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Hollow silica spheres (HSS) with special interior spaces, high specific surface area and excellent adsorption and permeability performance were synthesized via micelle-template method using cetyl trimethyl ammonium bromide (CTAB) micelles as soft template and tetraethoxysilane (TEOS) as silica precursor. SEM, TEM, FT-IR, XRD, DLS and BET-BJH were carried out to characterize the morphology and structure of as-obtained samples. The results demonstrated that the samples were amorphous with a hollow structure and huge specific surface area. The growth of HSS was an inward-growth mechanism along template. Notably, we have provided a new and interesting fundamental principle for HSS materials by precisely controlling the ethanol-to-water volume ratio. In addition, the as-obtained HSS were mixed with waterborne polyurethane (WPU) to prepare WPU/HSS composite membrane. Various characterizations (SEM, TEM, FT-IR and TGA) revealed the morphology, polydispersity and adherence between HSS and WPU. Performance tests showed that the introduction of HSS can improve the water vapor permeability of composite membrane, promoting its water resistance and mechanical performance at the same time.
Polyurethane (PU) is widely used in coating industry for its excellent wear resistance, low temperature flexibility, and good physical and chemical stability1,2,3. However, the PU membrane suffers several defects, such as yellowing, poor permeability, and the release of organic solvent, which hinder its further development. Specifically, the poor permeability will lead to low air permeability and water vapor permeability, so as to severely degrade sanitation performance4. Primarily, the water vapor permeability is of great importance when PU membrane is used as the coating of synthetic leather for shoes and garments5. It allows the sweat to evaporate promptly, especially when human bodies are in hot environments. Moreover, in order to adapt to the development of coating industries, waterborne polyurethane (WPU) with outstanding comprehensive performance and environmentally-friendly characteristics is generally taking place of traditional PU. Even though the water vapor permeability of WPU shows a slight promotion, but still in poor condition and the mechanical property dropped simultaneously.
Previous researches have shown that there are several important factors affecting the water vapor permeability of polymer membrane6. Among them, hydrophilic nature of polymer chain7 and free volume in polymer membrane8 are the decisive forces. First and foremost, from a chemical point of view, hydrogen bonds will be formed between water vapor molecules and hydrophilic groups in polymer membrane. With the vibrating of polymer chains, water vapor molecules diffuse from a region of greater to one of less concentration9. Furthermore, from a physical point of view, the free volume theory is widely applied to expound the relationship between mass transfer in a polymer film and water vapor dependence on number, shape and size of free volume10.
The above statements have been verified by theoretical analysis and experimental results. In Mondal et al.’s work11, they observed that water vapor permeability of PU was influenced by presence of both hydrophilic groups content as well as soft segment crystal melting. Zhang et al.12 reported a method of adding white wood flours with different ratio to polyurethane, and the experimentation results showed that the air and water vapor permeability of polyurethane membrane were obviously enhanced.
However, the generalisability of much published research on this issue is problematic. Most studies on the filler materials of PU membrane have only focused on solid materials of macro-range and overlooked hollow micro-nano materials with mesoporous structure13, which resulted in an insufficient performance improvement. The usage of inorganic nanoparticles would be desirable filler materials to overcome the aforementioned limitations. Because, polymer/inorganic nanocomposites showed a series of preeminent functionalities as compared with conventional polymer composites, such as improved mechanical strength, wear resistance, yellowing resistance, water resistance, antimicrobial behavior, self cleaning, hygienic properties and so on.
Among a variety of inorganic nanoparticles, hollow structured silica spheres have been widely concerned in the past few years due to the ingenious combination of hollow architecture with the excellent characteristics of silica materials14,15,16. Benefitting from the merits of low density, large specific surface area, the huge void space, special photoelectric properties and good biocompatibility17, hollow silica spheres (HSS) present promising application prospects in catalysis18, waste removal19, adsorption, storage20, and sustained/controlled release of agents with various functionalities21,22,23,24,25,26. Different methods have been employed to prepare HSS, including template-assisted synthesis27,28, self-templating method29,30, spray drying31,32 and hydrothermal synthetic method33,34. Among them, templating method is one of the most commonly used approaches. Usually, core-shell structured spherical composites are synthesized by coating silica on spherical template cores such as polymer based templates35,36,37, inorganic templates38,39,40 and emulsion templates41. Then, the template cores are removed by either high-temperature calcination in air or chemical etching with solvent to obtain hollow structure. However, this is time-consuming and may cause air pollution and the collapse of hollow structure. Therefore, there is a great challenge to develop a simple, effective and environmental friendly way for synthesizing HSS42.
