Biomineralization of soil with crude soybean urease using different calcium salts

Calcium salt is an important contributing factor for calcium-based biomineralization.To study the effect of calcium salt on soil biomineralization using crude soybean urease,the calcium salts,including the calcium chloride (CaCl_(2)),calcium acetate ((CH_(3)COO)_(2)Ca) and calcium nitrate (Ca(NO_(3))_(2)),were used to prepare the biotreatment solution to carry out the biomineralization tests in this paper.Two series of biomineralization tests in solution and sand column,respectively,were conducted.Scanning electron microscopy (SEM) and X-ray diffraction (XRD) were performed to determine the microscopic characteristics of the precipitated calcium carbonate (CaCO_(3)) crystals.The experimental results indicate that the biomineralization effect is the best for the CaCl2 case,followed by (CH_(3)COO)_(2)Ca,and worst for Ca(NO_(3))_(2) under the test conditions of this study (i.e.1 mol/L of calcium salt-urea).The mechanism for the effect of the calcium salt on the biomineralization of crude soybean urease mainly involves: (1) inhibition of urease activity,and (2) influence on the crystal size and morphology of CaCO_(3).Besides Ca^(2+) ,the anions in solution can inhibit the activity of crude soybean urease,and NO_(3)− has a stronger inhibitory effect on the urease activity compared with both CH_(3)COO^(−) and Cl^(−) .The co-inhibition of Ca^(2+) and NO_(3)− on the activity of urease is the key reason for the worst biomineralization of the Ca(NO_(3))_(2) case in this study.The difference in biomineralization between the CaCl_(2) and (CH_(3)COO)_(2) Ca cases is strongly correlated with the crystal morphology of the precipitated CaCO_(3).

氯盐环境下水泥基材料中Friedel’s盐的生成规律与稳定性研究

为了研究氯盐环境下水泥基材料中Friedel’s盐的生成规律及其稳定性影响因素,通过改变试件水灰比和浸泡液氯化钠浓度、pH,采用X射线衍射、热分析、离子色谱测试Friedel’s盐含量变化,分析不同条件下Friedel’s盐的生成规律和氯离子浓度、pH对Friedel’s盐稳定性的影响。结果表明:大水灰比试件水化程度高,熟料中更多的C4AF水化提供铝相吸附氯离子生成Friedel’s盐。溶液环境pH≥12时,Friedel’s盐能稳定存在;pH增大到13.5时,水化产物中钙矾石溶解,导致生成更多的Friedel’s盐;环境溶液氯离子浓度降低时,Friedel’s盐将会溶解;提高溶液的pH能抑制Friedel’s盐溶解。

Recent Advances of Transition Metal Basic Salts for Electrocatalytic Oxygen Evolution Reaction and Overall Water Electrolysis

Electrocatalytic oxygen evolution reaction(OER)has been recognized as the bottleneck of overall water splitting,which is a promising approach for sustainable production of H_(2).Transition metal(TM)hydroxides are the most conventional and classical non-noble metal-based electrocatalysts for OER,while TM basic salts[M^(2+)(OH)_(2-x)(A_(m^(-))_(x/m),A=CO_(3)^(2−),NO_(3)^(−),F^(−),Cl^(−)]consisting of OH−and another anion have drawn extensive research interest due to its higher catalytic activity in the past decade.In this review,we summarize the recent advances of TM basic salts and their application in OER and further overall water splitting.We categorize TM basic salt-based OER pre-catalysts into four types(CO_(3)^(2−),NO_(3)^(−),F^(−),Cl^(−)according to the anion,which is a key factor for their outstanding performance towards OER.We highlight experimental and theoretical methods for understanding the structure evolution during OER and the effect of anion on catalytic performance.To develop bifunctional TM basic salts as catalyst for the practical electrolysis application,we also review the present strategies for enhancing its hydrogen evolution reaction activity and thereby improving its overall water splitting performance.Finally,we conclude this review with a summary and perspective about the remaining challenges and future opportunities of TM basic salts as catalysts for water electrolysis.

