Response of Rice Growth and Nutrient Absorption in a SalineAlkali Paddy to Different Nitrogen Fertilizer Applications

Nitrogen(N),phosphorus(P)and carbon(C)are essential nutrients for rice growth and development,but the response of nutrient absorption by rice plants to different types of nitrogen fertilizer(N-fertilizer)under saline-alkali conditions is unclear.This study conducted a 147-day field-scale experiment to evaluate rice biomass and nutrient absorption capacity with five N-fertilizer applications.The results showed that the biomass.

The Decarbonization of Construction—How Can Alkali-Activated Materials Contribute?

1.Introduction and context Enormous emphasis is currently being paid to the decarbonization of the global built environment as a leading priority for the engineering community and related industrial sectors[1].One of the main contributors to the overall emissions footprint of the built environment-and thus a cornerstone of efforts to achieve decarbonization-is the emissions profile of construction materials during their production and utilization.The cement and concrete sector is the largest-volume contributor to the emissions incurred in meeting the world’s construction material needs and is therefore targeted in the discussion of the deep,rapid decarbonization that must be achieved in order to minimize irreversible damage to the Earth and its ecosystems.

Synthesis and microwave absorption performance of heat-treated RF/SiO_(2)aerogels

The well-designed composite with satisfactory electromagnetic microwave absorption at high temperatures remains a serious challenge.Herein,we fabricated a resorcinol-formaldehyde/silica dioxide composite aerogel(RF/SiO_(2))with a three-dimensional network structure using sol-gel,atmospheric pressure drying technique as well as heat-treated processes to achieve enhanced microwave absorption capabilities in the low frequency range.The pristine RF/SiO_(2)aerogel presented a typical micropores structure with a surface area,porous volume,and density of 146.82 m^(2)/g,62.40%,and 0.28 cm^(3)/g,respectively.Remarkably,the RF/SiO_(2)aerogel showed an effective absorption bandwidth of 3.56 GHz and a minimum reflection loss value of-46.10 d B at 2.25 mm after being heat-treated at 1500°C,while the maximum effective absorption bandwidth was 3.60 GHz at 2.30 mm.The intricate three-dimensional networks possessed remarkable impedance matching,multiple attenuation mechanisms,interfacial polarization,and dielectric loss,which were attributed to the exceptional ability to absorb electromagnetic microwaves.It offered a fresh approach to creating adaptable and effective microwave absorption materials in military defense.

Insight into the Alkali Resistance Mechanism of CoMnHPMo Catalyst for NH_(3) Selective Catalytic Reduction of NO

The existence of alkali metals in fl ue gases originating from stationary sources can result in catalyst deactivation in the low-temperature selective catalytic reduction(SCR)of nitrogen oxides(NO_(x)).It is widely accepted that alkali metal poisoning causes damage to the acidic sites of catalysts.Therefore,in this study,a series of CoMn catalysts doped with heteropolyacids(HPAs)were prepared using the coprecipitation method.Among these,CoMnHPMo exhibited superior catalytic performance for SCR and over 95%NO_(x) conversion at 150-300.Moreover,it exhibited excellent catalytic activity and stability after alkali poisoning,demonstrating outstanding alkali metal resistance.The characterization indicated that HPMo increased the specifi c surface area of the catalyst,which provided abundant adsorption sites for NO_(x) and NH_(3).Comparing catalysts before and after poisoning,CoMnHPMo enhanced its alkali metal resistance by sacrifi cing Brønsted acid sites to protect its Lewis acid sites.In situ DRIFTS was used to study the reaction pathways of the catalysts.The results showed that CoMnHPMo maintained high NH_(3) adsorption capacity after K poisoning and then reacted rapidly with NO intermediates to ensure that the active sites were not covered.Consequently,SCR performance was ensured even after alkali metal poisoning.In sum-mary,this research proposed a simple method for the design of an alkali-resistant NH_(3)-SCR catalyst with high activity at low temperatures.

