In Situ Synthesis of NaY Zeolite with Coal-Based Kaolin

NaY zeolites were in-situ synthesized from coal-based kaolin via thehydrothermal method. The effects of various factors on the structure of the samples were extensivelyinvestigated. The samples were characterized by N_2 adsorption, XRD, IR and DTG-DTA methods, andthe results show that the crystallization temperature and amount of added water play an importantrole in the formation of the zeolite structure. The 4A and P zeolites are the competitive phasepresent in the resulting product. However, NaY zeolites with a higher relative crystallinity,excluding impure crystals and the well hydrothermal stability, can be synthesized from coal-basedkaolin. These zeolites possess a larger surface area and a narrow pore size distribution, and thismeans that optimization of this process might result in a commercial route to synthesize NaYzeolites from coal-based kaolin.

Improvement of Rice Plant Root by Kaolin Application in Iron Toxicity Condition at Zoukougbeu (Central-West of Côte d’Ivoire)

In the tropics, lowland rice cultivation is often confronted with the problem of iron toxicity. The solution proposed by research in general is the use of industrial silicon. However, the high cost of industrial silicon limits its adoption by farmers. A study was carried out in Zakogbeu;Center-West of Côte d’Ivoire, to assess the potential of kaolin to mitigate the effect of this soil constraint on the root of the rice plant. Five kaolin-based treatments were analyzed (T0 = 0 kg kaolin ha−1, T1 = 366 kg kaolin ha−1, T2 = 736 kg kaolin ha−1, T3 = 1097 kg kaolin ha−1 and T4 = 1465 kg kaolin ha−1 are 0, 200, 400, 600 and 800 kg SiO2 ha−1) in a device in complete random blocks, with 5 repetitions. The results obtained show that kaolin supply increases the length of the root tissue as well as the number of branching of the root of the rice plant. Root tissue increased from 10 cm with T0 treatment to more than 15 cm with treatment T4. The microscopic observation of the roots shows that in the treatment T0, the roots present only primary ramifications and the tertiary and quaternary ramifications are observed with the treatments T3 and T4. The contribution of kaolin is an alternative to inhibit the effect of iron toxicity on the rice plant root development in iron toxicity condition.

Development of Kaolin and Glass Fiber Reinforced Composites for Thermal Insulating Panels

In our modern world, where conserving energy is highly valued, thermal insulation panels play a crucial role in reducing heat transfer between two spaces, surfaces, or materials. They are used to enhance the energy efficiency of various industrial applications by minimizing heat loss and temperature control. These panels function as silent protectors, aiding in reducing energy consumption and making things more sustainable and better for the environment. This is where composite materials come in;they are known for their lightweight nature, high strength-to-weight ratio, and excellent thermal insulation properties and have gained significant attention. Researchers are actively engaged in various studies aimed at enhancing these materials further. This research project focuses on the development of kaolin and glass fiber-reinforced composites for thermally insulating panels, to which natural strengthening materials like corn husk and bamboo fibers are added. The aim is to create cost-effective and efficient composite materials for thermal insulation applications by incorporating these components with a binder consisting of potassium silicate, hydroxide, and distilled water. This project involves conducting compression tests, bending tests, impact tests, thermal conductivity measurements, and microscopic analysis to evaluate the mechanical and thermal properties of the developed composites. The profound impact of these engineered composites on thermal insulation panels stands to revolutionize energy conservation efforts, offering a potent avenue to minimize heat loss and enhance overall energy efficiency across an array of industrial sectors.

A review of the synthesis and application of zeolites from coal-based solid wastes

Zeolite derived from coal-based solid wastes(coal gangue and coal fly ash)can overcome the environmental problems caused by coal-based solid wastes and achieve valuable utilization.In this paper,the physicochemical properties of coal gangue and coal fly ash are introduced.The mechanism and application characteristics of the pretreatment processes for zeolite synthesis from coal-based solid wastes are also introduced.The synthesis processes of coal-based solid waste zeolite and their advantages and disadvantages are summarized.Furthermore,the application characteristics of various coal-based solid waste zeolites and their common application fields are illustrated.Finally,we propose an alkaline fusion-assisted supercritical hydrothermal crystallization as an efficient method for synthesizing coal-based solid waste zeolites.In addition,more attention should be given to the recycling of alkaline waste liquid and the application of coal-based solid waste zeolites in the field of volatile organic compound adsorption removal.

