热响应性聚合物包覆铜纳米粒的研制和性能

以聚乙烯亚胺(PEI)、N-异丙基丙烯酰胺(NIPAM)为单体,无皂乳液聚合法制备了热响应性聚乙烯亚胺(PNIPAM-PEI),分散于一定浓度Cu2+溶液,原位还原,制得温敏性聚合物包覆铜的复合颗粒。扫描电镜观察发现,复合颗粒形态规则、分布均匀,较低Cu2+浓度制备颗粒粒径比较高浓度的小。热分析显示,复合颗粒最终残留物质量分别可达35%和47%,表明有较好聚合物包覆率。红外光谱、X衍射对样品组成分析发现,样品中有未被完整包覆的Cu颗粒存在。紫外可见分光光度仪测定复合颗粒分散液温敏性显示,吸光度随温度有明显变化,显示较好的温度响应性。

自组装形成的透明质酸-铜-槲皮素配位聚合物纳米粒子对乳腺癌的协同治疗作用

目的:探讨自组装形成的具有协同治疗作用的透明质酸-铜-槲皮素配位聚合物纳米粒子(HCQ NP)对乳腺癌的协同治疗作用。方法:采用自组装方法合成HCQ NP,并通过透射电镜、动态光散射、红外光谱分析和电感耦合等离子体质谱对其进行表征;采用亚甲蓝紫外吸收法测定HCQ NP与不同浓度的过氧化氢(H_(2)O_(2))反应生成羟基自由基(·OH)的能力;在模拟肿瘤微环境下,采用CCK-8法分别评价不同浓度的HCQ NP对乳腺癌MDA-MB-231细胞的抑制效果。结果:自组装形成的HCQ NP具有形状类似球形、大小均一的特点,并对乳腺癌MDA-MB-231细胞具有显著的协同抑制作用。结论:自组装形成的HCQ NP对乳腺癌MDA-MB-231细胞具有协同抑制作用。

微乳液法制备纳米铜粒的条件探究

本文以液体石蜡为油相,硝酸铜溶液为水相,Span-80、Tween-80为表面活性剂,正丁醇为助表面活性剂配制W/O型微乳液,采用微乳液法结合热处理的方式制备纳米铜粒子,并对其进行XRD表征,探究了热处理温度和硝酸铜浓度对纳米铜粒径的影响。研究表明,本文在热处理温度250℃、硝酸铜浓度0.5mol/L的条件下,制得的纳米铜粒径最小,为23.6nm。

Cu^2+/DSF共载型给药系统的制备与体外评价

目的将二油酰磷脂酸(dioleoylphosphatydic acid,DOPA)包衣的磷酸铜(copper phosphate,CuP)纳米粒(CuP/DOPA,约20 nm)和双硫仑(disulfiram,DSF)共载于脂质微球(lipid microspheres,LMs,约200 nm)中,并包埋在透明质酸热敏凝胶内,制备Cu^2+/DSF共载型给药系统并评价其性能。方法通过高压乳匀法将DSF与采用乳化分散法制备的CuP/DOPA共载入LMs中并分散在透明质酸热敏凝胶中得到Cu^2+/DSF共载型给药系统。利用高效液相色谱法和紫外分光光度法测定含量和包封率,激光散射粒度测定仪测定粒径及分布,透射电镜观察形态结构,应用流变仪测定相转变温度及流变学特性,并进行体外释放和细胞毒性实验。结果成功制备了Cu^2+/DSF共载型给药系统,平均粒径为198.5 nm,铜离子和DSF的包封率分别为99.7%和98.2%;相转变温度为20.2℃;对人乳腺癌细胞株MCF-7的抑制作用明显强于Cu^2+孵育条件下的DSF溶液剂。结论 Cu^2+/DSF共载型给药系统可以在体内环境下形成药物贮库,具有良好的体外抗癌效果。

Preparation and tribological properties of surface modified Cu nanoparticles

Cu nanoparticles surface-modified by dioctylamine dithiocarbamate （DTC8） were synthesized using a two-phase extraction route. The size, morphology and structure of resultant surface-capped Cu nanoparticles （coded as DTC8-Cu） were analyzed by means of X-ray diffraction, transmission electron microscopy and infrared spectrometry. The tribological behavior of DTC8-Cu as an additive in liquid paraffin was evaluated with a four-ball machine, and the surface topography of the wear scar was also examined by means of scanning electron microscopy. Results show that Cu nanoparticles modified by DTC8 have a small particle size and a narrow size distribution. Besides, DTC8-Cu as an additive in liquid paraffin has excellent antiwear ability, due to the deposition of nano-Cu with low melting point on worn steel surface leading to the formation of a self-repairing protective layer thereon.

