CN105712335A - Physical stripping method for graphene - Google Patents

Physical stripping method for graphene Download PDF

Info

Publication number
CN105712335A
CN105712335A CN201410711077.XA CN201410711077A CN105712335A CN 105712335 A CN105712335 A CN 105712335A CN 201410711077 A CN201410711077 A CN 201410711077A CN 105712335 A CN105712335 A CN 105712335A
Authority
CN
China
Prior art keywords
graphene
parts
filter cake
physical separation
separation methods
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
CN201410711077.XA
Other languages
Chinese (zh)
Inventor
戴加龙
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
JIANGYIN TANGU TECHNOLOGY Co Ltd
Original Assignee
JIANGYIN TANGU TECHNOLOGY Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by JIANGYIN TANGU TECHNOLOGY Co Ltd filed Critical JIANGYIN TANGU TECHNOLOGY Co Ltd
Priority to CN201410711077.XA priority Critical patent/CN105712335A/en
Publication of CN105712335A publication Critical patent/CN105712335A/en
Pending legal-status Critical Current

Links

Landscapes

  • Battery Electrode And Active Subsutance (AREA)
  • Carbon And Carbon Compounds (AREA)

Abstract

The invention discloses a physical stripping method for graphene. The method comprises the steps of: S1. injecting graphite scale and a stripping solution into a stirrer equipped kettle body, starting a motor of the kettle body to perform stirring so as to mix materials evenly, wherein the stripping solution comprises 100 parts of an alcohol solvent, 3-20 parts of hydroxy acrylic resin, and 1-30 parts of sheet metal powder; S2. heating the kettle body, keeping the internal temperature of the kettle body at 50DEG C-80DEG C, the pressure at 1-3atm and the stirring shaft rotation speed at 1000-2000rpm/min, and carrying out reaction for 3-6h; S3. at the end of the reaction, discharging the upper suspension solution into a storage tank to perform standing; S4. transporting the graphene suspension solution into a centrifuge to conduct centrifugation, then taking the supernatant, and carrying out vacuum filtration to obtain a filter cake; and S5. washing the filter cake, and carrying out freeze drying, thus obtaining a graphene product. The stripping method can strip graphene, at the same time does not corrode equipment, and causes no damage to the graphene structure.

