The Distribution Characteristics of Soil pH Values of Tobacco-growing Areas in Dali City and Its Correlation with Soil Nutrients

[Objective] The aim was to study the distribution characteristics of soil pH values and its correlation with soil nutrients in tobacco-growing areas. [Method] Soil nutrients of 43 samples from tobacco-growing areas in Dali City were analyzed.[Results] The results showed that average pH value of tobacco-planting soil in Dali City was 6.52, soil samples which suited for flue-cured tobacco cultivation accounted for 72.09% of total soil samples. In four soil types of tobacco-growing areas, the pH values in a descending order were as follows： alluvial soil〉 paddy soil 〉purple soil〉 red soil. At the altitude range of 1 780-2 200 m, soil pH values showed a gradual decreasing trend. The average contents of soil organic matters were relatively abundant and generally suited for high-quality tobacco cultivation; the average contents of soil alkali-hydrolyzable nitrogen, available phosphorus, exchangeable calcium and exchangeable magnesium were generally at medium and abundant level, however,their rations under the medium level in some tobacco-growing areas were 6.98%,11.63%, 2.33% and 4.65%, respectively; moreover, soil with lower available potassium contents occupied a large proportion, namely 58.14%. [Conclusion] Soil pH values had significant correlation with exchangeable magnesium and exchangeable magnesium, however, they had no significant correlation with other soil nutrients.

Effects of temperatures and pH values on rheological properties of cemented paste backfill

In this study,different influence mechanisms associated with temperatures and pH values were investigated through cemented paste backfill(CPB)systems.CPB samples were prepared with temperatures ranging from 10 to 50℃ in 10℃ increments and pH values of 3,7,and 13.Then,the CPB mixture were subjected to rheological tests,thermogravimetric analysis(TG),derivative thermogravimetry analysis(DTG),Fourier-transform infrared spectroscopy(FT-IR),and scanning electron microscopy(SEM).Results demonstrated that the temperatures had significant effects on the rheological properties of CPB,whereas the effects of pH values were relatively unapparent.Higher temperatures(over 20℃)were prone to bring higher shear stress,yield stress,and apparent viscosity with the same pH value condition.However,an overly high temperature(50℃)cannot raise the apparent viscosity.Non-neutral conditions,for pH values of 3 and 13,could strengthen the shear stress and apparent viscosity at the same temperature.Two different yield stress curves could be discovered by uprising pH values,which also led to apparent viscosity of two various curves under the same temperatures(under 50℃).Microscopically,rheological properties of CPB were affected by temperatures and pH values which enhanced or reduced the cement hydration procedures,rates,products and space structures.

Effect of Cu and Ni on Growth, Mineral Uptake,Photosynthesis and Enzyme Activities of Chlorella vulgaris at Different pH Values

A pH dependent reduction in growth, Pigment, ATP content, O,' evolution, carbonfixation, Photosynthetic electron transport system, nutrient uptake (NO,' and NH4+),nitrate reductase, and ATPase activities and increase in K+ emux of Chlorella vulgaris wasnoticed following supplementation of Cu and Ni to the culture medium. PS II was foundto be more sensitive to both pH and metals than PS I. Though, nitrate reductase (NR) wasmore sensitive to both PH and metals, the ATPase was however, more sensitive t0 metalsbut less sensitive to acidic pH. Acid PH was found to dst the nutrient (NO,' and NH4+)uptake and nitrate reductase in a non-competitive manner. The inhibition Pnduced by thetest metals alone was of noncompetitive type for NO3' uptake, nitrate reductase andATPase and competitive for NH'+ uptake. Acidity not only inhibited the metabolicvariables directly but also through facilitated uptake of metals and increased membranepermeability. A very low sensitivity of ATPase to acidic pH seems to be resgnsible forthe survival of algae in acid environment.

Adsorption Kinetics of NH_4^+ by Purple Soils with Different pH Values

Ammonium adsorption and desorption properties by purple soils with dif- ferent pH were studied. The results showed that the adsorption and desorption amounts of NH4＋ by purple soils increased with the increase of NH4＋ concentration, regardless of soil pH values; the largest adsorption and desorption amounts of NH4＋ by purple soil at pH 6.0 were 10.3 and 7.96 mg/g, respectively; the largest adsorp- tion and desorption amounts of NH4＋ by purple soil at pH 7.2 were 12.8 and 4.62 mg/g, respectively; the largest adsorption and desorption amounts of NH4＋ by purple soil at pH 8.0 were 13.5 and 2.23 mg/g, respectively. The isothermal adsorption ki- netics of NH4＋ by purple soils fits the Freundlich equation best （R〉0.95）. This study shows that the adsorption of NH4＋ by purple soils with different pH values is multi- molecular layer uneven surface adsorption.