Micelle template method is used as an alternative approach wherein micelle templates are formed and silica is deposited on templates43,44. In this article, HSS with regular structure, hollow cavity, narrow particle size distribution and amorphous shell were conveniently fabricated by micelle template. The innovation points of our research were that we employed cetyl trimethyl ammonium bromide (CTAB) micelle as cavity and mesoporous templates, which was very easy to prepare and remove at ambient surrounding. In contrary to current soft template synthesizing strategies including emulsion or micro-emulsion templates, micelle template method had improved structural stability and monodispersity. Significantly, we systematically demonstrated the influence of factors on morphology by changing the synthetic parameters, such as CTAB dissolving methods and ethanol-to-water volume ratio. And the possible mechanism of morphological change of HSS was proposed according to the research results. Finally, the as-prepared HSS were introduced into WPU emulsion by physical blending method to prepare WPU/HSS composite emulsion and composite membrane. Importantly, the multi-functional composite membrane have potential applications in improving water vapor permeability of waterborne polyurethane coating.
Tetraethoxysilane (TEOS) and cetyl trimethyl ammonium bromide (CTAB) were purchased from Tianjin Kemiou Chemical Reagent Co., LTD. Ammonia (25wt% NH3 in water) was supplied by Tianjin Fuyu Fine Chemical Co., Ltd. Ethanol was obtained from Tianjin Hedong Hongyan Chemical Reagent Factory. All the reagents were of analytical grade and used as received without further purification. WPU (technical pure) was provided by Yantai Daocheng Chemical Co., Ltd. The deionized water was from our laboratory.
HSS were prepared via the hydrolysis and condensation of TEOS in an aqueous basic-ethanol medium. Typically, 0.08g of CTAB was dissolved in 50mL of mixed aqueous solution of water and ethanol with stirring. Then 0.5mL of TEOS and 0.5mL of ammonia were added sequentially. The resulting mixture was further stirred at 30°C for 6h to give a white suspension. After reaction, the suspension were centrifuged and washed with water and ethanol by two cycles to remove any residual organics and ammonia. The final particles were collected after drying over-night at 60°C.
WPU/HSS composite emulsion was obtained by physical blends of WPU resin and HSS. First, 0.09g of HSS was dispersed in 15mL of aqueous solution containing one-third of ethanol with 20min ultrasonation. Then the dispersion was added into a 100mL three-necked flask containing 30g of WPU resin. The blending process was kept at 75°C for 6h with stirring.
20g of WPU/HSS composite emulsion was poured into a square glass tank and laid on the horizontal surface until dried completely at ambient temperature to obtain WPU/HSS composite membrane.
The morphology of HSS and WPU/HSS composite were observed by Scanning Electron Microscope (SEM, S48000, Japan) and Transmission Electron Microscope (TEM, Hitachi, H-7650, Japan). For SEM, the HSS were scattered on the conductive adhesive of sample platform and sputter-coated with gold. The WPU/HSS composite membrane were breaked off in liquid nitrogen and then attached to the samples platform and sputter-coated with gold. For TEM, the samples were prepared by diluting HSS or composite emulsion with ethanol and dropping the obtained suspension on a copper grid.
The chemical structure of HSS and WPU/HSS composite membrane were analyzed by Fourier Transform Infrared Spectroscopy (FTIR, VECTOR22, Brucker, Germany). The powder samples were pressed into a transparent sheet together with potassium bromide (KBr) by a mould, whereby the samples and KBr should be dry.
Wide-angle X-ray Diffraction (XRD, Rigaku, D/max-2200, Japan) was used to determine the crystalline phase of HSS. Radial scans of intensity versus scattering angle were recorded from 10° to 70° using a Cu Kα radiation. And the samples were flattened in a sample container by a glass slide.
The average particle size distribution of micelles and HSS were obtained by dynamic light scattering (DLS) measurements at 25°C using a Zetasizer NanoZS (Malvern Instruments Ltd., UK).
The specific surface areas of HSS were measured with Brunauer-Emmett-Teller (BET) and Adsorption Analysis. Pore size distributions were calculated from desorption branches of isotherms by the Barrett-Joyner-Halenda (BJH) method. Before test, the powder samples were degassed at 300°C under vacuum for 3h.
