Experimental study on grain size and soluble salt of saline soil in western Jilin Province, China

Western Jilin Province is a typical seasonal frost region, and is also one of the severest salinization areas of China. In this study, we aim to examine the saline soil in Da＇an and Wukesong areas, western Jilin Province, and mainly analyze the granulometric composition and distribution of salt in soil profiles. Four sampling sites, two in Da＇an and two in Wukesong respectively, are chosen for study. The granulometric composition, especially silt and clay content change in different sites and soil depths are analyzed. Analysis of total and components of soluble salt shows that the surface soil is weak carbonate saline, in which the main cation is Na＋ and the main anion is HCO3-. The total amount of soluble salt presents a decreasing tendency with increasing depth. The comprehensive analysis ofgranulometric composition and soluble salt shows that the clay content and soluble salt content present similar variation tendency with an increase of depth.

Effect of Initial Soluble Salt Composition of Saline Soil on Salinity Tolerance of Barley Plant

A pot experiment was carried out on a marine saline soil to study the effect of initial soluble Na/Ca ratio of saline soil on the salinity tolerance of barley plant.The results showed that (1) the Na/Ca ratio affected significantly the dry weight of the plant at an earlier stage of growth,the critical values of initial Na/Ca ratio at which the plant could grow normally on soils containing salts of 2.5,3.5 and 4.5g kg^-1 were 30,20 and 15,respectively;(2)smaller Na/Ca ratio resulted in a considerable decrease in Na accumulation but a great increase in K accumulation in the barley plant;and (3) the plasmallema of barley leaf were badly injured when the Na/Ca ratio was more than 30 and the increase of Na content of plant caused an exudation of K from the leaf cells.Some critical indexes were suggested for the cultivation of barley plant on marine saline soils and could be used as reference in the biological reclamation of marine saline soils.

Influences of Soluble Salts on Adsorption Properties of Polycarboxylate Superplasticizers

Polycarboxylate（PC） superplasticizers with different chemical structures were synthesized through free radical co-polymerization reaction.A total organic carbon analyzer was used to investigate adsorption behaviors of PCs,and to evaluate influences of soluble salts on absorption properties of PCs.It is found that adsorption ratios of PCs on cement particles decrease greatly with the addition of Na2SO4;the adsorption ratio of ethers PC with Hydroxyethyl methacrylate（HEMA） group first increases then decreases with the addition of NaCl;the adsorption ratio of esters PC with short side chains first decreases then increases,while the adsorption ratio of ethers PC with HEMA group decreases with the addition of CaCl2;the adsorption ratio of esters PC with short side chains decreases with the addition of Ca（NO3）2;AlCl3 causes the decrease of the adsorption ratio of ethers PC with HEMA group.

Numerical Modelling of Dissolving and Driving Exploitation of Potash Salt in the Qarhan Playa——A Coupled Model of Reactive Solute Transport and Chemical Equilibrium in a Multi-component Underground Brine System

Firstly, the macroscopic chemical equilibrium state of a series of chemical reactions between intercrystal brine and its media salt layer （salt deposit） in Qarhan Salt Lake was studied by using the Pitzer theory. The concept of macroscopic solubility product and its relation with accumulated ore dissolving ratio were presented, which are used in the numerical model of dissolving and driving exploitation of potassium salt in Qarhan Salt Lake. And secondly, with a model forming idea of transport model for reacting solutes in the multi-component fresh groundwater system in porous media being a reference, a two-dimensional transport model coupled with a series of chemical reactions in a multi-component brine porous system （salt deposits） was developed by using the Pitzer theory. Meanwhile, the model was applied to model potassium/magnesium transport in Qarhan Salt Lake in order to study the transfer law of solid and liquid phases in the dissolving and driving process and to design the optimal injection/abstraction strategy for dissolving and capturing maximum Potassium/ Magnesium in the mining of salt deposits in Qarhan Salt Lake.

