Construction of a direct Z-scheme Cs3Bi2Cl9/g-C3N4 heterojunction composite for efficient photocatalytic degradation of various pollutants in water: Performance, kinetics and degradation mechanism.

The use of emerging composite materials has been booming to remove environmental pollutants. The aim of this research is to develop a new composite based on Cs3Bi2Cl9 perovskite and graphitic carbon nitride (g-C3N4) to investigate the photocatalytic performance under visible light irradiation. To achieve this, we produce the Cs3Bi2Cl9/g-C3N4 heterojunctions through a simple self-assembly synthesis. The as-synthesized composites are characterized using XRD, FTIR, FESEM, TEM, BET and EDX techniques. The photocatalytic performance of Cs3Bi2Cl9/g-C3N4 is examined in the degradation of various water contaminants, including 4-nitrophenol (4-NP), tetracycline antibiotic (TC), methylene blue (MB) and methyl orange (MO). The experimental results indicate the superior photocatalytic performance of the composites in the degradation of pollutants compared to pure Cs3Bi2Cl9 and g-C3N4. The 10% Cs3Bi2Cl9/g-C3N4 composite achieves the optimal degradation efficiency of 100, 92, 98.7, and 85.1% of 4-NP, TC, MB, and MO, respectively. This superior photocatalytic activity attributes to improved optical and electrochemical properties, including enhanced absorption ability, narrowing band gap, promoted separation efficiency of photogenerated carriers, and a high redox potential, which is confirmed by UV-vis DRS, PL, EIS, and CV analyses. The 10% Cs3Bi2Cl9/g-C3N4 composite also demonstrates high photocatalytic stability after four consecutive cycles. Radical trapping tests show that superoxide radicals (•O2-), holes (h+), and hydroxyl radicals (•OH) contribute to the photocatalytic process. Based on the obtained data, a direct Z-scheme heterojunction mechanism is proposed. Overall, this research offers a new stable photocatalyst with excellent prospect for photocatalytic applications.

Peroxisome proliferator-activated receptor gamma upregulation and dietary fat levels in laying hens.

The present study was conducted to investigate the effect of feeding the different levels of the dietary fat on the expression of genes encoding proteins involving energy metabolism, oxidative phosphorylation, and lipid synthesis including peroxisome proliferator-activated receptor gamma (PPARγ) of laying hens in the intestine. Birds fed diets with 3 levels of fat, that is, low (LF), medium (MF), and high fat (HF) were reared from 22 to 42 wk of age. Jejunum tissue was collected at week 42 for gene expression analysis. Dietary fat content as ether extract, net energy to AME ratio, and CP content of 3 treatment groups were as follows: LF: 25, 0.735, 187 (g/kg, DM); MF: 61, 0.739, 185 (g/kg, DM); HF: 73, 0.752, 181 (g/kg, DM). The BW, fat pad weight (g), fat pad-to-BW ratio (%) was the same for all the treatments (P > 0·05). Birds fed a diet containing HF increased the AME daily intake per metabolic BW (BW0.75) (P < 0.05). The expression of jejunal PPARγ was increased in the birds fed MF than that fed LF (P < 0.05). Dietary fat level did not affect the expression of other genes: protein kinase AMP-activated noncatalytic subunit gamma 2, NADH dehydrogenase subunit 2, succinate dehydrogenase complex flavoprotein subunit A, ubiquinol-cytochrome c reductase Rieske iron-sulfur polypeptide 1, cytochrome c oxidase subunit III, ATP synthase subunit alpha, avian adenine nucleotide translocator, and acetyl-CoA carboxylase alpha (P > 0·05). The mitochondrial count per cell showed no difference among the 3 groups with different dietary treatments (P > 0·05). The results suggest that PPARγ may be important to the energy expenditure during nutrient absorption, digestion, and metabolism, and respiratory chain complexes, and other genes involving mitochondrial energy metabolism and lipogenesis may be less responsive to dietary treatment.

Factors affecting energy metabolism and evaluating net energy of poultry feed.

Different energy evaluating systems have been used to formulate poultry diets including digestible energy, total digestible nutrients, true metabolizable energy, apparent metabolizable energy (AME), and effective energy. The AME values of raw materials are most commonly used to formulate poultry diets. The net energy (NE) system is currently used for pig and cattle diet formulation and there is interest for its application in poultry formulation. Each energy evaluating system has some limitations. The AME system, for example, is dependent on age, species, and feed intake level. The NE system takes AME a step further and incorporates the energy lost as heat when calculating the available energy for the production of meat and eggs. The NE system is, therefore, the most accurate representation of energy available for productive purposes. The NE prediction requires the accurate measurement of the AME value of feed and also an accurate measurement of total and fasting heat production using nutritionally balanced diets. At present, there is limited information on NE values of various ingredients for poultry feed formulation. The aim of this review is to examine poultry feed energy systems with the focus on the NE system and its development for chickens.

