Ash removal from inferior coal via ammonium fluoride roasting and simultaneous yield of white carbon black

The quality upgrading and deashing of inferior coal by chemical method still faces great challenges.The dangers of strong acid,strong alkali,waste water and exhaust gas as well as high cost limit its industrial production.This paper systematically investigates the ash reduction and desilicification of two typical inferior coal utilizing ammonium fluoride roasting method.Under the optimal conditions,for fat coal and gas coal,the deashing rates are 69.02%and 54.13%,and the desilicification rates are 92.64%and 90.27%,respectively.The molar dosage of ammonium fluoride remains consistent for both coals;however,the gas coal,characterized by a lower ash and silica content(less than half that of the fat coal),achieves optimum deashing effect at a reduced time and temperature.The majority of silicon in coal transforms into gaseous ammonium fluorosilicate,subsequently preparing nanoscale amorphous silica with a purity of 99.90%through ammonia precipitation.Most of the fluorine in deashed coal are assigned in inorganic minerals,suggesting the possibility of further fluorine and ash removal via flotation.This research provides a green and facile route to deash inferior coal and produce nano-scale white carbon black simultaneously.

Molybdenite-limestone oxidizing roasting followed by calcine leaching with ammonium carbonate solution

Oxidizing roasting of molybdenite with lime can significantly reduce SO2pollution compared with the traditional roastingwithout lime.However,the calcine is subsequently leached by sulfuric acid,resulting in serious equipment corrosion and abundantnon-recyclable CaSO4slag.In this work,a novel process,in which the molybdenite was roasted with CaCO3followed by(NH4)2CO3solution leaching,was proposed to improve the art of lime roasting-sulfuric acid leaching.Oxidizing roasting of molybdenite withCaCO3was investigated through thermodynamic calculation,thermogravimetric analysis and roasting experiments.The results showthat the products of the oxidizing reaction of MoS2in the presence of CaCO3and O2are CaSO4,CaMoO4and CO2at573-1000K.The MoS2conversion rate achieves approximately99%and the sulfur-retained rate attains approximately95%with aCaCO3-to-MoS2molar ratio of3.6at500°C for1h by adding5%mineralizer A(mass fraction).The leaching results show that theleaching rate of Mo reaches98.2%at85°C for7h with a(NH4)2CO3concentration of600g/L and a liquid-solid ratio of10mL/g.The results presented are potential to develop a novel cleaner technique for ammonium molybdate production.

Direct synthesis of propylene carbonate from propylene and carbon dioxide catalyzed by quaternary ammonium heteropolyphosphatotungstate–TBAB system

In this paper,we have developed a highly efficient method for the direct preparation of propylene carbonate from propylene and carbon dioxide（CO2） using quaternary ammonium heteropolyphosphatotungstate–quaternary ammonium halide catalytic system with anhydrous hydrogen peroxide as an oxidant through one-pot two-step process.The effects of the amount of tetrabutylammonium bromide（TBAB）,the concentration of hydrogen peroxide and other reaction conditions were investigated.The catalyst system gave an optimum propylene oxide yield（91%） at75°C in oxidation step and the highest propylene carbonate yield（99%） at 140°C and 3.0 MPa in cycloaddition step.Based on the results,a reaction mechanism has been proposed.

Dimethyl carbonate synthesis via transesterification catalyzed by quaternary ammonium salt functionalized chitosan

A quaternary ammonium salt covalently linked to chitosan was first used as a catalyst for dimethyl carbonate （DMC） synthesis by the transesterification of propylene carbonate （PC） with methanol. The effects of various reaction variables like reaction time, temperature and pressure on the catalytic performance were also investigated. 54% DMC yield and 71% PC conversion were obtained under the optimal reaction conditions. Notably, the catalyst was able to be reused with retention of high catalytic activity and selectivity. Consequently, the process presented here has great potential for industrial application due to its advantages such as stability, easy preparation from renewable biopolymer, and simple separation from products.

