CN102912625B - Preparation method of bacterial-cellulose-based generating fiber and yarn - Google Patents
Preparation method of bacterial-cellulose-based generating fiber and yarn Download PDFInfo
- Publication number
- CN102912625B CN102912625B CN201210412225.9A CN201210412225A CN102912625B CN 102912625 B CN102912625 B CN 102912625B CN 201210412225 A CN201210412225 A CN 201210412225A CN 102912625 B CN102912625 B CN 102912625B
- Authority
- CN
- China
- Prior art keywords
- bacteria cellulose
- cellulose
- solution
- bacterial
- preparation
- 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.)
- Expired - Fee Related
Links
Landscapes
- Artificial Filaments (AREA)
- Chemical Or Physical Treatment Of Fibers (AREA)
Abstract
Disclosed is a preparation method of bacterial-cellulose-based generating fiber. The preparation method includes performing vacuum sputtering by metal zinc or evaporation deposition to ultrafine ribbon of bacterial cellulose to obtain bacterial cellulose B, and extracting for standby; placing the bacterial cellulose B into amine salt solution for reaction for a certain time to obtain bacterial cellulose C; dipping the bacterial cellulose C in conductive solvent; and preparing bacterial cellulose fiber which has generation performance. The prepared finished product is bacterial-cellulose-based generating fiber and yarn, which can be deeply processed by the existing spinning and weaving technology. Mechanical generating components different in scale are formed, and the bacterial-cellulose-based generating fiber and yarn are widely applied to fields, which have requirements for different sizes and powers of self-generating components, such as environment monitoring, biochips implanted into bodies, cars, buildings and military industries.
Description
Technical field
The present invention relates to the preparation method of a kind of bacteria cellulose base generating fiber and yarn, particularly a kind ofly can be applied to the generate electricity preparation method of fiber and yarn of miniature, high-performance electronic apparatus and the bacteria cellulose base of the self-powered of sensor.
Background technology
Along with the development of economic society, electricity has been a part indispensable in society.The present power status of China is city short of electricity, remote without electricity, spring and autumn paddy, summer in winter peak.Although the engineering of transferring electricity from the west to the east has been opened by country, the power loss of long distance powedr transmission and high track laying expense make the cost of electric power go up not down.The data demonstration that China Electricity Council issues, within 2011, China's power consumption reaches 4.69 trillion kilowatt hours, increases by 11.7% on a year-on-year basis.Within 2010, the maximum breach of power supply and demand is 3,000 ten thousand kilowatts; Meeting maximum breach during the kurtosis summer is 2,500 ten thousand kilowatts.At present, generated energy far can not meet the demand of economic growth.
But capacity of installed generator also reducing year by year, within 2011, the newly-increased capacity of installed generator in the whole nation has exceeded 9,000 ten thousand kilowatts, but the scale in fact effectively increasing reduces.Thermoelectricity is China generating main force, but thermoelectricity loses year after year and make electricity enterprise lose investment drive and ability, and thermoelectricity investment declines continuously and healthily, is reduced to fast 1,054 hundred million yuan in 2011 by 2,271 hundred million yuan in 2005.The variation of weather causes occurring that extremely cold, very hot weather and electric coal price lattice continue the anxiety that run at high level has also aggravated electricity consumption.Therefore, a few years from now on electric power breach will continue to expand certainly, estimate will reach for 2012 5000 ten thousand kilowatts.Electric power supply is not enough causes " hard short of electricity " phenomenon unavoidable.Moreover from far-off regions due to landform and fund, a lot of local power supplies are restricted does not even also switch on.Military combat, interchange, traffic etc. when pleasure trip on foot are because entrained electric weight is limited and can not remain permanent, for meagrely-populated region, the supply of power equipment is also a problem, current all more complicated and big energy-consumings of large-scale TRT, the manufacture of small-sized electric generating apparatus, reclaim and improperly all can cause very large harm to environment.Therefore, the Technology Need that we are present, the self power generation of generating electricity, to improve electricity usage efficiency, reduces electric power conveying process, reduces costs, and from life, immediately obtains our needed electric energy.
