PREPARATION METHOD OF BACTERIAL CELLULOSE-DEFECTIVE MOLYBDENUM DISULFIDE HETEROJUNCTION MATERIAL FOR TREATING RADIOACTIVE WASTEWATER

Abstract

A preparation method of a bacterial cellulose-defective molybdenum disulfide (BC-MoS.sub.2-x) heterojunction material for treating radioactive wastewater is provided, including: preparing bacterial cellulose by the in situ growth technology of Acetobacter xylinum, and freeze-drying to obtain dried bacterial cellulose; carbonizing the dried bacterial cellulose to obtain carbonized bacterial cellulose; dispersing the carbonized bacterial cellulose into deionized water under an ultrasonic treatment; then adding thiourea and Na.sub.2MoO.sub.4.2H.sub.2O, dissolving under an ultrasonic treatment to obtain a reaction mixture, subjecting the reaction mixture to a hydrothermal reaction to obtain a BC-MoS.sub.2 heterojunction; and calcining the BC-MoS.sub.2 heterojunction in a tube furnace with an Ar/H.sub.2 atmosphere to obtain the BC-MoS.sub.2-x heterojunction.

Claims

1. A preparation method of a bacterial cellulose-defective molybdenum disulfide (BC-MoS.sub.2-x) heterojunction material for treating radioactive wastewater, comprising the following steps: step 1: preparing a liquid culture medium (per 150 mL) by dissolving and evenly mixing 5 wt % D-glucose, 0.5 wt % yeast extract, 0.2 wt % disodium hydrogen phosphate, 0.5 wt % peptone, 0.1 wt % citric acid, 0.1 wt % potassium dihydrogen phosphate and water, adjusting a pH value to 6.8, and performing a sterilization under a vapor pressure of 103.4 kPa and a temperature of 120-121.3° C. for 15-20 min; inoculating Acetobacter xylinum in the liquid culture medium and placing the liquid culture medium with the Acetobacter xylinum in a constant temperature incubator, incubating the Acetobacter xylinum in the liquid culture medium for 7 days at 293 K with a shaking speed of 120 rpm to obtain an Acetobacter xylinum-inoculated culture medium, and then rinsing the Acetobacter xylinum-inoculated culture medium to neutral with deionized water to obtain neutral Acetobacter xylinum; performing a freeze-drying on the neutral Acetobacter xylinum to obtain dried bacterial cellulose; wherein the Acetobacter xylinum is inoculated in the liquid culture medium according to a volume fraction of 3-8%; step 2: placing the dried bacterial cellulose in a tube furnace with a nitrogen/argon protective atmosphere, and heating the dried bacterial cellulose to 750-850° C. at a rate of 5° C./min, and keeping the dried bacterial cellulose at 750-850° C. for 2-3 h to obtain carbonized bacterial cellulose; step 3: dispersing the carbonized bacterial cellulose into deionized water under a first ultrasonic treatment to obtain dispersed carbonized bacterial cellulose; adding thiourea and Na.sub.2MoO.sub.4.2H.sub.2O to the dispersed carbonized bacterial cellulose for a dissolution under the first ultrasonic treatment to obtain a first reaction mixture, transferring the first reaction mixture into a Teflon-lined stainless steel autoclave, and conducting a first heat preservation on the first reaction mixture at 140-230° C. for 12 h; cooling the first reaction mixture naturally to obtain a first cooled reaction mixture, and collecting a bacterial cellulose-MoS.sub.2 (BC-MoS.sub.2) heterojunction from the first cooled reaction mixture by a first centrifugation; step 4: placing the BC-MoS.sub.2 heterojunction in a tube furnace with an Ar/H.sub.2 atmosphere, heating the BC-MoS.sub.2 heterojunction to 300° C. at a rate of 5-10° C./min, keeping the BC-MoS.sub.2 heterojunction at 300° C. for 0-200 min, and cooling the BC-MoS.sub.2 heterojunction naturally to obtain the BC-MoS.sub.2-x heterojunction, wherein 0≤X<2.

2. The preparation method of the BC-MoS.sub.2-x heterojunction material for treating the radioactive wastewater according to claim 1, wherein in step 3, a mass ratio of the carbonized bacterial cellulose to the deionized water is 1:600-800, a mass ratio of the carbonized bacterial cellulose to the thiourea is 1:0.3-0.4, and a mass ratio of the thiourea to the Na.sub.2MoO.sub.4.2H.sub.2O is 1:14-17.

3. The preparation method of the BC-MoS.sub.2-x heterojunction material for treating the radioactive wastewater according to claim 1, wherein in step 2, the carbonized bacterial cellulose is subjected to a pretreatment as follows: laying the carbonized bacterial cellulose on a bottom plate of a low-temperature plasma generator, wherein a thickness of the carbonized bacterial cellulose after being laid is 6-12 mm; adjusting a spacing between two plates of the low-temperature plasma generator to 25-65 mm; controlling an internal air pressure of the low-temperature plasma generator to 900-1,200 Pa, then introducing a gas into the low-temperature plasma generator; adjusting a working voltage and a current between the two plates of the low-temperature plasma generator to 50-220 V and 0.5-1.2 A, respectively, and treating the carbonized bacterial cellulose for 30-60 min to obtain pretreated carbonized bacterial cellulose.

