scholarly journals Boron Fertilizer Product and Concentration Influence Spray Water pH

2000 ◽  
Vol 10 (2) ◽  
pp. 350-353
Author(s):  
Frank J. Peryea ◽  
Jennifer M. Lageschulte
Keyword(s):  
Boric Acid ◽  
Natural Waters ◽  
Agricultural Chemicals ◽  
Solution Ph ◽  
Initial Water ◽  
Multiple Products ◽  
Ph Values ◽  
Water Composition ◽  
Water Ph ◽  
The Stability

Farmers often mix fertilizers, pesticides and other agricultural chemicals together in a spray tank to allow applications of multiple products in a single spray. Because polyborate-based B fertilizers may increase solution pH, adding B to tank-mixed sprays may impair the stability and efficacy of alkalinity-sensitive pesticides and growth regulators if an acidifier is not included. We conducted a laboratory experiment to determine the influence of 10 commercial B fertilizer sources in factorial combination with B concentrations ranging from 0 to 4 lb/100 gal (4.8 g·L-1) on solution pH values of distilled water and two natural waters. Two boric acid-based compounds produced acidic reactions relative to background water pH at all tested B concentrations. Their pH responses were influenced by initial water composition. Seven B products produced moderately to strongly alkaline reactions at all but the highest B concentration, regardless of the form of B (polyborate vs. boric acid) initially present in the formulated products. One polyborate product formulated with an acidifier showed intermediate pH behavior. The dependence of solution pH on B rate of the polyborate-containing products was identical in all three waters. The maximum pH values generated by all products occurred in the B concentration range <0.1 to 0.25 lb/100 gal (0.12 to 0.3 g·L-1). Solution pH values declined with increasing B concentration above this range. The pH responses qualitatively conformed to known aqueous chemical behavior of B and the product additives. The complexity of the interaction between initial water chemistry, B concentration, and B fertilizer product reinforces the need to measure the pH of B-amended spray water before adding pH-sensitive compounds.

The kinetics of the reaction of boric acid with salicylic acid

1977 ◽  
Vol 55 (16) ◽  
pp. 3035-3039 ◽  
Author(s):  
Alan Queen
Keyword(s):  
Salicylic Acid ◽  
Boric Acid ◽  
Kinetic Data ◽  
Similar Process ◽  
Stopped Flow ◽  
Ph Values ◽  
The Stability ◽  
Kinetics Of ◽  
Protonated Ligand ◽  
Salicylate Ion

Salicylic acid forms a 1:1 complex with boric acid, the reaction involving both the fully protonated ligand, and the salicylate ion. The kinetics of this reaction have been studied by the stopped-flow method. The stability constant for the reaction involving salicylate ion has been calculated from measurements of the absorbances of solutions at equilibrium and is the same as that obtained from the kinetic data. The kinetic results at pH values in the range 3.45–4.63 suggest that, when salicylic acid is the ligand, the complex is formed in two steps. A similar process may also occur with salicylate ions.

scholarly journals Comparison of stability properties of poly(acrylic acid) adsorbed on the surface of silica, alumina and mixed silica-alumina nanoparticles — application of turbidimetry method

2014 ◽  
Vol 12 (4) ◽  
pp. 476-479 ◽  
Author(s):  
Małgorzata Wiśniewska ◽  
Teresa Urban ◽  
Agnieszka Nosal-Wiercińska ◽  
Vladimir Zarko ◽  
Vladimir Gun’ko
Keyword(s):  
Acrylic Acid ◽  
Colloidal Suspensions ◽  
Alumina Nanoparticles ◽  
Solution Ph ◽  
Ph Values ◽  
Silica Alumina ◽  
Effective Stabilizer ◽  
The Stability ◽  
Over Time ◽  
Poly Acrylic Acid

AbstractThe influence of anionic poly(acrylic acid) — PAA addition on the stability of synthesized silica, alumina and mixed silica-alumina suspensions as a function of solution pH was studied. The turbidimetry method was used to monitor the changes of the examined systems stability over time. The calculated stability coefficients enabled estimation of polymer adsorption influence on stability of metal oxide suspension. It was shown that the alumina suspension without the polymer is the most unstable at the pH values 6 and 9, whereas the silica polymer was most unstable at pH 3. PAA with higher molecular weight (240 000) is a relatively effective stabilizer of all investigated adsorbents (except silica at pH 3). These properties of poly(acrylic acid) are highly desirable in many branches of industry (e.g. production of cosmetics, pharmaceuticals, paints) where polymers are widely used as effective stabilizers of colloidal suspensions.

