JPH02229893A - Composition for wire covering - Google Patents

Composition for wire covering

Info

Publication number
JPH02229893A
JPH02229893A JP2021894A JP2189490A JPH02229893A JP H02229893 A JPH02229893 A JP H02229893A JP 2021894 A JP2021894 A JP 2021894A JP 2189490 A JP2189490 A JP 2189490A JP H02229893 A JPH02229893 A JP H02229893A
Authority
JP
Japan
Prior art keywords
composition
soap
weight
total
sodium
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
JP2021894A
Other languages
Japanese (ja)
Inventor
Daburiyu Taru Toomasu
トーマス ダブリュ.タル
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.)
Nihon Parkerizing Co Ltd
Original Assignee
Nihon Parkerizing 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 Nihon Parkerizing Co Ltd filed Critical Nihon Parkerizing Co Ltd
Publication of JPH02229893A publication Critical patent/JPH02229893A/en
Pending legal-status Critical Current

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    • C10M173/00—Lubricating compositions containing more than 10% water
    • C10M173/02—Lubricating compositions containing more than 10% water not containing mineral or fatty oils
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    • C10M103/00—Lubricating compositions characterised by the base-material being an inorganic material
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    • C10N2040/245—Soft metals, e.g. aluminum
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00—Specified use or application for which the lubricating composition is intended
    • C10N2040/20—Metal working
    • C10N2040/244—Metal working of specific metals
    • C10N2040/246—Iron or steel
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00—Specified use or application for which the lubricating composition is intended
    • C10N2040/20—Metal working
    • C10N2040/244—Metal working of specific metals
    • C10N2040/247—Stainless steel
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2050/00—Form in which the lubricant is applied to the material being lubricated
    • C10N2050/01—Emulsions, colloids, or micelles
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2050/00—Form in which the lubricant is applied to the material being lubricated
    • C10N2050/015—Dispersions of solid lubricants
    • C10N2050/02—Dispersions of solid lubricants dissolved or suspended in a carrier which subsequently evaporates to leave a lubricant coating

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  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Lubricants (AREA)
  • Metal Extraction Processes (AREA)
  • Superconductors And Manufacturing Methods Therefor (AREA)
  • Paints Or Removers (AREA)
  • Ropes Or Cables (AREA)
  • Communication Cables (AREA)
  • Application Of Or Painting With Fluid Materials (AREA)
  • Detergent Compositions (AREA)
  • Nonmetallic Welding Materials (AREA)

Abstract

PURPOSE:To obtain the subject composition having an excellent crystal structure, soap-lubricant pull-in and pull-out properties and low moisture absorption and capable of ready cold pultrusion by blending K2SO4, etc., with a specified alkaline soap in a specified ratio. CONSTITUTION:An objective composition containing (A) 95-99.99wt.% K2SO4 and/or Na2SO4 and (B) 0.01-5wt.% one or more alkaline soaps selected from potassium soap, ammonium soap and sodium soap and having <=50wt.% total Na ion in the composition based on the sum of the total K ion and the total NH3 ion.

Description

【発明の詳細な説明】 [産業上の利用分野] 本発明は、線材の冷間引抜き加工に用いられる改良され
た被覆用組成物、特に水溶性塩被覆剤に関する。
DETAILED DESCRIPTION OF THE INVENTION [Industrial Field of Application] The present invention relates to an improved coating composition, particularly a water-soluble salt coating, for use in cold drawing of wire rods.

[従来の技術] 水溶性塩被覆剤は、引抜き加工に先立つ′C水溶液の形
で鋼線に被覆されることが多い。このように溶液被覆さ
れた鋼線を乾燥し、その結果得た塩被覆鋼線を、乾燥石
鹸潤滑剤を用いて通常の引抜きダイスで引抜き加工する
ことは、周知の方法である。水溶性塩被覆物は、潤滑剤
のキャリアーとして働く。つまり、この作用で乾燥石鹸
容器箱(ダイスボックス)の潤滑剤をダイスに引込み、
潤滑性を付与する。このような鋼線上で乾燥する水溶性
塩被覆剤は、ダイスに潤滑剤を引き込むという特性があ
り、従来石灰やはう砂のような被覆剤が用いられている
。鋼(通常はステンレス鋼)線の被覆に用いられる典型
的な可溶性塩組成物には、硫酸ナトリウムとはう砂の両
方が含まれている。このような可溶性塩組成物を用いる
と、優れた結晶構造を有する被覆が得られ、被覆鋼線を
石鹸箱を通過させるときに良好な石鹸潤滑剤引込み性が
発揮されるので、優れた引抜き性が得られることになる
。
[Prior Art] Water-soluble salt coatings are often coated onto steel wire in the form of an aqueous solution prior to drawing. It is a well-known method to dry such solution-coated steel wire and to draw the resulting salt-coated steel wire in a conventional drawing die using a dry soap lubricant. The water-soluble salt coating acts as a carrier for the lubricant. In other words, this action draws the lubricant from the dry soap container box (dice box) into the die,
Provides lubricity. The water-soluble salt coating that dries on the steel wire has the property of drawing lubricant into the die, and conventionally coatings such as lime or sand have been used. Typical soluble salt compositions used to coat steel (usually stainless steel) wire include both sodium sulfate and sand. Using such a soluble salt composition, a coating with an excellent crystal structure is obtained, and when the coated steel wire is passed through a soapbox, good soap lubricant drawing properties are exhibited, resulting in excellent drawing properties. will be obtained.

