CN110983313A - Phosphate after-loading salt for PC line and use process thereof - Google Patents
Phosphate after-loading salt for PC line and use process thereof Download PDFInfo
- Publication number
- CN110983313A CN110983313A CN201911363160.1A CN201911363160A CN110983313A CN 110983313 A CN110983313 A CN 110983313A CN 201911363160 A CN201911363160 A CN 201911363160A CN 110983313 A CN110983313 A CN 110983313A
- Authority
- CN
- China
- Prior art keywords
- salt
- phosphating
- percent
- sodium
- wire
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C22/00—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals
- C23C22/05—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
- C23C22/00—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals
- C23C22/73—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals characterised by the process
Landscapes
- Chemical & Material Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
Abstract
The invention discloses a post-phosphating salt for a PC wire, which comprises the following raw material components in percentage by mass: 10 to 30 percent of sodium stearate, 65 to 85 percent of borax, 1 to 5 percent of sodium tripolyphosphate and 1 to 5 percent of sodium nitrite. The post-loaded salt for PC wire phosphating is characterized by comprising the following raw material components in percentage by mass: 10 to 30 percent of sodium stearate, 65 to 85 percent of borax, 1 to 5 percent of sodium tripolyphosphate and 1 to 5 percent of sodium nitrite. The quality of the surface of the wire rod after the salt loading treatment is greatly improved, and the wire rod does not rust after being placed for one month at normal temperature.
Description
[ technical field ] A method for producing a semiconductor device
The invention relates to the field of chemical industry, in particular to post-phosphating carried salt for a PC (polycarbonate) line and a preparation method thereof.
[ background of the invention ]
At present, borax, lime or saponification treatment is used for rust prevention after acid pickling and phosphorization of a PC wire, but a wire rod treated by the borax is easy to get damp, and when air humidity is high, water drops appear on the surface of the wire rod after the wire rod is placed for a period of time, so that the powder carrying of wire drawing powder is influenced during drawing, and the drawing efficiency and the drawing quality of the wire rod are also seriously influenced. If lime is used for treatment after phosphorization, the steel wire with too low pH value control is easy to return rust, the surface of the wire rod with too high pH value control is easy to yellow, the tank liquor is difficult to control, and the antirust effect is poor. If saponification is adopted after phosphorization, the hard sodium hyaluronate layer formed on the saponified surface is too smooth, so that the wire rod is easy to loose and slip in the stacking process, and serious safety risk exists.
It can be seen that providing an improved method is a problem that needs to be addressed in the art.
[ summary of the invention ]
The invention aims at the problems and provides a post-phosphating salt for a PC (polycarbonate) wire and a preparation method thereof.
In order to solve the problems, the invention provides a post-loaded salt for PC wire phosphating, which comprises the following raw material components in percentage by mass: 10 to 30 percent of sodium stearate, 65 to 85 percent of borax, 1 to 5 percent of sodium tripolyphosphate and 1 to 5 percent of sodium nitrite.
Further, the salt loading after the phosphating of the PC wire comprises the following preparation steps: sodium stearate, borax, sodium tripolyphosphate and sodium nitrite are weighed according to the quantity and added into a stirring kettle, and the mixture, namely the salt is obtained after full stirring.
Further, the stirring time is 20-40 minutes.
Further, pouring a certain amount of water into a working tank, heating to a certain temperature, adding 3% -10% of salt, fully stirring and reacting for a period of time, and then soaking the PC wire.
Further, the heating temperature is 70-85 ℃.
Further, the stirring time is 0.5 to 1.5 hours.
Further, the soaking time is 3-10 minutes.
Compared with the prior art, the invention has the following advantages:
1. the concentration range of the carried salt after the phosphorization of the PC line is wide, the process is easy to control, and the phenomena of yellowing and the like are not easy to occur.
2. The quality of the surface of the wire rod after the salt loading treatment is greatly improved, and the wire rod does not rust after being placed for one month at normal temperature.
3. The surface roughness of the dish elements after salt loading treatment is higher than that of the dish elements after saponification, and the phenomenon of loose rolling and slipping of the dish elements in the transportation and stacking process can be avoided.
[ detailed description ] embodiments
The PC wire phosphating post-loading salt comprises the following steps:
according to the mass percentage, 10 to 30 percent of sodium stearate, 65 to 85 percent of borax, 1 to 5 percent of sodium tripolyphosphate and 1 to 5 percent of sodium nitrite are provided. Sodium stearate, borax, sodium tripolyphosphate and sodium nitrite are weighed according to the quantity and added into a stirring kettle, and the mixture is fully stirred for 20-40 minutes to obtain a mixture, namely the salt-carrying mixture.
