Development of a void ratio-moisture ratio-net stress framework for the prediction of the volumetric behavior of unsaturated granular materials

Despite extensive research on the behavior of unsaturated fine-grained materials, there is still a lack of understanding of the volumetric behavior of unsaturated granular materials. In this research, a model has been developed to predict the fundamental volumetric behavior of unsaturated granular materials through loading and wetting state paths. In this regard, a loading-wetting surface was developed in a space of void ratio-moisture ratio-net stress. A distinctive feature of the proposed model is the relative simplicity in obtaining the model parameters using conventional geotechnical testing equipment. Two types of recycled granular materials, commonly applied in unbound pavements were used, namely, recycled crushed brick (CB) and excavation waste rock (WR). The uniqueness of the developed surface was evaluated by employing a number of loading and wetting state paths. The results indicate that the developed surface is unique in its loading state paths; however, it only shows uniqueness in its wetting state paths for stress levels greater than 2000 kPa. The proposed model seeks to introduce the application of the unsaturated soil mechanics theory, for predicting the behavior of granular materials in the field, by providing a practical and cost-effective methodology.     

Fluidizing effects of polymers with various anchoring groups in cement pastes and their sensitivity to environmental temperatures

We synthesized various polymers with different functional groups of ─COO⁻, ─SO₃⁻, and ≡N⁺─ to study the impact of the environmental temperature (25, 50, and 80 °C) on the dispersing capability by measuring the fluidity of fresh cement paste, total organic carbon, ζ potential, and isothermal calorimetry. The results show that no adsorption was observed for the cement pastes containing acrylic acid, 2-acrylamido-2-methyl propane sulfonic acid, and [3-(methacryloylamino)propyl] trimethyl ammonium chloride, probably because of the trace amount of adsorption, whereas the fluidity of the pastes was indeed improved by the addition of these chemicals. Generally, for the polymers containing various functional groups, the adsorption capability was in the order ─COO⁻ > ─SO₃⁻ > ≡N⁺─. The dispersing capability for the carboxylate superplasticizer was robust to the change in the temperature, whereas it was dramatically weakened by the increase in temperature for sulfonate superplasticizer, although the adsorption amount increased along with the temperature rise. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47494.     

羧基含氟聚合物纳米纤维膜的制备及对铜(II)的吸附性能

以甲基丙烯酸十二氟庚酯(DFHMA)和甲基丙烯酸(MAA)为单体,通过溶液聚合法制备出共聚物DFHMA-co-MAA,将DFHMA-co-MAA与聚偏氟乙烯(PVDF)按一定质量共混,采用静电纺丝方法,制备出羧基含氟聚合物(PVDF-DM)纳米纤维膜,用以吸附溶液中Cu(II)。讨论了PVDF和DFHMA-co-MAA的质量配比对纤维微观形貌和对Cu(II)吸附性能的影响,得出当PVDF与DFHMA-co-MAA的质量比为1∶2时,纤维的微观直径较均一且吸附性能最佳,故实验采用该质量配比制备PVDF-DM。使用红外光谱对PVDF-DM进行表征,显示出PVDF-DM纤维膜中含有—OH和C＝O等活性吸附基团。以PVDF-DM纳米纤维膜为吸附剂,探讨了吸附剂用量、吸附pH值和吸附时间对Cu(II)吸附性能的影响,并研究了吸附过程的动力学模型。结果表明,室温下,当吸附剂用量为0.03g,pH=5时,吸附60min达到吸附平衡,吸附率和吸附量分别为94.37%和62.91mg/g,PVDF-DM纳米纤维膜对Cu(II)的吸附过程同时满足拟一级动力学和拟二级动力学模型,说明该吸附过程包含了化学吸附和物理吸附。PVDF-DM纳米纤维膜循环使用5次后,吸附能力仅降低16.23%,说明PVDF-DM纳米纤维膜具有很好的再生使用能力。     

Evaluation and validation of an automatic jaw movement recorder (RumiWatch) for ingestive and rumination behaviors of dairy cows during grazing and supplementation

