Preparation Method of Rice Straw Biochar Loaded with Bacillus cereus and Use Thereof
20250122128 ยท 2025-04-17
Inventors
- Bing Li (Yaan City, CN)
- Jie Li (Yaan City, CN)
- Changchun Feng (Yaan City, CN)
- Changquan Wang (Yaan City, CN)
- Rong Huang (Yaan City, CN)
- Yulan Chen (Yaan City, CN)
- Qi Tao (Yaan City, CN)
Cpc classification
C05F11/08
CHEMISTRY; METALLURGY
International classification
C05F11/08
CHEMISTRY; METALLURGY
Abstract
A preparation method of a rice straw biochar loaded with Bacillus cereus, comprising: (1) washing, drying, grinding and sieving rice straws; (2) performing anaerobic pyrolysis treatment on the rice straws treated in the step (1) at 300-700 C. to obtain a biochar; (3) treating the biochar obtained in the step (2) with hydrochloric acid, then washing until a washing solution is neutral, drying, grinding, sieving and sterilizing to obtain a sterilized biochar; and (4) performing mixed culture on the sterilized biochar and a solution of Bacillus cereus subjected to activation culture, and then centrifuging after the end of culture to remove supernatant, so as to obtain a rice straw biochar loaded with Bacillus cereus having a carbon immobilizing capability.
Claims
1. A preparation method of a rice straw biochar loaded with Bacillus cereus having a carbon immobilizing capability, comprising the following steps: (1) washing, drying, grinding and sieving rice straws; (2) performing anaerobic pyrolysis treatment on the rice straws treated in the step (1) at 300-700 C. to obtain a biochar; (3) treating the biochar obtained in the step (2) with hydrochloric acid, then washing until a washing solution is neutral, drying, grinding, sieving and sterilizing to obtain a sterilized biochar; and (4) performing mixed culture on the sterilized biochar obtained in the step (3) and a Bacillus cereus liquid subjected to activation culture, and then centrifuging after the end of culture to remove supernatant, so as to obtain a rice straw biochar loaded with Bacillus cereus, the Bacillus cereus being Bacillus cereus deposited under accession No.: CGMCC 1.15914.
2. The preparation method according to claim 1, wherein in the step (1), the sieving refers to passing through a 20-mesh sieve.
3. The preparation method according to claim 1, wherein in the step (2), the anaerobic pyrolysis refers to pyrolysis under the protection of nitrogen.
4. The preparation method according to claim 1, wherein in the step (2), the program of anaerobic pyrolysis is as follows: the temperature is raised to 300, 500 or 700 C. at a rate of 10 C./min and then maintained for 2 h.
5. The preparation method according to claim 1, wherein in the step (3), a hydrochloric acid treatment method is as follows: the biochar is soaked for 4 h using 0.5 mol/L hydrochloric acid, and the sieving refers to passing through a 60-mesh sieve.
6. The preparation method according to claim 1, wherein in the step (4), a mixed ratio of a Bacillus cereus liquid to sterilized biochar is 1 g:10 ml; and the culture time is 24 h.
7. The preparation method according to claim 6, wherein in the step (4), the OD.sub.600 value of the Bacillus cereus liquid is 1.
8. Use of the rice straw biochar obtained by the preparation method according to claim 1 in increasing the content of soil organic carbon, achieving the stable input of Bacillus cereus into soil, or enhancing the stability of soil organic carbon.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
[0021]
[0022]
[0023]
[0024]
[0025]
[0026]
[0027]
DETAILED DESCRIPTION OF THE EMBODIMENTS
[0028] Experimental methods in examples below, unless specified stated, are all conventional methods. Experimental materials used in examples below, unless specified stated, are all commercially available.
[0029] Bacillus cereus used in the present disclosure is commercially available from China General Microbiological Culture Collection Center under accession No.: CGMCC1.15914.
