A novel catalytic two-step process for the preparation of rigid polyurethane foams: synthesis, mechanism and computational studies
文献情報
Loredana Maiuolo, Fabrizio Olivito, Fortuna Ponte, Vincenzo Algieri, Matteo Antonio Tallarida, Antonio Tursi, Giuseppe Chidichimo, Emilia Sicilia, Antonio De Nino
Polyurethanes (PUs) are very versatile and popular polymers that play a key role in the automotive, construction and non-food consumable sectors. In general, two-step polyurethane synthetic procedures involve the addition of catalysts also in the second phase of the reaction with problems of high environmental impact and disposal. In this work, an innovative eco-sustainable and very cheap procedure for the production of high-quality rigid polyurethane (PU) foams was developed, starting from polyethylene glycol (PEG 400) and diisocyanates as reagents and using common inorganic salts as catalysts, such as sodium chloride. In particular, our innovatory method is based on a single initial addition of a very cheap catalyst that is proved to be effective for both the prepolymer formation and polyurethane chain elongation. Moreover, simultaneous with the formation of final polyurethane, the salt was restored for a new catalytic cycle. Then, our strategy for polyurethane foam synthesis can surely represent a valid alternative as a very inexpensive and eco-compatible process, also for the industrial field. Finally, detailed mechanistic hypotheses were formulated and supported by DFT calculations.
関連文献
Reaction pathways for hydrogen desorption from magnesium hydride/hydroxide composites: bulk and interface effects
F. Leardini, J. R. Ares, J. Bodega, J. F. Fernández, I. J. Ferrer, C. Sánchez
DOI: 10.1039/B912964B
Impedance spectroscopy of H and OH adsorption on stepped single-crystal platinumelectrodes in alkaline and acidic media
K. J. P. Schouten, M. J. T. C. van der Niet, M. T. M. Koper
DOI: 10.1039/C0CP00104J
A suggested periodic table up to Z ≤ 172, based on Dirac–Fock calculations on atoms and ions
Pekka Pyykkö
DOI: 10.1039/C0CP01575J
Synthesis and transverse electromechanical characterization of single crystalline ZnO nanoleaves
Ya Yang, Qingliang Liao, Junjie Qi, Wen Guo
DOI: 10.1039/B918326D
Solvent-assisted optical modulation of FRET-induced fluorescence for efficient conjugated polymer-based DNA detection
Mijeong Kang, Okhil Kumar Nag, Sungu Hwang, Inhong Kim, Haesik Yang, Kwangseuk Kyhm
DOI: 10.1039/C0CP01025A
Ionic liquid silver salt complexes for propene/propane separation
Friederike Agel, Fee Pitsch, Florian Felix Krull, Peter Schulz, Matthias Wessling, Thomas Melin, Peter Wasserscheid
DOI: 10.1039/C0CP01104E
Selective internuclear coupling estimation in the solid-state NMR of multiple-spin systems
Andrea C. Sauerwein, Maria Concistrè, Malcolm H. Levitt
DOI: 10.1039/C0CP01262A
Thermal and photochemical oxidation of self-assembled monolayers on alumina particles exposed to nitrogen dioxide
Jonathan D. Raff, János Szanyi, Barbara J. Finlayson-Pitts
DOI: 10.1039/C0CP01041C
こちらもおすすめ
「邻羟基阿托伐他汀内酯标准品」に適用される法規ガイドelinesは何ですか?
CAS番号163217-74-1の「邻羟基阿托伐他汀内酯标准品」は、GHS分類では危険物に分類されず、主にREACH規則とFDA/EPAの管理対象となります。R...
メチル(3R)-3-アミノ-2,3-ジヒドロ-1-ベンゾファンラニン-5-カルボイル酸塩塩酸塩の主な用途は何ですか?
メチル(3R)-3-アミノ-2,3-ジヒドロ-1-ベンゾファンラニン-5-カルボイル酸塩塩酸塩は、医薬品や合成化学の研究に広く用いられます。また、特定の薬物の前...
トランス-4-メチルピロリジン-3-オール塩酸塩はどのように合成されますか?
トランス-4-メチルピロリジン-3-オール塩酸塩は、4-メチルピロリジンの塩酸塩化によって合成されます。一般的な合成方法では、4-メチルピロリジンを塩酸に加えて...
硫雜環丁烷-1,1-二氧化物は安全ですか?
硫雜環丁烷-1,1-二氧化物は安全ではありません。毒性は報告されていませんが、高温下で分解し、可燃性があるため、高圧ガスは注意が必要です。密閉した容器で保管し、...
9-ヒドロキシエリプチシネ塩酸塩はどのように合成されますか?
9-ヒドロキシエリプチシネ塩酸塩は、エリプチシネから塩酸を添加することで合成されます。選択性は高いですが、収率は約70%です。
5-塩素-2-(メチルアミノ)フェニル-(2-塩素フェニル)メタン酮の物理化学的性質は何ですか?
5-塩素-2-(メチルアミノ)フェニル-(2-塩素フェニル)メタン酮のCAS番号は5621-86-3です。この化合物は白色の結晶性粉末で、分子量は415.03で...
1-[2-(4-甲氧基-苯氧基)-乙基]-哌嗪はどのように保存すればよいですか?
1-[2-(4-甲氧基-苯氧基)-乙基]-哌嗪は、直射日光を避けて暗所に、室温(15-25℃)で保管し、密閉容器に入れることで安定性を保つことができます。
2-[3-(4-甲氧基フェニル)プロピル]-4,4,5,5-四メチル-1,3,2-ドイボロロールアンの主な用途は何ですか?
2-[3-(4-甲氧基フェニル)プロピル]-4,4,5,5-四メチル-1,3,2-ドイボロロールアンは、医薬品の合成、有機合成化学、および新材料の研究で使用され...
掲載誌
Reaction Chemistry & Engineering

Reaction Chemistry & Engineering is an interdisciplinary journal reporting cutting-edge research focused on enhancing the understanding and efficiency of reactions. Reaction engineering leverages the interface where fundamental molecular chemistry meets chemical engineering and technology. Challenges in chemistry can be overcome by the application of new technologies, while engineers may find improved solutions for process development from the latest developments in reaction chemistry. Reaction Chemistry & Engineering is a unique forum for researchers whose interests span the broad areas of chemical engineering and chemical sciences to come together in solving problems of importance to wider society. All papers should be written to be approachable by readers across the engineering and chemical sciences. Papers that consider multiple scales, from the laboratory up to and including plant scale, are particularly encouraged.











![1,1',1'',1'''-[Disulfanediylbis(carbonothioylnitrilo)]tetraethane structure 1,1',1'',1'''-[Disulfanediylbis(carbonothioylnitrilo)]tetraethane structure](https://static.chemtradehub.com/structs/97-/97-77-8-f3e4.webp)


