抗硫化返原剂PK900在全地形轮胎胎面胶中的应用

研究抗硫化返原剂PK900在全地形轮胎胎面胶中的应用。结果表明:在全地形轮胎胎面胶中添加抗硫化返原剂PK900,胶料硫化速度变化不大,抗硫化返原性能提高,在过硫条件下硫化胶可保持较好的物理性能;成品轮胎的耐久性能提高,使用寿命延长。     

Improved oxidation resistance of expanded graphite through nano SiC coating

Expanded graphite with nano SiC and amorphous SiC_xO_y coating was successfully prepared through pyrolysing silane coupling agent (SCA), where the grafting of SCA dominated the final products. The results show that mainly amorphous SiC_xO_y coating covers expanded graphite at 1000 °C, regardless of the SCA concentration. In comparison, nano SiC coating can be synthesized at 1200 °C depending on the good dispersion of SCA (with a SCA concentration of 50 vol%). The formed SiC coating contributes to much higher peak oxidation temperature (812.1 °C) than 678.0 °C of the pure expanded graphite. Meanwhile, the oxidation activation energies of expanded graphite are remarkably improved from 149.15 kJ/mol to 176.16 kJ/mol (based on Kissinger method), attributing to the derived nano SiC and SiC_xO_y coating.     

Study on the relationship between the particle size distribution and the effectiveness of the K‐powder fire extinguishing agent

The relationship between the particle size distribution and the extinguishing effectiveness of the new K‐powder fire extinguishing agent has been studied experimentally, to explore the reason of the great extinguishing efficiency exhibited by the new K‐powder fire extinguishing agent on Class B fire (liquid fuel fire). The results of the experiment showed that the extinguishing effectiveness increased along with the decrease of the particle size distribution. In addition, a sharp discontinuity appeared around the limiting size, about 40 μm. The powder with the particle size below 40 μm exhibited highly effective extinguishing with the minimum effective extinguishing concentration C_xr = 23 g·m^?3, while the powder with the particle size above 40 μm exhibited little fire extinguishing efficiency. Compared with other fire extinguishing agents produced by different substances, the new K‐powder fire extinguishing has the bigger limiting size. That means, in the same particle size distribution, the new K‐powder fire extinguishing agent contains more highly effective powder than others contain, and is more effective.     

Effect of matrix−nanoparticle supramolecular interactions on the morphology and mechanical properties of polymer foams

In this study, we report the fabrication of supramolecular polymer nanocomposite foams with a uniform cell structure, high cell density and high expansion ratio using a soft matrix of poly(methyl acrylate‐co‐2‐hydroxyethyl methacrylate) and silica nanoparticle fillers, both functionalized with ureido‐pyrimidinone (UPy) supramolecular groups. Microcellular structures were formed using a batch foaming process at 90 °C under a 9 MPa nitrogen atmosphere. Nanocomposites were characterized and compared before and after the foaming process to investigate the effect of supramolecular interactions on the thermomechanical properties and morphology of the foams. TEM images revealed that while strong inter‐filler supramolecular interactions do not have a positive effect on their dispersion state, matrix?filler interactions derived from hydrogen bonding UPy motifs result in a rather uniform distribution of nanoparticles. Competing filler?filler and matrix?filler supramolecular interactions can be balanced and optimized by adjusting UPy populations along the chains and on the surface of nanoparticles. At a given chain functionality, increasing the nanoparticle loading up to an optimum concentration improves the mechanical properties and formability of the system. Above such concentration strong interactions between fillers, which are not compensated by the matrix, result in large aggregates and consequently undermine the material performance. Supramolecular polymer foams illustrate a similar thermal and viscoelastic behavior to that of neat samples but after foaming, due to the formation of a cellular structure and rearrangement or dissociation of UPy dimers under the foaming conditions, the elastic modulus is reduced. © 2018 Society of Chemical Industry     

Isothermal crystallization kinetics and subsequent melting behavior of β‐nucleated isotactic polypropylene/graphene oxide composites with different ordered structure