[発明が解決しようとする課題J しかしながら、このような可溶性塩被覆剤で被覆された
線材は、外気に曝すと、特に湿度が高い空気に曝すと、
過度に吸湿してしまいがちである。このような吸湿があ
ると、被覆された鋼線の引抜き加工が重大に阻害された
り、時には不可能になることさえある。他方においては
、吸湿度の低い可溶性塩被覆剤を用いると、結晶構造が
殆どないようなもの(つまり、非品質またはガラス質型
の被覆)となり、潤滑剤引込み性及び引抜き性は、共に
顕著に劣ったものになる。
[Problem to be Solved by the Invention J] However, when a wire coated with such a soluble salt coating agent is exposed to the outside air, especially when exposed to high humidity air,
It tends to absorb too much moisture. Such moisture absorption can seriously impede and sometimes even make the drawing process of the coated steel wire impossible. On the other hand, the use of soluble salt coatings with low moisture absorption results in coatings with almost no crystalline structure (i.e., non-quality or glassy type coatings), and both lubricant retraction and extraction properties are significantly reduced. become inferior.

本発明は、かかる欠点を改善し、優れた結晶構造、石鹸
潤滑剤引込み性及び引抜き性を有し、同時に、湿度の高
い日でさえも水分吸収性が低い、つまり低吸湿性を有す
る均一被覆剤を提供しようとするものである。
The present invention improves such drawbacks and provides a uniform coating with excellent crystal structure, soap lubricant retraction and pullability, and at the same time low moisture absorption, i.e., low hygroscopicity, even on humid days. The aim is to provide a drug.

[課題を解決するための手段] そして、新しく見いだされた本発明の組成物は、 (1)冷間引抜き加工を容易にするための線材被覆用組
成物であって、有効成分として (イ)K2S04及び/又はNa2SO4並びに ?口)カリウム石鹸、アンモニウム石鹸及びナトリウム
石鹸よりなる群から選ばれる1種以上のアルカリ石鹸 を、その成分全量に対しそれぞれ95〜99.99重量
%及び0.01〜5重量%含有し、しかも組成物中の全
ナトリウムイオンの量が全カリウムイオンの量と全アン
モニウムイオンの量との和の50重量%以下である組成
物。
[Means for Solving the Problems] The newly discovered composition of the present invention is (1) a wire coating composition for facilitating cold drawing, which contains (a) as an active ingredient; K2S04 and/or Na2SO4 and? (1) Contains 95 to 99.99% by weight and 0.01 to 5% by weight of one or more alkaline soaps selected from the group consisting of potassium soap, ammonium soap, and sodium soap, respectively, and has a composition A composition in which the total amount of sodium ions in the product is 50% by weight or less of the sum of the total amount of potassium ions and the total amount of ammonium ions.

(2)冷間引抜き加工を容易にするための線材被覆用組
成物であって、有効成分として (イ)K2SO4及びl又はNa2SO4、(イ′)K
2B4o7、Na2B407、KBO■及びNaBO2
よりなる群から選ばれる1種以上の硼酸塩並びに (口)力〜リウム石鹸、アンモニウム石鹸及びナトリウ
ム石鹸よりなる群から選ばれる1種以上のアルカリ石鹸 を、その成分全量に対しそれぞれ50〜99.98 N
 量%、0.01〜49.99重量%及び0.01〜5
重量%含有し、しかも組成物中の全ナトリウムイオンの
量が全カリウムイオンの量と全アンモニウムイオンの量
との和の50重量%以下である組成物、である。
(2) A composition for coating a wire rod to facilitate cold drawing processing, which contains (a) K2SO4 and l or Na2SO4 as active ingredients, (a') K
2B4o7, Na2B407, KBO■ and NaBO2
one or more borates selected from the group consisting of borates and one or more alkaline soaps selected from the group consisting of lithium soap, ammonium soap, and sodium soap, each in an amount of 50 to 99. 98N
% by weight, 0.01-49.99% by weight and 0.01-5
% by weight, and the amount of total sodium ions in the composition is 50% by weight or less of the amount of total potassium ions and the amount of total ammonium ions.

