Accumulation and residue of napropamide in alfalfa (Medicago sativa) and soil involved in toxic response

Napropamide belongs to the amide herbicide family and widely used to control weeds in farmland. Intensive use of the herbicide has resulted in widespread contamination to ecosystems. The present study demonstrated an analysis on accumulation of the toxic pesticide napropamide in six genotypes of alfalfa (Medicago sativa), along with biological parameters and its residues in soils. Soil was treated with napropamide at 3 mg kg(-1) dry soil and alfalfa plants were cultured for 10 or 30 d, respectively. The maximum value for napropamide accumulation is 0.426 mg kg(-1) in shoots and 2.444 mg kg(-1) in roots. The napropamide-contaminated soil with alfalfa cultivation had much lower napropamide concentrations than the control (soil without alfalfa cultivation). Also, the content of napropamide residue in the rhizosphere was significantly lower than that in the non-rhizosphere soil. M. sativa exposed to 3 mg kg(-1) napropamide showed inhibited growth. Further analysis revealed that plants treated with napropamide accumulated more reactive oxygen species (O(2)(-) and H(2)O(2)) and less amounts of chlorophyll. However, not all cultivars showed oxidative injury, suggesting that the alfalfa cultivars display different tolerance to napropamide.     

Insight into the binding of copper(II) by non-toxic biodegradable material (Oryza sativa): effect of modification and interfering ions

The present studies are focused on the use of non-toxic biodegradable straw from Oryza sativa in its simple and modified forms for the binding of copper(II) ions. A relatively new “green” method was adopted for modification with urea under microwaves. The studies have been performed by using the aqueous solution of Cu(II) ions with and without the presence of Cd(II) and Pb(II) as interfering ions. FTIR analysis showed the presence of oxygen- and nitrogen-containing functional groups in simple and modified materials. The emergence of new bands and shifts in the peaks confirmed the modification. The kinetics of the process was studied using the commonly employed mathematical models. Although Elovich model seemed to fit yet coefficient of determination did not reinforce it. Pseudo-second-order model was found to explain the kinetics of the binding of metal ions by simple and modified straw. The equilibrium was studied using the non-linear approach. Based on root mean square error values, it was found that Langmuir model was the most suitable model, followed by Temkin model. Surface areas were compared for single and multi-metal systems. The effect of pH was also studied. Under the studied set of conditions, the modification of straw caused a decrease in the equilibrium time of contact and increase in the biosorption capacities. The presence of other ions decreased the capacities drastically due the competition to bind with the materials.     

Effects of calcium competition on lead sorption by palm kernel fibre

The kinetics of sorption of a mono-solute of lead ions and of a bi-solute of lead and calcium ions onto palm kernel fibre was investigated in a batch system. The experimental data were analysed based on an intraparticle diffusion equation and a pseudo-second-order mechanism, in both the mono- and bi-solute sorption systems, in order to predict the rate constant of sorption, the equilibrium capacity, and the initial sorption rate. The results indicate that the sorption mechanism is described by a pseudo-second-order equation. Intraparticle diffusion was significant in the lower-concentration systems. In addition, a modified intraparticle diffusion equation was applied to the sorption systems.     

The competition growth of ZnO microrods and nanorods in chemical bath deposition process

Well-aligned ZnO nanorod arrays were synthesized on the c-axis orientated ZnO seed layer by chemical bath deposition (CBD) technique. Randomly distributed ZnO microrods with big diameter and growth speed were also formed simultaneously in the same process. The growth of the microrods followed the expected diffusion-limited Ostwald ripening mechanism reasonably well, while that of the nanorods was suggested to be controlled not only by the nutrition ions available but also by the density of nuclei site and the reaction kinetics on the growing surfaces, etc. The microstructure and optical properties of the well-ordered nanorod were also investigated.     

Effects of exposure time and co-existing organic compounds on uptake of atrazine from nutrient solution by rice seedlings (Oryza sativa L.)

