Acetyldiaminobutanoic acid,a potential lathyrogenic amino acid in leaves of Acacia angustissima

Acacia angustissima has potential in agroforestry systems for forage production in tropical environments. However, feeding trials indicate that the leaves are potentially toxic. Signs of toxicity in sheep are similar to those presented by sheep fed flatpea (Lathyrus sylvestris) hay which contains a high concentration of the non‐protein amino acid 2,4‐diaminobutanoic acid (DABA). Cation exchange chromatography, high‐performance liquid chromatography (HPLC) and NMR were used to isolate and identify the non‐protein amino acid in A angustissima leaves. A quantitative HPLC method was used to determine the content of the non‐protein amino acid in leaves from 20 accessions. The non‐protein amino acid was identified as 4‐N‐acetyl‐2,4‐diaminobutanoic acid (ADAB), previously reported to occur in seeds. The average and range in ADAB content were 16.8 and 10.6–25.4 mg g^?1 respectively. This content of ADAB is higher than the levels of DABA in flatpea hay that are toxic to sheep. © 2001 Society of Chemical Industry     

Chlorination byproducts, their toxicodynamics and removal from drinking water

No doubt that chlorination has been successfully used for the control of water borne infections diseases for more than a century. However identification of chlorination byproducts (CBPs) and incidences of potential health hazards created a major issue on the balancing of the toxicodynamics of the chemical species and risk from pathogenic microbes in the supply of drinking water. There have been epidemiological evidences of close relationship between its exposure and adverse outcomes particularly the cancers of vital organs in human beings. Halogenated trihalomethanes (THMs) and haloacetic acids (HAAs) are two major classes of disinfection byproducts (DBPs) commonly found in waters disinfected with chlorine. The total concentration of trihalomethanes and the formation of individual THM species in chlorinated water strongly depend on the composition of the raw water, on operational parameters and on the occurrence of residual chlorine in the distribution system. Attempts have been made to develop predictive models to establish the production and kinetics of THM formations. These models may be useful for operational purposes during water treatment and water quality management. It is also suggested to explore some biomarkers for determination of DBP production. Various methods have been suggested which include adsorption on activated carbons, coagulation with polymer, alum, lime or iron, sulfates, ion exchange and membrane process for the removal of DBPs. Thus in order to reduce the public health risk from these toxic compounds regulation must be inforced for the implementation of guideline values to lower the allowable concentrations or exposure.     

Effect of the composition of some sulphide minerals on cyanidation and use of lead nitrate and oxygen to alleviate their impact

An investigation was carried out on synthetic ores containing high purity pyrite, pyrrhotite and chalcopyrite and on two gold ores currently processed to evaluate the impact of cyanicides on cyanidation and to improve the leaching performance by using a pre-leaching, injecting oxygen and adding lead nitrate. With regard to the synthetic ores, it was found that pyrrhotite did not generate a high cyanide consumption while pyrite and chalcopyrite were detrimental. Pre-leaching was deleterious for the ore containing chalcopyrite while pre-leaching with lead nitrate was very efficient to decrease the reactivity of the ore containing pyrite. The two gold ores studied had very different compositions. The low sulphide ore had a low sulphide content (1.36% S), present as pyrrhotite while the second had a very high sulphide content (20.2% S), in the form of pyrite, pyrrhotite and chalcopyrite. The efficiency of the process conditions was peculiar to the ores. The high sulphide ore required a stronger, longer pre-leaching period (12 h) with greater amounts of lime (7.0 kg/t) and lead nitrate (600 g/t) than the low-sulphide ore. The ore with a low sulphide content required a pre-leaching of only 1 h with a small quantity of Pb(NO₃)₂ (50 g/t) and leaching can be performed at 360 ppm NaCN to allow a recovery of 96.4% Au and a low cyanide consumption at 0.18 kg/t. As for the high sulphide ore, cyanidation had to be conducted at 560 ppm NaCN to recover 88.4% Au with a cyanide consumption of 0.80 kg/t. An increase in the amount of lime enhanced oxidation of soluble sulphides. Lead nitrate stabilized copper and iron dissolution by forming a passivation layer at the surface of sulphide minerals. Lead nitrate also prevented the formation of a passive layer at the surface of gold.     