すなわち、本発明の組成物は、使用のために水で希釈す
る前は乾燥した混合物の形であるが、以下の成分を次の
ような量範囲で含有するのである。
That is, the composition of the present invention, which is in the form of a dry mixture prior to dilution with water for use, contains the following ingredients in the following amount ranges:

第1発明: (イ)K2SO4及びl又はNa2S04を95 〜9
9.99重量%、好ましくは99.0〜99.9重量%
(口)カリウム石鹸、アンモニウム石鹸及びナトリウム
石鹸よりなる群から選ばれる1種以上のアルカリ石鹸を
0.01〜5重量%、好ましくは0.1〜1.0重量% ここで、(イ)、(口)成分中に存在する全カリウムイ
オンの量と全アンモニウムイオンの量との和の最大50
重量%、好ましくは10重量%以下がナトリウムイオン
で置換されているが、より好ましくはナトリウムイオン
で実質的に置換されていないものである。
First invention: (a) K2SO4 and l or Na2S04 at 95 to 9
9.99% by weight, preferably 99.0-99.9% by weight
(1) 0.01 to 5% by weight, preferably 0.1 to 1.0% by weight of one or more alkaline soaps selected from the group consisting of potassium soap, ammonium soap, and sodium soap, where (a), (mouth) Maximum 50 of the sum of the amount of total potassium ions and the amount of total ammonium ions present in the ingredient
% by weight, preferably 10% by weight or less, is substituted with sodium ions, more preferably not substantially substituted with sodium ions.

第2発明: (イ)K2SO4及び/又はNa2S○4を50 〜9
9.98重量%、好ま[7くは70〜89.9重量%(
イ′)K2B407、Na2B4o7、KBO。及びN
aBO2,よりなる群から選ばれる1種以上の硼酸塩を
0.01〜49.99重量%、好ましくは10〜29.
9重量%(口)カリウム石鹸、アンモニウム石鹸及びナ
トリウム石鹸よりなる群から選ばれる1種以上のアルカ
リ石鹸を0.01〜5重景%、好ましくは0,1〜1.
0重量% ここで、(イ)、(口)成分中に存在する全カリウムイ
オンの量と全アンモニウムイオンの量との和の最大50
重量%、好ましくは10重量%以下がナトリウムイオン
で置換されているが、より好ましくはナトリウムイオン
で実質的に置換されていないものである。
Second invention: (a) K2SO4 and/or Na2S○4 at 50 to 9
9.98% by weight, preferably [7 or 70-89.9% by weight (
B') K2B407, Na2B4o7, KBO. and N
aBO2, 0.01 to 49.99% by weight, preferably 10 to 29.9% by weight, of one or more borates selected from the group consisting of aBO2.
9% by weight (by weight) of one or more alkaline soaps selected from the group consisting of potassium soap, ammonium soap and sodium soap, 0.01 to 5%, preferably 0.1 to 1.
0% by weight Here, (a) (1) The maximum amount of 50% of the sum of the total amount of potassium ions and the total amount of ammonium ions present in the component.
% by weight, preferably 10% by weight or less, is substituted with sodium ions, more preferably not substantially substituted with sodium ions.

なお、第2発明は、第1発明における(イ)成分の一部
を(イ′)成分で置き換えたものである。
Note that the second invention is obtained by replacing a part of the component (A) in the first invention with the component (A').

上記両発明において、ナトリウムイオンで置換されてい
ないものが好ましいというのは、ナトリウムイオンが多
く存在すればするほど吸湿性が高くなるからである。
In both of the above inventions, those not substituted with sodium ions are preferred because the more sodium ions present, the higher the hygroscopicity becomes.

ナトリウムイオンが存在する場合には、(イ)、(イ′
)及び(口)成分の中の一成分以一トに存在し得るので
、例えば、(口)成分が部分的に若しくは全部ナトリウ
ム石鹸でもよい。
If sodium ions are present, (a), (i′)
) and the (oral) component, for example, the (oral) component may be partially or wholly a sodium soap.

また、(イ)成分及びl又は(イ′)成分がナトリウム
塩又はカリウム塩、またはこれらの塩の混合物でもよい
。但し、ナトリウム塩の全量に対する前記の制限は維持
されるものとする。
Furthermore, component (a) and component l or (a') may be a sodium salt, a potassium salt, or a mixture of these salts. However, the above-mentioned limit on the total amount of sodium salt shall be maintained.

