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31.
Use of nanocomposites is a well-established approach in enhancing the mechanical and barrier properties of bionanocomposite film for food packaging applications. The seed mucilage of Ocimum basilicum was employed for the preparation of bionanocomposite films with montmorillonite (MMT) as nanofiller. The films were prepared by solvent-casting method at varied solution pH (1, 3, 5 and 9) and MMT loading (1%, 3%, 5%, 10%, 15% and 20%). The films were characterized for physical, mechanical and barrier properties in addition to microstructure and X-ray diffraction pattern. XRD analysis revealed the exfoliated dispersion of MMT at pH 9, confirming its effective interaction with the bionanocomposite film. Maximum film tensile strength was achieved at a lower MMT load of 5%. Water vapour permeability reduced with increase in MMT loading up to 5%, followed by an increase at higher MMT loadings. Film formed at pH 9 showed tensile strength of 17.3 ± 0.33 MPa and reduced water vapour permeability (WVP) of 0.21 g mm.m−2.hr−1.kPa−1.  相似文献   
32.
The presence of pathogenic bacteria in water is one of the important health concerns in the world. Herein, we report a new high-performance environmentally friendly poly (urethane-imide) (PUIm) containing β-cyclodextrin (β-CD) in its backbone to adsorb bacteria from water samples with significant heat resistance. New PUIm was prepared by bonding a diisocyanate as a new cross linking agent to β-CD and magnetic nanoparticles (MNPs). The effects of concentrations of bare polymer and polymer bounded to iron nanoparticles and contact times on the adsorption of staphylococcus aureus and Escherichia coli were considered at physiological pH. The adsorption capacity of this polymer is increased by binding it to MNPs and in addition it is possible to separate the polymer from aqueous sample with external magnetic field. A filter was also provided from polymer attached to iron nanoparticles and high percentages of bacteria were removed after filtering the real wastewater.  相似文献   
33.
In recent times, polyaniline (PANI), a conducting polymer, has been studied widely for environmental remediation application due to its controllable electric conductivity with high surface area, which makes it a suitable adsorbent material. But lower mechanical stability of PANI is considered to be a serious drawback for its large-scale industrial application. To improve the mechanical strength of PANI, in this study, hematite nanoparticles were impregnated onto PANI by oxidative polymerization method in order to fabricate a novel organometallic nanocomposite (hematite-PANI-NC). The hematite-PANI-NC was used as adsorbent for removal of methyl orange (MO) and eosin yellow (EY) dye from binary dye matrix under ultrasonic-assisted adsorption. Excellent MO and EY dye removal (more than 98%) was observed from binary matrix at a wide solution pH from 2.0 to 6.0, and under ultrasound wave the adsorption equilibrium was achieved within 15 min only. Both MO and EY dyes adsorption experimental data strictly followed Langmuir isotherm, and maximum monolayer adsorption capacity of 126.58 mg/g and 112.36 mg/g was observed for MO and EY dye, respectively. The uptake mechanism of MO and EY dyes onto hematite-PANI-NC is governed by electrostatic interaction, π-π bonding and hydrogen bonding between dye molecules and nanocomposite. Response surface methodology analysis reveals maximum MO and EY removal of 98.43% and 99.35% at optimum experimental conditions. This study implies that the hybrid organometallic material hematite-PANI-NC has high potential for quick and enhanced sono-assisted uptake of anionic dyes from water near neutral solution pH.  相似文献   
34.
A novel metal–organic framework material {[N(C2H5)3][Zn2(ptmda)22-H2O)]·(H2O)0.5}n { GUT-3 ; H2ptmda is 4,4′-([p-tolylazanediyl]bis [methylene])dibenzoic acid} was successfully synthesized using the hydrothermal method and characterized by X-ray diffraction, Fourier transform infrared spectroscopy, and X-ray photoelectron spectroscopy. GUT-3 has a two-dimensional network based on dinuclear [Zn2(ptmda)2(μ2-H2O)] building units which formed an eightfold interpenetration network in GUT-3 molecules. Hirshfeld surface analysis revealed that H–H, C–H, and O–H bonds accounted for the majority of intermolecular interactions. Moreover, the interactions between GUT-3 and As(V) – the form of As(V) is AsO43− – were analyzed in aqueous solutions in a batch system to study the effect of pH, concentration, adsorbent dose, adsorption time, adsorption temperature, and shaking speed. The kinetic and isotherm data of arsenic adsorption on GUT-3 were accurately modeled by pseudo-second-order, Langmuir (qm = 33.91 mg/g), and Freundlich models. The Box–Behnken response surface method was used to optimize the adsorption conditions of As(V) from the simulated arsenic-contaminated wastewater. The effect of various experimental parameters and optimal experimental conditions was ascertained using the quadratic model.  相似文献   
35.