Effect of Electrochemical Treatment in Aqueous Ammonium Bicarbonate on Surface Properties of PAN-based Carbon Fibers

The surface properties of PAN-based carbon fibers electrochemically treated in aqueous ammonium bicarbonate before and after treatment were characterized by X-ray photoelectron spectroscopy (XPS), atomic force microscopy (AFM) and Dynamic Contact Angle Analysis (DCAA). The results of characterization indicated that the oxygen and nitrogen contents in carbon fiber surface were significantly increased by electrochemical treatment, and amide groups was introduced onto it, which was related with the electrolyte. The AFM photographs illustrated that the roughness of the fiber surface was also increased. The wettibality of the fibers was improved after treatment because the surface energy especially the polar part of it was increased.

Preparation of ultrafine α-Al_2O_3 powders by catalytic sintering of ammonium aluminum carbonate hydroxide at low temperature

The precursor of ammonium aluminum carbonate hydroxide was synthesized by using aluminum sulfate（Al2（SO4）3） and ammonium carbonate（（NH4）2CO3）. The effects of α-Al2O3 seeds and mixture composed of α-Al2O3 and ammonium nitrate, as well as multiplex catalysts （AT） on phase transformation of alumina in sintering process were investigated respectively. The results show that the α-Al2O3 seeds and the mixture of α-Al2O3 and ammonium nitrate can lower the phase transformation temperature of α-Al2O3 to different extents while the particles obtained agglomerate heavily. AT has great potential synergistic effects on the phase transformation of alumina and reduces the phase transformation temperature of α-Al2O3 and the trends of necking-formation between particles. Therefore the dispersion of powder particles is improved significantly.

Furfural residues derived nitrogen-sulfur co-doped sheet-like carbon: An excellent electrode for dual carbon lithium-ion capacitors

The state-of-the-art lithium-ion capacitors (LICs),consisting of high-capacity battery-type anode and high-rate capacitor-type cathode,can deliver high energy density and large power density when comparing with traditional supercapacitors and lithium-ion batteries,respectively.However,the ion kinetics mismatch between cathode and anode leads to unsatisfied cycling lifetime and anode degradation.Tremendous efforts have been devoted to solving the abovementioned issue.One promising strategy is altering high conductive hard carbon anode with excellent structural stability to match with activated carbon cathode,assembling dual-carbon LIC.In this contribution,one-pot in-situ expansion and heteroatom doping strategy was adopted to prepare sheet-like hard carbon,while activated carbon was obtained involving activation.Ammonium persulfate was used as expanding and doping agent simultaneously.While furfural residues (FR) were served as carbon precursor.The resulting hard carbon (FRNS-HC) and activated carbon (FRNS-AC)show excellent electrochemical performance as negative and positive electrodes in a lithium-ion battery (LIB).To be specific,374.2 m Ah g^(-1)and 123.1 m Ah g^(-1)can be achieved at 0.1 A g^(-1)and 5 A g^(-1)when FRNS-HC was tested as anode.When combined with a highly porous carbon cathode (S_(BET)=2961 m^(2)g^(-1)) synthesized from the same precursor,the LIC showed high specific energy of147.67 Wh kg^(-1)at approximately 199.93 W kg^(-1),and outstanding cycling life with negligible capacitance fading over 1000 cycles.This study could lead the way for the development of heteroatom-doped porous carbon nanomaterials applied to Li-based energy storage applications.

Green and Effective Ammonium Carbonate-assisted Process for Drying Hemicellulose Obtained through Alkali Extraction of Bleached Bamboo Kraft Pulp

Hemicellulose has a wide range of applications,including that as an emulsifier for the food industry and raw material for the synthesis of bioethanol/biochemicals and biodegradable films.Hemicellulose is usually present as a spent liquor,such as the prehydrolysis liquor of the prehydrolysis kraft dissolving pulp production process and the alkali extraction liquor of the cold caustic extraction of pulp fibers.Due to its dilute nature,hemicellulose needs to be dried for practical utilization,and this is challenging.In this study,cellulose and hemicellulose in a bleached bamboo kraft pulp were separated using an alkali extraction process.Hemicellulose obtained from the extraction liquor was dried by an ammonium carbonate-assisted drying process.The effects of drying time and drying temperature were determined.Structure of the hemicellulose obtained by the ammonium carbonate-assisted drying process was similar to that of original hemicellulose,as revealed by detailed Fourier transform infrared and X-ray diffraction analyses.The novel drying method was more energy efficient and required a shorter drying time than the conventional freeze drying method,and the excellent solubility in alkaline solutions favored the chemical modification of hemicellulose.The dried hemicellulose can be used as a renewable raw material for the preparation of hydrogels and other substances such as bioethanol/biochemicals and biodegradable films.