The application process of the phosphate after-loading salt for PC line phosphating comprises the following steps: pouring a certain amount of water into a working tank, heating to 70-85 ℃, adding 3% -10% of salt, fully stirring for reaction for 0.5-1.5 hours, and soaking the PC wire for 3-10 minutes.
Example 1
The PC line phosphating afterloading salt and the using process thereof comprise the following steps:
according to the mass percentage of the raw materials, 10% of sodium stearate, 85% of borax, 2% of sodium tripolyphosphate and 3% of sodium nitrite are provided, the sodium stearate, the borax, the sodium tripolyphosphate and the sodium nitrite are weighed according to the quantity and are added into a stirring kettle, and the mixture is fully stirred for 20 minutes to obtain a mixture, namely a salt-carrying mixture; pouring a certain amount of water into a working tank, heating to 80 ℃, adding 10% of salt, fully stirring for reaction for 0.5 hour, and soaking the PC wire for 3 minutes.
Example 2
The PC line phosphating afterloading salt and the using process thereof comprise the following steps:
according to the mass percentage of the raw materials, 30% of sodium stearate, 60% of borax, 5% of sodium tripolyphosphate and 5% of sodium nitrite are provided, the sodium stearate, the borax, the sodium tripolyphosphate and the sodium nitrite are weighed according to the quantity and are added into a stirring kettle, and the mixture is fully stirred for 40 minutes to obtain a mixture, namely a salt-carrying mixture; pouring a certain amount of water into a working tank, heating to 70 ℃, adding 3% of salt, fully stirring for reaction for 1.5 hours, and soaking the PC wire for 10 minutes.
Example 3
The PC line phosphating afterloading salt and the using process thereof comprise the following steps:
according to the mass percentage of the raw materials, 30% of sodium stearate, 65% of borax, 4% of sodium tripolyphosphate and 1% of sodium nitrite are provided, the sodium stearate, the borax, the sodium tripolyphosphate and the sodium nitrite are weighed according to the quantity and are added into a stirring kettle, and the mixture is fully stirred for 30 minutes to obtain a mixture, namely a salt-carrying mixture; pouring a certain amount of water into a working tank, heating to 85 ℃, adding 3% of salt, fully stirring for reaction for 1.2 hours, and soaking the PC wire for 8 minutes.
Example 4
The PC line phosphating afterloading salt and the using process thereof comprise the following steps:
providing 22% of sodium stearate, 75% of borax, 1% of sodium tripolyphosphate and 2% of sodium nitrite according to the mass percentage of the raw materials, weighing the sodium stearate, the borax, the sodium tripolyphosphate and the sodium nitrite according to the quantity, adding the weighed materials into a stirring kettle, and fully stirring the materials for 28 minutes to obtain a mixture, namely a salt-carrying material; pouring a certain amount of water into a working tank, heating to 80 ℃, adding 5% of salt, fully stirring for reaction for 1 hour, and soaking the PC wire for 8 minutes.
Example 5
The PC line phosphating afterloading salt and the using process thereof comprise the following steps:
providing 20% of sodium stearate, 75% of borax, 2% of sodium tripolyphosphate and 3% of sodium nitrite according to the mass percentage of the raw materials, weighing the sodium stearate, the borax, the sodium tripolyphosphate and the sodium nitrite according to the quantity, adding the weighed materials into a stirring kettle, and fully stirring the materials for 40 minutes to obtain a mixture, namely a salt-carrying material; pouring a certain amount of water into a working tank, heating to 75 ℃, adding 5% of salt, fully stirring for reaction for 1 hour, and soaking the PC wire for 10 minutes.
Comparative example: according to the mass percentage of the raw materials, 45% of sodium stearate, 54% of borax, 0.5% of sodium tripolyphosphate and 0.5% of sodium nitrite are provided, the sodium stearate, the borax, the sodium tripolyphosphate and the sodium nitrite are weighed according to the quantity and are added into a stirring kettle, and the mixture is fully stirred for 28 minutes to obtain a mixture, namely salt-carrying; pouring a certain amount of water into a working tank, heating to 80 ℃, adding 5% of salt, fully stirring for reaction for 1 hour, and soaking the PC wire for 8 minutes.