Description

A kind of Graphene physical separation methods
Technical field
The present invention relates to Graphene production technical field, be specifically related to a kind of Graphene stripping means.
Background technology
Graphene is a kind of two-dimensional material with good flexibility, electrical property.You need to add is that, stricti jurise is said, Graphene is the lamellar of a kind of monolayer;But due to the preparation difficulty of single-layer graphene, generally also the form the few-layer graphene alkene with similar performance is also ranged in the category of Graphene.
At present, the method that prepared by Graphene mainly has: chemically grown method and physics stripping method.Low compared to efficiency, be not suitable for the chemically grown method of industrialized mass production; it is raw material that physics stripping method mainly adopts cheap graphite; make graphite layers peeling-off by graphite crystal is applied mechanical force; break the Van der Waals force of graphite layers; forming monolithic graphite alkene or form the few-layer graphene alkene, this physical separation methods has more industrial prospect and applicable large-scale production.
In Graphene stripping means, it is necessary to add some auxiliary agents to increase the interlayer distance of graphite or so-called intercalation, so that graphite is peeled off better.As adopted nitric acid, potassium permanganate, chromic acid or hydrogen peroxide as oxidant, concentrated sulphuric acid, as intercalator, introduces the oxy radicals such as hydroxyl, epoxide group and carboxyl at graphite layers or edge, increase graphite layers from, be beneficial to follow-up graphite layers and peel off.But this chemical substance intercalated technique acid consumption is big, production process has the pollution of the harmful gass such as SOx, NOx or heavy metal ion, product there is sulfur remain, the Graphene finally given is easily generated defect, and in the application equipment there is is corrosion, reduce the service life of equipment, add production cost.
Summary of the invention
It is an object of the invention to overcome the defect existed in prior art, it is provided that a kind of Graphene physical separation methods, the method can be efficiently peeled off graphite, and the structural deterioration of Graphene is little.
For realizing the purpose of the present invention, the technical scheme is that a kind of Graphene physical separation methods, the method comprises the following steps:
S1. by purity more than 98%, particle diameter is that 30 ~ 500 μm of graphite flakes and stripper inject in the kettle with agitator according to the weight ratio of 1:2~5, and the motor starting kettle is stirred, and makes mixing of materials uniform, wherein the consisting of of stripper:
Alcohols solvent 100 parts,
Hydroxylated acrylic resin 3~20 parts,
Flake metal powder 1~30 part;
Wherein, each component is in its parts by weight.
S2. heating kettle, keeping still body temperature is 50 DEG C ~ 80 DEG C, and pressure is 1-3atm, and agitator shaft speed is 1000 ~ 2000rpm/min, response time 3 ~ 6h;
S3. by discharging opening, upper strata suspension is expelled in storage tank after stopped reaction, stands 24h head product derived above;
S4. the graphene suspension in the storage tank obtained by step S3 is delivered in centrifuge, and centrifuge speed is 1000-6000rpm/min, and centrifugation time 10min-2h takes the supernatant, and in vacuum apparatus, vacuum is filtrated to get filter cake;
S5. filter cake step S4 obtained with appropriate distilled water wash, filter cake more than lyophilization 3h in freeze drying plant, namely obtain graphene product.
Preferred technical scheme is, in step sl, described alcohols solvent is one or more in ethanol, normal propyl alcohol, n-butyl alcohol, propylene glycol and terpineol.
Preferred technical scheme is, in step sl, described flake metal powder is one or more in zinc powder, nikel powder, argentum powder.
It is preferred that technical scheme be that in step sl, described flake metal powder is of a size of 3~10 microns.
Preferred technical scheme is, in step sl, the number-average molecular weight of described Hydroxylated acrylic resin is 10000~20000.
Prior art is compared, and Graphene physical separation methods of the present invention, by adopting special stripper for the stripping of Graphene, adopts flake metal powder as abrasive media, it is possible to produce uniform peeling force on graphite flake layer in this stripper;Flake metal powder coordinates the alcohols solvent and Hydroxylated acrylic resin that can penetrate in graphite flake layer, by forming hydrogen bond between alcohols solvent and Hydroxylated acrylic resin, grinding the heat produced or making hydrogen bond destroy by the mode of external heat, thus graphite linings is produced impulsive force, form inside and outside pincer attack, be effectively facilitated the stripping of Graphene.This stripping means is being peeled off while Graphene, and not etching apparatus does not damage graphene-structured.
Detailed description of the invention
Below in conjunction with embodiment, the specific embodiment of the present invention is further described.Following example are only for clearly illustrating technical scheme, and can not limit the scope of the invention with this.
Embodiment 1
The present invention is a kind of Graphene physical separation methods, and the method comprises the following steps:
