Organic acid mediated nutrient extraction efficiency in three calcareous soils

Soil Research ◽  
2009 ◽  
Vol 47 (2) ◽  
pp. 213 ◽  
Author(s):  
Z. Khademi ◽  
D. L. Jones ◽  
M. J. Malakouti ◽  
F. Asadi ◽  
M. Ardebili
Keyword(s):  
Organic Acids ◽  
Organic Acid ◽  
Acid Concentration ◽  
Extraction Efficiency ◽  
Solid Phase ◽  
Calcareous Soils ◽  
Ionic Form ◽  
High Concentrations ◽  
Extractant Solution ◽  
Nutrient Extraction

This study was conducted to evaluate the effects of organic acids on the concentrations of metals and anions in soil solution. Three soils with contrasting CaCO3 contents were extracted with organic acid solutions (citrate and oxalate) of different concentrations for different time periods and analysed for Fe, Mn, Zn, Cu, P, and Ca. The soils showed a significant change after the addition of the organic acids to the soil. The mobilisation of metals from the solid phase was dependent on concentration and ionic form of organic acid. High concentrations of citric acid were more effective than oxalate in mobilising Ca, Fe, Mn, and Zn. Overall; oxalate was slightly more effective than citrate in mobilising P. Generally, the higher the organic acid concentration of the extractant solution, the greater was the amount of elements extracted from the soil. Citrate tended to be more effective than oxalate at mobilising elements from the soil. All pH changes were dependent on organic acid concentration.

scholarly journals Fate of Citric Acid Addition on Mineral Elements Availability in Calcareous Soils of Jordan Valley

2021 ◽  
pp. 82-89
Author(s):  
Zohuir A. Al-balawna ◽  
Ideisan I. Abu-Abdoun
Keyword(s):  
Citric Acid ◽  
Plant Growth ◽  
Organic Acid ◽  
Calcareous Soils ◽  
Chemical Properties ◽  
Ionic Concentration ◽  
Ionic Form ◽  
Soil Density ◽  
Jordan Valley ◽  
Citric Acid Concentration

The variation in physical and chemical properties of calcareous soils in Jordan valley has been changed dramatically due to use large amount of fertilizers in regular manner. Addition of organic acid such as citric acid (CA), can greatly change the pH which can affects plant growth and production, the weakly ionized organic acid present in the calcareous soil mostly in the form of organic matter, can play major rule in soils to raise the availability of mineral nutrients that are essential for crops, by lowering soil density, reducing soil salinity and the effects of suspended particles in soil which may hinder plant growth. The reduction in the pH of the soil enhance the availability of nutrients such as Fe, Cu, Zn, ions, by converting the metallic insoluble state to ionic form, and thus nutrients are easily available for plants intake, the salinity of the soil did not change by increasing the citric acid concentration, while the pH of the soil decreases. Data are presented to show the effects of citric acid (CA) concentration, ionic concentration of iron, copper, Zinc and manganese and the decrease in soil PH and soil density.

scholarly journals Development of an online-coupled MARGA upgrade for the two-hourly quantification of low-molecular weight organic acids in the gas and particle-phase

2018 ◽  
Author(s):  
Bastian Stieger ◽  
Gerald Spindler ◽  
Dominik van Pinxteren ◽  
Achim Grüner ◽  
Markus Wallasch ◽  
...  
Keyword(s):  
Molecular Weight ◽  
Organic Acids ◽  
Organic Acid ◽  
Gas Phase ◽  
Solid Phase ◽  
Ambient Air ◽  
Low Molecular Weight ◽  
Gradient System ◽  
Particle Phase ◽  
Separation Columns