上記の組成物が鋼線に被覆されるときに良好な結晶構造
が付与されるということは、全く予期せざるものである
。何故ならば、(口)成分を含まない上記組成物は、鋼
線に対して不均一な皮膜を付与し、このような皮膜は、
石鹸潤滑剤引込み性も引抜き性も共に不満足なものであ
り、コーティング剤として有用でないからである。機構
は未知ながら、上記の石鹸が存在する場合、水溶液の形
の上記組成物を鋼線に適用し、これを人工と自然とを問
わず乾燥させると、少なくとも部分的に結晶性?均一・
な皮膜が得られる。
It is quite unexpected that the above composition imparts a good crystal structure when coated onto a steel wire. This is because the above-mentioned composition that does not contain (original) components imparts a non-uniform coating to the steel wire, and such coating is
This is because the soap lubricant has unsatisfactory retraction and extraction properties and is not useful as a coating agent. Although the mechanism is unknown, if the above soap is present, applying the above composition in the form of an aqueous solution to a steel wire, whether artificial or natural, causes it to become at least partially crystalline? Uniform/
A film with a clear texture can be obtained.

(イ)成分として用いられるK2SO4は、化学的に純
粋なものでも工業的純度のものでもよいが、コストの観
点からは、後者が好ましい。
The K2SO4 used as component (a) may be chemically pure or industrially pure, but the latter is preferred from the cost standpoint.

(イ′)成分として用いられるK2B407も、化学的
に純粋なものでも工業的純度のものでもよいが、一般に
は、四水塩(K2B40■・4 H20 )として市販
され、本発明にてもこの形で用いられる。同様に、KB
O2は、(一イ′)成分として皐独にも、あるいはK2
B40■ど一緒にどんな比率の混合物としても用いられ
るが、このKBO2も化学的に純粋なものでも工業的純
度のものでもよい。
K2B407 used as component (a') may be chemically pure or industrially pure, but it is generally commercially available as a tetrahydrate salt (K2B40 4 H20), and this invention also uses this K2B407. used in the form Similarly, K.B.
O2 can also be used as a (1) component, or K2
Although used as a mixture with B40■ in any proportion, this KBO2 may also be chemically pure or of industrial purity.

上記アンモニウム石鹸又はカリウム石鹸は、C,2〜C
2■脂肪酸一種以上のアンモニウム塩又はカリウム塩、
又は2二のような01■一022脂肪酸二種以上の混合
物のアンモニウム塩又はカリウム塩である。
The above ammonium soap or potassium soap is C,2-C
2 ■ Ammonium salt or potassium salt of one or more fatty acids,
or an ammonium salt or a potassium salt of a mixture of two or more 01-1-022 fatty acids such as No. 22.

これら脂肪酸は、一般に飽和でしかも直鎖のもので、本
発明に使用するにはステアリン酸アンモニウム又はスデ
アリ;・・酸カリウムが好ましい。もつ1冒)、二重結
合が一個又は二個の不飽和Cエ2〜C2■?肪酸も、単
独あるいはお互いに混合して、更に/或いは飽和脂肪酸
と混合して用いることも可能である。例えば、獣脂油や
椰子油、又はこれらの混合物の鹸化によって得た脂肪酸
混合物から誘導されるアンモニウム石鹸又はカリウム石
鹸を、(ロ)成分として有利に用いることができる。ま
た、分枝状あるいは脂環構造のものを一部に含む0■2
〜C2■脂肪酸のアンモニウム塩又はカリ・クム塩を、
単独あるいは直鎖の脂肪酸塩と混合して本発明に使用す
ることができる。また、ロジン酸、゛例えば、アビエチ
ン酸のアンモニウム塩またはカリ・クム塩も、(口)成
分として用いることができる。
These fatty acids are generally saturated and linear, with ammonium stearate or potassium stearate being preferred for use in the present invention. 1) with one or two double bonds, unsaturated C2~C2■? Fatty acids can also be used alone or in admixture with each other and/or in admixture with saturated fatty acids. For example, ammonium or potassium soaps derived from fatty acid mixtures obtained by saponification of tallow oil, coconut oil, or mixtures thereof can be advantageously used as component (b). In addition, 0■2 containing some branched or alicyclic structures
~C2■ Fatty acid ammonium salt or potassium cum salt,
It can be used in the present invention alone or in combination with a linear fatty acid salt. Also, ammonium or potassium cum salts of rosin acids, such as abietic acid, can be used as (oral) ingredients.