Solution behavior of ZnS and ZnO in eutectic Na_2CO_3-NaCl molten salt used for Sb smelting

The solution behavior, including solubility, reactivity and sedimentation, of ZnO and ZnS in a Na_2CO_3-NaCl molten salt used for Sb smelting was investigated in the temperature range of 700-1000 oC. The saturated amount of dissolved ZnO in the molten salt remained constant at 0.02% and was unaffected by temperature; additionally, ZnO did not react with the molten salt. In contrast, the saturated amount of dissolved ZnS in the eutectic molten salt increased with increasing temperature, and the content of ZnS was 0.53% at 1000 oC. In addition, ZnS reacted with Na_2CO_3 above 900 oC to give ZnO. The sedimentation rates of these three species in the molten salt followed the order of Sb>ZnS>ZnO. It was thus concluded that ZnO is an appropriate sulfur-fixing agent for low-temperature Sb smelting in a Na_2CO_3-NaCl molten medium, and that the optimal smelting temperature is below 900 oC.

PREPARATION AND PHOTOSENSITIVITY OF WATER SOLUBLE PHENOLIC RESINS CONTAINING ACRYLOYL AND QUATERNARY AMMONIUM CHLORIDE GROUPS

New water soluble and photocrosslinkable prepolymers containing acrylate and quaternary ammonium salt groups were synthesized from epoxy phenolic resin via ring-opening reaction with acrylic acid and with aqueous solution of triethylamine hydrochloride successively. The second reaction needs no phase transfer catalyst to accelerate, since the product formed can act as a phase transfer catalyst. The prepolymer obtained contains both photocrosslinkable acrylate groups and hydrophilic quaternary ammonium salt groups. Optimum conditions for these reactions were studied. The photosensitivity of the prepolymer was also investigated. The effects of different photoinitiators, different crosslinkable diluent monomers and amine accelerator on the photosensitivity of the prepolymer were compared. The photoinitiator of hydrogen abstraction type is still effective without using amine or alcohol as accelerator, because the prepolymer contains a H beside the OH groups formed in the ring-opening reactions.

Pharmaceutical salts: Theory, use in solid dosage forms and in situ preparation in an aerosol

In this article, the theoretical foundation for salts is given with an emphasis on the amount of drug in solution. Consideration is given for the solubility of the non-ionized form, acid dissociation constant and solubility product, which are the limiting constraints. For dissolution of nonionized drugs, the surface pH differs from the bulk pH, giving rise to a lower than expected rate. For salts, theoretical considerations are relatively complex, and an experimental approach to estimating the surface pH is more likely to be of value in predicting the dissolution rate. General guidelines are described for screening, preparing and characterizing drugs as salts, which critically depend on the goal of the product development.Thereafter, our work involving the preparation of salts as a means to generate aerosols from a solution is provided. The solubility of six structurally related compounds was determined in four acids. Thereafter, the amount of the compound in solution was determined as a function of pH, using the acid that provided the highest solubility. Because the pH required to achieve the needed concentration for aerosol generation was low, ammonia vapor was introduced into the air stream to neutralize aerosol droplets. Solvent was then removed from the aerosol by a silica column. The resulting aerosol had a concentration of 96 μg/l and a mass median particle size of 1.8 μm. The reported pharmacokinetic study substantiated the feasibility of evaluating its safety and efficacy of inhalation administration in the rat model.

Crystal Structure, Characterization and Enhanced Solubility of Ibuprofen by 2-Methylimidazolium Salt

Novel crystalline forms of ibuprofen(IBU) with 2-methylimidazole(2 MI) in a 1:1 molar ratio was synthesized by liquid-assisted grinding technique and characterized by single-crystal X-ray diffraction, infrared spectral(IR), powder X-ray diffraction(PXRD),differential scanning calormetry(DSC) and Hirshfeld surface analysis. The structure of IBU-2 MI salt is assembled via N(1)–H(1)+···O1 and N(2)–H(2)+···O(2) hydrogen bonds to form the zigzag-like 1 D chain structure. The original purpose was to solve the pH-dependent solubility defect of ibuprofen, and the result of pH dependent solubility experiments showed that the IBU-2 MI salt had a better solubility at the wide range of pH 4.00 to 9.18. Furthermore, the solubility of IBU-2 MI salt exhibits a dramatic increase(30-fold) in aqueous mediums.

