CN102121124A - Method for electroplating on surface of silica optical fiber - Google Patents

Method for electroplating on surface of silica optical fiber Download PDF

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Publication number
CN102121124A
CN102121124A CN 201010504621 CN201010504621A CN102121124A CN 102121124 A CN102121124 A CN 102121124A CN 201010504621 CN201010504621 CN 201010504621 CN 201010504621 A CN201010504621 A CN 201010504621A CN 102121124 A CN102121124 A CN 102121124A
Authority
CN
China
Prior art keywords
optical fiber
electroplating
plating
lanthanum trioxide
silica fibre
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
CN 201010504621
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Chinese (zh)
Inventor
孙义兴
张腊生
谭会良
许建国
廖郑洪
李炳惠
张华�
李涛
陈曲
谢河彬
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Chengdu Hengtong Optical Communication Co Ltd
Original Assignee
Chengdu Hengtong Optical Communication 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 Chengdu Hengtong Optical Communication Co Ltd filed Critical Chengdu Hengtong Optical Communication Co Ltd
Priority to CN 201010504621 priority Critical patent/CN102121124A/en
Publication of CN102121124A publication Critical patent/CN102121124A/en
Pending legal-status Critical Current

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Abstract

The invention relates to a method for electroplating on the surface of a silica optical fiber. In the method, an optical fiber on which Ni-P is chemically plated is taken as a cathode; a nickel anode is first cleaned by using sodium hydroxide with the concentration of 30 percent, is then neutralized by using sulfuric acid with the concentration of 10 percent and is finally cleaned by using distilled water; 1.5g of lanthanum oxide additive is added into every liter of conventional electroplating solution; and the electroplating solution is plated on the surface of the silica optical fiber at the temperature of 25 DEG C and the current density of 0.7A dm<-2>. In the method, the lanthanum oxide is added into the electroplating solution according to a certain proportion, so that the deposition rate and the current efficiency are improved.

Description

The method of silica fibre electroplating surface
Technical field
The present invention relates to the method for silica fibre electroplating surface, particularly the method for silica fibre electroplating nickel on surface.
Background technology
The optical fiber bragg grating sensor that silica fibre is made is detected temperatures and strain and many physical quantitys and the chemical indirect measurement of measuring relevant with temperature and strain directly.Rare earth element has than thick atom radius and particular electrical minor structure and is having good physical and chemical performance, and the rare earth element of matters is added in the electroplate liquid, can effectively change silica fibre surface metal electroplating efficiency.But because problem such as its process complexity, lack a kind of effective way of not only having accelerated film forming efficiency but also having improved film forming characteristics in the present electro-plating method.
Summary of the invention
In order to solve above-mentioned drawback, a kind of method of silica fibre electroplating surface is characterised in that: will be negative electrode with the optical fiber of chemical Ni-P plating, nickel anode elder generation be cleaned with 30% sodium hydroxide, and with the neutralization of 10% sulfuric acid, distilled water is cleaned afterwards again; The traditional tile special plating solution adds 1.5g/L lanthanum trioxide additive, 25 degrees centigrade of temperature of electroplating solution, current density 0.7Adm -2Carry out plating.
Wherein, the method for described silica fibre electroplating surface, lanthanum trioxide additive use dissolving with hydrochloric acid purity are 99.9% lanthanum trioxide acquisition.
Embodiment
Material choice:
Greater than 99%, sodium-chlor purity contains the alcohol amount greater than 59% greater than 99.5% sodium lauryl sulphate greater than 98.5% anhydrous sodium sulphate analytical pure for 99.9% purity lanthanum trioxide, six hydration nickel sulfate purity, and boric acid purity is greater than 99.5% chemical Ni-P plating silica fibre
To be negative electrode with the optical fiber of chemical Ni-P plating, nickel anode elder generation be cleaned with 30% sodium hydroxide, and with the neutralization of 10% sulfuric acid, distilled water is cleaned afterwards again; Traditional tile special plating solution (six hydration nickel sulfate 180g/L, anhydrous sodium sulphate 60g/L, sodium-chlor 9g/L, PH=5.2, sodium lauryl sulphate 0.07g/L, boric acid 32g/L) adds 1.5g/L lanthanum trioxide additive, 25 degrees centigrade of temperature of electroplating solution, current density 0.7Adm -2Carry out plating.
Wherein, the method for described silica fibre electroplating surface, the lanthanum trioxide additive uses the lanthanum trioxide of 1mol/L dissolving with hydrochloric acid mass concentration 1.5g/L to obtain.
Close cross section pattern use scanning electron microscopic observation to electroplating the top layer, coating is formed with equipment such as energy spectrometer and plasma emission spectrometer and various conventional method of analysis and is measured, discovery is electroplated with the nickel plating that doping lanthanum oxide additive not carries out and is compared, the present invention has improved nickel deposition speed (bringing up to 15.2 microns/hour by 14.2 microns/hour) and current efficiency, improved the nickel dam quality, density, microhardness is improved, average grain size, resistivity and wetting time are respectively by 12 microns, 27 micro-ohms centimetre and 5-6 reduce to 1.5 microns second, 23 micro-ohms centimetre and 2-3 second.
The invention is not restricted to the foregoing description; in design scope of the present invention; the description of book according to the above description, those of ordinary skill in the art also can make some conspicuous changes, but these changes all should fall within the protection domain of claim of the present invention.