本発明の被覆組成物で被覆される線材は、一般に鋼線で
あり、通常はステンレス鋼線である。しかし、他の線材
も本発明の被覆組成物で被覆可能で、これらの被覆可能
の線材としては、軟鋼、チタニウム、゛バナジウム、タ
ングステン、アルミニウム、銅、ニッケル、ジルコニウ
ムなど及びこれらの合金が挙げられる。線材への被覆は
、本発明の徂成物の水溶液を線、オに接触させ、得られ
た湿った被覆物をそのまま乾燥させることによって行わ
れるが、この時、加熱する場合も加熱しない場合もある
。本発明に用いられる水溶液は、水中に紹成物を一般に
75〜400g/l、好ましくは150〜250g/l
含有するものである。
The wire coated with the coating composition of the present invention is generally a steel wire, usually a stainless steel wire. However, other wire materials can also be coated with the coating composition of the present invention, including mild steel, titanium, vanadium, tungsten, aluminum, copper, nickel, zirconium, etc., and alloys thereof. . Coating the wire is carried out by bringing an aqueous solution of the invention's product into contact with the wire and drying the resulting wet coating, which may or may not be heated. be. The aqueous solution used in the present invention generally contains 75 to 400 g/l, preferably 150 to 250 g/l of the introduced product in water.
It contains.

線材を上記溶液に接触させるには、回分式でも連続式で
も便利な方法で行い、その後得た湿潤被覆線材を乾燥し
た後、貯蔵、出荷、あるいはダイスボックス(例えば、
通常の粉末石鹸潤滑剤を使用する)を有する通常の引抜
き装置で被覆処理した線材を引抜き加工する。線材上の
皮膜は、ダイスの中の乾燥粉末石鹸潤滑剤を運ぶキャリ
アーとして機能する。
Contacting the wire with the solution may be carried out in any convenient manner, either batchwise or continuously, and the resulting wet coated wire may then be dried before being stored, shipped, or placed in a die box (e.g.
The coated wire is drawn on conventional drawing equipment (using a conventional powdered soap lubricant). The coating on the wire acts as a carrier for the dry powder soap lubricant within the die.

本発明の標準的な線材処理工程は、以下の工程によるが
、本発明はこの工程に限定されるものではない。
The standard wire treatment process of the present invention is based on the following process, but the present invention is not limited to this process.

1,線材の清浄一洗浄用組成物は周知技術であり、本発
明の構成部分とはならない。
1. Cleaning of Wire Rods - Cleaning compositions are well known and do not constitute a component of the present invention.

2.水洗。2. Wash with water.

3.酸洗一酸洗用組成物は周知技術であり、酸洗用組成
物の選択は本発明のtI4成部分とはならない。
3. Pickling and pickling compositions are well known in the art, and the selection of the pickling composition is not part of the tI4 component of the present invention.

4.水洗。4. Wash with water.

5,前記のように本発明の被覆組成物による処理。5. Treatment with the coating composition of the invention as described above.

6.前記のように線材を乾燥し、本発明の被覆線材を得
る。
6. The wire is dried as described above to obtain the coated wire of the present invention.

この被覆処理した線材は前記のように引抜き加工するこ
とが可能になる。
This coated wire can be drawn as described above.

本発明の水溶液を調製するのに用いられる水は、好まし
くは、蒸留水が脱イオン水であるが、過度に硬度が高く
なく、溶解ナトリウム塩含有量が低い場合には、水道水
も用いることが可能である。
The water used to prepare the aqueous solution of the invention is preferably distilled or deionized water, but tap water may also be used if it is not too hard and has a low dissolved sodium salt content. is possible.

[実施例J 以下、本発明を実施例及び比較例をあげて説明するが、
本発明はこれらの実施例に限定されないものとする。
[Example J The present invention will be explained below with reference to Examples and Comparative Examples.
The invention is not limited to these examples.

皿工 以下の水溶液租成物をステンレス鋼のパネルに被覆して
、皮膜形態観察及び吸湿性試験を行った。ステンレス鋼
パネルを以下の各組成物で被覆するには、水溶液中にパ
ネルを浸漬した後、この水溶液からパネルを引上げ、パ
ネルを急速(空気)乾燥することによって行った。
A stainless steel panel was coated with an aqueous solution of a size smaller than a plate, and film morphology observation and hygroscopicity tests were conducted. Stainless steel panels were coated with each of the following compositions by immersing the panels in an aqueous solution, pulling the panels from the aqueous solution, and rapidly (air) drying the panels.

比較例a)脱イオン水11につきNa2SO475重量
%及び四硼酸ナトリウム・IOH20 25重量%の混
合物187.2 g.使用温度190°F(87°C)
。
Comparative Example a) 187.2 g of a mixture of 75% by weight of Na2SO4 and 25% by weight of sodium tetraborate.IOH20 in 11 parts deionized water. Operating temperature 190°F (87°C)
.

比較例b)脱イオン水1lにつきK2SO475重量%
及びK2B40。・4H2025重量%の混合物187
.2 go使用温度190°F(87°C)。
Comparative example b) 75% by weight of K2SO per liter of deionized water
and K2B40.・4H2025% by weight mixture 187
.. 2 go operating temperature 190°F (87°C).

