Esterification by the Plasma Acidic Water:Novel Application of Plasma Acid

This work explores the possibility of plasma acid as acid catalyst in organic reactions. Plasma acidic water was prepared by dielectric barrier discharge and used to catalyze esterification of n-heptanioc acid with ethanol. It is found that the plasma acidic water has a stable and better performance than sulfuric acid, meaning that it is an excellent acid catalyst. The plasma acidic water would be a promising alternative for classic mineral acid as a more environment friendly acid.

Dynamically-evolved surface heterojunction in iridium nanocrystals boosting acidic oxygen evolution and overall water splitting

Simultaneously realizing improved activity and stability of acidic oxygen evolution reaction(OER) electrocatalysts is highly promising for developing cost-effective sustainable energy in the splitting of water technique.Herein,we report iridium nanocrystals embedded into 3D conductive clothes(Ir-NCT/CC) as a low iridium electrocatalyst realizing ultrahigh acidic OER activity and robust stability.The well-designed Ir-NCT/CC requires a low overpotential of 202 mV to reach the current density of 10 mA cm^(-2)with a high mass activity of 1754 A g^(-1).Importantly,in acidic overall water splitting,Ir-NCT/CC merely delivers a cell voltage of 1.469 V at a typical current density of 10 mA cm^(-2)and also maintains robust durability under continuous operation.We identify that a low working voltage drives the formation of a highly stable amorphous IrOxactive phase over the surface of Ir nanocrystals(surface heterojunction IrOx/Ir-NCT) during operating conditions,which contributes to an effective and durable OER process.

Effects of Drinking Slightly Acidic Electrolytic Water on Growth Performance and Behavior of Broilers

[Objective]The paper was to study the effects of drinking slightly acidic electrolytic water on growth performance and behavior of Rose 308 broilers,and to provide reference for the application of slightly acidic electrolytic water in broiler breeding.[Method]A total of 300 healthy 10-day-old Rose 308 broilers with similar body weight were randomly divided into five groups,three replicates each group,20 broilers each replicate.The broilers in control group were supplied with normal drinking water,and the broilers in experimental groups consumed slightly acidic electrolytic water with 0.3,0.5,0.7,1.0 mg/L residual chlorine,respectively.The test lasted 21 d.[Result]At 10-30 days of age,the water consumption of broilers in 0.7 and 1.0 mg/L electrolytic water groups were increased by 9.27%and 7.67%respectively compared with the control group(M<0.05).The average daily feed intake(ADFI)of broilers in 0.7 and 1.0 mg/L electrolytic water groups were increased compared with the control group(Q0.05).The average daily gain(ADG)of broilers in 0.7 mg/L electrolytic water group was 11.99%lower than that in control group(M<0.05).The feed gain ratio(F/G)of broilers in 0.5 mg/L electrolytic water group was 12.29%lower than that in control group(M<0.05),and the mortality was the lowest in 0.5 mg/L electrolytic water group.The standing,feeding and drinking frequency of broilers in experimental groups were higher than that in control group,and the flapping behavior of broilers in 0.5 mg/L electrolytic water group was the lowest.[Conclusion]Drinking slightly acidic electrolytic water has positive effect on the growth and behavior of broilers.

Synergistic Ru/RuO_(2) heterojunctions stabilized by carbon coating as efficient and stable bifunctional electrocatalysts for acidic overall water splitting

The development of highly active and stable acidic water oxidation electrocatalysts is of great significant for promoting the industrial application of proton exchange membrane electrolyzers.Ru-based catalysts have broad application prospects in acidic water oxidation,but their limitations in stability and activity hinder their further application.Herein,a nitrogen-doped carbon(NC)coated porous Ru/RuO_(2) heterojunctional hollow sphere(Ru/RuO_(2)/NC)is designed as high-active and stable bifunctional electrocatalyst for acidic oxygen evolution reaction(OER)and hydrogen evolution reaction(HER).In synthesis,the key is to use mesoporous polydopamine spheres as a template for forming hollow spheres,a source of NC coating and a reducing agent for forming Ru/RuO_(2) heterojunction.The Ru/RuO_(2) heterojunction adjusts the electronic structure of Ru active sites,optimizing the adsorption of intermediate species.Furthermore,the NC coating and the interaction between NC and Ru/RuO_(2) effectively prevent Ru from over-oxidation and dissolution.The porous hollow structure provides more exposed active sites and promotes mass transfer.Impressively,Ru/RuO_(2)/NC exhibits outstanding OER and HER performance with low overpotentials of 211 and 32 mV at 10 mA·cm^(−2),respectively,and shows excellent stability.The acid water splitting electrolyzer,based on the bifunctional Ru/RuO_(2)/NC,requires low cell voltages of 1.46 and 1.76 V at 10 and 100 mA·cm^(−2),respectively,with good stability for over 100 h operation,surpassing Pt/C||RuO_(2) and most of the reported catalysts.

