Preparation and properties of waterborne siloxane-containing polyurethane for moisture permeable textile coating

e-Polymers ◽  
2011 ◽  
Vol 11 (1) ◽  
Author(s):  
Haibo Lei ◽  
Yunjun Luo ◽  
Zhen Ge ◽  
Xiaomeng Li ◽  
Shengpeng Wang

AbstractWaterborne siloxane-containing polyurethanes (WSPU) were prepared by polyaddition reaction using poly(tetramethylene oxide)glycol (PTMG), polyethylene glycol (PEG), and α,ω-aminopropyl polydimethylsiloxane (APDMS) as mixing soft segments; 2,2-di(hydroxymethyl)propionic acid, as a hydrophilic chain extender; 1,4-butanediol and isophorone diisocyanate as hard segment; triethylamine as a neutralization agent. The thermal properties of WSPU films were analyzed by differential scanning calorimetry (DSC), dynamic mechanical analysis (DMA) and thermal gravimetric analysis (TGA). The mechanical properties of WSPU film were also investigated. Water vapor permeability (WVP) was examined according to GB_T 12704-1991. The DSC and DMA results indicated that there is a micro-phase separation in the WSPU film. The incorporation of APDMS into PU made the thermal stability of hard segment worse while that of soft segment better. The elasticity of WSPU was improved when the APDMS content was not more than 10%, the vapor permeability of coated fabric increased firstly and then decreased as the APDMS content increased, which was resulted from the hydrophilicity change and microstructure change of membrane. When 10% APDMS was incorporated into the WSPU, the WVP of coated fabric was 2130.15 g/(m2·24h), equal to one coated with a widely used solvent-based PU sample (UECCOAT), and the water resistance (WR) reached 30.0 KPa.

2013 ◽  
Vol 11 (12) ◽  
pp. 2058-2065 ◽  
Author(s):  
Tsvetomir Tsonev ◽  
Michael Herzog ◽  
Sanchi Nenkova

AbstractShape memory polyurethanes (SMPUs) were synthesized by 4,4′-diphenylmethane diisocyanate (MDI), hexane-1,6-diol (HD), polypropylene glycol (PPG), and recycled polyvinyl butyral (PVB). Dynamic mechanical analysis, differential scanning calorimetry and Fourier transformation infrared attenuated total reflection spectroscopy was used to characterize the poly (vinylbutyral-urethanes). Micro-phase domain separation of hard and soft segments and phase inversion were investigated. Increasing the hard segment content, i.e., average hard segment molecular weight, leads to an increase in the degree of micro-phase separation, hard domain order and crystallinity. The crystalline hard segment structures combined with the elastic nature of soft segment matrix provide enough physical and chemical crosslinks to have shape memory effect.


2020 ◽  
Vol 0 (0) ◽  
Author(s):  
E. Irzmańska ◽  
M. Jurczyk-Kowalska ◽  
M. Bil ◽  
M. Płocińska

AbstractThe study involved laminated nylon and viscose nonwovens, both perforated and non-perforated, with a view to using them for packaging of powders in mineral warmers. The nonwovens were examined in terms of morphology as well as tensile strength in dry and wet states. Thermal properties were determined by differential scanning calorimetry. Dynamic mechanical analysis was carried out in a broad range of temperatures. Surface wettability and water vapor permeability were assessed. The findings were analyzed to determine the utility of the studied materials as mineral warmer packaging materials in cold work or living environments.


Polymers ◽  
2018 ◽  
Vol 10 (11) ◽  
pp. 1292 ◽  
Author(s):  
Jia-Wun Li ◽  
Hsun-Tsing Lee ◽  
Hui-An Tsai ◽  
Maw-Cherng Suen ◽  
Chih-Wei Chiu

In this study, novel biodegradable long-segment fluorine-containing polyurethane (PU) was synthesized using 4,4′-diphenylmethane diisocyanate (MDI) and 1H,1H,10H,10H-perfluor-1,10-decanediol (PFD) as hard segment, and polycaprolactone diol (PCL) as a biodegradable soft segment. Nuclear magnetic resonance (NMR) was used to perform 1H NMR, 19F NMR, 19F–19F COSY, 1H–19F COSY, and HMBC analyses on the PFD/PU structures. The results, together with those from Fourier transform infrared spectroscopy (FTIR), verified that the PFD/PUs had been successfully synthesized. Additionally, the soft segment and PFD were changed, after which FTIR and XPS peak-differentiation-imitating analyses were employed to examine the relationship of the hydrogen bonding reaction between the PFD chain extender and PU. Subsequently, atomic force microscopy was used to investigate the changes in the microphase structure between the PFD chain extender and PU, after which the effects of the thermal properties between them were investigated through thermogravimetric analysis, differential scanning calorimetry, and dynamic mechanical analysis. Finally, the effects of the PFD chain extender on the mechanical properties of the PU were investigated through a tensile strength test.


