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Functional thin fabric with highly efficient cold protection properties are attracting the great attention of long-term dressing in a cold environment. Herein, a tri-layered bicomponent microfilament composite fabric comprised of a hydrophobic layer of PET/PA@C6 F13 bicomponent microfilament webs, an adhesive layer of LPET/PET fibrous web, and a fluffy-soft layer of PET/Cellulous fibrous web is designed and also successfully been fabricated through a facile process of dipping, combined with thermal belt bonding. The prepared samples exhibit a large resistance to wetting of alcohol, a high hydrostatic pressure of 5530 Pa, and brilliant water slipping properties, owing to the presence of dense micropores ranging from 25.1 to 70.3 µm, as well as to the smooth surface with an arithmetic mean deviation of surface roughness (Sa) ranging from 5.112 to 4.369 µm. Besides, the prepared samples exhibited good water vapor permeability, and a tunable CLO value ranging from 0.569 to 0.920, in addition to the fact that it exhibited a very suitable working temperature range of -5 °C to 15 °C. Additionally, it also showed excellent clothing tailorability including high mechanical strength with a remarkably soft texture and lightweight foldability that suitable for cold outdoor clothing applications.
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Polyester/polyamide 6 hollow segmented pie bicomponent spunbond hydro-entangled microfiber nonwovens (PET/PA6) with a microfilament structure have recently emerged in many markets around the world due to their green, high-strength, and lightweight properties. However, PET/PA6 is highly hydrophobic, which inhibits its large-scale application at present. In order to enhance the hydrophilic performance of PET/PA6, many methods have been applied, but the effects are not obvious. Ultraviolet (UV) irradiation treatment has proven to be an effective method to improve the hydrophilicity of fabrics. Herein, the aim of this paper was to investigate hydrophilic modification of PET/PA6 by UV/TiO2/H2O2. The effect of H2O2, nano-TiO2, and UV irradiation time on the morphology, elemental composition, hydrophilic properties, and mechanical properties of PET/PA6 were systematically investigated. The results showed that the modified microfibers were coated with a layer of granular material on the surface. It was found that the C 1s peak could be deconvoluted into six components (C-C-C, C-C-O, O-C=O, N-C=O, N-C-C, and C-C=O), and a suitable mechanism was proposed. Moreover, the water contact angle of PET/PA6 modified by 90 min irradiation with UV/TiO2/H2O2 decreased to zero in 0.015 s, leading to the water vapor transmission rate and the water absorption reaching 5567.49 g/(m2·24 h) and 438.81%, respectively. In addition, the modified PET/PA6 had an excellent liquid wicking height of 141.87 mm and liquid wicking rate of 28.37 mm/min.
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The mechanism of the nanofiltration (NF) membrane separation of Mg2+ and Li+ needs to be further investigated, but some commonly used model theories are abstract, which makes them difficult to understand. More importantly, the relationship between the membrane charge and separation performance of Mg2+ and Li+ cannot be quantitatively analyzed. It is worth studying these challenges and providing a performance boost for Mg2+/Li+ filtration applications of NF membranes. Here, various NF membranes, with the membrane volumetric charge density increasing from -4.69 to 7.02 mol · m-3, were fabricated via interfacial polymerization. For these membranes, the separation factor S Mg,Li was decreased from 0.41 to 0.20. Importantly, the visual simulation results were consistent with the experimental results as a whole. The separation factor S Mg,Li decreased with the increase of volumetric charge density, and the minimum separation factor S Mg,Li of the NF membranes was 0.20 (experiment) and 0.17 (simulation), respectively. This meant that the performance of the positively charged NF membrane was not fully developed. Furthermore, we analyzed the relationship between the membrane charge and separation performance, and visualized the simulation of the NF membrane filtration and separation.
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Iron and steel production is one of the main anthropogenic sources of mercury (Hg) emission and release. Oxidized and particulate Hg discharged from iron and steel enterprises deposit into the surrounding soil, which accumulate and introduce environmental risks. Therefore, it is important to assess Hg pollution in the soil surrounding iron and steel enterprises. In this study, the Hg pollution, Hg distribution from steel plants and Hg fractionation in farmland soil around five typical steel plants were analysed in Tangshan of China. The Hg pollution indexes (Pi) of more than 90% soil samples were greater than 3 by the single factor pollution index method, which showed that most soil samples around the five steel plants were strongly contaminated by Hg. The Hg contents in soil increased first and then decreased, and the maximum content presented at 250-300â¯m away from the boundary of the steel plants. The order of Hg fraction proportion in the soil samples was extractable (35%-43%)â¯>â¯volatile (24%-36%)â¯>â¯residual (10%-26%)â¯>â¯reducible (0-15%)â¯>â¯oxidizable (0-12%). The distribution of Hg fraction in farmland soil had no regular trend with the distance from the steel plants. The volatile Hg and extractable Hg were dominant in farmland soil, and their combined proportion was greater than 60%. These two fractions of Hg are at risk of re-volatilization into the atmosphere or potential absorption by plants.