Nanostructured Pt@RuO_(x) catalyst for boosting overall acidic seawater splitting

In the domain of acidic water splitting,designing bifunctional catalysts that marry high activity with enduring stability is a formidable challenge.Herein,we have constructed platinum-containing ruthenium oxide nanoparticles(Pt@RuO_(x)NPs)to achieve excellent overall water splitting performance in acidic electrolytes.Pt@RuO_(x)NPs demonstrate exceptional catalytic activity for both the hydrogen evolution reaction(HER)and oxygen evolution reaction(OER)in acidic seawater,requiring overpotentials of only 20 and 157 mV,respectively to achieve a current density of 10 mA cm^(-2).Furthermore,in 0.5 M H_(2)SO_(4),this catalyst exhibits high HER(19 mV)and OER(236 mV)catalytic activities.The two-electrode water splitting system composed of bifunctional Pt@RuO_(x)NPs requires cell voltages of only 1.442 and 1.465 V to deliver a current density of 10 mA cm^(-2)in acidic seawater and 0.5 M H_(2)SO_(4).Remarkably,this catalyst displays remarkable stability in the water splitting process.It is shown that the introduction of Pt could augment oxygen vacancies and enhance catalytic activity significantly.The synergy between Pt and Ru further contributes to the improved performance.Additionally,we have observed that acidic seawater holds distinct advantages for acidic water splitting,along with a thorough exploration of the relationship between Cl^(-)concentration and catalytic performance.This study not only provides a strategy to improve the catalytic activity and stability of ruthenium-based catalysts for water splitting in acidic environments,but also unveils the promoting effect of Cl^(-)on the catalytic activity in acidic water splitting.

Acidithiobacillus ferrooxidans enhanced heavy metals immobilization efficiency in acidic aqueous system through bio-mediated coprecipitation

This study investigated the promotion effect of A.ferrooxidans on complex heavy metals coprecipitation process.A.ferrooxidans significantly enhanced the ferrous oxidation,which also promoted the formation of iron-oxyhydroxysulphate.Cu(II)concentration reduced to0.058mmol/L in A.ferrooxidans inoculated system,and Cd also reduced to the lowest concentration(0.085mmol/L).Pb was mainly immobilized as anglesite and iron-oxyhydroxysulphate promoted the removal of remanent Pb in solution.The precipitates are characterized by XRD,SEM,and FTIR analysis.The main component of the iron-oxyhydroxysulphate was well crystallized jarosite.A.ferrooxidans contributed to the formation of schwertmannite in later monovalent cation lack stage.Higher ferrous iron oxidation rate and Fe(III)supply rate in A.ferrooxidans inoculated system facilitated polyhedron crystal formation and the increase of particle diameter.Complex heavy metals could be incorporated into iron oxyhydroxysulphate crystal,and efficiently removed from acidic wastewater through A.ferrooxidans mediated coprecipitation.

Effects of high-pressure activated slightly acidic electrolyzed water on cleaning and sterilization of pig transfer vehicles