Polymers ◽  
2021 ◽  
Vol 13 (18) ◽  
pp. 3097
Author(s):  
Mónica Fuensanta ◽  
José Miguel Martín-Martínez

Thermoplastic polyurethanes (TPUs) were synthetized with blends of poly(propylene glycol) (PPG) and poly(1,4-butylene adipate) (PAd) polyols, diphenylmethane-4,4′-diisocyanate (MDI) and 1,4-butanediol (BD) chain extender; different NCO/OH ratios were used. The structure and viscoelastic properties of the TPUs were assessed by infrared spectroscopy, differential scanning calorimetry, X-ray diffraction, thermal gravimetric analysis and plate-plate rheology, and their pressure sensitive adhesion properties were assessed by probe tack and 180° peel tests. The incompatibility of the PPG and PAd soft segments and the segregation of the hard and soft segments determined the phase separation and the viscoelastic properties of the TPUs. On the other hand, the increase of the NCO/OH ratio improved the miscibility of the PPG and PAd soft segments and decreased the extent of phase separation. The temperatures of the cool crystallization and melting were lower and their enthalpies were higher in the TPU made with NCO/OH ratio of 1.20. The moduli of the TPUs increased by increasing the NCO/OH ratio, and the tack was higher by decreasing the NCO/OH ratio. In general, a good agreement between the predicted and experimental tack and 180° peel strength values was obtained, and the TPUs synthesized with PPG+PAd soft segments had potential application as pressure sensitive adhesives (PSAs).


2015 ◽  
Vol 05 (03) ◽  
pp. 1550018 ◽  
Author(s):  
P. Thomas ◽  
B. S. Dakshayini ◽  
H. S. Kushwaha ◽  
Rahul Vaish

Composites of poly(methyl methacrylate) (PMMA) and [Formula: see text] (STMO) were fabricated via melt mixing followed by hot pressing technique. These were characterized using X-ray diffraction (XRD), thermo gravimetric analysis (TGA), differential scanning calorimetry (DSC), thermo mechanical analysis (TMA) and impedance analyser for their structural, thermal and dielectric properties. The coefficient of thermal expansion (CTE) was measured between 40°C and 100°C for pure PMMA is 115.2 ppm/°C, which was decreased to 78.58 ppm/°C when the STMO content was increased to 50 wt.% in PMMA. There was no difference in the glass transition ([Formula: see text]) temperature of the PMMA polymer and their composites. However, the FTIR analysis indicated possible interaction between the PMMA and STMO. The density and the hardness were increased as the STMO content increased in the PMMA matrix. Permittivity was found to be as high as 30.9 at 100 Hz for the PMMA+STMO-50 wt.% composites, indicating the possibility of using these materials for capacitor applications. The thermal stability of polymer was enhanced by incorporation of STMO fillers.


2017 ◽  
Vol 196 ◽  
pp. 43-54 ◽  
Author(s):  
Kun Wang ◽  
Jiping Yang ◽  
Chen Gong ◽  
Hao Lu

An amino-terminated poly(propylene glycol)-modified tetraaryl-buta-1,3-diene derivative (TABDAA) was introduced to synthesize polyurethanes with different ratios of soft/hard segments. A mixture of TABDAA and poly(tetrahydrofuran) 1000 as the soft segments was reacted with 4,4-diphenylmethane diisocyanate and 1,4-butanediol as the hard segments in molar ratios of 1 : 2 : 1, 2 : 3 : 1, and 3 : 4 : 1 to give the desired polyurethanes named TMPU-211, TMPU-321 and TMPU-431, respectively. The three polyurethanes exhibited different aggregation-enhanced emission (AEE) behaviors because of their different soft/hard segment ratios. The polyurethanes with a higher soft segment content tended to form bigger particles in a DMF/water mixture solution, thus causing a sharper increase in their fluorescence intensity. In addition, the polyurethane films exhibited different fluorescence intensities after different heat treatments. After a quenching treatment of the soft segments in the polyurethane films, the fluorescence intensity dropped greatly. When these quenched polyurethane films were thermally annealed at 60 °C for 24 hours, their fluorescence intensity exceeded the initial intensity of the as-prepared films. Differential scanning calorimetry results showed that the polyurethane films in the quenched condition did not present the endothermal melting peak of the soft segments, and the melting peaks appeared again after thermal annealing. AFM experiments showed that an ordered arrangement was achieved after the heat treatment of these AEE polyurethane films. These results demonstrated that the polymer structure had a significant effect on the AEE properties of the polyurethane films, and more importantly, it is of great significance in improving the fluorescence emission of the AEE polymers and also for their potential application in fluorescent probes, stimuli-responsive materials, PLED devices and so on.


