JPS60162881A - Dyeing of molded polyamide product - Google Patents
Dyeing of molded polyamide productInfo
- Publication number
- JPS60162881A JPS60162881A JP59017163A JP1716384A JPS60162881A JP S60162881 A JPS60162881 A JP S60162881A JP 59017163 A JP59017163 A JP 59017163A JP 1716384 A JP1716384 A JP 1716384A JP S60162881 A JPS60162881 A JP S60162881A
- Authority
- JP
- Japan
- Prior art keywords
- dyeing
- polyamide
- parts
- dimelamine
- molded
- 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.)
- Granted
Links
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】 本発明は、ポリアミド成形品の染色方法に関する。[Detailed description of the invention] The present invention relates to a method for dyeing polyamide molded articles.
ポリアミドは染色性が一般に良好であるが、濃色に染色
しにくいとか、染魚むらがあるとかの欠点があった。Although polyamide generally has good dyeability, it has drawbacks such as difficulty in dyeing deep colors and uneven dyeing.
本発明者らは、ポリアミド成形品の染色方法について鋭
意研究を重ねた結果、特定のメラミン誘導体をポリアミ
ドに配合することにより、上記欠点が解消されることを
知り2本発明に到った。As a result of extensive research into dyeing methods for polyamide molded articles, the present inventors found that the above-mentioned drawbacks could be overcome by blending a specific melamine derivative into polyamide, leading to the invention.
本発明は、ポリアミドと 式 (式中R1は炭素数1〜15の炭化水素残基を示し。The present invention uses polyamide and formula (In the formula, R1 represents a hydrocarbon residue having 1 to 15 carbon atoms.
nはθ〜5の整数である。)で表わされるメラミン誘導
体とから構成される成形品を酸性染料で染色することを
特徴とするポリアミド成形品の染色方法である。n is an integer from θ to 5. ) is a method for dyeing a polyamide molded article, which is characterized by dyeing a molded article composed of a melamine derivative represented by the following with an acid dye.
本発明において使用されるポリアミドの具体例としては
、ナイロン61 ナイロン11.ナイロン12などのポ
リラクタム類、ナイロン66、ナイロン610.ナイロ
ン612などのジカルボン酸とジアミンとから得られる
ポリアミド類、ナイロン6/66、ナイロン6/66/
610などの共重合ポリアミド類、これらの混合物など
が挙げられる。Specific examples of polyamides used in the present invention include nylon 61, nylon 11. Polylactams such as nylon 12, nylon 66, nylon 610. Polyamides obtained from dicarboxylic acids and diamines such as nylon 612, nylon 6/66, nylon 6/66/
Examples include copolyamides such as 610, mixtures thereof, and the like.
本発明において使用されるメラミン誘導体の代表例とし
ては、メチレンジメラミン、エチレンジメラミン、トリ
メチレンジメラミン、テトラメチレンジメラミン、ヘキ
サメチレンジメラミン、デカメチレンジメラミン、ドデ
カメチレンジメラミン、1.3−シクロヘキシレンジメ
ラミン、p−フユニレンジメラミン、p−キシリレンジ
メラミン。Representative examples of melamine derivatives used in the present invention include methylene dimelamine, ethylene dimelamine, trimethylene dimelamine, tetramethylene dimelamine, hexamethylene dimelamine, decamethylene dimelamine, dodecamethylene dimelamine, 1.3 - Cyclohexylene dimelamine, p-fuylylene dimelamine, p-xylylene dimelamine.
4.4′−ジチレンジメラミン、ジエチレントリメラミ
ン、トリエチレンテトラメラミン、テトラエチレンペン
タメラミン、ヘキサエチレンへブタメラミンなどが挙げ
られる。これらメラミン誘導体は単独で使用してもよく
、2種以上を併用してもよい。これらのメラミン誘導体
はポリアミドとの相溶性が良好であり、成形品の染色時
及び使用時にブリートアウトすることがない。4.4'-ditylene dimelamine, diethylene trimelamine, triethylene tetramelamine, tetraethylene pentamelamine, hexaethylene hebutamelamine, and the like. These melamine derivatives may be used alone or in combination of two or more. These melamine derivatives have good compatibility with polyamide and do not bleed out during dyeing or use of molded articles.