Abstract. A method is presented to quantify the low-molecular weight organic acids formic, acetic, propionic, butyric, pyruvic, glycolic, oxalic, malonic, succinic, malic, glutaric, and methanesulfonic acid in the atmospheric gas and particle phase in a two-hourly time resolution, based on a combination of the Monitor for AeRosols and Gases in ambient Air (MARGA) and an additional ion chromatography (IC) instrument. A proper separation of the organic target acids was initially tackled by a laboratory IC optimization study, testing different separation columns, eluent compositions and eluent flow rates both for isocratic and for gradient elution. Satisfactory resolution of all compounds was achieved using a gradient system with two coupled anion exchange separation columns. Online pre-concentration with an enrichment factor of approximately 400 was achieved by solid phase extraction consisting of a methacrylate polymer based sorbent with quaternary ammonium groups. The limits of detection of the method range between 7.1 ng m−3 for methanesulfonate and 150.3 ng m−3 for pyruvate. Precisions are below 1.0 %, except for glycolate (2.9 %) and succinate (1.0 %). Comparisons of inorganic anions measured at the TROPOS research site in Melpitz, Germany, by the original MARGA and the additional organic acid IC systems are in agreement with each other (R2 = 0.95 − 0.99). Organic acid concentrations from May 2017 as an example period are presented. Monocarboxylic acids were dominant in the gas phase with mean concentrations of 553 ng m−3 for acetic acid, followed by formic (286 ng m−3), pyruvic acid (182 ng m−3), propionic (179 ng m−3), butyric (98 ng m−3) and glycolic (71 ng  m−3). Particulate glycolate, oxalate and methanesulfonate were quantified with mean concentrations of 63 ng  m−3, 74 ng m−3 and 35 ng m−3, respectively. Elevated concentrations in the late afternoon of gas phase formic acid and particulate oxalate indicate a photochemical formation.

Electrospun nanofibers prepared using polystyrene (PS) with polymeric additives for the determination of nicotine in cigarette mainstream smoke

2014 ◽  
Vol 6 (14) ◽  
pp. 5120-5126 ◽  
Author(s):  
Zhifeng Guo ◽  
Xiaoyang Wu ◽  
Jingjing Dong ◽  
Hiudan Su ◽  
Ru Cai
Keyword(s):  
Solid Phase Extraction ◽  
Extraction Efficiency ◽  
Solid Phase ◽  
Electrospun Nanofibers ◽  
Phase Extraction ◽  
Mainstream Smoke ◽  
Polymeric Additives ◽  
Cigarette Mainstream Smoke

The objective of this paper is to use electrospun nanofibers as the adsorbents in solid phase extraction (SPE) to improve the extraction efficiency.

LC–MS-MS Method for the Determination of Antidepressants and Benzodiazepines in Meconium

2020 ◽  
Vol 44 (6) ◽  
pp. 580-588
Author(s):  
A López-Rabuñal ◽  
E Lendoiro ◽  
M Concheiro ◽  
M López-Rivadulla ◽  
A Cruz ◽  
...  
Keyword(s):  
Extraction Efficiency ◽  
Solid Phase ◽  
Gradient Methods ◽  
Reversed Phase ◽  
Process Efficiency ◽  
Limit Of Quantification ◽  
Mode 2 ◽  
Positive Mode ◽  
Compound Method