The development of microelectronics and micro-fabrication technology makes the micro-system such as wireless sense network and microactrator be widely used in environmental monitoring, body and is implanted into biochip, automobile, building, the key areas such as military.Along with going deep into of research, the pursuit to function of MEMS is more and more stronger, more and more lower to the requirement of power consumption, the research that volume and size have been entered to nanoscale.
Nanometer technology, as the important emerge science technical field of 21 century, is just experiencing high speed development in theory and practice.A large amount of novel nano device and materials are constantly developed, for people's life brings more facility.Meanwhile, be also that we have brought the clean technologies that solve energy crisis from microelectric technique research aspect.
But Nano-technology Development is to today, large quantity research is all to concentrate on to develop high sensitivity, high performance nano-device, almost without any the research of the power-supply system about nanoscale.But the nano-sensor that is applied to the aspects such as biological national defence is urgent all the more because of the lifting of technology to the demand of this power supply.In general the power supply of these devices is all directly or indirectly to derive from battery.Sensor can provide power supply to oneself from own in object, thereby the miniaturization that simultaneously realizes device and power supply is the target of researcher's Recent study.
Since Curie brother finds that in quartz crystal piezo-electric effect starts, people are just devoted to mechanical energy to be converted into the research of electric energy always.Conventional piezoelectric, because of its electric property, although can form potential change, can not form the Schottky barrier with unilateral conduction as metal, thereby can not reach this process of release that gathers of energy.Thereby piezoelectric circuit generally needs a complicated external circuits to complete the output of electric energy now.And conventional piezoelectric causes piezoelectric structure can not accomplish miniaturization because crystal structure is too complicated, say nothing of the high-quality piezoelectric structure of nanoscale.But when the metal oxide such as zinc oxide and silica enters after the research category of piezoelectric fabric, its simple chemical composition and crystal structure bring up the easy control of its purity, size, pattern.It becomes rapidly the important materials of current piezoelectric research as the electric conductivity of metal oxide with as the power generation performance of piezoelectric excellence.
The scientist Wang Zhonglin leader's of Chinese origin of the georgia ,u.s.a Institute of Technology in 2006 scientific research group develops a kind of novel plated zinc oxide nanofiber that can produce electric energy, and at motor driving because piezo-electric effect produces electric energy; The U.S. in 2011 and Chinese scientist's joint study have gone out taking zinc oxide nanowire as basic a kind of piezoelectric nano generator, realized on nanoscale mechanical energy is converted into electric energy.But present material, because of the sharply reduction mediocre and efficiency under wet environment of its overall work efficiency, can not come into operation well.
Summary of the invention
Order of the present invention is to provide the preparation method of a kind of bacteria cellulose base generating fiber and yarn.The prepared nanometer bacteria cellulose base of the present invention generating fiber and yarn can be applied to environmental monitoring, body and be implanted into biochip, automobile, building, the important field that needs microdevice miniature self-generating source corresponding thereto such as military.
For achieving the above object, the technical solution used in the present invention is as follows:
The preparation method of bacteria cellulose base generating fiber of the present invention, comprises the steps:
(1) bacterial cellulose wet-coating after bleaching is placed between a pair of gripping roller, according to the speed feeding of 10 mm ~ 100 m/ minutes;
(2) puncture, isolate and combing effect at a high speed through licker-in surface acupuncture from the cellulose membrane of exporting between roller, bacterial cellulose wet-coating is become to bacteria cellulose fibre; Bacteria cellulose fibre, through filter press press filtration processing, is prepared to bacteria cellulose superfine fibre bar; Take out postlyophilization, stand-by;
(3) bacteria cellulose superfine fibre bar is carried out to metallic zinc vacuum sputtering or vapor deposition treatment, obtain bacteria cellulose B, take out stand-by;
(4) bacteria cellulose B is put into amine salt solution, reaction a period of time, form bacteria cellulose C, take out postlyophilization, then in 60-100 DEG C of thermal environment, place, stand-by;
(5) bacteria cellulose C is carried out to solution immersion treatment; Prepare the bacteria cellulose fibre with power generation performance.
The diameter of the gripping roller using in step (1) is 20 ~ 3000mm.
In step (2), the moisture content of the bacteria cellulose super fiber of process press filtration processing is between 15% ~ 50000%, and the diameter of superfine fibre is at 10 ~ 500nm, and superfine fibre length is between 200nm ~ 200mm.
