一次盐水三氯化铁加入量实验

通过对一次盐水中三氯化铁加入量进行实验分析,得出三氯化铁最佳(最大)加入量为35.9 mg/L,过量的三氯化铁对絮凝过程起反作用,但量效关系影响缓慢。

高纯稀土镱配合物中痕量氧化钙及氧化铁的测定

采用标准加入法测定高纯稀土镱配合物中痕量的氧化钙和氧化铁,有效避免基体干扰。当钙元素分析谱线为393.366 nm和396.847 nm,铁元素分析谱线为259.940 nm和261.187 nm,硝酸酸度控制在5%,基体浓度为6 g/L时,高纯稀土镱配合物中痕量氧化钙和氧化铁的含量能准确测量。铝、镁、钠、硅、钾、锌、镍、铜、磷等元素对测定基本无干扰。该方法具有较好的精密度和准确度,CaO的相对标准偏差为4.29%,加标回收率在91.0%~105.5%之间;Fe_2O_3的相对标准偏差为5.88%,加标回收率在96.0%~104.0%之间。

普硅水泥在彩色混凝土中应用及颜料最优掺量研究

针对普通水泥混凝土外观色彩单调、灰暗,无法满足市场对混凝土装饰应用需求的缺点,研发性能优良的彩色混凝土。使用普硅水泥进行混凝土配制,观察确定混凝土着色,解决兰州白水泥短缺而无法配制高效彩色混凝土的问题,对彩色混凝土配合比进行优化,通过4种氧化铁掺量设计出着色好、抗压强度高及耐久性优良的彩色混凝土,确定了合理的颜料掺量范围。

Fe-Beta zeolite for selective catalytic reduction of NO_x with NH_3:Influence of Fe content

Fe doped Beta zeolite with different Fe contents were prepared by ion exchange by changing the volume or the concentration of a Fe salt solution. For a particular mass of Fe salt precursor, the concentration of the metal salt solution during ion exchange influenced the ion exchange capacity of Fe, and resulted in different activities of the Fe-Beta catalyst. Fe-Beta catalysts with the Fe contents of （2.6, 6.3 and 9） wt% were synthesized using different amounts of 0.02 mol/L Fe salt solution. These catalysts were studied by various characterization techniques and their NH3-SCR activities were evaluated. The Fe-Beta catalyst with the Fe content of 6.3 wt% exhibited the highest activity, with a temperature range of 202-616℃ where the NOx conversion was 〉 80%. The Fe content in Beta zeolite did not influence the structure of Beta zeolite and valence state of Fe. Compared with the Fe-Beta catalysts with low Fe content （2.6 wt%）, Fe-Beta catalysts with 6.3 wt% Fe content possessed more isolated Fe3. active sites which led to its higher NH3-SCR activity. A high capacity for NH3 and NO adsorption, and a high activity for NO oxidation also contributed to the high NH3-SCR activity of the Fe-Beta catalyst with 6.3 wt%. However, when the Fe content was further increased to 9.0 wt%, the amount of FexOy nanoparticles increased while the amount of isolated Fe3＋ active sites was unchanged, which promoted NH3 oxidation and decreased the NH3-SCR activity at high temperature.

冲天炉熔炼铸铁基础知识问答50题

作者编译了部分日本技工考工定级的有关冲天炉熔炼基础知识的教材,可作为铸造行业熔炼技工的基础理论教育、培训资料或考试的试题.

Influence of coal blending on mineral transformation at high temperatures

Transformation of mineral matter is important for coal utilization at high temperatures.This is especially true for blended coal.XRD and FTIR were employed together to study the transformation of mineral matter at high temperature in blended coals.It was found that the concentration of catalytic minerals, namely iron oxides, increases with an increasing ratio of Shenfu coal, which could improve coal gasification.The transformation characteristics of the minerals in blended coals are not exactly predictable from the blend ratio.This was proved by comparing the iron oxide content to the blending ratio.The results from FTIR are comparable with those from XRD.FTIR is an effective method for examining variation in mineral matter.