4. The preparation method of the BC-MoS.sub.2-x heterojunction material for treating the radioactive wastewater according to claim 3, wherein the gas is one selected from the group consisting of air, oxygen and carbon dioxide.

5. The preparation method of the BC-MoS.sub.2-x heterojunction material for treating the radioactive wastewater according to claim 1, wherein step 3 is replaced by the following step: adding the carbonized bacterial cellulose into a ball mill, and adding the thiourea and the Na.sub.2MoO.sub.4.2H.sub.2O into the ball mill simultaneously to obtain a mixture; introducing liquid nitrogen into the ball mill to immerse the mixture in the liquid nitrogen, and keeping a liquid level of the liquid nitrogen stable; preforming a ball milling on the mixture after keeping a constant temperature for 15-30 min to obtain milled materials, wherein the constant temperature in the ball mill is −155° C. to −180° C.; placing the milled materials at 40-60° C. for 90-120 min; dispersing the milled materials into deionized water under a second ultrasonic treatment to obtain a second reaction mixture, transferring the second reaction mixture into the Teflon-lined stainless steel autoclave, and conducting a second heat preservation on the second reaction mixture at 140-230° C. for 12 h; cooling the second reaction mixture naturally to obtain a second cooled reaction mixture, and collecting the BC-MoS.sub.2 heterojunction from the second cooled reaction mixture by a second centrifugation.

6. The preparation method of the BC-MoS.sub.2-x heterojunction material for treating the radioactive wastewater according to claim 5, wherein a time of the ball milling is 60-90 min, and a speed of the ball milling is 500-650 rpm.

7. The preparation method of the BC-MoS.sub.2-x heterojunction material for treating the radioactive wastewater according to claim 5, wherein in step 3, a mass ratio of the carbonized bacterial cellulose to the deionized water is 1:600-800, a mass ratio of the carbonized bacterial cellulose to the thiourea is 1:0.3-0.4, and a mass ratio of the thiourea to the Na.sub.2MoO.sub.4.2H.sub.2O is 1:14-17.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0020] FIG. 1 is a scanning electron microscopy (SEM) diagram showing the BC-MoS.sub.2-x heterojunction prepared in embodiment 1 of the present invention;

[0021] FIG. 2 is a high resolution transmission electron microscopy (HRTEM) diagram showing the BC-MoS.sub.2-x heterojunction prepared in embodiment 1 of the present invention;

[0022] FIG. 3 is a SEM diagram showing the carbonized bacterial cellulose prepared in embodiment 1 of the present invention;

[0023] FIG. 4 is a diagram showing Fourier transform infrared spectroscopy (FTIR) spectra of the bacterial cellulose, the carbonized bacterial cellulose, the BC-MoS.sub.2 heterojunction and the BC-MoS.sub.2-x heterojunction prepared in embodiment 1 of the present invention;

[0024] FIG. 5 is a diagram showing X-ray diffraction (XRD) patterns of the bacterial cellulose, the carbonized bacterial cellulose, the BC-MoS.sub.2 heterojunction and the BC-MoS.sub.2-x heterojunction prepared in embodiment 1 of the present invention;

[0025] FIG. 6 is a diagram showing electron paramagnetic resonance (EPR) spectra of the BC-MoS.sub.2 heterojunction and the BC-MoS.sub.2-x heterojunction prepared in embodiment 1 of the present invention;

[0026] FIG. 7 is a diagram showing adsorption kinetic curves (under dark conditions) of U(VI) by the carbonized bacterial cellulose, the BC-MoS.sub.2 heterojunction and the BC-MoS.sub.2-x heterojunction prepared in embodiment 1 of the present invention;

[0027] FIG. 8 is a diagram showing adsorption kinetic curves (under sunlight conditions) of U(VI) by the carbonized bacterial cellulose, the BC-MoS.sub.2 heterojunction and the BC-MoS.sub.2-x heterojunction prepared in embodiment 1 of the present invention;

[0028] FIG. 9 is a diagram showing X-ray photoelectron spectroscopy (XPS) spectra of the BC-MoS.sub.2-x heterojunction (prepared in embodiment 1) in U 4f region under dark conditions and simulated sunlight irradiation;

[0029] FIG. 10 is a diagram showing adsorption effects of the BC-MoS.sub.2-x heterojunction prepared in embodiment 1 on U(VI) (different addition amounts of the BC-MoS.sub.2-x heterojunction);

[0030] FIG. 11 is a diagram showing adsorption effects of the BC-MoS.sub.2-x heterojunction prepared in embodiment 1 on U(VI) (different initial concentrations of the U(VI));

[0031] FIG. 12 is a diagram showing adsorption kinetic curves (under sunlight conditions) of U(VI) by the BC-MoS.sub.2-x heterojunctions prepared in embodiments 3-6;

[0032] FIG. 13 is a diagram showing partial enlarged curves of FIG. 12;