Amine salt solution described in step (4) is a kind of of hexa, urea, ammoniacal liquor, monoethanolamine, diethanol amine, triethanolamine solution or their mixed solution, in solution, amine ion concentration is 0.01mol/L, bacteria cellulose B is 1:1-1:10 with the mass ratio of the amine salt solution of putting into, 20 ~ 100 DEG C of reaction temperatures, the reaction time is 2 ~ 72 hours.
Step is carried out solution immersion treatment by bacteria cellulose C described in (5), described solution is that CNT, Graphene, polyaniline nano fiber, poly-pyrene are coughed up a kind of in the alcoholic solution of nanofiber or their mixed liquor, the mass concentration of solution is 1%, the mass ratio of solution and bacteria cellulose fibre is 1:1, and the immersion treatment time is 24 ~ 72 hours.
Adopt bacteria cellulose base generating fiber spinning of the present invention to obtain bacteria cellulose base generating yarn of the present invention.
Adopt bacteria cellulose base generating fiber spinning of the present invention to obtain yarn.The made finished product of the present invention is bacteria cellulose base generating fiber and yarn, can carry out deep processing by existing weaving weaving technology.Can form the mechanical electrification component of different scales yardstick, be widely used in environmental monitoring, body and be implanted into biochip, automobile, building, the field that self power generation assembly is had to different size power requirement such as military.
Detailed description of the invention
Below in conjunction with specific embodiment, further set forth the present invention.
Embodiment 1
(1) bacterial cellulose wet-coating after bleaching is placed between a pair of gripping roller, according to the speed feeding of 10 mm ~ 100 m/ minutes; The diameter of the gripping roller using is 20 ~ 3000mm.
(2) puncture, isolate and combing effect at a high speed through licker-in surface acupuncture from the cellulose membrane of exporting between roller, bacterial cellulose wet-coating is become to bacteria cellulose fibre; Bacteria cellulose fibre, through filter press press filtration processing, is prepared to bacteria cellulose superfine fibre bar; Take out postlyophilization, stand-by; The moisture content of the bacteria cellulose super fiber of process press filtration processing is between 15% ~ 50000%, and the diameter of superfine fibre is at 10 ~ 500nm, and superfine fibre length is between 200nm ~ 200mm.
(3) bacteria cellulose superfine fibre bar is carried out to metallic zinc vacuum sputtering or vapor deposition treatment, obtain bacteria cellulose B, take out stand-by;
(4) bacteria cellulose B is put into amine salt solution, reaction a period of time, form bacteria cellulose C, take out postlyophilization, then in 60-100 DEG C of thermal environment, place, stand-by; Described amine salt solution is a kind of of hexa, urea, ammoniacal liquor, monoethanolamine, diethanol amine, triethanolamine solution or their mixture, bacteria cellulose B is 1:1-1:10 with the mass ratio of the amine salt solution of putting into, 20 ~ 100 DEG C of reaction temperatures, the reaction time is 2 ~ 72 hours.
(5) bacteria cellulose C is carried out to solution immersion treatment; Prepare the bacteria cellulose fibre with power generation performance, described solution is that CNT, Graphene, polyaniline nano fiber, poly-pyrene are coughed up a kind of in nanofiber alcoholic solution or their mixed liquor, the mass concentration of solution is 1%, the mass ratio of solution and bacteria cellulose fibre is 1:1, and the immersion treatment time is 24 ~ 72 hours.
The bacteria cellulose base generating fiber spinning that employing obtains obtains bacteria cellulose base generating yarn of the present invention.The yarn of one section of 10 centimeter length, under ultrasonic oscillation disposition, detects the current output signal of 35nA through galvanometer.
Embodiment 2
(1) bacterial cellulose wet-coating after bleaching is placed between a pair of gripping roller, according to the speed feeding of 10 mm m/ minutes; The diameter of the gripping roller using is 20mm.