scholarly journals A Study of Dispersed, Thermally Activated Limestone from Ukraine for the Safe Liming of Water Using ANN Models

Energies ◽  
2021 ◽  
Vol 14 (24) ◽  
pp. 8377
Author(s):  
Yuliia Trach ◽  
Roman Trach ◽  
Marek Kalenik ◽  
Eugeniusz Koda ◽  
Anna Podlasek
Keyword(s):  
Surface Water ◽  
Loss Function ◽  
Validation Dataset ◽  
Ann Model ◽  
Initial Water ◽  
Water Parameters ◽  
Thermally Activated ◽  
Ph Values ◽  
Water Ph ◽  
Ann Models

Liming surface water is a fairly popular method of increasing the pH values and decreasing the concentration of phosphates and heavy metals. According to the Environmental Protection Agency (EPA) recommendations, the increase of water pH should not exceed 1.5. If surface water is the source of water supply, liming is a process that reduces water contamination. This should prevent the creation of an additional load for the water treatment plants in urban settlements. This article is an interdisciplinary research study aiming to (1) determine and compare the doses of new dispersed, thermally activated limestone and natural limestone, (2) find the relation between dose value and initial water parameters (pH, Eh and total mineralization), and (3) create an artificial neural network (ANN) model to predict changes in water pH values according to EPA recommendations. Recommended doses were obtained from experimental studies, and those of dispersed, thermally activated limestone were lower than the doses of natural limestone. Neural networks were used to predict the changes in water pH values when adding different doses of limestone with different initial water parameters using the ANN model. Four ANN models with different activation functions and loss function optimizers were tested. The best results were obtained for the network with the ReLU activation function for hidden layers of neurons and Adam’s loss function optimizer (MAPE = 14.1%; R2 = 0.847). Further comparison of the results of the loss function and the results of calculating the quality metric for the training and validation dataset has shown that the created ANN can be used to solve the set research issue.

UV Curable Organic-Inorganic Hybrid Materials

2000 ◽  
Vol 628 ◽  
Author(s):  
Guang-Way Jang ◽  
Ren-Jye Wu ◽  
Yuung-Ching Sheen ◽  
Ya-Hui Lin ◽  
Chi-Jung Chang
Keyword(s):  
Hybrid Materials ◽  
Colloidal Silica ◽  
Sol Gel ◽  
Solution Ph ◽  
Uv Curable ◽  
Inorganic Hybrid ◽  
Degradation Temperature ◽  
Sol Gel Process ◽  
The Stability ◽  
Thermal Degradation Temperature

This work successfully prepared an UV curable organic-inorganic hybrid material consisting of organic modified colloidal silica. Applications of UV curable organic-inorganic hybrid materials include abrasion resistant coatings, photo-patternable thin films and waveguides. Colloidal silica containing reactive functional groups were also prepared by reacting organic silane and tetraethyl orthosilicate (TEOS) using sol-gel process. In addition, the efficiency of grafting organic moiety onto silica nanoparticles was investigated by applying TGA and FTIR techniques. Experimental results indicated a strong interdependence between surface modification efficiency and solution pH. Acrylate-SiO2 hybrid formation could result in a shifting of thermal degradation temperature of organic component from about 200°C to near 400°C. In addition, the stability of organic modified colloidal silica in UV curable formula and the physical properties of resulting coatings were discussed. Furthermore, the morphology of organic modified colloidal silica was investigated by performing TEM and SEM studies‥

scholarly journals Adsorptive and Coagulative Removal of Trace Metals from Water Using Surface Modified Sawdust-Based Cellulose Nanocrystals

J ◽  
2021 ◽  
Vol 4 (2) ◽  
pp. 193-205
Author(s):  
Opeyemi A. Oyewo ◽  
Sam Ramaila ◽  
Lydia Mavuru ◽  
Taile Leswifi ◽  
Maurice S. Onyango
Keyword(s):  
Trace Metals ◽  
Adsorption Capacity ◽  
Cellulose Nanocrystals ◽  
Inductively Coupled Plasma ◽  
Electrostatic Interactions ◽  
Natural Waters ◽  
Maximum Adsorption Capacity ◽  
Solution Ph ◽  
Major Drawback ◽  
Surface Modified