Production of Potash and N-Mg Compound Fertilizer via Mineral Shoenite from Kunteyi Salt Lake:Phase Diagrams of Quaternary System(NH_(4))_(2)SO_(4)-MgSO_(4)-K_(2)SO_(4)-H_(2)O in the Isothermal Evaporation and Crystallization Process

Based on the requirement of the new technology for producing potassium sulfate and N-Mg compound fertilizer,boussingaultite,by the reaction of the mineral shoenite from Kunteyi Salt Lake,Qinghai province,and the industrial by-product ammonium sulfate,the solubilities of the quaternary system(NH_(4))_(2)SO_(4)-MgSO_(4)-K_(2)SO_(4)-H_(2)O at 25.0℃in the isothermal evaporation and crystallization process were measured using the isothermal evaporation method,and the corresponding phase diagrams were plotted.According to the diagram,this system contains six saturation points and six solid phase fields of crystallization,which correspond to(K1-m,(NH_(4))m)_(2)SO_(4),(NH_(4))_(2)SO_(4)·MgSO_(4)·6H_(2)O,K_(2)SO_(4)·MgSO_(4)·6H_(2)O,MgSO_(4)·6H_(2)O,(K1-n,(NH_(4))n)_(2)SO_(4)·MgSO_(4)·6H_(2)O and MgSO_(4)·7H_(2)O,respectively.By analyzing and calculating the isothermal evaporation and dissolution phase diagram of this quaternary system at 25.0℃,K_(2)SO_(4)and(NH_(4))_(2)SO_(4)·MgSO_(4)·6H_(2)O can be separated via K_(2)SO_(4)·MgSO_(4)·6H_(2)O and(NH_(4))_(2)SO_(4)as raw materials.Theoretical calculations about the proposed process were carried out and verified by experiment,which indicated that the yield of potassium sulfate was improved and the magnesium resources were fully utilized.

Bioavailability and Solubility of Different Calcium-Salts as a Basis for Calcium Enrichment of Beverages

Background: When usual calcium consumption patterns were analysed most people in the U.S. and Europe consume less than the recommended daily allowance. Supplements and fortified foods offer alternative and additional sources of calcium to traditional food. Calcium carbonate is the most common supplement but it is less soluble in water and, therefore, not suitable for enrichment of beverages. New organic calcium salts have a better solubility but less is known about their bioavailability. In the present study, we assessed the solubility and bioavailability of the new organic calcium salts, calcium lactate citrate and calcium lactate malate, in comparison to the traditional supplements, calcium carbonate and calcium gluconate. Design: Randomized, single-blind, four way cross-over study comparing single doses of 500 mg calcium in the form of four different calcium-salts. Subjects were advised to consume 25 μg vitamin D3 daily two weeks prior to the start of the study and during the whole study period. Subjects: 20 healthy young men, Methods: Blood samples were drawn immediately before and 2, 4, 6, 8, 12 and 24 h after ingestion of the calcium preparation. Concentration of total calcium and intact parathyroid hormone were measured in the serum. Urine was collected at baseline and during the intervals 0-3, 3-6, 9-15 and 15-24 h and excretion of calcium, sodium and creatinine was examined. Results: The tested new salts were easily water soluble, significantly better than calcium gluconate. Calcium carbonate is almost insoluble. The bioavailability of the four different calcium salts was found to be almost identical. The maximum total serum calcium increased by 7.6 % two hours after ingestion calcium lactate citrate, by 7.4 % after calcium lactate malate, by 5.5 % after calcium carbonate, and by 5.8 % after calcium gluconate. Intact parathyroid hormone concentration showed the expected depression for calcium lactate citrate, calcium lactate malate and calcium carbonate, whereas the serum level was significantly higher after ingestion of calcium gluconate. Conclusion: Given an almost equivalent bioavailability of the four tested calcium salts, we conclude that the new salts calcium lactate citrate and calcium lactate malate are well suited for fortification of beverages and thus to increase the average daily calcium intake.

