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991.
M. Nagy 《Colloid and polymer science》1985,263(3):245-265
992.
Yoichi M.A Yamada 《Tetrahedron》2004,60(18):4087-4096
A novel catalyst PWAA, an assembled complex of phosphotungstic acid (H3PW12O40) and a non-cross-linked copolymer of N-isopropylacrylamide with an ammonium, was developed. It is an amphiphilic, cross-linked, and supramolecular insoluble complex and showed catalytic activity on oxidation with aqueous hydrogen peroxide. PWAA, used in 2.7×10−5-2.0×10−3 mol equiv., catalyzed oxidation of allylic alcohols, amines, and sulfides efficiently. The turnover number (TON) of PWAA reached up to 35,000. PWAA showed a good stability in organic/aqueous media and was reused three to five times. 相似文献
993.
Alexandros P. SiskosAlison M. Hill 《Tetrahedron letters》2003,44(4):789-792
Labeled glycerol is a widely used biochemical probe to investigate biosynthetic pathways. A highly efficient synthesis of [1-13C, 18O]- and [1-13C, 2H2]-glycerol is described in which the 13C label is introduced using cyanide. The 18O label was introduced by a Pinner synthesis and reduction of the ester 5 allowed incorporation of the 2H labels. 相似文献
994.
Ryashentseva M. A. Egorova E. V. Trusov A. I. Antonyuk S. N. 《Russian Chemical Bulletin》2002,51(9):1698-1701
The activity and selectivity of mono- and bimetallic catalysts containing copper and rhenium on sibunite were studied in the decomposition of methanol to methyl formate (MF), water, H2, CO, and CO2at 200—400 °C. Methane is also formed on rhenium-containing catalysts at 300—400 °C. The dehydrogenating activity and selectivity to form MF are higher on the copper-sibunite catalysts than on the rhenium-sibunite samples. The introduction of 0.25% Re into the 4% copper-containing catalyst enhances its total activity and stability. 相似文献
995.
Földvári M. Kovács-Pálffy P. Nagy N. M. Kónya J. 《Journal of Thermal Analysis and Calorimetry》1998,53(2):547-558
Various cation-exchanged montmorillonites (Li+, Na+, Ba2+, Mg2+, Ca2+, Mn2+, Co2+, Cu2+, Ag+, Cd2+, Hg2+, Al3+, Pb2+ and NH4+)
were prepared from calcium montmorillonite and their properties were studied by means of X-ray diffraction and thermal analysis.
The two methods give information on the cation exchange in the interlayer space only. X-ray diffraction studies at room temperature
are mainly suitable for estimation of the exchange of cations of different valencies. At 500°C, when the structure is completely
collapsed, the d value of montmorillonite depends on the non-hydrated ionic radius of the interlayer cation, but the measurement
interval is limited for fine interpretation. The thermoanalytical method is suitable for a better distinction of different
exchangeable cations of higher hydration energy on the basis of the DTG or DDTG curve.
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
996.
997.
利用等温和非等温方法详细研究了芳香族聚酯──热致型聚合物对,对’-联苯二甲酸二辛酯的结晶相和液晶相形成机理,并计算了相变过程中的表面自由能与温度系数,研究结果表明:从介晶相开始的结晶过程是二维异相成核、三维线性增长的,而从各向同性液相开始的液晶相形成过程则是二维异相成核二维线性增长的.对两个晶化过程的表面自由能的研究表明,该聚合物液晶相形成过程的相转变表面自由能比结晶过程小得多,预示了它将具有更大的晶化速率.研究还发现,该聚合物的液晶相形成过程具有比结晶过程大得多的温度敏感性. 相似文献
998.