Observation of ingestive and rumination behaviors of dairy cows may assist in detecting diseases, controlling reproductive status, and estimating intake. However, direct observation of cows on pasture is time consuming and can be difficult to realize. Consequently, different systems have been developed to automatically record behavioral characteristics; among them is the RumiWatch System (RWS; Itin and Hoch GmbH, Liestal, Switzerland). Until now, the RWS has not been thoroughly validated under grazing conditions. The aim of the current study was to validate the RWS, against direct observation, in measuring ingestive and rumination behaviors of dairy cows during grazing and supplementation in the barn. A further objective was to examine whether it is possible to refine the algorithm used by the evaluation software RumiWatch Converter 0.7.3.2 to improve the accuracy of the RWS. The data were collected from an experiment carried out with 18 lactating Holstein cows in a crossover block design including 3 treatments and 3 measuring periods. All cows grazed night and day, 19 h/d, and were either unsupplemented or supplemented, with chopped whole-plant corn silage, or chopped whole-plant corn silage mixed with a protein concentrate. During the measuring periods, cows were equipped with the RumiWatch Halter, and their ingestive and rumination behaviors were recorded concurrently by the RumiWatch Halter and by direct observation (690 × 10 min). Comparison of concurrently measured data shows that the RWS detected jaw movements reliably, but classification errors occurred. A low relative prediction error of ≤0.10 for the number of rumination boluses, rumination chews, and total eating chews was found. A high relative prediction error of >0.10 was found for the number of prehension bites and time spent in prehension and eating. Both converter versions performed equally well in differentiating ingestive and rumination behaviors when cows were supplemented in the barn or when grazing and supplementation activities were combined. For grazing cows, with no supplementation, more reliable results for the total number of eating chews, rumination chews, prehension bites, and time spent in these activities were obtained, by using the RumiWatch Converter 0.7.3.11. In light of these findings, further research is warranted to improve the accuracy of the RWS and to allow a differentiation between mastication chews and prehension bites while eating.     

Colloidal processing of Al2O3-doped zirconia ceramics with CaO–P2O5–SiO2 glass as additive

Well-dispersed concentrated aqueous suspensions of Al₂O₃-doped Y-TZP (AY-TZP), AY-TZP with 5.4 vol% of CaO–P₂O₅–SiO₂ (CaPSi) glass (AY-TZP5) and 10.5 vol% CaPSi glass (AY-TZP10), with ammonium polyacrylate (NH₄PA) dispersant were prepared to produce slip cast compacts. The rheological properties of 35 and 40 vol% slips were studied. The densification, microstructure as well as hardness and fracture toughness were investigated as a function of CaPSi glass content at 1300°C-1500°C. The optimum NH₄PA concentration of 35 vol% AY-TZP5 and AY-TZP10 slips at pH ~9 was found to be about 43% and 67% greater than that of AY-TZP slips; this behavior was related to the greater amounts of Ca²⁺ ions leached out from the CaPSi glass surface. The viscosity of stabilized 40 vol% slips with NH₄PA attained a minimum value at 5.4 vol% CaPSi glass addition, and resulted in a more dense packing of cast samples. AY-TZP5 can be sintered at a lower temperature (1300°C) compared to that of AY-TZP. AY-TZP5 exhibited a fine microstructure of tetragonal ZrO₂ (grain sizes below 0.3 µm), and ZrSiO₄–Ca₂P₂O₇ particles homogeneously distributed within the zirconia matrix. It presented similar fracture toughness and a slightly lower hardness compared to those of AY-TZP.     

非晶Fe粉掺杂Al-12Si合金的高温压缩变形行为

为提高Al-12Si合金的热变形抗力,并探索非晶Fe粉掺杂对Al-12Si合金热压缩行为的影响和掺杂非晶Fe粉热压缩中的晶化温度等,采用连续挤压技术制备了掺杂10wt%非晶Fe粉与不掺杂非晶Fe粉的Al-12Si合金试样,对试样进行了不同温度和应变速率下的热压缩试验,分析了试样在热压缩中的组织转变,以及采用双曲正弦关系构建了试样的热流变应力方程。结果表明:非晶Fe掺杂试样在450 ℃及以下的热压缩时,Fe维持非晶态,500 ℃时,则已发生晶化;掺杂10wt%非晶Fe粉使Al-12Si合金的热抗变形能力显著提高,其热压缩激活能Q=211.29 kJ/mol,比未掺杂非晶Fe粉的Al-12Si合金试样高40.78 kJ/mol,且热压缩过程中存在动态回复和动态再结晶;利用双曲正弦关系构建试样的热流变应力方程为ε·=4.42×10¹⁴[sinh(0.016 6σ)]^6.13exp(-211 290/RT),线性回归系数高达0.99,即可为非晶Fe粉掺杂试样的热加工提供一定的理论指导。     

