CN109440453A - A kind of preparation method of Cu-Ni-Gd-B-P electronic fabric - Google Patents

A kind of preparation method of Cu-Ni-Gd-B-P electronic fabric Download PDF

Info

Publication number
CN109440453A
CN109440453A CN201811226924.8A CN201811226924A CN109440453A CN 109440453 A CN109440453 A CN 109440453A CN 201811226924 A CN201811226924 A CN 201811226924A CN 109440453 A CN109440453 A CN 109440453A
Authority
CN
China
Prior art keywords
concentration
solution
sodolin
solute
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.)
Pending
Application number
CN201811226924.8A
Other languages
Chinese (zh)
Inventor
朱琳
吕银祥
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.)
Fudan University
Original Assignee
Fudan University
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 Fudan University filed Critical Fudan University
Priority to CN201811226924.8A priority Critical patent/CN109440453A/en
Publication of CN109440453A publication Critical patent/CN109440453A/en
Pending legal-status Critical Current

Links

Classifications

    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M11/00Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising
    • D06M11/83Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with metals; with metal-generating compounds, e.g. metal carbonyls; Reduction of metal compounds on textiles
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M13/00Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
    • D06M13/50Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with organometallic compounds; with organic compounds containing boron, silicon, selenium or tellurium atoms
    • D06M13/51Compounds with at least one carbon-metal or carbon-boron, carbon-silicon, carbon-selenium, or carbon-tellurium bond
    • D06M13/513Compounds with at least one carbon-metal or carbon-boron, carbon-silicon, carbon-selenium, or carbon-tellurium bond with at least one carbon-silicon bond
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M2101/00Chemical constitution of the fibres, threads, yarns, fabrics or fibrous goods made from such materials, to be treated
    • D06M2101/02Natural fibres, other than mineral fibres
    • D06M2101/04Vegetal fibres
    • D06M2101/06Vegetal fibres cellulosic

Landscapes

  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Chemical & Material Sciences (AREA)
  • Inorganic Chemistry (AREA)
  • Organic Chemistry (AREA)
  • Electroplating And Plating Baths Therefor (AREA)

Abstract

The invention belongs to field of electronic materials, are related to a kind of preparation method of Cu-Ni-Gd-B-P electronic fabric.Preparation method proposed by the present invention is to select sodolin as substrate, and depositing one layer of Cu-Ni-Gd-B-P alloy layer technique on its surface using the technique of chemical plating includes surface alkali process, and surface is modified, adsorption of metal ions, in-situ reducing, metal co-deposition etc..Anti-corrosion electric conducting fabric prepared by the present invention has the advantage that (1) flax substrate, sweat-absorbing breathable, health environment-friendly.(2) adhesive force between fabric substrate and metal coating can be improved by alkali process and silane coupler modified in sodolin.(3) the entire technological process of production is easy, is suitble to produce in enormous quantities, is able to satisfy the market demand.