The presence of toxic metals in surface and natural waters, even at trace levels, poses a great danger to humans and the ecosystem. Although the combination of adsorption and coagulation techniques has the potential to eradicate this problem, the use of inappropriate media remains a major drawback. This study reports on the application of NaNO2/NaHCO3 modified sawdust-based cellulose nanocrystals (MCNC) as both coagulant and adsorbent for the removal of Cu, Fe and Pb from aqueous solution. The surface modified coagulants, prepared by electrostatic interactions, were characterized using Fourier transform infrared, X-ray diffraction (XRD), and scanning electron microscopy/energy-dispersive spectrometry (SEM/EDS). The amount of coagulated/adsorbed trace metals was then analysed using inductively coupled plasma atomic emission spectroscopy (ICP-AES). SEM analysis revealed the patchy and distributed floccules on Fe-flocs, which was an indication of multiple mechanisms responsible for Fe removal onto MCNC. A shift in the peak position attributed to C2H192N64O16 from 2θ = 30 to 24.5° occurred in the XRD pattern of both Pb- and Cu-flocs. Different process variables, including initial metal ions concentration (10–200 mg/L), solution pH (2–10), and temperature (25–45 °C) were studied in order to investigate how they affect the reaction process. Both Cu and Pb adsorption followed the Langmuir isotherm with a maximum adsorption capacity of 111.1 and 2.82 mg/g, respectively, whereas the adsorption of Fe was suggestive of a multilayer adsorption process; however, Fe Langmuir maximum adsorption capacity was found to be 81.96 mg/g. The sequence of trace metals removal followed the order: Cu > Fe > Pb. The utilization of this product in different water matrices is an effective way to establish their robustness.

scholarly journals Measurement of the Intestinal pH in Mice under Various Conditions Reveals Alkalization Induced by Antibiotics

Antibiotics ◽  
2021 ◽  
Vol 10 (2) ◽  
pp. 180
Author(s):  
Kouki Shimizu ◽  
Issei Seiki ◽  
Yoshiyuki Goto ◽  
Takeshi Murata
Keyword(s):  
Antibiotic Treatment ◽  
High Protein Diet ◽  
Intestinal Bacteria ◽  
High Protein ◽  
Protein Diet ◽  
Germ Free ◽  
Treatment Regimens ◽  
Ph Values ◽  
Specific Pathogen ◽  
The Stability

The intestinal pH can greatly influence the stability and absorption of oral drugs. Therefore, knowledge of intestinal pH is necessary to understand the conditions for drug delivery. This has previously been measured in humans and rats. However, information on intestinal pH in mice is insufficient despite these animals being used often in preclinical testing. In this study, 72 female ICR mice housed in SPF (specific pathogen-free) conditions were separated into nine groups to determine the intestinal pH under conditions that might cause pH fluctuations, including high-protein diet, ageing, proton pump inhibitor (PPI) treatment, several antibiotic treatment regimens and germ-free mice. pH was measured in samples collected from the ileum, cecum and colon, and compared to control animals. An electrode, 3 mm in diameter, enabled accurate pH measurements with a small amount of gastrointestinal content. Consequently, the pH values in the cecum and colon were increased by high-protein diet, and the pH in the ileum was decreased by PPI. Drastic alkalization was induced by antibiotics, especially in the cecum and colon. The alkalized pH values in germ-free mice suggested that the reduction in the intestinal bacteria caused by antibiotics led to alkalization. Alkalization of the intestinal pH caused by antibiotic treatment was verified in mice. We need further investigations in clinical settings to check whether the same phenomena occur in patients.

Spray-Tank-Mix Compatibility of Manganese, Boron, and Fungicide: Solution pH and Precipitation1

1993 ◽  
Vol 20 (1) ◽  
pp. 44-49 ◽  
Author(s):  
N. L. Powell
Keyword(s):  
Boric Acid ◽  
Foliar Application ◽  
Water Solution ◽  
Inorganic Salts ◽  
Well Water ◽  
Manganese Sulfate ◽  
Solution Ph ◽  
Deep Well ◽  
Cupric Hydroxide ◽  
Disodium Octaborate Tetrahydrate