比較例C)  a)のように調製した水溶液にステアリ
ン酸ナトリウムを5 g/i添加。使用温度190°F
0実施例d)  b)のように調製した水溶液にステア
リン酸アンモニウムを5g/l添加。使用温度190°
F0上記組成物で被覆したステンレス鋼パネルの部分に
ついて、次に皮膜形態観察及び吸湿度試験を行った。試
験結果は、以下の第1表に示す。第1表において、RH
は相対湿度を意味する。
Comparative Example C) Addition of 5 g/i of sodium stearate to the aqueous solution prepared as in a). Operating temperature 190°F
Example 0 d) Addition of 5 g/l ammonium stearate to the aqueous solution prepared as in b). Operating temperature 190°
F0 The portion of the stainless steel panel coated with the above composition was then subjected to film morphology observation and a moisture absorption test. The test results are shown in Table 1 below. In Table 1, RH
means relative humidity.

第1表 本 被覆物中の平均水分バーセント。水分増加率は、空
気暴露の前と後の無被覆パネルと被覆パ木ルとの重量差
によって測定。
Table 1: Average percentage of moisture in the coating. Moisture gain was determined by the weight difference between the uncoated panel and the coated panel before and after air exposure.

第1表から分かるように、本発明の組成物、っまリd)
組成では、良好な結晶性と共に低い吸湿性が得られた。
As can be seen from Table 1, the composition of the invention,
The composition yielded good crystallinity and low hygroscopicity.

彰旦 本例は、水溶性塩被覆物の吸湿性に及ぼすナト;ノウム
とカリウムの相対比の影響を示す。第2表に示される以
下の組成の水溶液を用いて、例工の方法によってステン
レス鋼パネルを被覆した。なお、第2表には試験結果も
示す。ちなみに第2表において、 M=モル濃度つまり溶液11当たりのグラムモル数で、 RH=相対湿度である。
This example shows the effect of the relative ratios of sodium and potassium on the hygroscopic properties of water-soluble salt coatings. An aqueous solution having the following composition as shown in Table 2 was used to coat stainless steel panels by the method of Example Co., Ltd. Note that Table 2 also shows the test results. Incidentally, in Table 2, M=molar concentration, ie, number of grams of moles per solution 11, and RH=relative humidity.

例II1 木片例は、既知のナトリウムベースの塩組成物と本発明
の低ナトリウム塩組成物とからの被覆物および石灰被覆
物の相対吸湿性を示す。これら被覆物は、以下の水溶液
組成物を用いて、例工の方法に従い、ステンレス鋼線材
の試料の上に被覆したものである。
Example II1 The wood chip example shows the relative hygroscopicity of coatings and lime coatings from known sodium-based salt compositions and the low sodium salt compositions of the present invention. These coatings were coated on stainless steel wire samples using the following aqueous solution composition according to the method of Example Co., Ltd.

比較例j)脱・fオン水11につきNa2SO475重
量%及び四硼酸ナトリウム・IOH20 25重量%の
混合物187.2 g 0使用温度190°F0実施例
k)脱イオン水11につきK2S0479重量%、四硼
酸ナトリウム・10H2o20重量%、及びステアリン
酸アンモニウム1重景%の混合物187.2go使用温
度190°F0 比較例1)脱イオン水中の石灰3重量%。使用温度19
0°Fo 比較例m)脱イオン水中の石灰6重量%。使用温度19
0°F。
Comparative example j) 187.2 g of a mixture of 75% by weight of Na2SO4 and 25% by weight of sodium tetraborate/IOH20 in 11 parts of deionized water 0 Working temperature 190° F0 Example k) 479 parts by weight of K2S0 in 11 parts of deionized water, tetraboric acid Mixture of 20% by weight of sodium 10H2O and 1% by weight of ammonium stearate 187.2go Working temperature 190°F0 Comparative Example 1) 3% by weight of lime in deionized water. Operating temperature 19
0°Fo Comparative Example m) 6% by weight of lime in deionized water. Operating temperature 19
0°F.

第3表 上記の第3表から分かるように、本発明c6k)組成は
、石灰被覆物1)及びm)に対比して顕著に低い吸湿性
を有した。
Table 3 As can be seen from Table 3 above, the composition according to the invention c6k) had a significantly lower hygroscopicity compared to the lime coatings 1) and m).

例■ 異なった十種の被覆浴相成物について、水分増加量、皮
膜形態、皮膜の均一性、及び1インチ当たりの結晶数を
ステンレスパネルを用いて評価した。
Example ■ Ten different coating bath phase compositions were evaluated for moisture gain, film morphology, film uniformity, and number of crystals per inch using stainless steel panels.