Alkali Tolerance of Concrete Internal Curing Agent Based on Sodium Carboxymethyl Starch

Internal curing agents (ICA) based on super absorbent polymer have poor alkali tolerance and reduce the early strength of concrete.An alkali tolerate internal curing agent (CAA-ICA) was designed and prepared by using sodium carboxymethyl starch (CMS) with high hydrophilicity,acrylic acid (AA) containing anionic carboxylic group and acrylamide (AM) containing non-ionic amide group as the main raw materials.The results show that the ratio of CAA-ICA alkali absorption solution is higher than that existing ICA,which solves the low water absorption ratio of the ICA in alkali environment.The water absorption ratio of CAA-ICA in saturated Ca(OH)_(2) solution is 95.8 g·g^(-1),and the alkali tolerance coefficient is 3.4.The application of CAA-ICA in cement-based materials can increase the internal relative humidity and miniaturize the pore structure.The compressive strength of mortar increases up to 12.95%at 28 d,which provids a solution to overcome the reduction of the early strength.

Residual alkali-evoked cross-linked polymer layer for anti-air-sensitivity LiNi_(0.89)Co_(0.06)Mn_(0.05)O_(2)cathode

High-energy density lithium-ion batteries(LIBs)with layered high-nickel oxide cathodes(LiNi_(x)Co_(y)Mn_(1-x-y)O_(2),x≥0.8)show great promise in consumer electronics and vehicular applications.However,LiNi_(x)Co_(y)Mn_(1-x-y)O_(2)faces challenges related to capacity decay caused by residual alkalis owing to high sensitivity to air.To address this issue,we propose a hazardous substances upcycling method that fundamentally mitigates alkali content and concurrently induces the emergence of an anti-air-sensitive layer on the cathode surface.Through the neutralization of polyacrylic acid(PAA)with residual alkalis and then coupling it with 3-aminopropyl triethoxysilane(KH550),a stable and ion-conductive cross-linked polymer layer is in situ integrated into the LiNi_(0.89)Co_(0.06)Mn_(0.05)O_(2)(NCM)cathode.Our characterization and measurements demonstrate its effectiveness.The NCM material exhibits impressive cycling performance,retaining 88.4%of its capacity after 200 cycles at 5 C and achieving an extraordinary specific capacity of 170.0 mA h g^(-1) at 10 C.Importantly,this layer on the NCM efficiently suppresses unfavorable phase transitions,severe electrolyte degradation,and CO_(2)gas evolution,while maintaining commendable resistance to air exposure.This surface modification strategy shows widespread potential for creating air-stable LiNi_(x)Co_(y)Mn_(1-x-y)O_(2)cathodes,thereby advancing high-performance LIBs.

Fundamental Study on Alkali-Activated Slag System with Sodium Carbonate or Calcium Hydroxide

Cement as a building material, has high fluidity, compressive strength, and durability, but carbon dioxide emissions during cement production are a major problem. As one of the countermeasures, alkali-activated cement using blast furnace slag powder with alkaline stimulants is considered to be a very promising solution for reducing carbon dioxide emissions, but there is a lack of information about the fundamental properties of alkali-activated materials. This study presents an experimental investigation of the fundamental properties of an alkali-activated slag system with sodium carbonate (NC) and calcium hydroxide (CH). The effects of calcium sulfo-aluminate (CSA) and shrinkage reducing agent (SRA) on the properties of blast furnace slag (BFS) based alkali-activated mixture were also investigated. In the experiments, fundamental characteristics including compressive strength, drying shrinkage, and water penetration tests of mortar were evaluated. Porosity, pH, and ignition loss were measured to verify the effectiveness of the materials. The experimental investigation revealed that the compressive strength was increased with the increasing replacement rates of NC in the BFS mortar, and in the case of water to BFS ratio of 0.45 with sodium carbonation addition contents 10 wt.%, the compressive strength for 28 days of curing reaches more than 50 MPa. Low water to BFS ratio and higher addition ratio of NC had a positive effect on the compressive strength development of mortar. Incorporating NC into BFS would affect the decrease in porosity and increase in ignition loss, leading to higher compressive strength. There was a negligible change to the compressive strength, porosity, pH, and ignition loss of BFS samples made with CH, thus, the addition rates of CH to BFS have no or little significant effect on the fundamental properties of alkali-activated cement. From the results of drying shrinkage and water penetration tests, the addition of NC and CH only to BFS exhibited poor drying shrinkage and water penetration characteristics. However, these problems may be overcome due to the use of CSA or SRA in the alkali-activated system made with NC or CH.