Formation Process of Crystalline Ammonium Yttrium Carbonate Double Salt

The research was mainly based on the formation condition of crystalline ammoniu yttrium carbonate and the variation characteristics of PH value during the crystallization in which NH4HCO3 was used to precipitate yttrium ion. It is found that the crystallization process is always associated with the descent of pH. The pH of solution is controlled by the crystallization reaction of ammonium yttrium carbonate and the hydrolysis of NH4HCO3. Based on the pH variation, it can be judged whether the crystallization reaction occurs or not and the speed and the degree of crystallinity can be deterolfned. The precipitates were characterized by X- ray powder diffraction and differential thermal -thermogravimetric analysis. The results show that the crystallization is the process of NH4Y(CO3)2 formation and it is effected by feed ratio and feed method.

Solvent Extraction of Nickel and Cobalt from Ammonia-Ammonium Carbonate Solution by Using LIX 84-ICNS

In the present paper, separation of nickel and cobalt in ammonia-ammonium carbonate solution that simulates pregnant leach solution of Caron Process by solvent extraction using LIX 84-ICNS was studied. LIX 84-ICNS is a novel extractant which is still being studied, especially for nickel and cobalt separation in ammonia-ammonium carbonate solution. A series of solvent extraction tests were performed at various equilibrium pH, temperature, extractant concentration, and volume ratio of organic to aqueous solution (O/A ratio). The investigation results show that the highest nickel and cobalt extraction percentages of 99.8% and 90.3% were obtained from the extraction test at equilibrium pH of 8.75, temperature of 55°C, extractant concentration of 40% (v/v) and O/A ratio of 1/1, respectively. Oxidation of cobalt in aqueous solution prior to extraction is needed to minimize co-extraction of cobalt. Co-extracted cobalt can be decreased from 90.3% to 30.3% by mixing 1% (v/v) H2O22 in aqueous solution prior to the extraction stage. It was found that nickel and cobalt extractions by LIX 84-ICNS are endothermic processes with enthalpy changes of +171.03 and +7.64 kJ/mole, respectively. Based on constructed McCabe-Thiele Diagram, nickel extraction level of more than 99.9% can be obtained in 2 stages at O/A ratio of 0.5. The highest stripping percentages of nickel and cobalt of 98.82% and 3.16% respectively were obtained at 200 g/l H2SO4 stripping agent.

Binding tendency with oligonucleotides and cell toxicity of cetyltrimethyl ammonium bromide-coated single-walled carbon nanotubes

Functionalized carbon nanotubes （CNTs） were made for the delivery of genes and drugs and CNT-based biosensors. The basis of CNTs is for binding with biomolecules in biomedical applications. The binding tendency with small interfering RNA oligonucleotides and cytotoxicity of cetyltrimethyl ammonium bromide （CTAB）-coated single-walled carbon nanotubes （SWNTs） were studied. The field emission scanning electron microscopy and transmission electron microscopy results show that a SWNT suspension in CTAB solution was well-dispersed and stable. CTAB is the cross-linker between SWNTs and oligonucleotides. The CTAB-coated SWNTs have less cytotoxicity to human umbilical vein endothelial cells than single SWNTs and the cytotoxicity of CTAB-coated SWNTs depended on the concentration of CTAB-coated SWNTs.

Effect of inorganic carbon on anaerobic ammonium oxidation enriched in sequencing batch reactor

The present lab-scale research reveals the enrichment of anaerobic ammonium oxidation microorganism from methanogenic anaerobic granular sludge and the effect of inorganic carbon(sodium bicarbonate)on anaerobic ammonium oxidation.The enrichment of anammox bacteria was carried out in a 7.0-L sequencing batch reactor(SBR)and the effect of bicarbonate on anammox was conducted in a 3.0-L SBR.Research results,especially the biomass,showed first signs of anammox activity after 54 d cultivation with synthetic wast...

