Related Experiment Video
Updated: Feb 6, 2026

Depolymerizable Olefinic Polymers Based on Fused-Ring Cyclooctene Monomers
Published on: December 16, 2022
Polymer coatings based on sulfonated-poly-ether-ether-ketone films for implant dentistry applications
R S Brum1, P R Monich2, M C Fredel2
1Center for Research on Dental Implants (CEPID), School of Dentistry (ODT), Federal University of Santa Catarina (UFSC), Florianopolis/SC, 88040-900, Brazil. renatasbrum@live.com.
This study developed sulfonated poly-ether-ether-ketone (SPEEK) coatings on PEEK substrates for biomedical uses. While SPEEK coatings modified PEEK surfaces, they did not demonstrate significant bioactivity in simulated body fluid, requiring further development.
Area of Science:
- Biomaterials Science
- Polymer Chemistry
- Surface Engineering
Background:
- Poly-ether-ether-ketone (PEEK) is a widely used biocompatible polymer in biomedical applications.
- Sulfonation of PEEK (SPEEK) has been explored to enhance its properties for enhanced biomedical utility.
- Developing functionalized PEEK surfaces is crucial for improving implant performance and osseointegration.
Purpose of the Study:
- To synthesize and characterize sulfonated PEEK (SPEEK) coatings on PEEK substrates.
- To evaluate the physicochemical properties and surface characteristics of the modified PEEK materials.
- To assess the bioactivity of SPEEK-coated PEEK in simulated body fluid (SBF).
Main Methods:
- Biomedical grade PEEK was functionalized with sulfuric acid to produce SPEEK.
- SPEEK was dissolved in Dimethyl sulfoxide (DMSO) or Dimethylformamide (DMF) and coated onto PEEK substrates (bars and cylinders).
- Characterization involved FTIR, XRD, SEM, contact angle measurements, and bioactivity assessment in SBF with subsequent analysis (SEM, EDX, FTIR).
Main Results:
- FTIR and XRD confirmed the successful sulfonation and semicrystallinity of PEEK and SPEEK.
- SPEEK/DMF coatings showed significant physicochemical modifications, while SPEEK/DMSO coatings resulted in more regular, hydrophobic surfaces.
- Calcium precipitates formed on both SPEEK/DMSO and SPEEK/DMF coated samples in SBF, but bioactivity was not confirmed.
Conclusions:
- SPEEK coatings on PEEK substrates exhibit interesting surface properties, with DMF and DMSO influencing surface characteristics differently.
- The formation of calcium precipitates suggests some interaction with biological fluid, but the materials were not deemed bioactive.
- Further improvements in SPEEK film production and comprehensive biological testing are necessary to optimize these coatings for biomedical applications.
Related Concept Videos
Ethers from Alcohols: Alcohol Dehydration and Williamson Ether Synthesis
Ethers can be prepared from organic compounds by various methods. Some of them are discussed below,
Preparation of Ethers by Alcohol Dehydration
In this method, in the presence of protic acids, alcohol dehydrates to produce alkenes and ethers under different conditions. For example, in the presence of sulphuric acid, dehydration of ethanol at 413 K yields ethoxyethane, whereas it yields ethene at 443 K.
Crown Ethers
Structure and Nomenclature of Ethers
Ethers are organic compounds with an ether functional group which is characterized by an oxygen atom connected to two — identical or different — alkyl, aryl, or vinyl groups. The C–O–C linkage in dimethyl ether — the simplest ether — has an approximately tetrahedral bond angle of 110.3 degrees. The oxygen atom is sp3- hybridized, with the C–O distance being about 140 pm.
Classification of Ethers
Based on their attached substituent...
Physical Properties of Ethers
An ether molecule has a net dipole moment due to the polarity of C–O bonds. Subsequently, boiling points of ethers are lower than those of alcohols of comparable molecular weight and slightly higher than those of hydrocarbons of comparable molecular weight (Table 1).
Ethers can act as hydrogen bond acceptors, making them more water-soluble than hydrocarbons, but since ethers cannot act as hydrogen bond donors, they are much less soluble in water than alcohols. Ethers are considered...
Autoxidation of Ethers to Peroxides and Hydroperoxides
Ethers to Alkyl Halides: Acidic Cleavage

