Functionalized hybrid nanotube C@MoS.SUB.2./SnS.SUB.2 .and preparation method and application thereof

Abstract

The invention discloses a functionalized hybrid nanotube C@MoS.sub.2/SnS.sub.2 and preparation method and application thereof. Dissolving ammonium molybdate tetrahydrate in water under ultrasound, adding ethylenediamine with stirring, and then adding dilute hydrochloric acid dropwise to react to obtain MoO.sub.3-EDA nanowires; adding L-cysteine and glucose into water containing MoO.sub.3-EDA nanowires, and obtaining a dispersion by ultrasonication; heating the dispersion and then centrifuging, then drying the solid matter and then calcining to obtain C@MoS.sub.2 nanotubes; adding C@MoS.sub.2 nanotubes into water containing SnCl.sub.4.5H.sub.2O and KSCN, and hydrothermally reacting to obtain functionalized hybrid nanotubes C@MoS.sub.2/SnS.sub.2. The invention realizes photocatalytic reduction of heavy metal ions to achieve treatment of heavy metal ion solution.

Claims

1. A preparation method of a functionalized hybrid nanotube C@MoS.sub.2/SnS.sub.2, comprising the following steps: (1) dissolving ammonium molybdate tetrahydrate in water under ultrasound, adding ethylenediamine with stirring, and then adding dilute hydrochloric acid dropwise to react to obtain MoO.sub.3-EDA nanowires; (2) adding L-cysteine and glucose into water containing MoO.sub.3-EDA nanowires, and obtaining a dispersion by ultrasonication; heating the dispersion and then centrifuging, then drying the solid matter and then calcining to obtain C@MoS.sub.2 nanotubes; (3) adding C@MoS.sub.2 nanotubes into water containing SnCl.sub.4.5H.sub.2O and KSCN, and hydrothermally reacting to obtain functionalized hybrid nanotubes C@MoS.sub.2/SnS.sub.2.

2. A preparation method of C@MoS.sub.2 nanotubes, comprising the following steps: (1) dissolving ammonium molybdate tetrahydrate in water under ultrasound, adding ethylenediamine with stirring, and then adding dilute hydrochloric acid dropwise to react to obtain MoO.sub.3-EDA nanowires; (2) adding L-cysteine and glucose into water containing MoO.sub.3-EDA nanowires, and obtaining a dispersion by ultrasonication; heating the dispersion and then centrifuging, then drying the solid matter and then calcining to obtain C@MoS.sub.2 nanotubes.

3. A method for photocatalytic treatment of heavy metal ions, comprising the following steps: (1) dissolving ammonium molybdate tetrahydrate in water under ultrasound, adding ethylenediamine with stirring, and then adding dilute hydrochloric acid dropwise to react to obtain MoO.sub.3-EDA nanowires; (2) adding L-cysteine and glucose into water containing MoO.sub.3-EDA nanowires, and obtaining a dispersion by ultrasonication; heating the dispersion and then centrifuging, then drying the solid matter and then calcining to obtain C@MoS.sub.2 nanotubes; (3) adding C@MoS.sub.2 nanotubes into water containing SnCl.sub.4.5H.sub.2O and KSCN, and hydrothermally reacting to obtain functionalized hybrid nanotubes C@MoS.sub.2/SnS.sub.2; (4) adding the functionalized hybrid nanotubes C@MoS.sub.2/SnS.sub.2 to a solution containing heavy metal ions and is irradiated to realize photocatalytic treatment of heavy metal ions.

4. The method according to claim 1, wherein in step (1), the mass ratio of ammonium molybdate tetrahydrate and ethylenediamine is (1.5 to 1.6):1; the concentration of dilute hydrochloric acid is 1 mol/L; the reaction temperature is 50° C., and the reaction time is 2 hours.

5. The method according to claim 1, wherein in step (2), the mass ratio of the L-cysteine, glucose, and MoO.sub.3-EDA nanowires is (5-6):3:2; heating for 12 h at 200° C.; calcination is carried out for 2 h at 700° C. under nitrogen.

6. The method according to claim 1, wherein in step (3), the mass ratio of SnCl.sub.4.5H.sub.2O, C@MoS.sub.2 nanotubes, and KSCN is (6.5-7):5:10; the hydrothermal reaction is carried out for 20 hours at 180° C.