ポリアミドとメラミン誘導体との構成割合は。What is the composition ratio of polyamide and melamine derivative?
ポリアミド100重量部当シ、メラミン誘導体0.01
重量部以上5重量部未満、特に、0.1重量部〜ろ重量
部であることが好ましい。メラミン誘導体の構成割合が
過度に少ないとポリアミドに十分な易染性を付与するこ
とができず、その構成割合が過度に多いと得られるポリ
アミド成形品の物性が低下する。100 parts by weight of polyamide, 0.01 parts by weight of melamine derivative
It is preferably at least 5 parts by weight, and particularly preferably from 0.1 parts by weight to 0.1 parts by weight. If the proportion of the melamine derivative is too small, it will not be possible to impart sufficient dyeability to the polyamide, and if the proportion of the melamine derivative is too large, the physical properties of the resulting polyamide molded article will deteriorate.
本発明において、ポリアミド成形品は公知の方法によっ
て製造することができる。たとえば、ポリアミドとメラ
ミン誘導体とをトライブレンドまたは溶融混線により混
合し、ついで押出成形、射出成形などの公知の成形方法
によって製造される。In the present invention, the polyamide molded article can be manufactured by a known method. For example, polyamide and a melamine derivative are mixed by triblending or melt mixing, and then manufactured by a known molding method such as extrusion molding or injection molding.
本発明のポリアミド成形品は、そのほかに、酸化防止剤
、滑剤、無機質充填剤などの公知の添加剤を含むことが
できる。The polyamide molded article of the present invention can also contain known additives such as antioxidants, lubricants, and inorganic fillers.
本発明で用いられる酸性染料は7通常、普通酸性染料、
金属錯塩染料、酸性媒染染料筆キる。The acid dyes used in the present invention are 7 usually ordinary acid dyes,
Metal complex dyes and acidic mordant dyes can be brushed.
酸性染料による染色は9通常の方法において行なわれる
。例えば、値酸アンモニウムあるいは酢酸、ギ酸などの
酸を0.1重量%〜1,5重量%加えた40〜45°C
の水溶液に成形品を浸し、酸性染料を0.1〜1重量%
加えて、30〜60分かけて。Dyeing with acid dyes is carried out in a conventional manner. For example, at 40-45°C, add 0.1% to 1.5% by weight of acid such as ammonium acid or acetic acid or formic acid.
Soak the molded product in an aqueous solution of 0.1 to 1% by weight of acid dye.
In addition, it takes 30 to 60 minutes.
80〜100°Cに昇温して60分から60分間保持す
ることによって行なうことができる。染色後は常法に従
い洗浄、乾燥を行なう。This can be carried out by raising the temperature to 80 to 100°C and holding it for 60 to 60 minutes. After dyeing, wash and dry according to conventional methods.
つぎに、実施例および比較例を示す。なお、実施例およ
び比較例中の「部」は「重量部」を意味する。Next, Examples and Comparative Examples will be shown. Note that "parts" in Examples and Comparative Examples mean "parts by weight."
実施例1〜4
数平均分子量が13,000のナイロン6(宇部興産■
製;1013B)ペレット98部に、第1表に記載の粒
径1〜20μのメラミン誘導体2部をブレンドし、押出
機を用いてペレットを得た。このペレットから射出成形
により、染色性観察用の成形試験片(55X19X3.
