二苯碳酰二肼分光光度法测定磁性材料中的铬(Ⅵ)

在硫酸介质中,二苯碳酰二肼可与铬(VI)发生显色反应生成紫红色的络合物,该络合物在540 nm波长处有最大吸收峰,由此建立测定磁性材料中铬(VI)含量的分光光度分析方法。本文对测定波长、显色pH值、显色剂用量以及显色时间等实验条件进行优化,在最佳实验条件下,络合物在540nm处的吸光度值与铬(VI)的浓度在0～0.3mg/L范围内呈良好的线性关系,其线性方程为A=0.839C-0.0048(c∶mg/L),相关系数r=0.9999;检出限为3.85×10~(-4)mg/L,回收率为94%～105%。采用碱浸煮方法提取磁性材料中的铬(VI),并用该方法对样品中铬(VI)的含量进行测定,并与SGS测得的结果进行对比。结果表明,该法的测定结果与SGS测得的结果相一致。该方法具有操作简便、快捷的优点,用于磁性材料中铬(VI)的测定,所得结果令人满意。     

Facile Fabrication and Superparamagnetism of Silica‐Shielded Magnetite Nanoparticles on Carbon Nitride Nanotubes

Using conventional methods to synthesize magnetic nanoparticles (NPs) with uniform size is a challenging task. Moreover, the degradation of magnetic NPs is an obstacle to practical applications. The fabrication of silica‐shielded magnetite NPs on carbon nitride nanotubes (CNNTs) provides a possible route to overcome these problems. While the nitrogen atoms of CNNTs provide selective nucleation sites for NPs of a particular size, the silica layer protects the NPs from oxidation. The morphology and crystal structure of NP–CNNT hybrid material is investigated by transmission electron microscopy (TEM) and X‐ray diffraction. In addition, the atomic nature of the N atoms in the NP–CNNT system is studied by near‐edge X‐ray absorption fine structure spectroscopy (nitrogen K‐edge) and calculations of the partial density of states based on first principles. The structure of the silica‐shielded NP–CNNT system is analyzed by TEM and energy dispersive X‐ray spectroscopy mapping, and their magnetism is measured by vibrating sample and superconducting quantum interference device magnetometers. The silica shielding helps maintain the superparamagnetism of the NPs; without the silica layer, the magnetic properties of NP–CNNT materials significantly degrade over time.     

Temperature‐Sensitive Nanocapsules for Controlled Drug Release Caused by Magnetically Triggered Structural Disruption

Self‐assembled nanocapsules containing a hydrophilic core and a crosslinked yet thermosensitive shell are successfully prepared using poly(ethylene‐oxide)‐poly(propylene‐oxide)‐poly(ethylene‐oxide) block copolymers, 4‐nitrophenyl chloroformate, gelatin, and 1‐ethyl‐3‐(3‐dimethylaminopropyl) carbodiimide. The core is further rendered magnetic by incorporating iron oxide nanoparticles via internal precipitation to enable externally controlled actuation under magnetic induction. The spherical nanocapsules exhibit a hydrophilic‐to‐hydrophobic transition at a characteristic but tunable temperature reaching 40 °C, triggering a size contraction and shrinkage of the core. The core content experiences very little leakage at 25 °C, has a half life about 5 h at 45 °C, but bursts out within a few minutes under magnetic heating due to iron oxide coarsening and core/shell disruption. Such burst‐like response may be utilized for controlled drug release as illustrated here using a model drug Vitamin B12.     

Surface Modification of Exfoliated Layered Gadolinium Hydroxide for the Development of Multimodal Contrast Agents for MRI and Fluorescence Imaging

A novel method for modifying the surface of magnetic‐resonance‐contrasting layered gadolinium hydroxide (LGdH) is developed providing them with water‐ and bio‐compatibility and acid‐resistance, all of which are essential for medical applications. A stable colloid of exfoliated layers is synthesized by exchanging interlayer anions of LGdH with oleate ions. The delaminated layers are successively coated with phospholipids with poly(ethylene glycol) tail groups, and their effectiveness as a contrast agent for magnetic resonance imaging (MRI) is demonstrated. The adaptability of this surface modification approach for incorporating functional molecules and fabricating a fluorescent colloid of LGdH, which has the potential utility as a multimodal probe, is also demonstrated. This result provides a novel approach for expanding the applications of layered inorganic materials and developing a new class of MRI contrast agents.     

Nanoshells with Targeted Simultaneous Enhancement of Magnetic and Optical Imaging and Photothermal Therapeutic Response

Integrating multiple functionalities into individual nanoscale complexes is of tremendous importance in biomedicine, expanding the capabilities of nanoscale structures to perform multiple parallel tasks. Here, the ability to enhance two different imaging technologies simultaneously—fluorescence optical imaging and magnetic resonance imaging—with antibody targeting and photothermal therapeutic actuation is combined all within the same nanoshell‐based complex. The nanocomplexes are constructed by coating a gold nanoshell with a silica epilayer doped with Fe₃O₄ and the fluorophore ICG, which results in a high T₂ relaxivity (390 mM ^?1 s^?1) and 45× fluorescence enhancement of ICG. Bioconjugate nanocomplexes target HER2+ cells and induce photothermal cell death upon near‐IR illumination.     