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Monitoramento Ambiental/métodos , Mercúrio/análise , Metalurgia , Poluentes do Solo/análise , Solo/química , Fracionamento Químico , China , Fazendas , Ferro , Aço , VolatilizaçãoRESUMO
OBJECTIVE: Common findings are to be found from 144 different type of medical device manufacturers' audit reports which are from Jan. 2017 to Jun. 2019. Advise is to be provided for medical device manufacturers on continual improvement. METHODS: Classify and analyze the on-site audit findings from different type of medical device manufacturers. RESULTS: The frequency of findings from chapter production management, buildings and facilities, quality control are comparatively high. CONCLUSIONS: The key to improve the quality management system is to cultivate the staff sense of continual improvement of quality system, improve the staff ability of finding and solving problems, encourage staff participation in quality system, fit the quality system on product realization.
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Indústrias , Controle de Qualidade , Fatores de TempoRESUMO
The effects of salinity on survival, growth, special activity of digestive enzymes, nonspecific immune response, and muscle fatty acid composition were evaluated in the American shad (Alosa sapidissima). Juveniles of 35 days after hatching were reared at 0 (control), 7, 14, 21, and 28 ppt for 60 days. At the end of the experiment, juvenile American shad presented higher survival and specific growth rate (SGR) in salinity group (7, 14, and 21 ppt) than control group (P < 0.05). The special activity of trypsin and chymotrypsin was highest in fish reared at 21 ppt, while the highest lipase special activity was obtained in control group (P < 0.05). The special activity of alkaline phosphatase (ALP), lysozyme (LZM), superoxide dismutase (SOD), and catalase (CAT) showed significant increases in salinity group (14 and 21 ppt) compared to control group (P < 0.05). Lower muscle ash contents were detected in salinity group (14, 21, and 28 ppt) than control group (P < 0.05), while the contents of crude lipid and crude protein were significantly higher than control group (P < 0.05). The level of monounsaturated fatty acids (MUFA) exhibited a decreasing trend, while an increased level of polyunsaturated fatty acids (PUFA) was detected with the increase of salinity. Among the PUFA, the content of n-3 fatty acids in muscle tissue was found to be increasing with the increasing salinity, especially eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA). Results indicate that appropriate increase in salinity was reasonable and beneficial for juvenile American shad culture after a comprehensive consideration, especially salinity range from 14 to 21 ppt.
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Ácidos Graxos/metabolismo , Peixes/fisiologia , Trato Gastrointestinal/enzimologia , Músculo Esquelético/metabolismo , Salinidade , Animais , Aquicultura , Imunidade Inata , Músculo Esquelético/química , Análise de SobrevidaRESUMO
With the continuous improvement of the standard of living, people are increasingly inclined towards natural, green, and environmentally friendly products. Plant-based products that are safe, natural, non-toxic, and beneficial to human health are often more favored. Poly(lactic acid) (PLA) is a polymer obtained through lactate polymerization using renewable plant resources such as corn and has excellent biocompatibility and biodegradability. It is widely used in the field of food packaging. Wormwood oil (WO) is an oil extracted from the stems and leaves of Artemisia plants, and it has broad-spectrum antibacterial properties. In this article, through electrospinning technology, wormwood oil was directly incorporated into PLA, giving the PLA nanofiber membrane antioxidant and antibacterial functions. Various parameters such as voltage (11 KV, 13 KV, 15 KV), spinning solution concentration (8%, 10%, 12%), distance (15 cm, 17 cm, 19 cm), and feeding rate (0.4 mL/h, 0.5 mL/h, 0.6 mL/h) were explored, and the resulting spun fibers were characterized. Through SEM characterization, it was found that when the spinning voltage was 13 KV, the spinning solution concentration was 10%, the distance was 17 cm, and the feeding rate was 0.5 mL/h, the nanofiber membrane had a smooth morphology without bead formation, with an average diameter of 260 nm. The nanofiber membrane was characterized using FTIR, TG, and SEM, confirming the successful incorporation of artemisia essential oil into PLA. The prepared antimicrobial nanofilm was subjected to antimicrobial testing, and the results showed that as the concentration of the essential oil increased, the inhibition zones also increased. When wormwood oil concentration was 4%, the diameter of the inhibition zone for Staphylococcus aureus increased from 1.0 mm to 3.5 mm, while the diameter of the inhibition zone for Escherichia coli increased from 2.0 mm to 4.5 mm.
