γ-射线辐照对尼龙6纤维结构的影响

<正> 过去的大多数研究表明,高能射线辐照会引起聚乙烯及聚丙烯等稀烃类聚合物分子链交联及降解,而且会导致结晶度下降。张利华等人最近的研究表明,对于尼龙1010塑料,仅当辐照剂量高到一定程度后,辐照才会破坏结晶。此外,Stowe等人曾经研究过近紫外线对尼龙66纤维结构的影响,结果表明,在空气气氛中的近紫外辐照主要导致尼龙66纤维降解,并使纤维结晶度提高。有关高能射线辐照对高度取向的合成纤维结构及性能的影响的研究尚不多见。本工作将讨论γ-射线对于尼龙6纤维结构的影响。     

同步辐射白光全反射XRF在痕量元素检测的初步应用研究

叙述了同步辐射白光全反射Ｘ射线荧光分析的实验装置，给出了几种标准物质ＴＸＲＦ实验的检出限，并对实验结果进行了讨论。     

Carboxylic acid functionalization of nylon 6 by radiation grafting and conversion to zinc salts: Effects on physical properties

 Functionalization of polymers by grafting monomeric species on to the backbone of molecular chains with the use of γ-radiation has been used extensively. In this work methacrylic acid was grafted onto a commercial grade of polycaproamide (Nylon 6) by preirradiating the polymer granules to 15 kGy at a rate of 1.0 kGy per hour and subsequently immersing these in a 10% aqueous solution of methacrylic acid in the presence of small quantities of FeSO₄ as homopolymerization inhibitor. The polymer was subsequently neutralized by mixing it with zinc acetylacetonate in a laboratory scale melt mixing device. The acid-grafting polymer modification resulted in an increase in glass transition temperature, while the addition of zinc acetylacetonate gave rise to two transitions: The lower transition corresponds to a miscible mixture of free polyamide and acid-grafted polymer, both plasticized with undecomposed zinc compound, while the upper transition corresponds to the zinc salt of the acid grafted polyamide. Through rheological measurements it was shown that both the acid-grafted polymer and the derived zinc salt have a branched structure, possibly containing also some crosslinked domains. Large improvements in solvent resistance were observed for both type of polymer modifications. Received: 13 December 1996 Accepted: 10 February 1997     

Taking snapshots of photoexcited molecules in disordered media by using pulsed synchrotron X-rays

Photoexcited molecules are quintessential reactants in photochemistry. Structures of these photoexcited molecules in disordered media in which a majority of photochemical reactions take place remained elusive for decades owing to a lack of suitable X-ray sources, despite their importance in understanding fundamental aspects in photochemistry. As new pulsed X-ray sources become available, short-lived excited-state molecular structures in disordered media can now be captured by using laser-pulse pump, X-ray pulse-probe techniques of third-generation synchrotron sources with time resolutions of 30-100 ps, as demonstrated by examples in this review. These studies provide unprecedented information on structural origins of molecular properties in the excited states. By using other ultrafast X-ray facilities that will be completed in the near future, time-resolution for the excited-state structure measurements should reach the femtosecond time scales, which will make "molecular movies" of bond breaking or formation, and vibrational relaxation, a reality.     

Nanostructure evolution studies of bulk polymer materials with synchrotron radiation: progress in method development

The prospects of a modern analysis of nanostructure evolution during the processing of polymer materials by means of scattering from synchrotron radiation are demonstrated in examples. The beam sources have gained stability, shortages are located in beamline setups and in method development for the quantitative analysis of voluminous data sets.By using the proposed multidimensional chord distribution function (CDF) analysis method, nanostructure information from small-angle X-ray scattering (SAXS) data are extracted and visualised. The method can be automated if the beamline setup is able to deliver a full data set with simple constraints. In this case even a simultaneous data evaluation is possible (while one pattern is accumulated, the previous one is analysed). The advantages of the method are demonstrated in a study of the straining of a thermoplastic elastomer. The possibilities of an automated analysis are demonstrated in an investigation of the crystallisation behaviour of high-pressure injection-moulded polyethylene (HPIM-PE). The achievable results of nanostructure analysis of polymer materials are discussed. It is shown that the time-resolved SAXS of polymer materials studied during a transformation and analysed by the CDF method is not just a powerful tool to investigate the relationship between structure and properties of materials; the information that can be gained concerning the processes that control nanostructure evolution is equally important. In the future the enlightenment of such relationships may help to tailor polymer materials with respect to their properties and, beyond that, to improve assessments concerning their aging.     