Alumina Solubility in Na_3AlF_6-K_3AlF_6-AlF_3 Molten Salt System Prospective for Aluminum Electrolysis at Lower Temperature

The alumina solubility in the title system within the composition range of KR{m（K3AlF6）/[m（K3AlF6）＋ m（Na3AlF6）]} 10%―50%, a ternary Na3AlF6-K3AlF6-AlF3 molten system with 23%―29%（mass fraction） AlF3 was investigated by measuring the mass loss of a rotating sintered corundum disc. And the following empirical equation was derived when superheat degree was no more than 60 °C： w（Al2O3）sat=A×（T/1000）B, where A= –1.85774＋ 26.754234w（AlF3）–0.3683–0.00783KR2.363＋0.010266KR2.3048＋0.7902w（AlF3）0.00652, B=112.4625–53.2567w（AlF3）0.4236＋ 5.1079w（AlF3）0.9241＋0.01542w（AlF3）1.3540. Considering both higher alumina solubility and not too high superheat de gree are required, alumina solubility of different compositions at not the same temperature but the same superheat degree was studied, which will be more industrial helpful for selecting prospective compositions. The results show that the composition deserved to be further tested in lower temperature cells is 10%―30% KR and 23%―26%（mass fraction） AlF3.

Apparatus for determining permeability of hydrogen isotopes in molten-salt

In order to provide data on diffusion coefficients and solubility constants of tritium in molten salts for the critical issue of tritium control in the Thorium Molten Salt Reactor(TMSR)program,a two-chamber permeability apparatus separated by a nickel plate had been developed for determining the permeability of hydrogen isotope in molten salts.Descriptions on the permeability apparatus,experimental procedure and the analytical method for determining the diffusivity and solubility of hydrogen isotope in molten salts were presented in this paper.To assess the performance of the apparatus,the blank tests without molten salt were conducted at300-700℃.The results showed that the nickel plate acting as the window for hydrogen isotope permeation in the apparatus seemed to have less effect on experiments of determining the permeability of hydrogen isotope in molten slat at 500-700℃.Furthermore,the applicability of the apparatus with molten salt was also evaluated experimentally,with test experiments of molten Flinak(LiF-NaF-KF)at 500℃,600℃and 700℃.Diffusion coefficients and solubility constants of hydrogen in molten Flinak can be derived from those test experiments,which were correlated to D_(Flinak-H)=7.06×10^(-5)e^(-54.9/(R_gT))m^2/s and s_(Flinak-H)=1.67×10^(-7)e^(27.0/(r_gt))mol-H_2/(m^3 Pa).

THE SOLUBILITY OF FERROALLOYED NEODYMIUM IN MOLTEN SALT CONTAINING NEODYMIUM TRICHLORIDE

The solubility of ferroalloyed neodymium in molten salt containing neodymium trichloride and the de- pendence of solubility on temperature and composition of the melt are determined by means of electrochemical method.The data obtained are in good agreement with result of chemical analysis of the quenched molten salt samples.

