Addition Of Acid Research Articles

The properties of Chinese Baijiu distilled spent grain-derived hydrochar: effect of in situ deep eutectic solvents formation during hydrothermal carbonization

Distilled spend grain with rice husk (DSGH), a by-product of Chinese Baijiu, can be used as a solid fuel after hydrothermal carbonization (HTC) treatment. To enhance carbonization during HTC, a new strategy based on the addition of lactic acid to DSGH and AlCl3 is proposed for the in situ formation of deep eutectic solvents (DESs). The results show that in situ DES formation significantly enhanced the recovery of organic matter, thereby increasing the yield of hydrochar. Moreover, in situ DES formation effectively hindered the reaction between NH4+ and polysaccharides. Additionally, DES disrupted the protein structure in DSGHP, thereby intensifying protein hydrolysis and deamination. Furthermore, the DES altered the HTC process of the DSGHP. In summary, the incorporation of in situ DESs significantly influenced the HTC of DSGHP, leading to notable improvements in the recovery and quality of hydrochar. This study provides valuable insights into the potential of DESs in enhancing HTC processes, particularly for biomass such as DSGHP.

Analysis of protein profile and reducing sugar content of cassava plants (Manihot esculenta Crantz) results of induced resistance with salicylic acid

Cassava (Manihot esculenta Crantz) is an important food commodity in Indonesia, and in the future this commodity will play an increasingly strategic role in people's lives and the country's economy. But until now there are still many obstacles, one of which is fusarium wilt disease. Fusarium wilt disease can be controlled by using superior cultivars that are resistant to the disease, by applying salicylic acid. The aim of this study was to analyze the protein profile and reducing sugar content in cassava plants after being induced with salicylic acid and compare them with controls. This research used a Completely Randomized Design (CRD) with one factor, namely the addition of salicylic acid consisting of 5 concentration levels, namely 0 ppm, 80 ppm, 100 ppm, 120 ppm, and 140 ppm. Each concentration was repeated 5 times. This research data is in the form of qualitative data and quantitative data. Qualitative data is presented in comparative descriptive form and presented in the form of photographs. Quantitative data was tabulated with different concentration factors and analyzed using Analysis of Variance then further tested with the Honestly Significant Difference Test (BNJ) at the 5% level. The research results showed that there was a missing protein band, namely a band at a molecular weight of 115, and there was also the appearance of a new band, namely a molecular weight of 85 kDa, as well as an increase in the reducing sugar content in cassava plants along with increasing salicylic acid concentrations.

Effect of organic acids on fermentation quality and microbiota of horseshoe residue and corn protein powder

This experiment aimed to investigate the impact of malic acid (MA) and citric acid (CA) on the nutritional composition, fermentation quality, rumen degradation rate, and microbial diversity of a mixture of apple pomace and corn protein powder during ensiling. The experiment used apple pomace and corn protein powder as raw materials, with four groups: control group (CON), malic acid treatment group (MA, 10 g/kg), citric acid treatment group (CA, 10 g/kg), and citric acid + malic acid treatment group (MA, 10 g/kg + CA, 10 g/kg). Each group has 3 replicates, with 2 repetitions in parallel, subjected to mixed ensiling for 60 days. The results indicated: (1) Compared to the CON group, the crude protein content significantly increased in the MA, CA, and MA + CA groups (p < 0.05), with the highest content observed in the MA + CA group. The addition of MA and CA effectively reduced the water-soluble carbohydrate (WSC) content (p < 0.05). Simultaneously, the CA group showed a decreasing trend in NDFom and hemicellulose content (p = 0.08; p = 0.09). (2) Compared to the CON group, the pH significantly decreased in the MA, CA, and MA + CA groups (p < 0.01), and the three treatment groups exhibited a significant increase in lactic acid and acetic acid content (p < 0.01). The quantity of lactic acid bacteria increased significantly (p < 0.01), with the MA + CA group showing a more significant increase than the MA and CA groups (p < 0.05). (3) Compared to the CON group, the in situ dry matter disappearance (ISDMD) significantly increased in the MA, CA, and MA + CA groups (p < 0.05). All three treatment groups showed highly significant differences in in situ crude protein disappearance (ISCPD) compared to the CON group (p < 0.01). (4) Good’s Coverage for all experimental groups was greater than 0.99, meeting the conditions for subsequent sequencing. Compared to the CON group, the Shannon index significantly increased in the CA group (p < 0.01), and the Simpson index increased significantly in the MA group (p < 0.05). However, there was no significant difference in the Chao index among the three treatment groups and the CON group (p > 0.05). At the genus level, the abundance of Lentilactobacillus in the MA, CA, and MA + CA groups was significantly higher than in the control group (p < 0.05). PICRUSt prediction results indicated that the metabolic functional microbial groups in the CA and MA treatment groups were significantly higher than in the CON group (p < 0.05), suggesting that the addition of MA or CA could reduce the loss of nutritional components such as protein and carbohydrates in mixed ensilage. In conclusion, the addition of malic acid and citric acid to a mixture of apple pomace and corn protein powder during ensiling reduces nutritional losses, improves fermentation quality and rumen degradation rate, enhances the diversity of the microbial community in ensiled feed, and improves microbial structure. The combined addition of malic acid and citric acid demonstrates a superior effect.

