纳米凹凸棒土/炭黑复合填料对天然橡胶/丁苯橡胶/顺丁橡胶并用胶性能的影响

研究纳米凹凸棒土/炭黑N770/炭黑N330复合填料中纳米凹凸棒土/炭黑N770用量比对天然橡胶(NR)/丁苯橡胶(SBR)/顺丁橡胶(BR)并用胶性能的影响。结果表明:采用纳米凹凸棒土/炭黑N770/炭黑N330复合填料时,随着凹凸棒土用量增大,并用胶的F_L和F_(max)增大,硫化速度减慢,物理性能、耐磨性能和耐屈挠性能提高;纳米凹凸棒土/炭黑N770用量比为30/15时,并用胶的综合性能较优异。与添加其他无机填料(陶土、轻质碳酸钙和白炭黑)/炭黑复合填料的并用胶相比,添加纳米凹凸棒土/炭黑复合填料的并用胶拉伸强度和撕裂强度较高,耐屈挠性能较好,耐磨性能稍差。     

丁苯橡胶／蒙脱土纳米复合材料在半钢子午线轮胎胎面胶中的应用

对在中试装置上制备的丁苯橡胶（SBR）／蒙脱土（MMT）纳米复合材料——乳液共沉胶在半钢子午线轮胎胎面胶中的应用进行研究。结果表明,SBR／MMT乳液共沉胶是一种插层型纳米复合材料;与SBR纯胶相比,其拉伸强度、撕裂强度、回弹性等相当,耐磨性能大幅度提高,可以替代SBR及部分炭黑用于半钢子午线轮胎胎面胶中。     

SBR/有机蒙脱土纳米复合材料的结构与性能研究

通过控制加入芳烃油、相容剂，采用乳液插层法制得了2种不同亚微观结构的SBR／有机蒙脱土（0MMT）纳米复合材料。透射电镜显示制得了插层型和半剥离型纳米复合材料。实验结果表明：炭黑N330的加入，降低了复合材料的延迟硫化现象，改善了复合材料的加工性能；SBR／OMMT／N330纳米复合材料具有优异的力学性能，其耐磨性能下降。     

天然橡胶/丁苯橡胶/反式丁戊橡胶并用胶的性能研究

研究反式丁戊橡胶（TBIR）对天然橡胶（NR）/丁苯橡胶（SBR）并用胶性能的影响。结果表明：用15份TBIR替代NR,NR/SBR/TBIR并用胶的NR与SBR相容性改善,拉伸强度和定伸应力略有降低,耐磨性能、耐压缩疲劳性能和耐屈挠疲劳性能提高;用15份TBIR替代SBR,NR/SBR/TBIR并用胶的NR与SBR相容性明显改善,拉伸性能变化不大,耐磨性能、耐压缩疲劳性能和耐屈挠疲劳性能提高;用15份TBIR替代NR/SBR并用胶,NR/SBR/TBIR并用胶的大部分性能介于TBIR单独替代NR与SBR并用胶的性能之间,抗湿滑性能提高,滚动阻力降低;在NR/SBR并用胶中直接加入6份TBIR,NR/SBR/TBIR并用胶的NR与SBR相容性改善,耐磨性能、耐压缩疲劳性能和耐屈挠疲劳性能提高,抗湿滑性能和滚动阻力降低。     

蒙脱土/SBR纳米复合材料在轮胎内胎中的应用

试验研究蒙脱土（MMT）用量和加工助剂种类对MMT／SBR纳米复合材料性能的影响，探讨MMT／SBR纳米复合材料用于制备轮胎内胎的可行性。结果表明，加入2份三乙醇胺、MMT用量为20份的MMT／SBR纳米复合材料的加工性能和物理性能与工厂内胎胶差别不大，耐热老化性能和气体阻隔性较好，可用于制备轮胎内胎。     

炭黑/黏土/丁苯橡胶纳米复合材料的性能

研究了用1份(质量,下同)或2份黏土替代5份或10份炭黑对炭黑/黏土/丁苯橡胶纳米复合材料性能的影响。结果表明,用少量黏土非等量替代炭黑后,复合材料的物理机械性能变化不大;复合材料的耐磨性能随炭黑用量的减少而降低,耐屈挠疲劳性能随黏土用量增加而提高。当炭黑与黏土的填充量分别为45份和2份时,复合材料的物理机械性能和动态生热与填充50份炭黑时相当。     