长江三角洲北翼更新世以来的水土环境地球化学特征及其环境指示意义

江苏沿海平原是江苏省域水资源脆弱带,地下水咸化已成为较为严重的生态环境问题。为了解析长江三角洲北翼地区更新世以来地下水的补给及其盐分来源,布设一口275 m的深井HYRD1,全孔连续采集易溶盐样品、土工样品、水样。在区域采集地表水、浅层与深层地下水、海水样品。采用易溶盐指标结合土工指标(含水率、湿密度、比重)获取了HYRD1高精度孔隙水的水化学特征。采用Piper三线图、Gibbs图、离子比值法等结合δD、δ^(18)O数据、^(14)C测年数据解析了更新世以来地下水的补给及其盐分来源。结果表明:土体盐分主要为NaCl,盐渍土占比为25%。盐渍土主要分布在Q_(p3)弱透水层、 Q_(p2)地层与Q_(p1)上段地层。孔隙水水化学类型为Cl-Na型(仅Q_(p1)下段个别点为HCO~-_3-Ca·Na),微咸水占比7%,咸水占比49%,盐水占比44%。微咸水主要分布在Q_(p1)下段砂层中。潜水的δ^(18)O、δD说明潜水来源为大气降水,且受到了较为强烈的蒸发作用。弱透水层孔隙水、承压水的δ^(18)O、δD投点位于标准海水稀释线附近,且随着深度的增加,δ^(18)O、δD有减小趋势,说明海水混合作用随着深度的增加而减小。Q_(p1)弱透水层多见钙质结核,说明了Q_(p1)地层成土后受到了强烈的蒸发作用。HYRD1 Q_(p1)上段及上覆地层盐分主要来源于5期海侵、蒸发盐岩与硅酸盐风化溶解,Q_(p1)下段地层盐分主要来源为地壳源。地下水化学成分受到了水岩作用、蒸发浓缩作用与人类活动等的影响。

可溶性钾盐主要成分分析前处理技术与分析方法研究

钾盐是中国最紧缺的矿产资源之一,为农业三大肥料中钾肥的主要原料,当前具有开发利用价值的主要是可溶性钾盐资源。而目前可溶性钾盐尚无国家标准物质和标准分析方法,本文对称样量、固液比、溶解温度、溶解时间、搅拌条件、超声时间和功率等条件进行实验研究,利用电热板和超声振荡两种溶解方式,建立了可溶性钾盐中主要成分钾、钠、钙、镁、氯和硫酸根离子的分析方法。采用电感耦合等离子体发射光谱仪测定样品中的Ca^(2+)、Mg^(2+)、K^(+)和Na^(+)的含量,离子色谱仪测定样品中Cl^(-)和SO_(4)^(2-)的含量,两种溶解方法分析可溶性钾盐样品中上述离子的实验结果基本吻合。电热板溶解方法精密度为0.52%~3.19%(RSD,n=11),超声振荡溶解方法精密度为0.55%~3.07%(RSD,n=11),两种方法检出限为0.01~0.05μg/g。利用主要成分百分含量加和、加标回收率、阴阳离子平衡验证方法准确性,两种溶解方法的主要成分加和在99.0%~101.0%之间,加标回收率在95.3%~103.8%,阴阳离子平衡在-3%~3%之间,均满足DZ/T 0130.3—2006质量管理规范中的分析要求。两种可溶性钾盐的溶解方法均可在日常检测中应用,对于较大批的钾盐样品分析,电热板溶解法整体工作效率较高,更适用于实验室内批量样品分析;超声振荡器溶解方法与电热板溶解方法相比,更为简单快速,对于少量样品的分析,效率更高,且超声波振荡器方便野外携带,使用在钾盐的野外现场勘探工作中,可较大地提高工作效率,实时指导找矿行动顺利开展。

某东南沿海电厂钢结构腐蚀影响因素分析

目的 对比腐蚀环境因子分布和钢结构腐蚀事件分布,分析影响火力发电厂钢结构腐蚀的主要环境因素,探讨火力发电厂钢结构腐蚀的机理。方法 以东南沿海某火力发电厂为例,对电厂厂区进行网格化,利用便携式温湿度计进行逐网格温、湿度监测,逐网格收集结构物表面灰尘,并分析其中氯离子、可溶盐、酸碱含量等,开展腐蚀环境监测。统计从2012年至2022年10年间该电厂每一网格内的腐蚀防护工程,如腐蚀防护器件、装备、材料购置等项目的施工或应用次数。结果 温度、湿度及钢结构表面灰尘中氯离子含量、可溶盐含量、灰尘浸渍水p H等因子受海洋环境、厂区结构分布、生产活动多重原因的影响,随距海距离增加呈带状分布,或围绕生产设施点呈辐射分布。结论 环境因子对钢铁结构腐蚀的影响大小顺序为结构物灰尘含盐量>结构物灰尘浸渍水p H>相对湿度>结构物灰尘氯离子含量>温度。电厂钢结构腐蚀机理为雨水或大气凝结水溶出结构物表面灰尘的可溶性盐,含盐水经涂层缺陷输运至金属表面,成为钢铁腐蚀原电池的离子导路,导致钢结构发生电化学腐蚀。