Abstract An LC–MS-MS method for the determination of 14 benzodiazepines (BZDs) (alprazolam, α-hydroxyalprazolam, clonazepam, bromazepam, diazepam, nordiazepam, lorazepam, lormetazepam, oxazepam, flunitrazepam, 7-aminoflunitrazepam, triazolam, midazolam and zolpidem) and 15 antidepressants (ADs) (amitriptyline, nortriptyline, imipramine, desipramine, clomipramine, norclomipramine, fluoxetine, norfluoxetine, sertraline, norsertraline, paroxetine, venlafaxine, desmethylvenlafaxine, citalopram and desmethylcitalopram) in meconium was developed and validated. Meconium samples (0.25 ± 0.02 g) were homogenized in methanol and subjected to mixed-mode cation exchange solid-phase extraction. Chromatographic separation was performed in reversed phase, with a gradient of 0.1% formic acid in 2 mM ammonium formate and acetonitrile. Two different chromatographic gradient methods were employed, one for the separation of ADs and another for BZDs. Analytes were monitored by tandem mass spectrometry employing electrospray positive mode in MRM mode (2 transitions per compound). Method validation included: linearity [n = 5, limit of quantification (LOQ) to 400 ng/g], limits of detection (n = 6, 1–20 ng/g), LOQ (n = 9, 5–20 ng/g), selectivity (no endogenous or exogenous interferences), accuracy (n = 15, 90.6–111.5%), imprecision (n = 15, 0–14.6%), matrix effect (n = 10, −73 to 194.9%), extraction efficiency (n = 6, 35.9–91.2%), process efficiency (n = 6, 20.1–188.2%), stability 72 h in the autosampler (n = 3, −8.5 to 9%) and freeze/thaw stability (n = 3, −1.2 to −47%). The method was applied to four meconium specimens, which were analyzed with and without hydrolysis (enzymatic and alkaline). The authentic meconium samples tested positive for alprazolam, α-hydroxyalprazolam, clonazepam, diazepam, nordiazepam, fluoxetine, norfluoxetine, clomipramine and norclomipramine. Therefore, the present LC–MS-MS method allows a high throughput determination of the most common BZDs and ADs in meconium, which could be useful in clinical and forensic settings.

scholarly journals Fe3O4@C Nanoparticles Synthesized by In Situ Solid-Phase Method for Removal of Methylene Blue

Nanomaterials ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 330
Author(s):  
Hengli Xiang ◽  
Genkuan Ren ◽  
Yanjun Zhong ◽  
Dehua Xu ◽  
Zhiye Zhang ◽  
...  
Keyword(s):  
Methylene Blue ◽  
Solid Phase ◽  
Raw Materials ◽  
Phase Method ◽  
Maximum Adsorption Capacity ◽  
High Catalytic Activity ◽  
Solid Phase Reaction ◽  
Phase Reaction ◽  
High Concentrations

Fe3O4@C nanoparticles were prepared by an in situ, solid-phase reaction, without any precursor, using FeSO4, FeS2, and PVP K30 as raw materials. The nanoparticles were utilized to decolorize high concentrations methylene blue (MB). The results indicated that the maximum adsorption capacity of the Fe3O4@C nanoparticles was 18.52 mg/g, and that the adsorption process was exothermic. Additionally, by employing H2O2 as the initiator of a Fenton-like reaction, the removal efficiency of 100 mg/L MB reached ~99% with Fe3O4@C nanoparticles, while that of MB was only ~34% using pure Fe3O4 nanoparticles. The mechanism of H2O2 activated on the Fe3O4@C nanoparticles and the possible degradation pathways of MB are discussed. The Fe3O4@C nanoparticles retained high catalytic activity after five usage cycles. This work describes a facile method for producing Fe3O4@C nanoparticles with excellent catalytic reactivity, and therefore, represents a promising approach for the industrial production of Fe3O4@C nanoparticles for the treatment of high concentrations of dyes in wastewater.

scholarly journals PSVIII-16 The effects of adding two organic acid blends with or without high levels of zinc or copper, on post-weaning pig performance

2020 ◽  
Vol 98 (Supplement_3) ◽  
pp. 209-210
Author(s):  
Casey L Bradley ◽  
Jon Bergstrom ◽  
Jeremiah Nemechek ◽  
J D Hahn
Keyword(s):  
Phosphoric Acid ◽  
Benzoic Acid ◽  
Organic Acids ◽  
Organic Acid ◽  
Factorial Design ◽  
Sodium Butyrate ◽  
Weaned Pigs ◽  
Weaning Pig ◽  
Pig Performance ◽  
Dietary Treatments