(2) puncture, isolate and combing effect at a high speed through licker-in surface acupuncture from the cellulose membrane of exporting between roller, bacterial cellulose wet-coating is become to bacteria cellulose fibre; Bacteria cellulose fibre, through filter press press filtration processing, is prepared to bacteria cellulose superfine fibre bar; Take out postlyophilization, stand-by; The moisture content of the bacteria cellulose super fiber of process press filtration processing is between 15%, and the diameter of superfine fibre is at 10nm, and superfine fibre length is between 200nm.
(3) bacteria cellulose superfine fibre bar is carried out to metallic zinc vacuum sputtering or vapor deposition treatment, obtain bacteria cellulose B, take out stand-by;
(4) bacteria cellulose B is put into amine salt solution, reaction a period of time, form bacteria cellulose C, take out postlyophilization, then in 60 DEG C of thermal environments, place, stand-by; Described amine salt solution is hexa solution, and bacteria cellulose B is 1:1 with the mass ratio of the amine salt solution of putting into, 20 DEG C of reaction temperatures, and the reaction time is 72 hours.
(5) bacteria cellulose C is carried out to solution immersion treatment; Prepare the bacteria cellulose fibre with power generation performance, described solution is CNT alcoholic solution, and the mass concentration of solution is 1%, and the mass ratio of solution and bacteria cellulose fibre is 1:1, and the immersion treatment time is 24 hours.
The bacteria cellulose base generating fiber spinning that employing obtains obtains bacteria cellulose base generating yarn of the present invention.The yarn of one section of 10 centimeter length, under ultrasonic oscillation disposition, detects the current output signal of 38nA through galvanometer.
Embodiment 3
(1) bacterial cellulose wet-coating after bleaching is placed between a pair of gripping roller, according to the speed feeding of 100 m/ minutes; The diameter of the gripping roller using is 3000mm.
(2) puncture, isolate and combing effect at a high speed through licker-in surface acupuncture from the cellulose membrane of exporting between roller, bacterial cellulose wet-coating is become to bacteria cellulose fibre; Bacteria cellulose fibre, through filter press press filtration processing, is prepared to bacteria cellulose superfine fibre bar; Take out postlyophilization, stand-by; The moisture content of the bacteria cellulose super fiber of process press filtration processing is between 50000%, and the diameter of superfine fibre is at 500nm, and superfine fibre length is between 200mm.
(3) bacteria cellulose superfine fibre bar is carried out to metallic zinc vacuum sputtering or vapor deposition treatment, obtain bacteria cellulose B, take out stand-by;
(4) bacteria cellulose B is put into amine salt solution, reaction a period of time, form bacteria cellulose C, take out postlyophilization, then in 100 DEG C of thermal environments, place, stand-by; Described amine salt solution is urea liquid, and bacteria cellulose B is 1:10 with the mass ratio of the amine salt solution of putting into, 100 DEG C of reaction temperatures, and the reaction time is 2 hours.
(5) bacteria cellulose C is carried out to solution immersion treatment; Prepare the bacteria cellulose fibre with power generation performance, described solution is Graphene and alcohol, and the mass concentration of solution is 1%, and the mass ratio of solution and bacteria cellulose fibre is 1:1, and the immersion treatment time is 24 ~ 72 hours.
The bacteria cellulose base generating fiber spinning that employing obtains obtains bacteria cellulose base generating yarn of the present invention.The yarn of one section of 10 centimeter length, under ultrasonic oscillation disposition, detects the current output signal of 42nA through galvanometer.
Embodiment 4
(1) bacterial cellulose wet-coating after bleaching is placed between a pair of gripping roller, according to the speed feeding of 20 m/ minutes; The diameter of the gripping roller using is 300mm.
(2) puncture, isolate and combing effect at a high speed through licker-in surface acupuncture from the cellulose membrane of exporting between roller, bacterial cellulose wet-coating is become to bacteria cellulose fibre; Bacteria cellulose fibre, through filter press press filtration processing, is prepared to bacteria cellulose superfine fibre bar; Take out postlyophilization, stand-by; The moisture content of the bacteria cellulose super fiber of process press filtration processing is between 200%, and the diameter of superfine fibre is at 100nm, and superfine fibre length is between 100mm.
