On N-widths in Ip

In this paper we prove that (1<p<+∞), give the characteristics of x^o and the optimal subspace for n-width d_n in space X=l _n ^N . Where d_n in the n-width, in the sense of Kolmogorov, ofD in X, dⁿ is the n-width ofD with respect to X, in the sense of Gel'fand, δ is the linear n-width ofD with respect to X.     

Na2SnO3系催化剂在甲烷氧化偶联反应中的催化性能及表面碱性的探讨

1982年Keller和Bhasin以金属氧化物为催化剂从甲烷制得少量乙烯和乙烷的工作引起了各国研究工作者的重视,此后报道了许多有研究价值的催化剂,其中添加碱金属对提高催化性能所起的作用引起了普遍的关注.Lunsford等首先用添加Li~+的MgO作催化剂,发现催化剂表面碱性增强的同时,生成C_2烃类产物的选择性明显增加.随后Iwamatu等在MgO中添加Na~+及Rb~+盐,Jones等在Mn~(4+)/SiO_2中添加Na~+,Otsuka等在Sm_2O_3中添加LiCl作为甲烷氧化偶联催化剂进行了研究,这些结果均表明,因添加碱金属使催化剂呈现     

Covalent attachment of phospholipid analogous polymers to modify a polymeric membrane surface: a novel approach

A novel method for the surface modification of a microporous polypropylene membrane by tethering phospholipid analogous polymers (PAPs) is given, which includes the photoinduced graft polymerization of N,N-dimethylaminoethyl methacrylate (DMAEMA) and the ring-opening reaction of grafted poly-(DMAEMA) with 2-alkyloxy-2-oxo-1,3,2-dioxaphospholanes. Five 2-alkyloxy-2-oxo-1,3,2-dioxaphospholanes, containing octyloxy, dodecyloxy, tetradecyloxy, hexadecyloxy, and octadecyloxy groups in the molecular structure, were used to fabricate the PAP-modified polypropylene membranes. The attenuated total reflectance FT-IR spectra of the original, poly(DMAEMA)-grafted, and PAP-modified membranes confirmed the chemical changes on the membrane surface. Scanning electron microscope pictures showed that, compared with the original membrane, the surface porosities ofpoly(DMAEMA)-grafted and PAP-modified membranes were somewhat reduced. Water contact angles measured by the sessile drop method on PAP-modified membranes were slightly lower than that on the original polypropylene membrane, but higher than those on poly(DMAEMA)-grafted membranes with the exception of octyloxy-containing PAP-modified membranes. However, BSA adsorption experiments indicated that the five PAP-modified membranes had a much better protein-resistant property than the original polypropylene membrane and the poly(DMAEMA)-grafted membranes. For hexadecyloxy- and octadecyloxy-containing PAP-modified membranes, almost no protein adsorption was observed when the grafting degree was above 6 wt %. It was also found that the platelet adhesion was remarkably suppressed on the PAP-modified membranes. All these results demonstrate that the described approach is an effective way to improve the surface biocompatibility for polymeric membranes.     

冲击波处理的结晶MgO的化学分析正电子谱研究

冲击波处理的结晶ＭｇＯ的化学分析正电子谱研究＊张菊郑小明（杭州大学催化研究所，杭州３１００２８）常志向（抚顺石油化工研究院，抚顺１１３００１）关键词冲击波，化学分析正电子谱，结晶氧化镁，丁烯，脱氢冲击波是在介质中以超音速传播的压力脉冲．气体中的冲击波...     

过渡金属钼钒砷杂多化合物的合成与TPR,TPD研究

Seven transition metal molybdovanadoarsenic heteropoly compounds have been synthesized and characterized using IR, UV, TG-DTA, pH potential titration techniques. The molecular formulae of these compounds are pro-posed to be H_xM_yAsMO₁₀V₂O₄₀·zH₂O(x=1～3, y=1,2, M=Cr, Mn, Fe, Co, Ni, Cu, Zn).They are all keggin structure. Surface nature of these compounds have been investigated by temperature programmed desorption and temperature programmed reduction techniques. NH₃-TPD results show that in TPD profiles of the compounds there are two desorption peaks corresponding to weak acid sites of desorption, respectively. Desorbing activativon energy and preexponential factor of weak acid site of desorption for compounds have been calculated. H₂-TPR re-sults show that introducting transtion metal to molybdovanarsenic acid, the reduction peak temperatures of H₂-TPR shift regularly with increasing d electron numbers of transition metals. In addition, Zn and Cu heteropoly com-pounds have yet apparent effect of hydrogen spill over.     

ZrO_2对CuO-ZnO-ZrO_2催化剂低压合成甲醇的促进作用

我们曾报道CO_2/H_2在CuO-ZnO及CuO-ZnO-ZrO_2催化剂上低压合成甲醇的反应,指出CuO-ZnO-ZrO_2对CO_2/H_2制甲醇具有较高的活性和选择性。本文通过TPD-MS测试研究了第3组分ZrO_2的加入对CO_2/H_2在CuO-ZnO-ZrO_2催化剂上低压合成甲醇的促进作用。 1 实验部分 催化剂的评价在恒压流动反应系统内进行。用色谱仪分析产物(Porapak Q柱,4 mm×3m,柱温120℃,CO、CO_2、CH_3OH、H_2O的保留时间分别为0.55、0.84、4.72、6.6 min),热     

有机钛氢化物的化学

本文综述了有机钛氢化物化学的最近进展,包括:合成方法,反应及其在有机合成中的应用。     

Spectroscopic evidence for triplet excitation energy transfer among carotenoids in the LH2 complex from photosynthetic bacterium <Emphasis Type="Italic">Rhodopseudomonas palustris</Emphasis>

The LH2 complex from Rhodopsudomonas (Rps.) palustris is unique in the heterogeneous carotenoid compositions. The dynamics of triplet excited state Carotenoids (³Car* has been investigated by means of sub-microsecond time-resolved absorption spectroscopy both at physiological temperature (295 K) and at cryogenic temperature (77K). Broad and asymmetric T _n ←T ₁ transient absorption was observed at room temperature following the photo-excitation of Car at 532 nm, which suggests the contribution from various carotenoid compositions having different numbers of conjugated C=C double bonds (N_c=c). The triplet absorption bands of different carotenoids, which superimposed at room temperature, could be clearly distinguished upon decreasing the temperature down to 77 K. At room temperature the shorter-wavelength side of the main T_n04T₁ absorption band decayed rapidly to reach a spectral equilibration with a characteristic time constant of ∽1 μs, the same spectral dynamics, however, was not observed at 77 K. The aforementioned spectral dynamics can be explained in terms of the triplet-excitation transfer among heterogeneous carotenoid compositions. Global spectral analysis was applied to the time-resolved spectra at room temperature, which revealed two spectral components peaked at 545 and 565 nm, and assignable to the T_n04 T₁ absorption of Cars with Nc=c=11 and Nc=c=13, respectively. Surprisingly, the decay time constant of a shorter-conjugated Car, i.e. 0.72 ώs (aerobic) and 1.36 ώs (anaerobic), is smaller than that of a longer-conjugated Car, i.e. 2.12 us (aerobic) and 3.75 ώs (anaerobic), which is contradictory to the general rule of carotenoids and relative polyenes. The results are explained in terms of triplet-excitation transfer among different types of Cars. It is postulated that two Cars with different conjugation lengths coexist in an α, β-subunit in the LH2 complex.