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Electromagnetic (EM) metamaterial is a composite material with EM stealth properties, which is constructed by artificially reverse engineering metal split resonance rings (SRR). However, the greatest limitation of EM metamaterials is that they can only stealth at a fixed and lower frequency of EM waves, and modern processing techniques still cannot meet the accuracy requirements to fabric nano-size structural unit. Nano-sized and even ultra-small SRR at molecular level are promising arrays to realize the ability of EM stealth function at a higher frequency, although it has proven challenging to synthesize long, straight, connected molecular SRR, and also difficult to arrange those molecular SRR into a strict array. Here, the study overcomes this challenge and demonstrates that the fabric of polypyrrole molecular SRR achieves an ultra-small inner diameter of 2.49 Å and realizes the arrays arrangement at molecular level. Furthermore, the study exploits the EM stealth function and verifies that such arrays of molecular SRR with 2.49 Å have the ability to reach high-performance EM stealth in the range of 106 -1016 Hz. This design concept opens a pathway for developing new metamaterials with broadband EM wave stealth and also serves the wider range of new applications.
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Ultra-fine fibers derived from sea-island fibers have attracted great attention due to their excellent overall performance. However, green and efficient splitting of sea-island fibers is still a challenging task. In this work, thermoplastic polyvinyl alcohol (TPVA) was prepared by the physical blending of plasticizer. The modified TPVA showed a high decomposition temperature (285 °C) and a wide thermoplastic processing window. This made TPVA match well with polyamide 6 (PA6) to form conjugated melts at 250 °C. Corresponding PVA/PA6 sea-island fibers were first reported to realize water-splitting instead of alkali-extraction of "sea" polymers. The effects of sea/island mass ratios and different spinning speeds on the properties of PVA/PA6 sea-island pre-oriented yarn (POY) were investigated. A higher spinning speed enhanced the orientation-induced crystalline behavior of fiber, therefore increasing the tensile strength of fibers. As the increase of spinning speed from 1000 to 1500 m/min, the crystalline degree of corresponding POYs increased from 9.9 to 14.3%. The plasticizer in PVA did not diffuse to the PA matrix during spinning. However, PVA could induce the crystallization of PA6 via interfacial hydrogen bonding. When the spinning speed was 1500 m/min, and PVA/PA6 was 7:3, the tensile strength reached the highest value of 1.67 cN/dtex. The uniform diameters of ultra-fine PA6 fibers (2-5 µm) were obtained by an environment-friendly water-splitting process. The "sea" phase (TPVA) in sea-island fiber could be removed quickly by boiling water treatment in 3 min. This green and energy-saving sea-island fiber splitting technique is of great significance in reducing CO2 emissions during the preparation of super-fine fibers.
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To coordinate the trade-off between the separation and permeation of the nanofiltration membrane for the separation of Mg2+/Li+, we regulated poly(ethyleneimine)/piperazine interface polymerization parameters to construct a positively/negatively charged ultrathin Janus nanofiltration membrane at a free aqueous-organic interface. At the optimized interfacial polymerization parameters, 0.03 wt % of piperazine reacted with trimethylbenzene chloride prior to poly(ethyleneimine), forming a primary polyamide layer with fewer defects or limiting large-scale defects of the polyamide layer. The controlled subsequent reaction of poly(ethyleneimine) and trimethylbenzene chloride results in a Janus nanofiltration membrane, with one side enriched with the carboxyl groups, the other side enriched with the amine groups, and a dense polyamide structure in the middle. Under the optimum conditions, the positive potential of the rear surface of the prepared membrane was 14.57 mV, and the water contact angle reached 71.31°, while the negative potential of the front surface was -25.48 mV, and the water contact angle was 12.93°, confirming a Janus membrane with opposite charges and large hydrophilicity differences in the front and rear surfaces. With a high cross-linking degree, a 40 nm thick polyamide layer is 29.09% more thinner than the traditional polyamide membrane. The ultrathin Janus nanofiltration membrane showed an excellent separation factor (SLi,Mg of 18.26), stability, and water permeability flux (10.6 L·m-2·h-1·bar-1). The rejections to MgCl2, CaCl2, MgSO4, and Na2SO4 are measured above 90% at a nearly constant permeability of 10.6 L·m-2·h-1·bar-1, particularly stable rejections to MgCl2 and Na2SO4.