[0033] FIG. 14 is a diagram showing adsorption kinetic curves (under dark conditions) of U(VI) by the BC-MoS.sub.2-x heterojunctions prepared in embodiments 3-6;

[0034] FIG. 15 is a diagram showing cyclic adsorption effects of U(VI) by the BC-MoS.sub.2-x heterojunctions and the carbonized bacterial cellulose prepared in embodiments 3-6;

[0035] FIG. 16 is a diagram showing adsorption effects of the BC-MoS.sub.2-x heterojunction prepared in embodiment 1 on U(VI) (under different pH conditions);

[0036] FIG. 17 is a diagram showing XPS spectra of the bacterial cellulose, the carbonized bacterial cellulose, the BC-MoS.sub.2 heterojunction and the BC-MoS.sub.2-x heterojunction prepared in embodiment 1; and

[0037] FIG. 18 is a diagram showing XPS spectra (S 2p) of the BC-MoS.sub.2 heterojunction and the BC-MoS.sub.2-x heterojunction prepared in embodiment 1.

DETAILED DESCRIPTION OF THE EMBODIMENTS

[0038] The present invention is further described in detail in combination with the drawings, so that those skilled in the art can implement it with reference to the specification.

[0039] It is to be understood that terms such as “have”, “include” and “contain” as used herein do not imply the presence or addition of one or more other elements or combinations thereof.

Embodiment 1

[0040] A preparation method of a bacterial cellulose-defective molybdenum disulfide (BC-MoS.sub.2-x) heterojunction material for treating radioactive wastewater includes the following steps.

[0041] Step 1: a liquid culture medium (per 150 mL) is prepared by dissolving and evenly mixing 5 wt % D-glucose, 0.5 wt % yeast extract, 0.2 wt % disodium hydrogen phosphate, 0.5 wt % peptone, 0.1 wt % citric acid, 0.1 wt % potassium dihydrogen phosphate and water, adjusting a pH value to 6.8, and performing a sterilization under a vapor pressure of 103.4 kPa and a temperature of 120° C. for 20 min. Acetobacter xylinum is inoculated in the liquid culture medium and placed in a constant temperature incubator, incubated for 7 days at 293 K with a shaking speed of 120 rpm, and then rinsed to neutral with deionized water. A freeze-drying is performed to obtain dried bacterial cellulose. The Acetobacter xylinum is inoculated in the liquid culture medium according to a volume fraction of 5%.

[0042] Step 2: the dried bacterial cellulose is placed in a tube furnace with a nitrogen/argon protective atmosphere, and heated to 800° C. at a rate of 5° C./min, and kept at 800° C. for 2 h to obtain carbonized bacterial cellulose. FIG. 3 is the SEM diagram showing the carbonized bacterial cellulose, where the staggered arrangement of tubular hyphae indicates that hyphae is an ideal growth platform for MoS.sub.2.

[0043] Step 3: 100 mg of the carbonized bacterial cellulose is dispersed into 70 mL of deionized water under an ultrasonic treatment; 0.5 mmol of thiourea and 2.5 mmol of Na.sub.2MoO.sub.4.2H.sub.2O are added and dissolved under the ultrasonic treatment to obtain a reaction mixture. The reaction mixture is transferred into a Teflon-lined stainless steel autoclave, and kept at 200° C. for 12 h. After being cooled naturally, a BC-MoS.sub.2 heterojunction is collected by a centrifugation.

