A method of preparing natural graphene cellulose blended spunbond nonwoven fabric, which comprises the following steps: (a) combining a graphite powder with a solution comprising 1 to 10 wt. % of a first 5 compound selected from the group consisting of sulfuric acid (H 2 S O 4), hydrochloric acid (HCl), perchloric acid (HC l O 4), hydrogen iodide (HI), hydrofluoric acid (HF), and nitric acid (H NO 3), then stirring for 30 minutes in an ice bath environment; (b) adding a solution comprising 1 to 20 wt. % potassium permanganate (KMnO 4) to 10 the product of step (a), stirring for 1 to 2 hours, and adding distilled water, wherein the potassium permanganate solution is continuously added until none of the purple smoke generated by reacting with the potassium permanganate is formed from the distilled water; (c) adding a solution comprising 1 to 10 wt.% hydrogen peroxide (H 2 0 2) to the product 15 of step (b), wherein the hydrogen peroxide solution is added until no bubbles are formed and the mixture becomes dark green, then filtering the dark green solution into a cake; (d) rinsing the cake of step (c) with a solution comprising 5 wt.% hydrochloric acid (HCl) to remove sulfate ions, then washing the cake with distilled water; 20 (e) drying the cake of step (d) in an oven at 40 ° C for 2 hrs to obtain a dried solid graphite oxide; (f) adding distilled water to the dried solid graphite oxide of step (e), wherein the distilled water is added up to 200 m l s per 0.06 to 1.0 g of the dried solid graphite-21-oxide, then treating by ultrasonic vibration for 30 minutes to obtain a graphite oxide solution having a graphite oxide concentration of 0.03 wt. % to 0.5 wt. %; (g) adding a solution comprising 1 to 10 wt. % of a second compound selected from the group consisting of sodium borohydride (NaBH 4), potassium borohydride (KBH 4), 5 lithium aluminum hydride (LiA l H 4), and sodium citrate (C 6 H S Na 3 O 7) to the graphite oxide solution of step (f), then treating by ultrasonic vibration for 30 to 60 minutes, wherein in the resulting solution, the ratio of graphene oxide to the second compound is 1:1 to 1:5 by weight; (h) filtrating the product of step (g), washing the filtrate with water 3 to 5 times to 10 remove the second compound, then back-filtrating to obtain a graphene solution; (i) adding the graphene solution of step (h) to a slurry solution formed by mixing a pulp with N-methylmorpholine N-oxide (NMMO) and a stabilizer in an expansion dissolving tank, then mixing at 60 to 80 ° C, wherein the graphene solution of step (h) is added in a ratio of 0.11 to 5.0 wt. %, the pulp is selected from the group 15 consisting of wood pulp, cotton pulp, bamboo pulp and a mixture of cotton and bamboo pulp, the pulp comprises a-cellulose in an amount of 65 % or more with a polymerization degree of 500 to 1500; and the NMMO has a concentration of 50 % to 78 %; (j) removing water from the product of step (i) using a Thin Film Evaporator (TFE) 20 and heating at 80 to 130 ° C, wherein the water is removed to 5% to 13% within 5 minutes and the cellulose is dissolved to form a spinning dope, and the amount ratio of each component among the components comprised in the dope is: water (H 2 0) 5 % to 15 %, N-methylmorpholine N-oxide (N M MO) 70 % to 90 %, and -22-cellulose 5 % to 15 %; (k) Squeezing the spinning dope of step () from a spinning orifice by using a spunbond process to form a natural graphene cellulose blended filament strand, which comprises pressuring the spinning dope by a metering pump, filtering and 5 degassing by a continuous filter (CPF), transporting the spinning dope into a spinning tank, and stretching the spinning dope outward by air gap cooling through the spinning orifice, to form a natural graphene cellulose blended filament strand; and (1) feeding the natural graphene cellulose blended filament strand of step (k) into a 10 coagulation liquid, solidifying and regenerating the filament strand, stretching the filament strand under high pressure and high speed by an air stream drafting device, stacking the filament strand on a collection web to form a fibrous network structure, and washing, water needle punching, drying, oiling and coiling the fibrous network structure to form a natural graphene cellulose blended spunbond nonwoven fabric, 15 wherein the concentration of the coagulation liquid is between 2. 0% to 10.0 %, and after washing, the amount of residual N MM O solvent is less than 0.1 %.