これらのステンレス鋼パネルは、第4表に示される被覆
組成物及び被覆浴で、例■に用いられた方法に従って被
覆した。但し、湿潤被覆パネルは、250 ’F (約
120°C)で10分間加熱乾燥した。水分増加率は、
それぞれ温度80°F(27°C)及び湿度92%の恒
温室内で測定した。サートロン3サーフェース ブロビ
ロメータ−( Surtronic 3 surfac
epropb.ylometer )を用いて被覆1イ
ンチ当たりの結晶の数を測定した。皮膜性状と皮膜外観
は、目視によって決定した。
These stainless steel panels were coated according to the method used in Example 2 with the coating composition and coating bath shown in Table 4. However, the wet coated panels were heat dried at 250'F (approximately 120C) for 10 minutes. The moisture increase rate is
Each was measured in a constant temperature room at a temperature of 80°F (27°C) and a humidity of 92%. Surtronic 3 surface brovirometer (Surtronic 3 surfac
epropb. The number of crystals per inch of coating was determined using a ylometer. Film properties and film appearance were determined visually.

第4表において、S)、L)、及びW)被覆組成物は、
本発明による組成物であり、一方、n)、0)、p)、
q)、r)、U)、及びV)組成物は比較組成物である
。第4表から分かるように、S)、t)、及びW)組成
物は、均一な皮膜を生成するとともに低吸湿性を示した
。均一な皮膜を形成した比較組成物は、0)組成物のみ
であったが、吸湿性が高く許容に足るものでなかった。
In Table 4, the coating compositions S), L), and W) are:
a composition according to the invention, while n), 0), p),
Compositions q), r), U), and V) are comparative compositions. As can be seen from Table 4, compositions S), t), and W) produced uniform films and exhibited low hygroscopicity. Composition 0 was the only comparative composition that formed a uniform film, but it had high hygroscopicity and was not acceptable.

実際、n)、0)、及びp)組成物は全て、許容できな
いほど高い吸湿性を示I〜、従って湿度の高い環境では
線材引抜き性が劣るものであった。r)被覆組成物は、
ステアリン酸ナトリウム石鹸が過度の量存在しているこ
とを除いで、本発明に従って硫酸カリウムとステアリン
酸ナトリウムとを含有するものであるが、その結果とし
て、不均一かつ大部分ガラス質の皮膜となり、線材引抜
き特性は許容し得るものではない。石鹸が存在していな
いことを除いて本発明に従うカリウム塩組成物であるq
)、U)、及び■)組成物は、許容し得ない程の不均一
皮膜となり、従って線材引抜き特性がバラバラで許容し
得るものではない。本発明の8)、t)、及びW}被覆
組成物を比較すると、四硼酸アルカリ金属塩を含有する
W)組成物が、最も結晶性の高い皮膜となった。従って
、本発明の被覆組成物に四硼酸塩を存在させておくこと
は、選択的ではあるが、極めて好ましいことである。
In fact, compositions n), 0), and p) all exhibited unacceptably high hygroscopicity and therefore poor wire drawability in humid environments. r) The coating composition is:
containing potassium sulfate and sodium stearate according to the invention, except that sodium stearate soap is present in excessive amounts, resulting in a non-uniform and largely glassy film; The wire drawing properties are not acceptable. A potassium salt composition according to the invention except that no soap is present.
), U), and (2) compositions result in unacceptably non-uniform coatings and, therefore, the wire drawing properties are inconsistent and unacceptable. Comparing the coating compositions 8), t), and W} of the present invention, the W) composition containing an alkali metal tetraborate salt had the highest crystallinity. Therefore, the presence of tetraborate in the coating compositions of the present invention, although optional, is highly preferred.

[発明の効果] 以上の説明及び比較実験の結果からもわかるように、本
発明の組成物は、従来のこの種組成物に比べてより優れ
た結晶構造、石鹸潤滑剤引込み性及び引抜き性を有し、
かつ吸湿性も低く、極めて有用なものということができ
よう。
[Effects of the Invention] As can be seen from the above explanations and the results of comparative experiments, the composition of the present invention has a better crystal structure, soap lubricant drawing property, and drawing property compared to conventional compositions of this type. have,
It also has low hygroscopicity, making it extremely useful.

Claims (3)