Effect of Ferric Chloride on the Properties of Biological Sludge in Co-precipitation Phosphorus Removal Process

This paper studied the effect of ferric chloride on waste sludge digestion,dewatering and sedimentation under the optimized doses in co-precipitation phosphorus removal process.The experimental results showed that the concentration of mixed liquid suspended solid(MLSS) was 2436 mg.L-1 and 2385 mg.L-1 in co-precipitation phosphorus removal process(CPR) and biological phosphorous removal process(BPR),respectively.The sludge reduction ratio for each process was 22.6% and 24.6% in aerobic digestion,and 27.6% and 29.9% in anaerobic digestion,respectively.Due to the addition of chemical to the end of aeration tank,the sludge content of CPR was slightly higher than that of BPR,but the sludge reduction rate for both processes had no distinct difference.The sludge volume index(SVI) and sludge specific resistance of BPR were 126 ml.g-1 and 11.7×1012 m.kg-1,respectively,while those of CPR were only 98 ml.g-1 and 7.1×1012 m.kg-1,indicating that CPR chemical could improve sludge settling and dewatering.

Optimum blending of iron ore from Choghart stockpiles by using goal programming

Iron and steel industry is an important sector of Iran's economy.Choghart iron ore mine is an important iron ore producer of Iran steel industry.Phosphorous contained in the iron ore concentrates of Choghart mine has a detrimental effect on the steel making process,whereby this causes cracks to form in the refractory lining of blast furnaces.In the past,about 1.43 Mt of low-grade and 4.53 Mt of high-phosphorous materials had been transported to low grade and high phosphorous stockpiles,respectively,for future beneficiation.As a result of the progressive depletion of high-grade ore and establishment of beneficiation plant in Choghart,exploitation of these two stockpiles in this mine became an important issue.In this work,a linear goal programming(GP) model was developed in order to determine the optimum iron ore blend in terms of quality from low grade and high phosphorous stockpiles of Choghart mine.The model was solved by the SOLVER V.9 program.Results show that feeding with acceptable quality(w(Fe)≥50% and w(P)≤1.2%,mass fraction) materials can be blended from stockpiles that satisfy the needs of the Choghart processing line.

Ni(OH)_(2)quantum dots as a stable cocatalyst modifiedα-Fe_(2)O_(3) for enhanced photoelectrochemical water-splitting

Depositing a cocatalyst has proven to be an important strategy for improving the photoelectrochemical(PEC)water-splitting efficiency of photoanodes.In this study,Ni(OH)2 quantum dots(Ni(OH)2 QDs)were deposited in situ onto anα-Fe_(2)O_(3)photoanode via a chelation-mediated hydrolysis method.The photocurrent density of the Ni(OH)2 QDs/α-Fe_(2)O_(3)photoanode reached 1.93 mA·cm^(−2)at 1.23 V vs.RHE,which is 3.5 times that ofα-Fe_(2)O_(3),and an onset potential with a negative shift of ca.100 mV was achieved.More importantly,the Ni(OH)2 QDs exhibited excellent stability in maintaining PEC water oxidation at a high current density,which is attributed to the ultra-small crystalline size,allowing for the rapid acceptance of holes fromα-Fe_(2)O_(3)to Ni(OH)_(2)QDs,formation of active sites for water oxidation,and hole transfer from the active sites to water molecules.Further(photo)electrochemical analysis suggests that Ni(OH)_(2)QDs not only provide maximal active sites for water oxidation but also suppress charge recombination by passivating the surface states ofα-Fe_(2)O_(3),thereby significantly enhancing the water oxidation kinetics over theα-Fe_(2)O_(3)surface.

