Effects of Catalyst Complex on In Situ Polymerization and Formation Processes of Reactive Polyurethane Coatings

Reactive polyurethane (RPU) coatings are prepared via simultaneous polymerization and formation without any solvent. Therefore, it not only lowers the total organic carbon (TOC) emissions but also reduces energy consumption. However, its polymerization rate is relatively low at room temperature, and the whole process takes longer than 120 min. Although heating can enhance the rate, it also makes controlling the reaction more difficult. In addition, the present single catalyst is very sensitive to humidity. At high humidity, polyaddition of RPU cannot be efficiently achieved, significantly limiting mechanical properties. To overcome these drawbacks, the effects of selected catalysts on the microstructure evolution during the in situ polymerization and formation process of RPU coatings are investigated. Although the whole process still contains three stages as chain extension, gelation, and microphase separation, the polymerization rate of RPU coatings can be controlled by optimizing the mass ratio of the catalyst complex containing dibutyltin dilaurate (DBTDL) and 1,4-diazabicyclo[2.2.2]octane (DABCO). When the mass ratio of DBTDL to DABCO is 1:1, the polymerization rate is 44% faster than with the single catalyst DBTDL. Simultaneously, the breaking strength (14.56 MPa) and breaking elongation (813%) of the RPU coatings prepared by the catalyst complex are almost unchanged. The acceleration is mainly caused by the steric hindrance effect of the catalyst complex, which improves the catalytic selectivity and the interaction between -NCO and -OH groups in polyol. Moreover, the preparation process is less sensitive to humidity when the catalyst complex is applied. Even at 60% humidity, the final gel content can reach 92.1 ± 1.3%, 9.5% higher than that with the single catalyst DBTDL (84.1 ± 1.0%). Thus, the present catalyst complex can significantly shorten processing time and reduce humidity-related effects during preparation, thereby benefiting the PU industry.

Authors

Institutions

Publication Details

Journal
Langmuir
Published
2026-04-16
DOI
https://doi.org/10.1021/acs.langmuir.6c00770
Primary Topic
Polymer composites and self-healing
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Effects of Catalyst Complex on In Situ Polymerization and Formation Processes of Reactive Polyurethane Coatings

Neng Hu, Bin Zhao, Peter Müller‐Buschbaum, Junfeng Zhang et al.
Langmuir
Polymer composites and self-healing
article

Effects of Catalyst Complex on In Situ Polymerization and Formation Processes of Reactive Polyurethane Coatings

Neng Hu, Bin Zhao, Peter Müller‐Buschbaum, Junfeng Zhang, Lie Zhao, Dongming Qi, Zhuo Wang
article en

Abstract

Reactive polyurethane (RPU) coatings are prepared via simultaneous polymerization and formation without any solvent. Therefore, it not only lowers the total organic carbon (TOC) emissions but also reduces energy consumption. However, its polymerization rate is relatively low at room temperature, and the whole process takes longer than 120 min. Although heating can enhance the rate, it also makes controlling the reaction more difficult. In addition, the present single catalyst is very sensitive to humidity. At high humidity, polyaddition of RPU cannot be efficiently achieved, significantly limiting mechanical properties. To overcome these drawbacks, the effects of selected catalysts on the microstructure evolution during the in situ polymerization and formation process of RPU coatings are investigated. Although the whole process still contains three stages as chain extension, gelation, and microphase separation, the polymerization rate of RPU coatings can be controlled by optimizing the mass ratio of the catalyst complex containing dibutyltin dilaurate (DBTDL) and 1,4-diazabicyclo[2.2.2]octane (DABCO). When the mass ratio of DBTDL to DABCO is 1:1, the polymerization rate is 44% faster than with the single catalyst DBTDL. Simultaneously, the breaking strength (14.56 MPa) and breaking elongation (813%) of the RPU coatings prepared by the catalyst complex are almost unchanged. The acceleration is mainly caused by the steric hindrance effect of the catalyst complex, which improves the catalytic selectivity and the interaction between -NCO and -OH groups in polyol. Moreover, the preparation process is less sensitive to humidity when the catalyst complex is applied. Even at 60% humidity, the final gel content can reach 92.1 ± 1.3%, 9.5% higher than that with the single catalyst DBTDL (84.1 ± 1.0%). Thus, the present catalyst complex can significantly shorten processing time and reduce humidity-related effects during preparation, thereby benefiting the PU industry.

LangmuirVol. 42(16)
Zhejiang Sci-Tech University (CN), Zhejiang Institute of Modern Textile Industry (CN), Nano Carbon (Poland) (PL), Technical University of Munich (DE), Kuraray (United States) (US)
Openalex Percentile: Top 19%
Polymer composites and self-healing
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.