CN1464131A - Process for manufacturing coloration additive for producing positive ionic dye dyeable polypropylene - Google Patents
Process for manufacturing coloration additive for producing positive ionic dye dyeable polypropylene Download PDFInfo
- Publication number
- CN1464131A CN1464131A CN 02112052 CN02112052A CN1464131A CN 1464131 A CN1464131 A CN 1464131A CN 02112052 CN02112052 CN 02112052 CN 02112052 A CN02112052 A CN 02112052A CN 1464131 A CN1464131 A CN 1464131A
- Authority
- CN
- China
- Prior art keywords
- tpa
- terephthalic acid
- molar ratio
- sodium sulfonate
- 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
Links
Abstract
The preparation process of the dyeing additive includes the ester exchange reaction of 5-sodium sulfodimethyl isophthalate and glycol in the presence of catalyst to obtain 5-sodium sulfodihydroxyethyl isophthalate; the esterification reaction of terephthalic acid and glycol in the presence of catalyst and stabilizer to obtain dihydroxyethyl terephthalate; the pre-polycondensation of 5-sodium sulfodihydroxyethyl isophthalate and dihydroxyethyl terephthalate at 210-240 deg.c; the polycondensation of the reactant system at 240-290 deg.c and vacuum degree lower than 100 Pa and final casting and pelletizing to obtain the additive product. The additive product has high 5-sodium sulfodimethyl isophthalate content and may be used in mixing melt spinning process to produce dyeable polypropylene fiber capable of being dyed with cationic dye in high dyeing degree.
Description
Technical field
The present invention relates to by terephthalic acid (TPA), 5-sodium sulfonate dimethyl isophthalate and the ethylene glycol method by the copolymerization modified poly ester, this modified poly ester is as the coloration additive of dyeable polypropylene.
Background technology
Polypropylene fibre have light specific gravity, intensity height, warmth retention property good, breathe freely, lead moist good, plurality of advantages such as chemical resistance is strong, and it is abundant, cheap to make raw material sources, development in recent years is rapid, its Application Areas also constantly enlarges.But because crystalling propylene degree height, structure is tight, and does not have the polar group that can combine with dye molecule on the strand, promptly lacks and dyes seat, so that can't dye with the method for routine.Usually people adopt original liquid coloring or Masterbatch method of colouring to make the colored fibre of heavy colour, but this can have high dyeing flexibility and color diversity not as fiber or fabric printing after all, is subjected to people's attention deeply so improve the dyeability of polypropylene fibre always.
In the prior art, be the method for improving the polypropylene fibre dyeability comparatively commonly used with blending modification method.It will have the dyeing group on the molecule, and can be well be incorporated in the polypropylene with the coloration additive of acrylic resin blended melting and goes, and carries out blend melt spinning then.This method is easy to implement technically, and less to the mechanical property influence of fiber.In the prior art, being considered to optimal coloration additive is modified poly ester, it is normally introduced in polyester and contains the group that can combine with dyestuff, and as United States Patent (USP) 5,576,366 are introduced.Adopt this coloration additive and acrylic resin to carry out blend melt spinning, the fiber that makes has good dyeability.Yet, this good dyeability can only realize with disperse dyeing usually in the prior art, with cationic dyeing and have the but rare report of higher dye-uptake, and we know no matter cation dyes all are better than DISPERSE DYES from the vividness of color, the diversity and the COLOR FASTNESS of color.
Summary of the invention
Technical problem to be solved by this invention provides a kind of preparation method of dyeable polypropylene coloration additive, and its coloration additive that makes is used for blend melt spinning technology, and the dyeable polypropylene of producing can be used cationic dyeing, and has higher dye-uptake.
Below be the technical scheme that the present invention solves the problems of the technologies described above:
A kind of preparation method who is used to produce the coloration additive of cationic dye dyeable polypropylene fiber, this method may further comprise the steps:
1) 5-sodium sulfonate dimethyl isophthalate and ethylene glycol carry out ester exchange reaction and obtain the two hydroxyl ethyl esters of 5-sodium sulfonate M-phthalic acid in the presence of the anti-agent sodium acetate of catalyst acetic acid calcium and ether, reaction temperature is 80～175 ℃, the molar ratio of 5-sodium sulfonate dimethyl isophthalate and ethylene glycol is 1: 6.0～7.5, and the reaction time is 2～3 hours;
2) terephthalic acid (TPA) and ethylene glycol carry out esterification and obtain bishydroxyethyl terephthalate in the presence of catalyst acetic acid cobalt and antimonous oxide and stabilizing agent trimethyl phosphate, reaction temperature is 240～260 ℃, the molar ratio of terephthalic acid (TPA) and ethylene glycol is 1: 0.61～1.22, and the reaction time is 3～4 hours;
3) two hydroxyl ethyl esters of 5-sodium sulfonate M-phthalic acid and bishydroxyethyl terephthalate carry out prepolymerization reaction under 210～240 ℃ temperature, the molar ratio of two hydroxyl ethyl esters of 5-sodium sulfonate M-phthalic acid and bishydroxyethyl terephthalate is 1: 0.08～0.17, and the reaction time is 1～3 hour;
4) system was warming up to 240～290 ℃ after precondensation finished, and hierarchy of control vacuum≤100Pa carries out polycondensation reaction, and the reaction time is 2～4 hours, and polymer obtains the coloration additive product after the granulation of Cast Strip.