Abstract Foliar application of manganese and boron mixed with pesticides in water solution is a common practice for peanut (Arachis hypogaea L.) production. This study was conducted to determine the compatibility of mixing manganese, boron, and leafspot fungicides using water from three sources. Spray mixtures of the chelated manganese salt of ethylene diamine tetra-acetate and the inorganic salts of manganese as manganese sulfate(TECMANGAMTM), manganese sulfate monohydrate, manganese chloride, and manganese nitrate were developed using deep-well water, shallow well water, or distilled water. Boron was added to these mixtures using boric acid or disodium octaborate tetrahydrate. In addition, all combinations were mixed with the leafspot fungicides chlorothalonil or cupric hydroxide plus sulfur. Mixtures were equivalent to recommended rates of manganese, boron, and fungicide applied to the foliage in 140 L ha-1 of spray volume. Measurements were made of solution pH and manganese remaining in solution after filtration. Development of precipitates was noted. In the deep-well water solution (pH = 8.0), addition of manganese sulfate, manganese sulfate monohydrate and manganese chloride caused precipitates to form. Manganese nitrate and chelated manganese solutions did not form precipitates. Addition of disodium octaborate tetrahydrate increased the tank-mix pH for all waters source, and caused increased precipitation of the manganese inorganic salts, but not the chelated manganese. Use of boric acid in the water lowered solution pH, and all manganese sources remained in solution. Spray-tank-mix pH was critical in keeping all manganese inorganic salts in solution. For all pH levels studied (pH 4.6 to 8.4) the chelated manganese remained in solution without formation of a precipitate. Chemical analyses of the filtrate showed that only 75 to 80% of the inorganic salts of manganese remained in solution with disodium octaborate tetrahydrate, while 100% of the chelated manganese salt remained in solution. Inorganic salts of manganese and disodium octaborate tetrahydrate should not be mixed with chlorothalonil, and none of the manganese materials should be mixed with cupric hydroxide plus sulfur as a spray-tank-mixture for foliar application.

Study on Influence of Silicate Morphology Based on pH Value

2012 ◽  
Vol 454 ◽  
pp. 324-328
Author(s):  
Yan He ◽  
Ya Jing Liu ◽  
Yong Lin Cao ◽  
Li Xia Zhou
Keyword(s):  
Silicic Acid ◽  
Ph Value ◽  
Colorimetric Method ◽  
Absorption Spectrometry ◽  
Degree Of Polymerization ◽  
Raw Material ◽  
X Ray Diffraction ◽  
X Ray ◽  
Ph Values ◽  
The Stability

Infra-red absorption spectrometry, X-ray diffraction observations and characterization tests based on silicon molybdenum colorimetric method were used to investigate the optimal pH value controlling the stability of the silicic acid form. The experiment process was done by using sodium silicate as raw material. The results showed that the solution of silicate influenced the polymerization. The active silicic acid solution with a certain degree of polymerization was obtained by controlling the pH values.

672 An Investigation of Antibiotic Loading and Release in Acid-precipitated Keratin Proteins to Treat Topical Burn Infections

2021 ◽  
Vol 42 (Supplement_1) ◽  
pp. S192-S193
Author(s):  
Marc A Thompson ◽  
Robert J Christy
Keyword(s):  
Proteolytic Enzymes ◽  
Diglycidyl Ether ◽  
Water Soluble ◽  
Bacterial Colony ◽  
Freeze Dried ◽  
Antibiotic Compounds ◽  
Water Ph ◽  
Stable Product ◽  
Antibiotic Release ◽  
The Stability