A new copper (II) coordination complex formulated as [Cu (dipic)(phen)(2-MePy)]. 2H2O ( 1 ) where phen = 1, 10-phenanthroline, dipic2− = pyridine-2,6-dicarboxylato and 2-MePy = 2-methyl pyrrole was synthesized through a simple and environment-friendly reaction under ultrasound irradiation. Also, complex 1 was synthesized by hydrothermal process at 120 °C for 3 days. The corresponding structure of complex 1 was characterized by elemental analysis, atomic absorption spectroscopy (AAS), inductively coupled plasma (ICP), conductivity measurement, Fourier-transform infrared spectroscopy (FT-IR), Raman spectroscopy, ultraviolet–visible spectroscopy (UV–Vis), thermal gravimetric analysis (TGA), differential thermal analysis (DTA), scanning electron microscopy (SEM), vibrating sample magnetometer (VSM) and fluorescence. The crystal structure of the hydrothermally synthesized complex was characterized by single crystal X-ray diffraction (SC-XRD(, which revealed a triclinic structure. In the remainder of this study, the Cu2O nanoparticles have been prepared via thermal decomposition of hydrothermal and ultrasound complexes and characterized by ICP, FT-IR, powder X-ray diffraction (XRD), SEM and N2 adsorption/desorption. Adsorption and visible-light-driven photocatalytic capabilities of two synthetic Cu2O were investigated in the removal of MB from water. The result showed that the synthesized catalysts have good catalytic activity and the photocatalytic degradation is more effective in dye removal of MB compared with the adsorption.  相似文献   
36.
为实现较少试验次数下固化土无侧限抗压强度(qu)的准确预测, 提出了基于支持向量机(SVM)的固化土qu的预测模型. 以固化剂各组分掺入比、龄期、初始含水量、固化剂掺量等因素为输入量, 固化土的qu作为输出量, 以径向基为核函数, 采用网格搜索法和交叉验证法进行参数优化, 建立了基于SVM的固化土qu的预测模型. 算例分析表明: 该模型适用于任意条件下固化土qu的精确预测, 且在较小试验成本下实现与响应面法相当的预测精度.  相似文献   
37.
For B2 NiAl and NiTi intermetallic compounds, the ideal stress–strain image is lack from the perspective of elastic constants. We use first-principles calculation to investigate the ideal strength and elastic behavior under the tensile and shear loads. The relation between the ideal strength and elastic constants is found. The uniaxial tension of NiAl and NiTi along <001> crystal direction leads to the change from tetragonal path to orthogonal path, which is driven by the vanishing of the shear constant C(66). The shear failure under {110}{111} shear deformation occurring in process of tension may result in a small ideal tensile strength(~ 2 GPa) for NiTi. The unlikeness in the ideal strength of Ni Al and Ni Ti alloys is discussed based on the charge density difference.  相似文献   
38.
头发的弹性和抵抗意外拉断的能力是人们非常关注的指标。为了迎合这一需求,有些厂商推出了具有所谓“强韧”发质功效的洗发水,但其实并不清楚是否真能使头发变“强韧”。为此,针对市场上常见的一种标称具有“强韧”功效的洗发水,通过拉伸力学实验对头发洗护前后的力学性能进行了对比研究。结果表明,用洗发水处理后的头发,屈服应力下降,意味着头发更容易过早进入塑性变形;抗拉强度、最大应变减小,意味着头发抵抗外力拉断的能力下降;杨氏模量下降,说明头发抵抗弹性变形的能力变差。综上,所研究的洗发水对“强韧”发质没有帮助。 关键词: 头发,洗发水,力学性能,强度,韧性  相似文献   
39.
针对RC梁开裂荷载计算方法尚未统一的现状,首先,结合18根RC梁试验数据对比了已有的6种RC梁开裂弯矩计算公式,发现开裂弯矩理论计算值与试验值的偏差大小和混凝土强度有关;然后,通过提出塑性变形发展程度系数k,推导新的RC梁开裂弯矩计算公式,并进一步基于k值和塑性影响系数计算值γk进行改进;最后,选取12根RC试验梁验证改进公式的准确性,证明改进公式的计算值与试验值吻合更好且偏于安全。  相似文献   
40.
In this study, core‐shell structures of magnetite nanoparticles coated with CMK‐8 ordered mesoporous carbon (Fe3O4@SiO2‐CMK‐8 NPs) have been successfully synthesized for the first time by carbonizing sucrose inside the pores of the Kit‐6 mesoporous silica. The nano‐sized mesoporous particles were characterized by X‐ray diffraction, Fourier transform‐infrared spectroscopy, scanning electron microscope, dynamic light scattering, vibrating‐sample magnetometer, Brunauer–Emmett–Teller (BET) and transmission electron microscopy instruments. The obtained nanocomposite was used for removal of Reactive Yellow 160 (RY 160) dye from aqueous samples. The N2 adsorption–desorption method (at 77 K) confirmed the mesoporous structure of synthesized Fe3O4@SiO2‐CMK‐8 NPs. Also, the surface area was calculated by the BET method and Langmuir plot as 276.84 m2/g and 352.32 m2/g, respectively. The surface area, volume and pore diameter of synthesized nanoparticles (NPs) were calculated from the pore size distribution curves using the Barrett–Joyner–Halenda formula (BJH). To obtain the optimum experimental variables, the effect of various experimental parameters on the dye removal efficiency was studied using Taguchi orthogonal array experimental design method. According to the experimental results, about 90.0% of RY 160 was removed from aqueous solutions at the adsorbent amount of 0.06 g, pH 3 and ionic strength = 0.05 m during 10 min. The pseudo‐second order kinetic model provided a very good fit for the RY 160 dye removal (R2 = 0.999). The Langmuir, Freundlich, Temkin and Dubinin–Radushkevich models were applied to describe the equilibrium isotherms, and the Langmuir isotherm showed the best fit to data with the maximum adsorption capacity of 62.893 mg/g. Furthermore, the Fe3O4@SiO2‐CMK‐8 NPs could be simply recovered by external magnet, and exhibited recyclability and reusability for a subsequent six runs.  相似文献   
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