Reversion of Bioluminescent Bacteria (Mutatox^(TM)) toTheir Luminescent State upon Exposure to OrganicCompounds, Munitions, and Metal Salts

Mutatox is a new genotoxicity bioassay which uses as the endpoint the bioluminescence produced on reversion of a dark strain of the marine bacterium Vibrio fischeri ±S9.Reversion can occur by several mechanisms, including base substitution, frame-shift, SOS induction, and DNA intercalation. For screening, Mutatox provides many advantages over the Salmonella trphimurium (Ames) assay: it requires minimal sterility, employs a shorter incubation period, and does not require culture maintenance. Eighteen organic chemicals (phenol, polynuclear aromatic hydrocarbons, nitrotoluenes, others), Na3PO4, and 4 genotoxic metals (Cu2+, Ni2+, As3+, Cd2+) were tested. Most of the organic compounds positive in S. typhimurium assays were positive in Mutatox. None of the metals was genotoxic in V. fischeri, possibly due to poor uptake from the saline medium

The Negative Effect of Heavy Metal Salts on the Body of Mammal Animals

The main purpose of this presented article was to explain the need to study the amount of heavy metal salts in the environment where animals live, in the water, in air, and in the food and fodder consumed. This article presents materials from the literature on the effects of heavy metal salts on the body of animals and the environment in which they live. The cited analytical data showed that the general information on the negative effects of heavy metal salts on the body is sufficient, but their effects on the digestive tract and morpho-functional properties of rabbits should be studied in depth. Therefore, we planned to focus our scientific work on this topic. The article mainly refers to salts of heavy metals cadmium, lead, and mercury (Cd, Pb, Hg). It is noted in the literature that heavy metal salts have a negative effect on the body of animals. We focused mainly on data on the effects of heavy metals on farm animals, including rabbits. But it is clear that the authors referred to were referring to experimental animals. These negative effects are manifested in the form of disorders of digestive functions, disorders of neurovegetative processes, increasing incidence of cardiovascular disease, rapid heart failure, deterioration of calcium metabolism, as well as impaired haemoglobin metabolism. Disorders of protein metabolism manifest themselves in the form of cases of hyperproteinaemia and dysproteinaemia. The results of the evaluation of the organism of healthy animals in chemically and radioactively contaminated areas showed the accumulation of significant levels of chemical elements in their organism. We mainly looked at the effects of heavy metal salts on farm animals. The cited analytical data showed that the general information on the negative effects of heavy metal salts on the body is sufficient, but the effects on the activity of organ systems in the body (respiration, blood and blood circulation, digestion, reproduction, productivity and immunological systems) have not been comprehensively studied.

Recent Advances of Transition Metal Basic Salts for Electrocatalytic Oxygen Evolution Reaction and Overall Water Electrolysis

Electrocatalytic oxygen evolution reaction(OER)has been recognized as the bottleneck of overall water splitting,which is a promising approach for sustainable production of H_(2).Transition metal(TM)hydroxides are the most conventional and classical non-noble metal-based electrocatalysts for OER,while TM basic salts[M^(2+)(OH)_(2-x)(A_(m^(-))_(x/m),A=CO_(3)^(2−),NO_(3)^(−),F^(−),Cl^(−)]consisting of OH−and another anion have drawn extensive research interest due to its higher catalytic activity in the past decade.In this review,we summarize the recent advances of TM basic salts and their application in OER and further overall water splitting.We categorize TM basic salt-based OER pre-catalysts into four types(CO_(3)^(2−),NO_(3)^(−),F^(−),Cl^(−)according to the anion,which is a key factor for their outstanding performance towards OER.We highlight experimental and theoretical methods for understanding the structure evolution during OER and the effect of anion on catalytic performance.To develop bifunctional TM basic salts as catalyst for the practical electrolysis application,we also review the present strategies for enhancing its hydrogen evolution reaction activity and thereby improving its overall water splitting performance.Finally,we conclude this review with a summary and perspective about the remaining challenges and future opportunities of TM basic salts as catalysts for water electrolysis.

Ultrathin porous graphitic carbon nanosheets activated by alkali metal salts for high power density lithium-ion capacitors

Graphitic carbons with reasonable pore volume and appropriate graphitization degree can provide efficient Li+/electrolyte-transfer channels and ameliorate the sluggish dynamic behavior of battery-type carbon negative electrode in lithium-ion capacitors(LICs).In this work,onion-like graphitic carbon materials are obtained by using carbon quantum dots as precursors after sintering,and the effects of alkali metal salts on the structure,morphology and performance of the samples are focused.The results show that alkali metal salts as activator can etch graphitic carbons,and the specific surface area and pore size distribution are intimately related to the description of the alkali metal salt.Moreover,it also affects the graphitization degree of the materials.The porous graphitic carbons(SGCs)obtained by NaCl activation exhibit high specific surface area(77.14 m^(2)·g^(-1))and appropriate graphitization degree.It is expectable that the electrochemical performance for lithium-ions storage can be largely promoted by the smart combination of catalytic graphitization and pores-creating strategy.High-performance LICs(S-GCs//AC LICs)are achieved with high energy density of 92 Wh·kg^(-1)and superior rate capability(66.3 Wh·kg^(-1)at10 A·g^(-1))together with the power density as high as10020.2 W·kg^(-1).