(3) bacteria cellulose superfine fibre bar is carried out to metallic zinc vacuum sputtering or vapor deposition treatment, obtain bacteria cellulose B, take out stand-by;
(4) bacteria cellulose B is put into amine salt solution, reaction a period of time, form bacteria cellulose C, take out postlyophilization, then in 70 DEG C of thermal environments, place, stand-by; Described amine salt solution is ethanolamine solutions, and bacteria cellulose B is 1:5 with the mass ratio of the amine salt solution of putting into, 80 DEG C of reaction temperatures, and the reaction time is 36 hours.
(5) bacteria cellulose C is carried out to solution immersion treatment; Prepare the bacteria cellulose fibre with power generation performance, the alcoholic solution that described solution is polyaniline nano fiber, the mass concentration of solution is 1%, and the mass ratio of solution and bacteria cellulose fibre is 1:1, and the immersion treatment time is 24 ~ 72 hours.
The bacteria cellulose base generating fiber spinning that employing obtains obtains bacteria cellulose base generating yarn of the present invention.The yarn of one section of 10 centimeter length, under ultrasonic oscillation disposition, detects the current output signal of 40nA through galvanometer.
Embodiment 5
(1) bacterial cellulose wet-coating after bleaching is placed between a pair of gripping roller, according to the speed feeding of 65 m/ minutes; The diameter of the gripping roller using is 680mm.
(2) puncture, isolate and combing effect at a high speed through licker-in surface acupuncture from the cellulose membrane of exporting between roller, bacterial cellulose wet-coating is become to bacteria cellulose fibre; Bacteria cellulose fibre, through filter press press filtration processing, is prepared to bacteria cellulose superfine fibre bar; Take out postlyophilization, stand-by; The moisture content of the bacteria cellulose super fiber of process press filtration processing is between 780%, and the diameter of superfine fibre is at 350nm, and superfine fibre length is between 200nm ~ 200mm.
(3) bacteria cellulose superfine fibre bar is carried out to metallic zinc vacuum sputtering or vapor deposition treatment, obtain bacteria cellulose B, take out stand-by;
(4) bacteria cellulose B is put into amine salt solution, reaction a period of time, form bacteria cellulose C, take out postlyophilization, then in 60-100 DEG C of thermal environment, place, stand-by; Described amine salt solution is the mixed solution of diethanol amine and triethanolamine solution, and bacteria cellulose B is 1:6 with the mass ratio of the amine salt solution of putting into, 85 DEG C of reaction temperatures, and the reaction time is 32 hours.
(5) bacteria cellulose C is carried out to solution immersion treatment; Prepare the bacteria cellulose fibre with power generation performance, described solution is that CNT, Graphene, polyaniline nano fiber, poly-pyrene are coughed up the mixed liquor in the alcoholic solution of nanofiber, the mass concentration of solution is 1%, the mass ratio of solution and bacteria cellulose fibre is 1:1, and the immersion treatment time is 24 ~ 72 hours.
The bacteria cellulose base generating fiber spinning that employing obtains obtains bacteria cellulose base generating yarn of the present invention.The yarn of one section of 10 centimeter length, under ultrasonic oscillation disposition, detects the current output signal of 36nA through galvanometer.
Embodiment 6
(1) bacterial cellulose wet-coating after bleaching is placed between a pair of gripping roller, according to the speed feeding of 30m/ minute; The diameter of the gripping roller using is 50mm.
(2) puncture, isolate and combing effect at a high speed through licker-in surface acupuncture from the cellulose membrane of exporting between roller, bacterial cellulose wet-coating is become to bacteria cellulose fibre; Bacteria cellulose fibre, through filter press press filtration processing, is prepared to bacteria cellulose superfine fibre bar; Take out postlyophilization, stand-by; The moisture content of the bacteria cellulose super fiber of process press filtration processing is between 350, and the diameter of superfine fibre is at 200nm, and superfine fibre length is between 200nm.
(3) bacteria cellulose superfine fibre bar is carried out to metallic zinc vacuum sputtering or vapor deposition treatment, obtain bacteria cellulose B, take out stand-by;
(4) bacteria cellulose B is put into amine salt solution, reaction a period of time, form bacteria cellulose C, take out postlyophilization, then in 75 DEG C of thermal environments, place, stand-by; Described amine salt solution is the mixed solution of hexa, urea, ammoniacal liquor, monoethanolamine, diethanol amine, triethanolamine solution, and bacteria cellulose B is 1:4 with the mass ratio of the amine salt solution of putting into, 30 DEG C of reaction temperatures, and the reaction time is 26 hours.
