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. 2018 Jul 5;19:2253–2259. doi: 10.1016/j.dib.2018.06.120

MoO3NPs/ZIF-8 composite material prepared via RCVD for photodegradation of dyes

Matteo Ciprian a, Peng Xu a, Somboon Chaemchuen a, Rong Tu a, Serge Zhuiykov b, Philippe M Heynderickx b,d, Francis Verpoort a,b,c,
PMCID: PMC6141516  PMID: 30229101

Abstract

Toxic wastewaters from the textile industry have made its way into rivers and other waterways, posing a serious health treat on both human and wildlife. Herein, this data set presents the potential use of MoO3 nanoparticles supported on ZIF-8 in the photodegradation of a cationic dye molecule. The data presented in this article report a concise description of experimental conditions for the spray-dried ZIF-8 synthesis and subsequent deposition of MoO3 nanoparticles via rotary chemical vapor deposition (RCVD). The photodegradation and analysis data reviled that the MoO3-NPs@ZIF-8 3 wt% displayed the ability of degrading methylene blue up to 82% and 95% after 180 and 300 min, respectively.


Specifications Table

Subject area Chemistry, Environmental Sciences and Engineering
More specific subject area Photodegradation
Type of data Table, image, graph, figure
How data was acquired
  • Dye concentration measurement: Monitored by UV–vis absorption spectroscopy (UV-1800 Shimadzu, Japan)

  • Catalyst stability: Diffraction spectra were acquired using PXRD spectroscopy (Rigaku Ultima III, Japan), the molecular integrity was analyzed by FT-IR spectroscopy (Nicolet 6700, Thermo Scientific) and the morphology was confirmed by Scanning electron microscope (SEM – Phenom, Ted Pella Inc.)

  • Metal content: Monitored by Inductive coupled plasma atomic Emission (ICP-AES, Optima 4300 DV, PerkinElmer Inc.)

Data format Analyzed
Experimental factors Activation of MoO3-NPs/ZIF-8 prior to the BETs measurements were achieved by evacuating at 180 °C under vacuum for 6 h.
Experimental features
  • Spry-dried ZIF-8 was synthesized as reported in the original article [“Submitted to Microporous and Mesoporous Materials.”] and literature procedure [1]. The MoO3 nanoparticles were deposited onto the ZIF-8 powder by rotary chemical vapor deposition to obtain the final composite material.

  • The photocatalysts were mixed with the dye aqueous solution and monitored for their photodegradation capacity.

Data source location Wuhan, P.R. China
Data accessibility Data are accessible with article
Related research article Matteo Ciprian, Peng Xu, Somboon Chaemchuen, Rong Tu, Serge Zhuiykov, Philippe Heynderickx, Francis Verpoort, MoO3nanoparticle formation on zeolitic imidazolate frameworks-8 by rotary chemical vapor deposition “Submitted to Microporous and Mesoporous Materials.”

Value of the data

  • The use of the rotary chemical vapor deposition can encourage researchers to efficiently deposit other compounds on metal-organic frameworks.

  • The as-synthesized MoO3-NPs/ZIF-8 exhibits good photodegradation properties towards the removal of dye from polluted environment.

  • To understand the relationship between an alternative nanoparticle deposition technique and the subsequent properties of the composite material.

1. Data

Nanoparticles deposition and coating of powders have been accomplished with numerous techniques including chemical vapor deposition (CVD) [2] and sol-gel [3]. The combination of a fluidized bed and CVD has been extensively used for coating powders. However, operational limits are imposed due to particle size and density of the powders. Rotary chemical vapor deposition (RCVD) is an alternative method that allows us to remove previous operational restrictions and achieve a uniform nanoparticle deposition [4]. A schematic representation and pictures of the apparatus are reported in Fig. 1, Fig. 2.

Fig. 1.

Fig. 1

Schematic of RCVD equipment.

Fig. 2.

Fig. 2

Pictures of the RCVD apparatus, (a) highlight the precursor chamber with the O2 inlet, the tubular furnace and the rotating reactor (detail in c). In section (b) the rotating gear and the vacuum probe are displayed.

Due to the harmful effects of industrial dye emission to the environment and human health [5], [6], the following data set demonstrate the photocatalytic potential of the as-synthesized MoO3-NPs/ZIF-8 on a cationic dye molecule. In Fig. 2 is shown the structure of the methylene blue (MB). A change in maximum absorbance at 664 nm was used to monitor the dye׳s degradation [7]. The UV–vis spectra for the methylene blue photodegradation are illustrated in Fig. 3 (Fig. 4).

Fig. 3.

Fig. 3

Chemical structure of cationic dye methylene blue.

Fig. 4.

Fig. 4

Spectral evaluation of MB degradation using ZIF-8 (a), MoO3-NPs/ZIF-8 1, 2 and 3 wt% (b,c,d).

