Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Novel vinylidene fluoride copolymers and processes for production thereof

A technology of vinylidene fluoride and a manufacturing method, applied in 1 field, can solve problems such as defective heat resistance and reduced commercial value, and achieve the effects of good adhesion and excellent pollution resistance

Inactive Publication Date: 2014-07-16
KUREHA KAGAKU KOGYO KK
View PDF9 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0009] However, these 1,1-difluoroethylene copolymers having esters or modified products thereof have defects in heat resistance, and in melt molding, there is a problem that the molded product is colored and the commercial value is lowered, so the improvement of coloring resistance is expected improve

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Novel vinylidene fluoride copolymers and processes for production thereof
  • Novel vinylidene fluoride copolymers and processes for production thereof
  • Novel vinylidene fluoride copolymers and processes for production thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0120] [Example 1] (1,1-difluoroethylene / dimethylmethylenemalonate=99 / 1 (mass ratio))

[0121] 1024 g of ion-exchanged water, 0.6 g of methylcellulose, 1.2 g of ethyl acetate, 8.6 g of 50% by weight diisopropyl peroxydicarbonate-chlorofluorocarbon 225cb solution, 1, 396 g of 1-difluoroethylene (VDF), 4.0 g of dimethyl methylene malonate, and suspension polymerization were performed at 29° C. for 22 hours until the pressure dropped to 1.5 MPa. After the polymerization was completed, the polymer slurry was heat-treated at 95° C. for 30 minutes to deactivate the polymerization initiator, and the polymer was filtered, dehydrated and washed with water, and then dried at 80° C. for 20 hours to obtain a polymer powder. The yield was 86%, and the inherent viscosity of the obtained polymer was 1.29 dl / g.

Embodiment 2~4、 comparative example 1~3

[0123] In Examples 2 to 4 and Comparative Examples 1 to 3, except that the ratio of 1,1-difluoroethylene (VDF) to comonomer and the type of comonomer were changed as described in Table 1, the same method as in Example was adopted. 1 in the same way. In addition, Comparative Example 1 is a homopolymer of vinylidene fluoride.

[0124] Furthermore, regarding Example 2, as figure 2 and image 3 shown by the resulting polymer in the 1 In the H-NMR spectrum, it was observed around 3.7ppm that originated from COOCH 2 The signal of R (R=H in embodiment 1,2,4, comparative example 2,3, R=Me in embodiment 3), and in IR spectrum in 1740cm -1 A signal derived from C=O stretching vibration was observed nearby, confirming that a copolymer of methylene malonate was obtained. pass 1 The area ratio in the H-NMR spectrum calculates the ratio (molar ratio) of the vinylidene fluoride unit to the vinylidene malonate unit contained in the vinylidene fluoride copolymer. In addition, the ratio...

Embodiment 5

[0140] 125 ml of N,N-dimethylformamide and 1.17 g of lithium bromide were added to a 500 ml three-necked flask equipped with a magnetic stirring bar and a Dimro cooling tube to prepare a solution. To this solution was added 5.05 g of the 1,1-didene fluoride copolymer of the present invention obtained in Example 2, followed by heating and stirring at 100° C. for 9 hours. After naturally cooling to room temperature, the reaction solution was reprecipitated using dilute hydrochloric acid. The resulting solid was filtered and fractionated, dehydrated and washed with water, and then dried at 80° C. for 20 hours. Measure the resulting solid 1 H-NMR spectrum, results attributed to COOCH 3 The change of the integrated value of the signal (near 3.7ppm) confirms that about 41% of the total number of ester groups in the copolymer is hydrolyzed (refer to Figure 5 and Image 6 ).

[0141] [table 3]

[0142] Mn / 10 5 Mw / 10 5 Mn / Mw Tm(°C) Tc(°C) Example 5 ...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

PropertyMeasurementUnit
melting pointaaaaaaaaaa
melting pointaaaaaaaaaa
crystallization temperatureaaaaaaaaaa
Login to View More

Abstract

The present invention relates to a product having 99.9 to 90 mol% of vinylidene fluoride monomer units, 0.1 to 10 mol% of methylene malonate monomer units, and 0 to 10 mol of monomer units other than the above-mentioned monomer units %, 1,1-difluoroethylene copolymer with a weight average molecular weight of 200,000 or more, and a modified product obtained by hydrolyzing 10 to 90% of the total number of ester groups contained in the methylene malonate monomer unit , 1-difluoroethylene copolymers, and methods for their manufacture.

Description

technical field [0001] The present invention relates to a 1,1-difluoroethylene copolymer which is excellent in heat resistance, weather resistance, chemical resistance, and stain resistance, has good adhesiveness, and has reduced coloring during molding, and the 1,1-difluoroethylene copolymer. Process for the manufacture of ethylene copolymers. The 1,1-vinylidene fluoride copolymer obtained by the present invention is useful in the fields of various molded products, adhesives, paints, and the like. Background technique [0002] Polyvinylidene fluoride resin composed of 1,1-vinylidene fluoride unit is excellent in chemical resistance, weather resistance, stain resistance, etc., and can be used for producing various films and molded products by melt molding s material. In addition, it can also be used as a paint or an adhesive, but since the adhesive strength between polyvinylidene fluoride resin and substrates such as metals is low, improvement of the adhesive strength is d...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Patents(China)
IPC IPC(8): C08F214/22C08F8/12
CPCC08F2800/10C08F222/10C08F214/205C08F8/12C08F214/225C08F2/00C08F214/22
Inventor 佐藤圭介堺勇树
Owner KUREHA KAGAKU KOGYO KK
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products