Related Experiment Video
Updated: Sep 7, 2025

Method Development for Contactless Resonant Cavity Dielectric Spectroscopic Studies of Cellulosic Paper
Published on: October 4, 2019
Diatomite Modified with an Alkyl Ketene Dimer for Hydrophobicity of Cellulosic Paper
Zicheng Chen1,2, Guangyuan Fan1, Xiangyang He1
1School of Chemical Engineering, Northeast Electric Power University, Jilin 132012, Jilin Province, P. R. China.
Abstract:
Multifunctionalization of papermaking chemicals is one of the main developing strategies. Fillers and internal sizing agents are often mutually restricted in practice. Therefore, it is feasible to prepare a new papermaking chemical by combining the functions of both. A process of diatomite modified with an alkyl ketene dimer (AKD) was developed in this study. The modified diatomite (AD) can concurrently play the role of a mineral filler and sizing agent in the papermaking process. With the equal dosage of AKD, the AD showed better sizing and retention performance than the commercial AKD emulsion in the case of cationic polyacrylamide (CPAM) and the CPAM/bentonite retention system. The sizing mechanism of the AD can be interpreted to be due to numerous hydrophobic sites and the microsurface structure of the paper sheet caused by the AD. Since ketones were not detected in Fourier-transform infrared spectra of the paper sheet filled by the AD, the chemical reaction may not be indispensable for its sizing performance. What is more, an interesting "sticky" hydrophobicity phenomenon was observed when filling with AD. The approach in this study to prepare the "sticky" hydrophobic paper sheet can find its applications in some nontraditional application fields of cellulosic paper.
More Related Videos
Related Concept Videos
Regioselectivity and Stereochemistry of Acid-Catalyzed Hydration
Aldehydes and Ketones with Water: Hydrate Formation
The formation of hydrates is a reversible reaction. Hydrate formation is influenced by steric and electronic factors accompanying the alkyl substituents on the carbonyl group: The rate of hydrate formation increases with a decrease in the number of alkyl groups attached to the carbonyl carbon. Hence,...
Alkenes via Reductive Coupling of Aldehydes or Ketones: McMurry Reaction
Olefin Metathesis Polymerization: Acyclic Diene Metathesis (ADMET)
Similar to cross-metathesis, ADMET also involves the formation of metallacyclobutane intermediate by [2+2] cycloaddition of one of the double bonds of a terminal diene with...