[0044] Step 4: the BC-MoS.sub.2 heterojunction is placed in a tube furnace with an Ar/H.sub.2 atmosphere, heated to 300° C. at a rate of 10° C./min, and kept at 300° C. for 30 min, and cooled naturally to obtain the BC-MoS.sub.2-x heterojunction. FIG. 1 shows the SEM diagram of the BC-MoS.sub.2-x heterojunction, where the dense MoS.sub.2 nanoparticles are uniformly dispersed on the mycelium skeleton. FIG. 2 shows the HRTEM diagram of the BC-MoS.sub.2-x heterojunction, indicating distinct lattice fringes with an interplanar spacing of 0.62 nm. FIG. 4 shows the FTIR diagrams of the bacterial cellulose, the carbonized bacterial cellulose, the BC-MoS.sub.2 heterojunction and the BC-MoS.sub.2-x heterojunction. The BC-MoS.sub.2-x heterojunction retains several typical characteristic peaks corresponding to —OH, —OH from carboxyl, —C═O (amide I), —CO, and —COOH respectively, thus providing a basis for the effective removal of U(VI). FIG. 5 shows the XRD patterns of the bacterial cellulose, the carbonized bacterial cellulose, the BC-MoS.sub.2 heterojunction and the BC-MoS.sub.2-x heterojunction. The BC-MoS.sub.2-x heterojunction has seven broad peaks at 13.98°, 33.48°, 39.61°, and 59.21°, corresponding to (002), (100), (103), and (110) facets of 2H—MoS.sub.2 (JCPDS card No. 75-1539), respectively. In addition, a weak diffraction peak at 2θ=23.51° is ascribed to the (002) facet of graphene, which indicates the graphitization of bacterial cellulose. FIG. 6 shows the EPR spectra of the BC-MoS.sub.2 heterojunction and the BC-MoS.sub.2-x heterojunction. In order to further verify the details of features of the vacancy in the BC-MoS.sub.2/BC-MoS.sub.2-x heterojunctions, the EPR analysis is performed on the BC-MoS.sub.2/BC-MoS.sub.2-x heterojunctions. As shown in FIG. 6, the BC-MoS.sub.2 heterojunction exhibits a weak electron spin resonance (ESR) signal at 3514 G, indicating a low concentration of natural S-vacancies. However, the BC-MoS.sub.2-x heterojunction shows a strong ESR signal, which is caused by the charge state of anion vacancies in MoS.sub.2 after H.sub.2/Ar mixed treatment. The above results show that H.sub.2/Ar mixed high-temperature treatment is a feasible way to introduce anion vacancies. FIG. 17 shows the XPS spectra of the bacterial cellulose, the carbonized bacterial cellulose, the BC-MoS.sub.2 heterojunction and the BC-MoS.sub.2-x heterojunction. The wide-scan XPS spectra of BC-MoS.sub.2-x heterojunction show the C 1s, N 1s, O 1s, S 2p, and Mo 3d peaks at 285.2, 393.8, 530.1, 161.6, and 232.3 eV, respectively. Compared with the pure BC, obvious signals of N 1s, Mo 3d and S 2p are observed on the carbonized BC, the BC-MoS.sub.2 and the BC-MoS.sub.2-x heterojunctions. FIG. 18 shows the XPS spectra (S 2p) of the BC-MoS.sub.2 heterojunction and the BC-MoS.sub.2-x heterojunction prepared in embodiment 1. The S 2p XPS spectrum shows two main characteristic peaks at 162.8±0.1 eV and 161.6±0.1 eV, which are attributed to the S 2p1/2 and S 2p3/2 of S.sup.2−, respectively. Compared with the BC-MoS.sub.2 heterojunction, the two peaks of the BC-MoS.sub.2-x heterojunction are located at 162.5±0.1 and 161.4±0.1 eV, corresponding to S vacancies near the S 2p1/2 and S 2p3/2, respectively.

Embodiment 2

[0045] A preparation method of a bacterial cellulose-defective molybdenum disulfide (BC-MoS.sub.2-x) heterojunction material for treating radioactive wastewater includes the following steps.

[0046] Step 1: a liquid culture medium (per 150 mL) is prepared by dissolving and evenly mixing 5 wt % D-glucose, 0.5 wt % yeast extract, 0.2 wt % disodium hydrogen phosphate, 0.5 wt % peptone, 0.1 wt % citric acid, 0.1 wt % potassium dihydrogen phosphate and water, adjusting a pH value to 6.8, and performing a sterilization under a vapor pressure of 103.4 kPa and a temperature of 120° C. for 20 min. Acetobacter xylinum is inoculated in the liquid culture medium and placed in a constant temperature incubator, incubated for 7 days at 293 K with a shaking speed of 120 rpm, and then rinsed to neutral with deionized water. A freeze-drying is performed to obtain dried bacterial cellulose. The Acetobacter xylinum is inoculated in the liquid culture medium according to a volume fraction of 6%.

[0047] Step 2: the dried bacterial cellulose is placed in a tube furnace with a nitrogen/argon protective atmosphere, and heated to 850° C. at a rate of 5° C./min, and kept at 850° C. for 2.5 h to obtain carbonized bacterial cellulose.

[0048] Step 3: 100 mg of the carbonized bacterial cellulose is dispersed into 80 mL of deionized water under an ultrasonic treatment; 0.5 mmol of thiourea and 2.5 mmol of Na.sub.2MoO.sub.4.2H.sub.2O are added and dissolved under the ultrasonic treatment to obtain a reaction mixture. The reaction mixture is transferred into a Teflon-lined stainless steel autoclave, and kept at 230° C. for 12 h. After being cooled naturally, a BC-MoS.sub.2 heterojunction is collected by a centrifugation.

[0049] Step 4: the BC-MoS.sub.2 heterojunction is placed in a tube furnace with an Ar/H.sub.2 atmosphere, heated to 300° C. at a rate of 5° C./min, and kept at 300° C. for 45 min, and cooled naturally to obtain the BC-MoS.sub.2-x heterojunction.

Embodiment 3

[0050] A preparation method of a bacterial cellulose-defective molybdenum disulfide (BC-MoS.sub.2-x) heterojunction material for treating radioactive wastewater includes the following steps.

[0051] Step 1: a liquid culture medium (per 150 mL) is prepared by dissolving and evenly mixing 5 wt % D-glucose, 0.5 wt % yeast extract, 0.2 wt % disodium hydrogen phosphate, 0.5 wt % peptone, 0.1 wt % citric acid, 0.1 wt % potassium dihydrogen phosphate and water, adjusting a pH value to 6.8, and performing a sterilization under a vapor pressure of 103.4 kPa and a temperature of 120° C. for 20 min. Acetobacter xylinum is inoculated in the liquid culture medium and placed in a constant temperature incubator, incubated for 7 days at 293 K with a shaking speed of 120 rpm, and then rinsed to neutral with deionized water. A freeze-drying is performed to obtain dried bacterial cellulose. The Acetobacter xylinum is inoculated in the liquid culture medium according to a volume fraction of 5%.