A method of preparing natural graphene cellulose blended spunbond nonwoven fabric, which comprises the following steps: (a) combining a graphite powder with a solution comprising 1 to 10 wt. % of a first 5 compound selected from the group consisting of sulfuric acid (H 2 S O 4), hydrochloric acid (HCl), perchloric acid (HC l O 4), hydrogen iodide (HI), hydrofluoric acid (HF), and nitric acid (H NO 3), then stirring for 30 minutes in an ice bath environment; (b) adding a solution comprising 1 to 20 wt. % potassium permanganate (KMnO 4) to 10 the product of step (a), stirring for 1 to 2 hours, and adding distilled water, wherein the potassium permanganate solution is continuously added until none of the purple smoke generated by reacting with the potassium permanganate is formed from the distilled water; (c) adding a solution comprising 1 to 10 wt.% hydrogen peroxide (H 2 0 2) to the product 15 of step (b), wherein the hydrogen peroxide solution is added until no bubbles are formed and the mixture becomes dark green, then filtering the dark green solution into a cake; (d) rinsing the cake of step (c) with a solution comprising 5 wt.% hydrochloric acid (HCl) to remove sulfate ions, then washing the cake with distilled water; 20 (e) drying the cake of step (d) in an oven at 40 ° C for 2 hrs to obtain a dried solid graphite oxide; (f) adding distilled water to the dried solid graphite oxide of step (e), wherein the distilled water is added up to 200 m l s per 0.06 to 1.0 g of the dried solid graphite-21-oxide, then treating by ultrasonic vibration for 30 minutes to obtain a graphite oxide solution having a graphite oxide concentration of 0.03 wt. % to 0.5 wt. %; (g) adding a solution comprising 1 to 10 wt. % of a second compound selected from the group consisting of sodium borohydride (NaBH 4), potassium borohydride (KBH 4), 5 lithium aluminum hydride (LiA l H 4), and sodium citrate (C 6 H S Na 3 O 7) to the graphite oxide solution of step (f), then treating by ultrasonic vibration for 30 to 60 minutes, wherein in the resulting solution, the ratio of graphene oxide to the second compound is 1:1 to 1:5 by weight; (h) filtrating the product of step (g), washing the filtrate with water 3 to 5 times to 10 remove the second compound, then back-filtrating to obtain a graphene solution; (i) adding the graphene solution of step (h) to a slurry solution formed by mixing a pulp with N-methylmorpholine N-oxide (NMMO) and a stabilizer in an expansion dissolving tank, then mixing at 60 to 80 ° C, wherein the graphene solution of step (h) is added in a ratio of 0.11 to 5.0 wt. %, the pulp is selected from the group 15 consisting of wood pulp, cotton pulp, bamboo pulp and a mixture of cotton and bamboo pulp, the pulp comprises a-cellulose in an amount of 65 % or more with a polymerization degree of 500 to 1500; and the NMMO has a concentration of 50 % to 78 %; (j) removing water from the product of step (i) using a Thin Film Evaporator (TFE) 20 and heating at 80 to 130 ° C, wherein the water is removed to 5% to 13% within 5 minutes and the cellulose is dissolved to form a spinning dope, and the amount ratio of each component among the components comprised in the dope is: water (H 2 0) 5 % to 15 %, N-methylmorpholine N-oxide (N M MO) 70 % to 90 %, and -22-cellulose 5 % to 15 %; (k) Squeezing the spinning dope of step () from a spinning orifice by using a spunbond process to form a natural graphene cellulose blended filament strand, which comprises pressuring the spinning dope by a metering pump, filtering and 5 degassing by a continuous filter (CPF), transporting the spinning dope into a spinning tank, and stretching the spinning dope outward by air gap cooling through the spinning orifice, to form a natural graphene cellulose blended filament strand; and (1) feeding the natural graphene cellulose blended filament strand of step (k) into a 10 coagulation liquid, solidifying and regenerating the filament strand, stretching the filament strand under high pressure and high speed by an air stream drafting device, stacking the filament strand on a collection web to form a fibrous network structure, and washing, water needle punching, drying, oiling and coiling the fibrous network structure to form a natural graphene cellulose blended spunbond nonwoven fabric, 15 wherein the concentration of the coagulation liquid is between 2. 0% to 10.0 %, and after washing, the amount of residual N MM O solvent is less than 0.1 %.