Cytotoxicity effect assessment of acid purified carbon nanotubes modified with cetyltrimethyl ammonium bromide

The cytotoxicities of single-walled carbon nanotubes （SWNTs） and acid purified single-walled carbon nanotubes （SWNT-COOH） were investigated by spectroscopic analysis. Cell viability and cell apoptosis were applied to assessing the cytotoxicity of SWNT-COOH, cetyltrimethyl ammonium bromide （CTAB） and acid purified carbon nanotubes modified with cetyltrimethyl ammonium bromide （SWNT-COOH/CTAB）. The results indicate that SWNTs are more toxic than SWNT-COOH. Concentration and time-curve analyses indicate that cytotoxicity of SWNT-COOH/CTAB is more related to the toxicity of the surfactant CTAB. The cytotoxicity effect of CTAB and SWNT-COOH/CTAB is acceptable at low concentrations （0.5-25μg/mL）. The cytotoxicity observation suggests that SWNT-COOH/CTAB can safely applied to biomedical field at low concentrations （0.5-25μg/mL）.

Preparation of spherical cobalt carbonate from cobalt sulfate solution

A precursor of cobaltous dihydroxycarbonate was firstly prepared by precipitation reaction of cobalt sulfate solution and ammonium carbonate solution,and then a hydrothermal process for the precursor was conducted to obtain the spherical cobalt carbonate with low sulfur content.The experimental results show that the feeding method,final p H value of the precipitation reaction slurry and the concentration of the cobalt sulfate solution have obvious effects on the sulfur content,morphology and particle size distribution of the precursor.The sulfur content of the precursor is 0.0115 wt.%under the optimized conditions.The hydrothermal treatment with temperatures of 125-150℃can transform the precursor of cobaltous dihydroxycarbonate into spherical cobalt carbonate and decrease the sulfur content to 0.0030 wt.%in the obtained product.

Effects of soil nitrate:ammonium ratio on plant carbon:nitrogen ratio and growth rate of Artemisia sphaerocephala seedlings

Can soil nitrate： ammonium ratios influence plant carbon： nitrogen ratios of the early succession plant？ Can plant carbon： nitrogen ratios limit the plant growth in early succession？ To address these two questions, we performed a two-factor （soil nitrate： ammonium ratio and plant density） randomized block design and a uniform-precision rotatable central composite design pot experiments to examine the relationships between soil nitrate： ammonium ratios, the carbon： nitrogen ratios and growth rate of Artemisia sphaerocephala seedlings. Under adequate nutrient status, both soil nitrate： ammonium ratios and plant density influenced the carbon： nitrogen ratios and growth rate of A. sphaerocephala seedlings. Under the lower soil nitrate： ammonium ratios, with the increase of soil nitrate： ammonium ratios, the growth rates of plant height and shoot biomass of A. sphaerocephala seedlings decreased significantly; with the increase of plant carbon： nitrogen ratios, the growth rates of shoot biomass of A. sphaerocephala seedlings decreased significantly. Soil nitrate： ammonium ratios affected the carbon： nitrogen ratios of A. sphaerocephala seedlings by plant nitrogen but not by plant carbon. Thus, soil nitrate： ammonium ratios influenced the carbon： nitrogen ratios of A. sphaerocephala seedlings, and hence influenced its growth rates. Our results suggest that under adequate nutrient environment, soil nitrate： ammonium ratios can be a limiting factor for the growth of the early succession plant.

Preparation of Mesoporous ZSM-5 Zeolite under Double Ester Base Long Carbon Chains Organosilane Quaternary Ammonium Salt Template Agent

The pore sizes of traditional zeolites are in the range of0. 3-1. 5 nm,which strongly hinder the diffusion of large reactant and product molecules within the zeolite pores. To compensate for it,we tried to create mesopores in traditional microporous zeolites and retain all advantages of microporous zeolites. Mesoporous Zeolite Socony Mobile-Five( ZSM-5) zeolite was synthesized by a new double ester base long carbon chains organosilane quaternary ammonium salt as the soft template agent in hydrothermal method.The structure of the acquired zeolite crystals was confirmed by fieldemission scanning electron microscopy( FE-SEM), transmission electron microscopy( TEM), nitrogen adsorption-desorption measurements and X-ray diffraction( XRD),which indicated that their structure had the same characteristics as traditional ZSM-5 zeolites. Compared with traditional ZSM-5 zeolite,there were 4 nm and 15 nm mesopores in the crystal. The prepared hierarchical porous ZSM-5 zeolite was expected to be effective catalytic materials for chemical reactions involving large molecules.

