Performance evaluation and antifouling analyses of cellulose acetate/nanodiamond nanocomposite membranes in water treatment

In this study, nanocomposite membranes based on cellulose acetate (CA) and nanodiamond (ND) were prepared by applying phase inversion methods. In order to achieve efficient dispersion and more hydrophilic NDs, they were functionalized via heat treatment (ND‐COOH). The prepared nanocomposite membranes were characterized by Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), transmission electron microscopy (TEM), contact angle, porosity measurement, tensile strength, and abrasion resistance techniques. Furthermore, the governing fouling mechanisms were determined by using classic models as well as combined fouling models. Moreover, the effect of precoagulation with polyaluminum chloride (PAC) on the humic acid (HA) filtration was investigated. The obtained results showed that in the presence of ND‐COOH, the abrasion resistance of nanocomposite CA membrane was three times higher than that of pristine CA membrane. Besides, the nanocomposite membranes with 0.5 wt % of raw and functionalized ND exhibited excellent hydrophilicity and PWF. The analysis of fouling mechanism based on Hermia's model revealed that the cake formation is prevailing mechanism for CA and CA/ND (0.5 wt %) membranes while for CA/ND‐COOH (0.5 wt %) membrane, experimental results are fitted by combined cake filtration‐complete blocking (CFCB) model. It confirms that pretreatment with PAC can significantly mitigate fouling and improve HA removal. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 44873.     

High-density polyethylene membranes embedded with carboxylated and polyethylene glycol-grafted nanodiamond to be used in membrane bioreactors

In this work, neat and modified nanodiamond (ND) particles were embedded into high-density polyethylene (HDPE) membranes to improve hydrophilicity and antifouling properties. The membranes were prepared via thermally induced phase separation (TIPS) method and used for pharmaceutical wastewater treatment in membrane bioreactors (MBR) system. To prevent the agglomeration of ND, it was modified using two methods: thermal carboxylation (ND-COOH) and grafting with polyethylene glycol (ND-PEG). Membranes with different concentration of ND-COOH and ND-PEG nanoparticles ranging from 0.00 to 1.00 wt % were prepared and characterized using a set of analyses including water contact angle, pure water flux, tensile strength, differential scanning calorimeter, field emission scanning electron microscopy, and energy dispersive X-ray spectroscopy. It was found that the optimum contents of ND-COOH and ND-PEG nanoparticles were 0.50 wt % and 0.75 wt %, respectively. The interfacial interaction between nanoparticles and HDPE matrix was studied based on Pukanzsky model. To examine the performance of membranes, critical flux, filtration experiment in the MBR, and fouling analysis of membranes were carried out. The results showed that among the fabricated membranes, 0.75 wt % HDPE/ND-PEG membrane had the highest water flux and the best antifouling properties. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47914.     

Peroxopolyoxometalate nanoparticles blended PES membrane with improved hydrophilicity,anti-fouling,permeability, and dye separation properties

Poly(ethersulfone) (PES) is one of the polymers most widely used for the fabrication of ultrafiltration or nanofiltration membranes in various applications, but its membrane suffers from fouling. In this study, preparation, characterization, and performance of PES nanocomposite membrane comprising peroxopolyoxometalate nanoparticles was studied to provide improved permeability and anti-fouling properties. The high oxygen ratio of the PW₄ nanoparticles could enhance the hydrophilicity of the membranes. The PW₄ nanoparticles were characterized using Fourier transform infrared spectroscopy, scanning electron microscopy (SEM), energy dispersive X-ray (EDX), and X-ray diffraction analyses. The mixed matrix membranes were fabricated using a non-solvent induced phase-separation method. The fabricated membranes were characterized using atomic force microscopy, attenuated total reflection, SEM, EDX mapping, total average porosity, thermogravimetric analyze, and water contact angle experiments. The dye flux and rejection, pure water permeability and anti-fouling properties of the membranes were investigated. All of the membranes blended by different contents of the PW₄ nanoparticles presented better performance compared to the unmodified membrane. The filtration performance of the membranes in reactive green 19 (RG19) and reactive yellow 160 (RY160) dye separation showed that all of the PW₄ blended membranes possessed dye rejection greater than 86% and 96% for RY160 and RG19, respectively. The reusability test using bovine serum albumin (BSA) protein and RG19 dye solutions in five cycle experiments presented good reproductivity of the PW₄ blended membranes. The PES membrane containing 1 wt% of PW₄ nanoparticles showed the highest flux recovery ratio (75%) as well as reduced irreversible fouling ratio (8%) through BSA protein filtration.     