A method of preparing natural graphene cellulose blended spunbond nonwoven fabric, which comprises the following steps: (a) combining a graphite powder with a solution comprising 1 to 10 wt. % of a first 5 compound selected from the group consisting of sulfuric acid (H 2 S O 4), hydrochloric acid (HCl), perchloric acid (HC l O 4), hydrogen iodide (HI), hydrofluoric acid (HF), and nitric acid (H NO 3), then stirring for 30 minutes in an ice bath environment; (b) adding a solution comprising 1 to 20 wt. % potassium permanganate (KMnO 4) to 10 the product of step (a), stirring for 1 to 2 hours, and adding distilled water, wherein the potassium permanganate solution is continuously added until none of the purple smoke generated by reacting with the potassium permanganate is formed from the distilled water; (c) adding a solution comprising 1 to 10 wt.% hydrogen peroxide (H 2 0 2) to the product 15 of step (b), wherein the hydrogen peroxide solution is added until no bubbles are formed and the mixture becomes dark green, then filtering the dark green solution into a cake; (d) rinsing the cake of step (c) with a solution comprising 5 wt.% hydrochloric acid (HCl) to remove sulfate ions, then washing the cake with distilled water; 20 (e) drying the cake of step (d) in an oven at 40 ° C for 2 hrs to obtain a dried solid graphite oxide; (f) adding distilled water to the dried solid graphite oxide of step (e), wherein the distilled water is added up to 200 m l s per 0.06 to 1.0 g of the dried solid graphite-21-oxide, then treating by ultrasonic vibration for 30 minutes to obtain a graphite oxide solution having a graphite oxide concentration of 0.03 wt. % to 0.5 wt. %; (g) adding a solution comprising 1 to 10 wt. % of a second compound selected from the group consisting of sodium borohydride (NaBH 4), potassium borohydride (KBH 4), 5 lithium aluminum hydride (LiA l H 4), and sodium citrate (C 6 H S Na 3 O 7) to the graphite oxide solution of step (f), then treating by ultrasonic vibration for 30 to 60 minutes, wherein in the resulting solution, the ratio of graphene oxide to the second compound is 1:1 to 1:5 by weight; (h) filtrating the product of step (g), washing the filtrate with water 3 to 5 times to 10 remove the second compound, then back-filtrating to obtain a graphene solution; (i) adding the graphene solution of step (h) to a slurry solution formed by mixing a pulp with N-methylmorpholine N-oxide (NMMO) and a stabilizer in an expansion dissolving tank, then mixing at 60 to 80 ° C, wherein the graphene solution of step (h) is added in a ratio of 0.11 to 5.0 wt. %, the pulp is selected from the group 15 consisting of wood pulp, cotton pulp, bamboo pulp and a mixture of cotton and bamboo pulp, the pulp comprises a-cellulose in an amount of 65 % or more with a polymerization degree of 500 to 1500; and the NMMO has a concentration of 50 % to 78 %; (j) removing water from the product of step (i) using a Thin Film Evaporator (TFE) 20 and heating at 80 to 130 ° C, wherein the water is removed to 5% to 13% within 5 minutes and the cellulose is dissolved to form a spinning dope, and the amount ratio of each component among the components comprised in the dope is: water (H 2 0) 5 % to 15 %, N-methylmorpholine N-oxide (N M MO) 70 % to 90 %, and -22-cellulose 5 % to 15 %; (k) Squeezing the spinning dope of step () from a spinning orifice by using a spunbond process to form a natural graphene cellulose blended filament strand, which comprises pressuring the spinning dope by a metering pump, filtering and 5 degassing by a continuous filter (CPF), transporting the spinning dope into a spinning tank, and stretching the spinning dope outward by air gap cooling through the spinning orifice, to form a natural graphene cellulose blended filament strand; and (1) feeding the natural graphene cellulose blended filament strand of step (k) into a 10 coagulation liquid, solidifying and regenerating the filament strand, stretching the filament strand under high pressure and high speed by an air stream drafting device, stacking the filament strand on a collection web to form a fibrous network structure, and washing, water needle punching, drying, oiling and coiling the fibrous network structure to form a natural graphene cellulose blended spunbond nonwoven fabric, 15 wherein the concentration of the coagulation liquid is between 2. 0% to 10.0 %, and after washing, the amount of residual N MM O solvent is less than 0.1 %.