Root uptake of atrazine (ATR) by rice seedlings (Oryza sativa L.) from nutrient solution was investigated with exposure periods of 48, 96, and 240h. A similar ATR uptake was carried out with two co-existing organic compounds (o-chlorophenol (CP) and 2,4-dichlorophenol (DCP)) with 48h exposure. In contact with the seedlings, the ATR level in nutrient solution decreased sharply during the early exposure and then reached relatively steady levels after 48h. It was observed that the ATR levels within whole seedlings approached the estimated equilibrium partition limits in about 48h, according to the partition-limited model utilizing the measured plant water and organic matter contents and the ATR partition coefficients with whole seedlings. However, when roots and shoots were consisted separately, the detected ATR levels in roots were lower than estimated equilibrium limit while the levels in shoots exceeded the equilibrium limit. The data with roots suggested the occurrence of rapid ATR degradation in roots. The results with shoots are intrinsically consistent with the suggested complex formation of ATR with free metal ions in shoots. The ATR levels in roots and shoots varied to a moderate extent when the seedlings were exposed to different levels of ATR-CP-DCP mixtures. The variation results presumably from the interference of coexisting CP and DCP and the phytotoxicity of the mixed chemicals.     

Effects of temperature on ZnO hybrids grown by metal-organic chemical vapor deposition

The growth of three-dimensional ZnO hybrid structures by metal-organic chemical vapor deposition was controlled through their growth pressure and temperature. Vertically aligned ZnO nanorods were grown on c-plane of sapphire substrate at 600 °C and 400 Torr. ZnO film was then formed in situ on the ZnO nanorods at 100, 600, and 700 °C and 10 Torr. High-resolution X-ray diffraction measurements showed that the ZnO film on the nanorods/sapphire grew epitaxially, and that the ZnO film/nanorods hybrid structures had well-ordered wurtzite structures. The hybrid ZnO structure was shown to be about 3–5 μm by field-emission scanning electron microscopy. The hybrid formed at 600 °C showed better crystalline quality those formed at 100 °C or 700 °C. These structures have potential applicability as nanobuilding blocks in nanodevices.     

Effects of polycrystalline cu substrate on graphene growth by chemical vapor deposition

Chemical vapor deposition of graphene on Cu often employs polycrystalline Cu substrates with diverse facets, grain boundaries (GBs), annealing twins, and rough sites. Using scanning electron microscopy (SEM), electron-backscatter diffraction (EBSD), and Raman spectroscopy on graphene and Cu, we find that Cu substrate crystallography affects graphene growth more than facet roughness. We determine that (111) containing facets produce pristine monolayer graphene with higher growth rate than (100) containing facets, especially Cu(100). The number of graphene defects and nucleation sites appears Cu facet invariant at growth temperatures above 900 °C. Engineering Cu to have (111) surfaces will cause monolayer, uniform graphene growth.     

Effects of complexing agent on CdS thin films prepared by chemical bath deposition

CdS films have been prepared by chemical bath deposition (CBD) without stirring using weak and strong complexing agents, i.e., ammonia and ethylenediaminetetraacetic acid (EDTA). The optical, structural, and morphological properties of chemical bath deposited CdS films have been investigated. When the complexing agent is ammonia, five peaks in the X-ray diffraction (XRD) patterns from the CdS film, respectively, correspond to the interplanar spacing of 3.5498, 3.3429, 3.1449, 2.0574, and 1.7487 Å, which are definitely ascribed to hexagonal structure; unfortunately, this hexagonal CdS film is with poor morphology and its optical property in the visible region is not desirable for the solar cells. While, when the complexing agent is EDTA, three diffraction peaks in the XRD patterns from the CdS film, respectively, correspond to the interplanar spacing of 3.1164, 2.6716, and 1.8507 Å, indicating that the film is of a cubic structure. Furthermore, the CdS film has good morphology and its optical property in the visible region is compliant to the requirements of solar cells.     