乳液插层法制备丁苯橡胶/天然橡胶/蒙脱土纳米复合材料的研究

采用乳液插层法制备了丁苯橡胶/天然橡胶/蒙脱土（SBR/NR/MMT）纳米复合材料。采用透射电子显微镜研究了复合材料的亚微观形态,并对复合材料的性能进行了研究。透射电镜结果显示,制备出了插层型的SBR/NR/MMT复合材料。当蒙脱土含量较低时,SBR/NR/MMT纳米复合材料的力学性能随蒙脱土用量的增加而增大。SBR/NR/MMT复合材料的耐油性能随蒙脱土含量的增加而提高。蒙脱土的加入对纳米复合材料的耐磨性能没有太大影响。     

粘土/淀粉/炭黑/SBR复合材料的制备与性能研究

以少量淀粉和粘土等量替代炭黑,制备粘土/淀粉/炭黑/SBR复合材料,并对其性能进行研究。结果表明:与炭黑/SBR复合材料相比,淀粉/炭黑/SBR复合材料撕裂强度和抗湿滑性能提高,伸张疲劳次数增多,定伸应力和耐磨性能大幅下降,且压缩温升增大;与淀粉/炭黑/SBR复合材料相比,粘土/淀粉/炭黑/SBR复合材料定伸应力和耐磨性能提高,压缩生热降低且抗湿滑性能较好。     

用防老剂及并用防老剂提高轮胎胶料的耐屈挠疲劳和动态臭氧龟裂性能(续完)

(接上期) 3 用各种类型防老剂及其并用物改善NR/BR炭黑胎侧胶料动态屈挠及耐动态臭氧龟裂性能的评价 3.1 胎侧胶 典型的胎侧胶不是使用NR/BR,就是使用NR/BR/SBR,以改善耐割口增长、耐磨耗以及动态屈挠性能.胎侧暴露于外部环境中,因此需要进行防臭氧或氧化龟裂的保护.通常使用2.5～4.0份的烷基芳基对苯二胺,如6PPD或IPPD与混合蜡结合,用于静态和动态耐臭氧龟裂防护以及改善耐屈挠疲劳性能.此外,NR和顺式BR滞后损失小,行驶温度低,这种较低的行驶温度又可以改善屈挠疲劳性能.     

硅烷偶联剂KH-550对纳米晶纤维素/炭黑/天然橡胶复合材料性能的影响

试验研究硅烷偶联剂KH-550对纳米晶纤维素/炭黑/天然橡胶复合材料性能的影响。结果表明:加入硅烷偶联剂KH-550后,混炼胶的粘性模量和损耗因子减小,硫化胶的硬度和300%定伸应力增大,拉断永久变形减小,耐磨性能提高;当硅烷偶联剂KH-550用量为1~2份时,混炼胶的硫化特性和加工性能,硫化胶的交联密度、耐屈挠性能、压缩疲劳性能和耐磨性能明显改善。     

Wet Milling of Fe/Al/Al2O3 and Fe2O3/Al/Al2O3 Powder Mixtures

Wet milling of Al₂O₃-aluminide alloy (3A) precursor powders in acetone has been investigated by milling Fe/Al/Al₂O₃ and Fe₂O₃/Al/Al₂O₃ powder mixtures. The influence of the milling process on the physical and chemical properties of the milled powders has been studied. Particle refinement and homogenization were found not to play a dominant role, whereas plastic deformation of the metal particles leads to the formation of dislocations and a highly disarranged polycrystalline structure. Although no chemical reactions among the powder components in Fe₂O₃/Al/Al₂O₃ powder mixtures were observed, the formation of a nanocrystalline, ordered intermetallic FeAl phase in Fe/Al/Al₂O₃ powder mixtures caused by mechanical alloying was detected. Chemical reactions of Fe and Al particle surfaces with the atmosphere and the milling media lead to the formation of highly porous hydroxides on the particle surfaces. Hence the specific surface area of the powders increases, while the powder density decreases during milling. The fraction of Fe oxidized during milling was determined to be 0.13. The fraction of Al oxidized during milling strongly depends on the metal content of the powder mixture. It ranges between 0.4 and 0.8.     

