Water-soluble cationic chitosan derivative to improve pigment-based inkjet printing and antibacterial properties for cellulose substrates

The water-soluble N-(2-hydroxy)propyl-3-trimethylammonium chitosan chloride (HTCC) was prepared by chitosan and glycidyl trimethyl ammonium chloride. Fourier-transform infrared spectroscopic analysis spectrum confirmed that glycidyl trimethyl ammonium chloride was grafted to the amino groups of chitosan via substitution reaction (Zhao et al., Int J Pharm 2010, 393, 268; Montazer and Afjeh, J Appl Polym Sci 2007, 103, 178). The obtained chitosan derivative was used to modify cotton fabrics for improving aqueous pigment-based inkjet printing and antibacterial properties. Scanning electron microscope images showed that HTCC was adhered onto the cotton fabrics surface and formed film structure. The K/S value on printed cotton substrates increased from 3.20 to 4.87, which indicated that higher color yield was achieved in this way. Modified samples performed better crocking fastness and laundering fastness than the control cotton fabrics. The line definition of modified cotton fabrics respectively, improved 16.5% and 12.6% in the warp and weft direction as the specified line width was 0.5 × 10³ μm. Samples also showed good antibacterial potential, the inhibitory rate for Staphylococcus aureus and Escherichia coli were both more than 95% when the concentration of HTCC used in the pretreatment solution was 0.8%. The antibacterial effect was found to be durable for 20 laundering cycles. However, the hand feeling of modified cotton fabrics presented a slight decrease. © 2012 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Thermal properties of hyperbranched polyborate functionalized multiwall carbon nanotube/polybenzoxazine composites

Using a noncovalent functionalization strategy, hyperbranched polyborate (HBb) acts as a solubilizer for carbon nanotubes (CNTs), and a stable HBb‐CNT dispersion in N‐methyl‐pyrrolidone was produced. The thermal properties of the resulting HBb‐CNT/polybenzoxazine (B‐BOZ) composites and their carbonized structures were investigated. Scanning electron microscopy demonstrated that the fracture surface of HBb‐CNT/B‐BOZ composites was rather rough and plenty of plastic deformation was exhibited. Thermogravimetric analysis indicates an improvement in the thermal stability of the composite with CNTs, especially that of 2.0 wt% CNT modified composite. The increase in the thermal stability is due to the good nanotube dispersion and the effective polymer‐CNT interaction. Graphite‐like boron carbonitride ceramic compounds were found after the composites were carbonized at 1,100°C for 2 h, and there was more B‐C, B‐N, and C‐N bonds in the carbonized HBb‐CNT/B‐BOZ composite than that of HBb/B‐BOZ composite. The result implied that CNTs can promote the ceramic process of HBb/B‐BOZ composite, and the strategy of introducing ceramic precursor into polymer composites may be useful to improve their ablation properties. POLYM. COMPOS., 2011. © 2011 Society of Plastics Engineers     

Optimized process for the inclusion of carbon nanotubes in elastomers with improved thermal and mechanical properties

The effects of addition of reinforcing carbon nanotubes (CNTs) into hydrogenated nitrile–butadiene rubber (HNBR) matrix on the mechanical, dynamic viscoelastic, and permeability properties were studied in this investigation. Different techniques of incorporating nanotubes in HNBR were investigated in this research. The techniques considered were more suitable for industrial preparation of rubber composites. The nanotubes were modified with different surfactants and dispersion agents to improve the compatibility and adhesion of nanotubes on the HNBR matrix. The effects of the surface modification of the nanotubes on various properties were examined in detail. The amount of CNTs was varied from 2.5 to 10 phr in different formulations prepared to identify the optimum CNT levels. A detailed analysis was made to investigate the morphological structure and mechanical behavior at room temperature. The viscoelastic behavior of the nanotube filler elastomer was studied by dynamic mechanical thermal analysis (DMTA). Morphological analysis indicated a very good dispersion of the CNTs for a low nanotube loading of 3.5 phr. A significant improvement in the mechanical properties was observed with the addition of nanotubes. DMTA studies revealed an increase in the storage modulus and a reduction in the glass‐transition temperature after the incorporation of the nanotubes. Further, the HNBR/CNT nanocomposites were subjected to permeability studies. The studies showed a significant reduction in the permeability of nitrogen gas. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Surfactant‐assisted processing of polyimide/multiwall carbon nanotube nanocomposites for microelectronics applications