A Kinetic Spectrophotometric Method for the Determination of Iron (Ⅲ) in Water Samples

A new kinetic spectrophotometric method has been developed for the determination of iron （Ⅲ）. The method is based on the catalytic effect of iron （Ⅲ） on the oxidation of weak acid brilliant blue dye （RAWL） by KIO4 in acid medium. The advantages of the proposed method are that it is sensitive, accurate, rapid, inexpensive, can be operated under room temperature and has a large determination concentration range compared to other techniques. The obtained optimum conditions are： pH 3.15, RAWL （200 mgL^-1） 5.00mL, Potassium periodate solution （0.01 molL^-1） 0.30mL, phenanthroline （0.02 molL^-1） 1.00mL, reaction temperature 25℃ and reaction time 7 min. With this method iron could quantitively be determined in the range 0.00-0.02 mgL^-1, the detection limit being 4.10 × 10^10gmL^-1. The relative standard deviations （RSD） in five replicate determinations for 3 μgL^-1and 5 μgL^-1 iron （Ⅲ） are 3.1% and 1.9%, respectively. The method has been applied to the determination of iron （Ⅲ） in tap water samples and seawater samples （from the South China Sea）, the recovery rates being 98.0% and 100.5%, respectively.

Microwave-assisted hydroxylation of benzene to phenol with H_2O_2 over FeSO_4/SiO_2

Hydroxyl radicals HO are generated under Fenton-like (Fe2++H2O2→HO?+OH?+Fe3+) catalytic conditions upon microwave irradiation. Liquid-phase direct catalytic oxidation of benzene to phenol was obtained using FeSO4 supported on silica gel as a solid catalyst and hydrogen peroxide as the oxidant. The effects of various parameters, such as the different solvents, the amount of solvent used, the amount of catalyst used, the reaction time, the reaction temperature and the amount of hydrogen peroxide used on the yield of phenol were studied to identify optimum reaction conditions. Conventionally heated reaction gives a phenol yield of 0.6%. A higher phenol yield of 13.9% with a selectivity of 100% is obtained when the reaction mixture was irradiated with micro-wave energy. It is concluded that microwave irradiation offers more effective control of energy input for hydroxyl radical generation that is appropriate for various synthetic reactions.

Fe-TiO_2 and Fe_2O_3 quantum dots co-loaded on MCM-41 for removing aqueous rose bengal by combined adsorption/photocatalysis

Adsorption and photodegradation are promising approaches for removing organic pollutions.In this study,we combined these two processes by co-loading Fe-TiO2 and Fe2O3 quantum dots(QDs)on porous MCM-41,using a simple hydrolysis method.X-ray diffraction,high-resolution transmission electron microscopy,and X-ray photoelectron spectroscopy results indicated that Fe-TiO2 QDs are formed at low Fe precursor concentrations,while additional Fe2O3 QDs are formed at higher Fe precursor concentrations.The Fe2O3 and Fe-TiO2 QDs impart high adsorption capacity and high photoactivity to the porous MCM-41,respectively.Thus,their combination results in a synergic effect of the adsorption and photodegradation.The highest-performing sample exhibits excellent performance in removing rose bengal from aqueous solution.

Effect of reductant sodium bentonite content and reaction temperature in sponge iron production from composite pellets

In recent years,composite pellet production with added reductant has been developed instead of traditional iron production.Composite pellets produced by the addition of appropriate proportions of reductant produce sponge iron in the reductant melting process at high temperatures.The elements created in the structure by pellet production directly affect the quality of the product obtained by determining the chemical composition and the appropriate reaction temperature.In this study,sponge iron ore concentrate(scale)and reductant(coke coal dust and sodium bentonite)were mixed at certain proportions to produce composite pellet samples;the effects of addition rate of the reductant material of sodium bentonite(1 wt%−4 wt%)and variation in reaction temperature(900−1200℃)on the metallization and compressive strength properties of the produced composite pellet samples were investigated.The analysis results show that the highest compressive strength is obtained from pellet samples produced with 3%sodium bentonite at 1100℃.Additionally,SEM-EDS analysis results of the samples show that the morphologic structure has much lower porosity rates compared to samples produced under the other conditions which makes the samples denser and increases the metallization properties.