Fabrication of polysulfone nanocomposite membranes with silver‐doped carbon nanotubes and their antifouling performance

In this study, polysulfone (PSf)/silver‐doped carbon nanotube (Ag‐CNT) nanocomposite membranes were prepared by a phase‐inversion technique; they were characterized and evaluated for fouling‐resistant applications with bovine serum albumin (BSA) solutions. Carbon nanotubes were doped with silver nanoparticles via a wet‐impregnation technique. The prepared Ag‐CNT nanotubes were characterized with scanning electron microscopy (SEM)/energy‐dispersive X‐ray spectroscopy, X‐ray diffraction, Raman spectroscopy, and thermogravimetric analysis. The fabricated flat‐sheet PSf/Ag‐CNT nanocomposite membranes with different Ag‐CNT loadings were examined for their surface morphology, roughness, hydrophilicity, and mechanical strength with SEM, atomic force microscopy, contact angle measurement, and tensile testing, respectively. The prepared composite membranes displayed a greater rejection of BSA solution (≥90%) and water flux stability during membrane compaction with a 10% reduction in water flux values (up to 0.4% Ag‐CNTs) than the pristine PSf membrane. The PSf nanocomposite membrane with a 0.2% Ag‐CNT loading possessed the highest flux recovery of about 80% and the lowest total membrane resistance of 56% with a reduced irreversible fouling resistance of 21%. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 44688.     

Cellulose acetate ultrafiltration membranes customized with copper oxide nanoparticles for efficient separation with antifouling behavior

Cellulose acetate (CA) nanocomposite ultrafiltration membranes are fabricated with copper oxide (CuO) nanoparticles with the aim of improving efficient protein separation and antifouling performance. CuO nanoparticles are synthesized from cupric nitrate using a wet precipitation method and characterized by FTIR and XRD. CA/CuO nanocomposite membranes fabricated using 0.5, 1.0, and 1.5 wt% of CuO nanoparticles individually by simple phase inversion technique. The CA nanocomposite membrane with 0.5 wt% of hydrophilic CuO exhibited enhanced PWF of 118.6 Lm⁻² h⁻¹ due to the improvement in porosity and water uptake. This is in good agreement with the enhanced hydrophilicity of the CA/CuO nanocomposite membranes results observed in surface contact angle and morphological investigations. Further, 95.5% of BSA separation and 94.7% of flux recovery ratio (FRR) indicates its superior antifouling potential caused due to the presence of the hydration layer at the CA/CuO membrane surface. Among all the fabricated membranes, the CA-0.5 nanocomposite membrane with 0.5 wt% of CuO exhibited superiorly improved hydrophilicity, water permeation, BSA separation, and antifouling performance indicates its potential use in water and wastewater treatment applications.     

Removal of arsenic from aqueous media using zeolite/chitosan nanocomposite membrane

In this work, the removal of arsenic (III) using zeolite/chitosan nanocomposite membranes was studied and characterized using scanning electron microscopy (SEM), atomic force microscope (AFM), etc. The water contact angle of the membrane decreased from 74.2 to 59.2° and the porosity of the prepared membranes increased from 20.38 to 45.81% with an increase in the concentration of zeolite. The rejection of arsenic (III) increases with increase in the zeolite loading for 500 and 1000 µg/L; but at 100 and 150 µg/L, the trend was opposite. The membrane with 1.0 [Chi-Z (1.0)] and 1.25 [Chi-Z (1.25)] wt% zeolite showed the highest rejection (>94%) for 1000 µg/L concentration of arsenic trioxide aqueous solution.     