Migration behaviors and kinetics of phosphorus during coal-based reduction of high-phosphorus oolitic iron ore

To understand the migration mechanisms of phosphorus(P)during coal-based reduction,a high-phosphorus oolitic iron ore was reduced by coal under various experimental conditions.The migration characteristics and kinetics of P were investigated by a field-emission electron probe microanalyzer(FE-EPMA)and using the basic principle of solid phase mass transfer,respectively.Experimental results showed that the P transferred from the slag to the metallic phase during reduction,and the migration process could be divided into three stages:phosphorus diffusing from the slag to the metallic interface,the formation of Fe P compounds at the slag metal interface and P diffusing from the slag metal interface to the metallic interior.The reduction time and temperature significantly influenced the phosphorus content of the metallic and slag phases.The P content of the metallic phase increased with increasing reduction time and temperature,while that of the slag phase gradually decreased.The P diffusion constant and activation energy were determined and a migration kinetics model of P in coal-based reduction was proposed.P diffusion in the metallic phase was the controlling step of the P migration.

Adsorption and Regeneration of Volatile Organic Compounds(VOCs)on Coal-Based Activated Carbon by Ferric Nitrate Modification

In this study,the Heishan coal was used to prepare a series of activated carbon(AC)samples via a vapor deposition method.The effects of the Fe(NO_(3))3/coal weight ratio on the physicochemical properties of the activated carbon were systematically investigated,and the AC samples were analyzed by the N2 adsorption-desorption technique,the scanning electron microscopy,the X-ray diffraction,the Raman spectroscopy,and the Fourier transform infrared spectroscopy.Furthermore,the adsorption properties of ethyl acetate were investigated.The results indicated that as the Fe(NO_(3))3/coal mass ratio increased from 1:8 to 1:2,the specific surface area,the total pore volume and the micropore volume initially increased and then decreased.The specific surface area increased from 560.86 m^(2)/g to 685.90 m^(2)/g,and then decreased to 299.56 m^(2)/g.The total pore volume and micropore volume increased from 0.29 cm^(3)/g and 0.17 cm^(3)/g to 0.30 cm^(3)/g and 0.22 cm^(3)/g,and then decreased to 0.16 cm^(3)/g and 0.10 cm^(3)/g,respectively.The optimized ratio was 1:8.During the activation process,iron ions infiltrated the activated carbon to promote the development of the pore structure,the pore size of which was between 2.5 nm and 3 nm in daimeter.This approach could enhance the capacity for adsorption of ethyl acetate.It is worth noting that the ACs displaying the largest specific surface area and total pore volume(685.90 m^(2)/g and 0.30 cm^(3)/g)were formed under the optimized activation conditions(950℃,20%(volume)of CO_(2),ratio 1:5),and the maximum AC capacity for adsorption of ethyl acetate was 962.62 mg/g.After seven repeated thermal regeneration experiments,the saturated AC adsorption capacity was still above 90%.

Review on coal-based reduction and magnetic separation for refractory iron-bearing resources

The application of coal-based reduction in the efficient recovery of iron from refractory iron-bearing resources is comprehensively reviewed.Currently,the development and beneficiation of refractory iron-bearing resources have attracted increasing attention.However,the effect of iron recovery by traditional beneficiation methods is unacceptable.Coal-based reduction followed by magnetic separation is proposed,which adopts coal as the reductant to reduce iron oxides to metallic iron below the melting temperature.The metallic iron particles aggregate and grow,and the particle size continuously increases to be suitable for magnetic separation.The optimization and application of coal-based reduction have been abundantly researched.A detailed literature study on coal-based reduction is performed from the perspectives of thermodynamics,reduction kinetics,growth of metallic iron particles,additives,and application.The coal-based reduction industrial equipment can be developed based on the existing pyrometallurgical equipments,rotary hearth furnace and rotary kiln,which are introduced briefly.However,coal-based reduction currently mainly adopts coal as a reductant and fuel,which may result in high levels of carbon dioxide emissions,energy consumption,and pollution.Technological innovation aiming at decreasing carbon dioxide emissions is a new trend of green and sustainable development of the steel industry.Therefore,the substitution of coal with clean energy(hydrogen,biomass,etc.)for iron oxide reduction shows promise in the future.