The establishment of biosafety system is of enormous importance to the livestock and poultry production in terms of mitigating the transmission of diseases and implementing regional prevention and control measures.However,the current sterilization technology presents several drawbacks,including time-consuming procedures,chemical residues,and challenges in treating the sewage after rinsing.In this study,a novel cleaning and sterilization method that combines slightly acidic electrolyzed water and high pressure water-jet was developed.An orthogonal test was conducted to examine the correlation between high-pressure conditions and the various non-structural parameters on the efficacy of sterilization rate.In a field test,the effectiveness of the technology in cleaning pig transfer vehicles was evaluated by the total plate count and variations of community composition.The findings revealed that the combination of process parameters,including an available chlorine concentration of 200 mg/L,rinsing pressure of 170 bar,rinsing duration of 10 s,and residence time of 15 min,resulted in a removal rate of colony concentration on the surface of pig transfer vehicles of(96.50±0.91)%.Moreover,it was demonstrated to effectively inhibit a variety of pathogenic bacteria.The innovative cleaning system has the potential to replace traditional methods and reduces pollution while saving time and labor.It introduces a novel approach for sterilization of transportation in livestock and poultry farms as well as the biosafety construction of the animal husbandry.

Effect of ocean environmental factors on sound absorption by boric acid relaxation in sea water

By using the expressions for the maximum absorption per wavelength (αλ),and the relaxation frequency fr of the boric acid relaxation derived previously by the author and employing the related oceanographic literatures, the effects of pressure, temperature, pH and salinity on (αλ)r and ∫r of the boric acid relaxation in sea water have been estimated. Results show that ( αλ), not only increases with pH but also increases approximately linearly with pressure and temperature, and is nearly proportional to the 1. 35 power of salinity. However, pressure, pH and salinity have negligible effect on ∫r; therefore, ∫r, can be approximately expressed as a function of temperature only. Comparisons of the predicted with the measured ( αλ)r and ∫r in different ocean areas are given.

The buffering effects of aquatic sediments against acidic deposition

The cation exchange and the chemical weathering are two important processes for sedi-ments to buffer the acidification of surface water. In this paper, for sediments these two processeshave been studied. The relationship between BFC of sediments and ANC of the surface waters andthe weathering characteristics of sediments were discussed. The buffering effect and mechanism of sedi-ments against acidic deposition have also been studied. The results show that BFC of sediments arepositively correlative to ANC of the surface waters. the chemical weathering rate of sediments can beexpressed as R=k×[H￣ +]￣m.

Preliminary Study on the Control of Kiwifruit Canker by 6%Ascorbic Acid Water Aqua

[Objectives]This study was conducted to investigate the control efficacy of 6% ascorbic acid water aqua on kiwifruit bacterial canker. [Methods]The ascorbic acid water aqua was sprayed onto annual potted kiwifruit seedlings once every 5 d,for three times in total,and Pseudomonas syringae pv. Actinidiae was inoculated by needle punching 7 d later. Scab diameter and number of newly infected scab were investigated to analyze the control efficacy. [Results] Kiwifruit plants were treated with 6% ascorbic acid water aqua,and after 30 d,the 20 mg/L treatment showed an incidence rate of 25. 5%,and the 60 mg/L treatment exhibited an incidence rate only of 12. 1%; and after 60 d,the relative control efficacy reached 90. 7% at the mass concentration of 60 mg/L. [Conclusions] The6% ascorbic acid water aqua weakened the destruction and expansion of the pathogen in plants,effectively improved the resistance in kiwifruit plants,and had certain control efficacy on kiwifruit canker.

Experiment of Water Soluble Fertilizers Containing Humic Acid in Tomato Planting

As a natural macromolecular organic compound,humic acid can promote plant growth.Water soluble humic acid fertilizers refer to liquid or solid water soluble fertilizers made by adding appropriate amounts of nitrogen,phosphorus,potassium macroelements or zinc,boron,iron,molybdenum,manganese,copper and other trace elements or organic matter,based on humic acid in the required proportions for plant growth.In order to verify the application effect of humic acid containing water soluble fertilizer produced by Tai’an Gold Land Chemical Co.,Ltd.,in tomato production in Daiyue District,Tai’an City,a fertilizer effect application experiment of humic acid containing water soluble fertilizer on tomato planting was specially carried out.The results showed that the water soluble fertilizer containing humic acid could obviously improve the agronomic characters of tomato;the yield was significantly increased;the effect of increasing the income of tomato growers was obvious.