Examples of the experiments
The PC wire phosphating post-salt loading materials prepared in examples 1-5 and the comparative example are respectively subjected to performance tests, and the rust-proof performance of the PC wire phosphating post-salt loading treatment is mainly examined.
And (3) testing: the PC wires were treated with the salt-loaded materials prepared in examples and comparative examples, respectively, and the rust inhibitive performance of the salt-loaded materials was examined.
TABLE 1 Performance data for PC wire phosphating post-salt loading and comparative examples prepared in the examples
Item | Antirust property |
Example 1 | Does not rust after being placed for 20 days at normal temperature |
Example 2 | Does not rust after being placed for 25 days at normal temperature |
Example 3 | Does not rust after being placed for 25 days at normal temperature |
Example 4 | Does not rust after being placed for 23 days at normal temperature |
Example 5 | Does not rust after being placed for 28 days at normal temperature |
Comparative example | Does not rust after being placed for 10 days at normal temperature |
As can be seen from Table 1, in examples 1-5, the PC wire phosphating carried salt prepared by the invention is prepared by adding sodium stearate, borax, sodium tripolyphosphate and sodium nitrite into a stirring kettle in a quantitative manner and stirring, and the addition of sodium nitrite can also improve the rust resistance after phosphating, thereby solving the problem of easy rust return when only borax is used and the problem of stacking wire rods when sodium stearate is used.
Furthermore, it should be understood that although the present description refers to embodiments, not every embodiment may contain only a single embodiment, and such description is for clarity only, and those skilled in the art should integrate the description, and the embodiments may be combined as appropriate to form other embodiments understood by those skilled in the art.
Claims (7)
1. The post-loaded salt for PC wire phosphating is characterized by comprising the following raw material components in percentage by mass: 10 to 30 percent of sodium stearate, 65 to 85 percent of borax, 1 to 5 percent of sodium tripolyphosphate and 1 to 5 percent of sodium nitrite.
2. The post-phosphating salt for PC lines according to claim 1, characterized by comprising the following preparation steps: sodium stearate, borax, sodium tripolyphosphate and sodium nitrite are weighed according to the quantity and added into a stirring kettle, and the mixture, namely the salt is obtained after full stirring.
3. The afterloaded salt for PC line phosphating according to claim 2, characterized in that the stirring time is 20-40 minutes.
4. The post-phosphating salt for PC lines according to any one of claims 1 to 3, characterized in that the use process comprises the following steps: pouring a certain amount of water into a working tank, heating to a certain temperature, adding 3% -10% of salt, fully stirring for reaction for a period of time, and then soaking the PC wire.
5. A PC wire phosphating aftersalt according to claim 4, characterised in that the heating temperature is 70-85 ℃.
6. PC line phosphating aftersalt according to claim 4, characterized in that the stirring time is 0.5 to 1.5 hours.
7. PC line phosphating aftersalt according to claim 4, characterized in that the soaking time is 3-10 minutes.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201911363160.1A CN110983313A (en) | 2019-12-26 | 2019-12-26 | Phosphate after-loading salt for PC line and use process thereof |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201911363160.1A CN110983313A (en) | 2019-12-26 | 2019-12-26 | Phosphate after-loading salt for PC line and use process thereof |
Publications (1)
Publication Number | Publication Date |
---|---|
CN110983313A true CN110983313A (en) | 2020-04-10 |
Family
ID=70077069
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201911363160.1A Pending CN110983313A (en) | 2019-12-26 | 2019-12-26 | Phosphate after-loading salt for PC line and use process thereof |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN110983313A (en) |
Citations (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CH393871A (en) * | 1957-11-29 | 1965-06-15 | Parker Ste Continentale | Process for cold cleaning and cold phosphating of metal surfaces |
CA896508A (en) * | 1972-03-28 | Tuch Richard | Metal treating process | |
GB1294054A (en) * | 1970-04-20 | 1972-10-25 | Uss Eng & Consult | Method for the electrolytic removal of drawing or rolling lubricants on ferrous strands |