V.A. Ozeryanskii A.F. Pozharskii D.A. Shevchuk A.N. Chekhlov O.A. Dyachenko 《Tetrahedron》2005,61(17):4221-4232
A simple procedure for the synthesis of N,N,N′-trialkyl-1,8-diaminonaphthalenes is described. It consists in partial demethylation (dealkylation) of commercially available proton sponge [1,8-bis(dimethylamino)naphthalene] and some of its derivatives at heating with HBr-KI-DMF system. Limitation, scope and a possible mechanistic pathway for the reaction are discussed. For isomeric 8-dimethylamino-1-methylamino- and 1-dimethylamino-8-methylamino-4-nitronaphthalenes, X-ray measurements have been conducted. The first examples of complete realkylation reactions in the naphthalene proton sponges are reported. 相似文献
999.
水淬渣-累托石颗粒吸附材料的制备及应用 总被引:1,自引:0,他引:1
研究了水淬渣-累托石颗粒吸附材料制备工艺条件、再生方法及其去除铜冶炼工业废水中重金属的条件.试验结果表明,累托石与水淬渣的比例为1∶1,另加入10%的添加剂(IS)和50%的水,焙烧温度为400℃时,制成的颗粒吸附材料体积密度为1.06kg/m3,显气孔率为62.29%,吸水率为58.82%,抗压强度为2.22Mpa,吸附效果好,散失率较低.在未调节铜冶炼工业废水pH值的条件下,颗粒吸附材料用量为0.05g/cm3,反应时间为40min,吸附温度为25℃(常温)时,Cu2 、Pb2 、Zn2 、Cd2 、Ni2 的去除率分别为98.2%、96.3%、78.6%、86.2%、64.2%,处理后的水符合国家污水综合排放标准(GB8978-1996)一级标准.颗粒吸附材料对Zn2 、Cu2 有很好的选择性.吸附饱和的颗粒吸附材料用1mol/L氯化钠溶液再生效果好.该颗粒吸附材料具有分离容易、可重复使用、处理效果好、应用前景广阔的优点. 相似文献
1000.
Solution equilibrium studies on Cu(II)-, Ni(II)- and Zn(II)-N-Me-β-Alaninehydroxamic acid (N-Me-β-Alaha), -N-Me-α-alaninehydroxamic acid (N-Me-α-Alaha), -Imidazole-4-carbohydroxamic acid (Im-4-Cha), -N-Me-imidazole-4-carbohydroxamic acid (N-Me-Im-4-Cha) and -Imidazole-4-acetohydroxamic acid (Im-4-Aha) systems have been performed by pH-potentiometry, UV–Vis spectrophotometry, EPR, CD, ESI-MS and 1H NMR methods. According to the results: (i) the amino-N atoms are more basic in N-Me-α-Alaha and N-Me-β-Alaha than the hydroxamate function, but the trend is just the opposite between the imidazole-N(3) and hydroxamate. (ii) The metal ion anchor is always the hydroxamate part in the amino acid derivatives, while it is always the imidazole-N(3) in the studied imidazolehydroxamic acids. (iii) The three studied N-Me derivatives do not form metallacrowns. Only hydroxamate type chelate is formed with N-Me-β-Alaha, but with N-Me-α-Alaha a new type of coordination mode (via amino-N and hydroxamate-O) also exists. N-Me-Im-4-Cha also forms a dinuclear complex, [M2L3], with Cu(II) and Ni(II) (but not with Zn(II)). In this complex, one of the three ligands might bridge the two metal ions (five-membered hydroxamate-(O,O) plus five-membered (Nim, Ocarb) bridging bis-chelating mode), while each of the additional two ligands binds to one metal. (iv) The two studied N–H derivatives, having dissociable proton on the hydroxamic-N, are able to form metallacrown species. A pentanuclear complex, [M5L4H−4], is exclusively formed above pH 4 between Cu(II) and Im-4-Aha. Interestingly, this 12-metallacrown-4 type complex, although together with various mononuclear binding isomers, appears also with Ni(II) and Zn(II). Unfortunately, the complexes of Im-4-Cha are not soluble in water at physiological pH at all. 相似文献