Influence of heat-treatment on oxidation-resistance of phosphate-coating for C/C composite

Phosphate-coating was prepared for C/C composite using liquid-impregnation and different heat-treatment. The results show that the mass-loss rate of sample A with 1-2 ℃/min slow-cooling rate technology is 47%after oxidation at 700 ℃ for 20 h, while that of sample B with air-fast-cooling one is only 0.98%. SEM images reveal that the coating of sample A is full of micro-holes, micro-cracks and many piece-like crystal particles, while that of sample B is integrated and compacted in glassy state with a few of micro-cracks. The coating of sample A is almost exhausted only in 8 h oxidized-test at 700 ℃, while that of sample B remains integrated after 8 h test at 700 ℃ and becomes loose due to much small pores generated after 20 h test at 700 ℃.

Effect of Heat-Treatment Process on Properties of Rare Earth Mg-Based System Hydrogen Storage Alloys with AB_3-Type

The effect of heat-treatment process on the properties of Mm0.8Mg0.2(NiCoAlMn)3.5 hydrogen storage alloy was discussed . The electrochemical properties such as cycling stability, activation property, and the plateau voltage of the alloy which was heat-treated in various temperatures and times had different changes during the cycle process, the optimum heat-treatment conditions of this alloy were determined by this work.

Effects of Heat-treatment on Crystallization and Wear Property of Plasma Sprayed Fe-based Amorphous Coatings

The Fe-based amorphous coatings were produced by air plasma spraying. The as-sprayed coatings were heat-treated at the temperature of 573, 873, and 1 023 K, respectively. The crystallization and wear behavior of the heat-treated amorphous coatings were investigated. It was found that the amorphous- nanocrystalline transformation appeared when the as-sprayed coatings were treated at 853 K. The crystallization process had completed and a coating with microcrystallines was formed when the treatment temperature reached 1 023 K. The resultant amorphous and nanocrystalline composite coatings exhibited superior wear resistance compared to crystalline coating. It is attributed to fine grain strengthening of formed nanocrystallines.

Effects of Steam Heat-Treatment on Properties of Pinus massoniana Wood and Its Bonding Performance

Pinus massoniana wood was modified by steam heat-treatment at 160℃,180℃,200℃ and 220℃ respectively and effects of the changes of density,pH,surface wettability and apparent morphology of Pinus massoniana heat-treated wood on its bonding performance were studied in this paper.The results showed that Pinus massoniana wood underwent a series of physical and chemical changes during heat-treatment as the the following:(1)The degradation of hemicellulose and cellulose with low degree of polymerization,degradation and migration of the extract resulting in the decline of density and pH of heat-treated Pinus massoniana wood.(2)Brittle fracture occured on the cell wall surface,and the pit collapse,shrink and deformation,resulting in the formation of roughness and porosity on the wood surface.(3)The surface energy decreased with the improvement of temperature,the surface wettability of Pinus massoniana wood treated at 160℃–180℃ was good,while that at 200℃–220℃ showed hydrophobicity.(4)Changes of density,pH,surface roughness and porosity,and wettability resulted in a reduction in the bonding strength and reliability of heat-treated Pinus massoniana wood with MUF resin adhesive.(5)When the temperature was at 160℃–180℃,the better wettability of heat-treated Pinus massoniana wood could guarantee the better bonding performance.

Effect of Heat-treatment Temperature on HA-coated Titanium Materials

Homogeneous HA coating materials were prepared on porous titanium by the low-temperature combustion synthesis. It was found that the mechanical properties of the specimen depend on the coating process and the heat treatment, and the bending strength would be reduced during the coating process but could be improved by heat treatment. The effects of the temperature during heat- treatment on the phase composition and microstructure of the as-prepared coating, and the bending strength of the specimen were investigated by XRD and SEM. The experimental results show that in the coating process, slight oxidation of the substrate may give rise to a drop in bending strength ; however, it could be increased by the reaction of HA and TiO2 , and the sintering of the coating during heat treatment. The HA particles in the coating, with very fine sized particles. were pretty active and would decompose at 800℃.