S1. by purity more than 98%, particle diameter is in 30 ~ 500 μm of graphite flakes and the stripper injection kettle with agitator, the motor starting kettle is stirred, make mixing of materials uniform, wherein the consisting of of stripper: ethanol 100 parts by weight, Hydroxylated acrylic resin 3 parts by weight, zinc flake 1 parts by weight.Wherein, zinc flake is of a size of 3~10 microns;The number-average molecular weight of Hydroxylated acrylic resin is 10000~20000.The weight ratio of graphite flakes and stripper is 1:5.
S2. heating kettle, keeping still body temperature is 80 DEG C, and pressure is 1atm, and agitator shaft speed is 1000rpm/min, response time 3h.
S3. by discharging opening, upper strata suspension is expelled in storage tank after stopped reaction, stands 24h head product derived above.
S4. the graphene suspension in the storage tank obtained by step S3 is delivered in centrifuge, and centrifuge speed is 1000rpm/min, and centrifugation time 2h takes the supernatant, and in vacuum apparatus, vacuum is filtrated to get filter cake.
S5. filter cake step S4 obtained with appropriate distilled water wash, filter cake more than lyophilization 3h in freeze drying plant, namely obtain graphene product.
Embodiment 2
The present invention is a kind of Graphene physical separation methods, and the method comprises the following steps:
S1. by purity more than 98%, particle diameter is in 30 ~ 500 μm of graphite flakes and the stripper injection kettle with agitator, the motor starting kettle is stirred, make mixing of materials uniform, wherein the consisting of of stripper: normal propyl alcohol 100 parts by weight, Hydroxylated acrylic resin 10 parts by weight, Nickel Powder 20 parts by weight.Wherein, Nickel Powder is of a size of 3~10 microns;The number-average molecular weight of Hydroxylated acrylic resin is 10000~20000.The weight ratio of graphite flakes and stripper is 1:4.
S2. heating kettle, keeping still body temperature is 50 DEG C, and pressure is 3atm, and agitator shaft speed is 2000rpm/min, response time 6h.
S3. by discharging opening, upper strata suspension is expelled in storage tank after stopped reaction, stands 24h head product derived above.
S4. the graphene suspension in the storage tank obtained by step S3 is delivered in centrifuge, and centrifuge speed is 4000rpm/min, and centrifugation time 20min takes the supernatant, and in vacuum apparatus, vacuum is filtrated to get filter cake.
S5. filter cake step S4 obtained with appropriate distilled water wash, filter cake more than lyophilization 3h in freeze drying plant, namely obtain graphene product.
Embodiment 3
The present invention is a kind of Graphene physical separation methods, and the method comprises the following steps:
S1. by purity more than 98%, particle diameter is in 30 ~ 500 μm of graphite flakes and the stripper injection kettle with agitator, the motor starting kettle is stirred, make mixing of materials uniform, wherein the consisting of of stripper: n-butyl alcohol 70 parts by weight, propylene glycol 30 parts by weight, Hydroxylated acrylic resin 15 parts by weight, flake silver powder 30 parts by weight.Wherein, flake silver powder is of a size of 3~10 microns;The number-average molecular weight of Hydroxylated acrylic resin is 10000~20000.The weight ratio of graphite flakes and stripper is 1:3.
S2. heating kettle, keeping still body temperature is 60 DEG C, and pressure is 2atm, and agitator shaft speed is 1500rpm/min, response time 5h.
S3. by discharging opening, upper strata suspension is expelled in storage tank after stopped reaction, stands 24h head product derived above.
S4. the graphene suspension in the storage tank obtained by step S3 is delivered in centrifuge, and centrifuge speed is 6000rpm/min, and centrifugation time 10min takes the supernatant, and in vacuum apparatus, vacuum is filtrated to get filter cake.
S5. filter cake step S4 obtained with appropriate distilled water wash, filter cake more than lyophilization 3h in freeze drying plant, namely obtain graphene product.
Embodiment 4
The present invention is a kind of Graphene physical separation methods, and the method comprises the following steps:
S1. by purity more than 98%, particle diameter is in 30 ~ 500 μm of graphite flakes and the stripper injection kettle with agitator, the motor starting kettle is stirred, make mixing of materials uniform, wherein the consisting of of stripper: terpineol 100 parts by weight, Hydroxylated acrylic resin 20 parts by weight, flake silver powder 10 parts by weight, Nickel Powder 10 parts.Wherein, flake silver powder and Nickel Powder are of a size of 3~10 microns;The number-average molecular weight of Hydroxylated acrylic resin is 10000~20000.The weight ratio of graphite flakes and stripper is 1:1.
S2. heating kettle, keeping still body temperature is 70 DEG C, and pressure is 2.5atm, and agitator shaft speed is 1500rpm/min, response time 4h.
S3. by discharging opening, upper strata suspension is expelled in storage tank after stopped reaction, stands 24h head product derived above.
S4. the graphene suspension in the storage tank obtained by step S3 is delivered in centrifuge, and centrifuge speed is 2000rpm/min, and centrifugation time 1h takes the supernatant, and in vacuum apparatus, vacuum is filtrated to get filter cake.
S5. filter cake step S4 obtained with appropriate distilled water wash, filter cake more than lyophilization 3h in freeze drying plant, namely obtain graphene product.
The above is only the preferred embodiment of the present invention; it should be pointed out that, for those skilled in the art, under the premise without departing from the technology of the present invention principle; can also making some improvements and modifications, these improvements and modifications also should be regarded as protection scope of the present invention.

