Multi-objective planning and optimization of microgrid lithium iron phosphate battery energy storage system consider power supply status and CCER transactions

Lithium iron phosphate battery (LIPB) is the key equipment of battery energy storage system (BESS), which plays a major role in promoting the economic and stable operation of microgrid. Based on the advancement of LIPB technology and efficient consumption of renewable energy, two power supply planning strategies and the china certified emission reduction (CCER) model are proposed respectively. Based on it, the multi-objective planning optimization model with economic benefits, environmental benefits and power supply stability as the objective function is established for the first time, and the Newton Weighted Sum Frisch method (NWSFA) solution model is adopted. In the planning process, rain flow counting method is used to research the life of BESS, which improves the accuracy of energy storage annual cost calculation. A park in northern China is taken as a case study to demonstrate the application of this model. The simulation results show that the annual economic operating cost of BESS is decreased by 18.81%, the energy supply reliability is increased by 0.15%, and the optimal electricity price adjustment ratio of the system is 15%.     

The Innate Immune Glycoprotein Lactoferrin Represses the Helicobacter pylori cag Type IV Secretion System

Chronic infection with Helicobacter pylori increases risk of gastric diseases including gastric cancer. Despite development of a robust immune response, H. pylori persists in the gastric niche. Progression of gastric inflammation to serious disease outcomes is associated with infection with H. pylori strains which encode the cag Type IV Secretion System (cag T4SS). The cag T4SS is responsible for translocating the oncogenic protein CagA into host cells and inducing pro-inflammatory and carcinogenic signaling cascades. Our previous work demonstrated that nutrient iron modulates the activity of the T4SS and biogenesis of T4SS pili. In response to H. pylori infection, the host produces a variety of antimicrobial molecules, including the iron-binding glycoprotein, lactoferrin. Our work shows that apo-lactoferrin exerts antimicrobial activity against H. pylori under iron-limited conditions, while holo-lactoferrin enhances bacterial growth. Culturing H. pylori in the presence of holo-lactoferrin prior to co-culture with gastric epithelial cells, results in repression of the cag T4SS activity. Concomitantly, a decrease in biogenesis of cag T4SS pili at the host-pathogen interface was observed under these culture conditions by high-resolution electron microscopy analyses. Taken together, these results indicate that acquisition of alternate sources of nutrient iron plays a role in regulating the pro-inflammatory activity of a bacterial secretion system and present novel therapeutic targets for the treatment of H. pylori-related disease.     

Degradation mechanism of high alumina refractory bricks by reaction with deposits in a rotary kiln for fluxed iron ore pellets production

The formed deposits wear out of refractory wall linings in the rotary kiln and may cause production disturbances. This study describes the chemical composition and mineralogical phase components at the deposit/refractory interface in the rotary kiln for fluxed iron ore pellets production. The main phases of refractory bricks are corundum and mullite, while the deposits mainly contain hematite and silicates. The main phases in the deposit/refractory brick contact zone are hematite, anorthite (CaAl₂Si₂O₈), mullite, corundum, and silicates. Moreover, the hematite phases in the deposit/brick interface averagely contain 6.98 wt% Al and 1.38 wt% Ti. The silicates in the contact zone contain higher aluminium content and lower iron content than the silicates in the deposits. Finally, the thermodynamic analysis indicates that the main phases in the deposits can react with the refractory to form Al₂Fe₂O₆, CaAl₂Si₂O₈, feldspar, and liquid phases lead to the degradation of bricks in the kiln during the iron ore pellets production.     

球形木质素负载纳米零价铁去除溴酸盐的研究

以球形氰乙基木质素为原料通过液相还原法制备球形木质素负载纳米零价铁材料（LSAC-Fe），用于去除饮用水中微量的溴酸盐。采用场发射扫描电子显微镜（FESEM）、X射线衍射仪（XRD）、X射线光电子能谱仪（XPS）、氮气吸附法（BET）等对其结构进行表征，并探究了不同条件下LSAC-Fe对BrO-3的吸附效果及其热力学吸附和去除机理。研究表明，纳米零价铁可较为均匀地负载在球形木质素上，并且LSAC-Fe具有很高的表面活性；BrO-3的去除率随着初始溶液pH值的升高而降低，随着BrO-3初始溶液质量浓度的增加而降低；LSAC-Fe对BrO-3的吸附过程为吸热过程，升温可促进LSAC-Fe对BrO-3的吸附。     

等离子体改性海绵铁活化过硫酸盐处理含酚废水

采用低温等离子体技术对海绵铁表面进行改性，并将其用于活化过硫酸盐（PS）处理含酚废水。通过氮气等温吸附（BET）、X射线衍射（XRD）和扫描电子显微镜（SEM）等手段对改性前后的海绵铁进行表征分析。以苯酚为目标污染物，通过静态实验考察催化剂投加量、催化剂/PS摩尔比、pH和苯酚初始浓度对等离子体改性海绵铁活化PS处理含酚废水的影响。结果表明，改性后的海绵铁比表面积、孔容及孔径均有增大，活化PS能力显著提高；在最佳反应条件（等离子改性海绵铁的投加量为0.4g/L，催化剂/PS摩尔比为1∶15，溶液pH为2，苯酚的初始浓度为250mg/L）下，苯酚的去除率可达95%；反应过程符合二级反应动力学，主要是硫酸根自由基和羟基自由基起氧化作用。等离子体技术改性海绵铁活化过硫酸钠可有效去除水中苯酚，为实际含酚废水的处理提供一些思路。     