燃煤电厂氨法碳捕集浆液中捕集产物结晶行为研究

以燃煤电厂碳排放为背景,利用氨水吸收二氧化碳的结晶过程作为研究对象,基于经典的成核理论,采用温度、pH和电导率法研究了改变温度、搅拌转速、添加盐类添加剂前后碳酸氢铵结晶速率的变化,并通过扫描电镜(SEM)和X射线衍射(XRD)分析了有无添加剂对生成碳酸氢铵结晶的影响。结果表明:在水浴温度为25℃,搅拌转速为550 r/min的条件下,碳酸氢铵的结晶反应受到添加剂种类的影响,加入硫酸根离子会减缓反应的进行,加入氯化镁可以加快结晶的产生速率,并产生结构稳定的晶体。

γ-Al_(2)O_(3)载体的水热合成及其加氢性能

以ρ-Al_(2)O_(3)和NH4HCO3为原料,采用水热法合成出γ-Al_(2)O_(3)的前驱体碳酸铝铵(AACH),考察了原料配比和反应时间对合成产物的影响,利用X射线衍射仪、物理吸附分析仪、化学吸附仪对2种不同前驱体制得的载体进行表征,并对2种载体制得的催化剂进行了加氢脱硫脱氮性能评价。结果表明:在n(HCO_(3)^(-))/n(Al^(3+))为1.5∶1.0,100℃反应14 h下制得具有棒状结构、结晶度较好的AACH;相比由传统拟薄水铝石制得的载体,由AACH制得的载体具有较高比表面积和大孔容,有效孔径(4~10 nm)的孔容占比更高,且利于反应进行的中强酸更多,且所制备催化剂的脱硫脱氮活性更佳。

二氧化碳中和钨酸铵溶液制备细颗粒仲钨酸铵

采用二氧化碳中和钨酸铵溶液结晶制备细颗粒仲钨酸铵(APT),考察时间、温度、二氧化碳流量、钨酸铵溶液中三氧化钨质量浓度、氯化铵质量浓度和转速等因素对APT结晶的影响。研究结果表明:在一定范围内,增大二氧化碳流量、提高氯离子质量浓度和三氧化钨质量浓度有利于制备细颗粒APT;转速对APT粒度影响较小;延长结晶时间和提高反应温度,APT粒度会变大,不利于制备细颗粒APT。当反应时间为20 min、温度为90℃、二氧化碳流量为5 L/min、钨酸铵溶液中三氧化钨质量浓度为200 g/L、氯化铵质量浓度为62 g/L、转速为200 r/min时,该工艺制备的APT费氏(Fsss)粒度为15.5μm、粒度分布窄,其D(90)-D(10)/2D(50)为0.66且形貌完整。与工业上蒸发结晶工艺制备的APT相比,本工艺制备的APT粒度更小且粒度分布更窄,是制备超细钨粉和超细碳化钨粉的良好原料。

重晶石液相两次转化法制备碳酸钡新工艺

这是一篇冶金工程领域的论文。针对重晶石反应活性低、化学加工方法不多的局限,提出一种全新的纯碱转化法。首先探究了盐酸酸解法下重晶石反应粒度、温度、碳酸钠浓度对碳酸钡生成率的影响,结果表明:碳酸钠浓度对反应转化率的影响最大,在有限的实验条件下,当碳酸钠浓度达到28.57%时,碳酸钡的生成率最高达到90.05%。其次,在后续的反应中,选择氯化铵对重晶石转化产物进行再次转化制备碳酸铵,此法生产出的碳酸钡产率、纯度较高,作为重晶石与纯碱反应制备碳酸钡的新工艺,突破了传统硫酸钡不与纯碱反应的错误观念,本工艺操作流程简单可行,且氨气、二氧化碳可以回收循环利用,使整个工艺为一个大循环工艺,符合绿色环保理念,为重晶石制备碳酸钡提供了一种全新的生产工艺。