Description

A kind of preparation method of Cu-Ni-Gd-B-P electronic fabric
Technical field
The invention belongs to technical field of electronic materials, and in particular to a kind of preparation side of Cu-Ni-Gd-B-P electronic fabric Method.
Background technique
With the continuous development of the communications industry, miscellaneous electronic equipment answering in the fields such as traffic, medical treatment, scientific research With more and more extensive.However, while enjoying these electronic equipments is that daily life brings great convenience, great Jia Ye It is faced with the risk by electromagnetic radiation pollution.It is reported that Long Term Contact electromagnetic radiation can cause vision impairment, dysaudia and The illnesss such as arrhythmia cordis.Therefore, it prepares wearable electromagnetic shielding material and receives the extensive attention of all circles.In general, shielding material Material can be divided into two types: wave reflection, which dominates material and inhales wave, dominates material.Metal is that material is dominated in typical wave reflection, extensively Applied in electromagnetic shielding field.But, Metal Substrate shielding material (including metal laminate plate, wire mesh, metal foam and gold Belong to foil etc.) have the shortcomings that hard, weight is excessive, corrosion-vulnerable.In recent years, the research of Portable flexible Electromagnetically shielding fabrics by Concern.In fabric surface deposited metal coating, the flexibility of source textile can be possessed, it is considered to be prepare the one of Electromagnetically shielding fabrics Kind feasible scheme.Chemical plating is because the advantages that its is easy to operate, low in cost, is as fabric face metallized common method.Change It learns plating and generally includes three surface modification, catalytic activation and metal deposit steps.Studies have found that being added in chemical plating fluid micro- Rare earth is measured, deposition rate can be accelerated, refining grain size enhances corrosion resistance.Because rare earth has special 4f sub-layer rail Road electronics can accelerate electron transfer rate, and furthermore rare earth atom radius is larger, it is intended to be deposited on crystal boundary and fault location, drop Low surface tension and interfacial energy to improve deposition rate, and then obtain the metal coating of dense uniform, effectively prevent corroding The destruction of substance.
Generally, it is considered that rare earth element, which is added, can be improved the form compact and stable property of metal layer, to improve metallic cover type electricity The corrosion resistance of sub- fabric, but in this application, rare earth Gd is added, leads to the corrosion resistance of Cu-Ni-Gd-P electronic fabric Lower than Cu-Ni-P electronic fabric, and light element B is added, the corrosion resistance for obtaining Cu-Ni-Gd-B-P electronic fabric is better than Cu- Ni-P, i.e., in terms of electronic fabric corrosion resistance index, Cu-Ni-Gd-B-P > Cu-Ni-P > Cu-Ni-Gd-P, this is The phenomenon that other documents are not reported.
Summary of the invention
The purpose of the present invention is to provide a kind of preparation methods of Cu-Ni-Gd-B-P electronic fabric.
The present invention proposes the preparation method of Cu-Ni-Gd-B-P electronic fabric, selects sodolin as substrate, utilizes change The technique for learning plating deposits one layer of Cu-Ni-Gd-B-P alloy layer on its surface.Concrete technology flow process: including surface alkali process, table Face modification, adsorption of metal ions, in-situ reducing and metal co-deposition etc..
The preparation method of Cu-Ni-Gd-B-P electronic fabric proposed by the present invention, the specific steps are as follows:
(1) surface alkali process: sodolin is placed in aqueous slkali and is handled 10-30 minutes;
(2) surface is modified: the sodolin after step (1) alkali process being immersed in silane coupler solution 5-10 minutes, is put Enter baking oven drying, repeats the step 2-3 times;
(3) adsorption of metal ions: the sodolin after step (2) modification is placed in metal ion solution and impregnates 10-30 Minute, take out drying;
(4) sodolin that step (3) process adsorbing metal ions in-situ reducing: is put into reducing agent solution 10-30 points Clock takes out, and cleans;
(5) metal co-deposition: the sodolin after step (4) reduction is placed in alloy electroplating bath, in 50-90 DEG C of chemical plating It 0.5-2 hours, takes out and cleans, Cu-Ni-Gd-B-P electronic fabric is made in drying.
It is 1cm by area in the present invention2Cu-Ni-Gd-B-P electronic fabric be placed in 50ml concentration be 310g/L, pH= 12, free chlorine is to impregnate 48 hours in the sodium chloride solution of 40ppm in 25 DEG C, is surveyed with energy dispersion type Xray fluorescence spectrometer Try sodium chloride solution in concentration of heavy metal ion, measure copper ion≤0.20ppm, nickel ion≤0.15ppm, gadolinium ion≤ 0.10ppm。