2010 ◽  
Vol 150-151 ◽  
pp. 1396-1399 ◽  
Author(s):  
Xi Hong Li ◽  
Kuan Guo ◽  
Xiao Yan Zhao

This paper explains and demonstrates the effects of beeswax on functional and structural properties of soy protein isolate films, containing different glycerol. The results showed that percentage elongation at break, water vapor permeability, and transparency of soy protein isolate films decreased when the beeswax content increased, but tensile strength and oxygen permeability increased. The higher the glycerol content, the higher the film water vapor permeability, oxygen permeability, and transparency. The results of differential scanning calorimetry and Fourier transform infrared spectroscopy suggested that beeswax cross-linked with soy protein isolate molecules via connecting with glycerol, composed the film matrix.


2018 ◽  
Vol 31 (7) ◽  
pp. 820-830 ◽  
Author(s):  
Haifeng Wang ◽  
Zhenjiang Zhang ◽  
Puguang Ji ◽  
Xiaoyan Yu ◽  
Kimiyoshi Naito ◽  
...  

A novel vinylpyridine-based phthalonitrile monomer, 2,6-bis[3-(3,4-dicyanophenoxy)styryl]pyridine (BDSP), was resoundingly produced by a nucleophilic substitution reaction of 2,6-bis(3-hydroxystyryl)pyridine with 4-nitrophthalonitrile in the presence of potassium carbonate. The chemical structure of the synthesized BDSP was confirmed by proton (1H) and carbon (12C) nuclear magnetic resonance (NMR) as well as Fourier transform infrared (FTIR) analysis. The curing behavior of BDSP was investigated by FTIR and differential scanning calorimetry (DSC) analyses. The resin showed a low complex viscosity in the wide processing window between the monomer melting temperature and the curing temperature of the polymer, as discovered by rheological analysis. In addition, the properties of the polymer were studied by thermal gravimetric analysis (TGA) and dynamic mechanical analysis (DMA). Based on the test results, the BDSP polymer demonstrated superior processing performance, excellent thermal stability, outstanding mechanical properties, and low water uptake, and these advanced performance characteristics are critical to many fields.


Marine Drugs ◽  
2019 ◽  
Vol 17 (12) ◽  
pp. 662
Author(s):  
Yongliang Zhuang ◽  
Shiyan Ruan ◽  
Hanghang Yao ◽  
Yun Sun

Different composite films composed of tilapia skin collagen (TSC) with Pachyrhizus starch (PS) or rambutan peel phenolics (RPP) were prepared, and the physical properties of these films were determined. The effects of PS and RPP on TSC films were investigated, and our results indicated that PS and RPP could improve the physical properties of TSC films. Opacity and film thickness showed an enhanced trend with increasing PS and RPP contents in TSC films, whereas solubility in water, elongation-at-break (EAB), and water vapor permeability (WVP) showed declining trends. TSC film with 10% PS and 0.5% RPP had the highest tensile strength, and the tensile strength dropped drastically when the content of PS and RPP increased. The light transmittances of the films could decrease with the incorporation of PS and RPP. Differential scanning calorimetry (DSC) demonstrated that the addition of PS and RPP improved the thermal stability of TSC films. In addition, X-ray diffraction indicated that the crystallinity of the films decreased and the amorphous structure of the films tended to become more complex with the addition of PS and RPP. As shown by fourier transform infrared spectroscopy (FTIR) analysis, PS and RPP can strongly interact with TSC, resulting in a modification of its structure. Scanning electron microscope (SEM) analysis showed that there was a good compatibility between TSC, PS, and RPP. The results indicated that TSC film incorporated with 10% PS and 0.5% RPP was an effective method for improve the physical properties of the film. TSC–PS–RPP composite films can be used not only in biomedical applications, but also as active food packaging materials.


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