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101.
针对钙镁磷肥生产中高炉探料存在的问题 ,对原自动探料装置的电气控制回路及跟踪装置进行改造 ,增加了探料跟踪最大极限位置 ,获得成功。改造后的自动跟踪探料尺 ,动作准确可靠 ,运行稳定 ,效率高 ,节能降耗 ,直接经济效益每年约 2 5万元 ,提高台时产量间接经济效益每年可达 4 0万元 相似文献
102.
高碱值烷基苯磺酸钙的制备研究 总被引:1,自引:0,他引:1
以烷基苯磺酸、氢氧化钙、氧化钙和二氧化碳为原料,甲苯为溶剂,甲醇为促进剂,制备高碱值烷基苯磺酸钙,考查了原料配比、反应时间等对产品投入产出比和总碱值的影响,结果表明,合成工艺的最佳条件为:氧化钙和氢氧化钙与烷基苯磺酸的摩尔比为2.5∶1,氧化钙和氢氧化钙的摩尔比为1∶10,促进剂甲醇的用量为2.2 mol,中和反应时间为0.5 h,水加入量为8.4 mol,二氧化碳导入速率为100 mL/m in,二氧化碳导入量为1 mol。产品投入产出比大于70,总碱值接近400。 相似文献
103.
Calcium‐containing poly(urethane‐ester)s (PUEs) were prepared by reacting diisocyanate (HMDI or TDI) with a mixture of calcium salt of mono(hydroxybutyl)phthalate [Ca(HBP)2] and hydroxyl‐terminated poly(1,4‐butylene glutarate) [HTPBG1000], using di‐n‐butyltin‐dilaurate as catalyst. About six calcium‐containing PUEs having different composition were synthesized by taking the mole ratio of Ca(HBP)2:HTPBG1000:diisocyanate (HMDI or TDI) as 3:1:4, 2:2:4, and 1:3:4. Two blank PUEs were synthesized by the reaction of HTPBG1000 with diisocyanate (HMDI or TDI). The polymers were characterized by IR, 1H NMR, Solid state 13C‐CP‐MAS NMR, TGA, DSC, XRD, solubility, and viscosity studies. The Tg value of PUEs increases with increase in the calcium content and decreases with increase in soft segment content. The viscosity of the calcium‐containing PUEs increases with increase in the soft segment content and decreases with increase in the calcium content. X‐ray diffraction patterns of the polymers show that the HMDI‐based polymers are partially crystalline and TDI‐based polymers are amorphous in nature. The dynamic mechanical analysis of the calcium‐containing PUEs based on HMDI shows that with increase in the calcium content of polymer, modulus (g′ and g″) increases at any given temperature. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 1720–1727, 2006 相似文献
104.
J. J. Biernacki J. M. Richardson P. E. Stutzman D. P. Bentz 《Journal of the American Ceramic Society》2002,85(9):2261-2267
The reaction between ground granulated blast furnace slag (GGBFS) having an empirical formula of C7.88 S7.39 M3 A and calcium hydroxide (CH) was investigated. The kinetics of the reaction were explored. Thermogravimetric analysis was used to monitor the consumption of CH from which rate constants were determined. Based on Knudsen's kinetic model, activation energies of 14.5, 17.9, and 22.6 kJ/mol were determined for three different mass ratios of slag and CH reacted over a temperature range of 15° to 50°C and hydrated for a period of time from 0 to 32 days. A comparison of the kinetics of the slag/CH reaction was made with slag/portland cement hydration. The basic features of both appear similar. 相似文献
105.
粉煤灰水泥基材料的水化产物 总被引:15,自引:1,他引:15
用热重仪-差示扫描量热仪、扫描电子显微镜、透射电子显微镜、X射线能量散射、高分辩电子显微镜、压汞仪,测定了粉煤灰水泥基材料水化产物的形貌特征、微观结构、化学组成及水泥石的孔结构,讨论了水化产物性质及水泥石孔结构随粉煤灰掺量的变化规律。结果表明:粉煤灰的大量掺加,可以改善凝胶的化学组成。水化后期,粉煤灰与Ca(OH)2及由熟料水化生成的高n(Ca)/n(Si)的水化硅酸钙(C—S—H)凝胶发生二次水化反应,生成低n(Ca)/n(Si)的C—S—H凝胶,此种凝胶的固碱能力强,可减少碱-集料反应的危害性。同时,二次水化产物能够填充那些对水泥石强度和耐久性极为不利的孔隙空洞,使水泥石的结构更加致密,优化水泥石的孔结构,对提高水泥基材料的耐久性作用极大,为进一步提高工业废渣利用的技术水平奠定了基础。 相似文献
106.