Example 1 Study on Proliferation of Bacillus cereus on Rice Straw Biochar and Contents of Organic Carbon Components in Biochar
1. Specific Steps
1.1 Preparation of Bacteria-Loaded Biochar
[0030] Rice straws were washed, dried, grinded and passed through a 20-mesh sieve and then put in a muffle furnace, nitrogen was introduced in the muffle furnace, the above rice straws were heated to 300 C., 500 C. and 700 C. at a heating rate of 10 C./min, and the temperatures were maintained for 2 h, so as to obtain a 300 C. biochar, a 500 C. biochar and a 700 C. biochar. The above biochars were treated with 0.5 mol/L hydrochloric acid for 4 h, and the biochars were treated in hydrochloric acid to reduce hazardous substances. Subsequently, the treated biochars were washed until washing solutions were neutral. The washed biochars were dried, sieved, passed through the sieve and sterilized in sequence to obtain a 300 C. sterilized biochar, a 500 C. sterilized biochar and a 700 C. sterilized biochar. Bacillus cereus was cultured by using a glucose asparagine agar culture medium, the strains and sterilized biochars were mixed and cultured for 24 h separately in a ratio of 10 ml of bacterial liquid to each g of sterilized biochar after the OD.sub.600 value of the strains was adjusted to 1, and a 300 C. bacteria-loaded biochar, a 500 C. bacteria-loaded biochar and a 700 C. bacteria-loaded biochar were obtained after centrifuging and removing supernatant.
[0031] As shown in
TABLE-US-00001 TABLE 1 Properties of biochars prepared at different temperatures Easily Specific Average Total Micro- Meso- Dissolved oxidizable surface pore pore pore pore organic organic area diameter volume volume volume carbon carbon Biochar (m.sup.2/g) (nm) (cm.sup.3/g) (cm.sup.3/g) (cm.sup.3/g) (mg/kg) (mg/kg) 300 C. 43.33 4.05 0.04 0.03 0.01 1421.43 75.51 141.71 8.48 biochar 500 C. 116.01 3.12 0.09 0.06 0.03 424.34 41.01 86.31 4.22 Biochar 700 C. 262.68 2.41 0.16 0.07 0.08 129.94 20.27 80.85 11.73 Biochar
1.2 Culture of Bacteria-Loaded Biochar
[0032] After a bacteria-loaded biochar was dried in air on a clean bench, 35 g of bacteria-loaded biochar was cultured in a glass tissue culture bottle for 84 days at the culture temperature of 28 C., wherein the culture moisture content was 30% (moisture content based on weight). During the culture, a differential weight method was used to replenish the lost moisture.
1.3 Determination of Viable Counts
[0033] Viable counts of Bacillus cereus on a 300 C. biochar, a 500 C. biochar and a 700 C. biochar were determined by using a viable counting method.
1.4 Determination on Contents of Organic Carbon Components on Biochar
[0034] Dissolved organic carbon on a sample was taken by shaking with deionized water in a ratio of 1:20, and analyzed by using a total organic carbon (TOC) analyzer after an extracting solution passed through a 0.45 m filtration membrane. The content of easily oxidizable organic carbon was determined by using KMnO.sub.4, and the content of microbial biomass organic carbon was determined by using a CHCl.sub.3 fumigation-K.sub.2SO.sub.4 extraction method.
2. Experimental Results
2.1 Viable Counts of Bacillus cereus
[0035] It can be seen from results in
2.2 Change in Organic Carbon Components on Bacteria-Loaded Biochars at Different Temperatures
[0036] It can be seen from results in
Example 2 Comparison Study on Increase in Contents of Soil Organic Carbon by Biochar and Bacteria-Loaded Biochar
1. Specific Steps
1.1 Experimental Design
[0037] The preparation of a biochar and a bacteria-loaded biochar is as shown in the preparation of a bacteria-loaded biochar described in 1.1 of example 1. The prepared biochar and bacteria-loaded biochar were respectively mixed with calcareous purple soil developed from residual slope deposits weathered by Jurassic Penglaizhen Formation brownish purple sandstone and mudstone in a ratio of 1% and then cultured in a glass tissue culture bottle, meanwhile, a control group was set. The culture temperature was 28 C., the culture moisture content was 30% (moisture content based on weight), and during the culture, a differential weight method was used to replenish the lost moisture, with culture time of 63 days.
1.2 Analysis on Soil Organic Carbon Components
[0038] A potassium dichromate-concentrated sulfuric acid plus heating method was used to determine the content of soil organic carbon, and (NaPO.sub.3).sub.6 was used to determine the content of mineral bound organic carbon.
1.3 Microbial Diversity Analysis
[0039] Total DNA was extracted using a soil DNA rapid extraction kit. A primer pair, namely 338F:5-ACTCCTACGGGAGGCAGCA-3 and 806R:5-GGACTACHVGGGTWTCTAAT-3, was used to amplify V3-V4 regions of a bacterial 16s rRNA gene. Sequencing and analysis of amplifiers were performed on Illumina NovaSeq platform.
2. Experimental Results
2.1 the Contents of Soil Organic Carbon Components
[0040] It can be seen from results in
2.2 Abundance Analysis of Bacillus Genus
[0041] It can be seen from results in