(5) bacteria cellulose C is carried out to solution immersion treatment; Prepare the bacteria cellulose fibre with power generation performance, the alcohol that described solution is CNT closes liquid, and the mass concentration of solution is 1%, and the mass ratio of solution and bacteria cellulose fibre is 1:1, and the immersion treatment time is 24 ~ 72 hours.
The bacteria cellulose base generating fiber spinning that employing obtains obtains bacteria cellulose base generating yarn of the present invention.The yarn of one section of 10 centimeter length, under ultrasonic oscillation disposition, detects the current output signal of 39nA through galvanometer.
embodiment 7
By the bacteria cellulose after bleaching, feed between the gripping roller that a pair of diameter is 20mm according to the speed of 10mm.Then puncture, isolate and combing effect through the spiked roller surface needle-like combing acupuncture high speed through formation such as needle-like, superhard, elastic stainless steel silk or B alloy wire polishing wheels, bacterial cellulose wet-coating is become to bacteria cellulose fibre.Bacteria cellulose super fiber moisture content is after treatment 3%, and diameter is 400nm, and length is 150mm.Then by bacteria cellulose super fiber vacuum evaporation metallic zinc, form bacteria cellulose fibre B.Bacteria cellulose B is put into the amine salt solution of 80 degrees Celsius of constant temperature according to the mass ratio of 1:1, react and form bacteria cellulose fibre C after 36 hours.Bacteria cellulose fibre C is carried out after the carbon nano-tube solution immersion treatment of 24 hours, can obtain bacteria cellulose base generating fiber.
The bacteria cellulose base generating fiber spinning that employing obtains obtains bacteria cellulose base generating yarn of the present invention.The yarn of one section of 10 centimeter length, under ultrasonic oscillation disposition, detects the current output signal of 35nA through galvanometer.
embodiment 8
By the bacteria cellulose after bleaching, feed between the gripping roller that a pair of diameter is 50mm according to the speed of 30mm.Then puncture, isolate and combing effect through the spiked roller surface needle-like combing acupuncture high speed through formation such as needle-like, superhard, elastic stainless steel silk or B alloy wire polishing wheels, bacterial cellulose wet-coating is become to bacteria cellulose fibre.Bacteria cellulose super fiber moisture content is after treatment 2%, and diameter is 320nm, and length is 150mm.Then by bacteria cellulose super fiber vacuum sputtering metallic zinc, form bacteria cellulose fibre B.Bacteria cellulose B is put into the amine salt solution of 85 degrees Celsius of constant temperature according to the mass ratio of 1:1, react and form bacteria cellulose fibre C after 48 hours.Bacteria cellulose fibre C is carried out after the graphene solution immersion treatment of 36 hours, can obtain bacteria cellulose base generating fiber.
The bacteria cellulose base generating fiber spinning that employing obtains obtains bacteria cellulose base generating yarn of the present invention.The yarn of one section of 10 centimeter length, under ultrasonic oscillation disposition, detects the current output signal of 40nA through galvanometer.
Embodiment 9
By the bacteria cellulose after bleaching, feed between the gripping roller that a pair of diameter is 80mm according to the speed of 50mm.Then puncture, isolate and combing effect through the spiked roller surface needle-like combing acupuncture high speed through formation such as needle-like, superhard, elastic stainless steel silk or B alloy wire polishing wheels, bacterial cellulose wet-coating is become to bacteria cellulose fibre.Bacteria cellulose super fiber moisture content is after treatment 3%, and diameter is 250nm, and length is 150mm.Then by bacteria cellulose super fiber vacuum magnetic-control sputtering metallic zinc, form bacteria cellulose fibre B.Bacteria cellulose B is put into the amine salt solution of 90 degrees Celsius of constant temperature according to the mass ratio of 1:1, react and form bacteria cellulose fibre C after 60 hours.Bacteria cellulose fibre C is carried out after the polyaniline nano fiber solution immersion treatment of 48 hours, can obtain bacteria cellulose base generating fiber.