Enthalpies of formation of some solid hafnium nickel compounds and of the Ni-Rich HfNi liquid by direct reaction calorimetry

In the course of a systematic study of binary transition metal alloys, the enthalpies of formation of five Hf-Ni compounds were measured by direct reaction calorimetry: Hf_0.17Ni_0.83(l/6HfNi₅): Δ_fH(1323 K) = − 37,000 J/mole of atoms (±3200) Hf_0.22Ni_0.781/9Hf₂Ni₇): Δ_f(1623 K) = −50,700 J/mole of atoms (±2000) Hf_0.45Ni_0.55(l/2OHf₉Ni₁₁): Δ_fH(1473 K) = −54,500 J/mole of atoms (±2200) Hf_0.50Ni_0.50(l/2HfNi): Δ_fH(1573 K) = −47,900 J/mole of atoms (±1800) Hf_0.67Ni_0.33(l/3Hf₂Ni): ΔH(1423 K) = −36,700 J/mole of atoms (±1300) with reference to pure metals in their equilibrium states at the reaction temperatures. The Ni-rich Hf-Ni liquid was also studied by the dissolution of Hf in the liquid alloy of variable composition at 1743 and 1633 K. Results show that the enthalpy of formation of the liquid at a given composition depends strongly on temperature, and this point suggests the existence of associations in the liquid. The melting temperature of Hf_0.22Ni_0.78(Hf₂Ni₇) which was found (1705 K) is slightly lower than the one (1743 K) given in the literature. Formerly Senior Research Student with the Laboratoire de Thermodynamique Métallurgique, Université de Nancy Un, France     

Development of dieldrin,endosulfan, and hexachlorobenzene‐imprinted polymers for dye‐displacement array sensing

Due to the toxicity associated with the exposure to organochlorine pesticides, new materials capable of selectively capturing and detecting these compounds are highly desirable. In this study, imprinted polymers were prepared using three organochlorine pesticides—dieldrin (DE), endosulfan (EN), or hexachlorobenzene (HCB) as templates. The MIPs were polymerized via precipitation polymerization. The yields were over 90% with particle sizes ranging from 62 to 214 nm. Binding studies combined with GC‐ECD analysis showed that each template is more selective to its corresponding MIP compared with the other two structurally homologous templates. These results were consistent with those obtained using UV–vis where more bromocresol green (BCG) dye was released when higher template concentrations were introduced to the corresponding BCG‐impregnated MIPs. Since unique selectivity response pattern for each of the MIPs was obtained, this demonstrated that the MIPs were selective and can be potentially used in dye‐displacement array sensing. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 44401.     

Transparent ZnS Ceramics by Sintering of High Purity Monodisperse Nanopowders

We report an efficient way of preparing transparent ZnS ceramics using the hot‐pressing technique. It has been found that the transparency is highly dependent on the purity and the grain size distribution of the starting ZnS powders. Highly pure and monodisperse ZnS powders have been obtained by posttreatment of the precipitated powders in a H₂S/N₂ flow for 2 h at 600°C. The obtained ZnS ceramics show fully dense and homogeneous microstructure with average grain size of ~1 μm and smooth grain boundaries, leading to an excellent transmission of around 70% in the mid‐ and far‐ IR regions. The preparation technique described in this study is highly reproducible.     

Electroless ultrasonic functionalization of diamond nanoparticles using aryl diazonium salts

We report a novel and very handful strategy for the functionalization of diamond nanoparticles (NDs), based on the ultrasound-assisted grafting of aryl groups from the electroless reduction of diazonium salts. For this study, 4-nitrobenzenediazonium salt was used as a model molecule and the reaction was investigated in neutral and acidic aqueous media. Spectroscopic evidence for the successful attachment of aryl groups to nanodiamonds (NDs) was given by IR and XPS which clearly detect characteristic NO₂ peaks. Moreover, the absence of any peaks from the ⁺N≡N group in the IR spectra is a clear indication of the chemical reduction of the parent diazonium salt at the surface of NDs. This spontaneous chemical modification of NDs by aryl diazonium salts was confined to the surface of the ND particles; indeed, XRD measurements have shown that the crystalline structure of the bulk of the particles was unaffected. It opens up new possibilities towards the control of the surface chemical composition of NDs using simple protocols operated in very soft conditions, i.e. in water at room temperature. It shows conclusively that the chemistry toolbox of experts interested in nanodiamonds should contain aryl diazonium salts, given their versatility in forming active platforms.     

Dispersion of Nano-Sized γ-Alumina Powder in Non-Polar Solvents

To disperse nano-sized γ-alumina powders in non-polar solvents, the surface of γ-alumina has to be modified with unsaturated oleic acid, which forms aluminum-oleate on the surface. This changes the surface characteristics of γ-alumina powders from hydrophilic to hydrophobic in nature. A colloidally stable γ-alumina non-polar suspension is obtained when a critical amount of aluminum-oleate compound is formed on the surface. This is also evidenced by the results of adsorption and theoretical calculation of potential energies, which confirm the colloidal stability of organic γ-alumina suspension caused by the steric repulsion mechanism.