Health Consequences of Acid Rain in South West Sweden——Influence of Acid Well Water on Health and Hair Mineral Pattern

Acid rain leads to loss of essential elements from soils and bedrock, causing an imbalance in especially dug well waters, as essential element concentrations decrease and potentially toxic element concentrations increase. In this study 72 private dug wells from acid regions (pH 7.0) in South-western Sweden. Women, drinking the water for at least 5 years, were interviewed about their health and water and hair samples were collected. The concentrations of about 40 elements in water and hair were analysed, mostly by ICP-MS. The concentrations of essential elements such as Ca, Cr, Mo, Se, K, and SO4 as well as the body’s buffering agent HCO3 were significantly lower in acid than in alkaline water. The median Ca concentration was 6 times lower in acid waters, and also in hair compared to alkaline. Median HCO3 was 14 times lower in acid waters. Mg was similar in both populations, since the Swedish bedrock in general has low Mg content, even so limestone in the alkaline area. The concentrations of especially Ca, Cr, HCO3 and SO4, peaked at pH 7.0 - 8.0, due to precipitation of carbonates and sulphates in alkaline soils and leaching from acid soils. The levels of toxic metals such as Cd and Pb were significantly higher in acid well water. High Cu concentration from pipes, causing especially diarrhoea, is a serious acidification problem. The contribution of essential elements to the daily intake from these well waters, 2 Litres consumption per day, was from 0% to above 30% for some elements, clearly showing that 10%, which is generally predicted, can be exceeded for people with private well waters, as well as provide 0%, which is the case for many acid well waters. Water elements were mirrored in hair, e.g. Ca and Mo. The loss of essential minerals, and increased concentration of toxic elements in acid well water, caused mineral imbalances in the body, as mirrored in hair. Women living in the acid area reported more negative health changes than women in the alkaline district, during the time they had been drinking their well water. The number of reported heart, intestinal, muscle, and skin problems were between 2 and 9 times higher among women drinking acid than alkaline well water.

BASICITY ON ZEOLITE NAX AFTER WATER HANDLING STUDIED BY TPD OF ORGANIC ACID

In this paper the effect of ion-exchange simplified as water handling on basic zeolitewas studied.It was foond that the interaction between chemisorbed water and Na+-O2- couplewould increase the total number of basic sites, while weaken the intensity of each basic sites.Theprocess can be explained by the adsorb model of organic acid on NaX presented before.

Preparation and Characterization of CA-MA Eutectic/Silicon Dioxide Nanoscale Composite Phase Change Material from Water Glass via Sol-Gel Method

This work mainly involved the preparation of a nano-scale form-stable phase change material（PCM） consisting of capric and myristic acid（CA-MA） binary eutectic acting as thermal absorbing material and nano silicon dioxide（nano-SiO_2） serving as the supporting material. Industrial water glass for preparation of the nano silicon dioxide matrix and CA-MA eutectic mixture were compounded by single-step sol-gel method with the silane coupling agent. The morphology, chemical characterization and form stability property of the composite PCM were investigated by transmission electron microscopy（TEM）, scanning electron microscopy（SEM）, Fourier-transform infrared（FT-IR） spectroscopy and polarizing microscopy（POM）. It was indicated that the average diameter of the composite PCM particle ranged from 30-100 nm. The CA-MA eutectic was immobilized in the network pores constructed by the Si-O bonds so that the composite PCM was allowed no liquid leakage above the melting temperature of the CA-MA eutectic. Differential scanning calorimetry（DSC） and thermogravimetric analysis（TGA） measurement were conducted to investigate the thermal properties and stability of the composite PCM. From the measurement results, the mass fraction of the CA-MA eutectic in the composite PCM was about 40%. The phase change temperature and latent heat of the composite were determined to be 21.15 ℃ and 55.67 J/g, respectively. Meanwhile, thermal conductivity of the composite was measured to be 0.208 W·m^（-1）·K^（-1） by using the transient hot-wire method. The composite PCM was able to maintain the surrounding temperature close to its phase change temperature and behaved well in thermalregulated performance which was verified by the heat storage-release experiment. This kind of form-stable PCM was supposed to complete thermal insulation even temperature regulation by the dual effect of relatively low thermal conductivity and phase change thermal storage-release properties. So it can be formulated that the nanoscale CA-MA/SiO_2 composite PCM with the form-stable property, good thermal storage capacity and relatively low thermal conductivity can be applied for energy conservation as a kind of thermal functional material.