Metal salts with highly electronegative cations as efficient catalysts for the liquid-phase nitration of benzene by NO2 to nitrobenzene

Metal salts with highly electronegative cations have been used to effectively catalyze the liquid-phase nitration of benzene by NO2 to nitrobenzene under solventfree conditions. Several salts including FeCl3, ZrCl4, AlCl3, CuCl2, NiCl2, ZnCl2, MnCl2, Fe（NO3）3-9H2O, Bi （NO3）3·5H2O, Zr（NO3）4-SH2O, Cu（NO3）2.6H2O, Ni （NO3）2·6H2O, Zn（NO3）2·6H2O, Fe2（SO4）3, and CuSO4 were examined and anhydrous FeCl3 exhibited the best catalytic performance under the optimal reaction conditions. The benzene conversion and selectivity to nitrobenzene were both over 99%. In addition, it was determined that the metal counterion and the presence of water hydrates in the salt affects the catalytic activity. This method is simple and efficient and may have potential industrial application prospects.

Separation of chitin from shrimp shells enabled by transition metal salt aqueous solution and ionic liquid

Chitin is a widely used important industrial polymer mainly from shrimp shells, but its commercial preparation is under the great challenge of serious pollution due to the requirement of HCl and Na OH.Herein, we demonstrated that high purity chitin can be obtained from waste shrimp shells(WSSs) by cascade separation with transition metal salt aqueous solution and ionic liquid(IL). Firstly, calcium carbonate of WSSs was effectively removed in the metal salt aqueous solution driven by the ion exchange interaction. Subsequently, 1-butyl-3-methylimidazolium chloride([Bmim]Cl) had bifunctional abilities to remove residual protein and introduced metal salts simultaneously by hydrogen bonding and coordination interactions. The key experimental factors affecting the separation process were systematically studied, including the type of metal salts, temperature, and [Bmim]Cl loading. After sequential treatment with a 20%(mass) Ni SO4aqueous solution at 130 ℃ and [Bmim]Cl at 150 ℃, the purity of a-chitin can be up to 96.5%(mass) that meets commercial requirements. The use of metal salts with higher coordination ability makes the preparation of chitin no longer depend on the commonly acid-base reaction, which is conducive to the preservation of chitin structure.

Nonmetal-Metal Transition in Solutions of Metals in Molten Salts

Solutions of metals in molten salts present a rich phenomenology: localisatlon of electrons in disordered ionic media, activated electron transport increasing with metal concentration towards a nonmetal-metal (NM-M) transition, and liquid-liquid phase separation. A brief review of progress in the study of these systems is given in this article, with main focus on the NM-M transition. After recalling the known NM-M behaviour of the component elements in the case of expanded fluid alkali metals and mercury and of solid halogens under pressure, the article focuses on liquid metal-molten salt solutions and traces the different NM-M behaviours of the alkalis in their halides and of metals added to polyvalent metal halides.

The Influence of Nitrate Salts and Complex Metal Ion to Regio-Selective Synthesis of 2-Nitro-5,10,15,20-Tetra- (4-Methoxyphenyl)Porphyrinato Metal

A series of 2\|nitro\|5,10,15,20\|tetra(4\|methoxyphenyl) porphyrinato metals were regioselectively synthesized with nitrate salts as nitrating reagent in acetic acid/acetic anhydride for preparation of 2\|substituted porphyrin. The influence of nitrate salts and complex metal ion to the reaction were investigated. The extent of 2\|nitration increased with the electronegativity of the central metal. When Cu(NO 3 ) 2 · 3H 2O was used as nitrating reagent, almost quantitative yields of 2\|nitro porphyrin were obtained in the case of Cu(Ⅱ) or Ni(Ⅱ) chelates, while Zn(Ⅱ) or Mn(Ⅲ) chelates gave 50% and 30% yields respectively. If Zn(NO 3 ) 2 ·10H 2 O was used as nitrating agent, no product was found for Cu(Ⅱ) or Ni(Ⅱ) chelates, 12% was found for Zn(Ⅱ) chelates. The other metal ion and nitrate salts were also found in quite different influence.

