CN102965920A - Oiling agent for synthetic fiber, and preparation method thereof - Google Patents
Oiling agent for synthetic fiber, and preparation method thereof Download PDFInfo
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- CN102965920A CN102965920A CN 201210474166 CN201210474166A CN102965920A CN 102965920 A CN102965920 A CN 102965920A CN 201210474166 CN201210474166 CN 201210474166 CN 201210474166 A CN201210474166 A CN 201210474166A CN 102965920 A CN102965920 A CN 102965920A
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- synthetic fiber
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- acetone
- ethylhexyl
- coconut oil
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Abstract
The invention discloses an oiling agent for synthetic fiber, and a preparation method thereof. The oiling agent for the synthetic fiber comprises the components based on parts by weight: 10-20 parts of lauryl alcohol polyethylene glycol ester, 20-30 parts of isooctyl stearate, 3-6 parts of alkyl phosphate diethanolamine salt, 10-20 parts of coconut oil, 2-6 parts of 2-ethyl hexyl succinate sodium sulfonate, 3-8 parts of acetone and 20-30 parts of polyethylene glycol fatty acid ester. Compared with the prior art, the oiling agent for the synthetic fiber has the beneficial effects of (1) enabling the fiber to have good smoothness and flexibility; (2) enabling the fiber to have bundling property and the tow to have good adhesiveness and cohesive force; and (3) being good in heat resistance and non-volatile.
Description
Technical field
The invention belongs to the textile auxiliary technical field, more specifically relate to a kind of synthetic fiber finish and preparation method thereof.
Background technology
Synthetic fiber are high molecular polymers, and hygroscopicity is little, poorly conductive, and coefficient of friction is large.Synthetic fiber itself do not contain lipoid material, in spinning process, lack cohesive force, because synthetic fiber are non-conductors, no matter be long fiber or staple fibre, in various process again, often because friction produces electrostatic effect, cause single wire fracture in the tow and form lousiness, therefore, also need to use finish to improve the cohesive force of fiber, prevent electrostatic interaction, and increase flatness.
Summary of the invention
The object of the invention is to overcome the deficiency that prior art exists, a kind of synthetic fiber finish is provided.
Another object of the present invention is to provide the preparation method of these synthetic fiber with finish.
For achieving the above object, the present invention has taked following technical scheme:
A kind of synthetic fiber finish, in weight portion, composed of the following components:
The laruyl alcohol macrogol ester: 10～20, Ethylhexyl stearate: 20～30,
The alkyl phosphate diethanolamine salt: 3～6, coconut oil: 10～20,
2-ethylhexyl succinate sodium sulfonate: 2～6, acetone: 3～8,
Cithrol: 20～30.
Described a kind of synthetic fiber is characterized in that with the preparation method of finish, comprise the steps:
(1) by proportioning, cithrol, Ethylhexyl stearate are dissolved in the acetone, are warming up to 60～80 ℃, mix, reacted 1～3 hour;
(2) laruyl alcohol macrogol ester, alkyl phosphate diethanolamine salt and 2-ethylhexyl succinate sodium sulfonate are dissolved in the coconut oil, mix;
(3) product of step (1) and the product of step (2) are mixed, be cooled to room temperature, get final product to get product after stirring.
Compared with prior art, the present invention has following beneficial effect:
(1) can make fiber that good flatness and flexibility are arranged;
(2) can make fiber have convergence, tow has good cohesiveness and cohesive force;
(3) good heat resistance, non-volatile.
The specific embodiment
The invention will be further described below in conjunction with specific embodiment.
Embodiment 1
A kind of synthetic fiber finish, in weight portion, composed of the following components:
The laruyl alcohol macrogol ester: 10, Ethylhexyl stearate: 20,
The alkyl phosphate diethanolamine salt: 3, coconut oil: 10,
2-ethylhexyl succinate sodium sulfonate: 2, acetone: 3,
Cithrol: 20.
Embodiment 2
A kind of synthetic fiber finish, in weight portion, composed of the following components:
The laruyl alcohol macrogol ester: 20, Ethylhexyl stearate: 30,
The alkyl phosphate diethanolamine salt: 6, coconut oil: 20,
2-ethylhexyl succinate sodium sulfonate: 6, acetone: 8,
Cithrol: 30.
Embodiment 3
A kind of synthetic fiber finish, in weight portion, composed of the following components:
The laruyl alcohol macrogol ester: 16, Ethylhexyl stearate: 25,
The alkyl phosphate diethanolamine salt: 5, coconut oil: 16,
2-ethylhexyl succinate sodium sulfonate: 4, acetone: 6,
Cithrol: 25.
In above-described embodiment, described a kind of synthetic fiber comprise the steps: with the preparation method of finish
(1) by proportioning, cithrol, Ethylhexyl stearate are dissolved in the acetone, are warming up to 60～80 ℃, mix, reacted 1～3 hour;
(2) laruyl alcohol macrogol ester, alkyl phosphate diethanolamine salt and 2-ethylhexyl succinate sodium sulfonate are dissolved in the coconut oil, mix;
(3) product of step (1) and the product of step (2) are mixed, be cooled to room temperature, get final product to get product after stirring.