X-ray absorption near-edge structure study on the configuration of Cu2＋/histidine complexes at different pH values

The local configurations around metal ions in metalloproteins are of great significance for understanding their biolog- ical functions. Cu2＋/histidine （His） is a typical complex existing in many metalloproteins and plays an important role in lots of physiological functions. The three-dimensional （3D） structural configurations of Cu2＋/His complexes at different pH values （2.5, 6.5, and 8.5） are quantitatively determined by x-ray absorption near-edge structure （XANES）. Generally Cu2＋/His complex keeps an octahedral configuration consisting of oxygen atoms from water molecules and oxygen or nitrogen atoms from histidine molecules coordinated around Cu2＋. It is proved in this work that the oxygen atoms from water molecules, when increasing the pH value from acid to basic value, are gradually substituted by the Ocarboxy1, Nam, and Nim from hisitidine molecules. Furthermore, the symmetries of Cu2＋/His complexes at pH 6.5 and pH 8.5 are found to be lower than at pH 2.5.

Effect of pH values on extracellular protein and polysaccharide secretions of Acidithiobacillus ferrooxidans during chalcopyrite bioleaching

The effect of pH values on the extracellular protein and polysaccharide secretions of Acidithiobacillus ferrooxidans was comparatively investigated in different phases of bacterial growth during chalcopyrite bioleaching. The results indicate that the extracellular protein is always more than the extracellular polysaccharide secreted by attached cells on the chalcopyrite, on the contrary, and is always less than the extracellular polysaccharide secreted by free cells in the solution at bacterial adaptive phase, logarithmic phase and stationary phase whenever pH value is at 1.0, 1.5, 2.0 or 2.5; free cells are mainly through the secretion of extracellular polysaccharide rather than the extracellular protein to fight against disadvantageous solution environment, such as high concentration of metal ions and unsuitable pH solution; both amounts of polysaccharide and protein secreted by attached cells are mainly positively related to the solution acidity rather than the total concentration of soluble metal ions. The experimental results imply that bacteria are mainly through secreting more extracellular polysaccharide to fight against disadvantageous environment and the extracellular protein perhaps plays an important role in oxidation？reduction reactions in the bioleaching system.

Corrosion behaviour of die-cast AZ91D magnesium alloys in sodium sulphate solutions with different pH values

The corrosion behaviours of die-cast AZ91D magnesium alloys were investigated in 0.1 mol/L sodium sulphate （Na 2 SO 4 ） solutions with different pH values. The corrosion rates, morphologies, and compositions of the corrosion products were studied by means of scanning electron microscopy （SEM）, Fourier transform infrared spectroscopy （FTIR）, and X-ray diffractometry （XRD）. The results indicate that the order of corrosion rates in Na 2 SO 4 solutions with various pH values is pH 2pH 4pH 7pH 9pH 12. The corrosion rates in acidic solutions are higher than those in alkaline solutions, and the corrosion products are mainly magnesium hydroxide （Mg（OH） 2 ） and hydrated sulphate pickeringite （MgAl 2 （SO 4 ） 4 ·22H 2 O）. The results also indicate that the solution pH can influence the corrosion rate and morphology of corrosion products. Chloride ions and sulphate ions have different pitting initiation time.

Correspondence between Susceptibility to SCC of 7050 Aluminum Alloy and Passive Film-induced Stress at Various pH Values

The passive film-induced stress and the susceptibility to SCC of 7050 aluminum alloy in 3.5%sodium chloride solution at various pH values were investigated by slow strain rate testing（SSRT） and flowing stress differential method.The results showed that the passive film-induced stress and the susceptibility to SCC decreased with increasing pH values when pH≤7,while they increased with increasing pH values when pH7.However,the corrosion type was interpreted as exfoliation corrosion when pH=l and 14,and there was no film formed on the surface of the specimens.The whole variation plots of film-induced stress and the SCC susceptibility with pH values were both presented as a valley shape.The symbol and amount of the film-induced stress were related to the compositions of the passive film,which were analyzed using X-ray photoelectron spectroscopy（XPS）.