Synthesis and kinetics of 2,5-dicyanofuran in the presence of hydroxylamine ionic liquid salts

2,5-Dicyanofuran(DCF)is an important biomass-derived platform compound primarily used to prepare bio-based adiponitrile,which is the key precursor for the synthesis of nylon 66 and 1,6-hexanediisocyanate(HDI).In this study,one-pot,green and safe synthesis of DCF from 2,5-diformylfuran(DFF)and hydroxylamine ionic liquid salts was proposed.Eco-friendly hydroxylamine ionic liquid salts were used as the nitrogen source.Ionic liquid exhibited three-fold function of cosolvent,catalysis and phase separation.The conversion of DFF and yield of DCF reached 100%under the following optimum reaction conditions:temperature of 120℃ for 70 min,volume ratio of paraxylene:[HSO_(3)-b-Py]
HSO4 of 2:1,and molar ratio of DFF:(NH_(2)OH)_(2)
[HSO_(3)-b-Py]
HSO4 of 1:1.5.The reaction mechanism for the synthesis of DCF was proposed,and the kinetic model was established.The reaction order with respect to DFF and intermediate product 2,5-diformylfuran dioxime(DFFD)was 1.06 and 0.16,and the reaction activation energy was 64.07 kJ·mol^(-1) and 59.37 kJ·mol^(-1) respectively.After the reaction,the ionic liquid was easy to separate,recover and recycle.

Interconnected and high cycling stability polypyrrole supercapacitors using cellulose nanocrystals and commonly used inorganic salts as dopants

Polypyrrole(PPy)is wildly used as electrode material in supercapacitors due to its high conductivity,low cost,ease of handling,and ease of fabrication.However,limited capacitance and poor cycling stability hinder its practical application.After developing carboxylated cellulose nanocrystals(CNC-COO^(-))as immobile dopants for PPy to improve its cycling stability,we investigated the effect of different commonly used salts(KCl,NaCl,KBr,and NaClO_(4))as dopants during electrode fabrication by electropolymerization.The film’s capacitance increased from 160.6 to 183.4 F g^(-1)after adding a combination of KCl and NaClO_(4) into the electrodeposition electrolyte.More importantly,the porous and interconnected PPy/CNC-COO^(-)-Cl-(Cl O_(4)^(-))_0.5 electrode film exhibited an excellent capacitance of 125.0 F g^(-1)(0.78 F cm^(-2))at a high current density of 2.0 Ag^(-1)(20 m A cm^(-2),allowing charging in less than 1 min),increasing almost 204%over PPy/CNC-COO-films.A symmetric PPy/CNC-COO^(-)-Cl-(ClO_(4)^(-))_0.5 supercapacitor retained its full capacitance after 5000 cycles,and displayed a high energy density of 5.2 Wh kg^(-1)at a power density of 25.4 W kg^(-1)(34.5μWh cm^(-2) at 1752.3μW cm^(-2)).These results reveal that the porous structure formed by doping with CNC-COO-and inorganic salts opens up more active reaction areas to store charges in PPy-based films as the stiff and ribbon-like CNC-COO-as permanent dopants improve the strength and stability of PPy-based films.Our demonstration provides a simple and practical way to deposit PPy based supercapacitors with high capacitance,fast charging,and excellent cycling stability.

Study on the corrosion behavior of 316H stainless steel in molten NaCl–KCl–MgCl_(2) salts with and without purification

The corrosion behavior of 316H stainless steel(SS)in the impure and purified Na Cl–KCl–Mg Cl_(2) salt was investigated at700°C.Results indicate that the main deleterious impurity induced corrosion in the impure salt was the absorbed moisture,present in the form of Mg Cl_(2)·6H_(2)O.316H SS occurred severe intergranular corrosion with a corrosion depth of 130μm for1000 h in the impure Na Cl–KCl–Mg Cl_(2) salt.In contrast,the purification treatment of molten chloride salt by the dissolved Mg metal can remove the absorbed moisture,and the corresponding reactions were also discussed.As a result,the corrosiveness of Na Cl–KCl–Mg Cl_(2) salt is reduced significantly.316H SS occurred slight uniform corrosion with a depth of less than 5μm for 3000 h in the purified Na Cl–KCl–Mg Cl_(2) salt.