Characterization of triple electrospun layers of PVDF for direct contact membrane distillation process

Recently, electrospinning technique was applied successfully to fabricate porous hydrophobic membranes for MD applications. In this work, a novel triple layer configuration with diameter gradient for PVDF nanofiber membranes is proposed, with the objective of to minimize mass transfer resistance and heat loss. In outer layers of these membranes, the minimum concentration of PVDF (20 wt%) was used to produce bead-free nanofibers with thinner diameters and middle layers were composed of thicker nanofibers formed at higher polymer concentrations (21.5-26 wt%). Characterization of prepared membranes was conducted by the measurement of porosity, thickness, liquid entry pressure (LEP), scanning electron microscopy (SEM), contact angle, thermal and mechanical properties. Direct contact membrane distillation performance of fabricated membranes was tested using 42 g/L NaCl as feed solution. Water permeate flux of triple layer membranes (27.8-31.5 kg/m² h) was found to be considerably higher than that obtained from single layer membrane (15.4 kg/m² h), indicating the proposed configuration can effectively improve evaporation efficiency.     

Biocompatibility and strengthening of porous hydroxyapatite scaffolds using poly(l-lactic acid) coating

Hydroxyapatite (HA) is a well-known biocompatible bone substitute. Porous HA is more resorbable and osteoconductive compared with non-porous HA, and has been studied both experimentally and clinically. However, the mechanical strength of porous HA scaffolds is known to be weak. In this study, we developed a porous HA scaffold coated with a synthetic biodegradable polymer, poly(l-lactic acid) (PLLA), to strengthen the scaffold. PLLA-coated HA pellets were used to investigate the in vitro proliferation and alkaline phosphatase (ALP) activity of osteoblasts. PLLA-coated porous HA scaffolds were observed using scanning electron microscopy to investigate surface characteristics, porosity, and mechanical strength. PLLA coating concentration varied from 2 to 10 wt%. Osteoblast proliferation was higher in HA samples coated with PLLA compared with non-coated. ALP activity was highest on 8 wt% PLLA-coating after 3 days and on 4 wt% and 6 wt% PLLA after 9 and 12 days. Porous HA scaffolds with higher concentrations of PLLA were found to have a smoother, flatter surface. This enhanced proliferation and attachment of osteoblasts onto the porous HA scaffold. PLLA solution at a concentration of 10 wt% decreased scaffold porosity to half that of HA scaffolds with no PLLA coating. Scaffold mechanical strength was increased two-fold with a PLLA concentration of 2 wt%. Based on in vitro experimentation, it can be concluded that PLLA-coating on porous HA scaffolds enhances both the biocompatibility and the mechanical strength.     

Study on Morphology,Rheology and Mechanical Properties of Thermoplastic Elastomer Polyolefin (TPO)/Carbon Nanotube Nanocomposites with Reference to the Effect of Polypropylene-grafted-Maleic Anhydride (PP-g-MA) as a Compatibilizer

The structure–property relationships of polypropylene/ethylene-propylene-diene (PP/EPDM) (80/20) nanocomposites containing single-walled carbon nanotubes (SWCNTs) by melt-mixing process were investigated, the main focus being on the effect of SWCNTs concentration and compatilizer content. Morphological observations by scanning electron microscopy (SEM) are presented in conjunction with the mechanical, thermal, and rheological properties of these nanocomposites. The tensile modulus of nanocomposites was enhanced by increasing the SWCNTs concentration. A high level of toughness in the thermoplastic elastomer polyolefin (TPO)/SWCNTs nanocomposite was achieved with 0.5 wt% of SWCNTs and 1 wt% of polypropylene-grafted maleic anhydride (PP-g-MA). Differential scanning calorimetry (DSC) experiments confirmed the nucleation effect of nanotubes on the crystallization process of the TPO/SWCNTs composites. An appreciable viscosity upturn and a non-terminal low frequency storage modulus were observed in nanocomposites containing SWCNTs whose values increased in the presence of compatibilizer.     

Comparison of the performance of reduced graphene oxide and multiwalled carbon nanotubes based sulfonated polysulfone membranes for electrolysis application

A series of nanocomposites containing reduced graphene oxide (GO) versus multiwalled carbon nanotubes (MWCNTs) as filler contents anchored with sulfonated polysulfone (SPSF) polymer matrix have been successfully prepared by sol–gel technique with up to 0.5 wt%. The influence of reduced GO compared to MWCNTs to enhance conductivity of nanocomposite SPSF membranes for higher efficient water electrolysis applications has been studied. The nanocomposite membranes were characterized using scanning electron microscopy, atomic force microscopy, Raman spectroscopy, transmission electron microscopy, optical microscopy, electrical conductivity, and tensile testing. The membrane porous structure, porosity, and pores uniformity plus the uniformity of dispersion of mixture are investigated. The conductivity of the composite membranes for water electrolysis applications has been characterized using localized probes across the surface. The results show SPSF–GO nanocomposite membranes offer higher conductivity and improved performance than those of SPSF–MCNT. A uniform constant and high current density of 1.39 A/cm² has been achieved in SPSF–GO membrane at 60°C. POLYM. COMPOS. 36:475–481, 2015. © 2014 Society of Plastics Engineers     

