Effectiveness of Metal–Metal and Metal–Organic Compound Combinations Against Plutella xylostella: Implications for Plant Elemental Defense

Plants that contain elevated foliar metal concentrations can be categorized as accumulators or, if the accumulation is extreme, hyperaccumulators. The defense hypothesis suggests that these plants may be defended against folivore attack, and recent research has indicated that metal concentrations at or below the accumulator range may be defensively effective. This experiment explored the toxicity of four metals hyperaccumulated by plants (Cd, Ni, Pb, and Zn) and asked if combinations of metals, or metals and organic chemicals, might broaden the defensive effectiveness of metals. Metals were used alone and in certain metal + metal (Zn plus Ni, Pb, or Cd) and metal + organic defensive chemical (Ni plus tannic acid, atropine, or nicotine) combinations. Artificial diet amended with these treatments was fed to larvae of the crucifer specialist herbivore Plutella xylostella. Combinations of metals and metals + organic chemicals significantly decreased survival and pupation rates, compared to single treatments, for at least some concentrations in every experiment. Effects of combinations were additive rather than synergistic or antagonistic. Because Zn enhanced the toxicity of other metals and Ni enhanced the toxicity of organic defensive chemicals, our findings suggest that the defensive effects of metals are more widespread among plants than previously believed. They also support the hypothesis that herbivore defense may have led to the evolution of metal hyperaccumulation by increasing the preexisting defensive effects of metals at accumulator levels in plants.     

Preparation of Polymers Containing Metal–Metal Bonds along the Backbone Using Click Chemistry

The [(η⁵-C₅H₄(CH₂)₃OC(O)(CH₂)₂C≡CH)Mo(CO)₃]₂ complex (1) was synthesized and used to explore the feasibility of using the Huisgen cycloaddition reaction (a click reaction) to incorporate molecules with metal–metal bonds into polymer backbones. In a model reaction, coupling of 1 with benzyl azide was observed in 24 h using Cp*Ru(PPh₃)₂Cl as a catalyst. In contrast, the reaction of 1 with benzyl azide using a CuBr/ligand catalyst (where the ligand is either PMDETA or bipyridine), resulted in disproportionation of the Mo–Mo unit in 1. Complex 1 was also coupled with telechelic azide-terminated polystyrene oligomers. With either the CuBr/PMDETA or CuBr/bipyridine catalyst, disproportionation of the Mo–Mo bonded unit occurred before complete coupling was observed. The reaction was also slow when the Cp*Ru(PPh₃)₂Cl catalyst was used; however, no disproportionation products were observed and a high molecular weight polymer (M _n = 120,000 g/mol) was produced. The Cp*Ru(PPh₃)₂Cl catalyst was also used to couple 1 with azide-terminated poly(ethylene glycol). After 15 h, this reaction produced a polymer with M _n = 73,000 g mol⁻¹. It is concluded that, although somewhat slow, click chemistry using the Cp*Ru(PPh₃)₂Cl catalyst is an excellent method for synthesizing high molecular weight polymers with metal–metal bonds along the backbone.     

Metal Complexes of π-Conjugated Polymers

π-Conjugated chelating polymers such as poly(2,2′-bipyridine-5,5′-diyl), poly(1,10-phenanthroline-3,8-diyl), and salophen polymers have been prepared by organometallic polycondensations. The obtained polymers form metal complexes with various metal species such as [Ru(bpy)₂]²⁺ and CuCl₂. Metal complexes of π-conjugated ligands are also polymerized by dehalogenative organometallic polycondensations. Some of the metal complexes of π-conjugated polymers exhibit electrical conducting nature and show catalytic activity for redox reactions.     

Evaluation of the Effect of Nanosilica on Thermal and Mechanical Properties of Metal–Metal and Metal–Glass Canola-Based Polyurethane/Nanosilica Adhesives

Nanocomposites with different concentration of nanofiller were prepared by adding nanosilica to the canola-based polyurethane matrix via in situ polymerization. The effect of nanosilica on the mechanical properties of adhesives was evaluated by tensile tests. Adhesive characteristics on metal–metal and metal–glass bondings were also evaluated by lap shear strength tests. Incorporation of nanosilica into the canola-based polyurethane enhanced both tensile and lap shear strength of synthesized adhesives. Also the effect of nanoparticles on glass transition temperature and thermal stability was investigated by differential scanning calorimetry and thermogravimetric analysis, respectively. The increase of nanosilica content in the polyurethane adhesives, thermal property of the nanocomposites improved.     