Microstructure of nano precursors of La-Mg hydrogen storage alloy synthesized by sol-gel technology at different pH values

Sol-gel technology was employed to synthesize nanosized precursors of La-Mg hydrogen storage alloy at different pH values (0.5, 1.5, 8.0 and 9.0) of reaction solution. The effect of pH value on microstructure of the nano precursors of La-Mg hydrogen storage alloy was studied by infrared radiation (IR), thermo-gravimetric and differential thermal analysis (TG/DTA), X-ray diffraction analyzer (XRD) and transmission electron microscopy (TEM). IR results indicate that the chelating agent, citric acid, is not fully ionized, and carboxyl groups are not entirely used to complex metal ions in acidic solutions. The efficiency of complexing metal ions is enhanced in basic solutions. TG/DTA results show that the combustion may take place with low rate of the flame propagation that causes the longer combustion time when pH<1.5. On the contrary, the dry gel synthesized in basic solution combusts at low ignition temperature and combustion reaction is violent; it is easy to form fine particles. XRD and TEM results reveal that the precursor powders are mainly two-phase mixture of La 2 O 3 and MgO. The morphology of the particles is almost flake with the size of ~30 nm when pH is 8.0.

Morphology and photocatalytic performance of nano-sized TiO_2 prepared by simple hydrothermal method with different pH values

pH value is a key factor in the preparation of nano-sized TiO2 with hydrothermal method. Using Ti（SO4）2 as the titanium source, H2O2 as the complexing agent, NaOH and HCl as the pH value regulator, nano- sized TiO2 powder with various morphologies and sizes was synthesized. Changes in morphology, size and phase type with pH values of samples were characterized by X-ray diffraction （XRD） and transmission electron micro- scopy （TEM） measurements. Results show that under the present preparation conditions, TiO2 powder is an anatase phase with pH value less than 11, but is more likely to be a brookite phase with pH value more than 11. With the increase in pH value from 1 to 11 in hydrothermal envi- ronment, nano-sized anatase TiO2 gradually grows up in all directions. {001 }, { 101 } and { 100} groups of crystal plane are the exposed crystal planes of nano-sized anatase TiO2 for the （004）, （101） and （200） facets found in high-reso- lution TEM image. The photocatalytic performance of nano-sized TiO2 with different morphologies was com- pared by measuring their photocatalytic degradation rates for methylene blue under ultraviolet light. Results show that anatase TiO2 prepared under the alkalescenthydrothermal environment （pH = 9, 11） has a better pho- tocatalytic degrading performance. Different sizes and phases of nanoscaled TiO2 powders with different photo- catalytic performances can be prepared by the control of pH value of hydrothermal solutions.

Influence of pH value and chelating reagent on performance of Li_3V_2(PO_4)3/C cathode material

The Li3V2（PO4）3/C composite cathode material was synthesized via sol-gel method using three different chelating agents （citric acid, salicylic acid and polyacrylic acid） at pH value of 3 or 7. The crystal structure, morphology, specific surface area and electrochemical performance of the prepared samples were investigated by X-ray diffraction （XRD）, scanning electron microscopy （SEM）, cyclic voltammetry （CV）, electrochemical impedance spectroscopy （EIS） and galvanostatic charge/discharge test. The results show that the effects of pH value on the performance of the prepared materials are greatly related to the chelating agents. With salicylic acid or polyacrylic acid as the chelating reagent, the structure, morphology and electrochemical performance of the samples are greatly influenced by the pH values. However, the structure of the materials with citric acid as the chelating agent does not change as pH value changes, and the materials own uniform particle size distribution and good electrochemical performance. It delivers an initial discharge capacity of 113.58 mA·h/g at 10C, remaining as high as 108.48 mA·h/g after 900 cycles, with a capacity retention of 95.51%.

ZnO Additive Boosts Charging Speed and Cycling Stability of Electrolytic Zn–Mn Batteries

Electrolytic aqueous zinc-manganese(Zn–Mn) batteries have the advantage of high discharge voltage and high capacity due to two-electron reactions. However, the pitfall of electrolytic Zn–Mn batteries is the sluggish deposition reaction kinetics of manganese oxide during the charge process and short cycle life. We show that, incorporating ZnO electrolyte additive can form a neutral and highly viscous gel-like electrolyte and render a new form of electrolytic Zn–Mn batteries with significantly improved charging capabilities. Specifically, the ZnO gel-like electrolyte activates the zinc sulfate hydroxide hydrate assisted Mn^(2+) deposition reaction and induces phase and structure change of the deposited manganese oxide(Zn_(2)Mn_(3)O_8·H_(2)O nanorods array), resulting in a significant enhancement of the charge capability and discharge efficiency. The charge capacity increases to 2.5 mAh cm^(-2) after 1 h constant-voltage charging at 2.0 V vs. Zn/Zn^(2+), and the capacity can retain for up to 2000 cycles with negligible attenuation. This research lays the foundation for the advancement of electrolytic Zn–Mn batteries with enhanced charging capability.

