灰口铸铁阀体密封面镍基堆焊技术

详细介绍了一种改善旋转止回阀密封面性能的镍基堆焊工艺。针对阀体密封面的结构，设计了特殊焊接工艺，精确地完成了堆焊过程，达到厂家设计要求。     

Depth profiles of the Fermi level at an amorphous-carbon nitride/SiO2/n-type-Si heterojunction interface obtained by Kelvin probe force microscopy

To explore the work function of a typical amorphous-CN film containing a nitrogen concentration of 23.5 at.%, surface potential images were acquired using Kelvin probe force microscopy. Based on the Fermi level of the n-type Si and the contact potential difference between the amorphous-CN film and the n-Si substrate, the work function of the amorphous-CN film was estimated to be 5.2 ± 0.2 eV below its vacuum level. Using the surface potential depth profile for an etched amorphous-CN film, energy diagrams of the amorphous-CN/SiO₂/n-Si interface were constructed based on the positional relationship of the Fermi level. These band diagrams showed that band bending occurred at the amorphous-CN/SiO₂/n-Si interface despite the Fermi level pinning effect of surface trapping due to the SiO₂ insulator layer.     

Evaluation of amines for the selective catalytic reduction (SCR) of NOx from diesel engine exhaust

With a view to developing onboard generation of selective reductants for NO_x removal from diesel engine exhaust we compared the performance of a primary, secondary and tertiary amine to NH₃ using a typical mini core NH₃-SCR catalyst. Primary amines with short hydrocarbon chains, e.g. CH₃NH₂ (maximum NO_x conversion, 50%) approached the NO_x conversion obtained using NH₃ (maximum NO_x conversion, 70%). Increasing the amine to NO_x ratio greater than 1 results in NO_x conversions closer to those of NH₃ (maximum NO_x conversion increased to 60%). Secondary and tertiary amines had smaller NO_x conversions as a function of temperature and the drop in NO and NO_x conversion decreased with increasing amine hydrogen substitution. Also, the maximum NO_x conversion for each reductant tends to move to a lower temperature as the degree of substitution increases.Unlike NH₃, the amines can react in the gas phase at temperatures within the range of diesel engine exhaust. Due to this gas phase reactivity the NO_x conversions measured using the mini core SCR catalyst also contain a gas phase conversion component. Gas phase conversions were investigated by replacing the mini core SCR catalyst with an equivalent length of quartz beads. Subtraction of the two results highlighted the differences between the mini core catalytic and gas phase conversions measured in this manner over the temperature range investigated. These differential NO_x conversions for the three amines had maxima at about 375 °C.     

Rescheduling policies for large-scale task allocation of autonomous straddle carriers under uncertainty at automated container terminals

This paper investigates replanning strategies for container-transportation task allocation of autonomous Straddle Carriers (SC) at automated container terminals. The strategies address the problem of large-scale scheduling in the context of uncertainty (especially uncertainty associated with unexpected events such as the arrival of a new task). Two rescheduling policies–Rescheduling New arrival Jobs (RNJ) policy and Rescheduling Combination of new and unexecuted Jobs (RCJ) policy–are presented and compared for long-term Autonomous SC Scheduling (ASCS) under the uncertainty of new job arrival. The long-term performance of the two rescheduling policies is evaluated using a multi-objective cost function (i.e., the sum of the costs of SC travelling, SC waiting, and delay of finishing high-priority jobs). This evaluation is conducted based on two different ASCS solving algorithms–an exact algorithm (i.e., branch-and-bound with column generation (BBCG) algorithm) and an approximate algorithm (i.e., auction algorithm)–to get the schedule of each short-term planning for the policy. Based on the map of an actual fully-automated container terminal, simulation and comparative results demonstrate the quality advantage of the RCJ policy compared with the RNJ policy for task allocation of autonomous straddle carriers under uncertainty. Long-term testing results also show that although the auction algorithm is much more efficient than the BBCG algorithm for practical applications, it is not effective enough, even when employed by the superior RCJ policy, to achieve high-quality scheduling of autonomous SCs at the container terminals.     