In the above-mentioned steps 1, catalyst amount is calcium acetate/5-sodium sulfonate dimethyl isophthalate=0.64/10 with the molar ratio computing
3～0.75/10
3The anti-agent consumption of ether is sodium acetate/5-sodium sulfonate dimethyl isophthalate=3.61/10 with the molar ratio computing
3～4.21/10
3
Catalyst and stabilizing agent dosage are cobalt acetate/terephthalic acid (TPA)=1.41/10 with the molar ratio computing in the step 2
5～2.82/10
5, be preferably 1.88/10
5～2.82/10
5Antimonous oxide/terephthalic acid (TPA)=0.91/10
4～1.82/10
4, be preferably 1.21/10
4～1.82/10
4Trimethyl phosphate/terephthalic acid (TPA)=0.67/10
4～1.34/10
4, be preferably 0.90/10
4～1.34/10
4And the molar ratio of terephthalic acid (TPA) and ethylene glycol is preferably 1: 0.81～1.22.
The prepared dyeable polypropylene coloration additive of the present invention in fact also is a kind of modified poly ester, wherein introduced the monomer 5-sodium sulfonate dimethyl isophthalate that has with the fine group that combines of dyestuff, and characteristics of the present invention are that 5-sodium sulfonate dimethyl isophthalate content is higher in the coloration additive for preparing, this coloration additive is used for blend melt spinning technology, the not only available cationic dyeing of the dyeable polypropylene of producing, and have higher dye-uptake.
The specific embodiment
To enumerate some embodiment below and come further details of the present invention to be described, in an embodiment, the method for testing of polypropylene fibre dye-uptake and the definition of dye-uptake are as follows.
Method of testing:
Instrument: sample dyeing machine, 721 type spectrophotometers;
Reagent: peacock green, cation dyes (yellow 8GL, red 5GN, blue RL), acetic acid;
The dye liquor preparation: bath raio is 1: 100; The consumption of 1g fiber is 0.2% peacock green or cation dyes 5m1, is equipped with deionized water 95ml, and pH value is 4.5～5.5;
Dyeing condition: go into to dye for 70 ℃, be heated to 100 ℃ in 20 minutes, boil and dye 40 minutes, stop heating and kept 30 minutes, take out sample and be cooled to the room temperature after washing;
The mensuration of dyeing residual liquid optical density: get the 20ml dyeing residual liquid, merge the back with the stained specimens water lotion and move into volumetric flask, with its optical density of spectrophotometric instrumentation;
The mensuration of dyeing stoste optical density: get 20ml dyeing stoste, the deionized water dilution of immigration volumetric flask with stained specimens water lotion same amount is with its optical density of spectrophotometric instrumentation.
The preparation of [embodiment 1～8], coloration additive:
At first, with 5-sodium sulfonate dimethyl isophthalate, ethylene glycol, calcium acetate and sodium acetate with molar ratio Z: ethylene glycol/5-sodium sulfonate dimethyl isophthalate=1/6.0～7.5, calcium acetate/5-sodium sulfonate dimethyl isophthalate=0.64/10
3～0.75/10
3, sodium acetate/5-sodium sulfonate dimethyl isophthalate=3.61/10
3～4.21/10
3Join 2m
3Transesterification reactor, under normal pressure, 80～175 ℃ of temperature and impose to stir and carry out ester exchange reaction, the reaction time is 2.5 hours, generates the two hydroxyl ethyl esters of 5-sodium sulfonate M-phthalic acid.
