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61.
纤维复合材料已经研究了数十年了。他们有着比传统材料,如钢材,优秀的多的力学性能。然而,由于相对较低的产量,梭织、编织与其3D纤维结构的复合材料被认为较难大量生产。因此,近年来,针织物在复合材料界获得了较高的关注,它的高度可塑性使针织复合材料可以直接生产制造成各种复杂形状的复合材料如管状、圆锥型等,使得材料的浪费可以降到了最低。本文使用了有表面处理和没有表面处理的纬编平针碳纤维制成复合材料。对两种复合材料的经向和纬向分别做了拉伸试验。结果显示:有表面处理的材料具有更好的拉伸性能,尤其是在wale方向上,有表面处理的复合材料比没有表面处理的复合材料的拉伸强度提高75.68%。  相似文献   
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63.
Malaysian kenaf bast fiber was treated by acidic chlorite to be applied for a trunk polymer radiation‐induced graft copolymerization. The delignification conditions such as temperature, reaction time, and sodium chlorite (NaClO2) loading were optimized from the viewpoints of density, tensile strength, and reactivity of grafting. It was found that delignification condition at 80°C for 6 h with 0.5% NaClO2 gave 91% of lignin removal from the kenaf bast fibers. In this case, the density, fineness, and tensile strength of the kenaf fiber decreased about 46, 44, and 87%, respectively. Reactivity of grafting was evaluated using 4‐chloromethyl styrene to obtain widely available precursor materials. The partial delignified kenaf with residual lignin less than 2% resulted in degree of grafting of 134%, which is enough for precursor materials. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013  相似文献   
64.
Abstract

A method for low-temperature drying with high drying rate was developed for heat-sensitive foods and agricultural products. A freezing pretreatment was combined with fluidized bed drying under reduced pressure. Cylindrical carrot samples were frozen and then placed without thawing in a fluidized bed of hygroscopic porous silica gel particles that adsorbed water from the sample during the drying process. The effects of the freezing pretreatment and hygroscopicity of fluidizing particles on the drying characteristics of carrots were examined. A higher drying rate was achieved when carrots samples were subjected to freezing pretreatment than without it. At 12?kPa, the volume change was smaller in carrots subjected to freezing pretreatment than in untreated samples. A larger amount of water was absorbed during rehydration by carrots dried at 12?kPa than at 101?kPa within 120?min. The properties of dried carrots were affected not only by freezing pretreatment but also by the pressure applied during the drying process.  相似文献   
65.
Abstract