[0052] Step 2: the dried bacterial cellulose is placed in a tube furnace with a nitrogen/argon protective atmosphere, and heated to 800° C. at a rate of 5° C./min, and kept at 800° C. for 3 h to obtain carbonized bacterial cellulose.

[0053] Step 3: 10 g of the carbonized bacterial cellulose is dispersed into 6,000 mL of deionized water under an ultrasonic treatment; 4 g of thiourea and 60 g of Na.sub.2MoO.sub.4.2H.sub.2O are added and dissolved under the ultrasonic treatment to obtain a reaction mixture. The reaction mixture is transferred into a Teflon-lined stainless steel autoclave, and kept at 230° C. for 12 h; after being cooled naturally, a BC-MoS.sub.2 heterojunction is collected by a centrifugation.

[0054] Step 4: the BC-MoS.sub.2 heterojunction is placed in a tube furnace with an Ar/H.sub.2 atmosphere, heated to 300° C. at a rate of 5° C./min, and kept at 300° C. for 45 min, and cooled naturally to obtain the BC-MoS.sub.2-x heterojunction.

Embodiment 4

[0055] A preparation method of a bacterial cellulose-defective molybdenum disulfide (BC-MoS.sub.2-x) heterojunction material for treating radioactive wastewater includes the following steps.

[0056] Step 1: a liquid culture medium (per 150 mL) is prepared by dissolving and evenly mixing 5 wt % D-glucose, 0.5 wt % yeast extract, 0.2 wt % disodium hydrogen phosphate, 0.5 wt % peptone, 0.1 wt % citric acid, 0.1 wt % potassium dihydrogen phosphate and water, adjusting a pH value to 6.8, and performing a sterilization under a vapor pressure of 103.4 kPa and a temperature of 120° C. for 20 min. Acetobacter xylinum is inoculated in the liquid culture medium and placed in a constant temperature incubator, incubated for 7 days at 293 K with a shaking speed of 120 rpm, and then rinsed to neutral with deionized water. A freeze-drying is performed to obtain dried bacterial cellulose. The Acetobacter xylinum is inoculated in the liquid culture medium according to a volume fraction of 5%.

[0057] Step 2: the dried bacterial cellulose is placed in a tube furnace with a nitrogen/argon protective atmosphere, and heated to 800° C. at a rate of 5° C./min, and kept at 800° C. for 3 h to obtain carbonized bacterial cellulose. The carbonized bacterial cellulose is subjected to a pretreatment as follows: the carbonized bacterial cellulose is laid on a bottom plate of a low-temperature plasma generator with a thickness of 12 mm; a spacing between two plates of the low-temperature plasma generator is adjusted to 65 mm; an internal air pressure of the low-temperature plasma generator is controlled to 1,000 Pa, then a gas is introduced into the low-temperature plasma generator. A working voltage and current between the two plates of the low-temperature plasma generator are adjusted to 200 V and 1.2 A, and the pretreatment is performed for 45 min to obtain pretreated carbonized bacterial cellulose. The gas is carbon dioxide.

[0058] Step 3: 10 g of the pretreated carbonized bacterial cellulose is dispersed into 6,000 mL of deionized water under an ultrasonic treatment; 4 g of thiourea and 60 g of Na.sub.2MoO.sub.4.2H.sub.2 O are added and dissolved under the ultrasonic treatment to obtain a reaction mixture, the reaction mixture is transferred into a Teflon-lined stainless steel autoclave, and kept at 230° C. for 12 h; after being cooled naturally, a BC-MoS.sub.2 heterojunction is collected by a centrifugation.

[0059] Step 4: the BC-MoS.sub.2 heterojunction is placed in a tube furnace with an Ar/H.sub.2 atmosphere, heated to 300° C. at a rate of 5° C./min, and kept at 300° C. for 45 min, and cooled naturally to obtain the BC-MoS.sub.2-x heterojunction.

Embodiment 5

[0060] A preparation method of a bacterial cellulose-defective molybdenum disulfide (BC-MoS.sub.2-x) heterojunction material for treating radioactive wastewater includes the following steps.

[0061] Step 1: a liquid culture medium (per 150 mL) is prepared by dissolving and evenly mixing 5 wt % D-glucose, 0.5 wt % yeast extract, 0.2 wt % disodium hydrogen phosphate, 0.5 wt % peptone, 0.1 wt % citric acid, 0.1 wt % potassium dihydrogen phosphate and water, adjusting a pH value to 6.8, and performing a sterilization under a vapor pressure of 103.4 kPa and a temperature of 120° C. for 20 min. Acetobacter xylinum is inoculated in the liquid culture medium and placed in a constant temperature incubator, incubated for 7 days at 293 K with a shaking speed of 120 rpm, and then rinsed to neutral with deionized water. A freeze-drying is performed to obtain dried bacterial cellulose. The Acetobacter xylinum is inoculated in the liquid culture medium according to a volume fraction of 5%.