With terephthalic acid (TPA), ethylene glycol, cobalt acetate, antimonous oxide and trimethyl phosphate with molar ratio: terephthalic acid (TPA)/ethylene glycol=1: 0.81～1.22, cobalt acetate/terephthalic acid (TPA)=1.88/10
5～2.82/10
5, antimonous oxide/terephthalic acid (TPA)=1.21/10
4～1.82/10
4, trimethyl phosphate/terephthalic acid (TPA)=0.90/10
4～1.34/10
4Join 6m
3Reaction kettle of the esterification, under normal pressure, 240～260 ℃ of temperature and impose to stir and carry out esterification, the reaction time is 4 hours, generates bishydroxyethyl terephthalate.
The above-mentioned bishydroxyethyl terephthalate for preparing is moved into 6m
3The prepolymerization reaction still, impose the two hydroxyl ethyl esters of the 5-sodium sulfonate M-phthalic acid that stirs and will be incubated about 100 ℃ then to add at a slow speed, the molar ratio of two hydroxyl ethyl esters of 5-sodium sulfonate M-phthalic acid and bishydroxyethyl terephthalate is 1: 0.08～0.17, when two kinds of monomers fully mix and system temperature when reaching 235 ℃, material is moved into 8m
3Batch condensation polymerization reactor.Control reaction temperature is that 260～290 ℃, system vacuum carry out polycondensation reaction less than 100Pa, and the reaction time is 2.5 hours.After Cast Strip and granulation promptly get the coloration additive product.
This coloration additive inherent viscosity [η] that obtains is 0.3～0.5dL/g, and fusing point is 200～250 ℃.Two, the manufacturing of dyeable polypropylene:
The above-mentioned coloration additive that makes is sneaked into common acrylic resin with metering units after in the metering of required ratio, lacking melt spinning on the thread spinning plant then, produce polypropylene short fiber, its specification is 2.78dtex * 67mm (55000 hole) and 5.56dtex * 102mm (30000 hole).Spinning temperature is 230～290 ℃, and spinning speed is 80～120m/min, and the cooling wind-warm syndrome is 18～23 ℃.
The dyeability of coloration additive content, fiber sees Table 1 table 1. in each embodiment spinning material
| Dye-uptake (%) | Coloration additive content (wt%) | ||||
| Cationic yellow 8GL | Cationic red 5GN | Cationic blue RL | Peacock green | ||
| Embodiment 1 | ????70.6 | ????71.2 | ????72.6 | ????75.5 | ????8 |
| Embodiment 2 | ????72.5 | ????73.8 | ????75.0 | ????78.2 | ????10 |
| Embodiment 3 | ????74.7 | ????76.0 | ????77.3 | ????80.6 | ????10 |
| Embodiment 4 | ????75.2 | ????78.5 | ????80.0 | ????82.0 | ????11 |
| Embodiment 5 | ????78.9 | ????81.3 | ????82.5 | ????83.7 | ????11 |
| Embodiment 6 | ????80.1 | ????82.7 | ????83.6 | ????86.5 | ????12 |
| Embodiment 7 | ????86.8 | ????88.9 | ????90.0 | ????95.0 | ????12 |
| Embodiment 8 | ????86.7 | ????89.1 | ????90.2 | ????95.0 | ????12 |
Claims (5)
1, a kind of preparation method who is used to produce the coloration additive of cationic dye dyeable polypropylene fiber, this method may further comprise the steps:
1) 5-sodium sulfonate dimethyl isophthalate and ethylene glycol carry out ester exchange reaction and obtain the two hydroxyl ethyl esters of 5-sodium sulfonate M-phthalic acid in the presence of the anti-agent sodium acetate of catalyst acetic acid calcium and ether, reaction temperature is 80～175 ℃, the molar ratio of 5-sodium sulfonate dimethyl isophthalate and ethylene glycol is 1: 6.0～7.5, and the reaction time is 2～3 hours;
2) terephthalic acid (TPA) and ethylene glycol carry out esterification and obtain bishydroxyethyl terephthalate in the presence of catalyst acetic acid cobalt and antimonous oxide and stabilizing agent trimethyl phosphate, reaction temperature is 240～260 ℃, the molar ratio of terephthalic acid (TPA) and ethylene glycol is 1: 0.61～1.22, and the reaction time is 3～4 hours;
3) two hydroxyl ethyl esters of 5-sodium sulfonate M-phthalic acid and bishydroxyethyl terephthalate carry out prepolymerization reaction under 210～240 ℃ temperature, the molar ratio of two hydroxyl ethyl esters of 5-sodium sulfonate M-phthalic acid and bishydroxyethyl terephthalate is 1: 0.08～0.17, and the reaction time is 1～3 hour;
4) system was warming up to 240～290 ℃ after precondensation finished, and hierarchy of control vacuum≤100Pa carries out polycondensation reaction, and the reaction time is 2～4 hours, and polymer obtains the coloration additive product after the granulation of Cast Strip.