腾冲市茨竹地铁多金属矿成矿地质特征及控矿因素

腾冲市茨竹地铁多金属矿现目前是一座正在开采的以磁铁矿为主、共（伴）生锡钨矿的小型矿山。为了增加矿山资源储量、延长矿山服务年限，通过对矿区的地质特征阐述和对矿区地层岩性、构造、岩体等控矿因素的分析研究，总结了矿区成矿规律并形成了矿区的成矿模式，为矿区深部探矿、外围找矿提供了一定的理论依据。     

Microstructure,hardness, toughness and abrasive wear resistance of 16.0 wt. % chromium white iron after continuous and cyclic destabilisation treatment

Destabilisation of as-cast chromium white iron with 16 wt-% chromium are performed by continuous destabilisation treatment for 4 h and short duration (0.66 h) cyclic destabilisation treatment at 900, 950, 1000, 1050, and 1100 °C. Continuous destabilisation causes secondary carbides precipitation from austenite which on slow cooling transforms to pearlite matrix. Cyclic destabilisation treatment causes similar precipitation of finer secondary carbides following shorter period austenitisation and a matrix containing martensite and retained austenite on forced-air cooling. After continuous destabilisation, hardness falls below the as-cast value (HV622); whereas it rises to HV950 after cyclic destabilisation treatment. The as-cast notched impact toughness (4.0 J) increases to 8.5 J or more after both continuous and cyclic destabilisation at 1050 and 1100 °C. Abrasive wear resistance after continuous destabilisation improves only at higher wear load (49.0 N), while after cyclic destabilisation it supersedes the as-cast and Ni-Hard IV performance at both low (19.6 N) and high (49.9 N) wear load.     

甲烷/丙烷在氧化铁表面还原NO的红外原位研究*

利用漫反射红外傅里叶变换光谱仪(DRIFTS)对甲烷/丙烷在氧化铁表面还原NO的反应进行了原位研究,分析了不同气体在氧化铁表面的吸附特点以及在有O_2条件下甲烷/丙烷还原NO的中间产物生成特性。结果表明,氧化铁对NO有着较好的吸附能力,NO能够以不同桥式硝酸盐与硝基的形式吸附于氧化铁表面。这些吸附物种热稳定性各不相同,并且可能会被氧化铁中的晶格氧氧化产生新的吸附物种,对进一步与还原剂发生选择性催化反应有着重要的作用。甲烷与丙烷在氧化铁表面还原NO的微观反应机理通过一系列路径完成。还原剂吸附于氧化铁表面,与由NO吸附形成的含氮吸附物种相互反应,形成一系列碳氢中间产物,通过进一步反应还原NO;在氧气存在的情况下,O_2会参与碳氢还原剂与含氮吸附物种的竞争反应,并形成R—COO-、CH3COO-等更多活性中间物种,这些活性中间物种通过与NO不断的反应最终还原NO为N2。     

研磨介质形状对铁矿石磨矿动力学研究

以由粗到细的四种单粒级铁矿石为研究对象,基于磨矿动力学原理,解析了三种研磨介质(钢球、钢锻以及立方体)对铁矿石颗粒的破碎行为,探究了磨矿动力学参数k和m,获得了矿石在三种研磨介质下的比破碎速率。研究表明:随着单粒级铁矿石给料尺寸由小到大,矿石在三种研磨介质下的比破碎速率先增加后减小,其中,采用钢球为研磨介质时,矿石比破碎速率最大,钢锻次之,立方体的最小;不同给料尺寸下,采用钢球为研磨介质时的k和m始终最大,立方体的始终最小。     

Replacing Mg2+ by Fe2+ for RNA-Cleaving DNAzymes

It has been proposed that Mg²⁺ and Fe²⁺ are very similar in interacting with ribozymes and some protein-based enzymes, but their activities with DNAzymes have yet to be studied. Here, the activity of Fe²⁺ as cofactor for a few RNA-cleaving DNAzymes is investigated. 17E is a well-studied DNAzyme that is active in the presence of many different divalent metal ions; it is highly active with Fe²⁺ with an apparent K_d of 29.7±2.3 μm and a k_obs of 1.12±0.11 min⁻¹ in the presence of 1 mm Fe²⁺ at pH 7.5. Fe²⁺ has 21-fold higher activity than Mg²⁺. Six different DNAzymes are then tested, and only the DNAzymes active with Mg²⁺ (17E, 8–17, and E5) are active with Fe²⁺. Fe²⁺ has 25 and one- to twofold higher activity than Mg²⁺ for the 8–17 and E5 DNAzymes, respectively. In pH>7 buffer and in presence of air, 1 mm Fe²⁺ results in a nonspecific degradation of the DNA strand due to reactive oxygen species (ROS). Cleavage reactions in anoxic environment and antioxidant ascorbate can be used to overcome the effect of oxidation. The findings provide insights for potential DNAzyme catalysis in the early Earth, and they further support the similarity between Mg²⁺ and Fe²⁺ in enzyme catalysis.