Thermogravimetric analysis (TGA) curves of WPU/HSS composite membrane were carried out in a Perkin-Elmer thermogravimetric analyzer under air stream. The temperature gradient started from 25°C to 600°C at a heating rate of 10°C/min.
Water vapor permeability (WVP) of composite membrane was measured by permeability cup method, a National Standard test method in China. First, a permeability cup with area of 10cm2 was filled with 30g of deionized water. Then the composite membrane was sealed on the top of the cup. Keep the cup in an incubator with constant temperature (37°C) and humidity (90% RH) for 24h. The water vapor permeability was valued by the following formula:
where and are the total mass of permeability cup, composite membrane and water, weighted up promptly and after 24h respectively.
Three squares with size of 1.5cm×1.5cm were clipped from composite membrane and immerged in distilled water for 24h. Each one was weighed on analytical scale before and after immersion, denoted as m0 and m respectively. Water absorption (W) was calculated according to the following formula and 3 data were averaged for a more convincing result:
Tensile strength and elongation at break of composite membrane was measured using a functional materials examination machine made by Taiwan High Iron Science and Technology Stock Company with extending speed of 500mm/min and backhaul speed of 100mm/min. Composite membrane was sampled with the standard dumbbell-like mould. And before examination, all the samples were placed in desiccator of concentrated sulfuric acid for 24h for air conditioning.
Low-magnification SEM image (Fig. 1a) showed that the HSS samples were uniform in size with spherical shape, and the average size was ~500nm. Broken spheres prove the hollow nature of silica samples. Closer examination (Fig. 1b) indicated that the silica shell was rough, composed of many tiny silica particles. The thickness of the shell was about 150nm. These constituent silica particles were about 20nm in dimension, attaching to each other to form a relatively dense silica shell. The HSS could not be destroyed into individual silica particles even after fully grinded. So, strong chemical bonding is believed to be formed between the contacting lateral surfaces. Small-sized constituent silica particles are inclined to attach to each other to minimize the surface energy, forming hollow silica shell. Also for this reason, the adjacent HSS may further coagulate to form the twin-like structure, as observed in Fig. 1(a).
To furher confirm that HSS possess apparent hollow structure, the HSS samples were observed by TEM. As shown in Fig. 2, the typical TEM images of HSS clearly revealed that all those samples fabricated by micelle-template method were hollow in character and the shell thickness of the spheres was about 150nm. Meanwhile, the outer surface of HSS was smooth, while the inner surface was rough. These tendencies are same with the results of SEM observations.
Figure 3(a) showed the FT-IR spectrum of the obtained HSS samples. A distinctive Si-OH stretching vibration was displayed at about 3423cm−1. The strong absorption peak at 1082cm−1 was belonged to Si-O-Si asymmetric stretching. The peaks at 801cm−1 and 464cm−1 were assigned to symmetric stretching vibration of Si-O, and the peak at 964cm−1 was due to bending vibration absorption of Si-OH. Peak around 1635cm−1 was the bending vibration peak of H-O-H in water. The peaks at 2925cm−1 and 2854cm−1 were attributed to asymmetrical stretching vibration of -CH3 and -CH2-, which may be caused by the residual organic matter inside the samples. These results demonstrated that the as-obtained sample is silica. In addition, the powder XRD pattern in Fig. 3(b) showed a broad diffraction peak between 12° and 38°, indicating that the silica samples are of amorphous structure. This amorphous structure endowed HSS with loose and permeable silica shells.
To elucidate the importance of ethanol on the whole reaction system, the control experiment was carried out that using pure water as the initial solvent of CTAB. The SEM images (Fig. 4a) showed that when CTAB was dissolved in pure water, only nearly solid silica spheres were obtained with a smaller particle size. Because, when CTAB was dissolved in pure water system, the hydrophobic carbon chain with lower dielectric constant escaped from the water medium rapidly and entangled with each other. Then the smaller diameter micelles were formed and the surface energy of the system would be dropped to a minimum. On the other hand, the addition of ethanol was in favor of the formation of hollow structure. This is due to the fact that ethanol has lower dielectric constant than water. While ethanol and water were used as co-solvents, it is easier for ethanol to seep into the interior of the CTAB micelle to enlarge it, forming a rich-ethanol phase inside micelle and a rich-water phase outside micelles. Then the expanded micelle act as templates to direct the hydrolysis and assembly of silica precursor. The internal hydrophobic region of CTAB micelle allowed the organic precursor in and then provided place for precursor to hydrolyze. When exposed to alkaline condition, precursor hydrolyzed rapidly to form tiny silica seeds. Since negatively charged, these silica seeds attracted to the inner surface of positively charged CTAB micelle by electrostatic interactions, thus resulting a silica shell. After complete hydrolysis of precursor, HSS could be obtained (Fig. 4b). So, larger micelle is more conducive to the formation of hollow structure.