Application of poly (amide-<Emphasis Type="Italic">b</Emphasis>-ethylene oxide)/zeolitic imidazolate framework nanocomposite membrane in gas separation

Mixed matrix membranes (MMMs) are gaining increasing interest in academic and industrial research due to their combined, desirable properties of both polymers and organic/inorganic filler as important materials. In this work, synthesized zeolitic imidazolate framework (ZIF-8) suspension (10–50 wt%) was directly incorporated into a [poly (amide-b-ethylene oxide) Pebax^® 1657] matrix in order to improve the gas separation performance of the membrane. Dynamic light scattering (DLS) analysis showed an average diameter of 77.4 nm for the prepared nanoparticles. The transparent membranes were characterized by scanning electron microscopy (SEM), differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), Fourier transform infrared (FTIR) spectroscopy, and X-ray diffractometry (XRD). These indicated excellent dispersion of nanoparticles, which was achieved by ultrasonication before casting the solution. Incorporation of ZIF-8 as filler in the polymer matrix led to improved thermal and mechanical stability of the membranes. This was confirmed by TGA and tensile analyses, indicating good contacts provided at the polymer/filler interfaces. The effect of ZIF-8 loading (up to 50 wt%) on membrane performance was investigated and it showed an optimum loading of 30 %. Single gas (CO₂, N₂ and CH₄) permeation tests revealed rapid, enhanced permeability of the nanocomposite membranes without significant changes in selectivity (compared to those of the pristine polymeric membrane). The permeability increases for CO₂, CH₄ and N₂ in the optimum Pebax^® 1657/ZIF-8 (30 wt%) membrane were found in the stated order as 111, 88 and 99 %. The study revealed that Pebax^® 1657/ZIF-8 membranes displayed better gas permeation properties compared to those of Pebax^® 1657.     

Preparation and characterization of polyvinyl chloride based nanocomposite nanofiltration-membrane modified by iron oxide nanoparticles for lead removal from water

In this research (polyvinyl chloride-blend-cellulose acetate/iron oxide nanoparticles) nanocomposite membranes were prepared by casting technique to lead removal from wastewaters. The effect of blend ratio of polymer binder (PVC to CA) and Fe₃O₄ nanoparticles concentration on physico-chemical characteristics of membranes were studied. Water permeability and ionic rejection tests, water content and mechanical properties measurements and SEM analysis were carried out in membranes characterizations. Obviously, modified membrane containing 10 wt% CA and 0.1 wt% Fe₃O₄ nanoparticles showed better performance in lead removal compared to other modified membranes and also pristine ones.     

Enhanced mechanical and thermal properties of nanodiamond reinforced low density polyethylene nanocomposites

In this study, the reinforcement effects of low-content hydrophilic nanodiamond (ND) on linear low-density polyethylene (PE) nanocomposites were investigated. ND was incorporated in PE via simple solution blending. The obtained PE/ND nanocomposites were characterized using scanning electron microscopy, ultraviolet–visible spectra, X-ray diffraction, tensile test, thermogravimetry, and differential scanning calorimetry. Generally, PE/ND nanocomposites with poor interfacial interaction cause large agglomerates, resulting in brittle and poor mechanical properties. Owing to the different natures of non-polar PE and polar ND, the higher the ND content, the larger the agglomerates formed in the nanocomposites. However, PE/ND nanocomposites show unique mechanical properties, that is, the Young's modulus, tensile strength, elongation at break, and toughness increased upon the incorporation of ND. The Young's modulus of the PE/ND nanocomposites exceeded the theoretical value calculated using the Halpin–Tsai model. In addition, the toughness increased by 18% at only 0.5 wt% ND loading. Furthermore, there was an increase in the thermal degradation temperature, melting temperature, and crystallization temperature.     