Effect of Salt Spray Corrosion on Tribological Properties of HVOF Sprayed NiCr-Cr3C2 Coating with Intermediate Layer

The objective of the present work was to determine the influence of the neutral salt spray corrosion on the wear resistance of HVOF sprayed NiCr-Cr3C2 coating with intermediate layer. Ni-Zn-Al2O3 coatings as interlayers were prepared by low pressure cold spray（LPCS） between NiCr-Cr3C2 cermet coatings to form a sandwich structure to enhance the corrosion resistance properties. The tribological properties were examined using the UMT-3 fricition and wear tester by line-contact reciprocating sliding under dry and salt spray one week corrosion. The morphology, element distribution, and phase compositions of the coating and worn sufaces were analyzed by using scanning electron microscopy, energy dispersive spectrometry, and X-ray diffraction respectively. The corrosion behavior of the coating was studied by the open-circuit potential, the electrochemical impedance spectroscopy, potentiodynamic polarization, and salt spray corrosion methods. It is found that the sandwich structured coating has better corrosion resistance than the single layer coating. The results show that under dry wear conditions, the wear mechanism is abrasive and adhesive wear, whereas under salt spray corrosion conditions it becomes corrosion wear. The friction coefficient of the sandwich structured coating after salt spray corrosion is slightly lower than the dry friction coefficient, but the weight of the wear loss is lower than that under dry condition.

An Insight on Future Development Approaches of Salt Lake Magnesium Resources:from the Current Situation of China's Magnesium Industry

Magnesium-bearing minerals discovered on the earth so far occur mainly as solid or liquid.The former include magnesite(Mg CO3),dolomite(Mg CO3·Ca CO3),carnallite(Mg Cl2·KCl·6H2O),bischofite(Mg Cl2·6H2O)and

Mild hydrothermal preparation of a layered metal hydroxide salt with microtube/rod morphology

Microtubes/rods of the layered metal hydroxide salt compound Cd2（OH）3（DS）·nH2O, where DS stands for dodecyl sulfate sandwiched between two adjacent inorganic sheets, have been synthesized for the first time through a mild hydrothermal reaction route. The microtubes/rods have a diameter of about 1 μm and a length ranging from several microns to 20μm. The growth process of microtubes/rods under the experimental conditions employed follows a dissolution-recrystallization route.

Synthesis and Thermodynamic Properties of M2L[M=Li, Na; L=3,6-Bis（1H-1,2,3,4-tetrazol-5-yl-amino）-1,2,4,5-tetrazine]

Two novel energetic alkalic metal salts of 3,6-bis（1H-1,2,3,4-tetrazol-5-yl-amino）-l,2,4,5-tetrazine （BTATz）, Li2（BTATz）. 6H20（compound 1） and Na2（BTATz）. 2H20（compound 2）, have been synthesized by the reac- tion of BTATz with lithinnl hydroxide or sodium hydroxide in dimethylsulfoxide（DMSO） solution, respectively, and their structures were characterized by means of elemental analysis and Fourier transform infrared spectrometry（FTIR） Moreover, the single-crystal structure of compound 1 was determined by single crystal X-ray diffraction. It crystal- lizes in the monoclinic space group P1/c. Furthermore, their thermal decomposition behaviors were investigated by means of differential scanning calorimetry（DSC） and thermogravimetry-differential thermal gravimetry（TG-DTG）. The results show that the exothermic decomposition peak temperatures for compounds 1 and 2 were 642.65 and 644.46 K, respectively, and the kinetic equations of the main exothermic decomposition were also derived from non-isothermal method. Additionally, the thermal safety of the two compounds was evaluated by calculating self-accelerating decomposition temperature（TSADT） and critical temperature of thermal explosion（Tb）. The results（the TSADT and Tb values are 605.43 and 635.69 K for compound 1; 607.38 and 638.96 K for compound 2） reveal that the two compounds exhibit better thermal safety than BTATz.

Experimental Measurement of Both Kinetic and Total Mass Transfer Between Two Electromagnetically Stirred Molten Layers

In ladle metallurgical processing,two liquid layers,a metallic layer below a salty or oxide layer,are separated by an interface where mass exchanges occur by the way of a redox reaction.The mass transfer associated with such reaction is strongly dependent on the agitation of each phase as well of their interface.We use an experimental system able to melt separately metal and salt.Once these elements are molten a sampling system is used.The experimenter chooses the sampling times.Finally,the collected samples and the final metal and salt ingots are analyzed by Inductively Coupled Plasma Atomic Emission Spectroscopy(ICP-AES).During the experiments,both temperature and,intensity and frequency of the inducting current,are measured.Comparisons on experimental results are done varying the induction as well as the transferred element.