[0062] Step 2: the dried bacterial cellulose is placed in a tube furnace with a nitrogen/argon protective atmosphere, and heated to 800° C. at a rate of 5° C./min, and kept at 800° C. for 3 h to obtain carbonized bacterial cellulose. The carbonized bacterial cellulose is subjected to a pretreatment as follows: the carbonized bacterial cellulose is laid on a bottom plate of a low-temperature plasma generator with a thickness of 12 mm. A spacing between two plates of the low-temperature plasma generator is adjusted to 65 mm; an internal air pressure of the low-temperature plasma generator is controlled to 1,000 Pa, then a gas is introduced into the low-temperature plasma generator. A working voltage and current between the two plates of the low-temperature plasma generator is adjusted to 200 V and 1.2 A, and the pretreatment is performed for 45 min to obtain pretreated carbonized bacterial cellulose. The gas is carbon dioxide.

[0063] Step 3: 10 g of the pretreated carbonized bacterial cellulose is added into a ball mill, 4 g of thiourea and 60 g of Na.sub.2MoO.sub.4.2H.sub.2O are added simultaneously, liquid nitrogen is introduced into the ball mill to immerse all the materials in the liquid nitrogen, and a liquid level is kept stable; a ball milling is performed after a constant temperature is kept for 25 min, and the temperature in the ball mill is −175° C.; the milled materials are placed at 60° C. for 120 min. The milled materials are dispersed into 6,000 mL of deionized water under an ultrasonic treatment to obtain a reaction mixture, the reaction mixture is transferred into a Teflon-lined stainless steel autoclave, and kept at 230° C. for 12 h; after being cooled naturally, a BC-MoS.sub.2 heterojunction is collected by a centrifugation.

[0064] Step 4: the BC-MoS.sub.2 heterojunction is placed in a tube furnace with an Ar/H.sub.2 atmosphere, heated to 300° C. at a rate of 5° C./min, and kept at 300° C. for 45 min, and cooled naturally to obtain the BC-MoS.sub.2-x heterojunction.

Embodiment 6

[0065] A preparation method of a bacterial cellulose-defective molybdenum disulfide (BC-MoS.sub.2-x) heterojunction material for treating radioactive wastewater includes the following steps.

[0066] Step 1: a liquid culture medium (per 150 mL) is prepared by dissolving and evenly mixing 5 wt % D-glucose, 0.5 wt % yeast extract, 0.2 wt % disodium hydrogen phosphate, 0.5 wt % peptone, 0.1 wt % citric acid, 0.1 wt % potassium dihydrogen phosphate and water, adjusting a pH value to 6.8, and performing a sterilization under a vapor pressure of 103.4 kPa and a temperature of 120° C. for 20 min. Acetobacter xylinum is inoculated in the liquid culture medium and placed in a constant temperature incubator, incubated for 7 days at 293 K with a shaking speed of 120 rpm, and then rinsed to neutral with deionized water. A freeze-drying is performed to obtain dried bacterial cellulose. The Acetobacter xylinum is inoculated in the liquid culture medium according to a volume fraction of 5%.

[0067] Step 2: the dried bacterial cellulose is placed in a tube furnace with a nitrogen/argon protective atmosphere, and heated to 800° C. at a rate of 5° C./min, and kept at 800° C. for 3 h to obtain carbonized bacterial cellulose.

[0068] Step 3: 10 g of the carbonized bacterial cellulose is added into a ball mill, 4 g of thiourea and 60 g of Na.sub.2MoO.sub.4.2H.sub.2O are added simultaneously, liquid nitrogen is introduced into the ball mill to immerse all the materials in the liquid nitrogen, and a liquid level is kept stable. A ball milling is performed after a constant temperature is kept for 25 min, and the temperature in the ball mill is −175° C.; the milled materials are placed at 60° C. for 120 min. The milled materials are dispersed into 6,000 mL of deionized water under an ultrasonic treatment to obtain a reaction mixture, the reaction mixture is transferred into a Teflon-lined stainless steel autoclave, and kept at 230° C. for 12 h; after being cooled naturally, a BC-MoS.sub.2 heterojunction is collected by a centrifugation.

[0069] Step 4: the BC-MoS.sub.2 heterojunction is placed in a tube furnace with an Ar/H.sub.2 atmosphere, heated to 300° C. at a rate of 5° C./min, and kept at 300° C. for 45 min, and cooled naturally to obtain the BC-MoS.sub.2-x heterojunction.