Dendritic cell-specific intercellular adhesion molecule-3-grabbing nonintegrin (DC-SIGN) is a cellular receptor for delta inulin adjuvant.

Delta inulin, or Advax, is a polysaccharide vaccine adjuvant that significantly enhances vaccine-mediated immune responses against multiple pathogens and was recently licensed for use in the coronavirus disease 2019 (COVID-19) vaccine SpikoGen. Although Advax has proven effective as an immune adjuvant, its specific binding targets have not been characterized. In this report, we identify a cellular receptor for Advax recognition. In vitro uptake of Advax particles by macrophage cell lines was substantially greater than that of latex beads of comparable size, suggesting an active uptake mechanism by phagocytic cells. Using a lectin array, Advax particles were recognized by lectins specific for various carbohydrate structures including mannosyl, N-acetylgalactosamine and galactose moieties. Expression in nonphagocytic cells of dendritic cell-specific intercellular adhesion molecule-3-grabbing nonintegrin (DC-SIGN), a C-type lectin receptor, resulted in enhanced uptake of fluorescent Advax particles compared with mock-transfected cells. Advax uptake was reduced with the addition of ethylenediaminetetraacetic acid and mannan to cells, which are known inhibitors of DC-SIGN function. Finally, a specific blockade of DC-SIGN using a neutralizing antibody abrogated Advax uptake in DC-SIGN-expressing cells. Together, these results identify DC-SIGN as a putative receptor for Advax. Given the known immunomodulatory role of DC-SIGN, the findings described here have implications for the use of Advax adjuvants in humans and inform future mechanistic studies.

High-Yield Synthesis of Hierarchical SAPO-34 by Recrystallization Method for Efficient Methanol-to-Olefin Reactions.

Prolonging the lifetime of SAPO-34 catalysts and enhancing their olefin selectivity in methanol-to-olefin (MTO) reactions are critical yet challenging objectives. Here, a series of hierarchical SAPO-34 catalysts were synthesized using a straightforward recrystallization method. The incorporation of triethylamine into the recrystallization mother liquor facilitated the formation of mesopores, achieving a high solid yield of up to 90%. Notably, the addition of phosphoric acid and ammonium polyvinyl phosphate alcohol during the recrystallization process significantly enhanced the crystallinity and regularity of the hierarchical SAPO-34 crystals, consequently increasing the mesopore size. Due to the substantially improved mass transfer efficiency and moderated acidity, the SP34-0.14P-0.06R catalysts exhibited a prolonged operational life of 344 min and80.3%selectivity ofethylene and propylene at aWHSV of 2h-1. This performance markedly surpasses that of the parent SP34 catalyst, which demonstrated a lifetime of 136 min and a selectivity of 78.0%. Remarkably, the SP34-0.14P-0.06R maintained a lifetime of 166 minutes even at a high WHSV of 10h-1, which is more than 5-fold greater than that of the original microporous SP34. This research offers valuable insights into the design and development of hierarchically porous zeolites with high yields, enhancing the efficiency of MTO reactions and other applications.