In order to assess the structural stability of the MoO3-NPs/ZIF-8 3 wt% after its use, the catalyst has been recycled multiple times. The PXRD spectra (Fig. 5) and FT-IR spectra (Fig. 6) reveal that the photocatalyst remains stable under the reaction condition showing negligible degradation. Furthermore, MoO3-NPs/ZIF-8 3 wt% morphology was characterized after the 4th cycle by SEM (Fig. 7) and the metal content was assessed by ICP-AES (Table 1). The photocatalyst has been successfully recycled four times without evident decrease in performance, as shown in Fig. 8.

Fig. 5.

Fig. 5

PXRD pattern of MoO3-NPs/ZIF-8 before and after photocatalytic reaction.

Fig. 6.

Fig. 6

FT-IR spectra of MoO3-NPs/ZIF-8 before and after photocatalytic reaction.

Fig. 7.

Fig. 7

SEM pictures of MoO3-NPs/ZIF-8 3 wt% after use.

Table 1.

ICP-AES results for fresh and recycled MoO3-NPs/ZIF-8 3 wt%.

MoO3-NPs/ZIF-8 3wt% Metal loading (wt%)
Fresh 3.01
Recycled 2.63

Fig. 8.

Fig. 8

Number of catalyst recycles.

2. Materials, methods and experimental design

2.1. Materials

All reagents and solvents were purchased from commercial sources and used without further purification. The synthesis of the catalyst MoO3-NPs/ZIF-8 is detailed in the original paper, [“Submitted to Microporous and Mesoporous Materials.”] and are briefly discussed below.

2.2. Spray-dried ZIF-8 synthesis

The synthesis of ZIF-8 was achieved following literature procedure with minor modification [1].

Zn(OAc)2·2H2O (16 mmol) and 2-methylimidazole (16 mmol) are solubilized in 50 mL of methanol. The reaction mixture was spray-dried with a feed rate of 11.5 mL min−1, a flow rate of 4.6 × 106 mL min−1 and an inlet temperature of 180 °C. The product is collected as a white powder and suspended in methanol overnight. After centrifugation the ZIF-8 is dried at 60 °C in vacuum oven.

2.3. ZIF-8 functionalization by rotary chemical vapor deposition

MoO3 nanoparticles were deposited onto ZIF-8 with the use of a rotary chemical vapor deposition (RCVD) device (Fig. 1, Fig. 2) In brief, the key feature of the RCVD is the rotary reactor chamber. Equipped with four inner blades, can ensure a sufficient contact time between the powder and the reactant gasses. A fixed amount of metal precursor [Mo(CO)6] is placed in the evaporator chamber at 85 °C and carried into the rotary reactor by an oxygen flow of 8.3 × 10−7 m3 s−1. The ZIF-8 was loaded into the rotary chamber and the deposition is set at 250 °C to prevent any degradation of the supporting material. The nanoparticle deposition process took place under reduced pressure (1.0 × 104 Pa) and the deposition time (0.6 > t > 1.8 ks) was used to control the nanoparticles loading.

2.4. Photodegradation experiments

The photodegradation of methylene blue by MoO3-NPs/ZIF-8 was carried out as follows: 50 mg of as-synthesized catalyst were added into 200 mL dye aqueous solution (10 mg/L) and magnetically stirred for 30 minutes in a dark environment. Subsequently, the suspension is poured into a water-cooled jacked glass reactor to dissipate the intense heat sourcing from the solar lamp (PL-XQ 350 W Xenon). The solution aliquots were filtered through a 0.22 μm Millipore filter and analyzed by UV–vis absorption spectroscopy.

3. Data analysis

The MoO3-NPs/ZIF-8 photocatalytic performance is calculated based on the methylene blue photodegradation kinetics according to Eq. (1):

ln(C/C0)=kt (1)

where C is the MB concentration at any given time (t), C0 is the initial concentration and k is the rate constant.

Acknowledgments

The authors are grateful to the State Key Lab of Advanced Technology for Materials Synthesis and Processing for financial support (Wuhan University of Technology). F.V. acknowledges the support from the Tomsk Polytechnic University Competitiveness Enhancement Program grant (VIU-195/2018).

Footnotes

1

Matteo Ciprian, Peng Xu, Somboon Chaemchuen, Rong Tu, Seerge Zhuiykov, Philippe M. Heynderickx, Francis Verpoort, MoO3 nanoparticle formation on zeolitic imidazolate framework-8 by rotary chemical vapor deposition, Micropor. Mesopor. Mater, 2018, 267, 185-191.”

Transparency document

Transparency data associated with this article can be found in the online version at 10.1016/j.dib.2018.06.120.

Transparency document. Supplementary material

Supplementary material

mmc1.docx (9.7KB, docx)

References1

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Associated Data

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Supplementary Materials

Supplementary material

mmc1.docx (9.7KB, docx)

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