Preparation and properties of poly(Nε,Nε-dicarboxymethyl-l-lysine)

A new ampholytic homopolypeptide, $\text{poly}\text{(N}{}^{\mathrm{\epsilon }}\text{,N}{}^{\mathrm{\epsilon }}\text{-}\text{dicarboxy-methyl-}\text{l}\text{-lysine}\text{)}$, which has one tertiary amino and two carboxyl groups in the side chain has been derived from a hydrochloride salt of poly(L-lysine). The polymer in aqueous solution seems to be in the coil form with locally extended structure (LES) at neutral pH. In both the acidic and alkaline regions, the molar ellipticity of the polymer changes as a result of change in net charge on the side chain. The conformational changes may be from the coil with LES to other coiled forms. 5–7 M NaClO₄ and 80% aqueous methanol induce the α-helix in the polymer at neutral pH. Divalent cations, Cu²⁺ and Ca²⁺, do not induce any remarkably ordered structures such as α-helix or β-structure in the polymer in aqueous solution at any pH. Ultraviolet absorption studies show an absorption peak of the polymer-Cu²⁺ complex near 240 nm. Dependence of the peak intensity on pH at various q values ($\text{q =}\text{[}\text{Cu}{}^{\mathrm{2+}}\text{]}\text{[}\text{residue}\text{]}$) indicates the two steps of the complex formation. At q less than 0.64, the formation is described only with the first step. An average coordination number for Cu²⁺ at the first step was calculated to be about 2 by the method of Mandel and Leyte. The association constant of Cu²⁺ with the residue at the step was determined from the absorption data to be far smaller than that for the Cu²⁺-EDTA complex. The second step of the formation occurs in the case of large q but the absorption data for the second step cannot be obtained exactly due to precipitation.     

Sintering of Si3N4-Y2O3-Al2O3

Sintering kinetics of the system Si₃N4-Y2O₃-Al₂O3 were determined from measurements of the linear shrinkage of pressed disks sintered isothermally at 1500° to 1700°C. Amorphous and crystalline Si₃N₄ were studied with additions of 4 to 17 wt% Y₂O₃ and 4 wt% A1₂O₃. Sintering occurs by a liquid-phase mechanism in which the kinetics exhibit the three stages predicted by Kingery's model. However, the rates during the second stage of the process are higher for all compositions than predicted by the model. X-ray data show the presence of several transient phases which, with sufficient heating, disappear leaving mixtures of β ' -Si₃N₄ and glass or β '-Si₃N₄, α '-Si₃N₄, and glass. The compositions and amounts of the residual glassy phases are estimated.     

Participation of lewis base on vinyl chloride polymerization with Al(C2H5)3CCl4 catalyst system

The polymerization of vinyl chloride has been investigated using an $\text{Al}\text{(}\text{C}{}_2\text{H}{}_5\text{)}{}_3\text{CCl}{}_4$ catalyst system in the presence of various Lewis bases. Effective Lewis bases are γ-butyrolactone, diglyme and diethylenetriamine which are multidentate. The rate of polymerization is dependent not only on the basicity of the Lewis base used but also on a coordination number of one. The latter is the predominant factor. For the effect of polymeric amines, a tentative hypothesis is discussed.     

The System Si3N4-SiO2-Y2O3

Subsolidus phase relations were established in the system Si₃N₄-SiO₂-Y₂O₃. Four ternary compounds were confirmed, with compositions of Y₄Si₂O₇N₂, Y₂Si₃O₃N₄, YSiO₂N, and Y₁₀(SiO₄)₆N₂. The eutectic in the triangle Si₃N₄-Y₂Si₂O₇-Y₁₀(SiO₄)₆N₂ melts at 1500°C and that in the triangle Si₂N₂O-SiO₂-Y₂Si₂O₇ at 1550°C. The eutectic temperature of the Si₃N₄-Y₂Si₂O₇ join was ∼ 1520°C.     

Phase Relations in the Pseudobinary System Na2TiSi4O11-Na2Ti2Si2O9

The quenching technique was used to study subliquidus and subsolidus phase relations in the pseudobinary system Na₂ Ti₂Si₂ O₁₁-Na₂ Ti₂ Si₂ O₉. Both narsarukite (Na₂TiSi₄O₁₁) and lorenzenite (Na₂Ti₂Si₂O₉) melt incongruently. Narsarsukite melts at 911°±°C to SiO₂+liquid, with the liquidus at 1016°C. Lorenzenite melts at 910°±5°C to Na₂ Ti₆ O₁₃+liquid; Na₂ Ti₆ O₁₃ reacts with liquid to form TiO₂ and is thus consumed by 985°±5°C. The liquidus occurs at 1252°C.