КОФЕЙНАЯ КИСЛОТА СТИМУЛИРУЕТ СВЕЧЕНИЕ МИЦЕЛИЯ ВЫСШИХ ГРИБОВ NEONOTHOPANUS NAMBI, ARMILLARIA BOREALIS IN VIVO

In vivo experiments have shown that the addition of caffeic acid to the luminous mycelia of the higher fungi Neonothopanus nambi and Armillaria borealis stimulates a rapid and significant (by an order of magnitude or more) increase in the intensity of their light emission. It has been suggested that the observed effect of fungal luminescence activation may be mediated by the oxidation of caffeic acid by enzymes of the ligninolytic complex of basidiomycetes (in particular, by peroxidases) with the emission of visible light quanta. Comparative in vivo experiments showed that the addition of hispidin (the precursor of luciferin in the light emission reaction of higher fungi) did not affect the intensity of bioluminescence of the mycelia. At the same time, in vitro studies found that caffeic acid significantly suppressed the NADPH-hispidin-activated emission reaction of luminescent systems isolated from the mycelia of N. nambi and A. borealis. The inhibitory effect of caffeic acid is considered and discussed in the work from the standpoint of the classical biochemistry concept on enzyme inhibition by the reaction product according to the negative feedback principle. In general, the results obtained develop and supplement the understanding of the mechanisms of light emission in higher fungi and testify in favor of the fact that the generation of visible light quanta in basidiomycetes can be carried out by different biochemical pathways involving different enzymes (or enzyme systems). Clarifying the mechanism of stimulation of in vivo bioluminescence of higher fungi by caffeic acid is a priority for further research.

Studies on the Biomimetic Synthesis of Marine Ladder Polyethers via Endo‐Selective Epoxide‐to‐Epoxonium Ring‐Opening Cascades

Marine ladder polyethers have attracted the attention of chemists and biologists because of their potent biological activities. Synthetic chemists have attempted to construct their polyether frameworks by epoxide ring‐opening cascades, as Nakanishi hypothesis describes. However, Baldwin’s rules of ring closure state that exo‐selective intramolecular cyclization of epoxy alcohols is preferred over endo‐selective cyclization. Herein, we investigated epoxide ring‐opening cascades of polyepoxy alcohols in [EMIM]BF4/PFTB (1‐ethyl‐3‐methylimidazolium tetrafluoroborate /perfluoro‐tert‐butyl alcohol) and found that all‐endo products were formed via epoxide‐to‐epoxonium ring‐opening cyclizations (not restricted by Baldwin’s rules, which only apply to intramolecular hydroxyl‐to‐epoxide cyclizations). We determined that the key factor enabling polyepoxy alcohols to undergo a high proportion of all‐endo‐selective cyclizations was inhibition of exo‐selective hydroxyl‐to‐epoxide cyclization starting from the terminal hydroxyl group of a polyepoxy alcohol. By introducing a slow‐release protecting group to the terminal hydroxyl group, we could markedly increase the cyclization yields of polyether fragments with hydrogen atoms at the ring junctions. For the first time, we constructed consecutively fused six‐membered‐ring and fused seven‐, eight‐, and nine‐membered‐ring polyether fragments by epoxide‐to‐epoxonium ring‐opening cyclizations through the addition of a suitable Lewis acid. We also suggest that the biosynthesis of marine ladder polyethers may proceed via epoxide‐to‐epoxonium ring‐opening cyclization of polyepoxide.

Studies on the Biomimetic Synthesis of Marine Ladder Polyethers via Endo-Selective Epoxide-to-Epoxonium Ring-Opening Cascades.

Marine ladder polyethers have attracted the attention of chemists and biologists because of their potent biological activities. Synthetic chemists have attempted to construct their polyether frameworks by epoxide ring-opening cascades, as Nakanishi hypothesis describes. However, Baldwin's rules of ring closure state that exo-selective intramolecular cyclization of epoxy alcohols is preferred over endo-selective cyclization. Herein, we investigated epoxide ring-opening cascades of polyepoxy alcohols in [EMIM]BF4/PFTB (1-ethyl-3-methylimidazolium tetrafluoroborate /perfluoro-tert-butyl alcohol) and found that all-endo products were formed via epoxide-to-epoxonium ring-opening cyclizations (not restricted by Baldwin's rules, which only apply to intramolecular hydroxyl-to-epoxide cyclizations). We determined that the key factor enabling polyepoxy alcohols to undergo a high proportion of all-endo-selective cyclizations was inhibition of exo-selective hydroxyl-to-epoxide cyclization starting from the terminal hydroxyl group of a polyepoxy alcohol. By introducing a slow-release protecting group to the terminal hydroxyl group, we could markedly increase the cyclization yields of polyether fragments with hydrogen atoms at the ring junctions. For the first time, we constructed consecutively fused six-membered-ring and fused seven-, eight-, and nine-membered-ring polyether fragments by epoxide-to-epoxonium ring-opening cyclizations through the addition of a suitable Lewis acid. We also suggest that the biosynthesis of marine ladder polyethers may proceed via epoxide-to-epoxonium ring-opening cyclization of polyepoxide.