An investigation by electron spectroscopy for chemical analysis of chemical treatments of the (100) surface of n-type InP epitaxial layers for Langmuir film deposition

The surface chemistry of InP substrates used for the fabrication of electronic devices (MIS structures) was examined by ESCA. Spectroscopic data on related materials such as indium metal, plasma-oxidized indium metal, In₂O₃, InPO₄(xH₂O), P₄O₁₀, AlPO₄, (C₆H₅O)₃PO and (C₆H₅)₃P were collected so as to aid the assignment of components in the spectra of as-received and etched InP surfaces on the basis of the chemical shifts and the intensity ratios. Surface features of InP substrates from several batches were examined in the as-received and the chemically etched forms. The effectiveness of several types of etchants and the features thus produced on the substrate surface were evaluated and are discussed.     

Effects of hydrogen on the formation of aligned carbon nanotubes by chemical vapor deposition

Well-aligned carbon nanotubes with controllable properties were grown on porous silicon substrates by thermal chemical vapor deposition. The morphologies of the carbon nanotubes were varied with the introduction of H2 during the catalyst activation and/or carbon nanotube growth processes. It was found that H2 promotes the growth of carbon nanotubes while preventing the formation of spherical amorphous carbon particles. Without the introduction of H2 during the C2H2 thermal decomposition, aligned carbon nanotubes mixed with spherical carbon particles were formed on the substrate. However, with the introduction of H2, pure carbon nanotubes were synthesized. These nanotubes also had uniform diameters of 10-20 nm, which is much smaller than nanotubes synthesized without H2. The average growth rate of nanotubes was also affected by the introduction of hydrogen into the reaction chamber during nanotube growth. With the addition of hydrogen, the average growth rate changed from 78 nm/s to 145 nm/s. A possible growth mechanism, including the effect of a high ratio of H2 to C2H2, is suggested for the growth of these well-aligned carbon nanotubes with uniform diameters.     

Effects of ambient conditions on the quality of graphene synthesized by chemical vapor deposition

In this work, we investigated the effects of methane concentration and gas flow rate ratio between hydrogen and methane on the quality of graphene synthesized by chemical vapor deposition. It is found that a critical concentration of methane is needed to grow continuous graphene films, while discontinuous graphene flakes are formed at low methane concentrations. Under the condition without hydrogen, a graphene film in which monolayer areas are predominant is grown, whereas a great proportion of hydrogen causes thick graphene, which reduces the transmittance of the film. Our results present an instructive reference to the large-area synthesis of graphene for the potential applications in electronics.     

Biosynthesis of controllable size and shape gold nanoparticles by black seed (Nigella sativa) extract

We report on the use of black seed (Nigella sativa) extract, previously not exploited, in synthesis of gold nanoparticles. On treating aqueous chloroauric acid solution with black seed extract, the antioxidant activities critical roles of the various phytochemicals is observed leading to the formation of crystalline and poly shaped gold nanoparticles. In this research work, we developed a rapid and non-toxic method for the preparation of biocompatible gold nanoparticles by two different synthetic routes: microwave irradiation and thermo-induced procedures. The nanoparticles were characterized and investigated by ultraviolet-visible (UV-Vis) spectrophotometry, transmission electron microscopy (TEM), energy-dispersive X-ray (EDX) spectroscopy, and X-ray diffraction (XRD).The size and shape of the nanoparticles were found to be very sensitive to the quantity of the extract. As the amount of extract is increased, the stronger the interaction between the extract biomolecules and nascent nanoparticles, thus the yield of nanoparticles increased as shown by surface plasmon resonance bands in the UV-vis-NIR spectra. The reaction temperature has a significant role in production of gold nanoparticles with different shapes. The XRD studies reflect an interesting feature indicates that gold nanocrystals are highly anisotropic in nature, mainly triangular and hexagonal shapes, and that the particles are (111) oriented. The observed characteristics suggest the application of the biocompatible gold nanoparticles to future in vivo imaging and therapy.     

