废聚丙烯/废轮胎胶粉/废尼龙短纤维复合材料 Ⅰ.配方

用双螺杆挤出机制备了废聚丙烯/废轮胎胶粉/废尼龙短纤维(WPP/GRT/WSF)复合材料,通过正交实验得出了制备该复合材料的最佳配方,讨论了增容剂用量、氯化聚丙烯的含氯质量分数、GRT用量及其粒径、WSF用量及预处理对该复合材料力学性能的影响。结果表明,制备该复合材料的最佳配方(质量份,下同)是WPP100,GRT30,WSF8,二甲基二硫代氨基甲酸锌、二硫化二苯并噻唑、多乙烯多胺及重油用量依次为0.6,1.2,0.3,2,聚丙烯接枝马来酸酐、氯化聚丙烯用量依次为8,4;在最佳配方下,该复合材料的非缺口冲击强度为25.2kJ/m2,拉伸强度为13.6MPa;GRT用量为30份时,该复合材料的拉伸强度和非缺口冲击强度最大,GRT的最佳粒径为40目;WSF经D法预处理后,提高了该复合材料的力学性能,拉伸强度为16.3MPa,非缺口冲击强度为27.8kJ/m2。     

废聚丙烯/废轮胎胶粉/废尼龙短纤维复合材料Ⅱ.工艺条件

采用反应挤出方法制备了废聚丙烯／废轮胎胶粉／废尼龙短纤维(WPP／GRT／WSF)复合材料,讨论了螺杆转速、机头温度对WPP／GRT／WSF复合材料力学性能的影响。结果表明,当螺杆转速为15r／min,机头温度为185～195℃时,WPP／GRT／WSF复合材料的力学性能达到最佳,拉伸强度为13．6MPa,冲击强度为25．2kJ／m^2。按照最佳配方和工艺挤出管材的拉伸强度为4,6MPa,冲击强度为5．4kJ／m^2,爆破压力为0．69MPa。     

废PCB粉增强聚丙烯复合材料的力学性能

以废印刷电路板非金属粉(废PCB粉)为填料,采用熔融共混法制备了聚丙烯基复合材料,通过力学性能试验和冲击断面的微观形貌观察,研究了废PCB粉粒径、含量及改性剂PP-g-MAH对复合材料力学性能的影响。结果表明:细粒径的废PCB粉填充效果优于粗粒径粉;废PCB粉含量对复合材料力学性能影响较大,除弯曲强度外,复合材料的拉伸强度、无缺口冲击强度均随废PCB粉含量的增加呈降低趋势;PP-g-MAH接枝物能显著增强废PCB粉与PP的界面结合力,提高复合材料的力学性能,当废PCB粉粒径为150μm,填充质量分数为40%,PP-g-MAH加入量为4%时,复合材料的综合力学性能最佳。     

橡胶再生剂De-link在废轮胎胶粉增韧废PP复合材料中的应用研究

为了改善废轮胎胶粉（GRT）增韧废PP复合材料的力学性能,用橡胶再生剂De-link对废胶粉进行改性再生。结果表明,加入3份再生剂De-link,可使废PP／GRT复合材料的冲击强度和拉伸强度有很大的提高;复合材料的冲击断面扫描电镜分析显示,经再生剂改性后复合材料的分散相尺寸明显减小,相容性显提高。     

胶粉/LLDPE弹性体合金的研制

系统研究了废胶粉（GRT）／线型低密度聚乙烯（LLDPE）弹性体合金（GRT／LLDPE）的配方，以及粒径，GRT含量，相容剂和硫化剂（DCP）用量对共混物力学性能的影响，结果表明，采用两阶共混法，当GRT／LLDPE共混比为：60：40，DCP用量为2份，相容剂马来酸酐三单体接枝物用量为3－5份时，所得弹性体合金力学性能最佳，弹性体合金的拉伸强度从简单共混物的5．8Mpa上升到11．1MPa，撕裂强度从39．4kN/m，上升到63．4kN/m，断裂伸长率从180％增加到260％。     

马来酸酐接枝天然橡胶在废报纸粉填充聚氯乙烯材料中的应用

研究了马来酸酐接枝天然橡胶（MNR）作为改性剂，对废报纸粉（PF）填充聚氯乙烯（PVC）复合材料的力学性能和热学性能的影响。研究结果表明，MNR可以较好地改善PF与PVC基体的相容性，显著提高材料的冲击强度。当PF用量（质量份）为5份、MNR为4份时PF／PVC复合材料的综合性能最好，其拉伸强度为48．8MPa，缺口冲击强度达10．1kJ／m^2，后者比改性前提高了87％。热重分析表明：PF／MNR／PVC复合材料的耐热性比纯PVC树脂有所提高。而PF／PVC复合材料的维卡软化温度随着PF填充量的增加而提高，但随着MNR的增加而略有降低。冲击断面扫描电镜分析证实MNR改善了报纸粉与基体树脂的相容性。     