2, the preparation method of coloration additive according to claim 1 is characterized in that catalyst amount is calcium acetate/5-sodium sulfonate dimethyl isophthalate=0.64/10 with the molar ratio computing in the described step 1
3～0.75/10
3, the anti-agent consumption of ether is sodium acetate/5-sodium sulfonate dimethyl isophthalate=3.61/10 with the molar ratio computing
3～4.21/10
3
3, the preparation method of coloration additive according to claim 1 is characterized in that catalyst and stabilizing agent dosage are cobalt acetate/terephthalic acid (TPA)=1.41/10 with the molar ratio computing in the described step 2
5～2.82/10
5, antimonous oxide/terephthalic acid (TPA)=0.91/10
4～1.82/10
4, trimethyl phosphate/terephthalic acid (TPA)=0.67/10
4～1.34/10
4
4, the preparation method of coloration additive according to claim 3 is characterized in that catalyst and stabilizing agent dosage are cobalt acetate/terephthalic acid (TPA)=1.88/10 with the molar ratio computing in the described step 2
5～2.82/10
5, antimonous oxide/terephthalic acid (TPA)=1.21/10
4～1.82/10
4, trimethyl phosphate/terephthalic acid (TPA)=0.90/10
4～1.34/10
4
5, the preparation method of coloration additive according to claim 1 is characterized in that the molar ratio of terephthalic acid (TPA) and ethylene glycol is 1: 0.81～1.22 in the described step 2.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN 02112052 CN1464131A (en) | 2002-06-13 | 2002-06-13 | Process for manufacturing coloration additive for producing positive ionic dye dyeable polypropylene |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN 02112052 CN1464131A (en) | 2002-06-13 | 2002-06-13 | Process for manufacturing coloration additive for producing positive ionic dye dyeable polypropylene |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN1464131A true CN1464131A (en) | 2003-12-31 |
Family
ID=29742020
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN 02112052 Pending CN1464131A (en) | 2002-06-13 | 2002-06-13 | Process for manufacturing coloration additive for producing positive ionic dye dyeable polypropylene |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN1464131A (en) |
Cited By (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1304684C (en) * | 2005-03-07 | 2007-03-14 | 江苏群发化工有限公司 | Synthesis technology of polyester dying modifier SIPM |
| CN1329425C (en) * | 2004-06-16 | 2007-08-01 | 浙江工程学院 | Modified polyester and preparing method thereof |
| CN100345883C (en) * | 2004-05-10 | 2007-10-31 | （株）晓星 | Flame retardant polyesterpolymer able to dye by using cation pigment,its mfg.method and copolymer fiber using the same |
| CN100413907C (en) * | 2004-09-16 | 2008-08-27 | 洛阳高新技术开发区南峰聚酯有限公司 | Cation dye normal pressure deep dyeing estercopolymer and its preparing method |
| CN1825955B (en) * | 2005-02-11 | 2011-01-19 | 微软公司 | Detecting clock drift in networked devices through monitoring client buffer fullness |
| CN101765772B (en) * | 2007-05-31 | 2012-08-22 | 通用电气公司 | Method for determination of polymer concentration in water systems |
| CN106555251A (en) * | 2016-12-02 | 2017-04-05 | 江苏新瑞贝科技股份有限公司 | A kind of printing masterbatch of the imitative cellulose base fiber fabric suitable for printing shaping technology |
| CN107557902A (en) * | 2017-09-07 | 2018-01-09 | 江苏恒科新材料有限公司 | A kind of preparation method of cation dyeable polyester POY silks |
| CN108017779A (en) * | 2016-10-28 | 2018-05-11 | 中国石油化工股份有限公司 | A kind of easy dyeing polyester and preparation method thereof |
| CN109535041A (en) * | 2018-11-22 | 2019-03-29 | 青岛中科荣达新材料有限公司 | A kind of method that composite catalyst produces polyester modified dose of SIPE |
| CN110387596A (en) * | 2019-07-18 | 2019-10-29 | 新凤鸣集团股份有限公司 | A kind of preparation method of the CDP fabrics long filament |
-
2002
- 2002-06-13 CN CN 02112052 patent/CN1464131A/en active Pending
Cited By (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN100345883C (en) * | 2004-05-10 | 2007-10-31 | （株）晓星 | Flame retardant polyesterpolymer able to dye by using cation pigment,its mfg.method and copolymer fiber using the same |
| CN1329425C (en) * | 2004-06-16 | 2007-08-01 | 浙江工程学院 | Modified polyester and preparing method thereof |
| CN100413907C (en) * | 2004-09-16 | 2008-08-27 | 洛阳高新技术开发区南峰聚酯有限公司 | Cation dye normal pressure deep dyeing estercopolymer and its preparing method |