Quantitative assessment of ash effects on densifying lignocellulosic biomass with chemicals followed by autoclave (DLCA) pretreatment

Ash in lignocellulose is critical in interfering biomass pretreatment. Densifying Lignocellulosic biomass with Chemicals followed by Autoclave (DLCA) is a novel and efficient pretreatment method, whereas the specific effects of ash on DLCA pretreatment remain unclear. Herein, we quantitatively investigated the impacts of ash contents on the pretreatment effectiveness, enzymatic digestibility, and fermentability of DLCA pretreated corn stover (DLCA-CS). With the ash contents increasing from 3.36 % to 9.50 %, the DLCA-CS with addition of sulfuric acid (sa) showed decreased pretreatment efficiency and enzymatic digestibility, whereas these characteristics of DLCA-CS with addition of calcium hydroxide (ch) were improved with increasing ash contents. Further pH measurement during the biomass pretreatment revealed that the anions involved in ash neutralized the sulfuric acid, thus decreasing the pretreatment efficiency and enzymatic digestibility of DLCA(sa)-CS, while the anions can cooperated with the calcium hydroxide, thus increasing the pretreatment efficiency and enzymatic digestibility of DLCA(ch)-CS. The highest ethanol production of DLCA(sa)-CS (60.7 g/L) and DLCA(ch)-CS (66.5 g/L) at 25 % solid loading was achieved with a low ash content of 3.36 % without detoxification step. This study highlights the importance of controlling the ash contents for enhancing the efficiency of DLCA pretreatment.

Use of metal-tagged environmentally representative micro- and nanoplastic particles to investigate transport and retention through porous media using single particle ICP-MS

Microplastics and nanoplastics (collectively, MNPs) are increasingly entering soils, with potential adverse impacts to agriculture and groundwater. Environmental detection, characterization, and quantification of MNPs is difficult and subject to artifacts, often requiring labor-intensive separation from environmental matrices. These analytical challenges make it difficult to conduct experiments investigating specific MNP characteristics influencing their transport and fate, particularly when examining multiple plastic types at low concentrations. By synthesizing a suite of metal-tagged polymers, which are cryomilled to create polydisperse fragmented particle suspensions, single particle ICP-MS (spICP-MS) can be used to quantify MNP particle size and concentration in controlled fate and transport studies. Use of unique metal-polymer pairs enables accurate, simultaneous analysis of multiple MNP types which can be used to track total particle transport and retention within a variety of environmental matrices. This was demonstrated using saturated sand column transport experiments to quantify the movement of two plastics having different properties: tin-tagged polystyrene (Sn-PS) and tantalum-tagged polyvinylpyrrolidone (Ta-PVP). The behavior of these polydisperse, fragmented MNPs was compared to that of fluorescent, carboxylated monodisperse PS spherical microspheres (Fl-PS). Mobility of all MNP types increased with decreasing particle size, and hydrophilic Ta-PVP particles migrated more effectively than the hydrophobic Sn-PS particles. Furthermore, the addition of humic acid (HA) to the carrier solution increased the colloidal stability of both metal-tagged MNP suspensions, resulting in much greater elution from the column than in HA-free deionized water or moderately- hard water (ionic strength = 5mM). This combination of particle synthesis and spICP-MS analysis provides insights into the transport of MNP having physical properties that are representative of environmental MNPs and opens up a broad range of applications for study of MNP environmental fate and transport.

A Benign Synthesis Route to Terephthalic Acid via Two-Step Electrochemical Oxidation of P-xylene

Abstract Terephthalic acid is conventionally synthesized through the AMOCO process under harsh conditions, making milder electrosynthesis routes desirable. Electrooxidation of p-xylene has been demonstrated but the degree of oxidation is limited, resulting in low terephthalic acid yields. Here, we demonstrate a process with two electrochemical steps enabling the complete oxidation of p-xylene into terephthalic acid. The first electrochemical step achieves C-H activation of p-xylene using electrochemically generated bromine as a mediator, while the second electrochemical step does alcohol oxidation of 1,4-benzenedimethanol into terephthalate on NiOOH. The divided cell in the first step simultaneously generates acid and base that are utilized subsequently, negating the need of external acid and base addition and thus offering a cost competitive synthesis route. The competing bromide oxidation in the second step is suppressed by using constant voltage electrolysis at 0.50 V, where an optimal yield of terephthalic acid of 81% is achieved.