Figs 5 and and66 showed the SEM and TEM images of a series of HSS prepared at different ethanol-to-water volume ratio (Re/w), respectively. Diameters of HSS increased gradually from 150nm to 600nm when the Re/w changed from 0.3 to 0.6. Furthermore, the broken or fractured HSS in SEM images together with TEM images permit us to observe the inner space directly, indicating that the solid silica spheres were transformed to hollow silica spheres by increasing Re/w from 0.3 to 0.6. In this period, the hollow silica surface became smoother. The above morphological evolutions may due to the following reasons. When more ethanol was added, dielectric constant of the system reduced. More ethanol would enter into CTAB micelles, enlarging the template, to form larger HSS. Meanwhile, more TEOS species would enter into CTAB micelles together with ethanol due to increased solubility of TEOS in the rich ethanol system. The presence of ethanol also reduced the hydrolysis rate of precursor, creating HSS with smoother surface. However, further increasing the Re/w to 0.7, the ethanol content in the rich-water phase rose and the miscibility between TEOS and water increased greatly. A portion of TEOS was dissolved in rich-water phase outside the micelle, rather than into the micelle interior to further increase the template size. So, HSS with smaller hollow interior cavity and nearly invariable particle size were obtained, as shown in Figs 5(e) and 6(e).
It is known that the size of particles synthesized in a mixed aqueous solution of water and ethanol are governed by the amount of ethanol. Figure 7(a) revealed the hydrodynamic particle size distribution of HSS obtained at different Re/w, suggesting the increasing hydrodynamic diameter of HSS from 250nm to 800nm with the Re/w increasing from 0.3 to 0.6. Interestingly, it reached to a stable state with Re/w keeping on going up to 0.7. As a control, Fig. 7(b) showed the systematic DLS of micelle (CTAB) by varying Re/w, which indicated the similar tendency with Fig. 7(a). However, in contrast to the actual size in SEM and TEM images, all the samples in DLS results showed a larger population of particles with a large diameter, due to the little conglomeration and instability of particles.
The nitrogen sorption isotherms of HSS at different Re/w in Fig. 8(a) exhibited typical IV curves with a N2 hysteresis loop that gradually closed at a partial pressure near 0.4, revealing characteristics of obtained HSS with high surface areas and narrow pore size distribution45. The BET surface area and pore volume of HSS were calculated and compared in Fig. 8(b), which obviously indicated a gradual increase in specific surface area and pore volume of HSS when the Re/w changed from 0.3 to 0.7. For the optimization of HSS (Re/w=0.6), the BET surface area and the pore volume were found to be 600.05m2/g and 0.356cm3/g, respectively. When Re/w was up to 0.7, the BET surface area and the pore volume were calculated to be as high as about 957.97m2/g and 0.480cm3/g, both of them are larger than Re/w=0.6. At the same time, the detailed pore size distribution calculated based on the BJH method suggested that HSS prepared at different Re/w have uniform mesoporous size of about 3.8nm and narrow pore size distribution ranging from 3.2 to 4.5nm (Fig. 8c). Considering the aforementioned results that the diameter of HSS maintained a stable value but the hollow interior cavity decreased at Re/w=0.7. The highest surface area of HSS at Re/w=0.7 can probably be attributed to the greater numbers of pores in the shells.
Based on above morphological changes observed via the SEM images, an inward-growth mechanism involving sol-gel and electrostatic self-assembly of HSS was proposed in Fig. 9. First and foremost, cationic surfactant formed micelles in appropriate volume ratios of ethanol-water systems. Especially, a rich-ethanol phase was inside micelles and a rich-water phase was outside micelles owing to their differences in dielectric constant. Upon adding TEOS under stirring action, they would diffuse into the internal hydrophobic region of CTAB micelles together with ethanol because of their hydrophobic properties, they form an “oil-in-water” emulsion, in which the “oil” is TEOS in rich ethanol phase inside the micelles, and the “water” is rich-water phase outside the micelles. The “oil-in-water” emulsion act as a temporary template to define the morphology of HSS. Then ammonia catalyst was added to adjust the pH value and provide ideal reaction condition for silicon source. Lastly, under the catalysis of ammonia, the TEOS inside micelles hydrolyzed and condensed rapidly to form silica seeds46,47. During the sol-gel process, silica seeds with negative charge are drawn expeditiously to the hydrophilic end of cationic micelles by electrostatic interaction, which induced the synthesis of silica shell on the inner surface of the micelle. Since the hydrophobic interactions, the internal non-hydrolyzed TEOS will remain inside micelle interior until completion of hydrolysis. Although the silica shell formed earlier is loose with surface defects, the resulting silica seeds furtherly deposited inward, with continual increase in hollow silica shell thickness.
