Crystallization and chain conformation of semicrystalline and amorphous polymer blends studied by wide‐angle and small‐angle scattering

We examine the crystallization and chain conformation behavior of semicrystalline poly(ethylene oxide) (PEO) and amorphous poly(vinyl acetate) (PVAc) mixtures with wide‐angle X‐ray diffraction (WAXD), small‐angle X‐ray scattering (SAXS), and small‐angle neutron scattering (SANS) experiments. For blends with PEO weight fractions (wt_PEO) greater than or equal to 0.3, below the melting point of PEO, the WAXD patterns reveal that crystalline PEO belongs to the monoclinic system. The unit‐cell parameters are independent of wt_PEO. However, the bulk crystallinity determined from WAXD decreases as wt_PEO decreases. The scattered intensities from SAXS experiments show that the systems form an ordered crystalline/amorphous lamellar structure. In a combination of WAXD and SAXS analysis, the related morphological parameters are assigned correctly. With the addition of amorphous PVAc, both the average amorphous layer thickness and long spacing increase, whereas the average crystalline layer thickness decreases. We find that a two‐phase analysis of the correlation function from SAXS, in which the scattering invariant is linearly proportional to the volume fraction of lamellar stacks, describes quantitatively the crystallization behavior of PEO in the presence of PVAc. When wt_PEO is close to 1, the samples are fully spaced‐filled with lamellar stacks. As wt_PEO decreases from 1.0 to 0.3, more PVAc chains are excluded from the interlamellar region into the interfibrillar region. The fraction outside the lamellar stacks, which is completely occupied with PVAc chains, increases from 0 to 58%. Because the radius of gyration of PVAc with a random‐coil configuration determined from SANS is smaller than the average amorphous layer thickness from SAXS, we believe that the amorphous PVAc chains still persist with a random‐coil configuration even when the blends form an ordered structure. © 2001 John Wiley & Sons, Inc. J Polym Sci Part B: Polym Phys 39: 2705–2715, 2001     

HL-1M托卡马克中的中子通量和辐射剂量当量测量

用5台带有慢化剂(聚乙烯)的BF3₃正比计数管中子探测器测量中子通量和剂量当 量.4台 置于HL_1M装置的四周,分别测量了在氘等离子体条件下,因欧姆加热和波加热产生的热核聚 变中子产额、中子通量和剂量,以及氢等离子体条件下因高能x射线引起的光致核反应而产生 的光致中子. 另一台流动于其他6个观察点,主要监测中子剂量当量. 在D_D聚变条件下,实测 中子产额与计算值作比较,两者在数量级上大体一致. 中子辐射剂量当量远低于国家和部颁 标准,更低于国际防护委员会推荐的中子辐射允许剂量当量 关键词： 3正比计数管')" href="#">BF3₃正比计数管 光致中子 氘_氘聚变中子 剂量当量     

Temperature dependent small-angle neutron scattering of CTABr—magnetic fluid emulsion

Small-angle neutron scattering studies have been carried out to check the structural integrity of citryltrimethylammonium bromide (CTABr) micelles in a magnetic fluid for different magnetic fluid concentrations at two different temperatures 303 and 333 K. It is found that the CTABr micelles grow with increasing magnetic fluid concentration and there is a decrease in the micellar size with increase in temperature.     

Dynamics of thin polymer films: Recent insights from incoherent neutron scattering

Incoherent neutron scattering is presented as a powerful tool for interpreting changes in molecular dynamics as a function of film thickness for a range of polymers. Motions on approximately nanosecond and faster timescales are quantified in terms of a mean-square atomic displacement (〈u²〉) from the Debye–Waller factor. Thin-film confinement generally leads to a reduction of 〈u²〉 in comparison with the bulk material, and this effect becomes especially pronounced when the film thickness approaches the unperturbed dimensions of the macromolecule. Generally, there is a suppression (never an enhancement) of 〈u²〉 at temperatures T above the bulk calorimetric glass-transition temperature (T_g). Below T_g, the reduction in the magnitude of 〈u²〉 depends on the polymer and the length scales being probed. Polymers with extensive segmental or local mobility in the glass are particularly susceptible to reductions of 〈u²〉 with confinement, especially at the Q vectors probing these longer length scales, whereas materials lacking these sub-T_g motions are relatively insensitive. Moreover, a reduced 〈u²〉 value correlates with reduced mobility at long time and spatial scales, as measured by diffusion in these thin polymer films. Finally, this reduced thin-film mobility is not reliably predicted by thermodynamic assessments of an apparent T_g, as measured by discontinuities or kinks in the T dependence of the thermal expansion, specific volume, index of refraction, specific heat, and so forth. These measurements illustrate that 〈u²〉 is a powerful and predictive tool for understanding dynamic changes in thin polymer films. © 2004 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 42: 3218–3234, 2004     

SANS investigation on evolution of pore morphology for varying sintering time in porous ceria

Precipitates of ceria were synthesized by homogeneous precipitation method using cerium nitrate and hexamethylenetetramine at 80°C. The precipitates were ground to fine particles of average size ∼0.7 μm. Circular disks with 10 mm diameter, 2 and 3 mm thickness were prepared from the green compacts by sintering at 1300° C for three different sintering times. Evolution of the pore structures in these specimens with sintering time was investigated by small-angle neutron scattering (SANS). The results show that the peak of the pore size distribution shifts towards the larger size with increasing sintering time although the extent of porosity decreases. This indicates that finer pores are eliminated from the system at a faster rate than the coarser ones as sintering proceeds and some of the finer pores coalesce to form bigger ones.     