The bacteria cellulose base generating fiber spinning that employing obtains obtains bacteria cellulose base generating yarn of the present invention.The yarn of one section of 10 centimeter length, under ultrasonic oscillation disposition, detects the current output signal of 38nA through galvanometer.
Claims (6)
1. a preparation method for bacteria cellulose base generating fiber, is characterized in that, comprises the steps:
(1) bacterial cellulose wet-coating after bleaching is placed between a pair of gripping roller, according to the speed feeding of 10 mm ~ 100 m/ minutes;
(2) puncture, isolate and combing effect at a high speed through licker-in surface acupuncture from the cellulose membrane of exporting between roller, bacterial cellulose wet-coating is become to bacteria cellulose fibre; Bacteria cellulose fibre, through filter press press filtration processing, is prepared to bacteria cellulose superfine fibre bar; Take out postlyophilization, stand-by;
(3) bacteria cellulose superfine fibre bar is carried out to metallic zinc vacuum sputtering or vapor deposition treatment, obtain bacteria cellulose B, take out stand-by;
(4) bacteria cellulose B is put into amine salt solution, described amine salt solution is a kind of of hexa, urea, ammoniacal liquor, monoethanolamine, diethanol amine, triethanolamine solution or their mixed solution, reaction a period of time, form bacteria cellulose C, take out postlyophilization, then in 60-100 DEG C of thermal environment, place, stand-by;
(5) bacteria cellulose C is carried out to solution immersion treatment; Prepare the bacteria cellulose fibre with power generation performance; Step is carried out solution immersion treatment by bacteria cellulose C described in (5), described solution is a kind of in CNT, Graphene, polyaniline nano fiber alcoholic solution or their mixed liquor, the mass concentration of solution is 1%, the mass ratio of solution and bacteria cellulose fibre is 1:1, and the immersion treatment time is 24 ~ 72 hours.
2. the preparation method of bacteria cellulose base generating fiber according to claim 1, is characterized in that: the diameter of the gripping roller using in step (1) is 20 ~ 3000mm.
3. the preparation method of bacteria cellulose base generating fiber according to claim 2, is characterized in that: the diameter of the gripping roller using in step (1) is 30 ~ 300mm.
4. the preparation method of bacteria cellulose base generating fiber according to claim 4, it is characterized in that: in step (2), the moisture content of the bacteria cellulose superfine fibre bar of process press filtration processing is between 50% ~ 300%, the diameter of superfine fibre bar is between 30 ~ 200nm, and superfine fibre bar length is between 500nm ~ 100mm.
5. the preparation method of bacteria cellulose base generating fiber according to claim 1, it is characterized in that: in the amine salt solution described in step (4), amine ion concentration is 0.01mol/L, bacteria cellulose B is 1:1-1:10 with the mass ratio of the amine salt solution of putting into, 20 ~ 100 DEG C of reaction temperatures, the reaction time is 2 ~ 72 hours.
6. a preparation method for bacteria cellulose base generating yarn, is characterized in that: adopt bacteria cellulose base generating fiber spinning claimed in claim 1 to obtain yarn.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201210412225.9A CN102912625B (en) | 2012-10-25 | 2012-10-25 | Preparation method of bacterial-cellulose-based generating fiber and yarn |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201210412225.9A CN102912625B (en) | 2012-10-25 | 2012-10-25 | Preparation method of bacterial-cellulose-based generating fiber and yarn |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN102912625A CN102912625A (en) | 2013-02-06 |
| CN102912625B true CN102912625B (en) | 2014-10-22 |
Family
ID=47611177
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201210412225.9A Expired - Fee Related CN102912625B (en) | 2012-10-25 | 2012-10-25 | Preparation method of bacterial-cellulose-based generating fiber and yarn |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN102912625B (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN106917265A (en) * | 2017-02-23 | 2017-07-04 | 孙瑞宁 | A kind of preparation method of antimicrobial composite material |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0434030A (en) * | 1990-05-24 | 1992-02-05 | Oike Ind Co Ltd | Film-shaped material for gold and silver thread |