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The new composite product synthesized by zeolite P and bacteria consisting of nitrobacteria and denitrobacteria can efficiently and continuously remove ammonium in solution through zeolite adsorption and bacteria degradation. In this study, we used fly ash to prepared zeolite P, and then combined bacteria to synthesize the composite product. The adsorption efficiency and mechanism of products for ammonium were further studied by batch and dynamic experiments, and adsorption model. The zeolite P with a relative crystallinity of 84.7% was synthesized using fly ash by an alkali fusion-hydrothermal method. The synthetic zeolite P could combine with bacteria to be prepared an integral adsorption composite that had hierarchical pore structure including macropores, mesopores, and micropores, and its maximum compressive strength reached 106.2 N. The zeolite P could remove ammonium from solution, and Freundlich, Temkin, and Dubinin-Radushkevich models as well as thermodynamic models all showed that the ammonium adsorption by zeolite was mainly physical adsorption. Thus, the adsorbed ammonium was easy to be desorbed and became the nitrogen source for bacteria in composites. By batch experiments, the ammonium adsorption rate of composite product was significantly improved (P < 0.05) compared with zeolite P due to zeolite adsorption and the bacteria degradation. Through dynamic experiments, the composite product could efficiently and continuously remove ammonium from solution than zeolite P and bacteria alone. Therefore, the composite product could form a stable system for the adsorption, desorption, and degradation of ammonium in solution.
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Compostos de Amônio , Zeolitas , Zeolitas/química , Cinza de Carvão/química , Adsorção , Água , Bactérias , NitrogênioRESUMO
Effective personal thermal management is crucial for protecting human health during cold weather. Therefore, wearable heaters based on electric-heating membranes are one of the most promising devices to become essential appliances in our daily lives. The main challenge toward this goal is the development of electric-heating membranes with adequate breathable, flexible, and stretchable characteristics. In the work presented here, micro-nanofibrous fluffy electric-heating membranes were prepared by coating polyurethane/graphene nanoplatelet (PU@GNP) films onto melt-blown propylene-based elastomer (PBE) micro-nanofibrous membranes via a facile, cheap, and large-scale method consisting of a coating-compressing cyclic process. Investigation of the resulting PBE/PU@GNP membranes showed that the PU@GNP films were uniformly deposited onto the PBE micro-nanofiber surfaces, forming fluffy interconnected conducting channels. By applying a voltage of 36 V to the prepared PBE/PU@GNP membranes, the temperature increased to 69.7 °C, confirming excellent electric-heating features. Moreover, the porosity of the fabricated membrane could be tailored readily by adjusting the coating-compressing cycles. Benefiting from the conducting channels, the PBE/PU@GNP membranes exhibited efficiently regulated air permeability ranging from 212 to 60.2 mm/s, a prominent softness score of 53.8, and an excellent elastic recovery rate of 85.5%. These findings demonstrate that PBE/PU@GNP micro-nanofibrous fluffy membranes may well be suitable for application in electric-heating clothing. The cyclic coating-compressing preparation process may be attractive in industrial manufacturing.
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Medical protective materials have broadly drawn attention due to their ability to stop the spread of infectious diseases and protect the safety of medical staff. However, creating medical protective materials that combine excellent liquid shielding performance and outstanding mechanical properties with high breathability is still a challenging task. Herein, a polyester/polyamide 6 (PET/PA6) bicomponent microfilament fabric with tunable porosity for comfortable medical protective clothing was prepared via dip-coating technology and an easy and effective thermal-belt bonding process. The dip coating of the C6-based fluorocarbon polymer endowed the samples with excellent hydrophobicity (alcohol contact angles, 130-128°); meanwhile, by adjusting the temperature and pressure of the thermal-belt bonding process, the porosity of the samples was adapted in the range of 64.19-88.64%. Furthermore, benefitting tunable porosity and surface hydrophobicity, the samples also demonstrated an excellent softness score (24.3-34.5), agreeable air permeability (46.3-27.8 mm/s), and high hydrostatic pressure (1176-4130 Pa). Significantly, the created textiles successfully filter aerosol from the air and display highly tensile strength. These excellent comprehensive performances indicate that the prepared PET/PA6 bicomponent microfilament fabrics would be an attractive choice for medical protective apparel.