Au core-PtAu alloy shell nanowires for formic acid electrolysis

Inefficient electrocatalysts and high-power consumption are two thorny problems for electrochemical hydrogen(H2)production from acidic water electrolysis.Herein we report the one-pot precise synthesis of ultrafine Au core-Pt Au alloy shell nanowires(Au@PtxAu UFNWs).Among them,Au@Pt_(0.077) Au UFNWs exhibit the best performance for formic acid oxidation reaction(FAOR)and hydrogen evolution reaction(HER),which only require applied potentials of 0.29 V and-22.6 m V to achieve a current density of 10 m A cm^(-2),respectively.The corresponding formic acid electrolyzer realizes the electrochemical H2 production at a voltage of only 0.51 V with 10 m A cm^(-2) current density.Density functional theory(DFT)calculations reveal that the Au-riched Pt Au alloy structure can facilitates the direct oxidation pathway of FAOR and consequently elevates the FAOR activity of Au@Pt_(0.077) Au UFNWs.This work provides meaningful insights into the electrochemical H_(2) production from both the construction of advanced bifunctional electrocatalysts and the replacement of OER.

Modulating metal-organic frameworks for catalyzing acidic oxygen evolution for proton exchangemembrane water electrolysis

Proton exchangemembrane(PEM)water electrolysis represents one of the most promising technologies to achieve green hydrogen production,but currently its practical viability is largely affected by the slow reaction kinetics of the anodic oxygen evolution reaction(OER)in an acidic environment.While noble metal-based catalysts containing iridium or ruthenium are excellent catalysts for the acidic OER,their practical use in PEM electrolyzers is hindered due to their low abundance and high cost.Most recently,metal-organic frameworks(MOFs)have been demonstrated as a perfect platform to facilitate the design of acidic OER catalysts with both high efficiency and cost-effectiveness.Here,we pro-vide a timely and comprehensive overview of the recent progress on MOF-based acidic OER catalysts.The fundamental mechanisms of the acidic OER are first introduced,followed by a summary of the development of pristine MOFs and MOF derivatives as acidic OER catalysts.Importantly,a number of catalyst design strategies are discussed aiming at improving the acidic OER catalytic per-formance of MOF-based candidates.The integration of MOF-based catalysts into real PEM water electrolyzers is also included.Finally,future research directions are provided to achieve better MOF-based catalysts operational in acidic envi-ronments and PEM devices.

Efficiently coupled glucose oxidation for high-value D-glucaric acid with ultradurable hydrogen via Mn(III)in acidic solution

The electrooxidation of the alcohol and aldehyde molecules instead of water coupled with H2 production has been proven to be effective for producing high-value fine chemicals under alkaline conditions.It is also noteworthy that under acidic conditions,the stability of non-noble metal water oxidation catalysts remains a great challenge due to the lattice oxygen mechanism.Hence,we coupled the biomass-derived glucose oxidation for high-value D-glucaric acid(GRA)with ultra-durable hydrogen in acid solution over a Yb-MnO_(2)catalyst.The Mn^(3+)regulated by Yb atoms doped in MnO_(2)can effectively optimize the adsorption and desorption processes of the alcohol and aldehyde group and improve the intrinsic activity but cannot for H2O.The catalyst exhibited extremely high activity and stability after 50 h for glucose oxidation,inhibiting the lattice oxygen process and MnO4−formation,while the activity was quickly lost within 0.5 h for water oxidation.Density functional theory(DFT)calculations further demonstrated that glucose oxidation reaction proceeds preferentially due to the oxidation of aldehyde group with lower adsorption-free energy(−0.4 eV)than water(ΔG>0 eV),avoiding the lattice oxygen mechanism.This work suggests that biomass-derived glucose oxidation not only provides a cost-effective approach for high-value chemicals,but also shows an extremely potential as an alternative to acidic oxygen evolution reaction(OER)for ultradurable H2 production.

