固氟氯化铵焙烧法从包头稀土矿中回收稀土的动力学

研究了固氟氯化铵焙烧法分解包头混合型稀土精矿回收稀土的动力学.结果表明:固氟焙砂的氯化反应过程符合Bagdasarym提出的区域反应速率模型,氯化反应过程经过了两个串联反应步骤,且反应生成物的核按一个方向长大;反应速率方程遵从Erofeev方程的串联反应步骤模型,反应表观活化能Ea为36.831 KJ·mol-1,过程控制步骤是内扩散控制.     

二元稀土系AB5型贮氢电极合金的放电容量与晶胞体积和4f电子浓度的关系

制备了6个系列通式为AαA‘1-αB5的RE(NiCoMnTi)5贮氢电极合金(其中，AαA‘1-α为La，Ce，Pr，Nd4个元素中任意2个的组合)，测定了它们在100次循环中的最大放电容量Cmax及部分合金的晶胞体积Vcell．结果表明：Cmax主要由Vcell决定，Cmax先随Vcell的增大而增加，在Vcell≈85．66x10^-^3。nm^3时达到一极大值，然后又随Vcell的增大而减小；同时，Cmax还与4f电子浓度ne4f／naRE有关，A侧具有相同4f电子浓度的合金其Cmax随4f电子浓度的变化趋势相似．     

稀土元素对硬质合金高温性能的影响

采用动态热模拟试验技术，研究了添加微量稀土元素对硬质含金高温性能的影响。试验结果表明：添加微量稀土元素，能改善硬质合金高温性能，增加合金的塑性和高温韧性，降低硬质合金的热强性。     

稀土元素对钯室温电学性能的影响

研究了稀浓度(0.6at％以下)稀土元素(La、Ce、Pr、Nd、Sm、Eu、Gd、Tb、Dy、Er、Yb)对钯的室温电学性能的影响。所有稀土元素均提高钯的电阻率(p)、降低电阻温度系数(α),实验结果与理论分析证明(p·α)_((?)d-RE)d=(p·α)_(Pd)。Gd以前的稀土元素降低钯的对铜热电势(ε),其余重稀土元素增大钯的对铜热电势。按0.1at％RE归一化处理的实验数据表明,轻稀土元素对钯电阻率的影响稍大于重稀土,但Ce、Eu、Yb呈反常影响,化合价和尺寸因素是影响电学性能的主要因素。     

Reaction process of monazite and bastnaesite mixed rare earth minerals calcined by CaO-NaCl-CaCl2

The decomposition reactions of monazite and bastnaesite mixed rare earth minerals calcined by CaO-NaCl-CaCl2 were studied by means of TG-DTA and XRD. The results show that the process of the minerals decomposed by CaO involves two steps. The first step occurs in the temperature range of 425-540 ℃, and the main reactions are bastnaesite decomposition, i.e. REOF reacts with CaO to produce RE2O3 and CaF2, and Ce2O3 is oxidized to CeO2. During this step, CaCO3 is formed at about 500 ℃. The second step takes place in the temperature range of 610-700 ℃, and the reactions are monazite decomposition into RE2O3, Ca5F（PO4）3 and Ca3（PO4）2 by CaO and CaF2. In this process, the decomposition ability is improved because CaO from CaCO3 decomposing has high chemical activity. In calcining process, the new formed Ca5F（PO4）3 restrains fluorine that can escape in form of gaseous compound. The decomposition ratio of the mixed rare earth minerals reaches 90.8% at 700 ℃.     

Photocatalytic syngas synthesis from CO2 and H2O using ultrafine CeO2-decorated layered double hydroxide nanosheets under visible-light up to 600 nm

The rational design of photocatalyst that can effectively reduce CO₂ under visible light(l>400 nm),and simultaneously precise control of the products syngas(CO/H2)ratio is highly desirable for the Fischer-Tropsch reaction.In this work,we synthesized a series of CeO₂-decorated layered double hydroxides(LDHs,Ce-x)samples for photocatalytic CO₂ reduction.It was found that the selectivity and productivity of CO and H₂ from photoreduction of CO₂ in conjunction with Ru-complex as photosensitizer performed an obvious“volcano-like”trend,with the highest point at Ce-0.15 and the CO/H₂ ratio can be widely tunable from 1/7.7 to 1/1.3.Furthermore,compared with LDH,Ce-0.15 also drove photocatalytic CO₂ to syngas under 600 nm irradiation.It implied that an optimum amount of CeO₂ modifying LDH promoted the photoreduction of CO₂ to syngas.This report gives the way to fully utilize the rare earth elements and provides a promising route to enhance the photo-response ability and charge injection efficiency of LDH-based photocatalysts in the synthesis of syngas with a tunable ratio under visible light irradiation.     

