A method of preparing natural graphene cellulose blended fiber, which comprises the following steps: (a) combining a graphite powder with a solution comprising 1 to 10 wt % of a first compound selected from the group consisting of sulfuric acid (H 2 S O 4), hydrochloric acid (HCl), perchloric acid (HC lO 4), hydrogen iodide (HI), hydrofluoric acid (HF), and nitric acid (HNO 3), then stirring for 30 minutes in an ice bath environment; (b) adding a solution comprising 1 to 10 wt. % potassium permanganate (KMn O 4) to the product of step (a), stirring for 1 to 2 hours, and adding distilled water, wherein a stoichiometric amount of the potassium permanganate solution is added until reaction of the potassium permanganate and the product of step (a) and the distilled water is complete; (c) adding a solution comprising 1 to 10 wt. % hydrogen peroxide (H 2 0 2) to the product of step (b), wherein a stoichiometric amount of the hydrogen peroxide solution is added until reaction between the hydrogen peroxide and the product of step (b) is complete and the solution becomes green, then filtering the green solution into a cake; (d) rinsing the cake of step (c) with a solution comprising 5 to 10 wt. % hydrochloric acid to remove sulfate ions, then washing the cake with distilled water; (e) drying the product of step (d) at 40 to 60 ° C for 24 to 48 hours to obtain 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 g to 1.0 g of the dried solid graphite oxide, then treating by ultrasonic vibration for 30 to 60 minutes to obtain a graphite oxide solution having a graphite oxide concentration of 0.03 to 0.5 wt. %; (g) adding a solution comprising 1 wt. % to 10 wt. % of a second compound selected from the group consisting of sodium borohydride (NaBH 4), potassium borohydride (KBH 4), lithium aluminum hydride (LiA l H 4), and sodium citrate (C 6 H 5 Na₃ O 7) to the graphite oxide solution of step (f), then treating by ultrasonic vibration for 30 to 60 minutes; (h) filtrating the product of step (g), washing the filtrate with water 3 to 5 times to remove the sodium borohydride, potassium borohydride, lithium aluminum hydride, or sodium citrate, 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 is added in a ratio of 0.11 wt. % to 5.0 wt. %, the pulp is selected from the group 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 having 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) 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; (k) spinning the spinning dope of step (j) using a Dry-Jet Wet Spinning method, which comprises pressuring the spinning dope by a metering pump, filtering and degassing by a continuous filter (CPF), transporting the spinning dope into a spinning tank, forming a thin molten stream of the spinning dope by passing the spinning dope through a spinning orifice, then extruding the spinning dope through an air gap to form air-cured fibers; (1) delivering the air-cured fibers of step (k) into a coagulation bath, then regenerating and washing the fibers, wherein the coagulation bath has a concentration of 4.5 to 8.0%, and the amount of residual NMMO solvent remaining after washing is less than 0.1%; and (m) drying, oiling and winding the product of step (1) to form natural graphene cellulose blended fibers. Currently amended

A method of preparing natural graphene cellulose blended fiber, which comprises the following steps: (a) combining a graphite powder with a solution comprising 1 to 10 wt % of a first compound selected from the group consisting of sulfuric acid (H 2 S O 4), hydrochloric acid (HCl), perchloric acid (HC lO 4), hydrogen iodide (HI), hydrofluoric acid (HF), and nitric acid (HNO 3), then stirring for 30 minutes in an ice bath environment; (b) adding a solution comprising 1 to 10 wt. % potassium permanganate (KMn O 4) to the product of step (a), stirring for 1 to 2 hours, and adding distilled water, wherein a stoichiometric amount of the potassium permanganate solution is added until reaction of the potassium permanganate and the product of step (a) and the distilled water is complete; (c) adding a solution comprising 1 to 10 wt. % hydrogen peroxide (H 2 0 2) to the product of step (b), wherein a stoichiometric amount of the hydrogen peroxide solution is added until reaction between the hydrogen peroxide and the product of step (b) is complete and the solution becomes green, then filtering