Coordination states of metal ions in molten salts and their characterization methods

The macroscopic characteristics of molten salts are governed by their microstructures.Research on the structures of molten salts provides the foundation for a full understanding of the physicochemical properties of molten salts as well as a deeper analysis of the microscopic electrolysis process in molten salts.Information about the microstructure of matter can be obtained with the help of several speculative and experimental procedures.In this review,the advantages and disadvantages of the various test procedures used to determine the microstructures of molten salts are compared.The typical coordination configurations of metal ions in molten salt systems are also summarized.Furthermore,the impact of temperature,anions,cations,and metal oxides(O2-)on the structures of molten salts is discussed in detail.The accuracy and completeness of the information on molten salt structures need to be investigated by the integration of multiple methods and interdisciplinary fields.Information on the microstructure and coordination of molten salts deepens the understanding of the elementary elements of the microstructure of matter.This paper,which is based on the review of the coordination states of metal ions in molten salts,is hoped to inspire researchers to explore the inter-relationship between the microstructure and macroscopic properties of materials.

Wettability alteration of organo-vermiculites induced by layer charge and tailored bis-N-heterocyclic quaternary ammonium salts

Wettability is an important surface property that deserves to further explore the factors on its alteration.Series of bis-N-heterocyclic quaternary ammonium salts with different spacer length and N-heterocyclic headgroups(morpholinium(BMMB,BMMD and BMMH),piperidinium(BPMH)and piperazinium(BMPMH))have been synthesized and employed for altering the wettability of vermiculite and its derivates(Vts)treated by Li^(+)-saturated heating method.The results of X-ray diffraction(XRD),Fourier transform infrared spectroscopy(FT-IR),thermogravimetric analysis(TG-DTG),scanning electron microscopy(SEM)and N_(2)adsorption/desorption isotherms indicate that all of the bis-N-heterocyclic quaternary ammonium salts have been successfully inserted into the vermiculite layers,leading to the organic monolayer.The results of capillary rise tests combined with Lipophilic to Hydrophilic Ratio(LHR)values unveil the wettability alteration of the organo-Vts.As the layer charge decreases,the hydrophilicity of the organo-Vts gradually increases,which is probably caused by the decline in binding sites.As the result of the change in spacer length of modifier,the wetting properties of morpholinium-based organo-Vts change in order of BMMD-Vts>BMMH-Vts>BMMB-Vts,and difference in N-heterocyclic headgroups leads to the sequence of wettability:BMPMH-Vts>BPMH-Vts>BMMH-Vts.Layer charge of Vt,spacer length and the type of the N-heterocyclic headgroup of modifier have the synergistic effect on the regulation of the wettability.

Influence of Climate and Tectonics on the Crystallization of Carnallite and Related Salts in the Congolese Atlantic Basin during the Lower Cretaceous, Republic of Congo

Lithological, petrographic, and morphoscopic studies were conducted on cuttings and cores from three boreholes drilled in the Loemé salt, Kanga site, Republic of the Congo, to determine 1) the preferential conditions for crystallization of carnallite and associated salts and 2) to reconstruct paleoenvironmental and paleoclimatic conditions at the time of sedimentation. Sequential analysis of logs, sedimentary structures, carnallitite facies and associated salts concluded to the existence of a potassic carnallitite lagoon basin with low water cover, on a very wide and extensive plateau, affected by coastal waves and swells resulting from successive collapses. This basin evolved in two phases: confined and then open. The regular stratifications of halite, the rhythmicity of the halite-carnallitite elementary sequences are characteristic of salts that precipitated in relatively stable brines. These salts are therefore tectonosedimentary. The brecciated facies of the carnallitites sometimes associated with tachyhydrite result from the evolution of these deposits into salt crusts reworked by the surges into subaquatic allochemical gravelly cords under water. These crusts mark stages of partial and complete drying of the basin in a very hot and arid climate. Prolonged exposure of halite brines as well as their homogenization by surges accelerated evaporation and their abrupt evolution into carnallite brines obstructing the fossilization of sylvite. The precipitation of tachyhydrite marks the final stage of the successive complete drying of the basin.