In the present invention, the solvent of aqueous slkali described in step (1) is deionized water, and solute is sodium hydroxide or hydroxide Potassium, solute concentration 5wt%-10wt%.
In the present invention, the solvent of silane coupler solution described in step (2) is dehydrated alcohol, and solute is 3- aminopropyl Trimethoxy silane, solute concentration 1wt%-2wt%.
In the present invention, the solvent of metal ion solution described in step (3) is deionized water, and the solute of solution is cobaltous sulfate Or nickel sulfate, the molar concentration of metal ion are 0.5-2 mol/L.
In the present invention, the solute of reducing agent solution described in step (4) is potassium borohydride or sodium borohydride, solvent be go from Sub- water, the molar concentration of reducing agent are 0.5-1 mol/L.
In the present invention, the formula of alloy electroplating bath described in step (5) is that solvent is deionized water, and various solutes are in solution The concentration of copper sulphate is 2-5 g/L, and the concentration of nickel sulfate is 10-30 g/L, the concentration 10-30 g/L of sodium hypophosphite, lemon The concentration of sour sodium is 40-100 g/L, and the concentration of gadolinium chloride is 0.3-0.5 g/L, and the concentration of boric acid is 0.3-0.5 g/L, hydrogen-oxygen The concentration for changing sodium is 4-6 g/L.
In the present invention, if not boronic acid containing in the formula of alloy electroplating bath in step (5), the present invention also provides following technical sides Case is as a comparison:
By step (4) reduction after sodolin be placed in alloy electroplating bath, 50-90 DEG C chemical plating 0.5-2 hour, taking-up It cleans, Cu-Ni-Gd-P electronic fabric is made in drying.It is 1cm by area2Cu-Ni-Gd-P electronic fabric be placed in 50ml concentration It is to be impregnated 48 hours in 25 DEG C, in the sodium chloride solution of 40ppm with energy dispersion type X-ray for 310g/L, pH=12, free chlorine Fluorescence Spectrometer tests the concentration of heavy metal ion in sodium chloride solution, measures that copper ion concentration is 26ppm, nickel ion is concentration 48ppm, gadolinium ion concentration are 5.3ppm.
In the present invention, if not boronic acid containing and gadolinium chloride in the formula of alloy electroplating bath in step (5), the present invention also provides such as Lower technical solution is as a comparison:
By step (4) reduction after sodolin be placed in alloy electroplating bath, 50-90 DEG C chemical plating 0.5-2 hour, taking-up It cleans, Cu-Ni-P electronic fabric is made in drying.It is 1cm by area2Cu-Ni-P electronic fabric be placed in 50ml concentration and be In 310g/L, pH=12, the sodium chloride solution that free chlorine is 40ppm, impregnated 48 hours in 25 DEG C, it is glimmering with energy dispersion type X-ray Photothermal spectroscopic analyzer tests the concentration of heavy metal ion in sodium chloride solution, measures that copper ion concentration is 12ppm, nickel ion concentration is 29ppm, gadolinium ion concentration are 3.3ppm.
It can be seen from above-mentioned correlation technique scheme compared with Cu-Ni-P electronic fabric, contain in electroless alloy layer Rare-earth element gadolinium, then the metal ion flood rate of electronic fabric rises, i.e., rare earth element declines the corrosion resistance of alloy-layer; But gadolinium and boron element are added in alloy-layer, then the metal ion flood rate of electronic fabric is remarkably decreased, i.e. boron element and rare earth Element collective effect, so that the corrosion resistance of alloy-layer is promoted.I.e. technical solution of the present invention produces unexpected significant Technical effect has creativeness.
Cu-Ni-Gd-B-P prepared by the present invention cladding fabric has the advantage that (1) selects sodolin as substrate, It is its absorbing sweat, good permeability, harmless.(2) alkali process not only facilitates silane coupler modified, moreover it is possible to improve fabric substrate Adhesive force between metal coating.(3) precious metal activation is replaced with base metal, not only shortens the process time, but also reduce Process costs.Electronic fabric prepared by the present invention can be successfully applied to flexible wearable electronic product, wide market.
Specific embodiment
The invention is further illustrated by the following examples.
Embodiment 1