Inactivation efficiency of slightly acidic electrolyzed water against microbes on facility surfaces in a disinfection channel

Slightly acidic electrolyzed water(SAEW,pH 6.0-6.5)is an ideal and environmentally-friendly disinfectant,which was used to prevent and control bacterial infections on farms.This work aims to investigate the inactivation effectiveness of SAEW in inactivating microbes in a disinfection channel.The bactericidal efficiency of SAEW on equipment surfaces was compared to two commercial disinfectants,Kuei A bromide solution(KAS,5:1000 v/v)and Glutaraldehyde solution(GS,5:1000 v/v).The disinfection effectiveness of SAEW in inactivating Salmonella enteritidis(S.enteritidis)on equipment surfaces in the disinfection channel was evaluated,and a model was developed using multiple linear regression analysis.Results indicated that SAEW was significantly(p<0.05)more efficient than KAS and GS on kits and clothing in the disinfection channel at 1 min.The SAEW did not contribute as aggressively to respiratory difficulty as KAS and GS.Maximum reductions of 2.362 log10 CFU/cm^(2),2.613 log10 CFU/cm^(2) and 2.359 log10 CFU/cm^(2) for Salmonella enteritidis were obtained from clothing surfaces,iron materials,and kits treated with SAEW for 2.5 min at a chlorine concentration of 220 mg/L.Moreover,the established model had a good fit-quantified by the determination coefficient R^(2)(0.939)and a lack of fit test(p>0.05).In addition,available chlorine concentration(ACC)was an important factor than other factors,and the inactivation efficiency of Salmonella enteritidis sprayed by SAEW treatment was different between iron materials,kits and clothing surfaces(iron>kit>clothing).

Red cabbage washing with acidic electrolysed water:effects on microbial quality and physicochemical properties

The effects of acidic electrolysed water(AEW)as‘green’technology on the microbiological and physicochemical properties of fresh-cut red cabbages were studied.Fresh-cut red cabbages and artificially inoculated red cabbages with Salmonella typhimurium DT104 were washed with distilled water(DW)and different available chlorine concentrations(ACC)of AEW for different times.AEW treatments significantly reduced the populations of native aerobic bacteria,molds,and yeasts,and artificially inoculated S.typhimurium DT104 compared with the DW-treated and untreated red cabbage samples.The effectiveness of AEW treatments was greatly enhanced with increasing ACC and treatment times.S.typhimurium DT104 were not detected in the washing water that were collected after the red cabbages treated by AEW.The surface colour,pH,and total phenolic contents did not significantly change when the red cabbages were washed with DW and AEW containing 100 mg/L available chlorine for 3 min.The anthocyanin contents and antioxidant activities of red cabbage were significantly reduced by 18.5 per cent for cyanidin,22.1 per cent for pelargonidin,and 11.2 per cent for 2,2-diphenyl-1-picrylhydrazyl(DPPH)radical scavenging activity,however,the impacts on the nutritional benefits of red cabbage were considered as limited and acceptable.The optimal process condition of AEW for washing red cabbage was 100 mg/L ACC for 3 min.In these conditions,most of the native microflora were inactivated,and artificially inoculated S.typhimurium DT104 on the red cabbage were reduced by 40.2 per cent[3.67 log CFU/g(log10 colony-forming units per gram)]and with minimal losses of nutrients and antioxidant activity,as well as no requirement of decontamination treatment on the washing water after AEW treatment.

Preservative effects of the combined treatment of slightly acidic electrolyzed water and ice on pomfret

This study assessed the combined effect of slightly acidic electrolyzed water(SAEW)and slightly acidic electrolyzed water ice(SAEW-ice)on the quality of pomfrets over a period of 18 d of cold storage at 4°C.A presoak for 5 min in SAEW solution(22 mg/L)was used before the pomfrets were placed on SAEW-ice(pH:6.45;ORP:803 mV;ACC:18 mg/L);The changes in physicochemical properties(i.e.,pH,thiobarbituric acid,total volatile basic nitrogen and texture profile),microbial loads and sensory characteristics were all analyzed.Compared with the tap water(TW)group,the total bacterial counts of the SAEW group significantly decreased by 1.27 log10 CFU/g after immersion(p<0.05).The shelf life of the pomfrets was prolonged by 9 d by the combined treatment of SAEW and SAEW-ice during storage at 4℃.On the 18th day,the gumminess and chewiness values of the pomfrets in the SAEW+SAEW-ice group were 195 g and 3.97 mJ,respectively,which were significantly higher than those of the other groups(p<0.05).The results suggested that SAEW+SAEW-ice treatments have great potential as a novel method to maintain the quality and extend the shelf life of pomfrets during refrigerated storage.