.1mmol, 0.0308g) and dissolving in 1mL of distilled water, adding the cadmium nitrate solution into the ligand solution, uniformly mixing to obtain a transparent colorless solution, reacting in an oven at 90 ℃ for 1 day, cooling to room temperature to obtain a light yellow blocky crystal, wherein the yield is as follows: 51.4 percent. To pairThe product is subjected to infrared characterization, and the specific result is as follows: IR (KBr, cm)-1):3252(m),2358(w),1659(s),1581(s),1444(s),1363(m),1263(w),1147(m),1013(m),848(w),750(m),649(m),571(w)。
The infrared test results show that the product of this example is the same as the product of example 1.
Example 3: preparation of hydroxypyrazole cadmium carboxylate coordination polymer for visible light catalytic degradation of organic dye
Weighing 5-hydroxypyrazole-3-carboxylic acid (0.05mmol, 0.0064g) and dissolving in a mixed solution of 1.5mL of DMF and 2mL of distilled water to prepare a ligand solution, weighing cadmium nitrate (0.08mmol, 0.0246g) and dissolving in 1mL of distilled water, adding the cadmium nitrate solution into the ligand solution and uniformly mixing to obtain a colorless transparent solution, reacting in an oven at 100 ℃ for 1 day, cooling to room temperature to obtain a light yellow blocky crystal, wherein the yield is as follows: 53.2 percent. And (3) performing infrared characterization on the product, wherein the specific result is as follows: IR (KBr, cm)-1):3250(m),2361(w),1667(s),1580(s),1442(s),1360(m),1259(w),1148(m),1015(m),846(w),753(m),645(m),573(w)。
The infrared test results show that the product of this example is the same as the product of example 1.
The relevant crystallographic data for the Cd complex are as follows:
the complex is as follows: [ Cd (hpch)) (H2O)(DMF)]
The molecular formula is as follows: c7H11O5N3Cd
Molecular weight: 329.59
Crystal system: monoclinic
Space group: p21/c
Unit cell parameters:
Figure BDA0002554826890000041
90°、92.916(2)°、90°
volume:
Figure BDA0002554826890000042
and (3) performance testing: application of hydroxypyrazole cadmium carboxylate coordination polymer in photocatalytic degradation of methylene blue
A xenon lamp is used as a visible light source, and the cadmium coordination polymer obtained in example 1 is subjected to a photocatalytic degradation reaction of methylene blue, wherein the molecular formula of the methylene blue is shown as follows:
Figure BDA0002554826890000051
50mL of a methylene blue aqueous solution having a concentration of 5mg/L was put into a quartz reaction vessel, 30mg of the cadmium coordination polymer obtained in example 1 was added thereto, and the mixture was stirred in the dark for 30 minutes. After reaching the adsorption-desorption equilibrium, sampling is carried out once. Taking a xenon lamp as a visible light source to perform photocatalytic degradation reaction, sampling once every 10min for 10 times in total, centrifuging the taken suspension at a rotating speed of 10000r/min for 4min, and taking supernatant to measure the ultraviolet visible absorption spectrum (figure 2). The result shows that after 90min of photocatalytic degradation, the degradation rate of the cadmium coordination polymer on methylene blue reaches 96.7% (fig. 3). PXRD test results show that after 5 cycles, the structure of the cadmium coordination polymer photocatalyst is not obviously changed (figure 5), and the catalytic effect is not basically changed (figure 4), which shows that the cadmium coordination polymer photocatalyst not only has the characteristic of efficiently degrading methylene blue through photocatalysis, but also has high stability and can be recycled.
The foregoing illustrates and describes the principles, general features, and advantages of the present invention. However, the above description is only an example of the present invention, the technical features of the present invention are not limited thereto, and any other embodiments that can be obtained by those skilled in the art without departing from the technical solution of the present invention should be covered by the claims of the present invention.