Abstract A subset of 720 weaned pigs (6.44 ± 0.1 kg, PIC genetics, approximately 21-d of age) were used in a 42-d trial with a 2x3 factorial design evaluating the effects of adding organic acid (OA) blends [factor 1 = no organic acid (NO), Acid Pak 1 (AP1), Acid Pak 2 (AP2)] to diets with or without higher levels of Zn or Cu [factor 2 = +/-PZC] on pig performance. Pigs were allotted 10 pigs/pen to 12 weight blocks and randomly assigned the six dietary treatments. The +PZC diets contained 3000 ppm Zn (d 0-7), 2000 ppm Zn (d 8-21), and 250 ppm Cu (d 21-42) and -PZC diets contained 95 ppm Zn and 20 ppm Cu (d 0-42). The AP1 and AP2 diets used 0.9% of 2 acid premixes (d 0-21), and 0.45% of the premixes (day 22-42). AP1 provided 0.5% benzoic acid, 0.07% sodium butyrate, and 0.025% phosphoric acid (day 0-21) and half those levels (day 22-42). AP2 included the same acids as AP1 but at half the rate and combined with 7 other organic acids and carvacrol. From d 0-21, ADG, ADFI, and G:F were improved (P< 0.01) by +PZC compared to -PZC and by AP1 or AP2 compared to NO (P< 0.02). Overall (d 0-42), ADG and G:F were improved (P< 0.01) by +PZC compared to -PZC and by AP1 or AP2 compared to NO (P< .010). Data from this trial indicate that performance was improved by the addition of both OA and PZC. However, pigs fed OA and -PZC performed similarly to those fed NO and +PZC in the post-weaning period. In summary, regardless of the acid combination, organic acid supplementation has the potential to improve growth performance in weaned pigs.

scholarly journals Evolution of Food Safety Features and Volatile Profile in White Sturgeon Caviar Treated with Different Formulations of Salt and Preservatives during a Long-Term Storage Time

Foods ◽  
2021 ◽  
Vol 10 (4) ◽  
pp. 850
Author(s):  
Annalaura Lopez ◽  
Federica Bellagamba ◽  
Erica Tirloni ◽  
Mauro Vasconi ◽  
Simone Stella ◽  
...  
Keyword(s):  
Food Safety ◽  
Organic Acids ◽  
Solid Phase ◽  
Current Trend ◽  
Storage Period ◽  
Storage Conditions ◽  
Sensory Profile ◽  
Volatile Profile ◽  
Safety Parameters ◽  
Statistic Model

Caviar is a semi-preserved fish preparation in which cold storage (around 0 °C) and packaging under anaerobic conditions are fundamental to guarantee adequate safety parameters. Consumers seem to prefer caviar prepared with food salt only, but according to the needs of the different distribution channels, some preservatives are used in order to prolong its shelf life and to allow less restrictive storage conditions. Traditionally, the most common preservative was sodium tetraborate (borax), a salt that contributes to the sensory profile of caviar. However, due to its toxicity, borax has been banned in many countries, and the current trend is to reduce or eliminate its use. In this study, we evaluated the evolution of food safety parameters (pH, water activity, microbiological parameters) and the volatile profile during 14 months of storage in caviar samples treated with three different preservatives: I. exclusively NaCl, II. a mixture of borax and NaCl, and III. a mixture of organic acids and salts. Microbial presence was studied by means of plate counts; volatile organic compounds were identified on the sample headspace by means of solid phase microextraction with gas-chromatography and mass spectrometry. Results showed relevant differences among the three treatments investigated, with salt samples characterized by the highest viable counts and the greatest presence of volatile products driven by oxidative and spoilage processes, mainly occurring toward lipid and amino acids. On the contrary, the mixture of organic acids and salts showed the best response during the entire storage period. Finally, the employment of a multiparametric statistic model allowed the identification of different clusters based on the time of ripening and the preservative treatments used.