Influence of pH Value on Photocatalytic Activity of Bi4Ti3O12 Crystals Obtained by Hydrothermal Method

Bi4Ti3O12 （BIT） crystals were controllably synthesized via a facile hydrothermal process without adding any surfactant or template. The morphologies of BIT with nanosphere, nanoplate, nanobelt, and nanosheet can be selectively obtained by adjusting the pH value of the reactant. The formation mechanisms of these distinctive morphologies were then discussed based on the structural analysis of samples obtained at different pH values. BIT sample prepared at pH=1 showed the highest photocatalytic activity under visible light irradiation. The photocatalytic activities difference for the BIT samples synthesized at different pH values was studied based on their shape, size, and the variation of local structure.

Study on Pathogenicity Difference of Plasmodiophora brassicae Under Different Temperature and pH Conditions

[Objective] This study was conducted to investigate the pathogenicity of Plasmodiophora brassicae on cabbage grown under different temperature and soil pH conditions. [Method] The pathogenicity of P. brassicae were tested at seven different temperatures and at six different soil pH values with the resting spore concentration of lx108 （spores/g） in the soil. The plant survival rate and incidence rate of clubroot were investigated after 90 d. [Result] The incidence rate of clubroot on cabbage among the different temperature sets varied in a descending order as follows： 30 ℃〉25 ℃〉20 ℃〉35 ℃〉15 ℃〉10 ℃〉5 ℃ at soil pH value of 6, indicating that the pathogenicity of P. brassicae was weak at 5 and 10 ~（3. The incidence rate increased with soil temperature increasing from 15 to 30 ℃, but decreased at 35 ℃. The incidence rates of clubroot were 80.36%, 100%, 65%, 10.77%, 3.23% and 0% at soil pH 4, 5, 6, 7, 8 and 9 at 25 ℃, respectively. The growth of cabbage was inhibited and the survival rate was reduced at pH 4.The incidence rates of clubroot were low at pH value of 7 and 8, and was 0% at pH 9. The Chinese cabbage grew better at pH value of 5 and 6, but had high incidence rates of clubroot. [Conclusion] The results revealed that the incidence rate of clubroot on cabbage was closely related to the temperature and soil pH.

Changes and Correlations of Duroc Muscle pH,Glycogen,Lactic Acid and TBA under Different Storage Condition

The changes and correlations of muscle pH, glycogen, lactic acid and in- tramuscular fat oxidation in Duroc pigs 10 d after their slaughter, and the effects of different storage temperature and time on Duroc muscle pH value, water loss rate, glycogen, lactic acid and 2-thiobarbituric acid （TBA） were studied. The results showed that during the 10 h after the slaughter, the pH value was decreased rapid- ly, the lactic acid content was increased significantly, while the glycogen and TBA contents were remained stable. At the storage temperature of 4 ℃, storage time showed no significant effects on Duroc muscle pH value and glycogen, lactic acid and TBA contents. At the storage temperature of -20 ℃, storage temperature had significant effects on pH value, while no significant effects on other indicators. The correlation analysis demonstrated that during the 10 h after the slaughter, the TBA content was negatively related to glycogen content （P〈0.05）, but positively related to lactic content （P〈0.05）; the pH value was negatively related to lactic acid content （P〈0.05）. At the storage temperature of 4 ℃, the TBA content was negatively relat- ed to water loss rate （P〈0.01） and lactic acid content （P〈0.05）; the water loss rate was positively related to pH value （P〈0.01） and lactic acid content （P〈0.05）. At the storage temperature of -20 ℃, the TBA content was negatively related to pH value （P〈0.01） and positively related to water loss rate （P〈0.05）; the water loss rate was negatively related to pH value （P〈0.01） and lactic acid content （P〈0.05）.

The Stability of Endomorphin-1 Solution

Aim To study the most stable pH value of endomorphin-1 solution and toestimate the shelf-life of EM-1 solution. Methods The content of EM-1 in its solution was determinedby HPLC, and stability was studied by accelerated tests. Results The most stable pH value of EM-1solution was observed. By the accelerated tests we obtained the Arrhe-nius relationship and thepharmacokinetic parameters. Conclusion The most stable pH value of EM-1 solution is 4.5 -4.8. Thet_(1/2)(25℃) is 45 d.