Basic Characteristics of Synchrotron Radiation

Many advances have been made in chemical structure research over the past three decades using synchrotron radiation. Synchrotron radiation has a number of unique properties. They include high brightness, high collimation, broad energy spectrum, variable polarization, coherent power, and subnanosecond pulse width. The third-generation storage rings with wiggler and undulator sources and lower electron beam dimensions are delivering over 10¹² times higher brightness than laboratory-based sources. The future of synchrotron sources looks very promising with the development of energy recovery linac sources and free-electron laser sources. These will permit dynamic studies of chemical structure with subpicosecond time resolution. Commensurate with the development of X-ray sources, major progress has occurred in optical schemes to meet the challenging needs of chemical structure research. High-resolution monochromatization and submicron focusing of X rays present new avenues for the future.     

Time‐Resolved Synchrotron Radiation Excited Optical Luminescence: Light‐Emission Properties of Silicon‐Based Nanostructures

The recent advances in the study of light emission from matter induced by synchrotron radiation: X‐ray excited optical luminescence (XEOL) in the energy domain and time‐resolved X‐ray excited optical luminescence (TRXEOL) are described. The development of these element (absorption edge) selective, synchrotron X‐ray photons in, optical photons out techniques with time gating coincide with advances in third‐generation, insertion device based, synchrotron light sources. Electron bunches circulating in a storage ring emit very bright, widely energy tunable, short light pulses (<100 ps), which are used as the excitation source for investigation of light‐emitting materials. Luminescence from silicon nanostructures (porous silicon, silicon nanowires, and Si–CdSe heterostructures) is used to illustrate the applicability of these techniques and their great potential in future applications.     

Some Comments on the Matter Wave-light Wave Hypothesis

From the de Broglie matter wave hypothesis and Planck’s energy quantization law, and assuming conservation of energy in the absorption of a photon and its consequent conversion to kinetic energy of motion by a material particle initially at rest, one can deduce a simple mathematical relationship between the wavelength λ (or frequency ν), of the photon absorbed by the particle at rest, and the resulting de Broglie matter wave length, λ_D, of the particle with kinetic energy of motion of mv²/2. The relationship so deduced, λ_D∝√λ, suggests that visible wavelengths of light, from about 4000 ?, in the violet, to beyond about 7000 ?, in the red, on absorption by an electron at rest, lead to material electron wavelengths, λ_D, of the order of the size of the electron transfer proteins seen in the photosynthetic reaction centers of photosynthesizing organisms, at about a size of 50–100 ?. In addition to understanding the mechanism of photosynthesis as a material wave mediated phenomenon, further areas of importance of the relations pointed out in this paper are in the design of experiments to gain a deeper understanding of the basic tenets of wave mechanics, and in the use of tunable lasers to probe various properties of material waves, and to precisely control their properties for applications including lithography.     

Synergetic degradation of chitosan with gamma radiation and hydrogen peroxide

Chitosan samples were irradiated by ⁶⁰Co γ-rays in the presence of hydrogen peroxide with radiation dose from 10 kGy to 100 kGy. The degradation was monitored by gel permeation chromatography (GPC), revealing the existence of a synergetic effect on the degradation. Structures of the degraded products were characterized with Fourier-transform infrared spectra (FT-IR), ultraviolet-visible spectral (UV-vis) analysis, and X-ray diffraction (XRD). Results showed that the crystallinity of chitosan decreases with degradation, and the crystalline state of water-soluble chitosan is entirely different from that of water-insoluble chitosan. An elemental analysis method was employed to investigate changes in the element content of chitosan after degradation. Mechanism of chitosan radiation degradation with and without hydrogen peroxide was also discussed.     

Structure formation in heavy metal oxyhydrates at low rates of gel formation

Oxyhydrate gels have a hydrophilic surface, due to which they undergo destruction and secondary polymerization in aqueous media. Prolonged storage in aqueous solution gives rise to regions with selfsimilar helical ordering in gels. Structuring of this kind is also observed when synthesis is conducted under conditions that provide low gelation rates. Electromagnetic UV and visible radiation is another means to change the gel structure; it makes the oligomer species pass into the excited state, due to which one of the directions of structuring becomes dominant. This work summarizes the results of computer simulation of gel agglomerates. For oxyhydrate systems, helical ordering was found to be one of the local energy minima. The units of a macrohelix can lie at various angles relative to one another, and they can change, after absorption of energy, the helix pitch and the order of elements in the helix.