Adsorption behavior and adsorption mechanism of Cu(Ⅱ) ions on amino-functionalized magnetic nanoparticles

Amino-functionalized magnetic nanoparticle （NH2-MNP） were prepared by a sol-gel approach. The adsorption behavior of Cu（II） ions on NH2-MNP was discussed systematically by batch experiments. The effects of initial Cu（II） ions concentration, time, pH and temperature were investigated. In kinetic studies, the pseudo-second-order model was successfully employed, and the pseudo-first-order model substantiated that Cu（II） adsorption on NH2-MNP was a diffusion-based process. Langmuir model and Dubinin-Radushkevich model （R2〉0.99） were more corresponded with the adsorption isotherm data of Cu（II） ions than Freundlich model. The adsorption capacity was increased with the increment of temperature and pH. NH2-MNP remains excellent Cu（II） recoveries after reusing five adsorption and desorption cycles, making NH2-MNP a promising candidate for repetitively removing heavy metal ions from environmental water samples. According to the results obtained from adsorption activation energy and thermodynamic studies, it can be inferred that the main adsorption mechanism between absorbent and Cu（II） ions is ion exchange-surface complexation.

Synthesis of Cu2O/Ag Composite with Visible Light Photocatalytic Degradation Activity for in situ SERS Analysis

A multifunctional Cu2O/Ag micro-nanocomposite, which has the characteristics of high cat- alytic activities under the visible light and high surface-enhanced Raman scattering （SERS） activity, was fabricated via a facile method and employed for the in situ SERS monitoring of the photocatalytic degradation reaction of crystal violet. Through the variation of the AgNO3 concentration, Ag content on the Cu2O template can be controllably tuned, which has great influence on the SERS effect. The results indicate that Ag nanopartieles form on the Cu2O nanoframes to obtain the Cu2O/Ag nanoeomposite, which can act as an excellent bifunetional platform for in situ monitoring of photocatalytic degradation of organic pollutions by SERS.

Effects of reaction parameters on preparation of Cu nanoparticles via aqueous solution reduction method with NaBH_4

The preparation of Cu nanoparticles by the aqueous solution reduction method was investigated. The effects of different reaction parameters on the preparation of Cu nanoparticles were studied. The optimum conditions for preparing well-dispersed nanoparticles were found as follows: 0.4 mol/L NaBH4 was added into solution containing 0.2 mol/L Cu2+, 1.0% gelatin dispersant in mass fraction, and 1.2 mol/L NH3?H2O at pH 12 and 313 K. In addition, a series of experiments were performed to discover the reaction process. NH3?H2O was found to be able to modulate the reaction process. At pH=10, Cu2+ was transformed to Cu(NH3)42+ as precursor after the addition of NH3?H2O, and then Cu(NH3)42+ was reduced by NaBH4 solution. At pH=12, Cu2+ was transformed to Cu(OH)2 as precursor after the addition of NH3?H2O, and Cu(OH)2 was then reduced by NaBH4 solution.

Preparation of Cu nanoparticles with ascorbic acid by aqueous solution reduction method

Cu nanoparticles were prepared by reducing Cu2＋ ions with ascorbic acid through aqueous solution reduction method. The effects of solution pH and average size of Cu2O particles on the preparation of Cu nanoparticles were investigated. Cu particles were prepared at pH 3, 5 or 7, with the smallest Cu particles obtained at pH 7. However, Cu particles could not be prepared at pH 9 or 11. The average size of Cu2O particles can affect that of Cu particles. Larger Cu2O particles result in larger Cu particles. In addition, experiments were conducted to explore the reaction process by measuring the X-ray diffraction （XRD） patterns of specimens collected at different time points during the reaction. It was found that Cu（OH）2 was initially formed as a precursor, followed by the formation of Cu2O, which was finally reduced to Cu particles.