[0070] The adsorption-catalytic reduction experiment of U(VI) is carried out on the carbonized bacterial cellulose. The BC-MoS.sub.2 heterojunction and the BC-MoS.sub.2-x heterojunction prepared in embodiment 1.5 mg of samples (carbonized bacterial cellulose, BC-MoS.sub.2 heterojunction, and BC-MoS.sub.2-x heterojunction) are added into a 20 mL glass bottle containing 10 mL of U(VI) solution (8 mg/L, pH=5.0), respectively. The simulated sunlight is irradiated on the glass bottle from a 300-W Xe lamp with AM 1.5G filter (BL-GHX-V, China). A stirring is performed at 20° C. with a speed of 600 r/min, and the performance of the materials is characterized by measuring the concentrations of U(VI) in the solutions after different reaction time. Meanwhile, the same adsorption-catalytic reduction experiment of U(VI) is carried out under dark conditions. The U(VI) solution is prepared by uranyl nitrate. The concentrations of U(VI) in the solution before and after adsorption are determined by a double-beam UV-Vis spectrophotometer. All the experiments are performed in triplicate to take an average value. FIG. 7 shows the experimental results under dark conditions. FIG. 8 shows the experimental results under simulated sunlight irradiation conditions. FIG. 7 shows that the carbonized bacterial cellulose exhibits a relatively low U(VI) extraction capacity with a removal rate of only 34.9% under the dark conditions, while the removal rate of U(VI) by the BC-MoS.sub.2 and BC-MoS.sub.2-x heterojunctions are 40.9% and 48.1%, respectively, which are slightly higher than that of the carbonized bacterial cellulose. The results are ascribed to the electron transfer from MoS.sub.2/MoS.sub.2-x to the carbonized bacterial cellulose, thereby improving the adsorption of U(VI). As shown in FIG. 8, the U(VI) extraction capacity of the carbonized bacterial cellulose is substantially unchanged during the introduction of simulated sunlight into the reaction system. However, the BC-MoS.sub.2 heterojunction exhibits a promoted adsorption kinetics and the U(VI) extraction efficiency up to 79.3%. The above results confirm that the construction of heterojunctions effectively enhances the U(VI) extraction capability. Compared with the BC-MoS.sub.2 heterojunction, the BC-MoS.sub.2-x heterojunction shows excellent U(VI) extraction ability with the introduction of S-vacancies, and the removal rate is up to 91.8%. The above results show that the integration of Schottky junction and vacancies provides a feasible strategy to promote photoelectron transfer, thus improving the U(VI) extraction capability. In order to prove that the integration of Schottky junction and S-vacancies enhances the photocatalytic reduction of U(VI), the changes of uranium species on the BC-MoS.sub.2-x heterojunction under dark and sunlight conditions are further compared. In the U 4f XPS spectra, the presence of U(IV) and U(VI) species on the BC-MoS.sub.2-x heterojunction after U(IV) extraction confirms the reduction of U(VI), while U(IV) is absent under the dark conditions (as shown in FIG. 9). The results show that the integration of Schottky junction and S-vacancies enhances the photocatalytic reduction ability of the heterojunctions.

[0071] The adsorption-catalytic reduction experiment of U(VI) is carried out on the BC-MoS.sub.2-x heterojunction prepared in embodiment 1. 1 mg, 2 mg, 3 mg, 4 mg and 5 mg of samples (BC-MoS.sub.2-x heterojunction) are added into a 20 mL glass bottle containing 10 mL of U(VI) solution (8 mg/L, pH=5.0), respectively. The simulated sunlight is irradiated on the glass bottle from a 300-W Xe lamp with AM 1.5G filter (BL-GHX-V, China). A stirring is performed at 20° C. with a speed of 600 r/min for 60 min, and the concentrations of U(VI) in the solution before and after adsorption are measured to calculate removal rates. Removal rate=(C.sub.0−C.sub.t)/C.sub.0×100%, where C.sub.0 is an initial concentration and C.sub.t is a concentration after adsorption. The U(VI) solution is prepared by uranyl nitrate, and the concentrations of U(VI) in the solution before and after adsorption are determined by the double-beam UV-Vis spectrophotometer. All the experiments are performed in triplicate to take an average value. The results are shown in FIG. 10. With the increase of the solid-liquid ratio, the maximum extraction rate of U(VI) by the BC-MoS.sub.2-x heterojunction reaches 94%.

[0072] 5 mg of samples prepared by embodiment 1 (BC-MoS.sub.2-x heterojunction) are added into a 20 mL glass bottle containing 10 mL of U(VI) solution (C.sub.U(VI)=8 ppm, 20 ppm, 40 ppm, 60 ppm, 80 ppm and 100 ppm, pH=5.0), respectively. The simulated sunlight is irradiated on the glass bottle from a 300-W Xe lamp with AM 1.5G filter (BL-GHX-V, China). A stirring is performed at 20° C. with a speed of 600 r/min for 60 min, and the concentrations of U(VI) in the solution before and after adsorption are measured. The U(VI) solution is prepared by uranyl nitrate, and the concentrations of U(VI) in the solution before and after adsorption are determined by the double-beam UV-Vis spectrophotometer. All the experiments are performed in triplicate to take an average value. The results are shown in FIG. 11. The BC-MoS.sub.2-x heterojunction maintains a high removal rate of U(VI) over a wide range of U(VI) concentrations.