The dispersion and stability of carbon nanotubes (CNTs) inside a polymer matrix, especially with a high CNT content, are still big challenges. Moreover, the interaction between CNTs and the polymer matrix should be strong enough to improve the mechanical properties. The efficient dispersion of CNTs is essential for the formation of a uniform distribution of a CNT network in a polymer composite. Polyimide/multiwall CNT nanocomposites were synthesized by in situ polymerization with the aid of a surfactant. A Fourier transform infrared spectroscopy study proved that the surfactant did not hamper the polymerization of the polyimide. The microstructure, storage modulus and electrical conductivity of the nanocomposites were improved using a particular amount of the surfactant. Environmental stability test results showed that the polyimide with 1 wt% of CNTs produced with the aid of the surfactant possessed excellent reliability in high‐temperature and high‐humidity environments. Surfactants were successfully used to obtain fine‐structure polyimide/CNT nanocomposites by in situ polymerization. The enhancement of the mechanical properties was attributed to the incorporation of the surfactant. A percolation of electrical conductivity could be achieved with 1 wt% of CNTs. Copyright © 2010 Society of Chemical Industry     

Assessment of intertube interactions in different functionalized multiwalled carbon nanotubes incorporated in a phenoxy resin

In this work, about 1 wt% of different functionalized carbon nanotubes (CNTs), namely CNT? COOH (CNT with carboxylic groups), CNT? NH₂ (CNT with amine groups) and CNT? OH (CNT with hydroxyl groups), as well as nonfunctionalized CNTs were incorporated into a phenoxy resin via a melt mixing process. The extent of intertubes and polymer–tubes interactions and their influence on state of CNTs dispersion were assessed through determination of electrical, rheological, and morphological characteristics. CNT? NH₂ showed the lowest intertubes interactions followed by CNT? OH and CNT? COOH. Nanocomposite made from CNT? COOH showed the poorest state of CNTs dispersion and the biggest CNTs agglomerates and it remained nonconductive. The acid‐functionalized CNTs were not able to form strong polymer–tube interactions because of their high cohesive energy and therefore in the melt rheological investigations they exhibited the lowest storage modulus and complex viscosity as well as the highest loss factor among all the studied CNTs. A good balance between intertubes and polymer–tube interactions is necessary through proper selection of CNTs functional groups for achieving a good state of CNTs dispersion and consequently obtaining enhanced electrical and viscoelastic properties. POLYM. ENG. SCI., 2013. © 2012 Society of Plastics Engineers     

Quantification of carbon nanotube dispersion and its correlation with mechanical and thermal properties of epoxy nanocomposites

An experimental study is carried out to quantitatively assess the dispersion quality of carbon nanotubes (CNTs) in epoxy matrix as a function of CNT variant and weight fraction. To this end, two weight fractions (0.05% and 0.25%) of as-grown, oxidized, and functionalized CNTs are used to process CNT/epoxy nanocomposites. Scanning electron microscopy, X-ray diffraction, and Fourier transform infrared analysis of different variants of CNTs are used to establish the efficiency of purification route. While the relative change in mechanical properties is investigated through tensile and micro-hardness testing, thermal conductivity of different nanocomposites is measured to characterize the effect of CNT addition on the average thermal properties of epoxy. Later on, a quantitative analysis is carried out to establish the relationship between the observed improvements in average composite properties with the dispersion quality of CNTs in epoxy. It is shown that carboxylic (-COOH) functionalization reduces the average CNT agglomerate size and thus ensures better dispersion of CNTs in epoxy even at higher CNT weight fraction. The improved dispersion leads to enhanced interfacial interaction at the CNT/epoxy interface and hence provides higher relative improvement in nanocomposite properties compared to the samples prepared using as-grown and oxidized CNTs. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020 , 137, 48879.     

