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Hydrophobic–hydrophilic block copolymers were prepared by “living” anionic polymerization. They consist of polystyrene and poly(ethylene oxide) blocks, and are soluble in water. Their interfacial properties were investigated, employing aqueous solutions. The block copolymers lowered the surface tension of water in analogy with the low molecular weight surfactants such as sodium lauryl sulfate and heptaethylene oxide n‐dodecyl ether. Their aqueous solutions exhibited solubilization properties differing from those of polyethylene glycol. Therefore, it is thought that the polystyrene blocks produce solubilization phenomena. In samples of the same styrene content, the precipitation temperature of a high molecular weight copolymer in water was lower than that of a low molecular weight copolymer at the same concentration in the same solvent. The surface tension and precipitation temperature of aqueous solutions seem to be influenced by molecular weight and composition.

We investigated the effects of fluorescent illumination with a high red-to-far-red ratio (R:FR) on the resistance of cucumber (Cucumis sativus) seedlings to powdery mildew fungus (Sphaerotheca cucurbitae; PM). Seedlings were grown at a photosynthetic photon flux (PPF) of 300 μmol·m−2·s−1 provided by fluorescent lamps with high R:FR light (R:FR = 7.0; FLH) or low R:FR light (R:FR = 1.1; FLL) until cotyledons or the first foliage leaf were fully expanded. Spores of PM were then inoculated onto the leaves, and the seedlings were grown for 7 days (from cotyledon stage) or 9 days (from foliage–leaf stage) under FLH. The number of PM colonies on FLH seedlings was 0.80× (cotyledons) and 0.62× (foliage leaves) the number on FLL seedlings. The reduction on the FLH seedlings was probably the result of changes in leaf morphological characteristics such as a thicker epidermal tissue as a result of the higher R:FR illumination. The number of PM colonies on cotyledons of the FLH seedlings was also smaller than that on seedlings grown under metal-halide lamps providing a spectrum similar to that of natural light (R:FR = 1.2).

To evaluate the effect of fluorescent lamps with a high red:far-red (R:FR) light on the potential photosynthesis of transplants, we investigated the photosynthetic light responses of cucumber (Cucumis sativus L.) seedlings grown under fluorescent lamps with high R:FR light (FLH) and compared them with the responses of the seedlings grown under metal-halide lamps (ML) that provided a spectrum similar to that of natural light and under a fluorescent lamp with low R:FR light (FLL). The seedlings were grown under FLH (R:FR = 7.0), ML (R:FR = 1.2), or FLL (R:FR = 1.1) at a photosynthetic photon flux density (PPFD) of 350 μmol·m−2·s−1. The gross photosynthetic rate (Pg), quantum yield of photosystem II (ΦPSII), and photosynthetic electron transfer rate (ETR) of the foliage leaves were then evaluated at PPFDs ranging from 0 to 1000 μmol·m−2·s−1. The photosynthetic light response of FLH seedlings was similar to those of sun leaves, and the responses of ML and FLL seedlings were similar to those of shade leaves. The Pg, ETR, and ΦPSII of FLH seedlings at PPFD of 1000 μmol·m−2·s−1 was 1.38, 1.32, and 1.28 times, respectively, those of ML seedlings, and was 1.40, 1.23, and 1.22 times, respectively, those of FLL seedlings. The Pg was closely correlated with ETR in each treatment. FLH seedlings had thicker leaf and greater chlorophyll content per leaf area than ML and FLL seedlings. The greater Pg of FLH seedlings than in the other two groups of seedlings at high PPFD was probably the result of the improved ETR resulting from physiological and morphological changes in response to the high R:FR light.

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Hydration in a new semiaromatic polyamide, named polyamide 9-T (PA9-T), a copolymer of terephthalic acid with n-and iso-nonanediamine, is studied by dynamic viscoelastic analysis under controlled humidity conditions and wide-angle x-ray diffraction analysis in comparison with common polyamide nylon 6. The storage modulus of PA9-T is retained at up to 60 ºC with increasing humidity, then dropping with further increases in temperature past 70 ºC. The decrease in mechanical properties at 70 ºC due to moisture uptake is found to be substantially improved by annealing to develop molecular packing and/or crystallization. In contrast, the storage modulus of very highly crystallized (50% crystallinity) nylon 6 decreases markedly with humidity at low temperatures such as 20 ºC. Thus, PA9-T retains its mechanical properties in humid atmospheres at much higher temperatures than nylon 6. The crystalline x-ray diffraction peaks for nylon 6 corresponding to (002) + (202) of α form shift upon absorption of moisture, speculated to be due to the weakening of hydrogen bonds and the subsequent conformational disordering of the chains. Unlike nylon 6, the crystalline peaks of PA9-T do not shift due to moisture uptake. This is considered to be attributable to that the long aliphatic chain in PA9-T forms the large hydrophobic domain, rendering PA9-T less hygroscopic than nylon 6. Additionally, strong hydrogen bonds formed by terephthalamide residues together with a strong stacking force of phenylene groups may also repel water, preventing moisture bind with the amide groups of PA9-T crystals.