【特許請求の範囲】[Claims] (1)冷間引抜き加工を容易にするための線材被覆用組
成物であって、有効成分として (イ)K_2SO_4及び/又はNa_2SO_4並び
に (ロ)カリウム石鹸、アンモニウム石鹸及びナトリウム
石鹸よりなる群から選ばれる1種以上のアルカリ石鹸 を、その成分全量に対しそれぞれ95〜99.99重量
%及び0.01〜5重量%含有し、しかも組成物中の全
ナトリウムイオンの量が全カリウムイオンの量と全アン
モニウムイオンの量との和の50重量%以下である組成
物。
(1) A composition for coating a wire rod to facilitate cold drawing processing, the active ingredient being selected from the group consisting of (a) K_2SO_4 and/or Na_2SO_4 and (b) potassium soap, ammonium soap and sodium soap. The composition contains one or more alkaline soaps of 95 to 99.99% by weight and 0.01 to 5% by weight, respectively, based on the total amount of the ingredients, and the amount of total sodium ions in the composition is equal to the amount of total potassium ions. A composition in which the total amount of ammonium ions is 50% by weight or less.
(2)冷間引抜き加工を容易にするための線材被覆用組
成物であって、有効成分として (イ)K_2SO_4及び1又はNa_2SO_4、(
イ′)K_2B_4O_7、Na_2B_4O_7、K
BO_2及びNaBO_2よりなる群から選ばれる1種
以上の硼酸塩 並びに (ロ)カリウム石鹸、アンモニウム石鹸及びナトリウム
石鹸よりなる群から選ばれる1種以上のアルカリ石鹸 を、その成分全量に対しそれぞれ50〜99.98重量
%、0.01〜49.99重量%及び0.01〜5重量
%含有し、しかも組成物中の全ナトリウムイオンの量が
全カリウムイオンの量と全アンモニウムイオンの量との
和の50重量%以下である組成物。
(2) A composition for coating a wire rod to facilitate cold drawing processing, which contains (a) K_2SO_4 and 1 or Na_2SO_4, (
A') K_2B_4O_7, Na_2B_4O_7, K
One or more borates selected from the group consisting of BO_2 and NaBO_2 and (b) one or more alkaline soaps selected from the group consisting of potassium soap, ammonium soap and sodium soap, each containing 50 to 99% of the total amount of the ingredients. .98% by weight, 0.01 to 49.99% by weight, and 0.01 to 5% by weight, and the amount of total sodium ions in the composition is the sum of the amount of total potassium ions and the total amount of ammonium ions. 50% or less by weight of the composition.
(3)組成物が濃度70〜400g/lの水溶液である
請求項1又は2記載の組成物。
(3) The composition according to claim 1 or 2, wherein the composition is an aqueous solution having a concentration of 70 to 400 g/l.
JP2021894A 1989-02-07 1990-01-31 Composition for wire covering Pending JPH02229893A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US30764389A 1989-02-07 1989-02-07
US307643 1989-02-07

Publications (1)

Publication Number Publication Date
JPH02229893A true JPH02229893A (en) 1990-09-12

Family

ID=23190606

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2021894A Pending JPH02229893A (en) 1989-02-07 1990-01-31 Composition for wire covering

Country Status (11)

Country Link
EP (1) EP0382155B1 (en)
JP (1) JPH02229893A (en)
CN (1) CN1044774A (en)
AT (1) ATE92951T1 (en)
AU (1) AU621980B2 (en)
BR (1) BR9000543A (en)
CA (1) CA2009377A1 (en)
DE (1) DE69002649T2 (en)
DK (1) DK0382155T3 (en)
ES (1) ES2059847T3 (en)
ZA (1) ZA90917B (en)

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4440301A1 (en) * 1994-11-11 1996-05-15 Metallgesellschaft Ag Lubricant carrier salt for metal forming
CN102152069B (en) * 2011-01-30 2013-06-05 烟台鑫杰特钢有限公司 Method for producing steel sectional material of air valve
CN104593125B (en) * 2015-01-29 2017-07-11 南京工程学院 A kind of agglomeration resistance wire-drawing lubrication powder
IT202200006158A1 (en) 2022-03-29 2023-09-29 Condoroil Chemical S R L PROCESS TO PRODUCE A BORON-FREE COLD DEFORMATION COATING

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2957825A (en) * 1956-10-15 1960-10-25 Devex Corp Powdered soap lubricant containing inorganic sulfur salts
GB2003923A (en) * 1977-09-07 1979-03-21 Foseco Int Metal working lubricants

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CH670106A5 (en) * 1984-07-23 1989-05-12 Lonza Ag

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2957825A (en) * 1956-10-15 1960-10-25 Devex Corp Powdered soap lubricant containing inorganic sulfur salts
GB2003923A (en) * 1977-09-07 1979-03-21 Foseco Int Metal working lubricants

Also Published As

Publication number Publication date
EP0382155A1 (en) 1990-08-16
ES2059847T3 (en) 1994-11-16
AU621980B2 (en) 1992-03-26
BR9000543A (en) 1991-01-15
CN1044774A (en) 1990-08-22
ATE92951T1 (en) 1993-08-15
DE69002649D1 (en) 1993-09-16
CA2009377A1 (en) 1990-08-07
DK0382155T3 (en) 1993-09-20
AU4920990A (en) 1990-08-16
DE69002649T2 (en) 1993-12-16
EP0382155B1 (en) 1993-08-11
ZA90917B (en) 1990-11-28

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