The Xylem Sap of Maize Roots: Its Collection, Composition and Formation

1988 ◽  
Vol 15 (4) ◽  
pp. 557 ◽  
Author(s):  
MJ Canny ◽  
ME Mccully
Keyword(s):  
Amino Acids ◽  
Organic Acids ◽  
Organic Acid ◽  
Aspartic Acid ◽  
Xylem Sap ◽  
Great Variability ◽  
Reduced Pressure ◽  
Transpiration Stream ◽  
Maize Roots ◽  
Total Amino Acids

Three methods of sampling xylem sap of maize roots were compared: sap bleeding from the stem cut just above the ground; sap bleeding from the cut tops of roots still undisturbed in the ground; and sap aspirated from excavated roots under reduced pressure. The bleeding saps were often unobtainable. When their composition was measured with time from cutting, the concentrations of the major solutes approximately doubled in 2 h. Aspirated sap was chosen as the most reliable sample of root xylem contents. Solute concentrations of the saps showed great variability between individual roots for all solutes, but on average the concentrations found (in �mol g-1 sap) were: total amino acids, 1.8; nitrate, 1.8; sugars (mainly sucrose), 5.4; total organic acids, 18.3. Individual amino acids also varied greatly between roots. Glutamine, aspartic acid and serine were generally most abundant. The principal organic acid found was malic, approximately 8 �mol g-1. From these analyses the ratios of carbon in the fractions (sugars : amino acids : organic acids) = (44 : 6 : 50). 14Carbon pulse fed to a leaf appeared in the root sap within 30 min, rose to a peak at 4-6 h, and declined slowly over a week. During all this time the neutral, cation and anion fractions were sensibly constant in the proportions 86 : 10 : 4. The 14C therefore did not move towards the equilibrium of 12C-compounds in the sap. It is argued that the results do not support a hypothesis of formation of amino carbon from recent assimilate and reduced nitrate in the roots and an export of this to the shoot in the transpiration stream.

scholarly journals Characterization of Aerosol Composition, Aerosol Acidity and Organic Acid Partitioning at an Agriculture-Intensive Rural Southeastern U.S. Site

2018 ◽  
Author(s):  
Theodora Nah ◽  
Hongyu Guo ◽  
Amy P. Sullivan ◽  
Yunle Chen ◽  
David J. Tanner ◽  
...  
Keyword(s):  
Oxalic Acid ◽  
Organic Acids ◽  
Organic Acid ◽  
Organic Aerosol ◽  
Water Soluble ◽  
Molar Concentration ◽  
Particle Phase ◽  
Aerosol Composition ◽  
Phase Water ◽  
Acetic Acids

Abstract. The implementation of stringent emission regulations has resulted in the decline of anthropogenic pollutants including sulfur dioxide (SO2), nitrogen oxides (NOx) and carbon monoxide (CO). In contrast, ammonia (NH3) emissions are largely unregulated, with emissions projected to increase in the future. We present real-time aerosol and gas measurements from a field study conducted in an agricultural-intensive region in the southeastern U.S. during the fall of 2016 to investigate how NH3 affects particle acidity and SOA formation via the gas-particle partitioning of semi-volatile organic acids. Particle water and pH were determined using the ISORROPIA-II thermodynamic model and validated by comparing predicted inorganic HNO3-NO3− and NH3-NH4+ gas-particle partitioning ratios with measured values. Our results showed that despite the high NH3 concentrations (study average 8.1 ± 5.2 ppb), PM1 were highly acidic with pH values ranging from 0.9 to 3.8, and a study-averaged pH of 2.2 ± 0.6. PM1 pH varied by approximately 1.4 units diurnally. Formic and acetic acids were the most abundant gas-phase organic acids, and oxalate was the most abundant particle-phase water-soluble organic acid anion. Measured particle-phase water-soluble organic acids were on average 6 % of the total non-refractory PM1 organic aerosol mass. The measured molar fraction of oxalic acid in the particle phase (i.e., particle-phase oxalic acid molar concentration divided by the total oxalic acid molar concentration) ranged between 47 and 90 % for PM1 pH 1.2 to 3.4. The measured oxalic acid gas-particle partitioning ratios were in good agreement with their corresponding thermodynamic predictions, calculated based on oxalic acid’s physicochemical properties, ambient temperature, particle water and pH. In contrast, gas-particle partitioning of formic and acetic acids were not well predicted for reasons currently unknown. For this study, higher NH3 concentrations relative to what has been measured in the region in previous studies had minor effects on PM1 organic acids and their influence on the overall organic aerosol and PM1 mass concentrations.

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