Purpose of fructus citrus sarcodactylis volatile oil
A technology of volatile oil and bergamot, which is applied in the field of prevention and treatment of bergamot volatile oil on Chinese medicinal materials or crop root rot, can solve the problems of no bergamot volatile oil, etc., and achieve the effects of low residue, ecological environment protection, and low reagent cost
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Embodiment 1
[0019] Embodiment 1: the preparation of bergamot volatile oil
[0020] (1) Add 8 times the powder mass of water to 300 g of pulverized bergamot powder, soak for 2 hours, use steam to extract the volatile oil in male cloves by means of heating and distillation, and the extraction time is 6 hours, and condense to collect the effluent;
[0021] (2) The extracted volatile oil was dried with anhydrous sodium sulfate to remove the contained water, put into a brown sample bottle, sealed, and stored at -20°C until use.
Embodiment 2
[0022] Embodiment 2: the activation of pathogenic bacteria
[0023] (1) Isolate the root rot pathogenic bacteria from the roots of Panax notoginseng, purify and identify it as Fusarium oxysporum ( Fusarium oxysporum ), Fusarium solani ( Fusarium solani ) and Cylindrosporium destroyer ( Cylindrocarpon destructans ), inoculate the strains on the PDA medium for activation, after inoculating 4 times, take the vigorously growing strains for use;
[0024] (2) Potato dextrose agar medium (PDA): 200 g potato, 20 g glucose, 20 g agar, 1000 mL distilled water.
Embodiment 3
[0025] Embodiment 3: GC-MS measures the chemical composition of bergamot volatile oil
[0026] (1) GC conditions: Instrument model: Agilengt Technologies 7890B-5977B; Chromatographic column: HP-5MS 30 m×250μm×0.25μm;
[0027] (2) EI source Ionization source temperature: 230°C; quadrupole temperature: 150°C; scanning range: 30~500m / z; inlet temperature: 285°C; split ratio 10:1; injection volume: 1 μl; Electron energy: 70eV; column oven temperature rise program: 50°C for 4min, 5°C / min to 120°C, 1°C / min to 180°C, 10°C / min to 280°C and hold for 16min; The retention time of the continuous carbon (C9-C25) of alkanes is calculated, and the retention time and mass spectrum of the compound are compared with the NIST17.L database to determine the final compound. The test results are shown in the table below;
[0028]
[0029] a: retention time; b: relative peak area±relative deviation; c: retention index.
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