the green solution into a cake; (d) rinsing the cake of step (c) with a solution comprising 5 to 10 wt. % hydrochloric acid to remove sulfate ions, then washing the cake with distilled water; (e) drying the product of step (d) at 40 to 60 ° C for 24 to 48 hours to obtain 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 g to 1.0 g of the dried solid graphite oxide, then treating by ultrasonic vibration for 30 to 60 minutes to obtain a graphite oxide solution having a graphite oxide concentration of 0.03 to 0.5 wt. %; (g) adding a solution comprising 1 wt. % to 10 wt. % of a second compound selected from the group consisting of sodium borohydride (NaBH 4), potassium borohydride (KBH 4), lithium aluminum hydride (LiA l H 4), and sodium citrate (C 6 H 5 Na₃ O 7) to the graphite oxide solution of step (f), then treating by ultrasonic vibration for 30 to 60 minutes; (h) filtrating the product of step (g), washing the filtrate with water 3 to 5 times to remove the sodium borohydride, potassium borohydride, lithium aluminum hydride, or sodium citrate, 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 is added in a ratio of 0.11 wt. % to 5.0 wt. %, the pulp is selected from the group 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 having 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) 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; (k) spinning the spinning dope of step (j) using a Dry-Jet Wet Spinning method, which comprises pressuring the spinning dope by a metering pump, filtering and degassing by a continuous filter (CPF), transporting the spinning dope into a spinning tank, forming a thin molten stream of the spinning dope by passing the spinning dope through a spinning orifice, then extruding the spinning dope through an air gap to form air-cured fibers; (1) delivering the air-cured fibers of step (k) into a coagulation bath, then regenerating and washing the fibers, wherein the coagulation bath has a concentration of 4.5 to 8.0%, and the amount of residual NMMO solvent remaining after washing is less than 0.1%; and (m) drying, oiling and winding the product of step (1) to form natural graphene cellulose blended fibers. Currently amended

A method of preparing natural graphene cellulose blended fiber, which comprises the following steps: (a) combining a graphite powder with a solution comprising 1 to 10 wt % of a first compound selected from the group consisting of sulfuric acid (H 2 S O 4), hydrochloric acid (HCl), perchloric acid (HC lO 4), hydrogen iodide (HI), hydrofluoric acid (HF), and nitric acid (HNO 3), then stirring for 30 minutes in an ice bath environment; (b) adding a solution comprising 1 to 10 wt. % potassium permanganate (KMn O 4) to the product of step (a), stirring for 1 to 2 hours, and adding distilled water, wherein a stoichiometric amount of the potassium permanganate solution is added until reaction of the potassium permanganate and the product of step (a) and the distilled water is complete; (c) adding a solution comprising 1 to 10 wt. % hydrogen peroxide (H 2 0 2) to the product of step (b), wherein a stoichiometric amount of the hydrogen peroxide solution is added until reaction between the hydrogen peroxide and the product of step (b) is complete and the solution becomes green, then filtering the green solution into a cake; (d) rinsing the cake of step (c) with a solution comprising 5 to 10 wt. % hydrochloric acid to remove sulfate ions, then washing the cake with distilled water; (e) drying the product of step (d) at 40 to 60 ° C for 24 to 48 hours to obtain 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 g to 1.0 g of the dried solid graphite oxide, then treating by ultrasonic vibration for 30 to 60 minutes to obtain a graphite oxide solution having a graphite oxide concentration of 0.03 to 0.5 wt. %; (g) adding a solution comprising 1 wt. % to 10 wt. % of a second compound selected from the group consisting of sodium borohydride (NaBH 4), potassium borohydride (KBH 4), lithium aluminum hydride (LiA l H 4), and sodium citrate (C 6 H 5 Na₃ O 7) to the graphite oxide solution of step (f), then treating by ultrasonic vibration for 30 to 60 minutes; (h) filtrating the product of step (g), washing the filtrate with water 3 to 5 times to remove the sodium borohydride, potassium borohydride, lithium aluminum hydride, or sodium citrate, 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 