Preparation and photocatalytic performance of Cu-doped TiO_2 nanoparticles

Cu-doped TiO2 nanoparticles with different doping contents from 0 to 2.0% （mole fraction） were synthesized through sol-gel method. X-ray diffraction （XRD）, X-ray photoelectron spectroscopy （XPS） and field emission scanning electron microscope （FE-SEM） were used to characterize the crystalline structure, chemical valence states and morphology of TiO2 nanoparticles. UV-Vis absorption spectrum was used to measure the optical absorption property of the samples. The photocatalytic performance of the samples was characterized by degrading 20 mg/L methyl orange under UV-Vis irradiation. The results show that the Cu-doped TiO2 nanoparticles exhibit a significant increase in photocatalytic performance over the pure TiO2 nanoparticles, and the TiO2 nanoparticles doped with 1.0% Cu show the best photocatalytic performance. The improvement in photocatalytic performance is attributed to the enhanced light adsorption in UV-Vis range and the decrease of the recombination rate of photoinduced electron-hole oair of the Cu-doped TiO2 nanoparticles.

Octahedral Cu_2O-modified TiO_2 nanotube arrays for efficient photocatalytic reduction of CO_2

A photocatalyst composed of TiO 2 nanotube arrays（TNTs） and octahedral Cu2 O nanoparticles was fabricated,and its performance in the photocatalytic reduction of CO2 under visible and simulated solar irradiation was studied. The average nanotube diameter and length was 100 nm and 5 μm,respectively. The different amount of octahedral Cu2 O modified TNTs were obtained by varying electrochemical deposition time. TNTs modified with an optimized amount of Cu2 O nanoparticles exhibited high efficiency in the photocatalysis,and the predominant hydrocarbon product was methane. The methane yield increased with increasing Cu2 O content of the catalyst up to a certain deposition time,and decreased with further increase in Cu2 O deposition time. Insufficient deposition time（5 min） resulted in a small amount of Cu2 O nanoparticles on the TNTs,leading to the disadvantage of harvesting light. However,excess deposition time（45 min） gave rise to entire TNT surface being most covered with Cu2 O nanoparticles with large sizes,inconvenient for the transport of photo-generated carriers. The highest methane yield under simulated solar and visible light irradiation was observed for the catalysts prepared at a Cu2 O deposition time of 15 and 30 min respectively. The morphology,crystallization,photoresponse and electrochemical properties of the catalyst were characterized to understand the mechanism of its high photocatalytic activity. The TNT structure provided abundant active sites for the adsorption of reactants,and promoted the transport of photogenerated carriers that improved charge separation. Modifying the TNTs with octahedral Cu2 O nanoparticles promoted light absorption,and prevented the hydrocarbon product from oxidation. These factors provided the Cu2O-modified TNT photocatalyst with high efficiency in the reduction of CO2,without requiring co-catalysts or sacrificial agents.

Fabrication and photocatalytic properties of Cu_2S/T-ZnO_w heterostructures via simple polyol process

The Cu2S/tetrapod-like ZnO whisker（T-ZnOw） heterostructures were successfully synthesized via a simple polyol process employing the poly（vinyl pyrrolidone）（PVP） as a surfactant.The as-prepared heterostructures were characterized by X-ray diffraction（XRD）,field emission scanning electron microscopy（FESEM）,X-ray photoelectron spectroscopy（XPS） and Fourier transform infrared（FTIR）.The photocatalytic properties of Cu2S/T-ZnOw nanocomposites synthesized with different PVP concentrations were evaluated by photodegradation of methyl orange（MO） under UV irradiation.The results show that the Cu2S/T-ZnOw nanocomposites exhibit remarkable improved photocatalytic property compared with the pure T-ZnOw.The sample prepared with 3.0 g/L PVP shows an excellent photocatalytic property and the highest photodegradation rate of MO is 97% after UV irradiation for 120 min.Besides,the photocatalytic activity of the photocatalyst has no evident decrease even after four cycles,which demonstrates that the Cu2S/T-ZnOw photocatalyst exhibits an excellent photostability.Moreover,the photocatalytic mechanism of the Cu2S/T-ZnOw nanocomposites was also discussed.