Preparation,characterization and performance of cellulose acetate ultrafiltration membranes modified by charged surface modifying macromolecule

A charged surface modifying macromolecule (cSMM) was synthesized, characterized by FT-IR spectroscopy and blended into the casting solution of cellulose acetate (CA) to prepare surface modified UF membranes by phase inversion technique. With an increasing cSMM additive content from 1 to 4 wt%, pure water flux (PWF) and water content (WC) were increases whereas the hydraulic resistance decreases. Surface characteristic study reveals that the surface hydrophilicity increased in cSMM modified CA membranes. The pore size and surface porosity of the 4 wt% cSMM blend CA membranes increases to 41.26 Å and 0.015%, respectively. Similarly, the molecular weight cut-off (MWCO) of the membranes ranged from 20 to 45 kDa, depending on the various compositions of the prepared membranes. Lower flux decline rate (47.2%) and higher flux recovery ratio (FRR) (89.0%), exhibited by 4 wt% cSMM blend membranes demonstrated its fouling resistant characteristic compared to pristine CA membrane.     

Camphor Sulfonic Acid Doped Polyaniline-Titanium Dioxide Nanocomposite: Synthesis,Structural, Morphological,and Electrical Properties

A nanocomposite of polyaniline-titanium dioxide (PANi-TiO₂, 50 wt%) was doped with camphor sulfonic acid (CSA) by solid state reaction with increasing CSA content up to 50 wt% in a smooth agate mortar. CSA doped PANi-TiO₂ was dissolved in m-cresol and films were cast using a spin-coating technique. The doping effect of CSA on PANi-TiO₂ nanocomposite was characterized and evaluated by X-ray diffraction pattern (XRD), scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), and electrical conductivity measurement. The XRD spectra showed that the addition of CSA has no effect on crystallinity of PANi-TiO₂. SEM studies revealed that CSA has a strong effect on morphology of PANi-TiO₂. The FTIR spectra revealed the interaction between CSA and PANi-TiO₂ nanocomposite. Electrical conductivity measurements indicated that with the increasing content of CSA, the conductivity shows an orderly increase.     

Waterborne acrylic–polyaniline nanocomposite as antistatic coating: preparation and characterization

An antistatic and electrically conductive acrylic–polyaniline nanocomposite coating was successfully synthesized by interfacial polymerization of aniline in the presence of acrylic latex. The acrylic latex was prepared through emulsion polymerization, and aniline was polymerized by in situ interfacial polymerization at the interface of acrylic latex/chloroform phase. Fourier transform infrared spectroscopy (FTIR), UV–Vis spectroscopy and CHNS elemental analysis revealed the existence of 6.24 wt% emeraldine salt of polyaniline (PAni) in the dried film of the nanocomposite. Scanning electron microscopy (SEM) confirmed the presence of colloidal polymer particles in the aqueous phase which was confirmed to have some advantages, including prevention of aggregation of particles, dispersibility improvement and enhancement of the PAni nanofibers aspect ratio in the acrylic polymer matrix. According to SEM results, PAni fibers with the length ranging from 12 to 67 µm and diameters between 0.078 and 1 µm, highly dispersed in the acrylic polymer matrix, were successfully synthesized. Thermal, electrical and mechanical properties of the acrylic copolymer were significantly affected by PAni incorporation. The onset degradation temperature in thermogravimetric analysis revealed that the thermal stability of the nanocomposite was improved compared to that of the pure acrylic copolymer. The nanocomposite film showed electrical conductivity of about 0.025 S/cm at room temperature, along with satisfactory mechanical properties, attractive as an antistatic material in coating applications.     