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Poliésteres , Têxteis , Citoesqueleto de Actina , Caprolactama/análogos & derivados , Humanos , Polímeros , Porosidade , Tomografia por Emissão de Pósitrons , Roupa de ProteçãoRESUMO
In this paper, near-field direct-writing melt electrospinning technology was employed to fabricate a polycaprolactone/nano-hydroxyapatite (PCL/nHA) scaffold for future applications in tissue engineering. The influences of different fabrication parameters on the structural characteristics, mechanical properties, and thermal stability of the scaffolds were discussed. It was found that the moving speed of the receiving plate had the most significant effect on the scaffold performance, followed by the receiving distance and spinning voltage. The results also showed that these process parameters affected the fiber diameter, corresponding coefficient of variation, porosity of the composite scaffolds, and mechanical properties of the samples, including the tensile strength and fiber peeling strength. Moreover, the process parameters could influence the thermal degradation performance and melting process. Although the mass loss of the composite scaffolds was not obvious after degradation, the mechanical performance degraded severely. It was concluded that the more appropriate process parameters for preparing PCL/nHA scaffolds were a spinning voltage of -4 kV, receiving distance of 4 mm, moving speed of receiving plate of 5 mm/s, and melt temperature of 130 °C. This study proved that near-field direct-writing melt electrospinning technology is a good method to obtain PCL/nHA composite scaffolds with an excellent mechanical properties and desired morphology for future tissue engineering applications.
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As an effective way to obtain freshwater resources, atmospheric water harvesting (AWH) technology has been a wide concern of researchers. Therefore, hydrogels gradually become key materials for atmospheric water harvesters due to their high specific surface area and three-dimensional porous structure. Here, we construct a core-shell hydrogel-based atmospheric water harvesting material consisting of a shell sodium polyacrylate (PAAS) hydrogel with an open pore structure and a core thermosensitive poly N-isopropylacrylamide (PNIPAAm) hydrogel with a large pore size. Theoretically, the mutual synergistic hygroscopic effect between the core layer and the shell layer accelerates the capture, transport, and storage of moisture to achieve continuous and high-capacity moisture adsorption. Simultaneously, the integration of polydopamine (PDA) with the hydrogel realizes solar-driven photothermal evaporation. Therefore, the prepared core-shell hydrogel material possesses great advantages in water adsorption capacity and water desorption capacity with an adsorption of 2.76 g g-1 (90% RH) and a desorption of 1.42 kg m-2 h-1. Additionally, the core-shell structure hydrogel collects 1.31 g g-1 day-1 of fresh water in outdoor experiments, which verifies that this core-shell hydrogel with integrated photothermal properties can capture moisture in a wide range of humidity without any external energy consumption, can further sustainably obtain fresh water in remote water-shortage areas.
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Polycaprolactone (PCL) scaffold is a common biological material for tissue engineering, owing to its good biocompatibility, biodegradability and plasticity. However, it is not suitable for osteoblast adhesion and regeneration of bone tissue due to its non-biological activity, poor mechanical strength, slow degradation speed, smooth surface and strong hydrophobicity. To improve the mechanical properties and biocompatibility of PCL scaffold, the PCL/nHA scaffolds were prepared by melting and blending different proportions of nano-hydroxyapatite (nHA) with PCL by the near-field direct-writing melt electrospinning technology in this study. The morphology, porosity, mechanical properties and in vitro biocompatibility of the PCL/nHA scaffolds were studied. The results showed that when the proportion of nHA was less than or equal to 25%, PCL/nHA composite scaffolds were easily formed in which bone marrow mesenchymal stem cells proliferated successfully. When the proportion of nHA was 15%, the PCL/nHA composite scaffolds had excellent structural regularity, good fiber uniformity, outstanding mechanical stability and superior biocompatibility. The PCL/nHA composite scaffolds were ideal scaffold materials, which would broaden their applications for bone tissue engineering.
