Natural Operators Lifting Vector Fields to Bundles of Weil Contact Elements

Let A be a Weil algebra. The bijection between all natural operators lifting vector fields from m-manifolds to the bundle functor K ^A of Weil contact elements and the subalgebra of fixed elements SA of the Weil algebra A is determined and the bijection between all natural affinors on K ^A and SA is deduced. Furthermore, the rigidity of the functor K ^A is proved. Requisite results about the structure of SA are obtained by a purely algebraic approach, namely the existence of nontrivial SA is discussed.     

Extraction properties of octaethyltetraamidopyrophosphate (OETAPP)

The extraction of uranium was studied in the system of 0.1 M OETAPP in CHCl₃/HCl or HNO₃. The distribution coefficients of HCl and HNO₃ were calculated as a function of OETAPP concentration. The amount of OETAPP in the aqueous phase containing HCl and HNO₃ was found from the measurements of surface tension of this phase. The distribution of HCl and HNO₃ between an organic and aqueous phase was studied as a function of the concentration in the aqueous phase of the acid in question. The solvation energy of the extracted complexes was calculated on the basis of the measured potential differences. The cohesion and adhesion energies of the studied systems are given as well.     

Hypoxanthine,xanthine and theobromine complexes with palladium(II) and platinum(IV) chlorides

Summary Complexes of the general types Pd(L)(LH)Cl (LH=hxH, xnH, or tbH) and Pt(L)(LH)Cl₃ (LH=hxH, or xnH) are formed by boiling under reflux 21 molar mixtures of hypoxanthine (hxH), xanthine (xnH) or theobromine (tbH) and PdCl₂ or PtCl₄ in ethanol-triethyl orthoformate. These complexes appear to be linear chain polymeric species, characterized by single monoanionic L^– ligands bridging between adjacent Pd²⁺ or Pt⁴⁺ ions. Inclusion of one terminal neutral LH and one terminal chloro-ligand completes the coordination sphere in the square-planar Pd²⁺ complexes, while the Pt⁴⁺ complexes aretrans-octahedral, involving three terminal chloro and one terminal LH ligand per platinum. The possible binding sites of the bidentate bridging L^– and the unidentate terminal LH are discussed.     

Diethyl benzoylphosphonate as a ligand

Summary Complexes (2 : 1) of diethyl benzoylphosphonate (debp) with 3d metal perchlorates were synthesized and characterized by means of i.r. and electronic spectral, magnetic susceptibility and conductance measurements. In new complexes of the types [M(debp)₂(OClO₃)(OH₂)](ClO₄) (M = Fe, Co, Zn) and [Fe(debp)₂(OClO₃)(OH₂)](ClO₄)₂, both debp ligands function as bidentate chelating agents, coordinating through the P=O and C=O oxygens. In contrast, in the manganese(II) and nickel(II) complexes, which are of the [M(debp)₂(OClO₃)(OH₂)₂](ClO₄) type, one debp acts as a bidentate chelating ligand, while the second debp is unidentate, coordinating only through the P=O oxygen. Hexacoordination in the new cationic complexes is completed by coordination of aqua and unidentate perchlorato ligands, which are in competition for sites in the inner coordination sphere of the central metal ion with the weak debp ligand. On the other hand, debp, owing to its bulkiness, and especially the presence of the benzoyl substituent, introduces sufficiently severe steric hindrance during coordination. As a result of this, the formation of [M(debp)₃]ⁿ⁺ tris-chelate cationic complexes with the 3 d metal ions under study does not seem to be possible.     

On minimizing expected absorption times

A random walk with variable step size, depending on the location of the particle, is considered. Two cases are discussed: one with two absorbing boundaries, and another when one boundary is absorbing while the other cannot be reached. Generalization of the uniquess problem of a functional equation for the expected duration is proved. Also the optimal policy, i.e. step size for each location minimizing the expected duration, is discussed. The natural solution of the problem in case of two absorbing boundaries is verified, while for the case of one boundary a necessary and sufficient condition for the existence of optimal solution is developed, while specific policy still remains open.     

The natural operators lifting connections to higher order cotangent bundles

We prove that the problem of finding all Mf _m -natural operators C: Q ? QT ^r * lifting classical linear connections ? on m-manifolds M into classical linear connections C _M (?) on the r-th order cotangent bundle T ^r *M = J ^r (M, ?)₀ of M can be reduced to the well known one of describing all M f _m -natural operators D: Q ? ? ^p T ? ? ^q T* sending classical linear connections ? on m-manifolds M into tensor fields D _M (?) of type (p, q) on M.     

碱金属钾对Ni基催化剂纤维素水蒸气气化活性的影响

采用两段式催化气化方式研究了生物质热解气化过程中碱金属的挥发对Ni基催化剂活性的影响。实验结果表明,负载K盐的纤维素水蒸气催化气化过程中,K挥发后会在催化剂表面沉积,而少量K的存在和表面沉积不但能够提高镍基催化剂的抗积炭能力,而且有助于提高其催化活性,产生更多的氢气。然而纤维素中K的浓度过大,将会抑制Ni基催化剂的效果;K在催化剂上的沉积随催化剂循环次数的增加而增加,K的含量愈高,对催化剂的抑制效果愈明显,从而缩短了催化剂的使用寿命。