Two kinds of CACs with different monocalcium aluminate(CA) contents were used in the PC/CAC(PAC) mixtures. Effects of CA and CACs on the properties of PAC were analyzed by setting times and the compressive strength tests, and also by means of calorimetry, XRD, DTA-TG and ESEM. The experimental results show that the compressive strength of the PAC mortars decreases with increasing content of CAC while it declines sharply with a higher content of CA in CAC. Compared with neat PC paste, the content of calcium hydroxide in hydrates of PAC paste decreases significantly, and the hydration time of PC is prominently prolonged. Additionally, the higher the content of CA in CAC, the more obviously the hydration of PC is delayed, confi rming that the CA phase in CAC plays an important role in the delay of PC hydration. 相似文献
107.
This study aimed to improve the hydraulic potential properties of the slag. Therefore, a method of dynamic hydrothermal synthesis was applied to synthesize calcium silicate hydrate. The phases and nanostructures were characterized by XRD, FTIR, TEM, and BET nitrogen adsorption. The infl uence of alkalinity of steel slag on its structures and properties was discussed. The experimental results show that, the main product is amorphous calcium silicate hydrate gel with fl occulent or fi brous pattern with a BET specifi c surface area up to 77 m2/g and pore volume of 0.34 mL/g. Compared with low alkalinity steel slag, calcium silicate hydrate synthesized from higher alkalinity steel slag is prone to transform to tobermorite structure. 相似文献
108.
采用化学转化处理的方法,在AZ91D镁合金的表面制备了均匀致密的钙系磷化膜,其中磷化液配方中不含铬、氟及亚硝酸盐等对环境有害的离子。通过场发射扫描电子显微镜和X射线衍射仪研究了磷化时间及温度对磷化膜结构和相组成的影响。结果表明:磷化时间为20min,磷化温度为40℃时,所得到的磷化膜的致密性和均匀性较好。与空白基体相比,经磷化处理后的镁合金在3.5%NaCl溶液中的耐腐蚀性能明显提高。 相似文献
109.
In earlier work, we have observed discrepancies relating to the early hydration of calcium aluminate cement (CAC) when comparing data from heat flow calorimetry of CAC paste with results from mortar strength tests using the crushing method. Here, we investigated on this phenomenon and found that the sand which is used as a filler exerts a major influence on CAC hydration resulting in acceleration. Furthermore, in particular fine filler materials such as, for example, microsilica, fine limestone powder, and especially α- and γ-Al2O3 also produced a strong hydration accelerating effect which is dependent on their specific surface area. The mechanism underlying the acceleration is that under alkaline conditions their negative surface charge attracts calcium ions as was confirmed via inductively coupled plasma atomic emission measurements. Such a layer generates favourable conditions for the nucleation of CAC hydration products (C-A-H phases). The resulting crystalline hydrates which form on the surface of the filler particles submerged in CAC cement pore solution were visualized via SEM imaging. This way, specifically selected fillers can significantly accelerate CAC hydration and save precious lithium salts which are commonly used to boost the early strength of CAC. 相似文献
110.
以马来酸酐和二乙二醇醚为原料在无催化剂条件下制得二乙二醇醚马来酸酯(MD),此分子结构中具有酯基、醚键及碳碳双键,将此中间产物分别与乙酸钙、乙酸锌反应,制得二乙二醇醚马来酸酯钙/锌盐(MD?Ca/Zn)。通过傅里叶红外测试分析了热稳定剂产物的结构,分子中含有醚键、酯基、碳碳双键、羧酸盐结构,可作为PVC主效热稳定剂。通过刚果红法、热老化法、热失重法、电导率等检测方法,和市售硬脂酸钙/锌进行对比,验证了热稳定效果及性能,分析了热稳定机理,同时探究了与辅助热稳定剂β?二酮(硬脂酰苯甲酰甲烷)的协同作用。结果表明,当MD?Ca/Zn=2∶1(质量比,下同)时,对PVC的热稳定效果最好;初期白度可以达到40 min,静态热稳定时间为35 min;与热稳定剂总质量10 %的β?二酮复配后PVC的热稳定性能还可进一步提升。 相似文献