EFFECT OF HEAT-TREATMENT ON THE MECHANICAL PROPERTIES OF AIN/SICw(Y_2O_3+SiO_2)COMPOSITE

In the paper, the effect of heat-treatment on the strength and toughness of AIN-SiC whisker composites with Y2O3 + SiO2 additives have been studied. When the Sample confining 10wt% Y2O3+SiO2(.Y2O3/SiO2^l/0. 66) -was treated at 1330癈 in air for 140 hours ithe flexural strength of composites ivas raised from 481 MPa to 784 MPa the toughness ruas also enhanced slightly. The phase composi-tion infrastructure and grain boundary phase structure have been char-acterized by combining XDR, SEM, TEM/EDXA and HREM tech-niques, reinforcenent and toughening mechanism of the composites re-sults from the crystallization of glass phase in the grain boundary at the high temperature oxidizing atmosphere to form the crossing struc-ture of 2H?sialon fibrous phase and SiC whisker

Effects of biochar-amended alkali-activated slag on the stabilization of coral sand in coastal areas

Coral sand is widely encountered in coastal areas of tropical and subtropical regions.Compared with silica sand,it usually exhibits weaker performance from the perspective of engineering geology.To improve the geomechanical performance of coral sand and meet the requirement of foundation construction in coastal areas,a novel alkali activation-based sustainable binder was developed.The alkaliactivated slag(AAS)binder material was composed of ground granulated blast-furnace slag(GGBS)and hydrated lime with the amendment of biochar,an agricultural waste-derived material.The biocharamended AAS stabilized coral sand was subjected to a series of laboratory tests to determine its mechanical,physicochemical,and microstructural characteristics.Results show that adding a moderate amount of biochar in AAS could improve soil strength,elastic modulus,and water holding capacity by up to 20%,70%,and 30%,respectively.Moreover,the addition of biochar in AAS had a marginal effect on the sulfate resistance of the stabilized sand,especially at high biochar content.However,the resistance of the AAS stabilized sand to wet-dry cycles slightly deteriorated with the addition of biochar.Based on these observations,a conceptual model showing biochar-AAS-sand interactions was proposed,in which biochar served as an internal curing agent,micro-reinforcer,and mechanically weak point.

STUDY ON HEAT-TREATMENT OF AIN/SiC_w COMPOSITES AND EFFECTS ON MICROSTRUCTURE AND PROPERTIES

AlN-SiC whisker composites with Y2O3 and SiO2 additives were heat-treated at 1300 ℃ in air. The phase composition and microstrurture were analyzed using XRD, SEM and HREM techniques to study the effect of heat-treatment on the microstructure and properties of the composites. The results reveal that the mechanical properties and high temperature oxidation resistance of the composite of ivhich additives composition approaches the eutectic point of Y2O3-SiO2 can be improved through the heat-treatment. Glass phase in the grain boundary is observed to react with the surface composition of AlN forming fibrous 2Hδ Sialon, resulting a crossing structure produced by fibrous 2Hδ Sialon and SiC whiskers.

Effect of Seed Heat-Treatment on the Oxidative Stability of Canola Oil Body Emulsions

Enhancement of oxidative stability of canola oil extracted from seed subjected to prior heat-treatment has been attributed to heat-induced generation of antioxidants from phenolic precursors occurring in canola seed. Dispersion of aqueous extracts of intact seed oil bodies (OBs) in water is a novel and interesting way of producing natural and oxidatively stable food emulsions with minimal use of synthetic antioxidants and emulsifiers. As there is growing interest in natural food emulsions containing unsaturated oils, we investigated whether the oxidative stability of canola OB emulsions could be further improved by subjecting canola seed to heat-treatment prior to oil body extraction. Oil-in-water (5%, w/w) emulsions of OBs extracted from canola seed before and after heat-treatment were considerably more resistant to oxidation than emulsions prepared from refined canola oil and Tween? 40 emulsifier. However, only small amounts (0.9% - 4.5% by weight) of the phenolic compounds present in canola seed were transferred to the OBs after aqueous extraction, and consequently there was no discernible effect on oxidative stability as a result of prior heat-treatment of the seed. Thus, in contrast to oil, there is no oxidative stability benefit to be gained by subjecting canola seed to heat-treatment prior to extraction of OBs.

Orientational Separation of Sulfur in Petroleum Coke by Alkali Calcining and Reflux Washing

