Reactive-polymer-carrying porous film and process for producing the same
A reactive polymer, porous membrane technology, applied in the field of porous membranes, can solve the problems of difficult to adjust product quality, insufficient adhesion of electrodes and separators, reduce thermal shrinkage, etc., to achieve improved ion permeability, excellent battery characteristics, the effect of maintaining battery characteristics
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0106] (Production of Porous Membrane A)
[0107] The norbornene ring-opened polymer powder (Norsorex NB; product of Zeon Corporation, weight average molecular weight: more than 2,000,000) by 8 wt%, thermoplastic elastomer (TPE824; Sumitomo Chemical Co., Ltd. product) of 12 wt% and 80 wt% of 16 parts by weight of a polyethylene resin composition made of ultra-high molecular weight polyethylene with an average molecular weight of 3,500,000 and 84 parts by weight of liquid paraffin were mixed to form a slurry, and the mixture was melted and kneaded at a temperature of 160° C. for about 1 hour. Then, the obtained kneaded product was sandwiched between metal plates cooled to 0° C., rapidly cooled, and rolled into a sheet. Then, the sheet was hot-pressed at a temperature of 115° C. until the thickness of the sheet was 0.5 mm, and then biaxially stretched simultaneously at the same temperature in the longitudinal and transverse directions at a stretch ratio of 4.5, Heptane was used...
Embodiment 2
[0132] (Preparation of crosslinkable polymer B)
[0133] 40.0 g of methyl methacrylate, 20.0 g of 3-ethyl-3-oxetanyl methyl methacrylate, and 0.8 g of 2-hydroxyethyl methacrylate were placed in a 500 mL three-necked flask equipped with a reflux cooling tube. g, 19.2 g of butyl acrylate, 158 g of ethyl acetate, and 0.2 g of N,N'-azobisisobutyronitrile were stirred and mixed for 30 minutes under nitrogen gas, and then heated to 70° C. for 8 hours of radical polymerization. Thereafter, the resulting reaction mixture was cooled to 40°C. To this reaction mixture was added 0.2 g of N,N'-azobisisobutyronitrile, heated to 70°C again, and radical polymerization was performed for another 8 hours. Thereafter, the mixture was cooled to 40° C., 295 g of ethyl acetate was added, and then stirred until the mixture became uniform, thereby obtaining a polymer-forming ethyl acetate solution (concentration: 15 wt %).
[0134] Then, 100 g of the polymer solution was poured into 600 mL of methan...
Embodiment 3
[0139] (Production of porous membrane B)
[0140] 15 parts by weight of polyethylene resin formed from 20 wt% of EPDM (Espren 512F; product of Sumitomo Chemical Co., Ltd.; ethylidene norbornene content: 4 wt%) and 80 wt% of ultra-high molecular weight polyethylene with a weight average molecular weight of 1,500,000 The composition and 85 parts by weight of liquid paraffin were mixed into a slurry form, and the mixture was melted and kneaded at a temperature of 160° C. for about 1 hour using a small mixer. Then, the obtained kneaded product was sandwiched between metal plates cooled to 0° C., rapidly cooled, and rolled into a sheet. Then, the sheet was hot-pressed at a temperature of 115° C. until the thickness of the sheet was 0.4 mm, and then biaxially stretched at a stretch ratio of 4.0 in the longitudinal direction and the transverse direction at 123° C. at the same time. Heptane was desolvated. The porous membrane thus obtained was heated in air at 85° C. for 6 hours and...
PUM
Property | Measurement | Unit |
---|---|---|
thickness | aaaaa | aaaaa |
glass transition temperature | aaaaa | aaaaa |
glass transition temperature | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com