| CN101195940A (en) * | 2006-12-05 | 2008-06-11 | 上海申安纺织有限公司 | Regenerated cellulose fibre blending yarn and method for producing the same |
| CN101660265A (en) * | 2009-09-07 | 2010-03-03 | 江南大学 | Anti-bacterial fabric and preparation method thereof |
| CN102154832A (en) * | 2010-12-31 | 2011-08-17 | 泉州红瑞兴纺织有限公司 | Fabric coating finishing agent with electromagnetic shielding function and preparation method thereof |
-
2012
- 2012-10-25 CN CN201210412225.9A patent/CN102912625B/en not_active Expired - Fee Related
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0434030A (en) * | 1990-05-24 | 1992-02-05 | Oike Ind Co Ltd | Film-shaped material for gold and silver thread |
| CN101195940A (en) * | 2006-12-05 | 2008-06-11 | 上海申安纺织有限公司 | Regenerated cellulose fibre blending yarn and method for producing the same |
| CN101660265A (en) * | 2009-09-07 | 2010-03-03 | 江南大学 | Anti-bacterial fabric and preparation method thereof |
| CN102154832A (en) * | 2010-12-31 | 2011-08-17 | 泉州红瑞兴纺织有限公司 | Fabric coating finishing agent with electromagnetic shielding function and preparation method thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| CN102912625A (en) | 2013-02-06 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN103014888B (en) | Preparation method of bacterial cellulose based power generation fibers and yarns | |
| Rocha et al. | Multimaterial 3D printing of graphene-based electrodes for electrochemical energy storage using thermoresponsive inks | |
| Yang et al. | Te-Doped Black Phosphorus Field-Effect Transistors. | |
| Dong et al. | Simultaneous Production of High-Performance Flexible Textile Electrodes and Fiber Electrodes for Wearable Energy Storage. | |
| Liu et al. | High-quality graphene ribbons prepared from graphene oxide hydrogels and their application for strain sensors | |
| Wang et al. | Solid-state supercapacitor based on activated carbon cloths exhibits excellent rate capability. | |
| Meng et al. | Electro-induced mechanical and thermal responses of carbon nanotube fibers. | |
| CN102586922B (en) | Preparation method for macroscopic fiber of polyacrylonitrile grafted graphene | |
| Qiu et al. | Large-scale production of aligned long boron nitride nanofibers by multijet/multicollector electrospinning | |
| CN105741980A (en) | Flexible self-support graphene conductive thin film with microstructure pattern on surface and preparation method of flexible self-support graphene conductive thin film | |
| Fan et al. | Fabricating of high-performance functional graphene fibers for micro-capacitive energy storage | |
| CN102899886B (en) | Preparation method for bacterial cellulose based generating fiber and yarn | |
| CN102409462B (en) | Method for printing disordered micro nanofibers into ordered fiber array | |
| Al-Haddad et al. | Constructing Well-Ordered CdTe/TiO 2 Core/Shell Nanowire Arrays for Solar Energy Conversion. | |
| CN102912625B (en) | Preparation method of bacterial-cellulose-based generating fiber and yarn | |
| CN102899883B (en) | Preparation method of bacterial cellulose base power generating fibers and yarns | |
| Huang et al. | Electrochemical strategy for flexible and highly conductive carbon films: the role of 3-dimensional graphene/graphite aggregates | |
| CN109811328A (en) | A kind of preparation method of boron-doped diamond film | |
| CN102899887B (en) | Preparation method of bacterial cellulose base power generating fibers and yarns | |
| CN102912630B (en) | Preparation method of bacterial cellulose-based generating fiber and yarn | |
| CN102899889B (en) | Preparation method of bacterial cellulose base power generating fibers and yarns | |
| Guo et al. | Fabrication of ZnO nanofibers by electrospinning and electrical properties of a single nanofiber | |
| CN102912631B (en) | Method for preparing bacterial cellulose based generating fibers and yarns | |
| CN102912629B (en) | Preparation method of bacterial-cellulose-based generating fiber and yarn | |
| CN104532405A (en) | Vanadium nitride (VN) porous hollow nano-fiber and preparation method thereof |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| C14 | Grant of patent or utility model | ||
| GR01 | Patent grant | ||
| CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20141022 Termination date: 20171025 |
|
| CF01 | Termination of patent right due to non-payment of annual fee |