7. The method according to claim 3, wherein in step (4), the irradiation is irradiated by a xenon light source.

8. The method according to claim 2, wherein in step (1), the mass ratio of ammonium molybdate tetrahydrate and ethylenediamine is (1.5 to 1.6):1; the concentration of dilute hydrochloric acid is 1 mol/L; the reaction temperature is 50° C., and the reaction time is 2 hours.

9. The method according to claim 2, wherein in step (2), the mass ratio of the L-cysteine, glucose, and MoO.sub.3-EDA nanowires is (5-6):3:2; heating for 12 h at 200° C.; calcination is carried out for 2 h at 700° C. under nitrogen.

10. The method according to claim 3, wherein in step (1), the mass ratio of ammonium molybdate tetrahydrate and ethylenediamine is (1.5 to 1.6):1; the concentration of dilute hydrochloric acid is 1 mol/L; the reaction temperature is 50° C., and the reaction time is 2 hours.

11. The method according to claim 3, wherein in step (2), the mass ratio of the L-cysteine, glucose, and MoO.sub.3-EDA nanowires is (5-6):3:2; heating for 12 h at 200° C.; calcination is carried out for 2 h at 700° C. under nitrogen.

12. The method according to claim 3, wherein in step (3), the mass ratio of SnCl.sub.4.5H.sub.2O, C@MoS.sub.2 nanotubes, and KSCN is (6.5-7):5:10; the hydrothermal reaction is carried out for 20 hours at 180° C.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) FIG. 1. Scanning electron micrograph (SEM) of C@MoS.sub.2

(2) FIG. 2. Scanning electron micrograph (SEM) of C@MoS.sub.2/SnS.sub.2

(3) FIG. 3 shows the effect of C@MoS.sub.2/SnS.sub.2, C@MoS.sub.2 and SnS.sub.2 on the treatment of heavy metal ion solutions.

(4) FIG. 4 shows the cycle effect of C@MoS.sub.2/SnS.sub.2 hybrid nanotubes on heavy metal ion solution.

DETAILED DESCRIPTION OF THE INVENTION

(5) The invention successfully manufactures C@MoS.sub.2/SnS.sub.2 nano composite material, graphene-like molybdenum disulfide (MoS.sub.2) is a good option because it can adjust the photoresponse of TiO.sub.2 and improve its charge carrier transport properties. Meanwhile, carbon nanotubes (CNTs) have good mechanical strength and efficient electron transport capacity and are widely used as carriers in various catalysts, which can improve the efficiency of solar energy utilization and photocharge transport ,and has good photocatalytic ability for wastewater containing heavy metal ions.

(6) Implementation 1 Preparation of Precursor MoO.sub.3-EDA, the Specific Steps are as Follows:

(7) 2.48 g of ammonium molybdate tetrahydrate is dissolved in 30 mL of deionized water under ultrasound followed 1.6 g of ethylenediamine is added with stirring. And then 1 mol/L HCl is slowly added to the supernatant until a white solid is precipitated and precipitated in a large amount, and then the resulting dispersion is heated at 50° C. for 2 h under stirring. The white solid products are filtered and washed with water to obtain MoO.sub.3-EDA nanowires, which are then vacuum-dried at 50° C. for 12 h.

(8) Implementation 2 Preparation of C@MoS.sub.2/SnS.sub.2 Nanotubes and MoS.sub.2 Nanospheres, the Specific Steps are as Follows:

(9) 0.2 g of MoO.sub.3-EDA is dispersed in 30 mL of deionized water with ultrasonic assistance until a milky white solution is formed. 0.56 g of L-cysteine and 0.297 g glucose are added and then dissolved under ultrasonic treatment for 1 h. The obtained dispersion is then transferred into a 50 mL Teflon-lined autoclave, which is heated at 200° C. for 12 h. The black product is collected by centrifugation and washed several times with deionized water and ethanol, and then dried in a vacuum oven at 60° C. for 12 h. To obtain highly crystalline C@MoS.sub.2 and MoS.sub.2 nano-flowers, the above samples are calcined in a 700° C. tube furnace under N.sub.2 protection for 2 h.

(10) The preparation process of MoS.sub.2 microflowers is identical to that of C@MoS.sub.2 nanotubes except for the absence of glucose. Among them, glucose mainly plays the role of carbonization, which makes the MoS.sub.2 nano-microspheres carbonized at high temperature into C@MoS.sub.2 nano-tubes.