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Selective isolation, molecular identification and AFLP were used to investigate the distribution of the various species of endophytic and epiphytic Trichoderma associated with banana roots and to compare and contrast their genetic structure. Three specific groups of Trichoderma were observed in the roots of banana. Group one, which made up the largest population, comprised T. asperellum, T. virens, and Hypocrea lixii, which were isolated from both inside and on the surface of the banana roots, while group two, made up of T. atroviride and T. koningiopsis, existed on the surface only. Group three, comprising only T. brevicompactum was isolated from the inside of the roots. The AFLP analysis revealed Nei's diversity indices of 0.15 and 0.26 for epiphytic T. asperellum and T. virens, respectively. The index values of 0.11 and 0.11 were obtained for endophytic T. asperellum and T. virens, respectively. The genetic diversity within endophytic T. asperellum and T. virens was lower than that within the epiphytes. This suggests that endophytic Trichoderma has a higher genetic conservation and is compatible with the relatively stable microenvironments inside roots.
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Musa/microbiologia , Filogenia , Raízes de Plantas/microbiologia , Microbiologia do Solo , Trichoderma/genética , Análise do Polimorfismo de Comprimento de Fragmentos Amplificados , DNA Fúngico/genética , Variação Genética , Análise de Sequência de DNA , Trichoderma/crescimento & desenvolvimento , Trichoderma/isolamento & purificaçãoRESUMO
Life preservers often play a vital role in ensuring passenger safety in water-related accidents, while the difficulty of donning life preservers has been repeatedly proved even in a donning test. To evaluate the influencing factors for life preserver donning tests, 109 college students and 42 villagers were chosen as subjects. A total of fourteen variables with seven categorical variables and seven continuous variables were considered as potential influencing factors. T-test and one-way analysis of variance (ANOVA, for three or more categories) were used to judge whether grouping in categorical variables had a significant effect on the donning performance. Then all variables were offered into the stepwise linear regression (SLR) to evaluate the influential factors for life preserver donning tests. Results showed that four of fourteen variables, including gender, instruction condition, age group, and tool test time (representing the subject's flexibility), had a significant effect on the donning performance. To evaluate the relationship between the donning performance and influencing factors, models of the retrieving time, the opening time, and the donning time were built based on the SLR analysis. The paper also highlights recommendations for modification of the donning test procedure, which helps to improve the validation and reliability of life preserver donning tests.
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Afogamento/prevenção & controle , Equipamentos de Proteção/estatística & dados numéricos , Equipamentos de Proteção/tendências , Adulto , Aeronaves , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Roupa de Proteção/estatística & dados numéricos , Roupa de Proteção/tendências , Reprodutibilidade dos TestesRESUMO
Medical research reveals that keeping the skin surface dry can effectively prevent a variety of fungal skin diseases. Therefore, it is of great practical significance to develop a light, thin, comfortable and breathable functional garment fabric with efficient one-way water transmission for people's requirements. Here, we successfully prepared a three-layer stacking sandwich coating to construct a Janus nonwoven material with efficient unidirectional water transport function, viz. PDMS-ormosil-PDMS@nonwoven fabric (PDMS-ormosil-PDMS@NF). Theoretical analysis showed that the loading of ormosil particles could enhance the surface roughness, while PDMS could strengthen the hydrophobic properties and bondability between the ormosil particles and fabric, thus acting as an environmentally friendly fluorine-free treating agent. The results revealed that the hydrophilic-hydrophobic PDMS-ormosil-PDMS@nonwoven fabric maintained excellent hydrophobic stability and good air permeability even after abrasion, which solved the existing problems of aerogel poor deposition and PDMS poor permeability, benefiting the application of textiles with unidirectional water transport performance.
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This paper reports a novel thin-film nanocomposite (TFN) membrane with a dense, flat, and hydrophilic polyamide (PA) layer. The atypical PA structure was obtained by the cross-linking reaction of graphene oxide quantum dots containing amino groups (NH2-GOQDs) with triacyl chloride and polyamide oligomers. And the resulting TFN membrane showed a flat (small-scale ridge structure) and smooth surface. Meanwhile, the introduction of oxygen-containing and amino functional groups increased surface hydrophilicity. The reaction of amino groups on the NH2-GOQDs with acid chloride groups and the carboxyl groups (in the linear part of the polyamide) enhanced the degree of cross-linking of the PA layer, forming a compact surface. Owning to the dense surface structure, excellent hydrophilicity, and small water transmission distance, the optimized TFN membrane exhibited an enhanced water flux of 26.57 Lâ m-2â h-1 with a low reverse salt flux of 6.0 gâ m-2â h-1. Furthermore, nano-indentation/scratch results showed the interface adhesion between substrate and PA layer was improved due to the physical anchoring of NH2-GOQDs in the substrate. And in the long-term FO test, the TFN membrane showed stable selectivity. This work proves that the targeted structural design of the PA layer at the nanoscale will have a positive impact on desalination field.