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991.
992.
The forces needed to remove irregularly-shaped, 8 μm diameter, polyester particles from a polyester substrate were measured using an ultracentrifuge. Measurements were also made on a second set of similar particles where nanometer-size silica clusters had been placed on their surfaces. These silica clusters acted as spacers, reducing direct contact between the particle and the substrate. It was found that the separation forces for the bare particles were consistent with predictions of the JKR theory of adhesion, but were much larger than could be accounted for from simple electrostatic interactions associated with either uniformly-charged particles or particles with localized charged patches. It was found, however, that the forces needed to effect separation decreased with increasing silica concentration. For particles with 2% by weight silica clusters on their surfaces, the separation force was only about 5% of the separation forces of the bare particles. At this concentration of silica, the estimates of the separation forces obtained from JKR theory, from the uniformly-charged model, and from the localized-charged-patch model are all about equal. The numerical estimates are consistent with the experimentally-obtained values. 相似文献
993.
This study reports a new method of producing high-purity monoacylglycerols (MAGs) by glycerolysis of fully hydrogenated palm oil (FHPO) catalyzed by hydrotalcite loaded with K2CO3 (K2CO3/HT). The effects of reaction temperature, reaction time, catalyst (K2CO3/HT) loading, and mass ratio of FHPO to glycerol on glycerolysis were investigated. The selected conditions included a reaction temperature of 200°C, K2CO3/HT loading at 0.8 wt.% (FHPO mass), a 5:2 mass ratio of FHPO to glycerol, and a reaction time of 2 h. Under these selected conditions, the yield of MAGs in the acylglycerol phase reached 46.8 wt.%. A two-stage molecular distillation was introduced to purify MAGs, and the final MAG product was obtained with a purity of 96.6 wt.% and a recovery of 96.8%. Furthermore, the recycled K2CO3/HT was reactivated with restored catalytic efficiency through impregnation, carbonation, and recalcination. 相似文献
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Abstract In two previous studies, optimal conditions were identified for two‐step steam pretreatment of SO2‐ and H2SO4‐impregnated softwood. In the present study the yield of sugar and ethanol was determined in a process development unit where pretreatment was performed in a 10‐L reactor and simultaneous saccharification and fermentation (SSF) or enzymatic hydrolysis (EH) were performed in 30‐L reactors. The study showed that a steam pretreatment reactor should be larger than 2 L to yield acceptable results. Two pretreatment combinations were studied. In the H2SO4 case, the first pretreatment step was at 180°C for 10 min with 0.5% H2SO4 and the second step at 210°C for 2 min with 1% H2SO4. In the SO2 case, first step was at 190°C for 2 min followed by a second step at 210°C for 5 min. The concentration of SO2 was 3% in both steps. EH and SSF were performed on the whole slurry after the second pretreatment step to determine the yield of sugars and ethanol. The liquid after the first pretreatment step was also analyzed and fermented. When SSF and EH were performed at the same dry matter content and enzymatic activity, the ethanol yield in SSF exceeded the yield obtained with EH in both pretreatment cases, even when 100% yield in the fermentation step was assumed. Thus SSF is a better process if yield is the main priority. Comparison of the yields with the two acid catalysts showed higher yields with SO2 in both SSF and EH. The overall ethanol yield following SSF of SO2‐impregnated and pretreated wood reached 81% of the theoretical, that is, 357 liters per metric ton of dry raw material. 相似文献
997.
Novel, star-shaped multifunctional poly(methyl methacrylate) (PMMA) macromonomers with well-defined average number of pendant methacrylate groups were synthesized by copolymerizing MMA with 2-hydroxyethyl methacrylate (HEMA) via quasiliving ATRP with a tetrafunctional initiator in methanol at 10 °C, followed by methacrylation of the hydroxyl groups of the HEMA units. The resulting tailor-made poly(methyl methacrylate-co-2-methacryloylethyl methacrylate), P(MMA-co-MEMA), multifunctional macromonomers were used as cross-linking agents in photocuring of MMA, a solvent for its own polymer, and thus chemically homogeneous PMMA networks were formed in which the tetrafunctional initiator moiety provides inherent, additional branching points in the resulting cross-linked materials. This approach, even in the presence of relatively low amounts of macromonomers of ∼35–45%, provides sol-free products and up to ∼40% less polymerization shrinkage than that by curing of MMA with a conventional low molecular weight bifunctional methacrylate. These new, unique star-shaped PMMA macromonomers are potential cross-linkers in a variety of solvent-free applications where low curing shrinkage and high conversions are critical requirements, such as in several engineering materials, coatings, dental fillings and restorations, bone cements etc. 相似文献
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