Programmed cooling crystallization of potassium sulphate solutions

The crystal size distribution from a batch cooling crystallizer is predicted by the numerical solution of a mathematical model which uses empirical kinetics of nucleation and crystal growth. The predictions clearly point out the potential advantages of controlled cooling at a constant nucleation rate for improving the product crystal size over that obtained by either natural or linear cooling.Experimental runs following programmed cooling curves for seeded potassium sulphate solutions showed reasonable agreement with the theoretical predictions. A size dispersion of the crystals was observed which contributes to a slight deviation from theory. Nevertheless, controlled cooling significantly reduced the quantity of nuclei formed and improved the product crystal size distribution.     

基于工作流导向的“网络信息安全”实训教材建设

针对"网络信息安全"教材建设的现状进行分析,提出建设基于工作流导向的任务式实训模式教材的必要性,并从教材的指导思想、整体结构、内容结构及其特色等方面进行了阐述。实践证明,该新型教材的建设和使用能够激发学生学习网络安全知识的兴趣,提升动手能力,有效提高教学质量和效率。     

Airborne differences in odors emitted byRattus norvegicus in response to reward and nonreward

To test the hypothesis that rats (Rattus norvegicus) emit airborne, differential odors in response to reward and nonreward, donor rats received random sequences of rewarded and nonrewarded placements in small compartments and an airstream transported odors from these compartments to test rats in a separate chamber. When donors remained in the compartments during, or were removed just prior to, air transport, test rats utilized transported odors as discriminative cues signaling their own reward and nonreward for a lever-press response. When the airstream was passed through a clean compartment containing paper flooring extracted from donor compartments, test rats were not able to discriminate. Test trials to assess for control by food odors suggest that donor-produced odors, rather than food odors per se, provided the discriminative signals for test rats. Results confirm the existence of somewhat volatile, although apparently stable, odors emitted in response to reward and nonreward, and implicate a differential in amount and/or type of odor produced by donors to these two events as the source of discriminative control.     

Preparation of phenolic resin derived 3-D ordered macroporous carbon

Three-dimensionally ordered long-range macroporous carbon structures were prepared using commercially available phenolic resin by utilizing sacrificial colloidal silica crystalline arrays as templates that were subsequently removed by HF etching after pyrolysis in an argon atmosphere. SEM, TEM, and BET were employed to characterize the morphology and the surface area of the porous carbon structures. The pore size (150–1000 nm) and BET surface area, which reflect pore volume (298.6 m²/g (1.32 cm³/g) ∼ 93.7 m²/g (0.12 cm³/g)), of the macroporous carbon structures produced were approximately proportional to the size (150–1000 nm) of the sacrificial silica sphere templates used (annealing temp. 550°C). The achieved 550 nm porous carbon structures were examined to function as potential catalyst carriers and were successfully impregnated with Ag or Pt-Ru on their inner walls after borohydride reduction at room temperature. In addition, porous carbon patterns were fabricated using the ‘micromolding in capillary’ technique, which has potential applications in the microreaction technology.     

Performance relationships in PVC–plasticizer dry blending

The phenomenon of plasticizer acceptance by poly(vinyl chloride) (PVC) in hotprocess dry blending is examined via scanning electron microscopy, mercury intrusion porosimetry, and torque rheometer measurements. The effects of granule porosity, resin molecular weight, and synthesis recipe in PVC manufacture by the suspension process are related to the rate of plasticizer acceptance. For a PVC resin to dry blend, i.e., to become a free-flowing powder when mixed with plasticizer under hot-processing conditions, the resin granules must be porous. Porosity arises from interstices between primary PVC particles. At a given granule porosity, an increase in primary particle agglomeration adversely affects dry blend performance. At constant molecular weight and for resins manufactured by a given recipe, dry-blend performance is quantitatively described by granule porosity. With an increase in resin molecular weight, a greater granule porosity is required to maintain an equivalent dry-blend time (DBT). Accordingly, for most suspending agent recipes, DBT is dependent directly upon granule porosity and inversely upon molecular weight. However, if the suspending agent used in resin manufacture is an excessively rapid film former, dry-blend performance with molecular weight variation is dependent upon the suspending agent's concentration, not upon granule porosity, which must be adequate, nor upon the resin's molecular weight. An interfacial film-forming suspending agent enhances fusion of primary PVC particles at the suspension granule—water interface, increasing the granule's “pericellular membrane” thickness. This membrane, a PVC skin, does not significantly influence dry-blend performance with low- or intermediate-viscosity plasticizers. The particle skin does impede dry-blend rates with high-viscosity, poorly solvating plasticizers, but this effect can be negated in part by increasing the diameter of pore openings in the topographical skin. Dry blending occurs below the glass transition temperature (T_g) of PVC with low-viscosity plasticizers and above the T_g with high-viscosity, poorly solvating modifiers. The influence of resin and plasticizer variables indicates the dry-blend phenomenon to be a diffusion-controlled process. The rate of dry blending is dependent upon two mechanisms: (1) the rate of pore penetration—which exposes the plasticizer to a much greater surface area than if it remained exterior, encapsulating the granule—and (2) the rate of plasticizer diffusion into the PVC matrix.     