Prospect of Refractory for Hot Metal Pretreatment

The paper describes the recent developing situation and the latest research achievements of refractory for hot metal pretreatment. The relationship among desiliconization, dephosphorization and desulphurization techniques and the main corrosion reactions by various treating agents is analyzed. Some improving measures for several problems in practice are put forward while we anticipate the future developing direction of refractory for hot metal pretreatment.     

A Strategy for Preparing Star Polymers Containing Metal–Metal Bonds Along the Polymeric Arms Using Click Chemistry

The [(η⁵-C₅H₄(CH₂)₃N₃)Mo(CO)₃]₂ dimer (3) was prepared and used to determine if the Huisgen cycloaddition reaction could be used to synthesize high molecular weight star polymers with metal–metal bonds in the arms. Several different click catalysts were examined. Cp*Ru(PPh₃)₂Cl (Cp* = η⁵-C₅(CH₃)₅) was previously shown to catalyze the formation of metal–metal bond-containing polymers using click chemistry; however, this catalyst underwent a Staudinger reaction with dimer 3 when a model coupling reaction was attempted with phenylacetylene. In order to avoid the Staudinger reaction, Cp*Ru(COD)Cl was used as the catalyst in the reaction of 3 with phenylacetylene, and coupling was observed after 14 h. Synthesis of a star polymer was attempted with 3 and 1,3,5-triethynylbenzene. Instead of coupling, Cp*Ru(COD)Cl reacted with the 1,3,5-triethynylbenzene. A third catalyst, Cu(IMes)Cl (IMes = 1,3-dimesityl-imidazol-2-ylidene) was used to couple 3 with 1,3,5-triethynylbenzene in 48 h. Both a high molecular weight polymer (M _n  = 77,000 g mol^?1) and a tripodal star core (M _n  = 1,800 g mol^?1) were successfully prepared with this catalyst.     

Metal–support interactions on rhodium model catalysts

Metal–support interactions on supported rhodium catalysts were studied by using specially prepared Rh/TiO₂/Mo model systems. For their characterization and the analysis of modifications due to various heat treatments several surface analytical methods were applied: low-energy ion scattering, X-ray photoemission spectroscopy and thermal desorption spectroscopy. Heating in ultrahigh vacuum to 670 K leads to Rh agglomeration followed (above 720 K) by encapsulation including the formation of reduced titanium oxide species. These morphological and chemisorption changes are reversible upon reoxidation and low-temperature reduction and thus exhibit the characteristic features of strong metal–support interactions. For the effective mechanism a reaction is suggested that involves oxygen chemisorption on the Rh clusters and partial reduction of the surrounding support oxide.     

Metal–thermoplastic urethane hybrids in environmental exposure

The long-term properties of injection moulded metal–thermoplastic urethane (TPU) hybrids were studied. The hybrids manufactured with different metal substrates, namely copper, stainless steel and aluminium, were compared, using two surface modifications for copper and stainless steel. N-(β-aminoethyl)-γ-aminopropyltrimethoxysilane was used as coupling agent. It is concluded that the bond mechanism of the silane on different substrate differs, affecting the long-term behaviour of the respective hybrids. The thick layers of silane coupling agent on copper and stainless steel are sensitive to hydrolysis; thus the resistance in humid conditions is quite low. The high temperature exposure increased the bond strength and the fraction of cohesive failure in TPU in copper–TPU, aluminium–TPU and polished steel–TPU hybrids. The last one has native mixed oxide, contrary to controlled oxidised stainless steel, where adhesion decreased after any long-term experiments. This is suggested to derive from hydrogen bonding of the coupling agent to the surface Fe₂O₃ oxide.     

