Regional allocation of public investment

Conclusion In the previous Sections, we have observed the following interesting properties of the optimum solution to this regional allocation problem.First, as indicated by assumptions (33) (34), and (35), public investment in one of the regions will be justified during some phase of the planning period, even if it is less productive than the private investment in the same region. The reason is that the central government can directly control the interregional flow of public fundsoutside the market mechanism and can concentrate its public investment on the region with greater growth potential.Second, as seen by equation (41), the value of (T–t ^*), the length of the second phase of planning, is independent from the length of planning horizonT provided thatT>T–t ^*. Then, the relative significance of the second phase will be less and less asT becomes larger and larger. This is one of the characteristics which have been observed in the dynamic programming problems with linear form. Therefore, ifT is very large, the public investment should be almost persistently concentrated to the second region, as far as there is no change in the values of relevant parameters.Third, the resultant optimum solution is very sensitive to the relative sizes of such parameters ass _i, _i , _i (i=1, 2), and . Then, if there is some slight change in them by means of social overhead investment, for instance, which was analyzed earlier in this paper, we may observe a drastic change of the optimum solution. Such being the case, it may be possible for us to utilize some combination of those two kinds of public investment policy in order to attain theoptimum optimorum in the set of feasible growth paths.The author is a postdoctoral fellow with the University of Pennsylvania. The present paper is a product of his research on the basic theory of regional growth which has been supported by a grant from the Ford Foundation. This support is gratefully acknowledged. He is indebted to Professors W. Isard, B. H. Stevens, and J. Kissin for their valuable comments on the earlier draft of this paper. Of course, the author alone is responsible for any remaining errors.     

Effects of photo-induced graft polymerization of 2-methacryloyloxyethyl phosphorylcholine on physical properties of cross-linked polyethylene in artificial hip joints

Osteolysis caused by wear particles from polyethylene in the artificial hip joints is a serious issue. We have used photo-induced radical graft polymerization to graft 2-methacryloyloxyethyl phosphorylcholine (MPC) polymer onto the surface of cross-linked polyethylene (CLPE-g-MPC) in order to reduce friction and wear at the bearing surface of the joint. The physical and mechanical properties of CLPE and CLPE-g-MPC were not significantly different, expect that the friction coefficient of untreated CLPE cups was 0.0075, compared with 0.0009 for CLPE-g-MPC cup, an 88% reduction. After 3.0 × 10⁶ cycles in the hip joint simulator test, we could not observe any wear of CLPE-g-MPC cups. We concluded that the advantage of photo-induced radical graft polymerization technique was that the grafted MPC polymer gave a high lubricity only on the surface and has no effect on the bulk properties of the CLPE substrate.     

Preparation of CdS-doped Glasses from Gels Containing Diethyldithiocarbamatocadmium

CdS-doped SiO₂ glasses were prepared via silica gels containing diethyldithiocarbamatocadmium Cd(S₂CN(C₂H₅)₂)₂. Heat treatment of the gels gave transparent yellow SiO₂glasses doped with hexagonal CdS crystals. In optical absorption and fluorescence spectra, the optical absorption edge and the emission peak clearly exhibited a blue shift, which was attributed to the quantum size effect of the carrier confinement, as the CdS content was decreased. In the fluorescence spectra of the CdS-doped silica glasses, the emission peak was observed only near 500 nm and not observed at longer wavelengths which were known to be present if there were sulfur vacancies.     

Developments in asymmetric hydrogenation from an industrial perspective

Examples of developments in asymmetric hydrogenation from various perspectives, in an effort to improve efficiency, are reported. Discussed in this Account are (1) the improved synthesis of BINAP ligands, (2) the design of SEGPHOS ligands for higher enantioselectivity, (3) a new protocol with fewer reaction steps to synthesize beta-aminoesters, and (4) a novel asymmetric hydrogenation mediated by a copper catalyst.     

Fate of the chlorine and fluorine in a sub-bituminous coal during pyrolysis and gasification

The fate of the chlorine and fluorine present in a sub-bituminous coal from Indonesia during pyrolysis and gasification has been studied with fixed and entrained bed reactors. The rate profile for HCl evolved in the temperature programmed pyrolysis exhibits the main and shoulder peaks at 480 and 600 °C, respectively. Model experiments and subsequent Cl 2p XPS measurements show that HCl reacts with metal impurities and carbon active sites at 500 °C to be retained as inorganic and organic chlorine forms, from which HCl evolves again at elevated temperatures. It is suggested that the HCl observed in the coal pyrolysis may originate from the above-mentioned chlorine functionalities formed by secondary reactions involving the nascent char. In the CO₂ gasification of the 900 °C char at 1000 °C and 2.5 MPa, any measurable amounts of HCl and HF could not be detected even at a high conversion of 75 wt% (daf), suggesting the accumulation of these halogens in the residual char. When the coal is injected into an O₂-blown, entrained bed gasifier at 1200-1400 °C under 2.6 MPa, the partial oxidation proceeds to a larger extent at a higher O₂/coal ratio, whereas the chlorine and fluorine are enriched in the remaining char, and the extent of the enrichment at the latter stage of gasification is larger with the fluorine. The XPS measurements of the chars reveal the presence of the broad F 1 s peak, which can cover a wide range of binding energies attributable to inorganic and organic fluorine. The halogen enrichment during gasification is discussed in terms of secondary reactions of HCl and HF with char.     

Fire Safety Performance of Japanese Traditional Wood/Soil Walls and Implications for the Restoration of Historic Buildings in Urban Districts

Grass-root research activities to clarify fire safety performance of Japanese traditional wooden construction are introduced. The activities aim to resolve conflict between the restoration of historic buildings and the reduction of risk and hazard of urban fires. Among various activities, scope and results of fire resistance tests on traditional soil wall assemblies supported by timber frame are reported in detail. The test results indicate an encouraging prospect for the rational fire safety assessment of historic buildings and further development of fire-safe traditional constructions for the restoration of historic buildings and historic urban districts.     

Decarboxylation of the 6-nitrobenzisoxazole-3-carboxylate anion catalyzed by cross-linked poly(4-vinylpyridinium) salts

Summary Catalysis of cationic polyelectrolytes for the decarboxylation of 6-nitrobenzisoxazole-3-carboxylate anion was studied in a buffer solution (pH=9.0). Cross-linked poly (4-vinylpyridinium) salts prepared from 4-vinylpyridine and , -dibromides were used as cationic catalysts. The cross-linked catalysts were found to accelerate markedly the decarboxylation in comparison with the linear water-soluble analogues. Effect of the polymer structure such as the length of (CH₂)_x linkages between positive charges on the catalytic activity was examined. It was suggested that the acceleration by the cross-linked polymer catalysts would be due to the hydrophobic microenvironment around the catalytic sites.