Claims (5)

1.一种可见光催化降解有机染料的羟基吡唑羧酸镉配位聚合物,其特征在于,该镉配位聚合物的化学表达式为[Cd(hpcH)(H2O)(DMF)]n,式中hpcH3为5-羟基吡唑-3-羧酸,它的每个不对称单元含有1个金属Cd2+离子、1个去质子化有机配体(hpcH2-)、1个配位水分子以及1个配位DMF分子,Cd2+离子通过5-羟基吡唑-3-羧酸配体连接形成二维层状结构,其分子结构如下所示:1. a hydroxypyrazole carboxylate cadmium coordination polymer for visible light catalytic degradation of organic dyes, is characterized in that, the chemical expression of this cadmium coordination polymer is [Cd(hpcH)(H 2 O)(DMF)] n , where hpcH 3 is 5-hydroxypyrazole-3-carboxylic acid, and each asymmetric unit of it contains 1 metal Cd 2+ ion, 1 deprotonated organic ligand (hpcH 2- ), 1 Coordinated water molecule and one coordinated DMF molecule, Cd 2+ ions are connected by 5-hydroxypyrazole-3-carboxylic acid ligands to form a two-dimensional layered structure, and its molecular structure is as follows:
Figure FDA0003390440830000011
Figure FDA0003390440830000011
该镉配位聚合物可高效光催化降解亚甲基蓝偶氮染料,且在循环使用数次后能保持结构和催化效果稳定。The cadmium coordination polymer can efficiently photocatalyze the degradation of methylene blue azo dye, and can maintain stable structure and catalytic effect after being recycled for several times.
2.如权利要求1所述的可见光催化降解有机染料的羟基吡唑羧酸镉配位聚合物,其特征在于,该配位聚合物属于单斜晶系,P21/c空间群,晶胞参数为:
Figure FDA0003390440830000012
α=90°,β=92.916(2)°,γ=90°,
Figure FDA0003390440830000013
2. The cadmium hydroxypyrazole carboxylate coordination polymer for visible light catalytic degradation of organic dyes as claimed in claim 1, wherein the coordination polymer belongs to monoclinic crystal system, P21/c space group, and unit cell parameter for:
Figure FDA0003390440830000012
α=90°, β=92.916(2)°, γ=90°,
Figure FDA0003390440830000013
3.如权利要求1-2中任一项所述的可见光催化降解有机染料的羟基吡唑羧酸镉配位聚合物的制备方法,其特征在于,具体制备步骤为:将5-羟基吡唑-3-羧酸溶于蒸馏水和DMF的混合液中,硝酸镉溶于蒸馏水中,然后将两种溶液混合均匀,于密闭烘箱中进行加热反应,反应结束后,自然冷却至室温,即可得到该镉配位聚合物。3. the preparation method of the hydroxypyrazole carboxylate cadmium coordination polymer of visible light catalytic degradation organic dye as described in any one of claim 1-2, it is characterized in that, concrete preparation step is: 5-hydroxypyrazole -3-Carboxylic acid is dissolved in a mixture of distilled water and DMF, and cadmium nitrate is dissolved in distilled water. Then the two solutions are mixed evenly and heated in an airtight oven. After the reaction is completed, naturally cool to room temperature to obtain The cadmium coordination polymer. 4.如权利要求3所述的可见光催化降解有机染料的羟基吡唑羧酸镉配位聚合物的制备方法,其特征在于,5-羟基吡唑-3-羧酸与硝酸镉的摩尔比为1:1.5~1:2,蒸馏水与DMF的体积比为2:1~3:1。4. the preparation method of the hydroxypyrazole carboxylate cadmium coordination polymer of visible light catalytic degradation organic dye as claimed in claim 3, is characterized in that, the mol ratio of 5-hydroxypyrazole-3-carboxylic acid and cadmium nitrate is 1:1.5~1:2, the volume ratio of distilled water and DMF is 2:1~3:1. 5.如权利要求3所述的可见光催化降解有机染料的羟基吡唑羧酸镉配位聚合物的制备方法,其特征在于,烘箱温度为80~100℃,加热反应时间为1~2天。5 . The method for preparing a cadmium hydroxypyrazole carboxylate coordination polymer for catalyzing the degradation of organic dyes by visible light as claimed in claim 3 , wherein the oven temperature is 80-100° C., and the heating reaction time is 1-2 days. 6 .
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