Inferring from above, we draw information that the amount of TEOS and reaction time would certainly determine the shell thickness but has had no effect on particle size. Remarkably, an appropriate amount of ethanol can stabilize the template, so that the silica condensation can take place without interruption. Ethanol can also enter into micelles to expand the template, producing larger silica spheres with hollow interior. However, it is worth noting that when an excess amount of ethanol was added, they would spread into water phase due to the excellent inter solubility of ethanol and water. This leads to the increased solubility of TEOS in rich-water phase outside the micelles, resulting in smaller HSS formation.
In order to understand the interaction force between WPU chains and HSS, the FT-IR measurements of composite membrane were carried out. As shown in Fig. 10(a), the FT-IR spectrum of WPU membrane showed two apparent peaks at 1725cm−1 and 1250cm−1, which can be assigned to the stretching vibration of C=O group and C-N group respectively, clearly indicating the characteristic frameworks in a hard segment of PU. While the peak position of C=O group in the FT-IR spectrum of WPU/HSS was at 1715cm−1, this shift suggested that there were some strong interactions in C=O and Si-OH of WPU/HSS composite membrane. Additionally, the band located at 972cm−1 was associated with the Si-OH stretching vibration, which implied the existence of HSS in the composite membrane. However, compared to the bending vibration absorption of Si-OH located at 964cm−1 in FT-IR spectrum of HSS (Fig. 3a), this slight shift was also attributed to the interaction between C=O and Si-OH. Figure 10(b,c) presented the typical TGA and DGT curves of WPU and WPU/HSS composite membrane. The weight loss in temperature range of 350–500°C was shown that the thermal decomposition behavior of WPU/HSS composite membrane slightly shifted toward the higher temperature range compared with that of pure WPU. This confirmed the enhancement of thermal stability of hybrid WPU. The hybrid system may have an interpenetrated network nature and lead to the increase in the thermal stability, due to HSS acted as restriction sites to limit the segmental movement of WPU chains48. These above analyses indicate that rich hydroxyl groups on the surface of HSS could be interacted with WPU chains via H-bond force.
In order to further test the dispersibility of HSS in polymer matrix, the morphology of the as-prepared hybrid materials was examined by SEM and TEM. As shown in Fig. 11, we could clearly identify that a certain number of HSS dispersed in the cross-section of WPU membrane, showing a variant individual dispersion at different Re/w. When Re/w was 0.6 (Fig. 11e), as expected, the as-synthesized HSS possessed apparent internal hollow cavity and better monodispersion in WPU. Moreover, it also can be revealed from the TEM images as shown in Fig. 12, severe aggregation was observed when HSS made at Re/w=0.4 (Fig. 12c), which was consistent with the SEM study. With the increasing of Re/w, HSS indicated good individual dispersion in WPU and remained a clear hollow microstructure simultaneously. These facts demonstrate that the as-made WPU/HSS composite membrane would be suitable for the permeability of water vapor.
HSS were introduced into WPU resin by physical blends to prepare WPU/HSS composite membrane. To make the HSS well-dispersed into polymer matrix for performance improvement of WPU, ultrasonic processing was carried out. Figures 13, ,14,14, ,1515 showed the performances of composite membrane when 1wt% HSS prepared at different Re/w was incorporated into WPU. In comparison with pure WPU membrane, water vapor permeability, water resistance and mechanical properties of WPU/HSS composite membrane have been improved.