Making Ferronickel from Laterite Nickel Ore by Coal-Based Self-Reduction and High Temperature Melting Process

Based on the process of coal-based self-reduction and melting separation at high temperature, it was investigated that the effect of process factors on the reduction of iron and nickel oxide, the metal yield and the nickel content in ferronickel about the laterite nickel ore, was from Philippines and contented low nickel, high iron and aluminum. The results showed that if the C/O mole ratio was not higher than 0.5 and the reduction temperature was kept as 1200°C and then increased up to 1500°C, the metal could not separate from molten slag for the A series of experiments, which were only added CaF2. However, when the C/O ratio was added up to 0.6 - 0.8, the metal could separate well from the slag, and the yields of Fe and Ni increased gradually. But the nickel content in the metal declined from 1.79% to 1.34%. When the C/O ratio increased to 1.2, and the temperature of melting products obtained at 1200°C and rose to 1550°C, the separation of metal from slag could not be realized in B group of tests, which were only added hydrated lime. However, when both of CaF2 and hydrated lime were added, the metal could separate from slag in C group. In order to increase the content of nickel in the metal, it is necessary to restrain the reduction of iron oxide. When the C/O mole ratio is 0.6, the nickel content of metal could be 1.79%, which was higher than the theoretical ratio 1.65% of Ni/(Ni + Fe) of the latcritic nickel ore, but the yield of nickle was only 71.3%.

土性对工程泥浆固化强度影响规律及微观机理

本文开展了一系列不同液限高分子吸水树脂固化工程泥浆无侧限抗压强度试验,探讨了泥浆土液限对固化效率的影响规律,对比研究了掺入高岭土对泥浆固化强度的改进程度,最后基于XRD和SEM试验揭示了液限和高岭土对固化泥浆强度影响的微观机理。结果表明:随着泥浆土液限的增大,固化泥浆土强度逐渐降低,固化效率随着泥浆土液限增大显著衰减,当液限增加10%,固化泥浆土强度qu平均减少48.2%。然而高岭土的掺入则显著提升了固化泥浆土的强度,并且强度增长率随着龄期逐渐增大,对于龄期为90天时,增加40%高岭土能够提升固化泥浆土强度qu 1.17倍。微观结构试验表明泥浆土液限变化对水化产物产量的影响较小,固化泥浆土强度随泥浆土液限减小主要是由于固化泥浆土孔隙随着泥浆土液限增大而增多,使得微观结构松散从而导致强度降低。高岭土的掺入则显著提升了固化泥浆土的水化产物产量,增强了固化泥浆土胶结强度,从而提升了固化泥浆土强度。因此,在实际工程中,一方面可以通过调配泥浆土液限来提高固化效率;另一方面可以通过掺入高岭土或者一些高岭土基废弃物(如高岭土尾矿)来提高固化强度,实现“以废制废”绿色环保的理念。

基于高岭土增韧环氧树脂水泥基材料的多强度组合指标配比优化法

煅烧高岭土能有效改善环氧树脂水泥基材料的力学性能,实验表明:煅烧高岭土可大大提高环氧树脂水泥基材料的3 d早期抗折、抗压强度,当高岭土掺量为30%时,改性环氧树脂水泥基材料的抗折及抗压强度分别提高了134.28%、106.25%;当高岭土掺量小于30%时,改性环氧树脂水泥基材料具有二次抗折强度,且抗折强度残余率大于50%。根据不同高岭土掺量对改性环氧树脂水泥基材料抗压强度、抗折强度、二次抗折强度的影响规律,提出了适用于不同结构工程受力特点的多强度组合指标配比优化法,获得了考虑二次抗拉强度影响的不同最大拉应力和最大压应力组合条件下最优的高岭土配比,为实际不同结构体不同部位不同受力特征的高岭土改性环氧树脂水泥基材料制备提供了理论依据。

高吸油量煅烧高岭土的制备与性能表征

通过插层剂二甲基亚砜、接枝剂甲醇和剥离试剂十六烷基三甲基溴化铵协同超声震荡辅助作用,将层状煤系高岭土剥离为超细片状煤系高岭土。通过X射线衍射(XRD)、傅里叶红外(FT-IR)、N_(2)吸附-脱附及扫描电镜(SEM)与能谱分析(EDS)等技术手段对煤系高岭土进行表征。结果表明,其层间距由层状煤系高岭土的0.708 nm扩大到片状煤系高岭土的1.12 nm,内部孔隙增加,形成了裂隙形状的介孔且孔径分布均匀。煅烧高岭土较煤系高岭土的吸油性能大幅提升,其吸油量从60~73 g/100 g煤系高岭土增至70~79 g/100 g煅烧高岭土。整个制备工艺流程中无引入强酸强碱等腐蚀性物质,提供了一种环境友好型煅烧高岭土制备技术。