Properties of ink‐jet printed,ultraviolet‐cured pigment prints in comparison with screen‐printed,thermo‐cured pigment prints

A collection of printed fabrics for men’s shirts was designed and prepared using computer‐aided design/computer‐aided manufacturing technology. The colours for designs were ink‐jet printed on cotton fabrics with pigments and ultraviolet‐cured. These prints represented the target colours for subsequent flat‐screen printing, which was performed using pigment printing pastes and thermal curing. For an exact transfer of colours of the ink‐jet‐printed standard into the screen‐printing process, a computer recipe prediction method was used. A comparison of colorimetric parameters of fabrics printed with both printing techniques shows minimal and acceptable differences in the CIELab colour values. A comparison of colour fastness properties proves that very good colour fastness is achieved on the pigment‐printed fabrics produced with both printing techniques. The flat‐screen‐printed fabrics show better colour fastness to washing, perspiration and rubbing, while ink‐jet‐printed fabrics show better colour fastness to dry‐cleaning and light. The fabrics printed with both printing techniques have high rigidity and non‐elastic properties. The mechanical and physical parameters are strongly dependent upon the amount of the dry substance of the printing media applied on the cotton fabric surface, which is higher on screen‐printed fabrics. The ink‐jet‐printed fabrics show better air permeability than flat‐screen‐printed fabrics.     

Electrical and mechanical properties of acrylonitrile‐butadiene‐styrene/multiwall carbon nanotube nanocomposites prepared by melt‐blending

The electrical properties in polymer/carbon nanotube (CNT) nanocomposites are governed not only by the degree of dispersion but also to a greater extent on the aspect ratio of the CNTs in the final composites. Melt‐mixing of polymer and CNTs at high shear rate usually breaks the CNTS that lowers the aspect ratio of the nanotubes. Thus, homogeneous dispersion of CNTs while retaining the aspect ratio is a major challenge in melt‐mixing. Here, we demonstrate a novel method that involves melt‐blending of acrylonitrile‐butadiene‐styrene (ABS) and in situ polymerized polystyrene (PS)/multiwalled CNT (MWCNT) nanocomposites, to prepare electrically conducting ABS/MWCNT nanocomposites with very low CNT loading than reported. The rationale behind choosing PS/MWCNT as blending component was that ABS is reported to form miscible blend with the PS. Thus, (80/20 w/w) ABS/(PS/MWCNT) nanocomposites obtained by melt‐blending showed electrical conductivity value ≈1.27 × 10^?6 S cm^?1 at MWCNT loading close to 0.64 wt %, which is quite lower than previously reported value for ABS/MWCNT system prepared via solution blending. Scanning electron microscopy and differential scanning calorimetry analysis indicated the formation of homogenous and miscible blend of ABS and PS. The high temperature (100°C) storage modulus of ABS (1298 MPa) in the nanocomposites was increased to 1696 MPa in presence of 0.64 wt % of the MWCNT. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Wrinkle resistant properties and antibacterial efficacy of cotton fabrics treated with glyoxal system and with combination of glyoxal and chitosan system

This study examined the possibility of using glyoxal and chitosan in one‐step finishing to impart both durable press performance and antibacterial efficacy on cotton fabrics. Glyoxal treatment provided good wrinkle resistant property and fair antibacterial activity on the finished fabrics, but the loss of breaking strength retention of the finished fabrics was a main problem of this treatment. Chitosan added in the combination of glyoxal and chitosan system also provided comparable results in wrinkle resistant and antibacterial properties on the finished fabrics as the glyoxal did. The advantage of chitosan in the combination of glyoxal and chitosan system was the improvement of the breaking strength retention of the finished fabrics without affecting the durable press property of the finished fabrics. However, the yellowing of the finished fabric was still a problem when the finished fabrics were treated with the combination of glyoxal and chitosan system. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 1372–1377, 2006     

Ultradrawing properties of ultrahigh‐molecular weight polyethylene/functionalized carbon nanotube fibers and transmittance properties of their gel solutions

