In situ synthesis of CO 2 adducts of modified polyethylenimines in polyether polyols for polyurethane foaming
CO 2 adducts from hydrophobically-modified polyethylenimines (PEIs) in powder form are newly-developed environment-friendly blowing agents for polyurethanes (PUs). However, they are difficult to disperse into foaming systems that usually contain polyether polyols as the PU soft segments. Herein, we...
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Veröffentlicht in: | Journal of cellular plastics 2022-01, Vol.58 (1), p.103-120 |
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creator | Yuan, Shuai Long, Yuanzhu Xie, Xingyi |
description | CO 2 adducts from hydrophobically-modified polyethylenimines (PEIs) in powder form are newly-developed environment-friendly blowing agents for polyurethanes (PUs). However, they are difficult to disperse into foaming systems that usually contain polyether polyols as the PU soft segments. Herein, we employ mixtures of di(propylene glycol) monomethyl ether-grafted polyethylenimines (DPG-PEIs) and poly(propylene glycol) (PPG) polyols to absorb CO 2 , with in situ formation of the CO 2 adduct particles as PU blowing agents. Their CO 2 saturation degrees, revealed by thermogravimetry, scatter in the range of 93–98%. The DPG side chains tend to be exposed at the particle–matrix interface to stabilize the particles. In addition, some PPG oligomers in the matrix might entangle with the CO 2 adduct macromolecules during the in situ particle formation. The entangled PPG chains could further stabilize the suspending particles. The high grafting rate and high molecular weight of the PEI backbones could result in small particles, which largely thicken the foaming systems. The optimized blowing agents, with grafting rates between 5% and 8% and PEI backbone molecular weights not higher than 10k Da, show particle sizes from several hundreds of nanometers to ∼1 μm. The resultant foams demonstrate densities below 50 kg/m 3 and compressive strengths over 200 kPa, comparable to the values from industrial foams. This in situ CO 2 adduction has potential as a universal method suitable for PU foaming at an industrial scale. |
doi_str_mv | 10.1177/0021955X20987153 |
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However, they are difficult to disperse into foaming systems that usually contain polyether polyols as the PU soft segments. Herein, we employ mixtures of di(propylene glycol) monomethyl ether-grafted polyethylenimines (DPG-PEIs) and poly(propylene glycol) (PPG) polyols to absorb CO 2 , with in situ formation of the CO 2 adduct particles as PU blowing agents. Their CO 2 saturation degrees, revealed by thermogravimetry, scatter in the range of 93–98%. The DPG side chains tend to be exposed at the particle–matrix interface to stabilize the particles. In addition, some PPG oligomers in the matrix might entangle with the CO 2 adduct macromolecules during the in situ particle formation. The entangled PPG chains could further stabilize the suspending particles. The high grafting rate and high molecular weight of the PEI backbones could result in small particles, which largely thicken the foaming systems. The optimized blowing agents, with grafting rates between 5% and 8% and PEI backbone molecular weights not higher than 10k Da, show particle sizes from several hundreds of nanometers to ∼1 μm. The resultant foams demonstrate densities below 50 kg/m 3 and compressive strengths over 200 kPa, comparable to the values from industrial foams. 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The optimized blowing agents, with grafting rates between 5% and 8% and PEI backbone molecular weights not higher than 10k Da, show particle sizes from several hundreds of nanometers to ∼1 μm. The resultant foams demonstrate densities below 50 kg/m 3 and compressive strengths over 200 kPa, comparable to the values from industrial foams. 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However, they are difficult to disperse into foaming systems that usually contain polyether polyols as the PU soft segments. Herein, we employ mixtures of di(propylene glycol) monomethyl ether-grafted polyethylenimines (DPG-PEIs) and poly(propylene glycol) (PPG) polyols to absorb CO 2 , with in situ formation of the CO 2 adduct particles as PU blowing agents. Their CO 2 saturation degrees, revealed by thermogravimetry, scatter in the range of 93–98%. The DPG side chains tend to be exposed at the particle–matrix interface to stabilize the particles. In addition, some PPG oligomers in the matrix might entangle with the CO 2 adduct macromolecules during the in situ particle formation. The entangled PPG chains could further stabilize the suspending particles. The high grafting rate and high molecular weight of the PEI backbones could result in small particles, which largely thicken the foaming systems. The optimized blowing agents, with grafting rates between 5% and 8% and PEI backbone molecular weights not higher than 10k Da, show particle sizes from several hundreds of nanometers to ∼1 μm. The resultant foams demonstrate densities below 50 kg/m 3 and compressive strengths over 200 kPa, comparable to the values from industrial foams. This in situ CO 2 adduction has potential as a universal method suitable for PU foaming at an industrial scale.</abstract><doi>10.1177/0021955X20987153</doi><tpages>18</tpages><orcidid>https://orcid.org/0000-0003-2420-553X</orcidid></addata></record> |
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title | In situ synthesis of CO 2 adducts of modified polyethylenimines in polyether polyols for polyurethane foaming |
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