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61.
本文对模拟的含酚废水,采用新型技术对乳状液膜法脱酚进行了进一步的探讨。对所采用的制乳设备———撞击流-旋转填料床对制乳率、提取设备———旋转填料床对脱酚率、破乳设备———无机微孔膜法破乳的重要参数(如透过压方式、膜孔径等对膜通量和破乳率的影响)进行了研究。并且讨论了破乳后的油相回用情况。实验结果表明:撞击流-旋转填料床的制乳效率可达99.90 %以上,脱酚率可达99%左右,且瞬间完成;膜孔径越小,破乳率越高,膜通量越小;外压内抽方式的破乳效果优于单外压方式的破乳效果。对于粒径为5~2 5 μm乳液,用膜孔径为2 .0 μm的SiC微孔膜,在外压为6 0kPa、内负压为30kPa的外压内抽破乳方式下破乳,破乳率可达96 .4 % ,膜通量可达90 0L·(m2 ·h) -1。 相似文献
62.
无机颗粒增强聚乳酸复合材料能有效的改善聚乳酸的力学性能,并赋予其生物活性。本文系统介绍了各种无机颗粒增强聚乳酸复合材料的制备方法,并对其优劣性进行了初步探讨。 相似文献
63.
64.
The viscoelastic and peeling properties of polybutadiene/tackifying resin compatible blends have been studied in detail. Viscoelastic properties have been described through the variations of the complex shear modulus, G*(ω), as a function of frequency, ω and peeling properties through the variations of peeling force (F) as a function of peeling rate (V).
After showing the objective character of the peeling curves obtained, the variations of the peeling force and peeling geometry have been studied as a function of volume fraction of the tackifying resin.
In this first paper, the analysis is focused on the first domain of the peeling curves, i.e. the cohesive fracture region. In this region, the peeling properties have been related to the viscoelastic properties in the terminal region of relaxation. It is shown that the longest relaxation time, τo, is a reducing parameter of the peeling curves, so a peeling master curve-which is independent of temperature, resin volume fraction and polymer molecular weight-may be defined. Furthermore, the variations of the test geometry as a function of peeling rate have been investigated: the variations of the radius of curvature of the aluminium foil have been analyzed with respect to the viscoelastic behavior of the adhesive, which in fact governs the test geometry.
A detailed analysis of all these features leads to a model which allows one to calculate the peeling curves in the cohesive domain from the adhesive formulation. 相似文献
After showing the objective character of the peeling curves obtained, the variations of the peeling force and peeling geometry have been studied as a function of volume fraction of the tackifying resin.
In this first paper, the analysis is focused on the first domain of the peeling curves, i.e. the cohesive fracture region. In this region, the peeling properties have been related to the viscoelastic properties in the terminal region of relaxation. It is shown that the longest relaxation time, τo, is a reducing parameter of the peeling curves, so a peeling master curve-which is independent of temperature, resin volume fraction and polymer molecular weight-may be defined. Furthermore, the variations of the test geometry as a function of peeling rate have been investigated: the variations of the radius of curvature of the aluminium foil have been analyzed with respect to the viscoelastic behavior of the adhesive, which in fact governs the test geometry.
A detailed analysis of all these features leads to a model which allows one to calculate the peeling curves in the cohesive domain from the adhesive formulation. 相似文献
65.
Shear creep resistance of styrene–isoprene–styrene (SIS)‐based hot‐melt pressure‐sensitive adhesives
The effects of the properties of substrates and tackifier on the shear creep of SIS‐based HMPSAs were investigated. The holding power (tb) and shear adhesion failure temperature (SAFT) were measured. The relationship between the complex viscosity and the holding power was examined. The holding power and SAFT values of the triblock SIS blends were higher than those of the diblock‐containing SIS blends, perhaps because blends using triblock SIS have higher crossover temperature and complex viscosity than those using diblock‐containing SIS. Higher levels of aromatic resin‐modified aliphatic tackifier and rosin ester were found to decrease the holding power of the HMPSAs. This maybe due to the fact that rosin ester and aromatic‐modified aliphatic resin are compatible with both the ends and midblocks of SIS. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 825–831, 2006 相似文献
66.
The demand for ultraviolet (UV)‐crosslinkable pressure‐sensitive adhesives (PSAs) has rapidly been increasing. A variety of different PSAs containing new photoreactive pyridinium derivatives have been evaluated for their effectiveness in improving adhesion and cohesion in UV‐crosslinkable PSAs. PSAs have been evaluated with respect to the tack, peel adhesion, and shear strength. This article summarizes the breakthrough technology used to achieve better performances in UV‐crosslinkable acrylic PSAs. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2007 相似文献
67.
研究了HF +HCl消解样品 ,试液用ICP -AES法同时测定TAM胶粘剂中铅、镉、汞、铬、砷的新方法。在选定的最佳条件下测铅、镉、汞、铬、砷的检出限分别为 0 .0 0 15、0 .0 0 0 8、0 .0 0 11、0 .0 0 17、0 .0 0 0 9μg·L- 1 ,回收率为 93 .5 %~ 10 8.3 % ,RSD为 0 .62 %~ 5 .65 %。该法准确、快速、简便 ,应用于TAM胶粘剂的测定 ,结果满意 相似文献
68.
69.
在太阳能热发电技术中,硝酸盐类相变材料是使用最多的一种相变材料,但其最高使用温度仅为600 ℃,因此找到一种热容量大、工作温度范围宽、热损失低、价格便宜的相变储热材料是目前的研究重点。选取氯化锂和氯化钠两种高温熔盐相变材料按照不同的质量比混合制备了9种二元熔盐混合物,利用差式扫描量热仪(DSC)对其在600 ℃范围内的相变温度和相变潜热进行了研究。实验结果显示:由于氯化钠的熔点较高,当氯化锂和氯化钠的二元混合物中氯化钠的含量较多时,即氯化锂的含量较少时,少量的氯化锂不能将混合物的熔点降低至600 ℃以下,混合材料无法熔化;当氯化钠和氯化锂发生熔融时,无论何种比例其相变温度均保持在540 ℃左右,浮动±15 ℃;以质量配比为90%氯化锂-10%氯化钠的二元混合物的熔融温度与结晶温度相差较大,所以该二元混合熔盐可以应用于太阳能发电的传热和蓄热技术中。 相似文献
70.
Sung‐Jun Cho 《应用聚合物科学杂志》2003,88(8):1904-1910
The polymerization of ?‐caprolactam between the interlamellar spaces of the [TEACOOH]–montmorillonite intercalations complex was attempted using Na–montmorillonite and 10‐carboxy‐n‐decyltriethylammonium bromide to achieve [TEACOOH]–polycaprolactam–montmorillonite, in which montmorillonite (inorganic polymer) is chemically bonded with the polycaprolactam (organic polymer). The results of X‐ray and IR analysis for the samples obtained after polymerization showed that the polymerization reaction has been successfully accomplished. For the purpose of studying the polymeric reaction product more precisely, we have isolated the polymerized product from the silicate layers and analyzed it with X‐ray diffractometer and IR spectrometer. Comparison of the results of X‐ray and IR analysis between the isolated polymer and the polymer that was synthesized by the reaction of ?‐caprolactam only with the organic cation without montmorillonite showed that both obtained polymers are the same compounds. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 88: 1904–1910, 2003 相似文献