The influences of the dispersion level of carbon nanotubes (CNTs) and functionalized CNTs on the transmittance properties of ultrahigh‐molecular weight polyethylene (UHMWPE) gel solutions and on ultradrawing properties of their as‐prepared fibers are reported. The transmittance properties suggest that the dispersion level of functionalized CNTs in UHMWPE/functionalized CNTs gel solution is significantly better than plain CNTs in UHMWPE/CNTs gel solutions. The orientation factors, achievable draw ratios, tensile strength (σ_f), and modulus (E) values of UHMWPE/CNTs (F_xC_y) and UHMWPE/functionalized CNTs (F_xC_f‐y) as‐prepared fiber specimens reached a maximum value as their CNT and functionalized CNT contents approached optimum contents at 0.00015 and 0.0001 wt%, respectively. The σ_f and E values of both F_xC_0.0012 and F_xC_f‐0.001 series fiber specimens prepared at their optimum CNT and functionalized CNT contents reached another maximum as their UHMWPE approached optimum UHMWPE concentration of 1.7 wt%. Possible reasons accounting for these interesting properties are proposed. POLYM. ENG. SCI., 2011. © 2011 Society of Plastics Engineers     

Wear properties of 3‐aminopropyltriethoxysilane‐functionalized carbon nanotubes reinforced ultra high molecular weight polyethylene nanocomposites

Ultra high molecular weight polyethylene (UHMWPE) is extensively used as a material in various high‐end applications with superior mechanical properties. Carbon nanotubes (CNTs) reinforced UHMWPE (CNT/UHMWPE) nanocomposite is a promising material that can compensate for the weak durability of UHMWPE. In this study, multiwalled carbon nanotubes were oxidized and silanized using acid mixture and 3‐aminopropyltriethoxysilane, respectively, to improve the interfacial strength between CNTs and UHMWPE. The CNT/UHMWPE nanocomposite was fabricated using these oxidized and silanized CNTs. The treatment effect of CNTs on the wear behavior of the CNT/UHMWPE nanocomposites was investigated through wear tests. The oxidization and silanization of CNTs were confirmed by infrared spectroscopy. Scanning electron microscope analysis showed that the silane‐treated CNT/UHMWPE nanocomposites showed better dispersion and interfacial adhesion between UHMWPE and CNTs becaue of the newly formed functional groups on the CNTs. The friction coefficient and wear rate of silanized CNT/UHMWPE nanocomposite were also found to be lower than those of raw UHMWPE and oxidized CNT/UHMWPE nanocomposite. CNTs were functionalized using oxidation and silanization methods to improve the interfacial adhesion between CNTs and UHMWPE. POLYM. ENG. SCI., 2010. © 2010 Society of Plastics Engineers     

The effect of pH and ionic strength on the dispersion of carbon nanotubes in poly(acrylic acid) solutions

The dispersion of three kinds of acid‐treated carbon nanotubes (CNTs) in poly(acrylic acid) (PAA) aqueous solution of different pH and ionic strengths (varied by NaCl, KCl and ZnCl₂) was investigated by visual observation, zeta potential, particle size analysis, transmission electron microscopy and scanning electron microscopy. Visual observation revealed that the dispersion of CNTs acid treated at 60 °C for 3 h and at 80 °C for 2 h was poor in aqueous solutions with pH < 2 or pH > 12. The poor dispersion of acid‐treated CNTs may be improved by adding PAA. In particular, PAA improved the dispersion of CNTs with greater COOH content. In a low pH solution (pH 1.5), a higher PAA content resulted in poorer CNT dispersion while in a high pH solution (pH 12.5), a higher PAA content led to better CNT dispersion. For superior dispersion in a basic aqueous solution (pH 12.5), experimental data showed that a greater atomic radius or a higher cationic charge of the added salt may result in faster aggregation and thus precipitation of CNTs. Copyright © 2011 Society of Chemical Industry     

Study of nanoreinforced shape memory polymers processed by casting and extrusion

Multi‐walled carbon nanotubes (CNTs) and cellulose nanofibers (CNFs) reinforced shape memory polyurethane (PU) composite fibers and films have been fabricated via extrusion and casting methods. Cellulose nanofibers were obtained through acid hydrolysis of microcrystalline cellulose. This treatment aided in achieving stable suspensions of cellulose crystals in dimethylformamide (DMF), for subsequent incorporation into the shape memory matrix. CNTs were covalent functionalized with carboxyl groups (CNT‐COOH) and 4,4′‐methylenebis (phenylisocyanate) (MDI) (CNT‐MDI) to improve the dispersion efficiency between the CNT and the polyurethane. Significant improvement in tensile modulus and strength were achieved by incorporating both fillers up to 1 wt% without sacrificing the elongation at break. Electron microscopy was used to investigate the degree of dispersion and fracture surfaces of the composite fibers and films. The effects of the filler (type and concentration) on the degree of crystallinity and thermal properties of the hard and soft segments that form the PU sample were studied by calorimetry. Overall, results indicated that the homogeneous dispersion of nanotubes and cellulose throughout the PU matrix and the strong interfacial adhesion between nanotubes and/or cellulose and the matrix are responsible for the enhancement of mechanical and shape memory properties of the composites. POLYM. COMPOS., 2011. © 2011 Society of Plastics Engineers     