CN1059361A (en) * | 1990-08-22 | 1992-03-11 | 远东钢丝针布厂 | Wire cold-drawing lubricant and preparation method thereof |
US6068710A (en) * | 1996-11-27 | 2000-05-30 | Henkel Corporation | Aqueous composition and process for preparing metal substrate for cold forming |
US6376433B1 (en) * | 1999-07-13 | 2002-04-23 | Century Chemical Corporation | Process and product for lubricating metal prior to cold forming |
CN102230183A (en) * | 2011-06-24 | 2011-11-02 | 大连洁仕清洁用品有限公司 | Cleaning and antirust agent for secondary processing of casting parts and preparation method thereof |
CN105018913A (en) * | 2014-04-18 | 2015-11-04 | 石家庄正仁环保科技有限公司 | Rust prevention liquid for metal surfaces |
US20160236236A1 (en) * | 2015-02-16 | 2016-08-18 | Han Young Steel Wire Co., Ltd. | Method for manufacturing non-phosphate coated metal material for cold heading-plastic working process |
-
2019
- 2019-12-26 CN CN201911363160.1A patent/CN110983313A/en active Pending
Patent Citations (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA896508A (en) * | 1972-03-28 | Tuch Richard | Metal treating process | |
CH393871A (en) * | 1957-11-29 | 1965-06-15 | Parker Ste Continentale | Process for cold cleaning and cold phosphating of metal surfaces |
GB1294054A (en) * | 1970-04-20 | 1972-10-25 | Uss Eng & Consult | Method for the electrolytic removal of drawing or rolling lubricants on ferrous strands |
CN1059361A (en) * | 1990-08-22 | 1992-03-11 | 远东钢丝针布厂 | Wire cold-drawing lubricant and preparation method thereof |
US6068710A (en) * | 1996-11-27 | 2000-05-30 | Henkel Corporation | Aqueous composition and process for preparing metal substrate for cold forming |
US6376433B1 (en) * | 1999-07-13 | 2002-04-23 | Century Chemical Corporation | Process and product for lubricating metal prior to cold forming |
CN102230183A (en) * | 2011-06-24 | 2011-11-02 | 大连洁仕清洁用品有限公司 | Cleaning and antirust agent for secondary processing of casting parts and preparation method thereof |
CN105018913A (en) * | 2014-04-18 | 2015-11-04 | 石家庄正仁环保科技有限公司 | Rust prevention liquid for metal surfaces |
US20160236236A1 (en) * | 2015-02-16 | 2016-08-18 | Han Young Steel Wire Co., Ltd. | Method for manufacturing non-phosphate coated metal material for cold heading-plastic working process |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN107435144B (en) | Silane vitrification agent, vitrification working solution and method for preparing silane vitrification agent | |
CN110629209A (en) | Phosphating solution suitable for phosphating low-alloy steel wires and preparation method thereof | |
CN110818097A (en) | Phosphorus-free corrosion and scale inhibitor and preparation method thereof | |
EP3771704A1 (en) | Anti-caking agent used for nitrogen-based fertilizer, preparation method therefor and application thereof | |
CN105154181A (en) | Anti-rust wax for metal | |
CN115198259A (en) | Passivating solution for stainless steel and preparation method thereof | |
CN102676139A (en) | Micro paraffin inhibitor used for high-temperature high-salt oil well and preparation method thereof | |
GB2048961A (en) | Protective compositions for steel surfaces | |
CN110983313A (en) | Phosphate after-loading salt for PC line and use process thereof | |
CN110670058A (en) | Chromium-free passivator | |
CN110921857A (en) | Special scale inhibitor for MVR system and preparation method thereof | |
CN104451633A (en) | Rust-removing and rust-preventing solution and preparation method thereof | |
CN112725785A (en) | Blue passivator for steel parts and preparation method thereof | |
CN104388159A (en) | Antirust oil for metal pipelines | |
CN104450023A (en) | Rust-proof oil for metal processing molding | |
CN111676472B (en) | Chromium-free passivator with high corrosion resistance for batch hot galvanizing | |
CN104312671A (en) | Thin-layer high-permeability rust-preventive oil | |
CN111270231A (en) | Chromium-free passivator for powder zinc impregnation | |
CN112210783A (en) | Rust-removing and rust-preventing agent and application thereof | |
CN111850532A (en) | Chromium-free surface treatment liquid for electro-galvanized steel plate and preparation method thereof | |
US4214924A (en) | Method of improving surface characteristic of heat-treated metal | |
US3598756A (en) | Phosphate-and chromate-free corrosion inhibitor | |
CN104388158A (en) | Environment-friendly anti-rust oil | |
CN115433891B (en) | Annealing method of copper conductive material | |
US2410688A (en) | Method of making protective composition and resulting product |
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 | ||
RJ01 | Rejection of invention patent application after publication |
Application publication date: 20200410 |
|
RJ01 | Rejection of invention patent application after publication |