Electronic and geometric structure of the copper-ceria interface on Cu/CeO2 catalysts

The atomic structure of the active sites in Cu/CeO2 catalysts is intimately associated with the copper-ceria interaction. Both the shape of ceria and the loading of copper affect the chemical bonding of copper species on ceria surfaces and the electronic and geometric character of the relevant interfaces. Nanostructured ceria, including particles(polyhedra), rods, and cubes, provides anchoring sites for the copper species. The atomic arrangements and chemical properties of the(111),(110) and(100) facets, preferentially exposed depending on the shape of ceria, govern the copper-ceria interactions and in turn determine their catalytic properties. Also, the metal loading significantly influences the dispersion of copper species on ceria with a specific shape, forming copper layers, clusters, and nanoparticles. Lower copper contents result in copper monolayers and/or bilayers while higher copper loadings lead to multi-layered clusters and faceted particles. The active sites are usually generated via interactions between the copper atoms in the metal species and the oxygen vacancies on ceria, which is closely linked to the number and density of surface oxygen vacancies dominated by the shape of ceria.

Preparation of copper nanoparticles modified with [BMIm]BF_4 ionic liquid

Copper nanoparticles was prepared by ascorbic acid reducing CuC12 solution modified with [ BMIm ] BF4 ionic liquid. The size of copper nanoparticles was obviously affected by the concentration of Cu2＋ . The diameter of nanoparticles was smaller than 10 nm when the Cu2＋ concentration was smaller than 2× 10.2 moL/L. The pH and temperature of reductive reaction had no obvious effect on the size of copper nanoparticles.

Synthesis of Cu nanoparticles by chemical reduction method

Cu nanoparticles (CuNPs) have been synthesized through an easy route by chemical reduction at room temperature. The Cu^2+ ions were reduced and stabilized with sodium borohydride and polyvinylpyrrolidone, respectively. The effect of the variation of the reducing agent/precursor-salt (RA/PS) ratio on the size and morphology of the CuNPs was evaluated. The synthesized material was studied by ultraviolet-visible (UV-Vis) spectroscopy, X-ray diffraction (XRD), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). The UV-Vis spectra showed a CuNPs plasmon peak at 569 nm and another peak belonging to Cu2O at 485 nm. XRD analysis showed the fcc-Cu phase with a small amount of fcc-Cu2O compound. SEM and TEM studies displayed that small semispherical CuNPs of approximately 7 nm were obtained at the RA/PS ratio of 2.6. The excess of polyvinylpyrrolidone stabilizer played an essential role in preventing CuNPs oxidation. On the other side, Cu2O polyhedral particles with larger sizes up to 150 nm were identified in the RA/PS ratio range of 2.0-1.84. In addition, Cu2O particles having star morphologies with quantum confinement at their tips were obtained at the RA/PS ratio of 1.66.

Synthesis and size control of copper nanoparticles and their catalytic application

The synthesis and catalytic properties of copper nanoparticles（Cunps） were reported using L-ascorbic acid as reducing and capping agent in aqueous medium. The effect of different concentrations of L-ascorbic acid on the particle size of Cunps was investigated. The synthesized Cunps were characterized by UV-Visible spectrophotometer, scanning electron microscopy（SEM）, transmission electron microscopy（TEM） and Fourier transform infrared（FTIR） spectrophotometer. The result indicates that the size of copper nanoparticles decreases with the increase in concentration of L-ascorbic acid. L-Ascorbic acid plays an important role to protect the copper nanoparticles from oxidation and agglomeration which helps nanoparticles to get better stability for the application. The synthesized Cunps show excellent catalytic activity in the oxidation of serine（Ser） by peroxomonosulphate（PMS）. The catalytic activity of Cunps increases with the decrease in size of Cunps. The Cunps are expected to be suitable alternative and play an imperative role in the fields of catalysis and environmental remediation.