Sodolin is placed in aqueous slkali and is handled 10 minutes;Sodolin after alkali process is immersed in silane coupler solution In 5 minutes, be put into baking oven drying, repeat the step 2 time;Sodolin after step modification is placed in metal ion solution It is middle to impregnate 10 minutes, take out drying;The sodolin of processed adsorbing metal ions is put into reducing agent solution 10 minutes, is taken Out, it cleans;Sodolin after reduction is placed in alloy electroplating bath, 50 DEG C chemical plating 0.5 hour, take out clean, dry It is dry, Cu-Ni-Gd-B-P electronic fabric is made.Wherein, the solvent of aqueous slkali is deionized water, and solute is sodium hydroxide, and solute is dense Degree is 5wt%;The solvent of silane coupler solution is dehydrated alcohol, and solute is 3- TSL 8330, solute concentration For 1wt%;The solvent of metal ion solution is deionized water, and the solute of solution is cobaltous sulfate, and the molar concentration of metal ion is 0.5mol/L;The solute of reducing agent solution is potassium borohydride, and solvent is deionized water, and the molar concentration of reducing agent is 0.5 mol/L;The formula of alloy electroplating bath is that solvent is deionized water, and it is 2g/L, sulfuric acid that various solutes, which are the concentration of copper sulphate, in solution The concentration of nickel is 10g/L, and the concentration of the concentration 10g/L of sodium hypophosphite, sodium citrate are 40g/L, and the concentration of gadolinium chloride is 0.3g/L, the concentration of boric acid are 0.3g/L, and the concentration of sodium hydroxide is 4g/L.
It is 1cm by area2Cu-Ni-Gd-B-P electronic fabric be placed in that 50ml concentration is 310g/L, pH=12, free chlorine is In the sodium chloride solution of 40ppm, impregnated 48 hours in 25 DEG C, it is molten with energy dispersion type Xray fluorescence spectrometer test sodium chloride Concentration of heavy metal ion in liquid, measuring copper ion concentration 0.20ppm, nickel ion concentration 0.15ppm, gadolinium ion concentration is 0.10ppm。
Embodiment 2
Sodolin is placed in aqueous slkali and is handled 30 minutes;Sodolin after alkali process is immersed in silane coupler solution In 10 minutes, be put into baking oven drying, repeat the step 3 time;Sodolin after modification is placed in metal ion solution It impregnates 30 minutes, takes out drying;The sodolin of processed adsorbing metal ions is put into reducing agent solution 30 minutes, is taken Out, it cleans;Sodolin after reduction is placed in alloy electroplating bath, 90 DEG C chemical plating 2 hours, take out clean, dry, system Obtain Cu-Ni-Gd-B-P electronic fabric.Wherein, the solvent of aqueous slkali is deionized water, and solute is potassium hydroxide, and solute concentration is 10wt%;The solvent of silane coupler solution is dehydrated alcohol, and solute is 3- TSL 8330, and solute concentration is 2wt%;The solvent of metal ion solution is deionized water, and the solute of solution is or nickel sulfate, the molar concentration of metal ion are 2 mol/L;The solute of reducing agent solution is sodium borohydride, and solvent is deionized water, and the molar concentration of reducing agent is 1 mol/L;It closes The formula of golden plating solution is that solvent is deionized water, and it is 5 g/L, the concentration of nickel sulfate that various solutes, which are the concentration of copper sulphate, in solution For 30 g/L, 30 g/L of concentration of sodium hypophosphite, the concentration of sodium citrate is 100 g/L, and the concentration of gadolinium chloride is 0.5 g/ L, the concentration of boric acid are 0.5 g/L, and the concentration of sodium hydroxide is 6 g/L.
It is 1cm by area2Cu-Ni-Gd-B-P electronic fabric be placed in that 50ml concentration is 310g/L, pH=12, free chlorine is In the sodium chloride solution of 40ppm, impregnated 48 hours in 25 DEG C, it is molten with energy dispersion type Xray fluorescence spectrometer test sodium chloride Concentration of heavy metal ion in liquid, measures that copper ion concentration is 0.18ppm, nickel ion concentration 0.13ppm, gadolinium ion concentration are 0.08ppm。
Embodiment 3
Sodolin is placed in aqueous slkali and is handled 30 minutes;Sodolin after alkali process is immersed in silane coupler solution In 10 minutes, be put into baking oven drying, repeat the step 3 time;It is molten that sodolin after step modification is placed in metal ion It is impregnated 10 minutes in liquid, takes out drying;The sodolin of processed adsorbing metal ions is put into reducing agent solution 30 minutes, It takes out, cleans;Sodolin after reduction is placed in alloy electroplating bath, 90 DEG C chemical plating 2 hours, take out clean, dry It is dry, Cu-Ni-Gd-B-P electronic fabric is made.Wherein, the solvent of aqueous slkali is deionized water, and solute is sodium hydroxide, and solute is dense Degree is 5wt%;The solvent of silane coupler solution is dehydrated alcohol, and solute is 3- TSL 8330, solute concentration For 1.5wt%;The solvent of metal ion solution is deionized water, and the solute of solution is cobaltous sulfate, and the molar concentration of metal ion is 1.5mol/L;The solute of reducing agent solution is potassium borohydride, and solvent is deionized water, and the molar concentration of reducing agent is 0.75 mol/L;The formula of alloy electroplating bath is that solvent is deionized water, and it is 3g/L, sulfuric acid that various solutes, which are the concentration of copper sulphate, in solution The concentration of nickel is 12g/L, and the concentration of the concentration 12g/L of sodium hypophosphite, sodium citrate are 45g/L, and the concentration of gadolinium chloride is 0.4g/L, the concentration of boric acid are 0.4g/L, and the concentration of sodium hydroxide is 5g/L.