Abstract Introduction Human-hair derived keratin (KOS) protein has been selected in this investigation for its ability to bind antibiotic compounds and provide sustained release while withstanding harsh proteolytic environments such as inflamed, damaged tissue. The need to control local flora has been recognized as an imperative for wound healing, as recovery is significantly hampered by infection. This study investigates the synthesis of KOS-based particulate matter, developed using acid-precipitation, to load and release the water-soluble antibiotic ciprofloxacin (CIP). We hypothesize that ionically bound CIP release is tied to the degradation of KOS, therefore, bacterial metabolism, which produces proteolytic enzymes, will trigger CIP release thereby creating a novel self-extinguishing delivery system for contaminated skin wounds. Methods Ciprofloxacin hydrochloride was solubilized in deionized water (pH 5.3) under constant stirring. Freeze-dried KOS powder was added for an ultimately 5% w/v and 0.8% w/v solution of KOS and CIP, respectively. To improve the stability of KOS a water-soluble diglycidyl ether crosslinker was added to solutions and stirred for 24 hours. CIP-loaded protein was precipitated out by a hydrochloric acid induced pH reduction. Samples were collected and frozen at -20 °C prior to lyophilization, thus forming the stable product. Degradation of KOS and commensurate release of CIP were measured using a bicinchoninic acid (BCA) assay and fluorescent measurements of hydrated material supernatant. The reduction of bacterial colonies was validated by a broth inhibition assay whereby CIP-loaded KOS or unloaded KOS controls where hydrated in bacterial-laden broth cultures of Pseudomonas aeruginosa or Methicillin-resistant Staphylococcus aureus. Cultures were sampled at 24, 48, or 72 hours and plated to quantify colony-forming units. Results The presence of CIP in the KOS protein was confirmed and release rates follow similar patterns to that of KOS degradation. CIP-loaded proteins significantly reduce bacterial colony presence in concentrated inoculant solutions up to 72 hours. Conclusions CIP release does appear to coincide with KOS degradation, which is bolstered in the presence of infectious levels of bacteria. Ongoing studies aim to observe more robust models of infection and more controlled antibiotic release.

USING MALIC ACID SOLUTIONS FOR THE HYDRATION OF VEGETABLE OILS AND LECITHIN PRODUCTION

2020 ◽  
Author(s):  
Л.А. МАРЧЕНКО ◽  
Т.Н. БОКОВИКОВА ◽  
Е.В. ЛИСОВАЯ ◽  
С.А. ИЛЬИНОВА ◽  
Е.П. ВИКТОРОВА
Keyword(s):  
Malic Acid ◽  
Complex Compounds ◽  
Point Of View ◽  
Magnesium Ions ◽  
Ph Values ◽  
Calcium And Magnesium ◽  
The Stability ◽  
The Cost ◽  
Calcium And Magnesium Ions

Исследована возможность применения яблочной кислоты (ЯК) в качестве гидратирующего агента для перевода негидратируемых форм фосфолипидов в гидратируемые. Выбор ЯК обусловлен ее стоимостью, которая в 1,5 раза меньше стоимости янтарной кислоты, широко применяемой в качестве гидратирующего агента, а также большей доступностью с точки зрения промышленного производства. Исследование процесса комплексообразования и определение состава комплексных соединений ЯК с ионами кальция и магния осуществляли методом потенциометрического титрования. Установлено, что внесение в раствор ЯК ионов кальция и магния приводит к снижению значений рН, что свидетельствует о наличии комплексообразования в указанных системах. Наиболее устойчивыми являются комплексы ионов кальция и магния с непротонированным лигандом при соотношении Ме2 : лиганд 1 : 1. В процессе комплексообразования ионы Ca2 и Mg2 вытесняют протоны только карбоксильных групп ЯК, которая с ионами кальция образует более устойчивые комплексы, чем с ионами магния. Показано, что устойчивость комплексов ЯК с ионами кальция и магния значительно выше, чем устойчивость комплексов фосфатидилсеринов и фосфатидных кислот с указанными ионами. Использование водных растворов ЯК в качестве гидратирующего агента позволит повысить эффективность процесса гидратации и увеличить выход фосфолипидов и, следовательно, готового продукта лецитина. The possibility of using malic acid (MA) as a hydrating agent for converting non-hydrated forms of phospholipids into hydrated ones has been investigated. The choice of MA is due to its cost, which is 1,5 times less than the cost of succinic acid, as well as greater availability from the point of view of industrial production. The study of the complexation process and determination of the composition of complex compounds of MA with calcium and magnesium ions was carried out by the method of potentiometric titration. It was found that the introduction of calcium and magnesium ions into the MA solution leads to a decrease in pH values, which indicates the presence of complexation in these systems. Complexes of calcium and magnesium ions with an unprotected ligand at a ratio of ME2 : ligand 1 : 1 are the most stable. In the process of complexing, Ca2 and Mg2 ions displace protons only of the carboxyl groups of MA, which forms more stable complexes with calcium ions than with magnesium ions. It is shown that the stability of MA complexes with calcium and magnesium ions is significantly higher than the stability of phosphatidylserine and phosphatidic acid complexes with these ions. Using water solutions of MA as a hydrating agent will increase the efficiency of the hydration process and increase the yield of phospholipids and, consequently, the finished product lecithin.

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