Implementation of net energy evaluating system in laying hens: Validation by performance and egg quality.

Three experiments were conducted to determine the effect of different dietary net energy (NE) and AMEn ratios (NE:AMEn) on performance, egg quality, and heat production (HP) in laying hens. In experiment 1, 62 Hy-Line Brown hens were fed 2 treatments with 31 replicates from 44 to 54 wk of age. In experiment 2, 600 hens of the same strain were fed 3 treatments from 22 to 42 wk of age with 10 replicates. Both used a completely randomized design. Diets were based on corn, wheat, wheat bran, barley, soybean meal, canola meal, meat and bone meal, and canola oil. In both experiments, the NE:AMEn ratio of diets was increased with higher oil inclusion compared with T1 controls. The AMEn (kcal/kg), NE (kcal/kg), ether extract (g/kg), and CP (g/kg), respectively, on a DM basis in experiment 1 was T1: 3,011, 2,288, 42, 202 and T2: 3,023, 2,374, 81, 203; and in experiment 2, T1: 3,026, 2,324, 25, 187; T2: 2,949, 2,315, 61, 185; and T3: 3,026, 2,397, 73, 181. Increasing the ratio of NE:AMEn decreased feed intake (P < 0.001) and increased egg mass (P < 0.05) in experiment 2 and increased egg weight (P < 0.01), decreased feed conversion ratio (P < 0.01), increased egg albumen % (P < 0.001), and decreased yolk % (P < 0.05) and shell % (P < 0.05) compared with T1 controls in both experiments. Haugh units and yolk color scores were increased with high NE:AMEn in both experiments (P < 0.001; P < 0.01). Experiment 3 was conducted in calorimetry chambers to measure HP in birds fed experiment 2 diets. Increasing the NE:AMEn increased total retained energy (RE), RE as fat, and RE in the body (kcal/kg BW0.75/D) and NE:AME. The results indicate that using oil to increase the NE:AMEn results in improved performance and egg quality and more efficient energy utilization.

Metabolizable energy of corn, soybean meal and wheat for laying hens.

Feed formulation using apparent metabolizable energy (AME) corrected to zero nitrogen retention (AMEn) is widely used by poultry nutritionists. Most available tabulated data are from experiments using adult cockerels or growing broilers. Specific values are rarely available for laying hens. A study was conducted to evaluate AME, AMEn, and AMEs (AME adjusted to 50% nitrogen retention) of corn, soybean meal (SBM) and wheat in laying hens using the reference diet substitution and regression methods. Forty eight 42-wk-old Hy-Line Brown hens were used, 2 birds per cage with six replicates per diet. Test diets contained 30% test ingredient (as is basis) and 65.7% reference diet (as is basis) with limestone, other minerals, vitamins, and amino acids held constant across the reference and test diets. Using the reference diet substitution method, AME values obtained for corn, SBM, and wheat were 3,791, 2,621, and 3,565 kcal/kg (DM), respectively. The corresponding AMEn values were 3,722, 2,496, and 3,479 kcal/kg (DM), and AMEs were 3,784, 2,835, and 3,562 kcal/kg (DM), respectively. Calculation of AME, AMEn, and AMEs of ingredients using regression based on the inclusion rate (DM) of dietary ingredients and reference diet gave identical values to those obtained by the reference diet substitution method. In addition, the measured AMEn values of ingredients using laying hens in this study were close to those calculated from proximate composition using the European Union prediction equation based on adult cockerels.

Analysis of antibody levels in egg yolk for detection of exposure to Ascaridia galli parasites in commercial laying hens.

Ascaridia galli is one of the most abundant nematode parasites in poultry. A. galli infections can significantly impact the profitability of egg farms and have negative implications for bird health and welfare. The main objectives of this study were to determine whether A. galli specific antibodies in egg yolks can be used to detect prior or current exposure to A. galli in laying hens, and to distinguish between eggs obtained from caged and free-range hens. Twenty-two laying hen flocks from different production systems (10 free-range, 2 barn-housed, and 9 caged flocks) were enrolled in the study. An in-house enzyme-linked immunosorbent assay was used to analyze levels of A. galli specific antibodies in yolk. The numbers of A. galli eggs in hen excreta were also determined in a subset of farms. Free-range flocks had higher and also more variable levels of anti-A. galli antibodies in the egg yolk compared to those of the cage flocks (0.50 ± 0.39 vs. 0.16 ± 0.13 OD units) (P < 0.001). Results also confirmed that excreta from free-range and barn-housed flocks contained higher numbers of A. galli eggs than did excreta from caged flocks in which no A. galli eggs were detected. In conclusion, analysis of anti-A. galli antibodies in the egg yolk can be used to detect worm exposure in commercial layer flocks. However, the method used in this study cannot be used in isolation to distinguish between eggs from cage and free-range production systems as anti-A galli antibodies were detected in egg yolk samples from all production systems, and the range of antibody levels overlapped between production systems.