Fragrant finishing of cotton with microcapsules: comparison between printing and impregnation

Microencapsulated fragrance was used to produce a fragrant textile product. Melamine–formaldehyde polymer wall microcapsules with a lavender, rosemary and sage essential oil core were applied to a cotton fabric in two ways, i.e. byscreen printing and impregnation. The samples were dried and cured, and then the differences between them were analysed. The condition and distribution of applied microcapsules were observed by scanning electron microscopy, fragrance evaluation was performed on printed and impregnated samples after they had been washed several times, and their handle properties were investigated. Moreover, the influence of artificial light on the wall of microcapsules was examined, and possible antibacterial activity against Staphylococcus aureus and Escherichia coli was evaluated. The change in colour of all samples as a consequence of the addition of microcapsules to the paste or bath was checked. The results show that both application techniques are appropriate for the effective fragrant but on the other hand ineffective antibacterial finishing of cotton fabrics. Artificial light did not affect the microcapsules. There is an impact on colour only when the capsules are printed to fabric. Both of the techniques used, printing and impregnation, have advantages as well as drawbacks.     

Use of a biomaterial as a thickener for textile ink‐jet printing

The feasibility of using chitosan as a thickener in the pretreatment print paste for textile ink‐jet printing was explored. An orthogonal analysis was used to determine the optimum conditions for using chitosan as a thickener in the pretreatment print paste and the effects of different process factors for achieving the best color yield in textile ink‐jet printing. With the help of the orthogonal analysis, the importance of different process factors was found to be in the order of (1) the amount of urea used, (2) the amount of chitosan used, (3) the amount of sodium bicarbonate used, and (4) the steaming time. On the basis of the results of the orthogonal analysis, the optimum conditions for using chitosan as a thickener for the pretreatment print paste were concluded to be 40 mL of chitosan, 10 g of urea, 8 g of sodium bicarbonate, and 5 min of steaming. According to an analysis of the results of different color fastness tests, chitosan could principally work as a pretreatment print paste thickener. However, the final color yield obtained from chitosan‐containing cotton fabrics depended greatly on the stage of the chitosan application. Nevertheless, the color fastness properties and the outline sharpness of the prints of cotton fabric were greatly improved by the chitosan treatment. A two‐bath chitosan treatment was developed to separate the chitosan from sodium bicarbonate and urea before it was padded onto the fabric surface to minimize the neutralization effect. On the basis of the results for the highest color yield obtained on the cotton fabric, it was confirmed that the two‐bath chitosan treatment was successfully developed. In addition, chitosan could impart higher antibacterial properties with a slight reduction in the tensile strength of the cotton fabric. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Using carbon black nanoparticles to dye the cationic‐modified cotton fabrics

Carbon black (CB) aqueous dispersion was prepared and used to dye the cationic‐modified cotton fabrics through exhaust dyeing process. The effects of CB concentration, CB nanoparticles size, dyeing bath pH, dyeing time and dyeing temperature were investigated. The color yields of dyed fabrics were evaluated on Kubelka‐Munk value K/S. The surface morphologies of cationic modified and nonmodified cotton fabrics were measured by video microscope. The fabrics presented 18.9 of the color yield with the dyeing conditions: the dyeing solution contained 2% o.w.f. CB and dyeing at 80°C for 30 min with pH 13 using a 50 : 1 liquor ratio. The images of the video microscope demonstrated a clear surface profile for the cationic‐modified cotton fabrics dyed with smaller CB particle size solutions. These results indicated that CB nanoparticles were suitable for dyeing the cotton fabrics. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Fabrication and properties of CNT/Ni/Y/ZrB2 nanocomposites reinforced in situ