超细粉末压片法X荧光仪测定高岭土中主量元素

利用超细粉碎技术,将高岭土标准物质(含内部控制样)粉碎至微米级,建立起超细制样粉末压片X射线荧光光谱法的高岭土工作曲线,克服了粒度效应和矿物效应,测定高岭土的主量元素含量。扣除灼失含量校正,用归一化法计算,标准物质测定结果与标准值一致。方法准确度高,精密度好,极大提高了高岭土的检测效率,主元素铝的氧化物加标回收率在92.00%~110.00%之间。满足了高岭土主量元素的检测需求,减少了对环境的污染。

高岭土对含有Cu^(2+)和Pb^(2+)污水吸附性实验

这是一篇环境工程领域的论文。为了研究高岭土对含有Cu^(2+)和Pb^(2+)污水吸附性能的影响,开展了不同初始浓度、温度、吸附时间、高岭土掺量和pH值作用下高岭土吸附重金属离子实验,并分析了高岭土对Cu^(2+)和Pb^(2+)共同吸附实验结果。结果表明:高岭土吸附金属Pb^(2+)离子的效果要好于高岭土吸附金属Cu^(2+)离子的效果。结合实验结果和经济效益而言,在初始浓度为200 mg/L,pH值为6、温度为30℃,高岭土掺量为1.5 g,吸附时间为2.0 h时,高岭土对金属Pb^(2+)和Cu^(2+)离子的吸附效果较优,其中金属Pb^(2+)离子的吸附量分别达到了56.38、56.22、58.76、35.75、和42.42 mg/g,金属Cu^(2+)离子的吸附量45.99、47.45、47.27、25.26、22.52 mg/g。整体上,高岭土对共同吸附金属离子(Cu^(2+)、Pb^(2+))的吸附量要小于单一离子的吸附量,这是由于两个金属离子在吸附过程中会相互影响对方的吸附过程。Langmuir模型对实验曲线的拟合度要远远高于Freundlich模型对实验曲线的拟合度,这就说明了Langmuir等温吸附模型更加适用于高岭土吸附金属离子吸附量的变化规律,进而证明了高岭土吸附重金属离子属于表面吸附,被吸附的重金属离子都是相互独立存在的。

肯尼亚沃伊矿区高岭土矿床地质特征及成因探讨

本文在对肯尼亚沃伊矿区高岭土矿进行专项地质调查和综合研究的基础上,分析了高岭土矿床的地质特征和矿床成因,总结了找矿标志。研究认为:肯尼亚沃伊矿区高岭土矿床赋存于前寒武纪长英质变粒岩中,是优质的高岭土矿石,可满足各类工业应用要求;该矿床为风化残积型高岭土矿床;区内高岭土一般为白色高岭土,白色的黏土矿物为本区高岭土找矿直接标志,富含有长石的基岩为高岭土矿的间接找矿标志。研究结果为肯尼亚高岭土的找矿工作提供参考。

电动土工塑料排水板修复重金属污染高岭土试验研究

针对重金属锌和镉污染的低渗透性高岭土,采用电动土工塑料排水板(EKG)作为电极材料,通过自制模型试验装置研究了电动修复中电势梯度、通电时间、含水率对重金属去除率的影响,确定电动修复的最优试验条件。在最优试验条件下,开展了电极材料、电势梯度对不同种类重金属去除效果影响的试验研究。结果表明:随着修复时间的增长,阳极处重金属污染物逐渐减少,阴极处重金属污染物富集逐渐增加;试验条件相同情况下,重金属污染物Cd的除去率明显高于Zn;电势梯度越大,重金属Zn离子的去除率越高;电动土工塑料排水板作为电极的电动修复重金属污染土的效果要优于石墨电极。研究有助于揭示电动修复重金属污染土的效果和机理,为电动生态环境修复技术的应用提供技术支持。