A method of preparing natural graphene cellulose blended spunbond nonwoven fabric, which comprises the following steps: (a) combining a graphite powder with a solution comprising 1 to 10 wt. % of a first 5 compound selected from the group consisting of sulfuric acid (H 2 S O 4), hydrochloric acid (HCl), perchloric acid (HC l O 4), hydrogen iodide (HI), hydrofluoric acid (HF), and nitric acid (H NO 3), then stirring for 30 minutes in an ice bath environment; (b) adding a solution comprising 1 to 20 wt. % potassium permanganate (KMnO 4) to 10 the product of step (a), stirring for 1 to 2 hours, and adding distilled water, wherein the potassium permanganate solution is continuously added until none of the purple smoke generated by reacting with the potassium permanganate is formed from the distilled water; (c) adding a solution comprising 1 to 10 wt.% hydrogen peroxide (H 2 0 2) to the product 15 of step (b), wherein the hydrogen peroxide solution is added until no bubbles are formed and the mixture becomes dark green, then filtering the dark green solution into a cake; (d) rinsing the cake of step (c) with a solution comprising 5 wt.% hydrochloric acid (HCl) to remove sulfate ions, then washing the cake with distilled water; 20 (e) drying the cake of step (d) in an oven at 40 ° C for 2 hrs to obtain a dried solid graphite oxide; (f) adding distilled water to the dried solid graphite oxide of step (e), wherein the distilled water is added up to 200 m l s per 0.06 to 1.0 g of the dried solid graphite-21-oxide, then treating by ultrasonic vibration for 30 minutes to obtain a graphite oxide solution having a graphite oxide concentration of 0.03 wt. % to 0.5 wt. %; (g) adding a solution comprising 1 to 10 wt. % of a second compound selected from the group consisting of sodium borohydride (NaBH 4), potassium borohydride (KBH 4), 5 lithium aluminum hydride (LiA l H 4), and sodium citrate (C 6 H S Na 3 O 7) to the graphite oxide solution of step (f), then treating by ultrasonic vibration for 30 to 60 minutes, wherein in the resulting solution, the ratio of graphene oxide to the second compound is 1:1 to 1:5 by weight; (h) filtrating the product of step (g), washing the filtrate with water 3 to 5 times to 10 remove the second compound, then back-filtrating to obtain a graphene solution; (i) adding the graphene solution of step (h) to a slurry solution formed by mixing a pulp with N-methylmorpholine N-oxide (NMMO) and a stabilizer in an expansion dissolving tank, then mixing at 60 to 80 ° C, wherein the graphene solution of step (h) is added in a ratio of 0.11 to 5.0 wt. %, the pulp is selected from the group 15 consisting of wood pulp, cotton pulp, bamboo pulp and a mixture of cotton and bamboo pulp, the pulp comprises a-cellulose in an amount of 65 % or more with a polymerization degree of 500 to 1500; and the NMMO has a concentration of 50 % to 78 %; (j) removing water from the product of step (i) using a Thin Film Evaporator (TFE) 20 and heating at 80 to 130 ° C, wherein the water is removed to 5% to 13% within 5 minutes and the cellulose is dissolved to form a spinning dope, and the amount ratio of each component among the components comprised in the dope is: water (H 2 0) 5 % to 15 %, N-methylmorpholine N-oxide (N M MO) 70 % to 90 %, and -22-cellulose 5 % to 15 %; (k) Squeezing the spinning dope of step () from a spinning orifice by using a spunbond process to form a natural graphene cellulose blended filament strand, which comprises pressuring the spinning dope by a metering pump, filtering and 5 degassing by a continuous filter (CPF), transporting the spinning dope into a spinning tank, and stretching the spinning dope outward by air gap cooling through the spinning orifice, to form a natural graphene cellulose blended filament strand; and (1) feeding the natural graphene cellulose blended filament strand of step (k) into a 10 coagulation liquid, solidifying and regenerating the filament strand, stretching the filament strand under high pressure and high speed by an air stream drafting device, stacking the filament strand on a collection web to form a fibrous network structure, and washing, water needle punching, drying, oiling and coiling the fibrous network structure to form a natural graphene cellulose blended spunbond nonwoven fabric, 15 wherein the concentration of the coagulation liquid is between 2. 0% to 10.0 %, and after washing, the amount of residual N MM O solvent is less than 0.1 %.