Energy produced from plant residue composting has stimulated great interest in heat recovery and utilization. Composting is an exothermic process often controlled through temperature measurements. However, energy analysis of the overall composting system, especially the rotary bioreactors, is generally not well known and very limited. This study presents detailed energy analysis in a laboratory-scale, batch-operated, rotary bioreactor used for composting tomato plant residues. The bioreactor was considered as a thermodynamic system operating under unsteady state conditions. The composting process was described, the input generated and lost energy terms as well as the relative importance of each term were quantitatively evaluated, and the composting phases were clearly identified. Results showed that the compost temperature peaked at 72 h of operation reaching 66.7 °C with a heat generation rate of 9.3 W·kg⁻¹ of organic matter. During the composting process, the accumulated heat generation was 1.9 MJ·kg⁻¹ of organic matter; only 4% of this heat was gained by the composting material, and 96% was lost outside the bioreactor. Contributions of thermal radiation, aeration, cylindrical, and side-walls surfaces of the reactor on the total heat loss were 1%, 2%, 69%, and 28%, respectively. The information obtained is applicable in the design, management, and control of composting operations and in improvement of bioreactor effectiveness and productivity.

Juncus acutus, acknowledged through its indigenous nomenclature “samar”, is part of the Juncaceae taxonomic lineage, bearing considerable import as a botanical reservoir harboring conceivable therapeutic attributes. Its historical precedence in traditional curative methodologies for the alleviation of infections and inflammatory conditions is notable. In the purview of Eastern traditional medicine, Juncus species seeds find application for their remedial efficacy in addressing diarrhea, while the botanical fruits are subjected to infusion processes targeting the attenuation of symptoms associated with cold manifestations. The primary objective of this study was to unravel the phytochemical composition of distinct constituents within J. acutus, specifically leaves (JALE) and roots (JARE), originating from the indigenous expanse of the Nador region in northeastern Morocco. The extraction of plant constituents was executed utilizing an ethanol-based extraction protocol. The subsequent elucidation of chemical constituents embedded within the extracts was accomplished employing analytical techniques based on high-performance liquid chromatography (HPLC). For the purpose of in vitro antioxidant evaluation, a dual approach was adopted, encompassing the radical scavenging technique employing 2,2-diphenyl-1-picrylhydrazyl (DPPH) and the total antioxidant capacity (TAC) assay. The acquired empirical data showcase substantial radical scavenging efficacy and pronounced relative antioxidant activity. Specifically, the DPPH and TAC methods yielded values of 483.45 ± 4.07 µg/mL and 54.59 ± 2.44 µg of ascorbic acid (AA)/mL, respectively, for the leaf extracts. Correspondingly, the root extracts demonstrated values of 297.03 ± 43.3 µg/mL and 65.615 ± 0.54 µg of AA/mL for the DPPH and TAC methods. In the realm of antimicrobial evaluation, the assessment of effects was undertaken through the agar well diffusion technique. The minimum inhibitory concentration, minimum bactericidal concentration, and minimum fungicidal concentration were determined for each extract. The inhibitory influence of the ethanol extracts was observed across bacterial strains including Staphylococcus aureus, Micrococcus luteus, and Pseudomonas aeruginosa, with the notable exception of Escherichia coli. However, fungal strains such as Candida glabrata and Rhodotorula glutinis exhibited comparatively lower resistance, whereas Aspergillus niger and Penicillium digitatum exhibited heightened resistance, evincing negligible antifungal activity. An anticipatory computational assessment of pharmacokinetic parameters was conducted, complemented by the application of the Pro-tox II web tool to delineate the potential toxicity profile of compounds intrinsic to the studied extracts. The culmination of these endeavors underpins the conceivable prospects of the investigated extracts as promising candidates for oral medicinal applications.

In the present investigation, the phenolic compounds of Solanum elaeagnifolium were identified, and the plant’s anti-lipase and anti-glycation effects on hemoglobin were discovered through in vitro experiments, as well as its short-term antihyperglycemic and anti-inflammatory effects. The chemical compound composition was detected using HPLC-DAD, the anti-lipase activity was tested in vitro using 4-nitrophenyl butyrate as a substrate, and the antiglycation activity of the plant extracts was also tested in vitro using a haemoglobin model. The antihyperglycemic effect was determined by inhibiting pancreatic α-amylase and α-glycosidase activity and performing an in vivo glucose tolerance test on normal rats, and the anti-inflammatory activity was determined by inducing paw inflammation with carrageenan. In both the SEFR (fruit) and SEFE (leaf) extracts, chromatographic analysis revealed the presence of quercetin 3-O-β-D-glucoside, rutin, and quercetin. SEFR inhibited the pancreatic lipase enzyme more effectively, with an IC₅₀ of 0.106 ± 0.00 mg/mL. S. elaeagnifolium extracts demonstrated significant antiglycation activity, with 3.990 ± 0.23 mg/mL of SEFE and 3.997 ± 0.14 mg/mL of SEFR. When compared to positive and negative controls, plant extracts had very significant anti-diabetic and anti-inflammatory effects. The findings in this study and previous research on this plant encourage us to investigate other pharmacological activities of this plant besides its duiretic, cictrisant, and anti-ulcer activity.