Antimicrobial effect of plasma-activated water combined with tartaric acid against Staphylococcus aureus and its application on fresh-cut asparagus lettuce

Plasma-activated water (PAW) is increasingly recognized for its role in mitigating microbial contamination in fresh-cut produce, but its disinfection effectiveness can be limited under certain conditions. Notably, dissolving organic acids in PAW is an effective way to boost its antimicrobial properties through a synergistic effect. This study examined the enhanced antimicrobial efficacy of PAW when combined with tartaric acid against Staphylococcus aureus and its application on fresh-cut asparagus lettuce. Results demonstrated that PAW combined with tartaric acid showed stronger antimicrobial efficacy than PAW alone (p < 0.05). The addition of tartaric acid to PAW increased the oxidation-reduction potential and lowered the pH, contributing to its superior antimicrobial performance against S. aureus. The underlying antimicrobial mechanisms included the inactivation of Ca2+-Mg2+-ATPase and Na+-K+-ATPase accompanied by damage to bacterial cell membrane, enhanced oxidative damage due to the influx of extracellular reactive oxygen species such as H2O2, the disrupted energy metabolic activities, and the mitigated bacterial defense system constructed by antioxidant enzymes, such as superoxide dismutase and catalase. Furthermore, the synergistic treatment improved the quality of fresh-cut asparagus lettuce by retarding browning, curbing microbial spoilage, and lessening weight loss. The preservation of color was largely due to the decreased activities of polyphenol oxidase and peroxidase, along with controlled chlorophyll degradation. These findings suggest that PAW enhanced with tartaric acid could be a promising, cost-effective disinfection strategy for fresh-cut asparagus lettuce.

Natural soil as the peroxymonosulfate activator for efficient remediation and detoxification of bisphenol A: Nonradical-dominated mechanism and the change of soil properties

Peroxymonosulfate (PMS) has been extensively applied in soil refractory organics remediation, but studies without an activator were scarce. Besides, the role of soil as well as the interaction between the soil constituents and PMS remained unclear. Using bisphenol A (BPA) as a model contaminant, our findings demonstrated that soil could efficiently activate PMS for BPA abatement in water and slurry. Free Fe oxides, especially crystalline Fe oxides in soil, were primarily responsible for PMS activation through nonradical pathways (singlet oxygen) for BPA removal, but soil organic matter (SOM) might inhibit the process. Moreover, BPA elimination was almost not inhibited by the addition of anions (Cl−, NO3−, HCO3−, and SO42−) and humic acid, but could be promoted by cations (Fe3+ and Mn2+). PMS oxidation caused an insignificant impact on the bioavailability of heavy metals, except for Fe, Mn, SOM, pH, total phosphorus (TP) content, soil composition, and crystal structure have not changed obviously after PMS treatment. BPA decomposition pathways were proposed based on the intermediates identified. Furthermore, the phytotoxicity of BPA − polluted soil was significantly reduced after PMS remediation in terms of crop growth indexes. Overall, the study provided new insights into the crucial role of soil constituents in PMS activation and inspired more energy or catalyst − saving soil remediation strategies.

The Synthesis of Amino-Acid-Anchored Two-Dimensional Silicoaluminophosphates and Congo Red Adsorption Application.

Two-dimensional (2D) materials with nanometer thickness have the advantage of a large specific surface area and excellent surface accessibility. They have great potential for adsorption, catalysis, and many other applications. 2D zeolitic silicoaluminophosphates (SAPOs) can be synthesized through a dual structure directing agent (SDA) strategy. But the materials have been primarily used in their organic-free form. In this work, we demonstrate that the same synthesis strategy is effective for developing amino-acid-anchored 2D SAPOs through a one-step synthesis. Because of the addition of amino acids, the surficial amino and carboxylic groups serve as active sites for adsorption and catalysis. Congo red adsorption is used to evaluate the potential of using the organic functional groups as active adsorption sites. The 2D SAPO materials have demonstrated excellent Congo red removal efficiency with close to complete removal for certain concentrations. The effects of the amino acid concentration and hydrothermal synthesis time on material morphology development will be discussed. Thorough characterization by SEM, TEM, FTIR, XRD, and nitrogen adsorption has been done to reveal the properties of the amino-acid-anchored 2D SAPOs.