Relations between quantum correlations,purity and teleportation fidelity for the two-qubit Heisenberg XYZ system

Quantifying and understanding quantum correlations may give a direct reply for many issues regarding the interesting behaviors of quantum system. To explore the quantum correlations in quantum teleportation, we have used a two-qubit Heisenberg XYZ system with spin–orbit interaction as a quantum channel to teleport an unknown state. By using different measures and standard teleportation protocols, we have derived the analytical expressions for quantum discord, entanglement of formation, purity, and maximal teleportation fidelity of the system. We compare their different characteristics and analyze the relationships between these quantities.     

Oxidation of Thin Sheet Reaction-Sintered Silicon Nitride

Oxidation of reaction-sintered silicon nitride was studied in damp air. The formation of "passive" silica films was investigated at 1 atm and 700 to 1100°C and some limited work on weight loss behavior was performed in vacuo of 10⁻⁸ to 10⁻⁵ atm at 1050 to 1200°C. Passive behavior was dominated by reaction in the pore network. Oxidation was extensive at 900 to 1000° but slight at 700 to 800°C. At 1100°C a protective skin limited reaction. Weight loss in vacuo was slight at 1050°C. The vacuum pressure required to suppress the weight loss increased from 4 to 5 × 10⁻⁷ atm at 1050° to 1.5 to 2.5 × 10⁻⁵ atm at 1200°C.     

扎赉诺尔褐煤制取高炉喷吹料和中热值煤气研究 (Ⅰ)煤气、焦油产率及性质

本文是在10kg／h固体热载体干馏实验装置上用扎赉诺尔褐煤制取高炉喷吹料和中热值煤气的研究结果。在干馏温度450℃～650℃范围制得煤气110Nm3/t～400Nm3/t，煤气热值为14．7MJ／Nm3～17．5MJ／Nm3，属中热值煤气。可供民用，也可用于补充钢铁企业燃气不足，平衡能源。得低温焦油2％～9％，可加工成化工产品和燃料油。半焦可用于高炉喷吹。     

Dielectric relaxation of poly(chlorostyrenes) and their copolymers in the primary transition region

Dielectric relaxation measurements were carried out on a series of bulk poly(chlorostyrene) homopolymers and random copolymers over the frequency range from 50 to 100 kHz and at temperatures in the neighbourhood of the glass transitions of the polymers thus encompassing the α relaxation. Homopolymers examined were polystyrene (PS), poly(2-chlorostyrene) (P2CS), poly(3-chlorostyrene) (P3CS), and poly(4-chlorostyrene) (P4CS). Copolymers were poly(styrene-co-2-chlorostyrene) (PS2CS), poly(styrene-co-4-chlorostyrene) (PS4CS), and poly(2-chlorostyrene-co-4-chlorostyrene) (P2CS4CS). The dielectric data were analysed to yield dipole moments and Kirkwood—Fröhlich correlation parameters. The shapes of the dielectric loss curves were also taken into account. Glass transition temperatures were determined by differential scanning calorimetry (d.s.c.). It was concluded that the phenyl ring rotates freely in the α relaxation regions of PS, P4CS, and P3CS, but not in P2CS. The dipole moments of the copolymers are correlated with dyad distributions calculated from reactivity ratios.