Traditional view that the size and shape of free-volume holes available in membrane materials control its permeability is generally accepted49. According to the measurement principle, the porosity and permeability of composite membrane are related directly to the water vapor permeability. Following the “adsorption-diffusion-desorption” mechanism, the diffusion of water vapor molecules through membrane is via both the organic-inorganic interface and the pore of HSS (Fig. 16). HSS with large specific surface area and hollow interior offered a relatively “free” pathway for water vapor molecules diffusion from the inner surface to the outside surface of composite membrane. The introduction of HSS into WPU can disrupt network of polymer chains and shorten the diffusion path length of water vapor molecules, making them diffuse quickly from the WPU-HSS organic-inorganic interface. Also, due to the amorphous structure of HSS, water vapor molecules can pass through the silica shell and be stored in the internal cavity, causing the vapour pressure differences between inside and outside surfaces of composite membrane. When the water vapor pressure is high enough, water vapor molecules spread rapidly out of the silica shell to the outer surface of membrane, improving the water vapor permeability of composite membrane remarkably. In our previous research, we have reported HSS with smaller hollow size are conducive to increase the water vapor permeability of composite. However, the water vapor permeability decreased sharply when the size of HSS is getting very small6. This can be illustrated by the reunion of small HSS, which decreased their dispersion degree in composite. Herein, when the Re/w was 0.3, the obtained HSS with small particle diameter and unconspicuous hollow structure would agglomerate when blended with WPU, which hindered the transmission of water vapor molecules. By increasing the Re/w, the cavity volume of HSS became larger, which is more conducive to the diffusion of water vapor molecules, showing enhanced water vapor permeability (Fig. 13). In addition, the bigger the specific surface area of additives is, the better the water vapor permeability of membrane will be49. As the Re/w increased to 0.7, the diameter of HSS remains nearly unchanged, but the cavity volume of HSS sharply reduced instead of further increased. Eventhough specific surface area is higher, the hollow interior cavity seem to have a more significant impact on the properities. So, the water vapor permeability of WPU/HSS composite membrane slightly decreased.
Water molecules hardly penetrate through HSS without the effect of water vapor pressure, diffusing mainly through the free volume between polymer chains. Therefore, the mesoporous shell of HSS can allow water vapor molecules to pass through while act a barrier to water molecules. The absorbed water can only exist in the space not occupied by hollow silica. In addition, the introduction of hollow silica spheres would limit the swing amplitude of polymer chain and thereby the free volume between polymer chains decreased. Hence, the diffusion of water molecules in membrane is hindered and the total water absorption is decreased (Fig. 14).
Compared to the pure WPU membrane, ensile strength and elongation at break of the composite membrane has been improved (Fig. 15). This could be ascribed to the reinforcing and toughening effect of nanoparticles on polymer matrix. Due to the large specific surface area and rich hydroxyl groups on their surface, the HSS could be interacted with WPU chains via physical bond and acted as restriction sites for the movement of polymer chains. Thus the composite membrane incorporated with HSS showed high resistance against the plastic deformation and reinforced mechanical performance. However, agglomeration of HSS would cause stress concentration and weakened reinforcement in polymeric matrix. So introducing the HSS prepared at Re/w of 0.3 into WPU decreased the mechanical performance of composite membrane slightly.
In summary, we successfully prepared HSS by micelle-template method using CTAB micelles as soft template and TEOS as silica precursor. The HSS possess a significant cavity, regular structure, narrow particle size distribution and amorphous shell with mesoporous structure. Particularly, the mechanism for formation of HSS was illustrated in detail and showed that the way of growth was from outside to inside along micelle template. Size of HSS increased gradually with the increase of Re/w within a proper range due to the lower dielectric constant of ethanol, which can not only stabilize but also dissolve TEOS. Importantly, when HSS were introduced into WPU, rich hydroxyl groups on the surface of HSS could be interacted with WPU chains via H-bond force and showed good individual dispersion in WPU membrane. Performance tests indicated that the introduction of HSS can significantly improve the water vapor permeability of composite membrane, promoting its water resistance and mechanical performance at the same time. In future developments, the HSS/WPU hybrid membranes with excellent properties, in principle, could be as multifunctional coating and favorable for the actual production.
How to cite this article: Bao, Y. et al. Micelle-template synthesis of hollow silica spheres for improving water vapor permeability of waterborne polyurethane membrane. Sci. Rep. 7, 46638; doi: 10.1038/srep46638 (2017).
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This work was supported by Program for New Century Excellent Talents in University (NCET-13-0885), National Nature Science Foundation of China (No: 21376145) and Key Scientific Research Group of Shaanxi Province (No: 2013KCT-08).
The authors declare no competing financial interests.
Author Contributions T.W., Q.L.K.and C.H.S. carried out the experiments and characterizations under the guidance of Y.B. and J.Z.M.; T.W., Y.B. and C.H.S. wrote the manuscript and prepared Figures 1–16. All authors discussed the results and commented on the manuscript.