It is 1cm by area2Cu-Ni-Gd-B-P electronic fabric be placed in that 50ml concentration is 310g/L, pH=12, free chlorine is In the sodium chloride solution of 40ppm, impregnated 48 hours in 25 DEG C, it is molten with energy dispersion type Xray fluorescence spectrometer test sodium chloride Concentration of heavy metal ion in liquid, measuring copper ion concentration 0.14ppm, nickel ion concentration 0.11ppm, gadolinium ion concentration is 0.09ppm。
Embodiment 4
Sodolin is placed in aqueous slkali and is handled 20 minutes;Sodolin after alkali process is immersed in silane coupler solution In 8 minutes, be put into baking oven drying, repeat the step 3 time;Sodolin after modification is placed in metal ion solution and is soaked Bubble 20 minutes takes out drying;The sodolin of processed adsorbing metal ions is put into reducing agent solution 20 minutes, is taken out, It cleans;Sodolin after reduction is placed in alloy electroplating bath, 80 DEG C chemical plating 2 hours, take out clean, dry, be made Cu-Ni-Gd-B-P electronic fabric.Wherein, the solvent of aqueous slkali is deionized water, and solute is potassium hydroxide, and solute concentration is 8wt%;The solvent of silane coupler solution is dehydrated alcohol, and solute is 3- TSL 8330, and solute concentration is 2wt%;The solvent of metal ion solution is deionized water, and the solute of solution is or nickel sulfate, the molar concentration of metal ion are 1 mol/L;The solute of reducing agent solution is sodium borohydride, and solvent is deionized water, and the molar concentration of reducing agent is 1 mol/L;It closes The formula of golden plating solution is that solvent is deionized water, and it is 4 g/L, the concentration of nickel sulfate that various solutes, which are the concentration of copper sulphate, in solution For 25 g/L, 25 g/L of concentration of sodium hypophosphite, the concentration of sodium citrate is 90 g/L, and the concentration of gadolinium chloride is 0.5 g/L, The concentration of boric acid is 0.4 g/L, and the concentration of sodium hydroxide is 5 g/L.
It is 1cm by area2Cu-Ni-Gd-B-P electronic fabric be placed in that 50ml concentration is 310g/L, pH=12, free chlorine is In the sodium chloride solution of 40ppm, impregnated 48 hours in 25 DEG C, it is molten with energy dispersion type Xray fluorescence spectrometer test sodium chloride Concentration of heavy metal ion in liquid, measures that copper ion concentration is 0.19ppm, nickel ion concentration 0.12ppm, gadolinium ion concentration are 0.07ppm。
Embodiment 5
Sodolin is placed in aqueous slkali and is handled 26 minutes;Sodolin after alkali process is immersed in silane coupler solution In 8 minutes, be put into baking oven drying, repeat the step 2 time;Sodolin after modification is placed in metal ion solution and is soaked Bubble 22 minutes takes out drying;The sodolin of processed adsorbing metal ions is put into reducing agent solution 25 minutes, is taken out, It cleans;Sodolin after reduction is placed in alloy electroplating bath, 70 DEG C chemical plating 1.5 hours, take out clean, dry, system Obtain Cu-Ni-Gd-B-P electronic fabric.Wherein, the solvent of aqueous slkali is deionized water, and solute is potassium hydroxide, and solute concentration is 8wt%;The solvent of silane coupler solution is dehydrated alcohol, and solute is 3- TSL 8330, and solute concentration is 1.8wt%;The solvent of metal ion solution is deionized water, and the solute of solution is or nickel sulfate, the molar concentration of metal ion are 1.8 mol/L;The solute of reducing agent solution is sodium borohydride, and solvent is deionized water, and the molar concentration of reducing agent is 0.9 mol/L;The formula of alloy electroplating bath is that solvent is deionized water, and it is 4.8 g/L, sulphur that various solutes, which are the concentration of copper sulphate, in solution The concentration of sour nickel is 280 g/L, 26 g/L of concentration of sodium hypophosphite, and the concentration of sodium citrate is 95 g/L, gadolinium chloride it is dense Degree is 0.4 g/L, and the concentration of boric acid is 0.5 g/L, and the concentration of sodium hydroxide is 5 g/L.
It is 1cm by area2Cu-Ni-Gd-B-P electronic fabric be placed in that 50ml concentration is 310g/L, pH=12, free chlorine is In the sodium chloride solution of 40ppm, impregnated 48 hours in 25 DEG C, it is molten with energy dispersion type Xray fluorescence spectrometer test sodium chloride Concentration of heavy metal ion in liquid, measures that copper ion concentration is 0.17ppm, nickel ion concentration 0.15ppm, gadolinium ion concentration are 0.09ppm。