Thermal properties of phosphorylated nanodiamond reinforced polyimides

Recently, the preparation of nanodiamond–polymer composites has attracted the attention of materials scientists due to the unique properties of nanodiamonds. In this study, novel polyimide (PI)/phosphorylated nanodiamonds (PNDs) composites were prepared. PNDs were achieved from the reaction of methylphosphonic dichloride with nanodiamonds in dichloromethane. Precursor of polyimide, which is the poly(amic acid) (PAA), was successfully synthesized with 3,3′, 4,4′‐benzophenonetetracarboxylic dianhydride and 4,4′‐oxydianiline in the solution of N,N‐dimethylformamide. Different ratios of phosphorylated nanodiamond particles were added into PAA solution and four different nanocomposite films were prepared. The amount of PNDs in the composite films was varied from 0 wt% to 3 wt%. The structure, thermal and surface properties of polyimide films were characterized by scanning electron microscopy (SEM), ATR‐FTIR, thermogravimetric analysis (TGA), ultraviolet visible spectroscopy, and contact angle. SEM and FTIR results showed that the phosphorylated nanodiamond and PI/PNDs films were successfully prepared. Phosphorylated nanodiamonds were homogeneously dispersed in the polymer matrix and they displayed good compatibility. TGA results showed that the thermo‐oxidative stability of PI/PNDs films was increased with the increasing amount of phosphorylated nanodiamond. POLYM. COMPOS., 37:2285–2292, 2016. © 2015 Society of Plastics Engineers     

Improvement of mechanical and electrical properties of epoxy resin with carbon nanofibers

In the present research, the reinforcement effect of vapor grown carbon nanofiber (VGCNF) was studied in relation to the mechanical properties and electrical conduction behavior of fabricated nanocomposites. Different weight fractions of nanofillers into epoxy resin, from 0.05 to 1 wt% and up to 2 wt% for mechanical and electrical properties were investigated. It was found that the optimum improvement in mechanical properties of nanocomposite is obtained at 0.25 wt% of carbon nanofibers. At this filler content, 23 % enhancement in tensile strength and 10 % in flexural strength have been observed. The degree of the VGCNF dispersion has been monitored by means of viscosity variation of the suspension during the sonication process to obtain the optimum sonication time. Finally, the quality of the dispersion for post-cured nanocomposites is characterized by fractured surfaces using the scanning electron microscopy. Agglomerates had a direct effect on the reduction of tensile and flexural strength of nanocomposites. The electrical conductivity was obtained by means of surface measuring method. The optimum amount of filler for the generation of a fine electrical conductivity was found to be around 0.5 wt% of VGCNF. After the threshold point, the electrical conductivity of nanocomposites was slightly raised in spite of adding more filler contents.     

Fabrication of fullerenol-incorporated thin-film nanocomposite forward osmosis membranes for improved desalination performances

Development and use of novel membranes for forward osmosis (FO) applications have gained popularity throughout the world. To enhance FO membrane performance, a novel thin-film nanocomposite membrane was fabricated by interfacial polymerization incorporating Fullerenol (C₆₀(OH)_n) nanomaterial, having n in the range of 24–28 into the active layer. Different concentrations of fullerenol loading (100, 200, 400, and 800 ppm) were added to the top skin layer. The structural and surface properties of the pure thin-film composite membrane (TFC) and fullerenol-incorporated thin-film nanocomposite (FTFC) membranes, were characterized by ATR-FTIR, SEM, and AFM. FO performance and separation properties were evaluated in terms of water flux, reverse salt flux, antifouling propensity, water permeability and salt permeability for all TFC and FTFC membranes. Osmotic performance tests showed that FTFC membranes achieved higher water flux and reverse salt flux selectivity compared with those of TFC membranes. The FTFC membrane with a fullerenol loading of 400 ppm exhibited a water flux of 26.1 L m^?2 h^?1 (LMH), which is 83.03% higher than that of the TFC membrane with a specific reverse salt flux of 0.18 g/L using 1 M sodium chloride draw solution against deionized water in FO mode. The fullerenol incorporation in FTFC membranes also contributed to a decreased fouling propensity.     

聚氨酯/纳米金刚石纳米复合材料的性能研究

通过原位反应法制备了聚氨酯(PU)/纳米金刚石(ND)纳米复合材料,采用X射线衍射(XRD)、热失重分析(TGA)、扫描电子显微镜(SEM)和力学性能测试等手段系统研究了PU/ND纳米复合材料的力学性能、热性能和形态。研究结果表明,ND能够显著提高聚氨酯的力学性能。随着ND用量的增加,PU/ND纳米复合材料的拉伸强度、100%定伸应力、500%定伸应力和断裂伸长率先增加后减少。当ND质量分数为0.5%时,PU/ND纳米复合材料的力学性能最佳,拉伸强度和断裂伸长率分别提高了61.5%和39.1%。PU/ND纳米复合材料的T-剥离强度和耐热性也有提高。