A Review:Pre-lithiation Strategies Based on Cathode Sacrificial Lithium Salts for Lithium-Ion Capacitors

Similar to lithium-ion batteries(LIBs),during the first charge/discharge process of lithium-ion capacitors(LICs),lithium-intercalated anodes(e.g.,silicon,graphite,and hard carbon)also exhibit irreversible lithium intercalation behaviors,such as the formation of a solid electrolyte interface(SEI),which will consume Li^(+)in the electrolyte and significantly reduce the electrochemical performance of the system.Therefore,pre-lithiation is an indispensable procedure for LICs.At present,commercial LICs mostly use lithium metal as the lithium source to compensate for the irreversible capacity loss,which has the demerits of operational complexity and danger.However,the pre-lithiation strategy based on cathode sacrificial lithium salts(CSLSs)has been proposed,which has the advantages of low cost,simple operation,environmental protection,and safety.Therefore,there is an urgent need for a timely and comprehensive summary of the application of CSLSs to LICs.In this review,the important roles of pre-lithiation in LICs are detailed,and different pre-lithiation methods are reviewed and compared systematically and comprehensively.After that,we systematically discuss the pre-lithiation strategies based on CSLSs and mainly introduce the lithium extraction mechanism of CSLSs and the influence of intrinsic characteristics and doping amount of CSLSs on LICs performance.In addition,a summary and outlook are conducted,aiming to provide the essential basic knowledge and guidance for developing a new pre-lithiation technology.

Lacunary silicotungstic heteropoly salts as high-performance catalysts in oxidation of cyclopentene

The development of polyoxometalates for olefin oxidation is critical to achieving the green chemical process of the C5 fraction further processing.Di-lacunary silicotungstic anions were easily obtained by continuously adjusting the p H instead of the traditional step-by-step method,which exhibited excellent performance in the catalytic oxidation of cyclopentene(CPE)to aldehydes or alcohols.The 93.69%CPE conversion and 97.15%total product selectivity(41.38%for glutaraldehyde(GA)and 55.77%for 1,2-cyclopentanediol(1,2-diol)were achieved by using H_(2)O_(2)as the oxidant and acetonitrile as the solvent.Through complementary characterization,it was found that the optimized di-lacunary silicotungstic polyoxometalate retained a complete Keggin structure,and exhibited better catalytic activity and stability than the mono-lacunary or saturated silicodecatungstate because it exposed more catalytic active centers.Furthermore,in situ FT-IR spectra was utilized to monitor the reaction process,revealing the formation of the active species W(O_(2))on the di-lacunary silicotungstic polyoxometalate and the intermediate epoxycyclopentane during the catalytic oxidation of cyclopentene.

Research progress on protective coatings against molten nitrate salts for thermal energy storage in concentrating solar power plants

Concentrating solar power(CSP) has garnered considerable global attention as a reliable means of generating bulk electricity, effectively addressing the intermittent nature of solar resources.The integration of molten salt technology for thermal energy storage(TES) has further contributed to the growth of CSP plants;however, the corrosive nature of molten salts poses challenges to the durability of container materials, necessitating innovative corrosion mitigation strategies.This review summarizes scientific advancements in high-temperature anticorrosion coatings for molten nitrate salts, highlighting the key challenges and future trends.It also explores various coating types, including metallic, ceramic, and carbon-based coatings, and compares different coating deposition methods.This review emphasizes the need for durable coatings that meet long-term performance requirements and regulatory limitations, with an emphasis on carbon-based coatings and emerging nanomaterials.A combination of multiple coatings is required to achieve desirable anticorrosion properties while addressing material compatibility and cost considerations.The overall goal is to advance the manufacturing, assembly, and performance of CSP systems for increased efficiency, reliability, and durability in various applications.

氯离子体系铀溶液中铁、钍、稀土的去除研究

采用复盐沉淀法,用硫酸钠同时去除氯离子体系铀溶液中的铁、钍、稀土杂质离子,并研究了硫酸钠用量、反应温度、反应时间、体系pH等对除杂效果的影响。结果表明,反应的最佳条件为:硫酸钠用量为理论量的160%、反应温度95℃、反应时间2 h、体系pH=0.75~1.25。在此优化条件下,铁、钍和总稀土的平均去除率分别达到99.62%、99.42%和98.27%,铀的平均回收率为99.87%。方法具有除杂效果好、铀损失率低、易分离等优点。

葡萄响应盐胁迫的研究进展

在葡萄生产中,盐胁迫是常见的非生物胁迫之一。在发生盐胁迫时,葡萄的产量与品质常常会降低,因此提高葡萄对盐胁迫的耐受性,已成为葡萄栽培中迫在眉睫的问题。本文综述了盐胁迫对葡萄生长发育及生理生化影响的研究进展,探讨了葡萄响应盐胁迫的分子机制和缓解盐胁迫的应对措施,并展望了葡萄耐受盐胁迫研究的方向。以期为葡萄耐盐机理的解析及耐盐品种的选育提供理论依据,为缓解葡萄盐害的栽培技术提供新思路。