Effective Pyroelectric Coefficient and Polarization Offset of Compositionally Step-like Graded Ferroelectric Structures

In this paper, the effective pyroelectric coefficient and polarization offset of the compositionally step-like graded multilayer ferroelectric structures have been studied by use of the first-principles approach. It is exhibited that the dielectric gradient has a nontrivial influence on the effective pyroelectric coefficient, but has a little influence on the polarization offset; and the polarization gradient plays an important role in the abnormal hysteresis loop phenomenon of the co.mpositionally step-like graded ferroelectric structures. Moreover, the origin of the polarization offset is explored,which can be attributed to the polarization gradient in the compositionally step-like graded structure.

Energy Saving and Emission Reduction Estimations of Electrified Railways in China

Based on the annual production data collected by the Statistic Center of the Ministry of Railways of the People＇s Republic of China, we calculated the energy saving and direct emission reductions of CO2, soot, SO2, CO, NOx and CnHm of electrified railways, and analyzed their dynamic characteristics during the period of 1975 2007. The results show that during this period, the annual mean values of energy saving is 1.23×10^6 tce, and direct emission reduction of CO2, soot, SO2, CO, NOx and CnHm are 4.267×10^6 t, 20.5×10^3 t, 3.0×10^3 t, 9.6×10^3 t, 67.9×10^3 t, and 6.9×10^3 t per year, respectively. The annual average increasing rates of energy saving is 139×10^3 tce, and direct emission reduction of CO2, soot, SO2, CO, NOx and CnHm are 483×10^3 t, 2.3×10^3 t, 0.34×10^3 t, 1.1×10^3 t, 7.7 ×10^3 t and 0.78×10^3 t per year, respectively. The electrified railways have played an important role in decreasing the energy consumption and air pollutant emissions of China＇s railway system. The results of this study could provide some reference knowledge for future reductions of energy consumption and waste gas emission in China＇s railway transportation.

Synthesis of light hydrocarbons over Fe/AC catalysts

A series of Fe/AC catalysts for catalytic hydrogenation of CO to light hydrocarbons(LHCs) were prepared by decomposing Fe(CO)5 in an autoclave.The catalysts activities were tested in a high-pressure micro reactor.The results show that both CO conversion and LHCs selectivity were significantly affected by the amount of Fe loaded onto the catalysts.The optimum Fe content was determined to be 10% by weight of the catalyst.Over the corresponding catalyst(i.e.,10% Fe/C catalyst),the conversion of CO and the selectivity of LHCs were 94.8% and 59.2%,respectively,at 360 °C.Based on various catalyst characterization techniques,such as XRD,BET and SEM,the catalysts surface areas and pore volume decreased and the smaller particles agglomerated at the edges and corners in the outer region of the support with the increasing Fe content.The agglomerated particles increased greatly when the iron content of the catalyst was higher than 10%.The decrease of catalyst activity can be due to the agglomerated particles.

Nonalcoholic steatohepatitis in Asian Indians is neither associated with iron overload nor with HFE gene mutations

AIM: The pathogenesis of occurrence of liver inflammation and fibrosis in patients with nonalcoholic steatohepatitis (NASH) is not completely understood. Other than insulin resistance, iron abnormalities have been thought to be one of the triggering factors. Therefore, our aim was to study the role of iron abnormalities and HFE gene mutations in patients with NASH. METHODS: Thirty-one patients of NASH diagnosed on the basis of clinical examination biochemistry, ultrasonography and liver biopsy (n = 14) were included in the study. Serum iron parameters (n = 23) (iron, ferritin, total iron-binding capacity and transferrin saturation), Perls' iron staining on liver biopsies (n = 14) and HFE gene mutations (C282Y and H63D) (n = 16) were studied in these patients. The association between iron staining, necroinflammatory activity and fibrosis stage on liver biopsies was also determined. RESULTS: Elevated serum iron, ferritin and transferrin saturation above 55% were observed in 4.3% of patients. On histology, 71% of the patients had negative iron staining, 21.4% had 1+ staining, 7.2% had 2+ staining and none had 3+ or 4+ staining. There was no association between the degree of iron staining and necroinflammatory activity (P=0.55) and fibrosis stage (P= 0.09) on histology. None of the patients had C282Y HFE gene mutation and four patients (25%) were found to be heterozygotes for H63D gene mutation. CONCLUSION: Our study does not favor iron overload and HFE gene mutations as major factors in the pathogenesis of NASH in Asian Indians.