Porous Polymersomes with Encapsulated Gd‐Labeled Dendrimers as Highly Efficient MRI Contrast Agents

The use of nanovesicles with encapsulated Gd as magnetic resonance (MR) contrast agents has largely been ignored due to the detrimental effects of the slow water exchange rate through the vesicle bilayer on the relaxivity of encapsulated Gd. Here, the facile synthesis of a composite MR contrast platform is described; it consists of dendrimer conjugates encapsulated in porous polymersomes. These nanoparticles exhibit improved permeability to water flux and a large capacity to store chelated Gd within the aqueous lumen, resulting in enhanced longitudinal relaxivity. The porous polymersomes, ～130 nm in diameter, are produced through the aqueous assembly of the polymers, polyethylene oxide‐b‐polybutadiene (PBdEO), and polyethylene oxide‐b‐polycaprolactone (PEOCL). Subsequent hydrolysis of the caprolactone (CL) block resulted in a highly permeable outer membrane. To prevent the leakage of small Gd‐chelate through the pores, Gd was conjugated to polyamidoamine (PAMAM) dendrimers via diethylenetriaminepentaacetic acid dianhydride (DTPA dianhydride) prior to encapsulation. As a result of the slower rotational correlation time of Gd‐labeled dendrimers, the porous outer membrane of the nanovesicle, and the high Gd payload, these functional nanoparticles are found to exhibit a relaxivity (R1) of 292 109 mM ^?1 s^?1 per particle. The polymersomes are also found to exhibit unique pharmacokinetics with a circulation half‐life of >3.5 h and predominantly renal clearance.     

Some mechanisms concerning the electrical conductivity of magnetorheological suspensions in magnetic field

Iron carbonyl is decomposed, at the temperature of 473 K ± 10%, into a liquid matrix formed of silicone oil and stearic acid. For 3.703% and 1.886% stearic acid, magnetorheological suspensions (MRSs) are obtained. The iron particles in MRSs have the mean diameter of 0.356 μm. Magnetoresistors are achieved from MRSs with the dimensions of diameter and length equal to 5 mm. In longitudinal magnetic field, the resistance of the magnetoresistors is measured. Assimilating the resistance of the magnetoresistors with that of a linear resistor, the conductivity σ of MRS is determined. The duration t_c of onset of σ is determined. It is observed that t_c is considerably influenced by the intensity of the magnetic field applied and by the composition of MRSs. Experimental data are discussed, too.     

Influence of magnetic field upon the electric capacity of a flat capacitor having magnetorheological elastomer as a dielectric

The flat capacitor is built of two non-magnetic plates (with dimensions 0.065 m × 0.050 m) between which there is a layer of magnetorheological elastomer (MRE). The thickness of the layer is 0.0015 m ± 10%. MRE is based on silicone rubber and iron particles. The iron particles diameter ranges between 0.12 μm and 0.75 μm. The electric capacity, in absence of the magnetic field, is 377 ± 1 pF. In cross magnetic field with strengths up to 94 kA/m, the flat capacitor's capacity increases by up to 200%. For well chosen values of the intensity of the magnetic field, the capacity of the flat capacitor with MRE changes with time. The experimental results obtained in this manner are discussed.     

Preparation and characterization of magnetite/dextran nanocomposite used as a precursor of magnetic fluid

Magnetic nanoparticles were synthesized by the co-precipitation of Fe²⁺ and Fe³⁺ using ammonium hydroxide (NH₄OH). The obtained nanoparticles were characterized by X-ray powder diffraction, transmission electron microscopy, scanning electron microscopy, Fourier transform infrared (FT-IR) spectroscopy and vibrating sample magnetometer. In order to prepare a biocompatible water-based magnetic fluid, the nanoparticles were modified by dextran through a two-step method. The influences of dextran molecular weight on the size, morphology, coating efficiency and magnetic property of magnetite/dextran nanocomposite were investigated. The magnetite/dextran nanocomposite was dispersed in water to form a magnetic fluid by ball milling. The rheological property of magnetic fluids was investigated using a rotating rheometer.     

Size effects on charge ordering and magnetic properties in La0.25Ca0.75MnO3

The size effects on the charge ordering (CO) and magnetic properties in La_0.25Ca_0.75MnO₃ with mean particle size ranging from 40 to 2000 nm were studied. With decreasing particle size the CO transition temperature shifts to lower temperature and the transition width becomes increasingly wide, indicating the weakening of the CO state. Meanwhile the ferromagnetic (FM) cluster glass state appears and the magnetization at low temperature increases significantly. The behaviour is due to the increasing uncompensated surface spins which weaken the antiferromagnetic interaction and disfavour the formation of the CO state. The suppression of the CO state and appearance of the FM cluster glass state are also found in La_0.25Ca_0.75MnO₃ nanowires fabricated by a sol–gel template method. These results indicate that the CO state can be modulated effectively by varying particle size, which has an important implication for nano-device applications of manganites.