Photocatalytic TiO(2) deposition by chemical vapor deposition

Dip-coating, spray-coating or spin-coating methods for crystalline thin film deposition require post-annealing process at high temperature. Since chemical vapor deposition (CVD) process is capable of depositing high-quality thin films without post-annealing process for crystallization, CVD method was employed for the deposition of TiO(2) films on window glass substrates. Post-annealing at high temperature required for other deposition methods causes sodium ion diffusion into TiO(2) film from window glass, resulting in the degradation of photocatalytic efficiency. Anatase-structured TiO(2) thin films were deposited on window glass by CVD, and the photocatalytic dissociation rates of benzene with CVD-grown TiO(2) under UV exposure were characterized. As the TiO(2) film deposition temperature was increased, the (112)-preferred orientations were observed in the film. The (112)-preferred orientation of TiO(2) thin film resulted in a columnar structure with a larger surface area for benzene dissociation. Obviously, benzene dissociation rate was maximum when the degree of the (112) preferential orientation was maximum. It is clear that the thin film TiO(2) should be controlled to exhibit the preferred orientation for the optimum photocatalytic reaction rate. CVD method is an alternative for the deposition of photocatalytic TiO(2).     

Effects of organic solvents on hyaluronic acid nanoparticles obtained by precipitation and chemical crosslinking

Hyaluronic acid is a hydrophilic mucopolysaccharide composed of alternating units of D-glucuronic acid and N-acetylglucosamine. It is used in many medical, pharmaceutical, and cosmetic applications, as sponges, films, or particle formulations. Hyaluronic acid nanoparticles can be synthesized free of oil and surfactants by nanoprecipitation in organic solvents, followed by chemical crosslinking. The organic solvent plays an important role in particles size and structure. Therefore, this study aimed to investigate the influence of acetone, ethanol, and isopropyl alcohol on the synthesis and physico-chemical properties of hyaluronic acid nanoparticles. Particles were crosslinked with adipic hydrazide and chloride carbodiimide under controlled conditions. The nanoparticles obtained with all three studied solvents were moderately electrostatically stable. Experiments with acetone produced the smallest particle size (120.44 nm) and polydispersity (0.27). The size and polydispersity of hyaluronic acid nanoparticles correlated with the surface tension between water and the organic solvents, not with the thermodynamic affinity of water for the organic solvents.     

Effects of methane partial pressure on synthesis of single-walled carbon nanotubes by chemical vapor deposition

A series of experiments have been done to investigate the role of methane partial pressure in the synthesis of carbon nanotubes by catalyst chemical vapor deposition. It is supposed that there is a critical methane partial pressure (0.4 atm) for single-walled carbon nanotube (SWNT) synthesis at 850°C. When the methane partial pressure is higher than the critical value, the whole rate is decided by the carbon diffusion rate on the catalyst surface or in the bulk, contrariwise, the synthesis rate is proportional to the methane partial pressure.     

Factors affecting the chemical stability of carboxylic acid drugs in Enhanced Solubility System (ESS) Softgel Formulations Based on Polyethylene Glycol (PEG).

Drug decomposition in ESS softgel formulations of three monocarboxylic acid drugs was measured after accelerated storage of solutions at 105 deg C for 3 or 7 days. Drug decompostion occured primarily by reaction between the unionised carboxylic acid function of the drug and the alcoholic groupings of the components in the solvent (e.g. PEG, glycerin) to form mainly the corresponding mono-esters. The ionised form of the drug was relatively unreactive. Different solvents were evaluated and the corresponding drug decomposition rates were explained in terms of the alcoholic group content of the solvent components. The presence of water in the formulation decreased the reaction rate. A rate equation was derived and utilised to compare chemical stabilities of related formulations. The stabilities of similar ESS formulations of the three drugs were greatly different due to differences in the intrinsic reactivities of the drugs The findings of this study can be used to maximise chemical stability of ESS formulations of carboxylic acid drugs.     

定向碳纳米管的化学气相沉积制备法

报道了一种简便有效的合成定向碳纳米管 (CNTs)的化学气相沉积 (CVD)制备方法。以铁为催化剂 ,乙炔为碳源 ,采用单一反应炉 ,直接在石英基底上沉积催化剂颗粒薄膜 ,成功合成了定向性好、管径均匀的高质量大密度的碳纳米管