2m)を作製した。この成形試験片33部あたりに、水
1000部を加え、40〜45°Cで酢酸(100チ換
算)7部を加えた。10分後+ Am1nyl Blu
e E−2GL(Suminol Levellng
Blue AGG+住友化学■製)1部を加え、40〜
60分かけて85〜100°Cに昇温し、そのままの温
度で1時間染色を続けた。Examples 1 to 4 Nylon 6 with a number average molecular weight of 13,000 (Ube Industries ■
1013B) were blended with 2 parts of the melamine derivative having a particle size of 1 to 20 μm listed in Table 1 to obtain pellets using an extruder. This pellet was injection molded into a molded test piece (55 x 19 x 3.
2m) was produced. 1000 parts of water was added per 33 parts of this molded test piece, and 7 parts of acetic acid (calculated in 100 parts) was added at 40 to 45°C. 10 minutes later + Am1nyl Blue
e E-2GL (Suminol Levelng)
Add 1 part of Blue AGG + Sumitomo Chemical ■, 40~
The temperature was raised to 85-100°C over 60 minutes, and dyeing was continued at that temperature for 1 hour.
その後、染色された試験片をオーバーフロー水槽で、洗
浄し、常法により乾燥した。染色状態は目視で評価した
。Thereafter, the dyed test piece was washed in an overflow tank and dried in a conventional manner. The staining condition was visually evaluated.
比較例1
メラミン誘導体を配合しなかったほかは、実施例1を繰
返した。Comparative Example 1 Example 1 was repeated except that the melamine derivative was not blended.
上記実施例及び比較例の結果を第1表に示す。The results of the above Examples and Comparative Examples are shown in Table 1.
特許出願人 宇部興産株式会社Patent applicant Ube Industries Co., Ltd.
Claims (1)
体とから構成される成形品を酸性染料で染色することを
特徴とするポリアミド成形品の染色方法。[Claims] Polyamide. A molded article composed of a melamine derivative represented by the formula (wherein R1 represents a hydrocarbon residue having 1 to 15 carbon atoms, and n is an integer of 0 to 5) is dyed with an acid dye. Characteristic dyeing method for polyamide molded products.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP59017163A JPS60162881A (en) | 1984-02-03 | 1984-02-03 | Dyeing of molded polyamide product |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP59017163A JPS60162881A (en) | 1984-02-03 | 1984-02-03 | Dyeing of molded polyamide product |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS60162881A true JPS60162881A (en) | 1985-08-24 |
JPH0377311B2 JPH0377311B2 (en) | 1991-12-10 |
Family
ID=11936290
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP59017163A Granted JPS60162881A (en) | 1984-02-03 | 1984-02-03 | Dyeing of molded polyamide product |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS60162881A (en) |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB482345A (en) * | 1936-09-25 | 1938-03-25 | Of Chemical Industry Soc | Improvements in or relating to the production of dyed or printed materials |
US3097911A (en) * | 1963-07-16 | Process of reserving wool with bis-tri- | ||
JPS5271572A (en) * | 1975-12-05 | 1977-06-15 | Koppers Co Inc | Dyeing of mouldings containing resins of urea formaldehyde or melamine formaldehyde |
JPS536978A (en) * | 1976-07-05 | 1978-01-21 | Spradow & Co Apparatebau | Material feeding device of lon noise for bar material woking lathes |
-
1984
- 1984-02-03 JP JP59017163A patent/JPS60162881A/en active Granted
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3097911A (en) * | 1963-07-16 | Process of reserving wool with bis-tri- | ||
GB482345A (en) * | 1936-09-25 | 1938-03-25 | Of Chemical Industry Soc | Improvements in or relating to the production of dyed or printed materials |
JPS5271572A (en) * | 1975-12-05 | 1977-06-15 | Koppers Co Inc | Dyeing of mouldings containing resins of urea formaldehyde or melamine formaldehyde |
JPS536978A (en) * | 1976-07-05 | 1978-01-21 | Spradow & Co Apparatebau | Material feeding device of lon noise for bar material woking lathes |
Also Published As
Publication number | Publication date |
---|---|
JPH0377311B2 (en) | 1991-12-10 |
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