Factors Influencing the Acidification Trends in Agriculture Soils: A Case Study of Slovakia

This study aims to evaluate the development of soil reaction values in 15 key localities of soil Partial Monitoring System from 1994 to 2023, and to identify the most important regional drivers of pH value development. Soil samples were collected from the depth 0 - 0.10 m yearly in the spring (5 samples from each locality). In the dry soil, samples were determined actively and exchanged soil reaction. The most significant negative changes (decreases of soil reaction) were determined in Haplic Stagnosols group and Cambisols group. The pH value in topsoil is primarily controlled by soil type and soil substrate, soil management and land use, and to a lesser extent by climatic region.

Effect of humic substances on the precipitation of calcium phosphate

For phosphorus （P） recovery from wastewater, the effect of humic substances （HS） on the precipitation of calcium phosphate was studied. Batch experiments of calcium phosphate precipitation were undertaken with synthetic water that contained 20 mg/L phosphate （as P） and 20 mg/L HS （as dissolved organic carbon, DOC） at a constant pH value in the range of 8.0-10.0. The concentration variations of phosphate, calcium （Ca） and HS were measured in the precipitation process; the crystalline state and compositions of the precipitates were analysed by powder X-ray diffraction （XRD） and chemical methods, respectively. It showed that at solution pH 8.0, the precipitation rate and removal efficiency of phosphate were greatly reduced by HS, but at solution pH ≥9.0, the effect of HS was very small. The Ca consumption for the precipitation of phosphate increased when HS was added; HS was also removed from solution with the precipitation of calcium phosphate. At solution pH 8.0 and HS concentrations ≤3.5 mg/L, and at pH ≥ 9.0 and HS concentrations ≤ 10 mg/L, the final precipitates were proved to be hydroxyapatite （HAP） by XRD. The increases of solution pH value and initial Ca/P ratio helped reduce the influence of HS on the precipitation of phosphate.

Physical and Chemical Transformation of Hydroxyapatite Nanoparticles in Aqueous Sol after Preparation and in vitro

The co-precipitation method followed by ultrasound and heat treatment is a common way to prepare below 100 nm sized hydroxyapathe nanoparticles for biomedical studies and applications. The size and pH value of the obtained calcium phosphate nanoparticles in aqueous sol have a strong impact on the interactions with cells and tissue. The physical and chemical properties of material samples for in vitro and in vivo studies are often assumed to remain constant from the time after fabrication to the actual use. Only little attention is paid to eventual changes of the material over time or due to the different in vitro conditions. In this study, the physical and chemical transformation of calcium phosphate nanoparticles after preparation and in vitro was investigated. As the result showed, dispersed nano sized amorphons calcium phosphate precipitation as well as crystallized hydroxyapathe nanoparticles continue to crystallize even when kept at 4℃ leading to declining pH values and particle sizes. Due to the pH buffer in the medium the pH value of the cell culture remained stable after adding 20% nanoparticle sol in vitro. However, hydroxyapathe nanoparticles immediately became unstable in the presents of cell culture medium. The resulting loose agglomerations showed a size of above 500 nm.

Historical simulation and twenty-first century prediction of oceanic CO_2 sink and pH change

A global ocean carbon cycle model based on the ocean general circulation model POP and the improved biogeochemical model OCMIP-2 is employed to simulate carbon cycle processes under the historically observed atmospheric CO 2 concentration and different future scenarios （called Rep- resentative Concentration Pathways, or RCPs）. The RCPs in this paper follow the design of Inter- governmental Panel on Climate Change （IPCC） for the Fifth Assessment Report （AR5）. The model results show that the ocean absorbs CO 2 from atmosphere and the absorbability will continue in the 21st century under the four RCPs. The net air-sea CO 2 flux increased during the historical time and reached 1.87 Pg/a （calculated by carbon） in 2005; however, it would reach peak and then decrease in the 21st century. The ocean absorbs CO 2 mainly in the mid latitude, and releases CO 2 in the equator area. However, in the Antarctic Circumpolar Current （ACC） area the ocean would change from source to sink under the rising CO 2 concentration, including RCP4.5, RCP6.0, and RCP8.5. In 2100, the anthropogenic carbon would be transported to the 40 S in the Atlantic Ocean by the North Atlantic Deep Water （NADW）, and also be transported to the north by the Antarctic Bottom Water （AABW） along the Antarctic continent in the Atlantic and Pacific oceans. The ocean pH value is also simulated by the model. The pH decreased by 0.1 after the industrial revolution, and would continue to decrease in the 21st century. For the highest concentration sce- nario of RCP8.5, the global averaged pH would decrease by 0.43 to reach 7.73 due to the absorption of CO 2 from atmosphere.