福建大田县元山高岭土矿床成矿地质特征及开发利用前景

通过福建大田县元山高岭土矿床的成矿地质特征及开发利用价值的分析,认为:元山高岭土矿产出于流纹斑岩风化壳内,矿石质量尚佳,埋藏浅,适宜露天分台阶开采;矿物主要为高岭石和石英,高岭石多为集合体,少量为他形片状单体;高岭土应用领域广泛,元山高岭土矿床具有较大的经济价值,具有较好的开发利用前景。

改性高岭土处理模拟印染废水效果研究

本文采用煅烧方法活化高岭土,采用聚合硫酸铁处理煅烧活化后的高岭土,通过对比2种高岭土的表征,利用它们处理大红染料模拟印染废水的色度,分析2种高岭土表征对模拟印染废水色度处理效果的相关性。结果表明,聚合硫酸铁改性煅烧活化后的高岭土比煅烧活化高岭土在BET表面积、吸附体积及BJH吸附平均孔径的数据显示更优,而运用聚合硫酸铁改性煅烧活化后的高岭土处理模拟印染废水色度的去除率更高,可高达99.94%。

基于响应面法的煤矸石氯化焙烧除铁工艺参数优化

为解决煤矸石氯化焙烧除铁过程中氯化剂消耗量过高、焙烧时间掌握不准以及除铁率难以达到期望值的问题,以CaCl_(2)作为氯化剂对煤矸石进行氯化焙烧除铁,在焙烧温度分别为600℃,700℃,800℃,900℃,1000℃,CaCl_(2)添加量(质量分数)分别为5%,10%,15%,20%,25%,焙烧时间分别为90 min,120 min,150 min,180 min,210 min的单因素实验基础上,通过Design-Expert13.0.6软件设计和优化了煤矸石氯化焙烧除铁实验。通过方差分析、等高线分析、响应面分析证明了模型的可靠并分析了各变量之间的交互影响关系。运用响应面优化法以除铁率为指标优化了工艺参数。结果表明:焙烧温度与焙烧时间交互最为显著,CaCl_(2)添加量与焙烧时间交互最低。各影响因子按影响显著性由大到小依次为焙烧温度、CaCl_(2)添加量、焙烧时间;随着焙烧温度升高除铁率进一步提升,由于焙烧温度超过1000℃后产物会转为莫来石,因此控制焙烧温度不超过950℃,当CaCl_(2)添加量达到15%时除铁率最好,超过这一添加量会降低除铁率,焙烧时间达到180 min时除铁率基本上达到了最高值,继续延长焙烧时间对除铁率的影响不大;对响应面模型预测并优化后得到了最佳的工艺条件,即焙烧温度为915℃,CaCl_(2)添加量为15%,焙烧时间为175 min,在此条件下除铁率达到了95.23%,实验值与预测值基本一致。

两种UHMWPE/Kaolin复合材料在干摩擦条件下的滑动摩擦磨损性能研究

在 MM- 2 0 0型磨损试验机上分别对以釜内聚合和熔融机械混合方法制备的高岭土填充超高分子量聚乙烯基复合材料 (UHMWPE/ Kaolin)在干摩擦条件下与 45 #钢对摩时的摩擦磨损性能进行了研究 ,并用扫描电子显微镜和立体光学显微镜对其磨损表面进行了观察与分析 ,对材料的磨损机理进行了探讨 .结果表明 :引入适量的高岭土能明显降低 UHMWPE的摩擦系数和磨损率 ,用釜内聚合方法制备的 UHMWPE/ Kaolin复合材料的摩擦系数和磨损率比用机械混合方法制备的同样成分的复合材料的都低 ;2种复合材料均能在偶件钢试环表面形成转移膜 ,从而使复合材料的摩擦系数和磨损率比纯 UHMWPE的均有所降低 .但二者的转移膜特性存在差异 ,这也是 2种复合材料的摩擦磨损性能产生差异的原因之一 ;而聚合型和混合型 UHMWPE/

m-HDPE/Kaolin复合材料流变性质研究

对比研究了采用聚合填充法(Polymerization-filling)和熔融共混法(meltcompounding)制备的m-HDPE/Kaolin复合材料的流变性质.动态流变实验和毛细管挤出实验的结果表明,聚合填充的HDPE/Kaolin复合体系的熔体动态粘度、复数粘度、表观粘度均低于熔融共混复合体系和纯HDPE的相应值.聚合填充的Kaolin粒子与PE分子链的强相互作用及其良好的分散状态,是改善材料流变行为的原因所在.