is added in a ratio of 0.11 wt. % to 5.0 wt. %, the pulp is selected from the group 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 having 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) 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; (k) spinning the spinning dope of step (j) using a Dry-Jet Wet Spinning method, which comprises pressuring the spinning dope by a metering pump, filtering and degassing by a continuous filter (CPF), transporting the spinning dope into a spinning tank, forming a thin molten stream of the spinning dope by passing the spinning dope through a spinning orifice, then extruding the spinning dope through an air gap to form air-cured fibers; (1) delivering the air-cured fibers of step (k) into a coagulation bath, then regenerating and washing the fibers, wherein the coagulation bath has a concentration of 4.5 to 8.0%, and the amount of residual NMMO solvent remaining after washing is less than 0.1%; and (m) drying, oiling and winding the product of step (1) to form natural graphene cellulose blended fibers. Currently amended

A method of preparing natural graphene cellulose blended fiber, which comprises the following steps: (a) combining a graphite powder with a solution comprising 1 to 10 wt % of a first compound selected from the group consisting of sulfuric acid (H 2 S O 4), hydrochloric acid (HCl), perchloric acid (HC lO 4), hydrogen iodide (HI), hydrofluoric acid (HF), and nitric acid (HNO 3), then stirring for 30 minutes in an ice bath environment; (b) adding a solution comprising 1 to 10 wt. % potassium permanganate (KMn O 4) to the product of step (a), stirring for 1 to 2 hours, and adding distilled water, wherein a stoichiometric amount of the potassium permanganate solution is added until reaction of the potassium permanganate and the product of step (a) and the distilled water is complete; (c) adding a solution comprising 1 to 10 wt. % hydrogen peroxide (H 2 0 2) to the product of step (b), wherein a stoichiometric amount of the hydrogen peroxide solution is added until reaction between the hydrogen peroxide and the product of step (b) is complete and the solution becomes green, then filtering the green solution into a cake; (d) rinsing the cake of step (c) with a solution comprising 5 to 10 wt. % hydrochloric acid to remove sulfate ions, then washing the cake with distilled water; (e) drying the product of step (d) at 40 to 60 ° C for 24 to 48 hours to obtain 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 g to 1.0 g of the dried solid graphite oxide, then treating by ultrasonic vibration for 30 to 60 minutes to obtain a graphite oxide solution having a graphite oxide concentration of 0.03 to 0.5 wt. %; (g) adding a solution comprising 1 wt. % to 10 wt. % of a second compound selected from the group consisting of sodium borohydride (NaBH 4), potassium borohydride (KBH 4), lithium aluminum hydride (LiA l H 4), and sodium citrate (C 6 H 5 Na₃ O 7) to the graphite oxide solution of step (f), then treating by ultrasonic vibration for 30 to 60 minutes; (h) filtrating the product of step (g), washing the filtrate with water 3 to 5 times to remove the sodium borohydride, potassium borohydride, lithium aluminum hydride, or sodium citrate, 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 is added in a ratio of 0.11 wt. % to 5.0 wt. %, the pulp is selected from the group 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 having 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) 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; (k) spinning the spinning dope of step (j) using a Dry-Jet Wet Spinning method, which comprises pressuring the spinning dope by a metering pump, filtering and degassing by a continuous filter (CPF), transporting the spinning dope into a spinning tank, forming a thin molten stream of the spinning dope by passing the spinning dope through a spinning orifice, then extruding the spinning dope through an air gap to form air-cured fibers; (1) delivering the air-cured fibers of step (k) into a coagulation bath, then regenerating and washing the fibers, wherein the coagulation bath has a concentration of 4.5 to 8.0%, and the amount of residual NMMO solvent remaining after washing is less than 0.1%; and (m) drying, oiling and winding the product of step (1) to form natural graphene cellulose blended fibers. Currently amended