Sulfuric acid recovery from rare earth sulphate solutions by diffusion dialysis

1 Introduction As an important industrial chemical, sulfuric acids are widely used in metallurgical and chemical processes, in which some waste solutions containing free sulfuric acids and metallic ions are therefore produced[1, 2]. If these waste acids …     

Nanocomposites of CsPbBr3 perovskite quantum dots embedded in Gd2O3:Eu3+ hollow spheres for LEDs application

Gd₂O₃:Eu³⁺@CsPbBr₃ quantum dots (QDs) mesoporous hollow nanocomposites with good luminescent properties and high stability were built. Among which, the hollow Gd₂O₃:Eu³⁺ spheres and CsPbBr₃ QDs were prepared by urea homogeneous precipitation and hot-injection method, respectively. Finally, the Gd₂O₃:Eu³⁺@CsPbBr₃ QDs shell–core compounds were constructed through mechanical stirring. The structure, morphology, stability and luminescent properties were studied by Fourier transform infrared spectroscopy (FT-IR), differential scanning calorimetry/thermogravity (DSC/TG), X-ray diffraction (XRD), field-emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM), photoluminescence excitation/photoluminescence (PLE/PL) and life decay tools. Compared to the original CsPbBr₃ QDs, Gd₂O₃:Eu³⁺@CsPbBr₃ QDs display better photostability, thermal stability and current stability. The resulting Gd₂O₃:Eu³⁺@CsPbBr₃ QDs composite exhibits good yellow emission. The Gd₂O₃:Eu³⁺@CsPbBr₃ QDs mixed silicone resin was directly coated on the blue LED chip, then the w-LED device with the color coordinate of (0.31, 0.32) was successfully assembled. The Gd₂O₃:Eu³⁺@CsPbBr₃ QDs compounds with excellent luminescent properties and stability are expected to be widely used in lighting and display areas.     

Ce对440C不锈轴承钢夹杂物演变的影响

为探究稀土Ce对440C不锈轴承钢中夹杂物的改性作用,利用实验室MoSi₂电阻炉对440C不锈轴承钢进行稀土Ce处理,采用OM、SEM等系统分析了Ce的添加对440C不锈轴承钢脱氧及夹杂物演变的影响。结果表明,随着Ce加入量的增加,其收得率逐渐升高。Ce的加入使钢中TO质量分数由0.002 5%降低至0.001 2%。未加入Ce的钢中夹杂物主要为Al₂O₃、MnS以及镁铝尖晶石;加入质量分数为0.011 5%的Ce后,夹杂物被改性为以Ce-Al-O为主的夹杂物;当Ce的添加量达到0.036 4%时,夹杂物被完全改性为Ce-O-S夹杂物。适量的Ce可以降低夹杂物尺寸及面积比例,但过量加入会使夹杂物尺寸变大。在本试验条件下,当Ce质量分数为0.011 5%时,钢中夹杂物细小弥散效果最明显。以上结论可为Ce在高碳铬不锈轴承钢中的应用提供参考。     

耐腐蚀摩托艇ADC12-0.5La铝合金微观组织及制备

为改善ADC12铝合金的耐腐蚀性能,通过超声熔铸法制备ADC12-0.5La铝合金,并利用光学显微镜、扫描电镜、能谱分析仪、硬度计、浸泡腐蚀试验和电化学工作站研究了T6热处理和稀土La改性对ADC12铝合金的微观组织、硬度和耐腐蚀性能的影响。结果表明,T6态ADC12-0.5La铝合金微观组织明显细化,α-Al尺寸减小,形貌变圆整,共晶Si相和AlFeMnSi相细化为短棒状。相比于ADC12铝合金,T6态ADC12-0.5La铝合金硬度达到117.7HV,提高了26.8%,腐蚀电流密度降低了10.7%,腐蚀电位上升了64.4%,腐蚀速率降低了54.4%,腐蚀表面平坦且光滑,表现为较轻微的晶间腐蚀。T6态ADC12-0.5La铝合金提高了腐蚀电位,Al-La-Cu稀土相阻碍了电子移动,铝合金的耐腐蚀性能得到大幅度提高。