[0073] The adsorption-catalytic reduction experiment of U(VI) is carried out on the BC-MoS.sub.2-x heterojunction prepared in embodiment 1. 5 mg of samples (BC-MoS.sub.2-x heterojunction) are added into a 20 mL glass bottle containing 10 mL of U(VI) solution (C.sub.U(VI)=8 ppm, pH=3.1, 4.2, 5.0, 6.3, 7.5, 8.2, 9.1 and 10.5), respectively. The simulated sunlight is irradiated on the glass bottle from a 300-W Xe lamp with AM 1.5G filter (BL-GHX-V, China). A stirring is performed at 20° C. with a speed of 600 r/min for 60 min, and the concentrations of U(VI) in the solution before and after adsorption are measured. The U(VI) solution is prepared by uranyl nitrate, and the concentrations of U(VI) in the solution before and after adsorption are determined by the double-beam UV-Vis spectrophotometer. All the experiments are performed in triplicate to take an average value. The results are shown in FIG. 16. Under various pH conditions, the BC-MoS.sub.2-x heterojunction still maintains a high removal efficiency of U(VI).

[0074] The adsorption-catalytic reduction experiment of U(VI) is carried out on the BC-MoS.sub.2-x heterojunctions prepared in embodiments 3-6. 5 mg of samples (BC-MoS.sub.2-x, heterojunctions prepared in embodiments 3-6) are added into a 20 mL glass bottle containing 10 mL of U(VI) solution (8 mg/L, pH=5.0), respectively. The simulated sunlight is irradiated on the glass bottle from a 300-W Xe lamp with AM 1.5G filter (BL-GHX-V, China). A stirring is performed at 20° C. with a speed of 600 r/min, and the performance of the materials is characterized by measuring the concentrations of U(VI) in the solution after different reaction time. Meanwhile, the same adsorption-catalytic reduction experiment of U(VI) is carried out under dark conditions. The U(VI) solution is prepared by uranyl nitrate. The concentrations of U(VI) in the solution before and after adsorption are determined by the double-beam UV-Vis spectrophotometer. All the experiments are performed in triplicate to take an average value. FIGS. 12 and 13 show the adsorption-catalytic results of the BC-MoS.sub.2-x heterojunctions prepared in embodiments 3-6 under sunlight conditions, and FIG. 14 shows the adsorption-catalytic results of the BC-MoS.sub.2-x heterojunctions prepared in embodiments 3-6 under dark conditions. As can be seen from FIGS. 12 and 13, the BC-MoS.sub.2-x heterojunctions prepared in embodiments 3-6 have better adsorption-catalysis on U(VI). Under sunlight conditions, the removal rate of U(VI) by the BC-MoS.sub.2-x heterojunction prepared in embodiment 3 is 91.9%, the removal rate of U(VI) by the BC-MoS.sub.2-x heterojunction prepared in embodiment 4 is 92.7%, the removal rate of U(VI) by the BC-MoS.sub.2-x heterojunction prepared in embodiment 5 is 92.2%; and the removal rate of U(VI) by the BC-MoS.sub.2-x heterojunction prepared in embodiment 6 is 94.8%. It can be seen from FIG. 14 that under dark conditions, the removal rate of U(VI) by the BC-MoS.sub.2-x heterojunction prepared in embodiment 3 is 48.2%; the removal rate of U(VI) by the BC-MoS.sub.2-x heterojunction prepared in embodiment 4 is 53.2%; the removal rate of U(VI) by the BC-MoS.sub.2-x heterojunction prepared in embodiment 5 is 51.3%; and the removal rate of U(VI) by the BC-MoS.sub.2-x heterojunction prepared in embodiment 6 is 55.4%.

[0075] After the adsorption-catalytic reduction experiment of U(VI) is carried out on the BC-MoS.sub.2-x heterojunctions and the carbonized BC prepared in embodiments 3-6, the BC-MoS.sub.2-x heterojunction loaded with U(VI) is further treated with excessive NaOH or HC; (0.1 mol/L) for 4 h under ultrasonic conditions, and then rinsed with deionized water three times. After being dried, a cyclic adsorption is performed five times. The adsorption process of each time is the same as that of the first time, i.e., 5 mg of samples (BC-MoS.sub.2-x heterojunctions and carbonized bacterial cellulose prepared in embodiments 3-6) are added into a 20 mL glass bottle containing 10 mL of U(VI) solution (8 mg/L, pH=5.0), respectively. The simulated sunlight is irradiated on the glass bottle from a 300-W Xe lamp with AM 1.5G filter (BL-GHX-V, China). A stirring is performed at 20° C. with a speed of 600 r/min for 70 min. The U(VI) solution is prepared by uranyl nitrate, and the concentrations of U(VI) in the solution before and after adsorption are determined by the double-beam UV-Vis spectrophotometer. All the experiments are performed in triplicate to take an average value. The results are shown in FIG. 15. After five cycles, the carbonized bacterial cellulose and the BC-MoS.sub.2-x heterojunction maintain a relative high removal efficiency of U(VI) without a significant decrease.

[0076] Although the implementation modes of the present invention have been disclosed as above, they are not limited to the applications listed in the specification and embodiments. They can be applied to various fields suitable for the present invention. For those skilled in the art, additional modifications can be easily realized. Therefore, without departing from the general concept defined by the claims and equivalent scope thereof, the present invention is not limited to the specific details and the drawings shown and described here.