Huge quantities of palm tree residues are available annually in Saudi Arabia; they are often disposed of by burning, leading to large environmental pollution and health problems. Enclosed composting may be a successful method for utilizing these residues. Effective composting in a rotary bioreactor depends on the composting materials and the frequencies of the rotation–aeration process. Here, we attempted to determine the optimal method for composting these residues in a bioreactor. Four identical pilot-scale bioreactors (D1–D4) were used. The respective aeration–rotation frequencies were continuous (D1), and 20 min per 1 h (D2), 2 h (D3), and 3 h (D4); the rotation speed of the bioreactors was 3 rpm. Three periods were analyzed; their names and their respective lengths for D1, D2, D3, and D4 were as follows: the lag period was 10 h for each, the mesophilic periods were 13, 14, 89, and 231 h, and the thermophilic periods were 0, 55, 71, and 17 h. The peak compost temperatures (T_{c, max}) for D1, D2, and D3 were 65.2, 57.2, and 46.9 °C, and were achieved at 36, 71, and 108 h of operation, respectively. In D1, T_c quickly declined after reaching T_{c, max} due to limited microbial activity at T_c > 60 °C. In D2, a T_c of 50–57.2 °C was maintained for 61 h, and the highest organic matter degradation (OMD) of 0.30 was achieved. During the composting period, the carbon to nitrogen (C/N) ratio and moisture contents (MC) remained in the optimal ranges for microorganisms and did not affect the composting process. The results indicated that combined aeration–rotation for 20 min every hour (D2) gave the best results for composting palm tree residues, it ensured the hygiene safety of the end product, and it also consumed less power for aeration and rotation than D1.

A wide range of biological properties and a potent therapeutic and prophylactic effect on chronic diseases are all present in Argania spinosa L. press cake. The aim of this research is to valorize the anticrystallization properties against calcium oxalate crystals of Argania spinosa L. press cake fractions and identify its bioactive components. Chemical species identification was performed using GC–MS analysis. The turbidimetric model was used to investigate crystallization inhibition in vitro. Infrared spectroscopy technique was used to characterize the synthesized crystals. Furthermore, both DPPH and FRAP methods were used to assess antioxidant activity. The results show that the fractions are equally important in crystallization inhibition percentages of calcium oxalate crystals. For saponin and polyphenol fractions, the inhibition percentages are in the orders of 83.49% and 82.83%, respectively. The results of the antioxidant activity by DPPH method show that the two fractions are equally important in the elimination of free radicals; the inhibition percentages were 77.87 ± 4.21 and 89.92 ± 1.39 for both polyphenols and saponins, respectively. FRAP method showed that the absorbance increases proportionally with concentration, and the absorbance are almost similar for both fractions and reach maximum values in the orders of 0.52 ± 0.07 and 0.42 ± 0.03, respectively, for saponins and polyphenols. These findings demonstrate that both fractions are rich in bioactive chemicals and have an anticrystallization capacity, allowing them to be employed for the curative and prophylactic effects against urolithiasis.

The control of Parlatoria ziziphi (Lucas, 1853) was studied in citrus orchards at Mechraa Belksiri in the Gharb area of Morocco. Three concentrations of spirotetramat T0 = 0 L/Ha as a control experiment, T1 = 0.625 L/Ha, T2 = 0.755 L/Ha, and T3 = 1 L/Ha, were applied on 4 ha of Valencia late orchard (each dose for 1 ha of Valencia late). The effect of spirotetramat was evaluated on the mortalities and survival rates of P. ziziphin during the stages of larvae (first instar and second instar) and females (F1, F2, and F3). Results showed that the spirotetramat was effective on larvae and females of P. ziziphi. Among the 11,229 females recorded, 93% were inhibited, while only 7% were intact after the treatment period. Finally, our study highlights that all concentrations tested were effective on the P. ziziphi population; besides, all three concentrations of this product tested were equally effective on larvae and females of P. ziziphi. Thus, during the spread period, spraying a low concentration of this product (0.625 L/Ha) will better control this pest and reduce the environmental impact.