Claims (2)

1. the method for a silica fibre electroplating surface is characterised in that: will be negative electrode with the optical fiber of chemical Ni-P plating, nickel anode cleans with 30% sodium hydroxide earlier, neutralizes with 10% sulfuric acid again, and distilled water is clean afterwards; The traditional tile special plating solution adds 1.5g/L lanthanum trioxide additive, 25 degrees centigrade of temperature of electroplating solution, current density 0.7Adm -2Carry out plating.
2. the method for silica fibre electroplating surface as claimed in claim 1, wherein, lanthanum trioxide additive use finite concentration dissolving with hydrochloric acid purity is 99.9% lanthanum trioxide acquisition.
CN 201010504621 2010-10-13 2010-10-13 Method for electroplating on surface of silica optical fiber Pending CN102121124A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN 201010504621 CN102121124A (en) 2010-10-13 2010-10-13 Method for electroplating on surface of silica optical fiber

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN 201010504621 CN102121124A (en) 2010-10-13 2010-10-13 Method for electroplating on surface of silica optical fiber

Publications (1)

Publication Number Publication Date
CN102121124A true CN102121124A (en) 2011-07-13

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Family Applications (1)

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CN 201010504621 Pending CN102121124A (en) 2010-10-13 2010-10-13 Method for electroplating on surface of silica optical fiber

Country Status (1)

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CN (1) CN102121124A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104152899A (en) * 2014-08-05 2014-11-19 南昌大学 Manufacturing method for high-temperature resistant bundling optical fibers
CN107796752A (en) * 2016-09-06 2018-03-13 鞍钢股份有限公司 A kind of method for measuring steel hydrogen induced cracking (HIC) performance in hydrogen sulfide corrosion environment

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1637166A (en) * 2003-12-31 2005-07-13 罗姆和哈斯电子材料有限责任公司 Methods of metallizing non-conductive substrates and metallized non-conductive substrates formed thereby
CN1876897A (en) * 2005-06-08 2006-12-13 长沙力元新材料股份有限公司 Electroplating aqueous solution for quick nickel plating of porous substrate

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1637166A (en) * 2003-12-31 2005-07-13 罗姆和哈斯电子材料有限责任公司 Methods of metallizing non-conductive substrates and metallized non-conductive substrates formed thereby
CN1876897A (en) * 2005-06-08 2006-12-13 长沙力元新材料股份有限公司 Electroplating aqueous solution for quick nickel plating of porous substrate

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104152899A (en) * 2014-08-05 2014-11-19 南昌大学 Manufacturing method for high-temperature resistant bundling optical fibers
CN104152899B (en) * 2014-08-05 2017-04-05 南昌大学 A kind of manufacture method of high temperature resistant bundling optical fiber
CN107796752A (en) * 2016-09-06 2018-03-13 鞍钢股份有限公司 A kind of method for measuring steel hydrogen induced cracking (HIC) performance in hydrogen sulfide corrosion environment

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Application publication date: 20110713