Microstructural characteristic,outward-inward growth behavior and formation mechanism of MAO ceramic coating on the surface of ADC12 Al alloy with micro-groove

The ceramic coatings on the surface of aluminum alloy substrates with micro-grooves have been successfully fabricated in the silicate solution via micro-arc oxidation (MAO) approach. Microstructure characterization showed that the larger main discharge channels were located in the center of micro-groove, the smaller secondary discharge channels were located on both sides of main discharge channel; and a few irregular micro-pores existed in the vicinity of all discharge channels, which were mainly cause by the rapid cooling and solidification of discharge channels hindering the removal of gases produced via reaction. Moreover, the growing direction of coating in the initial stage was mainly outward-growth and resulted in the formation of inverted triangle coating structure, which was due to the sharp-angled effect. But in the final growing stage, the inward-growth behavior played a key role owing to the spark transfer. According to above results and discussion, the formation of smooth, uniform and homogeneous ceramic coating on the surface of whole trapezoidal micro-groove substrate contained four stages: anodic oxidation growth, sharp corner rapid growth, coating homogenization and groove self-filling.     

Logarithmic decrease of adhesion force with lateral dynamic revealed by an AFM cantilever at different humidities

Adhesion forces between a tipless cantilever and an Au film were determined to investigate the influence of lateral velocity by recording force curves with an atomic force microscope at 20%–90% relative humidities. The sample was moved laterally, forth and back, with a frequency of 0.001–100 Hz and scan distances of 0.8, 8, and 80 μm to achieve a velocity ranging over 7 orders of magnitude. Experimental results show that at low lateral velocities (between 1.6 nm/s and 1–10 μm/s), the adhesion force either increases or decreases or remains stable with the lateral velocity without a certain characteristic trend. However, after a critical velocity, the adhesion force decreases logarithmically with the lateral velocity (between 1–10 and 16,000 μm/s). The decreasing magnitude can be as large as 97.3% of the maximum adhesion force. This decrease is well-explained by the contact time dependence of water bridges formed by capillary condensation.     

Biodegradable Spheres Protect Traumatically Injured Spinal Cord by Alleviating the Glutamate‐Induced Excitotoxicity

New treatment strategies for spinal cord injury with good therapeutic efficacy are actively pursued. Here, acetalated dextran (AcDX), a biodegradable polymer obtained by modifying vicinal diols of dextran, is demonstrated to protect the traumatically injured spinal cord. To facilitate its administration, AcDX is formulated into microspheres (≈7.2 µm in diameter) by the droplet microfluidic technique. Intrathecally injected AcDX microspheres effectively reduce the traumatic lesion volume and inflammatory response in the injured spinal cord, protect the spinal cord neurons from apoptosis, and ultimately, recover the locomotor function of injured rats. The neuroprotective feature of AcDX microspheres is achieved by sequestering glutamate and calcium ions in cerebrospinal fluid. The scavenging of glutamate and calcium ion reduces the influx of calcium ions into neurons and inhibits the formation of reactive oxygen species. Consequently, AcDX microspheres attenuate the expression of proapoptotic proteins, Calpain, and Bax, and enhance the expression of antiapoptotic protein Bcl‐2. Overall, AcDX microspheres protect traumatically injured spinal cord by alleviating the glutamate‐induced excitotoxicity. This study opens an exciting perspective toward the application of neuroprotective AcDX for the treatment of severe neurological diseases.     

Polyoctadecylacrylate (POA) and resin-stabilized asphaltene synergistically improve the flow behavior of model waxy oils

In this paper, the effect of POA PPD together with resin-stabilized asphaltenes on the flow behavior of model waxy oils was investigated through rheological test, DSC, microscopic observation and asphaltenes precipitation test. Compared to the POA or asphaltenes alone, POA/asphaltenes cannot further decrease the wax appearance temperature of oils, but can dramatically decrease the pour point, gelation point, G′, G″ and apparent viscosity of oils. POA molecules can adsorb on the surface of asphaltenes, thus inhibiting the asphaltenes precipitation and forming the POA/asphaltenes composite particles. The composite particles can act as wax crystallization templates and then greatly change the wax crystals' morphology into large and spherical-like, thus improving the waxy oil flow behavior.