Heat transfer of copper/water nanofluid flow through converging-diverging channel

The main objective of this work is to investigate analytically the steady nanofluid flow and heat transfer characteristics between nonparallel plane walls. Using appropriate transformations for the velocity and temperature, the basic nonlinear partial differential equations are reduced to the ordinary differential equations. Then, these equations have been solved analytically and numerically for some values of the governing parameters, Reynolds number, Re, channel half angle, α, Prandtl number, Pr, and Eckert number, Ec, using Adomian decomposition method and the Runge-Kutta method with mathematic package. Analytical and numerical results are searched for the skin friction coefficient, Nusselt number and the velocity and temperature profiles. It is found on one hand that the Nusselt number increases as Eckert number or channel half-angle increases, but it decreases as Reynolds number increases. On the other hand, it is also found that the presence of Cu nanoparticles in a water base fluid enhances heat transfer between nonparallel plane walls and in consequence the Nusselt number increases with the increase of nanoparticles volume fraction. Finally, an excellent agreement between analytical results and those obtained by numerical Runge-Kutta method is highly noticed.

Preparation of Cu nanoparticles with NaBH_4 by aqueous reduction method

Cu nanoparticles were prepared by reducing Cu2＋ ions with NaBH4 in alkaline solution. The effects of NaBH4 concentration and dripping rate on the formation of Cu nanoparticles were studied. The optimum conditions are found to be 0.2 mol/L Cu2＋, solution with pH=12, temperature of 313 K and 1% gelatin as dispersant, to which 0.4 mol/L NaBH4 is added at a dripping rate of 50 mL/min. NH3-H2O is found to be the optimal complexant to form the Cu precursor. A series experiments were conducted to study the reaction process at different time points.

On the comparable activity in plasmonic photocatalytic and thermocatalytic oxidative homocoupling of alkynes over prereduced copper ferrite

Despite of extensive attention on the copper-based heterogeneous oxidative homocoupling of alkynes(OHA)to 1,3-diynes,the photocatalytic OHA is scarcely investigated.By screening copper-containing spinel catalysts,we discovered that a prereduced copper ferrite(CuFe2O4)not only can catalyze the thermocatalytic OHA but also is efficient for the photocatalytic OHA under visible light irradiation.It is found that the sol-gel combustion(SG)method and the partial reduction at 250 ℃ can result in the optimal CuFe2O4-SG-250 catalyst showing high activity and stability.Surface oxidized Cu2O is evidenced to be the active species for the thermocatalytic OHA,whereas metallic copper nanopaticles(CuNPs)are identified as the active sites for the photocatalytic OHA.The efficiency of photocatalytic OHA at ambient temperature is comparable to that of thermocatalytic OHA at 120 ℃,and the CuFe2O4-SG-250 catalyst can be magnetically separated and reused at least five times.The localized surface plasmon resonance effect of CuNPs contributes to visible light-induced photocatalytic OHA.

Preparation and characterization of polyvinylchloride membrane embedded with Cu nanoparticles for electrochemical oxidation in direct methanol fuel cell

Copper nanoparticles were prepared by the chemical reduction method.These copper particles were embedded into the polyvinylchloride(PVC)matrix as support and used as an electrode(PVC/Cu)for the oxidation of methanol fuel for improving the current response.The PVC/Cu electrodes were characterized by thermal gravimetric analysis(TGA)for thermal stability of the electrode,X-ray diffraction(XRD)for identification of copper nanoparticles in the electrode,Fourier transform infrared spectroscopy(FTIR)to identify the interaction between PVC and Cu and scan electron microscopy(SEM)with EDAX for the morphology of the electrode.The electrocatalytic activity of the electrode was characterized by the cyclic voltammetry,linear sweep voltammetry,and chronoamperometry techniques.An increase in the electrode activity was observed with the increase of copper quantity from 0.18 g(PVC/Cu-0.18 g)to 0.24 g(PVC/Cu-0.24 g)and the maximum was found at 0.24 g of copper in the electrode.Also,it was observed that the electrode achieved the maximum catalytic current in 0.5 mol/L CH3OH+1 mol/L Na OH solution.FTIR identified that water molecules,C—H group,copper nanoparticle and its oxide were available in the electrode.SEM images with EDAX showed that copper particles were properly embedded in the polyvinylchloride matrix.