Extraction of Eu(III) and Am(III) from HNO3 into the organic solvents using N,N,N′,N′‐tetraoctyl‐diglycolamide (TODGA) was investigated in order to study the detailed extraction reaction. The chemical species: 1:2 for metal:TODGA complex is present in polar diluents. On the other hand, the metal complexes need three or more TODGA molecules to remain stable in non‐polar diluents. The HNO3 concentration dependence on the distribution ratio suggests that HNO3 participates in the metal extraction. Infrared spectra indicate that the carbonyl oxygen coordinates with Eu(III), and luminescence lifetimes suggest that there are no water molecules in the inner coordination sphere of the extracted Eu‐complex.  相似文献   
66.
Acid oil is a by-product in the neutralization step of vegetable oil refining and is an alternative source of biodiesel fuel. A model substrate of acid oil, which is composed of TAG and FFA, was used in experiments on the conversion to FAME by immobilized Candida antarctica lipase. FFA in the mixture of TAG/FFA were efficiently esterified with methanol (MeOH), but the water generated by the esterification significantly inhibited methanolysis of TAG. We thus attempted to convert a mixture of TAG/FFA to FAME by a two-step process comprising methyl esterification of FFA and methanolysis of TAG by immobilized C. antarctica lipase. The first reaction was conducted at 30°C in a mixture of TAG/FFA (1∶1, wt/wt) and 10 wt% MeOH using 0.5 wt% immobilized lipase, resulting in efficient esterification of FFA. The reaction mixture after 24 h was composed of 49.1 wt% TAG, 1.3 wt% FFA, 49.1 wt% FAME, and negligible amounts of DAG and MAG (<0.5 wt%). The reaction mixture was then dehydrated and used as a substrate for the second reaction, which was conducted at 30°C in a solution of the dehydrated mixture and 5.5 wt% MeOH using 6 wt% immobilized lipase. The activity of the lipase increased gradually when the reaction was repeated by transferring the enzyme to a fresh substrate mixture. The activity reached a maximum after 6 cycles, and the content of FAME achieved was >98.5 wt% after a 24-h reaction. The immobilized lipase was very stable in the first-and second-step reactions and could be used for >100 d without significant loss of activity.  相似文献   
67.
This study aimed to optimize the ratio of dioctyl 4‐cyclohexene‐1,2‐dicarboxylate (DOTH) and di‐isononyl‐cyclohexane‐1,2‐dicarboxylate (DINCH®) for use as plasticizers in poly(vinyl chloride) (PVC) sheets. We also evaluated the biological safety of DOTH for its potential to be part of a safe PVC‐based blood container. The suppression of hemolysis in mannitol‐adenine‐phosphate / red cell concentrates (MAP/RCC) with DOTH/(DINCH®‐PVC) sheets and the elution of plasticizers from the sheets increased with higher DOTH compositions. The properties of the PVC sheet containing DOTH and DINCH® in the ratio of 25:33 parts against PVC 100 parts as a weight were almost identical to the PVC sheet made of di(2‐ethylhexyl) phthalate. From a subchronic toxicity test, DOTH did not show any adverse effects on all organs, including the testes, epididymis, liver, and kidneys. The no‐observed‐adverse‐effect level was 300 mg/kg body weight/day in a rat. These results suggest that DOTH/DINCH® (25:33) is a promising candidate for the replacement of di(2‐ethylhexyl) phthalate in blood containers. J. VINYL ADDIT. TECHNOL., 22:520–528, 2016. © 2015 Society of Plastics Engineers  相似文献   
68.
Porous alumina with a highly textured microstructure was fabricated by pulse electric current sintering (PECS) using alumina platelets. Highly oriented porous alumina with a porosity of 3%–50% was obtained by a pressure-controlled method of PECS. The properties of the highly textured porous alumina were measured in two directions. The nitrogen gas permeance and thermal conductivity at room temperature were higher in the direction along the platelet length due to the higher continuity of pores and the connectivity of alumina platelets, respectively. The anisotropy of the thermal conductivity at room temperature was investigated and explained by the effect of grain size of platelets as well as morphology and orientation of pores. The bending strength was higher with the loading direction along the platelet thickness. The thermal shock strength was clearly different in the two directions. The difference in the thermal shock strength was investigated by the measurement of properties and thermal stress analysis.  相似文献   
69.
To understand the adsorption properties of a styrene–divinylbenzene copolymer functionalized with N,N,N-trimethylglycine, AMP03, the adsorption behaviours for platinoid ions (Ru(III), Rh(III) and Pd(II)) were examined. Furthermore, we performed adsorption experiments using sample solutions by adding triethylamine, thiourea and N,N,N-trimethylglycine. Based on the adsorption data obtained in this study, we performed chromatographic experiments. The results indicated that all platinoid ions in the feed solution completely adsorbed on AMP03, and almost 80% of the adsorbed platinoid ions were recovered. These results show that AMP03 has the potential to recover Ru(III), Rh(III) and Pd(II) from high-level liquid waste.  相似文献   
70.
A straightforward method, which is termed novel handspinning, is reported for producing uniaxially aligned sPP nanofibers. As demonstrated by SEM analysis, the morphologies of handspun sPP nanofibers are strongly dependent upon the processing conditions such as spinning method and solvent system. Compared to the normal electrospun sPP nanofibers, the handspun sPP nanofibers show smoother morphologies. FT‐IR analysis demonstrates a significant difference in polymer chain conformation between the handspun and electrospun sPP nanofibers. Moreover, interestingly, the handspun sPP single nanofibers show higher Young's modulus and tensile strength than electrospun sPP single nanofibers.

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