Dick Cepek首次推出Gun Metal 7轮毂

美国《现代轮胎经销商》(www.moderntire-dealer.com)2012年4月19日报道:Dick Cepek Gun Metal Gray 7轮毂(见图1)有17和20英寸两种规格。     

Dick Cepek首次推出Gun Metal 7轮毂

美国《现代轮胎经销商》（www.moderntire-dealer.com）2012年4月19日报道： Dick Cepek Gun Metal Gray 7轮毂（见图1）有17和20英寸两种规格。     

Self-Assembly of Nanostructures on Surfaces Using Metal–Organic Coordination

Layer-by-layer (LbL) assembly of multilayers is an established method for the construction of layered nanostructures on surfaces, affording control of the thickness, composition, and organization in the vertical direction. Binding between layers is accomplished using various types of interactions, including electrostatic binding, hydrogen bonding, covalent bonding, metal–organic coordination, host–guest interactions, biospecific interactions, and others. Here we focus on LbL assembly using metal–organic coordination, and specifically on layered nanostructures based on bishydroxamate–M⁴⁺ binding. The coordination approach offers attractive features, such as a simple reaction, a defined geometry, and reversibility under certain conditions. The basic scheme includes self-assembly of a ligand (anchor) monolayer on the surface, followed by alternate binding of metal ions and multi-functional ligand layers, to form a coordination multilayer. This approach is demonstrated by the construction of a variety of coordinated nanostructures, including bilayers, multilayers, dendrimers, and nanoparticle assemblies, prepared on gold and oxide substrates.     

Metal–insulator transition in boron-ion implanted type IIa diamond

Electrical conductivity measurements for selected boron-ion dopant concentrations have been made on type IIa diamond specimens in the temperature range 1.5–30 K. Samples have been implanted using the CIRA (cold implantation–rapid annealing) process, in which small implantation increments were used followed by high-temperature annealing to achieve a significant reduction in the levels of implantation-induced radiation damage and to obtain maximum boron activation. Further post anneals at temperatures up to 1700°C were carried out. Using this procedure, we have recorded, for the first time, metallic conductivity behaviour in implanted surface layers in single-crystal diamond specimens with boron concentrations measured by secondary-ion mass spectrometry to be of the order of n=10²¹ cm⁻³. The occurrence of a metal–insulator transition in this system is discussed.     

Effect of Metal Additives on Performance of Low-Carbon Magnesia-Carbon Materials

In this paper,both oxidation and corrosion resistance of low-carbon magnesia-carbon materials containing 4.0wt% graphite with metallic Al and Mg-Al alloy powders as antioxidants were investigated.Meanwhile,the microstructures of samples corroded by slag were observed with optical microscope as well.The test results revealed the properties of oxidation and corrosion resistance of low-carbon magnesia-carbon materials could be improved obviously by adding metal Al powder and Mg-Al alloy powder.The rule of improving oxidation resistance was illegibility when metal Al powder and Mg-Al alloy powder were added together.It was harmful to corrosion resistance by mixed adding metal Al powder and Mg-Al alloy powder into the materials,at the same time,the corrosion resistance would decreased with the increasing of Mg-Al alloy content.The corrosion resistance of samples with 0.5wt% or 3.0wt% Mg-Al alloy was better. The oxidation resistance and corrosion resistance of materials with metal Al or Mg-Al alloy respectively were better than that with mixed metal Al and Mg-Al alloy. As a result, Mg-Al alloy was more suitable for low-carbon composite materials than metal Al as additives.     