废胶粉填充改性PP复合材料

采用熔融挤出共混的方法,选用三种废胶粉填充聚丙烯(PP),制备了PP/废胶粉复合材料,研究了废胶粉质量分数对复合材料力学性能的影响.结果表明:废旧三元乙丙橡胶粉可明显提高复合材料冲击强度和拉伸断裂应变,当其质量分数为60%时,简支梁缺口冲击强度可提高33%,拉伸断裂应变增大了26%,有显著的增韧效果:废旧杂胶粉的加入使...     

废纸浆/ABS复合材料的性能研究

研究了废纸浆、马来酸酐接枝苯乙烯-乙烯/丁烯-苯乙烯(SEBS-g-MAH)用量以及发泡对废纸浆/丙烯腈-丁二烯-苯乙烯(ABS)复合材料的力学性能和吸水率的影响;通过扫描电镜SEM分析了SEBS-g-MAH对未发泡和发泡废纸浆/ABS复合材料的增容效果.结果表明:废纸浆用量为30份和SEBS-g-MAH用量为20份时,未发泡和发泡复合材料的拉伸性能和缺口冲击强度都达到最佳;吸水率随纸浆用量的增加而增加,SEBS-g-MAH用量为20份时,未发泡和发泡材料吸水率都达到最低.发泡后的复合材料的拉伸强度降低,冲击性能和吸水率升高.SEBS-g-MAH能有效地改善ABS和纸浆的界面相容性.     

mPE-g-MAH对HDPE/木粉复合材料的改性

采用废木粉填充高密度聚乙烯（HDPE）制备木塑复合材料。采用马来酸酐接枝茂金属聚乙烯（mPE—g-MAH）对复合材料进行增容和增韧，并阐述了它的增容和增韧机理。讨论了mPE—g—MAH用量对复合材料的力学性能如拉伸强度、冲击强度、弯曲强度、弯曲模量的影响。结果表明，mPE—g—MAH不仅可明显提高复合材料的强度和韧性，而且也使材料的弯曲模量有了一定的提高。当其质量分数为16％时，复合材料的拉伸强度、冲击强度分别由原来的16．2MPa和4．5kJ／m^2提高到30．5MPa和9．8kJ／m^2。     

橡胶再生剂De-link在废轮胎胶粉增韧废PP复合材料中的应用研究

为了改善废轮胎胶粉(GRT)增韧废PP复合材料的力学性,用橡胶再生剂De-link对废胶粉进行改性再生.结果表明,加入3份再生剂De-link,可使废PP/GRT复合材料的冲击强度和拉伸强度有很大的提高;复合材料的冲击断面扫描电镜分析显示,经再生剂改性后复合材料的分散相尺寸明显减小,相容性显著提高.     

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.     

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.     

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.     

Synthesis and Characterization of Ti0.33Ta0.33Nb0.33C and Ti0.33Ta0.33Nb0.33CxN1-x Whiskers

Ta_0.33Ti_0.33Nb_0.33C and Ta_0.33Ti_0.33Nb_0.33C _x N_{1− x} whiskers were synthesized via a carbothermal vapor-liquid-solid growth mechanism in the temperature range 900°-1450°C in Ar or N₂. The optimum temperature was 1250°C. Whiskers were obtained in a yield of 70-90 vol%. The whiskers were 0.5–1 µm in diameter and 10–30 µm in length. The starting materials that produced the highest whisker yield were: TiO₂, Ta₂O₅, Nb₂O₅, C, Ni, and NaCl. C was added to reduce the oxides, and Ni to catalyze whisker growth. NaCl was used as a source of Cl for vapor-phase transportation of Ta and Nb oxochlorides and Ti chlorides to the catalyst. The catalyst metal was recycled several times during the synthesis and was transported as NiCl₂( g ) according to thermodynamic calculations. The rate of formation and the chemical composition of the whiskers depended on the synthesis temperature, the choice of catalyst, and the atmosphere. At low temperatures, the whiskers were enriched in Nb and Ta, whereas the Ti content increased with increased synthesis temperature.