The effects of ordered structure on isothermal crystallization kinetics and subsequent melting behavior of β‐nucleated isotactic polypropylene/graphene oxide (iPP/GO) composites were studied using differential scanning calorimetry. The ordered structure status was controlled by tuning the fusion temperature (T_f). The results showed that depending on the variation of crystallization rate, the whole T_f range could be divided into three regions: Region I (T_f > 179 °C), Region II (170 °C ≤ T_f ≤ 179 °C) and Region III (T_f < 170 °C). As T_f decreased from Region I to Region III, the crystallization rate would increase substantially at two transition points, due to the variation of the ordered structure status. Calculation of Avrami exponent n indicated that the ordered structure induced the formation of two‐dimensional growing crystallites rather than three‐dimensional growing crystallites. Moreover, in the case of isothermal crystallization, the ordered structure effect (OSE) can also greatly increase the relative content of β‐phase (β_c). In Region II, OSE took place, resulting in evident increase of β_c, achieving 92.4% at maximum. The variation of the isothermal crystallization temperature (T_iso) had little influence on the T_f range (Region II) of the OSE. The higher T_f in Region II was more favorable for the formation of higher β_c. The ordered structure was favorable for the improvement of the nucleating efficiency of β‐nucleating agent (β‐NE), and was more effective for the improvement of lower β‐NE. © 2018 Society of Chemical Industry     

Novel poly(aryl ether nitrile ketone) foams and the influence of copolymer structure on the foaming result

Novel poly(aryl ether nitrile ketone) foams were prepared through the batch foaming method with supercritical CO₂ as the blowing agent. Both temperature‐induced and pressure‐induced foaming methods were conducted to examine the influence of nitrile groups on the foaming result. The results indicated that nitrile groups influenced the foaming result by affecting both the viscoelasticity and CO₂ absorption of the polymers. In addition, the CO₂ solubility of the polymers increased with increasing CN content presumably because of the Lewis acid–base nature of the interaction between the CO₂ molecules and the nitrile groups. The cell growth process was assessed by analyzing the influence of foaming temperature and foaming time on the cell morphology. Nanocellular foams with a minimum size of 30–50 nm were achieved by the temperature‐induced foaming method. Moreover, highly expanded foams with a maximum expansion ratio of 23.6 were obtained by the pressure‐induced foaming method. © 2018 Society of Chemical Industry     

抗凝冰乳化沥青涂层的性能研究

为了研究自制融雪剂对抗凝冰乳化沥青涂层性能的影响,将自制固态型融雪剂按5%、10%、15%的比例加入乳化沥青制备涂层乳液,采用水煮法、摆式摩擦仪、电导率试验分别对涂层材料的粘附性、抗滑性能和抗凝冰性能进行了测试。结果表明:自制型融雪剂对乳化沥青与集料的粘附性影响不大;随着融雪剂掺配比例的增大,抗凝冰乳化沥青涂层的摩擦系数有所降低,但均满足规范要求;相比于普通沥青涂层,抗凝冰乳化沥青涂层的抗凝冰性能得到改善,且随着融雪剂掺配比例的增大,凝冰性能逐渐提高。     

Preparation of YSZ porous ceramics with precise porosity control

Conventional preparation of porous ceramics often hard to accurately control the porosity of the samples. In this paper, by improving the foaming method, the foaming process is placed in the limited space of the ball mill tank, and YSZ porous ceramics with different porosity are obtained by changing the amount of slurry. Initial results showed that the porosity of the sample varies linearly with the increasing of addition of slurry. From the microscopic morphology, it can be seen that the increase in slurry content will reduce the number of pore with little changed size, which lead to the decrease in porosity. Therefore, with simple calculation YSZ porous ceramics with 85%, 80%, 75%, 70%, and 65% porosity can be obtained using the method of foaming in limited space by ball milling.     

Effect of antimicrobial packaging on physicochemical and microbial quality of chicken drumsticks

The effects of antimicrobial agents (nisin, chitosan, potassium sorbate (PS) or silver substituted zeolite (AgZeo)) incorporated into low density polyethylene (LDPE) on the physicochemical and microbial quality of chicken drumsticks stored at 5 °C for 6 days were investigated. Active multilayer bags (LDPE/polyamide/LDPE-containing 2% antimicrobial agent) were used to pack chicken drumsticks under vacuum. Their efficiency in inhibiting total aerobic mesophilic bacteria (APC), total coliforms and total molds and yeasts were evaluated by comparison with control bag (LDPE-polyamide-LDPE). APC counts of samples packed in bags containing chitosan, nisin, AgZeo and PS were 1.03, 0.98, 0.51, and 0.17 log respectively were lower than those of samples packed in control bags. Samples packaged in active bags had lower microbial counts and thiobarbituric acid reactive substance (TBARS) values than those of samples packed in control bags. The pH, color and hardness of the samples were not affected significantly by use of different packaging films (p > 0.05). Therefore, the bag including chitosan or nisin can be suggested as a suitable packaging material for chicken drumstick to increase safety and quality.