PRODUCTION OF PIGMENT NANOPARTICLES USING A WET STIRRED MILL WITH POLYMERIC MEDIA

Pigment nanoparticles with a size range of 10-100 nm were produced from large agglonmerates via a stirred media mill operating in the wet-batch mode and using polymeric media,The effects of several operating variables such as the surfactant concentration,polystyrene media loading.and media size on the pigment size distribution of the product were studied.The process dynamics was also investigated.Dynamic light scattering and electron microscopy were used as the characerization techniques.The polymeric grinding media are found to be effective for the production of pigment nanoparticles.The experimental results suggest the existence of an optimum media size and surfactant concentration,A population balance model of the process reveals a transition from first-order breakage kinetice for rela-large agglomerates split in a first-order kinetics,with a delay period,for the smaller particles.The model implies that large agglomerates split in a first-order fashion whereas the breakage of individual naoparticles may depend on induced fatigue of the particles.     

Effect of molecular structure on polyethylene melt rheology. II. Shear-dependent viscosity

The investigation of the effect of molecular structural variables on the melt viscosity of polyethylene was extended to the shear dependent region by application of a reduced variables treatment following, in a formal sense, that of Bueche. Viscosity–shear rate data were obtained for a series of experimentally polymerized linear polyethylene samples having a range of molecular weights and molecular weight distributions as characterized primarily by gel permeation chromatography. These data could be superimposed on a single reduced variables flow curve using parameters which were a function only of temperature, limiting Newtonian viscosity, M?_w, and M?_w/M?_n. The same treatment was successfully applied also to branched (low-density) fraction data discussed in a previous paper, with additional correction for long-chain branching. However, different reduced variables curves were obtained for the branched and linear cases.     

Classical trajectory calculations with time-dependent forces in heavy-ion collisions

The applicability of a phenomenological time-dependent nucleus-nucleus potential to deep inelastic collisions is studied. We present its general shape and make a particular choice of the diabatic and adiabatic parts. From trajectory calculations we find that the angle-energy correlation is well described when a time-dependent friction force is used. We also compare our results to some TDHF calculations.     

A reiterative approach to 2,3-disubstituted naphthalenes and anthracenes

[reaction: see text] Simple bis(bromoethynyl)arenediynes are easily prepared by the desilylative halogenation of the corresponding trimethylsilyl derivatives. Cycloaromatization of these halogenated enediynes leads to the otherwise difficult to prepare 2,3-dibromoarenes in good yield. Alkynylation of the resulting haloaromatic compound regenerates the soluble enediyne system, homologated by one aromatic ring. This iterative methodology can be terminated by the cycloaromatization of the unsubstituted enediyne, providing the simple acene hydrocarbon.     

Trace sulfide determination in oxic freshwaters

A simplified method for determination of reduced sulfur species in natural waters is presented. Reduced sulfur species were separated from a natural water matrix, using purge-and-trap (PT), after reacting with acid (acid volatile sulfide—AVS) or Cr(II) in acidic medium (chromium reducible sulfur—CRS). Sulfide in the trapping medium (0.05 M NaOH), was analyzed spectrophotometrically after derivatization to form methylene blue (MB). AVS precision for Na₂S and zinc sulfide clusters in synthetic solutions was ≤8.5% RSD at concentrations ranging from 48 to 503 nM. Spike recoveries of zinc sulfide clusters were 75-98% in a variety of freshwaters using the AVS procedure. Spike recoveries of Cu sulfide colloids were 94-109% in the same freshwater samples using the CRS procedure. During the analytical procedure an interfering compound was produced due to the reaction of mixed diamine reagent with itself. Lowering the pH of the reaction mixture minimized the formation of this compound. Minimizing contamination from particulates was necessary to achieve sub-nanomolar detection limits. The detection limit for AVS in a 500 ml sample with a 10 cm spectrophotometer cell was 0.1-0.3 nM (3×S.D. blank). The CRS procedure was calibrated with a synthetic CuS colloid. Interferences to the CRS method included finely divided pyrite, polysulfide, thiosulfate, sulfite and some elemental sulfur. The Cr(II) reagent did not reduce sulfate under our experimental conditions. The degree to which zinc sulfide clusters were adsorbed on membrane filters during filtration was mitigated if the clusters were synthesized in the presence of natural organic matter. Examples of AVS and CRS concentrations determined in oxygenated waters using the PT method were comparable to those reported recently by other methods. This method offers greater simplicity than other methods for trace dissolved sulfide determination in natural waters.     

Determination of butyltin species in natural waters using aqueous phase ethylation and off-line room temperature trapping

Monobutyltin (MBT), dibutyltin (DBT) and tributyltin (TBT) were determined in natural water samples by aqueous phase ethylation with sodium tetraethylborate (STEB), room temperature trapping of the resulting volatile derivatives on Tenax TA^®, followed by gas chromatography-quartz furnace atomic absorption spectrometry (GC-QFAAS). Recoveries of butyltin spikes from natural water samples were 90-109% at concentrations of ∼100 ng Sn/l. The method precision at ∼100 ng Sn/l was ≤6% RSD for butyltins spiked into natural waters. The detection limits for 1 l water samples were <1 ng Sn/l for all butyltin species. Sample throughput of the method is high (greater than three samples per hour) due to the two-stage nature of the procedure, which allows derivatisation/trapping and GC-QFAAS quantitation to be performed separately. Off-line trapping is also advantageous as it extends the life of the GC column and quartz furnace to at least 12 months due to minimisation of carry-over of co-purged material.     

超声速化学反应流动中燃料预喷研究述评

研制基于超声速燃烧的高效吸气式推进装置(运行Mach数在3.5以上)需要寻求改善混合效率的有效机制, 这对于采用常规碳氢燃料(特别是可以增加密度的液体燃料)的装置尤为重要. 延长混合时间的一种途径是在飞行器燃料室的上游喷入部分燃料. 壁面喷射一直是超声速气动力学最具挑战性的课题, 这里包括使比冲损失最小、改善燃料-空气的混合、减少入口段/燃烧室的相互作用以及增进火焰稳定性等. 综述了超声速入口段或燃烧室的隔离器中液体燃料(个别情况下为气体燃料)喷射的研究进展. 在这些研究中, 燃料都是从后掠型细支架尾迹中的壁面处喷射出来的, 动压比很低($q_{\rm {jet}}/q_{\rm {air}}$=0.6$\sim$1.5). 它们涉及入口段和燃烧室的隔离器中单个支架/喷射器的几何结构及其组合方式、各种各样的喷射条件、不同的引射剂, 并且评估了这些因素对于燃料羽流喷散、比冲损失以及混合效率的影响. 述评引用了46篇参考文献.     

High throughput discovery of heteroaromatic-modifying enzymes allows enhancement of novobiocin selectivity

Glycosylated analogues of novobiocin, discovered using a broad library of enzymes, have 100-fold improved activity against breast, brain, pancreatic, lung and ovarian cancers and ablated associated off-target activity leading to an up to 2.7 × 10(4) fold increase in selectivity.     

Statistical Geometry and Lattices

Statistical geometry furnishes the tool that allows the transfer of results from a lattice with finite lattice parameter to the continuum. Since lattice simulations are simpler than continuum ones, this suggests that larger scale simulations for the continuum might be more effectively carried out on a lattice with finite lattice parameter followed by the indicated transfer. We also show that a statistical geometry, peculiar to hard particles on a lattice, can be developed. Among other things, this opens the possibility that a scaled particle theory on a lattice might be derived.