(11) FIG. 1 is a scanning electron micrograph of C@MoS.sub.2. It can be seen from the picture that C@MoS.sub.2 has a uniform particle size distribution and a surface layered structure of MoS.sub.2 nanosheets.

(12) 0.66 g of SnCl.sub.4.5H.sub.2O, and 1.0 g of KSCN are dissolved in 25 mL of water, add 500 mg prepared C@MoS.sub.2 nanotubes, and then transferred to a 50 mL stainless steel autoclave hydrothermal reaction at 180° C. for 20 h. The black product obtained after the reaction is completed is denoted C@MoS.sub.2/SnS.sub.2 hybrid nanotubes.

(13) FIG. 2 is a scanning electron micrograph of C@MoS.sub.2/SnS.sub.2. It can be seen from the picture that the surface of C@MoS.sub.2/SnS.sub.2 is rougher and the nanosheet layer increases.

(14) Implementation 3 Photocatalytic Treatment of Heavy Metal Ions, the Specific Steps are as Follows:

(15) The C@MoS.sub.2/SnS.sub.2 hybrid nanotubes, SnS.sub.2 and C@MoS.sub.2 nanotubes (50 mg) are added to 50 mg/L heavy metal ion with pH=2. Each sample is placed in a Xenon light source (300 W, λ>400 nm) for 90 min.

(16) The content of heavy metal ions in the solution is analyzed by UV-vis spectrophotometry after irradiation with a xenon lamp to compare the degradation effects.

(17) FIG. 3 is the reduction abilities of C@MoS.sub.2/SnS.sub.2, C@MoS.sub.2, and SnS.sub.2 for 50 mg/L Cr(VI) solutions, it could be found that the catalytic efficiency of C@MoS.sub.2/SnS.sub.2 for heavy metal ions in solution is significantly better than that of C@MoS.sub.2 and SnS.sub.2.

(18) Implementation 4 Heavy Metal Ions Removal, the Specific Steps are as Follows:

(19) In order to qualitatively study the visible light catalytic ability of C@MoS.sub.2/SnS.sub.2 hybrid nanotubes, different concentrations (50, 80, 100, 120, 150 mg/L) of Cr(VI) solution (50 mL) are poured into clear glass bottles and 50 mg of C@MoS.sub.2/SnS.sub.2 is added to each bottle. Then placed in a Xenon lamp light source (300 W, λ>400 nm) with stirring for 90 min. After the end of the reaction, the concentration of Cr(VI) in the solution is measured by usingl, 5-diphenylcarbazide colorimetric method. The results are as follows: for Cr(VI) solutions with concentrations of 50, 80, 100, and 120 mg/L, nearly 100% reduction could be achieved in 90 min. When the concentration of heavy metal ion solution reaches 150 mg/L, the catalytic removal rate can still be close to 87% in 90 min.

(20) Implementation 5 The Cycle of Heavy Metal Ion Removal by C@MoS.sub.2/SnS.sub.2 Hybrid Nanotubes, the Specific Steps are as Follows:

(21) In order to study the cycling performance of C@MoS.sub.2/SnS.sub.2 hybrid nanotubes in the treatment of wastewater containing Cr(VI), 50 mg of C@MoS.sub.2/SnS.sub.2 (cycled three times) is added to the Cr(VI) solution (50 mg/L, 50 mL), and irradiated with visible light for 90 min in the stirring. After the reaction, the content of Cr(VI) in the solution is measured using 1,5-diphenylcarbazide colorimetric method.

(22) The data for the cyclic degradation of 50 mg/L Cr(VI) solutions over the C@MoS.sub.2/SnS.sub.2 hybrid nanotubes are shown in FIG. 4. After three cycles using the same catalyst sample, Cr(VI) is completely reduced within 90 min. The second and third cycles of Cr(VI) degradation are less effective than the first, but the C@MoS.sub.2/SnS.sub.2 hybrid nanotubes still showed good degradation ability.

CONCLUSION

(23) Through the above analysis, the invention modified SnS.sub.2 onto the layered MoS.sub.2 by one-pot method and in-situ growth method, and successfully prepared the C@MoS.sub.2/SnS.sub.2 nanocomposite. Moreover, the composite material disclosed in the invention has a strong visible light catalytic reduction for heavy metal ions in an aqueous solution, and can almost achieve a removal rate of 100%. In addition, the manufacturing process of the invention is simple, convenient, economical and environmentally friendly, and therefore has a good application prospect in wastewater treatment.