Pyrolysis of sulfuric acid-treated chrome-tanned leather wastes: Kinetics, mechanism and evolved gas analysis.

Management and safe disposal of chrome-tanned leather wastes generated in leather industry are of great importance due to their potential health risks and environmental hazards. Herein, an integrated strategy was proposed for disposing of chrome-tanned leather scrap (CTLS). This method involves the separation of chromium salts from CTLS with sulfuric acid for recycling purpose, followed by pyrolysis of the acid-treated CTLS in an inert atmosphere. SEM/EDX analysis was employed to characterize the changes in composition and morphology of CTLS after acid treatment. CO2 and H2O are main pyrolysis gases of CTLS, while the acid treatment increases the relative content of aliphatic hydrocarbons and NH3 in evolved gases. The pyrolysis characteristics and kinetics of the acid-treated CTLS were investigated by thermogravimetric analysis (TGA) at three different heating rates. After 3 and 6 days of acid treatment, the average activation energy of CTLS (450.9 kJ/mol) obtained from the Flynn-Wall-Ozawa method decreased to 369.6 and 351.0 kJ/mol, respectively. It is assumed that the CTLS consists of two pseudocomponents: low-crosslinked collagen (LCol) and highly-crosslinked collagen (HCol). Using the generalized master plots method, random nucleation and nuclei growth model (An model) was found to be the most probable kinetic model for the pyrolysis process of LCol and HCol. The kinetic exponent for pseudocomponent pyrolysis varied between 3.00 and 3.90, and the pre-exponential factor ranged from 5.83 × 1012 to 2.93 × 1013 min-1. The results of the present study provide an alternative route and useful information for recycling and disposing of chrome-containing leather wastes.

Dietary l-arginine supplementation influences growth performance and B-cell secretion of immunoglobulin in broiler chickens.

Our previous study has shown that high levels of l-arginine (ARG) have reduced serum and mucosal antibody concentrations. In order to provide a better understanding in the application of ARG supplementation in the poultry industry, the study was conducted to investigate the effect of high levels of ARG on performance and B-cell secretion of immunoglobulin M (IgM) and IgG development in broiler chickens. A total of 192 1-day-old male Arbor Acres Plus broilers were randomly allocated into 4 groups (8 replicates per group, 6 birds per replicate) fed diets containing one of four ARG concentrations (analysed): 9.8, 14.7, 19.1 and 23.4 g/kg respectively. Growth performance was measured based on body weight gain (BWG), feed intake (FI) and feed conversion ratio (FCR). Increasing ARG quadratically increased (p < 0.05) BWG and FI with reaching plateau at 14.7 g/kg, while linearly decreased (p < 0.05) FCR, indicating that maximal performance required ARG no more than 14.7 g/kg in diets. Serum IgG and IgM concentrations were linearly reduced (p < 0.05) with increasing ARG. Chickens fed 19.1 g/kg or 23.4 g/kg ARG had lower (p < 0.05) serum IgG or IgM than chickens fed 9.8 g/kg ARG. As for the mRNA expression of bursal IgG and IgM, they were significantly downregulated with increasing ARG (p < 0.05). Chickens on ARG (>19.1 g/kg) had a lower (p < 0.05) IgG and IgM mRNA expression than chickens fed 9.8 g/kg. Activator of transcription 3 (STAT3) mRNA expression was linearly reduced with increasing ARG (p < 0.05), the transcriptional repressor B-cell lymphoma 6 (BCL6) mRNA expression was quadratically (p < 0.05) responded, and these cytokines had the lowest expression at 19.1 g/kg. ARG supplementation (>14.7 g/kg) did not significantly improve the growth performance, while it may have a potential negative regulatory effect on B-cell-mediated humoral immunity in chickens associated with suppression of the STAT3 expression associated with the JAK/STAT3 pathway.

Crystal structure of diethyl 3,3'-[(4-nitro-phen-yl)methyl-ene]bis-(1H-indole-2-carboxyl-ate).

In the title compound, C29H25N3O6, the mean planes of the two indole ring systems (r.m.s. deviations = 0.0115 and 0.0082 Å) are approximately perpendic-ular to one another, making a dihedral angle of 89.7 (5)°; the benzene ring is twisted with respect to the two indole ring systems by 52.6 (4) and 88.2 (3)°. In the crystal, pairs of N-H⋯O hydrogen bonds link the mol-ecules into the inversion dimers, which are further linked into supra-molecular chains along the b-axis direction. Weak C-H⋯O hydrogen bonds and C-H⋯π inter-actions are also observed in the crystal.