Application of K2CO3 catalysts in the coal gasification process using nuclear heat

Conventional gasification processes use coal not only as feedstock to be gasified but also for supply of energy for reaction heat, steam production, and other purposes. With a nuclear high temperature reactor (HTR) as a source for process heat, it is possible to transform the whole of the coal feed into gas. This concept offers advantages over existing gasification processes: saving of coal, as more gas can be produced from coal; less emission of pollutants, as the HTR is used for the production of steam and electricity instead of a coal-fired boiler; and a lower production cost for the gas. However, the process has the disadvantage that the temperature is limited to the outlet temperature (950 °C max) of the helium cooling gas of the HTR. Therefore the possibility of catalytic steam gasification was examined. Model calculations based on experimental results show that use of 3–4 wt% relative to coal of K²CO³ catalyst increases the throughput of a large scale nuclear gasification plant by ≈65%, while gas production costs decrease by ≈15%. Corrosion by catalysts is not significant at low concentration (< 5 wt%) and low temperature (< 900 °C).     

高铁酸钾去除饮用水源中盐酸四环素试验研究

利用提纯后的次氯酸钠溶液、硝酸铁、氢氧化钾制备高铁酸钾。并采用高铁酸钾氧化去除水中盐酸四环素（TC）,初步探讨了高铁酸钾去除TC的效果,研究了高铁酸钾投加量、pH值、氧化时间等对去除效率的影响。结果表明,高铁酸钾可以有效快速地去除水中的TC,在一定范围内,高铁酸钾投加越多,TC去除率越高,反应越快。pH值对反应影响较大,最优pH值范围为9～10。降解反应主要发生在前60S,在之后的10-20min内高铁酸钾与TC持续反应,TC得到进一步的降解。当高铁酸钾与TC摩尔比为1：1和1：5时,反应60S后的TC去除率约为100％。但反应液TOC下降幅度不大,说明大部分的TC仅转化为中间产物,未得到彻底矿化。     

Catalysis of Active Carbon Supporting Transition Metal Oxides for Pyrotechnical Reagent with Potassium Perchlorate

In order to improve the pyrotechnical reagent with potassium perchlorate,composite catalyst of active carbon supporting transition metal oxides (TMO),Fe2O3 and CuO,were prepared and added into pyrotechnical reagent with potassium perchlorate.Accelerating rate calorimeter (ARC) was used to study the catalysis of pyrotechnical reagent which is consisted of potassium perchlorate and composite catalyst.Composite catalyst of both Fe2O3 and CuO supported by active carbon can catalyze pyrotechnical reagent with potassium perchlorate.Furthermore,it can lower the apparent activation energy and accelerate the reaction with a smaller quantity than that with Fe2O3 and CuO.The maximal reaction rate of pyrotechnical reagent with potassium perchlorate mixed with Fe2O3/active carbon and CuO/active carbon is 8.31 min-1 and 9.13 min-1,which is 1.74 times and 1.91 times of pyrotechnical reagent mixed with no catalyst;time to maximal rate was 18.99 min and 1.96 min respectively,which is lower than pyrotechnical reagent mixed with no catalyst by 86.46% and 98.67% ;the apparent activation energy is 368.10 kJ·mol-1 and 325.29 kJ·mol-1,which is lower than pyrotechnical reagent mixed with no catalyst by 31.89% and 39.81% respectively.     

Preparation,characterization and salt-resistance of a coal based super absorbent composite

Potassium humate was extracted from brown coal.A novel super absorbent composite,poly (acrylic acid-co-acrylamide)/potassium humate (PAA-AM/KHA),was prepared by graft polymerization of acrylic acid,acrylamide and coal based potassium humate using N,N'-methylenebisacrylamide as a crosslinker and potassium peroxydisulfate as an initiator.The effects of reaction temperature,degree of neutralization of the poly (acrylic acid) and the amounts of crosslinker,initiator and potassium humate were investigated.Salt resistance tests were also carried out.The composite prepared under optimal conditions had a potassium humate content of 10% and exhibited a water absorption of 770 g/g in distilled water,and 349,286 and 41 g/g in 0.5 mol/L KC1,MgCl2 and AlCl3 solutions respectively.The results indicate that the salt resistance of PAA-AM/KHA was superior to that of poly (acrylic acid-co-acrylamide) because of the collaborative effect of functional groups of the coal based potassium humate.The PAA-AM/KHA micro powder was characterized by IR spectroscopy and the micrographic surface was characterized by scanning electron microscopy.Introduction of potassium humate into the poly (acrylic acid-co-acrylamide) structure creates a composite more suitable for use as a water-managing material in the renewal of arid and desert environments.The salt resisting property of the composite is improved,production costs are reduced and the growth stimulant effect is still present.     