Claims (7)

1. a kind of preparation method of Cu-Ni-Gd-B-P electronic fabric, it is characterised in that specific step is as follows:
(1) surface alkali process: sodolin is placed in aqueous slkali and is handled 10-30 minutes;
(2) surface is modified: the sodolin after step (1) alkali process being immersed in silane coupler solution 5-10 minutes, is put Enter baking oven drying, repeats the step 2-3 times;
(3) adsorption of metal ions: the sodolin after step (2) modification is placed in metal ion solution and impregnates 10-30 Minute, take out drying;
(4) sodolin that step (3) process adsorbing metal ions in-situ reducing: is put into reducing agent solution 10-30 points Clock takes out, and cleans;
(5) metal co-deposition: the sodolin after step (4) reduction is placed in alloy electroplating bath, in 50-90 DEG C of chemical plating It 0.5-2 hours, takes out and cleans, Cu-Ni-Gd-B-P electronic fabric is made in drying.
2. preparation method according to claim 1, it is characterised in that: the solvent of aqueous slkali described in step (1) be go from Sub- water, solute are sodium hydroxide or potassium hydroxide, solute concentration 5wt%-10wt%.
3. preparation method according to claim 1, it is characterised in that: silane coupler solution described in step (2) it is molten Agent is dehydrated alcohol, and solute is 3- TSL 8330, solute concentration 1wt%-2wt%.
4. preparation method according to claim 1, it is characterised in that: the solvent of metal ion solution described in step (3) For deionized water, the solute of solution is cobaltous sulfate or nickel sulfate, and the molar concentration of metal ion is 0.5-2 mol/L.
5. preparation method according to claim 1, it is characterised in that: the solute of reducing agent solution described in step (4) is Potassium borohydride or sodium borohydride, solvent are deionized water, and the molar concentration of reducing agent is 0.5-1 mol/L.
6. preparation method according to claim 1, it is characterised in that: the formula of alloy electroplating bath described in step (5) is molten Agent is deionized water, and it is 2-5 g/L that various solutes, which are the concentration of copper sulphate, in solution, and the concentration of nickel sulfate is 10-30 g/L, secondary The concentration 10-30 g/L of sodium phosphite, the concentration of sodium citrate are 40-100 g/L, and the concentration of gadolinium chloride is 0.3-0.5 g/L, The concentration of boric acid is 0.3-0.5 g/L, and the concentration of sodium hydroxide is 4-6 g/L.
7. preparation method according to claim 1, it is characterised in that: the Cu-Ni-Gd-B-P electronic fabric it is corrosion-resistant Property are as follows: by area be 1cm2Cu-Ni-Gd-B-P electronic fabric be placed in that 50ml concentration is 310g/L, pH=12, free chlorine is In the sodium chloride solution of 40ppm, impregnated 48 hours in 25 DEG C, it is molten with energy dispersion type Xray fluorescence spectrometer test sodium chloride Concentration of heavy metal ion in liquid, measure copper ion concentration≤0.20ppm, nickel ion concentration≤0.15ppm, gadolinium ion concentration≤ 0.10ppm。
CN201811226924.8A 2018-10-22 2018-10-22 A kind of preparation method of Cu-Ni-Gd-B-P electronic fabric Pending CN109440453A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201811226924.8A CN109440453A (en) 2018-10-22 2018-10-22 A kind of preparation method of Cu-Ni-Gd-B-P electronic fabric