Carbon nanotubes (CNTs) were synthesized in situ by chemical vapor deposition of methane over nano‐ZrB₂ matrix using Ni/Y catalysts. Well‐grown CNTs with tangled and long bodies and mainly composed of well‐crystallized graphite were obtained when the Ni content reaches 10 wt%. The CNT/ZrB₂ nanocomposites obtained by spark plasma sintering at 1400°C exhibited full density and optimal mechanical properties. The flexural strength and fracture toughness of the nanocomposites were 1184 ± 52 MPa and 10.8 ± 0.3 MPa·m^1/2, respectively. Results indicated that the dispersion of CNTs in situ can improve composite performance, rendering the mechanical properties of the CNT/ZrB₂ nanocomposites synthesized in situ considerably superior to those of monolithic ZrB₂ nanoceramics and CNT/ZrB₂ nanocomposites synthesized using the traditional method. The toughening mechanisms included crack deflection, crack bridging, CNT debonding, pull‐out, and fracture.     

Fabrication of high mechanical performance UHMWPE nanocomposites with high-loading multiwalled carbon nanotubes

Using conventional mixing techniques, the mechanical properties of prepared carbon nanotube (CNT)/polymer composites are not impressive enough, because of their aggregation problem at a high loading of CNTs. In this article, high mechanical performance ultrahigh molecular weight polyethylene (UHMWPE) nanocomposites with high loading of multiwalled CNTs were successfully fabricated by a new manufacturing technique. Specifically, the tensile strength and storage modulus at 25 °C of UHMWPE nanocomposites with 32 wt % of nanotubes prepared by the novel technique reaches 107.6 MPa and 6.0 GPa, respectively, about 4.7 times and 5.0 times of that of pure UHMWPE resin, which are also very high experimental results compared with polyethylene nanocomposite prepared by traditional hot-compression techniques. These attractive results suggest that the high-loading CNTs without sacrificing their dispersion and the impregnation quality of polymer-impregnated buckypapers are essential for fabricating CNTs/polymer composites with superior mechanical properties. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 137, 48667.     

Fabrication and toughening behavior of carbon nanotube (CNT) scaffold reinforced SiBCN ceramic composites with high CNT loading

Uniform dispersion, high loading and three-dimensional (3D) continuous network of carbon nanotube (CNT) are desired for high-performance nanocomposites to fully utilize the superior strength and toughness of CNTs. In this work, monolithic CNTs/SiBCN composites with high CNT loading (10 wt% and 20 wt%) were prepared from 3D scaffold-like CNT cottons and a liquid polyborosilazane (PBSZ) precursor through precursor infiltration and pyrolysis process. The 3D CNT scaffold in the nanocomposite can function as passive filler and gas path to ensure formation of monolithic bulks. Moreover, direct infiltration of PBSZ into the pores among CNT cotton can hinder agglomeration of CNTs and localize CNTs at the original sites, guarantee good alignment and high CNT concentration in the final nanocomposite. This highly concentrated 3D CNT reinforcement in the nanocomposite shows unique resistance to cracking under external stress related to the complex fracture behavior of CNT bundles during the cracking formation and extension process (including CNT bridging, aligning, pulling out and then breaking), which more favors for absorbing energies and enhance toughness of the ceramic composites.     

原子层沉积氧化锌功能化碳纳米管织物及其光催化特性

以二乙基锌和去离子水为前驱体,利用原子层沉积（ALD）在自支撑碳纳米管（CNT）织物上沉积氧化锌（ZnO）对其进行了功能化;考察了ALD沉积过程中功能化织物的微观形貌、晶型结构、表面性质及光催化性能。实验结果表明,ZnO最初在CNTs表面生长为纳米颗粒,随ALD循环次数的增加,逐渐形成包覆CNTs的保形生长层,改变ALD沉积条件可精确调控氧化物在CNT织物中的负载量,CNT织物逐渐由强疏水转变为高度亲水。CNTs与六方纤锌矿结构ZnO的结合有效增强了电子转移能力,同时降低了光生电子与空穴的复合几率,ALD功能化CNT织物展现出优异的光催化降解性能,表明ALD是一种能够拓展CNT织物应用领域的灵活且有效的功能化手段。