Utilization of blue panic (Panicum antidotale) as an alternative feed resource for feeding Barky sheep in arid regions.

This study aimed at elucidating effects of replacing sorghum with blue panic (BP) on total dry matter intake (TDMI), average daily gain (ADG), feed conversion ratio (FCR), apparent nutrient digestibility, blood biochemical constituents, rumen fermentation patterns and economic feasibility of Barky male lambs. Fifteen lambs (av. BW, 22.5 ± 1.6 kg) were randomly allotted into 3 treatments (n = 5/group). Control lambs were given a diet of concentrate mixture (CM) plus sorghum (S), BP50% lambs were given a diet of CM plus (S: PB 1:1) and BP100% lambs were given CM plus PB. The experiment lasted for 54 days. At the last week of the experiment, the apparent nutrient digestibility coefficients were determined using lignin contents of feeds and faeces as an internal marker. Blood samples were collected at weeks 3, 5 and 7 to determine serum biochemical parameters. Results showed that TDMI significantly (P < 0.05) influenced by diet, whereas ADG was not affected. Mean FCR values were 5.67, 5.46 and 5.86 for control, BP50% and BP100%, respectively. Neither nutrients digestibility nor ruminal fermentation parameters were affected (P > 0.05) by total replacement of sorghum with BP. Likewise, none of the serum biochemical constituents were different in BP than in control lambs. This study concluded that BP grass would be considered as one of the promising tropical green forages in the arid regions as an alternative feedstuff in case of shortage of green fodders.

Synthesis of recyclable carbon/lignin biocomposite sorbent for in-situ uptake of BTX contaminants from wastewater.

In this work, both palm-date pits and pulping black liquor industrial wastes were recycled as low-cost starting materials for the production of three series of granule activated carbon (gAC)/Kraft lignin (KL) (gAC/KLx, x = 33, 50 and 67%) biocomposites using a one-pot solid-state method. The gAC/KLx biocomposites with defined characteristics were examined towards batch adsorption of BTX (Benzene, Toluene, and Xylene) in multi-solute salty wastewaters. Optimization of adsorption performances under different experimental conditions were carried out using high performance liquid chromatography (HPLC). Adsorption modeling versus contact time (0-12 h) and BTX concentrations (150-2250 mg/L) were examined using non-linear forms of nine kinetic and five isotherm equations to best understand gAC/KL0.5 suitability for BTX sorption/recovery processing. Accordingly, the gAC/KLx at KL blended ratio of 50% was found to be the topmost to achieve the highest BTX capacity even at broad ranges of water salinity (0-100 g/L) and pH (3-9) values. The adsorption mechanism found to best described by physico-sorption (E ≈ 0.12-1.38 kJ/mol) via the hydrophobic interaction and diffusion mechanisms. In respect to gAC/KL0.5 affinities, the sorption capacity followed the descending sequence of X ≥ T > B. Particularly, the maximum theoretical BTX capacity using the best fitted Langmuir-Freundlich model (L-FM) for gAC/KL0.5 was found to be slightly higher than obtained by gAC (363.9 and 360.1 mg/g, respectively), along with higher initial sorption (h) rate (≈742.47 mg/g.h) than of gAC (≈559.85 mg/g.h) and KL (≈22.22 mg/g.h). Batch BTX sorption/recovery processes and estimated cost suggested the effective utilization of gAC/KL0.5 as a promising in-expensive sorbent (0.31 ±â€¯0.05 US$/kg) for commercial decontamination of petroleum hazardous (BTX) pollutants from wastewaters up to five reuse cycles.

Spectroscopic and electrochemical studies of ruthenium and osmium complexes of salicylideneimine-2-thiophenol Schiff base.

The reactions between [M(3)(CO)(12)], M = Ru and Os, and salicylideneimine-2-thiophenol Schiff base in THF under reflux gave [Ru(CO)(4)(satpH)] and [Os(CO)(3)(satpH(2))] complexes. Structures of the two complexes were proposed on the basis of spectroscopic studies. Magnetic study of [Ru(CO)(4)(satpH)] suggested that a change in oxidation state of the ruthenium atom from zero to +1 was achieved via oxidative addition of the SH group with a proton displacement to give a low-spin d(7) electronic configuration. UV-Vis spectra of the two complexes in different solvents exhibited visible bands due to metal-to-ligand charge transfer. Electrochemical investigation of the free ligand and complexes showed some cathodic and anodic irreversible peaks due to interconversions through electron transfer.