Use of biological cellulose gel as potted plant soil substitute
A technology of biocellulose and substitutes, which is applied in the field of biocellulose gel as a soil substitute for potted plants, which can solve the problems of poor soil water retention capacity, pollution of indoor environment, waste of water resources and nutrients, etc., and achieve good water retention Performance, interval extension, cost-saving effects
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Embodiment 1
[0017] Use natural ingredients coconut water as the medium, inoculate Gluconoacetobacter xylinum (inoculum size 8%), ferment and culture in a static tray at 30°C for 5 days, obtain a biocellulose gel wet film, and separate the wet film from solid and liquid , Soak it with alkaline solution to remove the adsorbed culture medium and impurities, and then wash it repeatedly with deionized water. The biocellulose wet film was then cut into small particles with a particle size of 1 cm. Put the small biocellulose gel particles into a flowerpot, and when the volume of the flowerpot is about 80%, plant the plants, continue to add the small biocellulose gel particles, and fix the plants.
Embodiment 2
[0019] Synthetic culture medium was formulated with carbon source, nitrogen source and other raw materials commonly used in the field, inoculated with Gluconacetoacetobacter xylinum (10% inoculum), and fermented in a static tray at 28°C for 7 days to obtain biocellulose gel wet The wet membrane is separated from solid and liquid, soaked in alkaline solution to remove the adsorbed culture medium and impurities, and then washed repeatedly with deionized water. The biocellulose wet film was then cut into small particles with a particle size of 0.5 cm. Put the small biocellulose gel particles into a flowerpot, and when the volume of the flowerpot is about 80%, plant the plants, continue to add the small biocellulose gel particles, and fix the plants.
Embodiment 3
[0021] Synthetic culture medium is formulated with carbon sources, nitrogen sources and other raw materials commonly used in this field, inoculated with Gluconacetobacter xylinum (10% inoculum), and cultured on a dynamic shaker at 28°C for 7 days to directly obtain small spherical biocellulose Gel particles, the gel particles are separated from solid and liquid, soaked in lye to remove the culture medium and impurities adsorbed on them, and then washed repeatedly with deionized water. The biocellulose wet film was then cut into small particles with a particle size of 0.8 cm. Put the small biocellulose gel particles into a flowerpot, and when the volume of the flowerpot is about 80%, plant the plants, continue to add the small biocellulose gel particles, and fix the plants.
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