PSV-11 In vitro screening of selected compounds to reduce ruminal methane production

Abstract Methane is a natural product of rumen fermentation and emissions from ruminant livestock represent a major environmental concern. Methane is not only a potent greenhouse gas but also represents a loss of energy efficiency for the host. The objective of this study was to perform in vitro screening of a range of compounds with potential anti-methanogenic activity, including polyphenols, flavonoids, fatty acids, amino acids, and salts. We aimed to select compounds conferring up to a 20% reduction in CH4 for further investigations. The substances tested included carvacrol, coumaric acid, coumarin, flavanone, gallic acid, glycerol monolaurate (GML), glycine, methylene blue, naringin, quercetin, quinic acid, resorcinol, rutin, tannic acid, vanillic acid, and zinc acetate. These substances varied in their mechanisms of action and were selected based on known antimicrobial or anti-methanogenic properties. The experiment was designed as a randomized block experiment, with treatments tested in triplicates across four batches (n = 228 samples) using the same treatments and experimental conditions. Fresh rumen contents were manually collected from two rumen-fistulated lactating Holstein cows, 3 h after their morning feeding. Rumen contents were blended at a 2:1 ratio, filtered through a four-layered cheesecloth, and added to McDougall’s solution at a 2:1 ratio. Final media (9 mL) was added to a 20 mL Bellco flask containing 150 mg of total mixed ration (TMR) ground to 1 mm. Each batch also had three flasks without TMR and no treatment (blank flasks), three flasks containing only TMR without treatment (negative control), and three flasks containing TMR and treated with chloroform (positive control), resulting in a total of 19 treatments. The end-products of in vitro batch fermentations were assessed after 24 h of incubation, and samples from each flask were collected for gas composition analysis using gas chromatography. Volatile fatty acids were determined using high-performance liquid chromatography (HPLC). The data were analyzed using R Studio, and the following model was applied: yij = µ + treatmenti + batchj + ℇij. Methane production (measured in parts per million, ppm) increased when GML, naringin, and quercetin were added compared with the negative control. In contrast, the addition of carvacrol, glycine, tannic acid, and methylene blue resulted in a decrease of up to 25% in methane production. These compounds show potential to alter ruminal fermentation and mitigate methane production and will be selected for evaluation of synergistic interactions and effects on the rumen microbial communities.

272 Effects of increasing folic acid on nursery pig growth performance and serum homocysteine

Abstract Barrows (n = 350; DNA 200×400; [n = 2,172; initial body weight (BW) = 6.0 ± 0.06 kg] were used in a 38-d growth trial to determine the effects of increasing folic acid on nursery pig growth performance and serum homocysteine. Pigs were weaned at 21 d of age and randomly allotted to 1 of 5 dietary treatments in a completely randomized design. A total of 70 pens were used with 5 pigs per pen and 14 replications per treatment. Dietary treatments were corn-soybean meal-based and consisted of increasing added folic acid: 0, 5, 10, 20, or 40 mg/kg. Treatment diets were fed in three phases from d 0 to 10 (phase 1), d 10 to 23 (phase 2), and d 23 to 38 (phase 3) after weaning. For phase 1, there were no differences (P &amp;gt; 0.10) in BW, average daily gain (ADG) and average daily feed intake (ADFI) across treatments (Table). However, increasing folic acid resulted in decreased gain to feed ratio (G:F; linear, P = 0.032). For phase 2, there was a marginally significant response in BW, ADG, and ADFI where performance was decreased as folic acid increased with the poorest performance observed when pigs were fed 20 mg/kg (quadratic, P ≤ 0.079). No treatment differences (P &amp;gt; 0.10) were observed for G:F. For phase 3 and overall (d 0 to 38), final BW, ADG, ADFI, and G:F were reduced with increasing folic acid with the poorest performance observed when pigs were fed 20 mg/kg (quadratic, P ≤ 0.049). No differences (P &amp;gt; 0.10) were observed for mortality or removals across treatments with a very low amount of overall mortality. On d 10 and 23, blood samples were collected from 70 pigs to determine serum homocysteine concentrations. A marginally significant treatment × d interaction was observed (linear folic acid × d, P = 0.069). An increase (linear, P = 0.037) in homocysteine concentrations was observed as folic acid increased from 0 to 40 mg/kg in the diet on d 10; however, no differences were observed across increasing folic acid treatments on d 23 (P = 0.450). Pigs had increased (P &amp;lt; 0.001) homocysteine concentrations on d 10 compared with d 23. In summary, the addition of folic acid resulted in reduced growth performance with the greatest impact observed when pigs were fed 20 mg/kg.