砂岩质文物内部毛细水运移过程微电极响应特征

盐结晶病害是砂岩质文物中最为常见的病害之一,可溶盐溶液在砂岩内部的毛细运移直接影响着文物保存的完整性。为了进一步了解不同因素影响下砂岩质文物内部中毛细水运移特征,以大足石刻砂岩材料为研究对象,自主设计了毛细吸水试验及微电极电阻率测试装置,定量分析孔隙结构、孔隙溶液、干湿循环及相对湿度对毛细运移和电阻率分布特征的影响。结果表明,松散的孔隙结构及较低的相对湿度对毛细运移有促进作用。毛细运移受可溶盐溶液表面张力影响明显,吸水量和运移速率随表面张力增加呈递增趋势。干湿循环作用导致内部孔隙扩张使毛细迁移速率加快,同时呈现出试样饱和度和砂岩电阻率的负相关性。可溶盐的存在极大降低了砂岩的电阻率,通过电阻率的时空分布特征,识别湿润锋的视电阻率范围与试样表层盐结晶劣化区域大致重合,整体趋势沿深度方向呈凹曲面变化。研究结果揭示了砂岩质文物内部毛细水运移规律,可为合理追踪盐害范围提供理论支撑。

馆藏汉代瓦当表面可溶盐的化学组成分析

采用离子色谱仪(IC),扫描电子显微镜-能谱仪(SEM-EDS),X射线衍射仪(XRD)和傅里叶变化显微红外光谱仪(FTIR)等现代分析仪器,对陕西历史博物馆馆藏的汉代瓦当表面可溶盐进行了鉴定,并分析了相关的化学组成。结果表明,瓦当表面可溶盐含有石膏(Ca SO_(4)·2H_(2)O)和有机酸钙盐[Ca_(3)(CH_(3)COO)_(3)Cl(NO_(3))_(2)·6H_(2)O]等成分。

Soluble salt deposit in the Nihewan beds and its environmental significance

Observation and experimental analysis of soluble salt deposit along four profiles across the strata deposited in Nihewan paleolake basin enabled us to recognize the nature and evolution stages of the Nihewan paleolake and its significance in stratigraphical division and pa-leo-environmental reconstruction. The Nihewan paleolake was at least a weak-saline to semi-saline lake and represents an intracontinental lake in the semi-arid region. The lower member of sedimentary strata in the paleolake contains gypsum layer and gypsum lamellae. Soluble salt is mainly composed of SO42- and Ca2+ ions, representing a trend of the paleolake evolvinginto a stage of sulfate lake. The upper member of the strata has predominantly Cl-, K+, and Na+ ions in soluble salt, indicating a starting development of the paleolake to chlorite lake, but no salt rock was deposited, indicating a drying trend of the area.

硒对水稻生长和盐胁迫耐受性的影响

为确定适合水稻生长发育的硒浓度,采用含不同亚硒酸钠浓度的木村B营养液对水稻苗进行培养、表型观察和生化测定。结果表明,2、4、8μmol/L硒均可促进水稻主根长度的增加,减少侧根数量,但不影响水稻地上部分生长;40、200μmol/L硒则引起水稻生长减慢或停止,总蛋白含量下降,SOD活性提高。采用8μmol/L亚硒酸钠+150 mmol/L氯化钠共同进行胁迫处理,结果显示,亚硒酸钠提高了水稻的盐胁迫耐受性,叶片中的可溶性蛋白含量显著高于对照,SOD的比活力则低于对照。