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71.
水煤浆添加剂及其研究进展   总被引:8,自引:0,他引:8  
介绍了水煤浆添加剂结构特征对煤成浆性能影响的研究情况及新型高效添加剂的研究进展。目前制浆添加剂主要分为阴离子表面活性剂和非离子表面活性剂;我国与国外的水煤浆添加剂技术相比,还存在一定的差距,特别是分散降粘性质方面,高效、价廉、适用性广的添加剂为数并不多。  相似文献   
72.
微波烧结Al2O3-TiC复合材料的研究   总被引:4,自引:0,他引:4  
以纳米级TiC、Al2 O3 为原料 ,用微波烧结制备Al2 O3 -TiC复合材料 ,并与常规烧结比较。分析了两种烧结方法对制备试样的力学性能的影响 ,并探讨了添加剂对Al2 O3 -TiC复合材料烧结性能的影响  相似文献   
73.
用硝酸铋分离磷酸根离子,在滤液中用EGTA-EDTA分别测定氧化钙,氧化镁较之传统方法简便效果好。  相似文献   
74.
The rheology of solutions of extracts from the bark of Pinus radiata was investigated in the presence of poly(ethylene glycol)s (PEGs) of different molecular weights. PEG with a molecular weight of 4600 (1% w/w) was sufficient to reduce the viscosity of a concentrated (40% w/w) pine tannin extract by one order of magnitude. The reduction of the viscosity was due to the inhibition of molecular association via hydrogen bonding and hydrophobic interactions between tannin and PEG and depended on the molecular weight of PEG. PEG effectively reduced the viscosity of polyphenolic tannins but retained high reactivity toward paraformaldehyde for adhesive formulations. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 97: 1254–1260, 2005  相似文献   
75.
Poly(vinyl alcohol) (PVA) can be dissolved in a nonaqueous medium in the presence of catalytic concentration of ethyl nitrate dimethyl sulfoxide, C2H5ONO2·DMSO. From the PVA solution, poly(vinyl propionate), PVPR was prepared by the homogeneous esterification of PVA with propionic acid. The ester thus formed contained some unconverted hydroxyl group. The formation of the ester was confirmed by the IR and 1H‐NMR spectra. The molecular weight of the ester was determined by GPC and intrinsic viscosity (η) was determined by viscometric method. Glass transition temperature, Tg, was obtained from differential scanning calorimetric (DSC) analysis. Thermal stabilities of the ester were checked by thermogravimetric analysis (TGA) and differential thermogravimetric (DTG) analysis. The efficiency of the ester as a flow improver of crude oil was also examined. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 5675–5679, 2006  相似文献   
76.
对直接法生产两钠(硝酸钠和业硝酸钠)的工艺过程作了简介,分析了原设计中尾气分离装置存在的缺陷,对尾气分离装髓进行了改造并取得了良好的效果。  相似文献   
77.
李明  刘渭萍  刘刚  孙蕊 《辽宁化工》2004,33(10):593-594
介绍了食品添加剂的定义、分类和作用 ,分析了国内外食品添加剂的现状、发展前景及存在的问题 ,综述了食品添加剂的安全性问题及监督管理办法。  相似文献   
78.
对米糠综合利用的途径进行了详细论述;并总结厂各种米糠精制产品在日用化工、医药工业、食品工业、精细化工领域的具体用途,包括米糠油的浸提技术,米糠油作为营养保健食品的开发利用,米糠油作为油脂化工原材料的深加工;米糠油精炼皂脚中提取游离脂肪酸及脂肪酸衍生物的制备;米糠脱水、脱臭、脱色的小皂化物提取谷甾醇、生育酚、谷维素的方法;米糠脱蜡副产物制备糠蜡和二十烷醇的利用及米糠饼(粕)提取植酸钙、植酸和肌醇的利用途径,最后提出了大力发展我国米糠产业的市场前景。  相似文献   
79.
Graft copolymers were synthesized by graft copolymerization of butyl acrylate (BA) onto sodium salt of partially carboxymethylated starch (Na‐PCMS). Ceric ammonium nitrate (CAN), a redox initiator, was used for initiation of graft copolymerization reaction. All the experiments were run with Na‐PCMS having degree of substitution, DS = 0.35. The grafting reaction was characterized by parameters such as % total conversion (%Ct), % grafting (%G), % grafting efficiency (%GE), and % add‐on. Graft copolymers were characterized by infrared spectral analysis and scanning electron microscopy. Variables affecting graft copolymerization reaction such as nitric acid concentration, reaction time, reaction temperature, and ceric ion concentration were investigated. The results revealed that 0.3M CAN as initiator, 0.3M HNO3, with reaction time 4–4.5 h at 25–30°C were found as suitable parameters for maximum yield of graft copolymerization reaction. © 2006 Wiley Periodicals, Inc. JAppl Polym Sci 102: 3334–3340, 2006  相似文献   
80.
Vinyl ester resin is a major thermoset polymer used in low‐temperature composite manufacturing processes such as the Seemann composite resin infusion‐molding process (SCRIMP). Volume shrinkage and residual styrene are important concerns for composites produced in such processes. A low‐shrinkage additive (LSA) is a typical agent added to control the volume shrinkage of vinyl ester resins during molding. In this study, the effects of LSA content and the temperature profile (the temperature gradient and peak temperature) on the volume shrinkage control of a vinyl ester resin were investigated. The reaction kinetics of the resin system were also studied. We achieved good volume shrinkage control if we raised the curing temperature slowly to allow sufficient time for phase separation and if the curing temperature reached a high value after phase separation to allow microvoid formation. On the basis of experimental results, we designed an improved SCRIMP to increase resin conversion, reduce resin shrinkage, and produce composites with better properties. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 90: 1486–1496, 2003  相似文献   
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