CMAS、CMAS+NaVO_(3)、CMAS+海盐作用下热障涂层的腐蚀行为与机理

环境沉积物(CaO-MgO-Al_(2)O_(3)-SiO_(2),CMAS)的高温腐蚀已成为航空发动机涡轮叶片热障涂层过早失效的重要原因之一。然而涡轮叶片工作环境复杂,熔盐、海盐常与CMAS耦合,一起对热障涂层造成多元复杂腐蚀,但目前关于CMAS与盐类的多元耦合腐蚀行为鲜有报道。针对Y2O_(3)部分稳定ZrO_(2)(YSZ)热障涂层在CMAS、CMAS+NaVO_(3)、CMAS+海盐作用下的腐蚀行为进行对比研究。通过XRD、SEM等方法对不同条件下腐蚀后的涂层进行表征,并分析热处理温度、腐蚀物种类对腐蚀行为的影响。结果表明:与CMAS相比,CMAS+NaVO_(3)、CMAS+海盐会在更低的温度下损伤涂层(1200℃)。当三种腐蚀物均能完全熔化时(1250℃),CMAS+NaVO_(3)、CMAS+海盐熔体则由于更大的流动性而大量渗入,腐蚀内部涂层。其中,CMAS+海盐熔体在涂层内的渗透性最强,1250℃热处理4 h后,渗透深度超过400μm。盐类的共存会改变CMAS的性质,增强熔体的渗透能力,增加涂层内部甚至底部失效的倾向。研究结果有助于理解盐类与CMAS耦合时混合熔体对热障涂层的破坏机理及潜在威胁。

我国盐穴资源评价及调查技术研究

在“双碳”目标大背景下,盐穴是实现地质储能、碳封存的重要方式之一,但我国盐穴资源数量、质量不明,盐穴调查技术体系不完善,严重制约盐穴资源开发利用。通过分析我国主要盐矿区地质勘探报告、储量核实报告、企业年报及文献报道等,形成了我国盐穴资源数量、可利用性的科学认识和基本判断;在盐穴集中区开展综合探测技术试验并结合前人试验成果,初步构建了盐穴资源调查技术体系。结果表明:(1)我国盐穴资源丰富,储量大、分布广、埋深适宜、具备规模化开发利用条件,其中华东和华中地区已有盐穴资源最为丰富。(2)通过建立盐穴资源可利用性评价体系,将全国盐穴资源分为Ⅰ、Ⅱ、Ⅲ3级,Ⅰ级已有盐穴资源占比约29.4%,主要分布在华东、华中地区的江苏、湖北、河南等省份,是开发利用的优选区;Ⅱ级已有盐穴资源占比约65.4%,广泛分布于华中、西北和西南地区,可作为开发利用远景区;Ⅲ级已有盐穴资源占比约5.2%,整体地质条件不适宜开发利用。(3)地面物探可查明盐矿区区域地质、盐层地质、水文地质及盐腔分布情况,指导盐穴建库选址;井中物探精度高,可获取盐矿品味、腔体结构等信息,服务储库建设及运行监测。研究结果可为我国盐穴资源规划及开发提供基础数据和技术支撑。

基于透射图像的高压脉动腌制咸鸭蛋含盐量检测

含盐量是衡量咸鸭蛋品质的重要指标。为了利用机器视觉技术实现高压脉动腌制咸鸭蛋含盐量的无损检测。该研究采用工业相机和透射光源搭建咸鸭蛋的透射图像采集装置。采用图像整体特征和长轴截面光强度特征两种特征提取方法,利用多元线性回归、支持向量机回归两种算法,建立对蛋清、蛋黄及全蛋含盐量以及蛋黄指数的定量预测模型。结果表明,随着咸鸭蛋腌制时间的增加,其透光性显著提高。同时,透射图像蛋黄的所在视野区域会随着含盐量的增加而呈现规律性的变化。基于图像整体特征建立的蛋清、蛋黄、全蛋含盐量模型较优,在蛋黄指数预测下基于长轴截面光强度特征所建模型较优。其中,基于图像整体特征所建立的蛋黄含盐量支持向量机回归(support vector regression,SVR)模型最优,测试集相关系数(test set correlation coefficient,Rp)、测试集均方根误差(root mean square error of prediction,RMSEp)、相对分析误差(residual predictive deviation,RPD)分别达到0.8460、0.3416、1.898;基于长轴截面光强度特征建立的蛋黄指数多元线性回归(multiple linear regression,MLR)模型最优,测试集相关系数Rp、均方根误差RMSEp、相对分析误差RPD分别为0.8318、0.0743、1.916。该研究结果为咸鸭蛋含盐量的快速检测提供理论依据和技术支持。