189 Combination of organic acid and monoglyceride blend improved growth performance in nursery pigs with and without added antibiotics and ZnO

Abstract This study was to investigate the effects of supplementing a combination of organic acid and monoglyceride additives in feed with and without added antibiotics and pharmacological levels of ZnO on growth performance of nursery pigs. Pigs (n = 1,008; 21 d of age with initial body weight (BW) = 5.8] were assigned to 4 treatments (n = 12, 21 pigs/pen, mixed sex) following 2 × 2 factorial experiment design and fed for 42 d in 4 phases (d 0-8, d 9-21, d 22-35, and d 36-42, respectively). Treatments were 1) Positive control (PC), basal diet with in-feed antibiotics in phase 1-3, and 3000 ppm of Zn in phase 1, 2000 ppm of Zn in phase 2 and 125 ppm of Zn in phase 3 and 4 (i.e., pharmacological levels); 2) PC supplemented with the combination of Acitra G20C (formic acid-based acid blend on inert carrier) and Entero-Nova 410C (blend of monoglycerides of short-chain and medium-chain fatty acids on inert carrier), Acitra G20C was added at 3 kg/MT in phase 1 diet and 1.5 kg/MT in phase 2 diet, while Entero-Nova 410C was added at 3 kg/MT in phase 1 and 2 diets, and 1 kg/MT in phase 3 and 4 diets; 3) Negative control (NC), basal diet without in-feed antibiotics and pharmacological levels of ZnO; and 4) NC supplemented with the combination of Acitra G20C and Entero-Nova 410C (same supplementation rate as Treatment 2). Diets contained nutrients meeting or exceeding NRC requirements. Growth performance was measured for each phase. Data were analyzed using JMP software with pen serving as the experimental unit and differences considered significant at P ≤ 0.05. Throughout the trial, pigs fed diets without in-feed antibiotics and pharmacological levels of ZnO had ess (P &amp;lt; 0.01) BW, average daily gain (ADG) and average daily feed intake (ADFI) than pigs fed diets added with antibiotics and pharmacological levels of ZnO. During the period of phase 2 and overall phase 1 and 2 of the trial, pigs fed diets supplemented with the combination of Acitra and Entero-Nova additives had greater (P &amp;lt; 0.05) ADG and ADFI and greater (P &amp;lt; 0.05) BW on d 22 of trial. In phase 3 and 4, there was no significant improvement on growth performance of pigs fed diet only supplemented with 1 kg/MT of Entero-Nova comparing with the pigs in control groups. In conclusion, under current trial conditions, the combination of Acitra G20C and Entero-Nova 410C improved growth performance of nursery pigs in phase 1 and 2 when supplemented at tested dosage comparing with pigs in control groups without the additives.

Selective removal of chromium from laterite residue with high content of iron by the co-operation of phosphoric acid and oxalic acid

With the rising demand for nickel and cobalt, laterite residue containing chromium is extensively generated through the laterite hydrometallurgical process, posing a significant burden on environmental protection and the sustainable development of the nickel industry. This study presents a novel and environmentally friendly method for selectively extracting chromium from laterite residue and yielding iron phosphate concentrate. In this method, iron, as the major component, is simultaneously transformed into iron phosphate as solid state, while chromium is extracted into solution by a minimal amount of phosphoric acid. The effects of phosphoric acid and oxalic acid usage, temperature, liquid-to-solid ratio, and leaching time on the transformation and removal were investigated. Thermodynamic analysis and experimental results indicated that the addition of oxalic acid promoted chromium extraction with minimal impact on the transformation of hematite and iron phosphate. The results of SEM, XPS, and XRD revealed the conversion of laterite residue to iron phosphate. At an oxalic acid dosage of 10 %, almost 90 % of the iron remained in the residue as iron phosphate, while over 60 % of the chromium was extracted into the solution, resulting in a chromium concentration of 1.1 g/L. The solution underwent a two-step treatment process, primarily to recycle the soluble iron species. The extracted chromium was captured by adding calcium hydroxide at pH ∼ 3.0 in the form of phosphate.