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201811226924.8A CN109440453A (en) 2018-10-22 2018-10-22 A kind of preparation method of Cu-Ni-Gd-B-P electronic fabric

Publications (1)

Publication Number Publication Date
CN109440453A true CN109440453A (en) 2019-03-08

Family

ID=65548034

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201811226924.8A Pending CN109440453A (en) 2018-10-22 2018-10-22 A kind of preparation method of Cu-Ni-Gd-B-P electronic fabric

Country Status (1)

Country Link
CN (1) CN109440453A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN112331378A (en) * 2020-11-19 2021-02-05 中国工程物理研究院应用电子学研究所 Flexible wearable conductive material with Joule heating performance and preparation method thereof
CN112647067A (en) * 2020-12-24 2021-04-13 西安稀有金属材料研究院有限公司 Gadolinium-plated tungsten/gadolinium-plated boron carbide powder and preparation method and application thereof
CN113881097A (en) * 2021-09-08 2022-01-04 复旦大学 Ultrahigh-performance terahertz absorption sponge and preparation method thereof

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6468478A (en) * 1987-09-07 1989-03-14 Agency Ind Science Techn Metal plating method using silver hydrosol
CN103114437A (en) * 2013-02-01 2013-05-22 东华大学 Method for chemically plating nickel at textile surface without using palladium
CN105256291A (en) * 2015-06-10 2016-01-20 上海大学 Method for preparing aramid fiber nickel/copper plating double-plating-layer composite conductive fibers
CN106049035A (en) * 2016-09-06 2016-10-26 复旦大学 Establishment method of conductive circuit on surface of flexible fabric
CN107385891A (en) * 2017-07-11 2017-11-24 复旦大学 A kind of preparation method of ternary alloy three-partalloy anti-corrosion electric conducting fabric
CN107513858A (en) * 2017-07-11 2017-12-26 复旦大学 A kind of preparation method of Co Ni P Nd alloy electromagnetic loomages

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6468478A (en) * 1987-09-07 1989-03-14 Agency Ind Science Techn Metal plating method using silver hydrosol
CN103114437A (en) * 2013-02-01 2013-05-22 东华大学 Method for chemically plating nickel at textile surface without using palladium
CN105256291A (en) * 2015-06-10 2016-01-20 上海大学 Method for preparing aramid fiber nickel/copper plating double-plating-layer composite conductive fibers
CN106049035A (en) * 2016-09-06 2016-10-26 复旦大学 Establishment method of conductive circuit on surface of flexible fabric
CN107385891A (en) * 2017-07-11 2017-11-24 复旦大学 A kind of preparation method of ternary alloy three-partalloy anti-corrosion electric conducting fabric
CN107513858A (en) * 2017-07-11 2017-12-26 复旦大学 A kind of preparation method of Co Ni P Nd alloy electromagnetic loomages