A Modified Method for Measuring Root Iron Reductase Activity Under Normal Laboratory Conditions

Based on the strong chelating property of bathophenanthroline disulfonic acid (BPDS) with root chelate reductase activity is usually measured with a spectrophotometer using MES (2-morpholinoethanesulfonic acid) or HEPES (2-(4-(2-Hydroxyethyl)-1-piperazinyl) ethanesulfonic acid) buffer in the dark because of high autoreduction rate of in the presence of light. However, the exclusion of light is inconvenient, especially when analyzing a large number of samples. The objective of this study was to develop a new method for determination of root reductase activity under normal laboratory conditions using a suitable buffer composition and concentration to eliminate the autoreduction of A modified method using a Tris (2-amino-2-hydroxymethyl-1,3-propanediol) buffer at pH 7.5 instead of MES or HEPES buffer and a decreased FeEDTA (Fe ethylene diamine tetraacetic acid) concentration of 50 μmol L-1 was developed. The autoreduction of using the Tris buffer was undetectable for temperatures at 4 and 28 °C and was also much lower than that using the other buffers even with sunlight during measurement of reduction. Furthermore, the differences in reductase activity among 5 plant species and 14 red clover cultivars (Trifolium pratense L.) could be easily detected with the modified method. The method developed in this study to measure root Fe chelate reductase activity was not only effective and reliable but also easily managed under normal laboratory light conditions.

Contribution of Iron and Aluminum Oxides to Electrokinetic Characteristics of Variable Charge Soils in Relation to Surface Charge

The contribution of iron and aluminum oxides to electrokinetic characteristics of variable charge soils was studied through determination of electrophoretic mobilities of the red soils treated with either removal of iron oxides or coating of aluminum oxides, and of those deferrated under natural conditions. After removal of the iron oxides, zeta potentials of the latosol and the red earth decreased obviously with a shift of IEP to a lower pH, from 6.4 to 5.3 and 4.1 to 2.4 for the former and the latter, respectively, and the electrokinetic change for the latosol was greater than for the red earth. Zeta potentials of the kaolinite sample increased markedly after coated with iron oxides. The striking effect of iron oxides on electrokinetic properties of the soils was also demonstrated by the electrokinetic differences between the samples from the red and white zones of a plinthitic horizon formed naturally, and between the samples from the gley and bottom horizons of a paddy soil derived from a red earth. The coatings of aluminum oxides on the latosol and the yellow earth made their zeta potentials rise pronouncedly and their IEPs move toward higher pHs, from 6.2 to 6.8 and 4.3 to 5.3 for the former and the latter, respectively. The samples with different particle sizes also exhibited some electrokinetic variation. The experiment showed that the effects of iron and aluminum oxides were closely related to the pH and type of the soils.

Influence of sulfur content in raw materials on oxidized pellets

The influence of sulfur content in raw materials on oxidized pellets was studied. The results show that most sulfur exists in the form of elementary sulfur in pyrite cinder, and over 95% sulfur is removed in producing pyrite cinder oxidized pellets. The compressive strength of fired pellets drops from 3 186 N to 2 405 N when the ratio of pyrite cinder increases from 40% to 70% under the conditions of preheating at 900℃ for 9 min and firing at 1 230 ℃ for 15 min. The porosity and microstructures of fired pellets prove that the higher ratio of pyrite cinder is given, and the more holes and cracks are achieved, leading to the better reducibility index （RI） and reduction swelling index （RSI）, and the lower compressive strength of fired pellets and the worse reduction degradation index （RDI）.