Claims (5)

1. a Graphene physical separation methods, it is characterised in that the method comprises the following steps:
S1. by purity more than 98%, particle diameter is that 30 ~ 500 μm of graphite flakes and stripper inject in the kettle with agitator according to the weight ratio of 1:2~5, and the motor starting kettle is stirred, and makes mixing of materials uniform, wherein the consisting of of stripper:
Alcohols solvent 100 parts,
Hydroxylated acrylic resin 3~20 parts,
Flake metal powder 1~30 part;
Wherein, each component is in its parts by weight;
S2. heating kettle, keeping still body temperature is 50 DEG C ~ 80 DEG C, and pressure is 1-3atm, and agitator shaft speed is 1000 ~ 2000rpm/min, response time 3~6h;
S3. by discharging opening, upper strata suspension is expelled in storage tank after stopped reaction, stands 24h head product derived above;
S4. the graphene suspension in the storage tank obtained by step S3 is delivered in centrifuge, and centrifuge speed is 1000-6000rpm/min, and centrifugation time 10min-2h takes the supernatant, and in vacuum apparatus, vacuum is filtrated to get filter cake;
S5. filter cake step S4 obtained with appropriate distilled water wash, filter cake more than lyophilization 3h in freeze drying plant, namely obtain graphene product.
2. Graphene physical separation methods as claimed in claim 1, it is characterised in that in described step S1, described alcohols solvent is one or more in ethanol, normal propyl alcohol, n-butyl alcohol, propylene glycol and terpineol.
3. Graphene physical separation methods as claimed in claim 1, it is characterised in that in described step S1, described flake metal powder is one or more in zinc powder, nikel powder, argentum powder.
4. Graphene physical separation methods as claimed in claim 3, it is characterised in that in described step S1, described flake metal powder is of a size of 3~10 microns.
5. Graphene physical separation methods as claimed in claim 1, it is characterised in that in described step S1, the number-average molecular weight of described Hydroxylated acrylic resin is 10000~20000.
CN201410711077.XA 2014-12-01 2014-12-01 Physical stripping method for graphene Pending CN105712335A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201410711077.XA CN105712335A (en) 2014-12-01 2014-12-01 Physical stripping method for graphene

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201410711077.XA CN105712335A (en) 2014-12-01 2014-12-01 Physical stripping method for graphene

Publications (1)

Publication Number Publication Date
CN105712335A true CN105712335A (en) 2016-06-29

Family

ID=56145846

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201410711077.XA Pending CN105712335A (en) 2014-12-01 2014-12-01 Physical stripping method for graphene

Country Status (1)

Country Link
CN (1) CN105712335A (en)

Similar Documents

Publication Publication Date Title
US10472243B2 (en) Industrial method for preparing large-sized graphene
CN104386678B (en) A kind of preparation method of Graphene
CN108529679B (en) Method for preparing molybdenum disulfide nanosheet through polyol stripping
CN105776193A (en) Method for preparing graphene nanoplatelets with pulsed high pressure water jet mill
Wen et al. Preparation of graphene by exfoliation and its application in lithium-ion batteries
CN105645383A (en) Efficient graphene stripping method
CN105712333A (en) Physical striping method of graphene
CN105712335A (en) Physical stripping method for graphene
CN106751263A (en) Stannic oxide/graphene nano lamella strengthens the preparation method of polyvinyl alcohol composite material
CN105712338A (en) Graphene preparation method
CN105712336A (en) Physical stripping production method for graphene
CN105712324A (en) Graphene viscous-state stripping production method
CN105712341A (en) High efficiency graphene stripping method
CN105712322A (en) Method for producing bulky graphene
CN105883768A (en) Extraction method of graphene
CN105883759A (en) Graphene industrial production method
CN105883776A (en) Method for producing graphene on large scale
CN105712342A (en) Graphene stripping method
CN105621397A (en) Large graphene stripping production method
CN105883770A (en) Graphene production method
CN105712326A (en) Method for producing graphene
CN105883763A (en) Efficient preparation method of graphene
CN105712325A (en) Method for stripping graphene
CN105712320A (en) Method for stripping graphene
CN105883764A (en) Macroscopic-quantity preparation method of graphene

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
WD01 Invention patent application deemed withdrawn after publication

Application publication date: 20160629

WD01 Invention patent application deemed withdrawn after publication