重铬酸钾氧化比色法和气相色谱法定量分析发酵液中乙醇的比较研究

为了比较重铬酸钾氧化比色法和气相色谱法测定乙醇体积分数的效果,采用这2种方法分别定量分析已知体积分数的标准液和未知体积分数的发酵液.分析和比较统计结果发现：定量分析发酵液乙醇体积分数时气相色谱法较准确,成本较高;重铬酸钾氧化比色法可以用于发酵液乙醇体积分数的批量分析,成本较低.     

1-丁基-3-甲基咪唑碘对染料敏化太阳电池的影响

采用季铵化反应合成了1-丁基-3-甲基咪唑碘([Bmim]I).以此制备了DSCs用液体电解质.通过对比不同浓度的1-丁基-3-甲基咪唑碘、碘化钾、碘,研究其对电池性能的影响.经过优化后,当cIL=0.9 mol.L-1、cKI=0.5 mol.L-1、cI2=0.12 mol.L-1时,所组装的离子液体DSCs在AM1.5,100 mW.cm-2下,DSCs的短路电流密度为15.97 mA.cm-2、开路电压为0.71 V、填充因子为0.55、光电转换效率可达6.34%.     

Potassium fertilization of broccoli transplants

Increased potassium fertilization may be important in broccoli transplant growth. Recommended amounts of water soluble 20N-8.7P-16.6K were supplemented with varying concentrations of K as KCl applied at intervals during broccoli transplant development. Transplant growth and subsequent broccoli yields were studied in greenhouse and field tests.Fertilization with supplemental K significantly increased broccoli transplant fresh and dry weight, leaf area, stem diameter and plant height over the control. Effect of number of applications was generally dependent on K concentration and age of the broccoli seedling at the first fertilization. High K concentrations (> 2098 ppm) applied two weeks after planting were detrimental to broccoli transplant growth.In two field tests, supplemental K applied to transplants had no effect on broccoli yield. No significant differences were found between supplementing fertilizer with K and hardening transplants in a cold frame for two weeks. Incidence of hollow stem was increased in one test by application of 1000ppm K. Two applications per week caused significant increases in yield, head diameter and hollow stem when compared with one application per week.     

Ni(Ⅳ)引发丙烯酸甲酯与三元尼龙接枝共聚反应的研究

以二过碘酸合镍(Ⅳ)钾〔Ni(Ⅳ)〕为氧化剂,共聚尼龙上的弱的还原基团(酰胺基)为还原剂,组成氧化还原引发体系,于碱性介质中直接在共聚尼龙分子骨架上产生接枝点,引发丙烯酸甲酯(MA)的接枝共聚合反应,获得了较高的接枝效率(可达90%以上)。探讨了引发剂浓度、单体浓度、反应温度对接枝参数的影响,结果表明:当c〔Ni(Ⅳ)〕=8×10-4mol/L,c(MA)=1 5mol/L,θ=35℃时,接枝效率和接枝百分比可达到最高值。用红外光谱、X射线衍射、扫描电镜对接枝共聚物进行了表征,提出了建立在镍(Ⅳ)还原为镍(Ⅱ)的过程为两步单电子转移的基础之上的引发机理。将所得接枝共聚物用作尼龙/聚甲基丙烯酸甲酯体系的增容剂,通过扫描电镜分析表明:该共混体系的相容性得到一定程度的改善。     

热复分解法制备硫酸钾的研究

利用热复分解法来制备硫酸钾。将硫酸铵和氯化钾按一定比例充分混合,在高于340℃下反应1~2 h。反应过程中副产物氯化铵(NH4C l)升华分离出去,从而留下主产物硫酸钾(K2SO4)。由于主产物中氯的含量较高,必须想法降低其氯含量,达到无氯钾肥的合格标准。     

Polymer electrolytes from PEO and novel quaternary ammonium iodides for dye-sensitized solar cells

Polymer electrolytes were prepared by blending high molecular weight poly(ethylene oxide) (PEO) and a series of novel quaternary ammonium iodides, the polysiloxanes with oligo(oxyethylene) side chains and quaternary ammonium groups. X-ray diffraction (XRD) measurements ensured relatively low crystallinity when the quaternary ammonium iodides were incorporated into the PEO host. The ionic conductivity of these complexes was improved with the addition of plasticizers. The improvement in the ionic conductivity was determined by the polarity, viscosity and amounts of plasticizers. A plasticized electrolyte containing the novel quaternary ammonium iodide was successfully used in fabricating a quasi-solid-state dye-sensitized solar cell for the first time. The fill factor and energy conversion efficiency of the cell were calculated to be 0.68 and 1.39%, respectively.