Static and dynamic properties of KCN<Subscript><Emphasis Type="Italic">x</Emphasis></Subscript>Cl<Subscript>1−<Emphasis Type="Italic">x</Emphasis></Subscript>

An extended three-body force shell model (ETSM) has been applied to investigate the static and dynamic properties of KCN _x Cl_1−x for the compositionx = 0.56 and 1.0 at 300 K. The phonon dispersion curves computed by us are compared with the single crystal neutron diffraction data. The unusual features of these curves are the upward curvature seen in some of the acoustic branches. This is a result ofK-dependent softening of the phonon due to translation-rotation coupling. The transverse acoustic branch is more soft near the zone centre.     

Radiation damage in Si photodiodes by high-temperature irradiation

Results are presented of a detailed study of the effects of high-temperature 4-MeV neutron irradiation on the performance degradation of Si pin photodiodes together with the radiation-induced defects, observed by deep level transient spectroscopy. The degradation of the device performance and the introduction rate of the lattice defects decrease with increasing sample temperature during irradiation. For a 250°C irradiation, the reduction of the reverse current is only 20% of the starting value. This result suggests that the creation and recovery of the radiation damage proceeds simultaneously at high temperatures. Carbon-related complex as hole capture levels is also mainly responsible for the device degradation for high-temperature neutron irradiation.     

Interferometry with entangled atoms

A quantum gravity-gradiometer consists of two spatially separated ensembles of atoms interrogated by pulses of a common laser beam. The laser pulses cause the probability amplitudes of atomic ground-state hyperfine levels to interfere, producing two, motion-sensitive, phase shifts, which allow the measurement of the average acceleration of each ensemble, and, via simple differencing, of the acceleration gradient. Here we propose entangling the quantum states of atoms from the two ensembles prior to the pulse sequence, and show that entanglement encodes their relative acceleration in a single interference phase which can be measured directly, with no need for differencing. Received 6 June 2002 / Received in final form 25 October 2002 Published online 28 January 2003     

Assessment of fast and thermal neutron ambient dose equivalents around the KFUPM neutron source storage area using nuclear track detectors

A set of five ²⁴¹Am–Be neutron sources are utilized in research and teaching at King Fahd University of Petroleum and Minerals (KFUPM). Three of these sources have an activity of 16 Ci each and the other two are of 5 Ci each. A well-shielded storage area was designed for these sources. The aim of the study is to check the effectiveness of shielding of the KFUPM neutron source storage area. Poly allyl diglycol carbonate (PADC) Nuclear track detectors (NTDs) based fast and thermal neutron area passive dosimeters have been utilized side by side for 33 days to assess accumulated low ambient dose equivalents of fast and thermal neutrons at 30 different locations around the source storage area and adjacent rooms. Fast neutron measurements have been carried out using bare NTDs, which register fast neutrons through recoils of protons, in the detector material. NTDs were mounted with lithium tetra borate (Li₂B₄O₇) converters on their surfaces for thermal neutron detection via and nuclear reactions. The calibration factors of NTD both for fast and thermal neutron area passive dosimeters were determined using thermoluminescent dosimeters (TLD) with and without a polyethylene moderator. The calibration factors for fast and thermal neutron area passive dosimeters were found to be 1.33 proton tracks and 31.5 alpha tracks , respectively. The results show variations of accumulated dose with the locations around the storage area. The fast neutron dose equivalents rates varied from as low as up to whereas those for thermal neutron ranged from as low as up to . The study indicates that the area passive neutron dosimeter was able to detect dose rates as low as 7 and from accumulated dose for thermal and fast neutrons, respectively, which were not possible to detect with the available active neutron dosimeters.     

断前粒子发射的同位素效应

用推广的裂变扩散模型研究了²⁸Si+^164,167,170Er→^192,195,198Pb反应中测量的断前中子、质子和α粒子多重性的激发函数.发现扩散模型能很好地拟合这些轻粒子多重性随裂变系统激发能和Pb同位素的变化趋势.表明断前粒子发射存在一个同位素效应.进而在一个考虑了裂变过程中摩擦效应的统计模型的框架内,在In和Er这两个元素的同位素链中,考察了同位素效应与裂变碎片质量不对称性和裂变系统尺度的关系.计算结果表明:同位素效应的存在不依赖于裂变系统的大小和不对称性.此外,当裂变系统具有高的中质比时,轻带电粒子发射将不再敏感于裂变延迟时间的长短,而中子发射则非常敏感.这个结果暗示对那些特别丰中子的裂变系统,轻带电粒子(质子和α粒子)的多重性对于研究热核裂变过程中的摩擦强度不是一个好的探针.