Effect of Phase Changes on Metal‐Particle Combustion Processes

This paper summarizes a series of experimental studies addressing combustion of single metal particles. Sets of freefalling monodisperse molten metal droplets were formed at repeatable initial temperatures and velocities in a pulsed microarc discharge ignited between a cold tool cathode and a consumable wire anode. The droplets formed in oxygenated environments immediately ignited and burned, while their temperature histories were studied using optical pyrometry. Burning particles were quenched at different combustion times using techniques providing variable cooling rates. Analyses of the quenched samples were used to recover the evolution of burning particle compositions for different metals. Experiments were conducted with Al, Mg, Zr, Ti, Ta, W, Mo, Fe, and Cu particles. In addition, similar combustion experiments were carried out with boron particles produced using an oxygenacetylene torch melting an edge of a vibrating boron filament. Most of the combustion experiments were conducted in air, while argon–oxygen, helium–oxygen, and carbondioxide environments were also used in some tests. A limited number of experiments on aluminumparticle combustion were conducted in microgravity. The experiments were aimed at identifying correlations between the burning particle temperature and composition histories. Dissolution of oxygen and other gases was observed to occur within the burning metal, leading to phase changes coinciding with sudden changes in metal combustion regimes. Equilibrium metal–gas phase diagrams were used to interpret the experimentally observed metal combustion behavior. Based on the experimental results, an expanded mechanism of metal combustion was suggested, emphasizing reactions and phase changes occurring within the burning metal in addition to reactions occurring on and above the metal surface.     

Bis-Aniline-Crosslinked Enzyme–Metal Nanoparticle Composites on Electrodes for Bioelectronic Applications

The electrical contacting of redox enzymes with electrodes is the most fundamental requirement for the development of amperometric biosensors and biofuel cell elements. We describe a novel method to prepare electrically contacted metallic nanoparticles (NPs) or carbon nanotubes (CNTs)/enzyme hybrid composites on electrodes that act as amperometric biosensors or as the constituents of biofuel cells. Au NPs or Pt NPs were modified with thioaniline electropolymerizable groups, and so were the enzymes glucose oxidase (GOx) or bilirubin oxidase (BOD). Electrochemical polymerization of the thioaniline-functionalized Pt NPs and GOx on a thioaniline monolayer-modified Au surface led to the formation of a bis-aniline-bridged Pt NPs/GOx composite electrode that enabled the analysis of glucose through the electrocatalyzed reduction of H₂O₂. Similarly, a Pt NPs/BOD composite-functionalized electrode showed electrocatalytic activity toward the reduction of O₂ to H₂O. Also, a Au NPs/GOx composite-functionalized electrode revealed direct electrical contacting between the enzyme and the electrode through the electrocatalytic reduction of the bis-aniline bridges, and this enabled the bioelectrocatalytic oxidation and the amperometric sensing of glucose. Finally, a biofuel cell consisting of an anode modified with Nile blue/NAD⁺/alcohol dehydrogenase on carbon nanotubes, and a cathode composed of the bis-aniline-crosslinked Pt NPs/BOD composite was constructed. The biofuel cell operates with a power output corresponding to 200 μW cm^-2.     

Preparation and Properties of Novel Quaternized Metal–Polymer Matrix Nanocomposites

A new class of PANI/Sn(II)SiO₃/FCNTs nanocomposite was synthesized by mixing polyaniline into the gel of Sn(II)SiO₃ followed by FCNTs (Polyaniline/Sn(II)SiO₃/Functionalized Carbon nanotubes). The physico-chemical characterization was carried out by scanning electron microscope, XRD (X-ray Diffraction), FTIR (Fourier Transform Infrared Spectroscopy), ultraviolet–visible spectroscopy, and simultaneous thermogravimetric analysis studies. The ion-exchange capacity (1.2 meq/g) and distribution studies were also determined to understand the ion-exchange capabilities. The DC electrical conductivity studies revile it in the range of 3–5 × 10^?3 S/cm. On the basis of distribution studies, ion-selective membrane electrode was designed for Hg(II). The analytical utility of this membrane was established by using it as an indicator electrode in electrometric titrations.     

Phosphonates Meet Metal−Organic Frameworks: Towards CO2 Adsorption

Here we report a new highly microporous zirconium phosphonate material synthesized under solvothemal conditions. The specific Brunauer-Emmett-Teller (BET) surface area of the “unconventional metal−organic framework” (UMOF) is measured to be ∼900 m²/g, after following an appropriate activation protocol. Diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) shows that the material bears a free −OH functionality on the phosphonate linker that may interact with CO₂. CO₂ adsorption isotherms were collected and a measured heat of adsorption of 31 kJ/mol was obtained. In addition, adsorption isotherms of CO₂, N₂, and CH₄ at 298 K combined with Ideal Adsorbed Solution Theory (IAST) show that the material can be expected to display high selectivities for uptake of CO₂ versus N₂ or CH₄.