燕麦对滨海盐渍土的适应性及纳盐改土效果

为探索燕麦植株对滨海盐渍土的适应性及纳盐改土效果,本试验以白燕2号为材料,在东营的3种类型滨海盐渍土上(轻度、中度、重度)设6个区顶凌播种,观测燕麦农艺性状及田间覆盖率,测定燕麦全株及籽粒产量和燕麦不同部位及收获期0~20 cm土层土壤可溶性盐和Na+含量。结果表明,白燕2号在3种滨海盐渍土壤中均能生长,但适应程度不同,全株产量为3.320~18.780 t·hm^(-2),籽粒产量为0.456~4.106 t·hm^(-2),基本趋势为轻度盐渍土>中度盐渍土>重度盐渍土;燕麦利用植株的储盐能力将盐渍土部分可溶性盐移出土壤,燕麦全株移出可溶性盐量为0.161~1.508 t·hm^(-2),籽粒移出可溶性盐量为2.961~43.242 kg·hm^(-2);春季返盐高峰后,裸露地土壤表层盐表聚严重,试验区燕麦收获期0~20 cm土层土壤可溶性盐和Na+含量均有不同程度的降低;燕麦植株不同部位的可溶性盐、Na+分配结果显示,燕麦秸秆含盐量最高,达96.954 g·kg^(-1),是根的3.576倍、籽粒的12.803倍,秸秆内Na+含量最高,为20.242 g·kg^(-1),是根的5.190倍、籽粒的55.763倍。可见,燕麦植株通过在不同部位间合理分配可溶性盐和Na+来提高燕麦的耐盐性。综上表明,燕麦植株通过吸盐、储盐、收获移盐等纳盐过程对滨海盐渍土的改良效果明显。

葡萄MYB转录因子基因VvMYB30的克隆及其耐盐性分析

MYB转录因子在响应各类非生物胁迫中发挥着重要作用。本研究以‘阳光玫瑰’葡萄为材料,鉴定了1个盐胁迫响应MYB转录因子基因VvMYB30,并对其特性及功能进行研究。该基因cDNA全长为984 bp,编码327个氨基酸。生物信息学分析发现,VvMYB30含有1个保守的R2R3蛋白结构域,与甜橙CsMYB30转录因子的同源性最高,相似度为64.75%,归属于SubgroupⅠ亚类。亚细胞定位及转录激活分析表明,VvMYB30定位于细胞核,且具有转录激活活性。qRT-PCR结果表明,VvMYB30受盐胁迫诱导,处理24 h表达量达到最高,为对照的6.86倍。将VvMYB30基因转化拟南芥,盐胁迫下VvMYB30转基因拟南芥种子萌发率和幼苗的成活率均显著高于野生型,表明过表达VvMYB30可增强转基因拟南芥的耐盐性。

中国大规模盐穴储氢需求与挑战

氢能是来源广泛且低碳清洁的能源,大力发展氢能产业是实现双碳目标和应对全球能源转型的重要举措。在氢能“制备―储存―运输―应用”全产业链中,储氢难问题长期制约着氢能产业高质量发展。盐穴储氢具有成本低、规模大、安全性高和储氢纯度高等突出优势,是未来氢能大规模储备的重要发展方向,也是我国能源低碳转型的重大战略需求。综合调研了我国制氢产业和氢能消费现状,分析了我国盐穴储氢的需求。调研了国外利用盐穴储存天然气和氢气的技术及工程现状,总结了我国盐穴储气库发展和建设历程。对比了利用盐穴储存天然气、氦气、压缩空气和氢气的异同点,提出我国盐穴储氢面临三大科技挑战:层状盐岩氢气渗透与生化反应、盐穴储氢库井筒完整性管控、储氢库群灾变孕育与防控。研究成果明确了我国氢气储备需求的快速增长趋势和大规模盐穴储氢的重点攻关方向。