Tailoring supramolecular solvents with phosphoryl groups for highly efficient extraction of chlorophenols in natural waters

BackgroundChlorophenols are routinely determined in aquatic systems to check compliance with the restrictive international legislations set for protection of human and aquatic life. Their control requires affordable analytical methods, particularly in labs at low- and medium-income countries. Liquid chromatography-UV detection is a convenient technique for this purpose, but the availability of suitable sample processing remains pending. Organic solvents are inefficient for extracting the whole range of chlorophenols whereas solid-phase extractions are expensive and labour-intensive. So, an efficient, fast and cheap extraction of chlorophenols, amenable to any lab, would help to cope with their worldwide analytical control in natural waters. ResultsA supramolecular solvent (SUPRAS) was tailored for providing mixed interaction mechanisms aimed at the efficient extraction of chlorophenols prior to LC-UV. The SUPRAS was synthesized from the self-assembly of hexylphosphonic acid under acidic conditions and consisted of sponge-like nanostructures made up of amphiphile and water. The phosphoryl (PO) group was selected as the major driver of the extraction because of its ability to act as halogen and hydrogen bond acceptor for chlorophenols. Additional interactions were hydrogen bonds from O–H amphiphilic groups and the surrounding water, and dispersion and CH-π interactions in the hydrocarbon chains. The number of binding sites in the SUPRAS could be modulated by addition of salt. The SUPRAS formed in situ in the sample, the extraction took 5 min, the concentration factor was around 220, quantification limits (0.1–0.3 μg L−1) were below the EU standards, and the method worked for natural waters. SignificanceA fast, low-cost, and organic solvent-free sample processing only requiring conventional lab equipment (stirrers and centrifuges) provided SUPRAS extracts that could be directly analyzed by LC-UV. SUPRAS synthesis occurred spontaneously in the water sample under addition of hexylphosphonic acid and the whole process required low skills. The method meets the analytical and operational performances for the analytical control of chlorophenols in natural waters and it is within the reach of any lab.

Medium-short chain fatty acids cannot spare the essential fatty acids of low marine diets in golden pompano (Trachinotus ovatus)

Based on the essential fatty acids (EFA) precision nutrition, a blend oil (BO) of fish oil and terrestrial oils was developed, and applied successfully to the low marine diets of golden pompano (Trachinotus ovatus). To evaluate whether medium- and short-chain fatty acids (MCFA and SCFA), efficient energy supplements for animals, can spare the dietary EFA, four iso-proteic (48%) and iso-lipidic (11%) low fishmeal (FM) diets (D1-D4, contained 6% FM) were formulated and fed T. ovatus juveniles (initial weight ∼8.50 g) for 9 weeks in sea cages. Control diets (D1) contained 8% BO, while the BO of diets D2-D4 were replaced 50% with coconut oil, coconut oil + sodium butyrate, and coconut oil + n-3 LC-PUFA enriched oil, respectively. The results showed that compared to the D1 group, the growth performance of D2 and D3 were significantly lower, while a comparable growth was detected in the D4 group. The muscle and hepatic n-3 PUFA levels in the D2 and D3 groups were significantly low, and these fatty acid contents were modified in the D4 group. Meanwhile, the muscle textural firmness of the D2-D4 groups was decreased. Regarding the health index of fish, compared to the D1 group, high serum triglyceride (TG) contents and low HDL/LDL ratio were detected in the D2-D4 groups, and high ACP, AST, and ALT activities were observed in these groups. Meanwhile, high HSI and low hepatic enzymatic activities of CAT and ALT were measured in the D2-D3 groups. Additionally, the mRNA levels of hepatic fatty acid synthesis-related genes (fas, acc, and pparγ) were significantly increased in D2-D4 groups, and the expression levels of lipid catabolism genes (cpt-1 and lpl) showed an upward trend. Moreover, the D2 group exhibited the lowest intestinal wall thickness, the mRNA levels of intestine anti-inflammatory cytokines (il-10) were up-regulated in the D2-D4 groups, and the highest mRNA levels of pro-inflammatory cytokines (il-8) were detected in the D2 group. In conclusion, the EFA deficiency leads to a decline in the growth and muscle quality of T. ovatus fed low marine diets, which cannot be mitigated by the addition of medium-short chain fatty acids. The results indicated that MCFA and SCFA cannot spare the EFA of low marine diets in T. ovatus.