| CN1825955B (en) * | 2005-02-11 | 2011-01-19 | 微软公司 | Detecting clock drift in networked devices through monitoring client buffer fullness |
| CN1304684C (en) * | 2005-03-07 | 2007-03-14 | 江苏群发化工有限公司 | Synthesis technology of polyester dying modifier SIPM |
| CN101765772B (en) * | 2007-05-31 | 2012-08-22 | 通用电气公司 | Method for determination of polymer concentration in water systems |
| CN108017779A (en) * | 2016-10-28 | 2018-05-11 | 中国石油化工股份有限公司 | A kind of easy dyeing polyester and preparation method thereof |
| CN108017779B (en) * | 2016-10-28 | 2021-07-02 | 中国石油化工股份有限公司 | Polyester easy to dye and preparation method thereof |
| CN106555251A (en) * | 2016-12-02 | 2017-04-05 | 江苏新瑞贝科技股份有限公司 | A kind of printing masterbatch of the imitative cellulose base fiber fabric suitable for printing shaping technology |
| CN107557902A (en) * | 2017-09-07 | 2018-01-09 | 江苏恒科新材料有限公司 | A kind of preparation method of cation dyeable polyester POY silks |
| CN109535041A (en) * | 2018-11-22 | 2019-03-29 | 青岛中科荣达新材料有限公司 | A kind of method that composite catalyst produces polyester modified dose of SIPE |
| CN109535041B (en) * | 2018-11-22 | 2021-08-10 | 青岛中科荣达新材料有限公司 | Method for producing polyester modifier SIPE (styrene-isoprene-styrene) by using composite catalyst |
| CN110387596A (en) * | 2019-07-18 | 2019-10-29 | 新凤鸣集团股份有限公司 | A kind of preparation method of the CDP fabrics long filament |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN100537631C (en) | Preparation process of copolyester capable of being dyed deeply with cationic dye | |
| CN1831028B (en) | Normal pressure cation dyeable polyester, textile product made from the same, and process for production of the same | |
| CN100567600C (en) | A kind of copolyester section of modification or fiber and preparation method thereof | |
| CN1464131A (en) | Process for manufacturing coloration additive for producing positive ionic dye dyeable polypropylene | |
| KR20190076960A (en) | Modified polyester masterbatch for textile application and method of making same | |
| CN101469060B (en) | Preparation of cationic dyeable poly(trimethylene terephthalate) | |
| CN105442078A (en) | Method for preparing colored polyester fibers through stock solution coloring | |
| CN101857671A (en) | High-shrinkage cation normal-pressure easy-to-dye polyester chip and preparation method thereof | |
| CN104499079A (en) | Method for preparing black polyester fiber by dope dyeing | |
| CN110820062B (en) | Composite fiber with accurate and controllable color | |
| CN101457413A (en) | Deep dye type polyester-nylon composite superfine fiber and manufacture method | |
| CN104480564A (en) | Super-bright light trefoil irregular FDY fiber and preparation method thereof | |
| CN103351462B (en) | A kind of normal atmosphere cation-dyeable wig polyester and fiber producing processes thereof | |
| CN101525784A (en) | Cationic dye deep dyeing copolyester at normal pressure and method for producing same | |
| CN102828422B (en) | Preparation method of environment-friendly high temperature leveling agent | |
| CN107129567A (en) | A kind of fire-retardant ECDP polyester slices of copoly type and preparation method thereof | |
| CN111019105B (en) | Modified polyester and preparation method thereof | |
| CN1036798C (en) | Method for mfg. disperse dye dyeable polypropylene fibre | |
| CN104532391A (en) | High-dye-uptake-rate polyester fiber and preparation method thereof | |
| CN102409428B (en) | Preparation method for polyester fiber with composite ultraviolet resisting and cationic dyeing functions | |
| CN106609474A (en) | Preparation method of eco-friendly high-temperature leveling agent | |
| CN1793450A (en) | Method for preparing depth dyeing type island composite superfine fibre | |
| CN1189605C (en) | Process for manufacturing dyeable polypropylene | |
| CN1448549A (en) | Manufacture of cationic dye dyeable polypropylene fiber | |
| CN103469613B (en) | A kind of colouring method of ionic type high-hydrophilicity polyester fiber |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C06 | Publication | ||
| PB01 | Publication | ||
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| C02 | Deemed withdrawal of patent application after publication (patent law 2001) | ||
| WD01 | Invention patent application deemed withdrawn after publication |