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN112331378A (en) * 2020-11-19 2021-02-05 中国工程物理研究院应用电子学研究所 Flexible wearable conductive material with Joule heating performance and preparation method thereof
CN112331378B (en) * 2020-11-19 2022-03-01 中国工程物理研究院应用电子学研究所 Flexible wearable conductive material with Joule heating performance and preparation method thereof
CN112647067A (en) * 2020-12-24 2021-04-13 西安稀有金属材料研究院有限公司 Gadolinium-plated tungsten/gadolinium-plated boron carbide powder and preparation method and application thereof
CN112647067B (en) * 2020-12-24 2022-10-14 西安稀有金属材料研究院有限公司 Gadolinium-plated tungsten/gadolinium-plated boron carbide powder and preparation method and application thereof
CN113881097A (en) * 2021-09-08 2022-01-04 复旦大学 Ultrahigh-performance terahertz absorption sponge and preparation method thereof
CN113881097B (en) * 2021-09-08 2023-08-29 复旦大学 Ultra-high-performance terahertz absorption sponge and preparation method thereof

Similar Documents

Publication Publication Date Title
CN109440453A (en) A kind of preparation method of Cu-Ni-Gd-B-P electronic fabric
Seifzadeh et al. Environmentally-friendly method for electroless Ni–P plating on magnesium alloy
CN102899890A (en) Aramid fiber surface metallization treatment method
CN108118528B (en) Flexible conductive textile
CN103334093A (en) Chemical copper-plating activating process of ceramic material
CN109161876A (en) A kind of silver-plated method of nylon fiber surface chemistry
CN106191825B (en) Based on SO42-Replacement-reduction electroless palladium plating solution of system
CN101886330A (en) Fe-Co magnetic alloy plated carbon fiber, preparation method and application thereof
CN103757617B (en) A kind of Ni-Cu-La-B quaternary alloy plating solution and the method for the plating of glass fibre chemistry
CN104797744B (en) The surface treatment method of copper foil and the copper foil being surface-treated by this method
CN109537275A (en) A kind of preprocess method of conductive dacron fibre, conductive dacron fibre and preparation method thereof
CN210826040U (en) Silver fiber electromagnetic shielding adhesive tape
CN101899690B (en) Multi-porous alloy material and method for preparing same
CN107868947A (en) A kind of activating solution and preparation method thereof and no-palladium activating chemical nickel plating method
CN101974741B (en) Method for performing chemical plating on surface of polytetrafluoroethylene thin film
Hui et al. Preparation of EMI shielding and corrosion-resistant composite based on electroless Ni-Cu-P coated wood
CN101555611B (en) Method for electroplating nickel on surface of magnesium alloy
CN100595326C (en) Ni-Fe-La-P four-component alloy plating solution for chemical plating on surface of fiberglass and method for preparing same
CN104910586A (en) Preparation method of electromagnetic protective composite material
CN102121100A (en) 'Copper/straw' electromagnetic wave shield composite material and preparation method thereof
CN107513858A (en) A kind of preparation method of Co Ni P Nd alloy electromagnetic loomages
CN101974769B (en) Alkaline non-cyanide copper plating solution taking amino methylene diphosphonic acid as main coordinating agent
CN101768736A (en) Formula for chemical plating of nickel-copper on calcium magnesium silicate mineral whisker surface and process thereof
CN101760734A (en) Tin-nickel chemical plating prescription and process on surface of glass fiber
CN109554917A (en) A kind of conduction aramid fiber preprocess method, conductive aramid fiber and preparation method thereof

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
WD01 Invention patent application deemed withdrawn after publication
WD01 Invention patent application deemed withdrawn after publication

Application publication date: 20190308