Assessment of gamma radiation from a limited area of forest floor using a cumulative personal dosimeter.

To elucidate long term changes in gamma radiation from a limited region of interest of the forest floor, a simple monitoring procedure using a cumulative personal dosimeter (D-shuttle) was examined from 2016 to 2017. The test site was in a small forest in Abiko, Japan, where the initial radiocesium contamination from the Fukushima Dai-ichi Nuclear Power Plant was 60-100 kBq m. Three experimental plots basically containing a set of two 5 × 5 m observation areas were arranged at the site.

Poly(n-alkylsilsesquioxane) liquids prepared by cosolvent-free hydrolytic polycondensation of n-alkyltrialkoxysilanes: effects of liquid-liquid phase separation during aging and alkyl chain length on structure and viscosity.

The effect of the alkyl chain length and alkoxy groups on the viscosity and related properties of polysilsesquioxanes (PSQs) prepared by cosolvent-free hydrolytic polycondensation from n-alkyltrialkoxysilane-water binary systems via aging was investigated. n-Alkyltrialkoxysilanes with ethyl, n-propyl, and n-butyl groups gave PSQ liquids, whereas those with methyl groups yielded gels. The viscosity of the PSQ liquids remained stable over a month at room temperature despite the presence of many SiOH groups, and decreased with an increase in the alkyl chain length.

Changes in the distribution of radiocesium in the wood of Japanese cedar trees from 2011 to 2013.

The changes in the distribution of (137)Cs in the wood of Japanese cedar (Cryptomeria japonica) trunks within three years after the Fukushima Dai-ichi Nuclear Power Plant (FDNP) accident in 2011 were investigated. Thirteen trees were felled to collect samples at 6 forests in 2 regions of the Fukushima prefecture. The radial distribution of (137)Cs in the wood was measured at different heights.

Intercalation of a surfactant with a long polyfluoroalkyl chain into a clay mineral: unique orientation of polyfluoroalkyl groups in clay layers.

Eight novel polyfluorinated surfactants (C(n)F(2n+1)CONH(CH2)2 N(+)(CH3)2C16H33 Br(-); abbreviated as CnF-S, where n = 1, 2, 3, 4, 5, 6, 8, 10) were synthesized and their intercalation into cation-exchangeable clay was investigated. All of the polyfluorinated surfactants intercalated in amounts exceeding the cation exchange capacity (CEC) of the clay. The C4F-S and C5F-S surfactants exhibited intercalation up to 480% of the CEC as a saturated adsorption limit.

Novel methodology to control the adsorption structure of cationic porphyrins on the clay surface using the "size-matching rule".

Saponite-type clays that have different cation exchange capacities were successfully synthesized by hydrothermal synthesis. The structure and properties were analyzed by X-ray diffraction, X-ray fluorescence, (27)Al NMR, FT-IR, thermogravimetric and differential thermal analysis, atomic force microscopy, and cation exchange capacity measurement. The intercharge distances on the synthetic saponite (SS) surfaces were calculated to be 0.

Order-order and order-disorder transitions in thin films of an amphiphilic liquid crystalline diblock copolymer.

In this study, we quantitatively investigated the temperature-dependent phase transition behaviors of thin films of an interesting amphiphilic diblock copolymer, poly(ethylene oxide)-b-poly(11-[4-(4-butylphenylazo)phenoxy]undecyl methacrylate) (p(EO)-b-p(MAAZ)) and the resulting morphological structures by using synchrotron grazing incidence X-ray scattering (GIXS) and differential scanning calorimetry. The quantitative GIXS analysis showed that the diblock copolymer in the homogeneous, isotropic melt state undergoes phase-separation near 190 degrees C and then forms a body-centered cubic (BCC) structure of spherical p(EO) domains in the p(MAAZ) matrix, at which point the p(EO) domains and the p(MAAZ) matrix are both in amorphous, liquid states. The BCC structure of spherical p(EO) domains is converted to a hexagonal cylinder structure near 120 degrees C, which is induced by the transformation of the isotropic phase of the p(MAAZ) matrix to the smectic A phase, which is composed of a laterally ordered structure of p(MAAZ) blocks with fully extended side groups.

Synthesis, liquid-crystalline properties, and supramolecular nanostructures of dendronized poly(isocyanide)s and their precursors.

A series of novel dendronized pi-conjugated poly(isocyanide)s were synthesized successfully by using a Pd-Pt mu-ethynediyl dinuclear complex ([ClPt{P(C2H5)3}2C[triple bond]CPt{P(C2H5)3}2Cl]) as the initiator. The polymerizations of the dendronized monomers follow first-order kinetics, indicating that living polymerization takes place. The obtained polymers exhibit narrow polydispersities in the range of 1.