The application of high-sulfur petroleum coke after desulfurization in aluminum electrolysis anodes is an important development trend. However, removing sulfur from high-sulfur petroleum coke is still a significant challenge.This study proposes alkali calcining and reflux washing to examine the impacts of temperature, particle size, the mass ratio of Na_(2)CO_(3) to NaOH, and total sodium addition on the desulfurization efficiency and mechanism. The results show that the desulfurization rate increases with increasing temperature, increasing total sodium content, and decreasing particle size. The addition of alkali can significantly reduce the opening-ring reaction temperature of thiophene and convert organic sulfur into inorganic sulfur(Na_(2)S). Three washing methods were compared, and reflux washing was selected to separate inorganic sulfur(Na_(2)S) from calcined petroleum coke. The sulfur content in petroleum coke decreased from 7.29% to 1.90%, with a desulfurization rate of 80.13% under optimal conditions. The petroleum coke was analyzed before and after desulfurization using X-Ray diffraction(XRD), Scanning Electron Microscopy(SEM), Infrared Spectroscopy(IR), Thermogravimetric Analysis and Differential Scanning Calorimetry(TG-DSC), Gaschromatography-mass Spectrometry(GC-MS). The results show that thiophene and benzothiophene in petroleum coke are decomposed and converted into octane and ethyl cyclohexane. These new observations are expected to provide further understanding and guidance for the utilization of highsulfur petroleum coke.

Genome-wide analysis of soybean DnaJA-family genes and functional characterization of GmDnaJA6 responses to saline and alkaline stress

Plant Dna JA proteins act as molecular chaperones in response to environmental stressors.The purpose of this study was to characterize the function and regulatory mechanisms of Dna JA genes in soybean.Gene expression profiles in various soybean tissues at various stages of development indicated that Gm Dna JAs function in the coordination of stress and plant hormone responses.Gm Dna JA6 was identified as a candidate regulator of saline and alkaline stress resistance and Gm Dna JA6 overexpression lines showed increased soybean saline and alkaline tolerance.Dna J interacted with Hsp70,and Gm Hsp70 increased the saline and alkaline tolerance of plants with chimeric soybean hairy roots.

Emerging Carbon Nanotube-Based Nanomaterials for Stable and Dendrite-Free Alkali Metal Anodes:Challenges,Strategies,and Perspectives

Alkali metals(Li,Na,and K)are promising candidates for high-performance rechargeable alkali metal battery anodes due to their high theoretical specific capacity and low electrochemical potential.However,the actual application of alkali metal anodes is impeded by the challenges of alkali metals,including their high chemical reactivity,uncontrolled dendrite growth,unstable solid electrolyte interphase,and infinite volume expansion during cycling processes.Introducing carbon nanotube-based nanomaterials in alkali metal anodesis an effective solution to these issues.These nanomaterials have attracted widespread attention owing to their unique properties,such as their high specific surface area,superior electronic conductivity,and excellent mechanical stability.Considering the rapidly growing research enthusiasm for this topic in the last several years,we review recent progress on the application of carbon nanotube-based nanomaterials in stable and dendrite-free alkali metal anodes.The merits and issues of alkali metal anodes,as well as their stabilizing strategies are summarized.Furthermore,the relationships among methods of synthesis,nano-or microstructures,and electrochemical properties of carbon nanotube-based alkali metal anodes are systematically discussed.In addition,advanced characterization technologies on the reaction mechanism of carbon nanotube-based nanomaterials in alkali metal anodes are also reviewed.Finally,the challenges and prospects for future study and applications of carbon nanotube-based AMAs in high-performance alkali metal batteries are discussed.

Quantitative Extraction of p-Coumaric Acid and Ferulic Acid in Different Gramineous Materials and Structural Changes of Residual Alkali Lignin

Ferulic acid(FA)and p-coumaric acid(pCA)in bagasse,wheat straw,corn straw,and corncob were extracted by alkaline hydrolysis and characterized by gas chromatography(GC)and gas chromatography-mass spectrometry(GC-MS).It was found that the FA and most of the pCA in gramineous biomass could be dissociated and released after being treated with 1 M NaOH at 100℃for 4 h.The yields of pCA/FA in bagasse,wheat straw,corn straw,and corncob determined by GC-FID are 39.8/11.5,13.7/11.0,28.0/11.0,and 35.1/14.5 mg/g,respectively.The raw materials and the treated solid residues were characterized by gel-state 2D Heteronuclear Single Quantum Coherence Nuclear Magnetic Resonance(2D HSQC NMR).It was found that only a small amount of lignin was detected in the residue after alkali treatment,indicating that the alkali treatment conditions can effectively cleave the FA and pCA.Additionally,the lignin in the alkali solution was recovered and characterized by 2D HSQC NMR.The FA was not able to be detected by NMR,whereas a small amount of pCA remained in the alkali lignin.This study reveals the structural change of residual lignins during the quantitative isolation of FA and pCA,which is essential for the selective isolation of pCA/FA and valorization of residual alkali lignin.