Claims (5)
1. a synthetic fiber finish is characterized in that, and is in weight portion, composed of the following components:
The laruyl alcohol macrogol ester: 10～20, Ethylhexyl stearate: 20～30,
The alkyl phosphate diethanolamine salt: 3～6, coconut oil: 10～20,
2-ethylhexyl succinate sodium sulfonate: 2～6, acetone: 3～8,
Cithrol: 20～30.
2. a kind of synthetic fiber finish according to claim 1 is characterized in that, and is in weight portion, composed of the following components:
The laruyl alcohol macrogol ester: 10, Ethylhexyl stearate: 20,
The alkyl phosphate diethanolamine salt: 3, coconut oil: 10,
2-ethylhexyl succinate sodium sulfonate: 2, acetone: 3,
Cithrol: 20.
3. a kind of synthetic fiber finish according to claim 1 is characterized in that, and is in weight portion, composed of the following components:
The laruyl alcohol macrogol ester: 20, Ethylhexyl stearate: 30,
The alkyl phosphate diethanolamine salt: 6, coconut oil: 20,
2-ethylhexyl succinate sodium sulfonate: 6, acetone: 8,
Cithrol: 30.
4. a kind of synthetic fiber finish according to claim 1 is characterized in that, and is in weight portion, composed of the following components:
The laruyl alcohol macrogol ester: 16, Ethylhexyl stearate: 25,
The alkyl phosphate diethanolamine salt: 5, coconut oil: 16,
2-ethylhexyl succinate sodium sulfonate: 4, acetone: 6,
Cithrol: 25.
5. a kind of synthetic fiber claimed in claim 1 is characterized in that with the preparation method of finish, comprise the steps:
(1) by proportioning, cithrol, Ethylhexyl stearate are dissolved in the acetone, are warming up to 60～80 ℃, mix, reacted 1～3 hour;
(2) laruyl alcohol macrogol ester, alkyl phosphate diethanolamine salt and 2-ethylhexyl succinate sodium sulfonate are dissolved in the coconut oil, mix;
(3) product of step (1) and the product of step (2) are mixed, be cooled to room temperature, get final product to get product after stirring.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN 201210474166 CN102965920A (en) | 2012-11-21 | 2012-11-21 | Oiling agent for synthetic fiber, and preparation method thereof |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN 201210474166 CN102965920A (en) | 2012-11-21 | 2012-11-21 | Oiling agent for synthetic fiber, and preparation method thereof |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN102965920A true CN102965920A (en) | 2013-03-13 |
Family
ID=47796337
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN 201210474166 Withdrawn CN102965920A (en) | 2012-11-21 | 2012-11-21 | Oiling agent for synthetic fiber, and preparation method thereof |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN102965920A (en) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN104975496A (en) * | 2015-06-30 | 2015-10-14 | 盐城工学院 | Complex oil agent for textile and preparation method thereof |
| CN105155259A (en) * | 2015-09-17 | 2015-12-16 | 宋新祥 | Preparation method for dacron oiling agent |
| CN105200769A (en) * | 2015-11-14 | 2015-12-30 | 安徽双帆高纤有限公司 | Dacron short fiber oiling agent |
| CN105239375A (en) * | 2015-09-16 | 2016-01-13 | 宋新祥 | Terylene spinning oil |
| CN105492688A (en) * | 2014-08-05 | 2016-04-13 | 松本油脂制药株式会社 | Treatment agent for synthetic fibers and use thereof |
| CN105603730A (en) * | 2016-02-25 | 2016-05-25 | 苏州三和开泰花线织造有限公司 | Oil solution special for environmentally-friendly efficient synthetic fiber and preparation method thereof |
-
2012
- 2012-11-21 CN CN 201210474166 patent/CN102965920A/en not_active Withdrawn
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN105492688A (en) * | 2014-08-05 | 2016-04-13 | 松本油脂制药株式会社 | Treatment agent for synthetic fibers and use thereof |
| CN105492688B (en) * | 2014-08-05 | 2017-05-24 | 松本油脂制药株式会社 | Treatment agent for synthetic fibers and use thereof |
| CN104975496A (en) * | 2015-06-30 | 2015-10-14 | 盐城工学院 | Complex oil agent for textile and preparation method thereof |
| CN105239375A (en) * | 2015-09-16 | 2016-01-13 | 宋新祥 | Terylene spinning oil |
| CN105155259A (en) * | 2015-09-17 | 2015-12-16 | 宋新祥 | Preparation method for dacron oiling agent |
| CN105200769A (en) * | 2015-11-14 | 2015-12-30 | 安徽双帆高纤有限公司 | Dacron short fiber oiling agent |
| CN105603730A (en) * | 2016-02-25 | 2016-05-25 | 苏州三和开泰花线织造有限公司 | Oil solution special for environmentally-friendly efficient synthetic fiber and preparation method thereof |
| CN105603730B (en) * | 2016-02-25 | 2018-02-02 | 东莞市联洲知识产权运营管理有限公司 | A kind of environment-friendly high-efficiency synthetic fibers are oil solution dedicated and preparation method thereof |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C04 | Withdrawal of patent application after publication (patent law 2001) | ||
| WW01 | Invention patent application withdrawn after publication |
Application publication date: 20130313 |