Surface acidity study of Mn+-montmorillonite clay catalysts by FT-IR spectroscopy: Correlation with esterification activity

A simple method for evaluating the surface acidity of different cation-exchanged montmorillonite (mont) clay catalysts, Mⁿ⁺-mont (Mⁿ⁺=Al³⁺, Fe³⁺, Cr³⁺, Zn²⁺, Ni²⁺, Cu²⁺, and H⁺), involving treatment with pyridine is described. After treating with pyridine, the samples were heated at 120 °C and the FT-IR spectra were directly recorded in the region 1650 and 1350 cm⁻¹. The data obtained show the presence of both Lewis and Brønsted acid sites. The activities of the catalysts to bring about Brønsted acid catalysed esterification of succinic acid with iso-butanol to yield di-(iso-butyl) succinate have been studied. The Brønsted acidity data obtained for Mⁿ⁺-mont correlated well with activity in the esterification reaction. The activities of the catalysts were found to decrease in the order of exchange ions Al³⁺ > Fe³⁺ > Cr³⁺ > Zn²⁺ > Ni²⁺ > Cu²⁺ > Na⁺-mont. They also correlated well with the charge to radius ratio of the cations. The catalysts exchanged with trivalent cations showed stronger absorption bands attributed to Brønsted acidity (1540 cm⁻¹) whereas those exchanged with divalent cations showed an increased Lewis acidity (1450 cm⁻¹) and reduced Brønsted acidity along with charge to radius ratio. Zn²⁺-, Cu²⁺- and Ni²⁺-exchanged clays showed an additional peak around 1605 cm⁻¹ which is attributed to the pyridine adsorption on surface sites through its π electrons. The method suggested here to evaluate the acidity is suitable for active sites which are thermally unstable such as water molecules in the hydration shell of a cation in exchanged clay.     

The potential for rapid coke making using microwave energy

This paper describes initial work into the production of coke from high volatile bituminous coal using microwave energy. A series of batch experiments were carried out using an 8 kW multimode microwave to heat 300 g of a UK high volatile bituminous coal, sized at −3 mm, at different treatment times of 10, 25 and 70 min. Devolatilisation started after 1 min of heating and was complete within 5 min. Subsequent heating yielded no further volatiles and the power was maintained to prolong the coking process. Characterization of each product was carried out using thermogravimetric analysis, microscopy and dielectric property measurement in order to investigate the impact of residence time and provide a comparison with coke material produced using conventional methods. The measured characteristics of each sample became increasingly similar to those of two conventional cokes as treatment time was increased.     

合成煤中钠对煤燃烧及灰特性影响

准东煤中钠含量高，燃用时锅炉会出现严重结渣问题。通过向准东煤为原料制取的超纯煤中添加灰的模型化合物，得到合成煤。并在此基础上利用热重-差示扫描量热分析法（TG/DTG/DSC）、X射线衍射仪（XRD）和灰熔融温度测定分析手段，研究Na₂O含量对煤燃烧特性和灰熔融性的影响。结果表明：钠主要影响合成煤的着火温度（T_i）与焦炭燃烧阶段，钠含量增加使T_i升高，并且Na₂O在灰中质量分数由5%升高至8%后，钠含量增加使焦炭燃烧速率先减小后加快，并能够改善煤粉燃尽特性。钠能够降低灰熔融温度，并在Na₂O质量分数高于5%后，温度下降更加明显。在三元相图中钠对莫来石的助熔作用是造成灰熔融温度降低的重要原因。XRD分析表明Na₂O含量增加，充当骨架作用的石英在钠的助熔作用下与难熔矿物硅钙石、MgO等生成低熔点长石类矿物，这类矿物在高温下有助熔作用，能够降低灰熔融温度。同时还生成助熔性含钠矿物霞石，加剧了灰熔融。     

Evaporative Heat Transfer of Annular Two-phase Flow of Air-water in a Small Vertical Tube

The evaporative heat transfer of the non-boiling annular two-phase flow of air-water in a small vertical tube with uniform wall heat flux was studied both theoretically and experimentally. A simplified two-phase flow boundary layer model was used to calculate the thickness of the water film attached to the wall, and from the liquid film thickness the evaporative heat transfer coefficients of the annular two-phase flow were obtained. Theoretical equations and semi-theoretical equations were proposed for predicting the evaporative heat transfer of the annular two-phase flow of air-water in a small vertical tube. The semi-theoretical prediction agrees well with the experimental data. The mechanism of the heat transfer enhancement is the evaporation of the thin liquid film attached on the wall.     

过渡金属离子掺杂纳米TiO2的相变与光催化活性

采用溶胶-凝胶法制备了掺杂Mo⁶⁺、Cr³⁺、Fe³⁺的改性纳米TiO₂光催化剂，并分别在550℃和580℃下对其进行了热处理，考察了热处理温度对掺杂纳米TiO₂相变和光催化活性的影响.通过光催化降解染料罗丹明B实验，对在不同热处理温度下Mo⁶⁺、Cr³⁺、Fe³⁺改性以及不同Mo⁶⁺掺杂量的TiO₂光催化活性进行了评价，发现掺杂离子对TiO₂光催化活性的影响与其对TiO₂相转变的作用是一致的，即抑制相转变的同时也提高了光催化活性.实验结果也进一步表明，Mo⁶⁺掺杂量为0.05％（摩尔分数）时的TiO₂具有最佳光催化活性.