Mark-Houwink-Sakurada coefficients for conventional poly(methyl methacrylate) in tetrahydrofuran

Summary Intrinsic viscosities [] in tetrahydrofuran (THF) at 30°C are reported for ten narrow molecular weight distribution poly(methyl methacrylate) (PMMA) samples covering nearly two orders of magnitude in molecular weight. By combining the viscosity results with absolute weight-average molecular weights determined via low-angle laser light scattering (LALLS) experiments, we have accurately determined the Mark-Houwink-Sakurada (MHS) parameters for this polymer-solvent pair (K=7.56x10⁵ and a=0.731, when [] is in dL g^-1).     

Synthesis and chain flexibility of poly(cyclohexylethyl methacrylate)

The synthesis and characterization of fractions of poly(cyclohexylethyl methacrylate) (PCHEM) are reported. A combination of low-angle laser light scattering and intrinsic viscosity experiments was employed to estimate the characteristic ratio (C_∞) of this polymer. The value of 10.7 obtained for PCHEM is similar to the value of 11.3 found previously for poly(phenylethyl methacrylate) but is smaller than values measured for poly(cyclohexyl methacrylate) and poly(cyclohexylmethyl methacrylate) (C_∞ = 11.6 and 11.9, respectively). Received: 28 October 1996/Revised: 16 December 1996/Accepted: 19 December 1996     

Dual diagnosis: a treatment model for substance abuse and major mental illness

The treatment of "dual diagnosis", co-occurring substance abuse and mental illness, calls for addressing two serious and often confounding problems. The authors introduce an expanded version of the transtheoretical model of change as formulated by J.O. Prochaska and C.C. DiClemente, and suggest that this new version offers a pragmatic approach to the conceptualization and treatment of dual diagnosis. The potential utility of the treatment model is presented through the authors' experiences in working with inner-city, chronic mentally ill individuals with substance abuse problems. Practical guidelines for dual diagnosis group therapy are discussed.     

Legal issues in sharing the benefits of biodiversity prospecting

The National Cancer Institute (NCI) is the US Government's principal agency for research on the prevention, diagnosis and treatment of cancer. A critical component of the Institute's mission is the identification and development of new and promising treatments for cancer and AIDS. For many years these efforts have included a program to investigate natural products for potential new therapeutic agents. In 1986, with the advent of new screening techniques, the National Cancer Institute stepped up its exploration of natural products and began world-wide collections of plants in tropical and subtropical regions. In recognition of the principles of the Biodiversity Treaty, NCI appreciates that continued access to the natural products of these countries depends on the Institute's ability to recognize the contributions of these source countries and their indigenous peoples, and to provide them adequate incentives to conserve their natural resources for the purposes of drug discovery. Accomplishing this goal presented several legal issues for the National Cancer Institute. As an agency of the US government, the NCI has an adjunct statutory mission to facilitate the transfer of technology developed through the Institute's programs into the private sector for further development and commercialization, and NCI operates under a national policy to use the patent system to transfer Federally supported research to the private domestic sector. Reliance on patent law may limit the Institute's ability to recognize the rights of source countries and their indigenous people and provide compensation for their contributions. However, other legal instruments, such as contracts, can serve as interim measures to provide compensation to source countries and indigenous populations. The National Cancer Institute's Letter of Collection agreement (LOC, formerly the "Letter of Intent'), is an example of an alternative means that "fills-in the gaps' created by patent law and through which source countries may share in the benefits of natural product development.     

Improving comparability of hydrogen storage capacities of nanoporous materials

We present results of investigations into improving methods by which gas sorption data are collected and reported. The focus is the accurate comparison of hydrogen storage capacities of different nanoporous materials. The aim is to produce a more rigorous approach to the assessment of the hydrogen storage capacities of different nanoporous materials through formulation of meticulous and systematic data collection routines for production of universally reproducible H₂ isotherms over a wide range of pressure and temperature conditions. Effects of a range of experimental variables are examined and recommendations for the optimisation of data collection routines are given.     

Dilute solution properties of randomly branched poly(methyl methacrylate)

Randomly branched poly(methyl methacrylate) samples were prepared by copolymerization with different amounts of ethylene dimethacrylate. The molecular weight distributions, radius of gyration distributions, and intrinsic viscosity distributions were measured by size exclusion chromatography with refractive index, multiangle light-scattering, and viscosity detectors. The effect of branching on the radius of gyration was compared with the effect on the intrinsic viscosity. It was found that the intrinsic viscosity contraction factor gⁱ scales with the radius of gyration contraction factor g, with the exponent, ϵ, having a value in the range 0.8–1.0. © 1996 John Wiley & Sons, Inc.     

Three-dimensional simulation of the coupled convective, conductive, and radiative heat transfer during decay heat removal in an HTR

A three-dimensional model has been constructed to simulate the passive heat removal in a modular prismatic-block high temperature reactor during a loss of active cooling accident. This model, developed using the STAR-CD general computational fluid dynamics code, solves the combined conductive, convective, and radiative heat transfer within a 30° section of the core and reactor vessel. To accommodate the different spatial scales, it uses homogeneous equivalent media to represent the coolant flow and the prismatic fuel blocks. A customized procedure that manages solving alternatively the dynamic and thermal fields permits the computation of very long transients, which typically are performed for 100 or more hours of simulated time.The global methodology and specific modeling procedures are explained, and key points of the CFD analysis are highlighted. Next, the results of several calculations are presented, and the physical phenomena represented are described. Two commonly investigated loss of active cooling scenarios are considered: depressurized conduction cooldown and pressurized conduction cooldown. The results for these two scenarios are compared to assess the effect of heat transfer via internal natural convection – which is negligible during the depressurized event – on the thermal behavior of the system. In addition, the evolution of the natural convection flow through the core and in the annular spaces is examined and discussed.     

Optimization of Co-content in C14 Laves phase multi-component alloys for NiMH battery application

The structural, electrochemical, and gas phase hydrogen storage properties of predominantly C14 crystalline phase alloys with partial replacement by Co (up to 2.5 at%) are reported. Minor phases, including C15 and cubic TiNi, were found by X-ray diffraction and contributed to the improved hydrogen diffusion through the alloy. The optimal Co-content of between 1.0 and 1.5 at% provides easy activation, high gas phase capacity, and a high discharge capacity. An optimized alloy formula also provided the smallest metallic nickel cluster size embedded in the surface oxide and the largest number of nickel clusters. In sealed cell studies, a Co-content of 1.5% gives the best performance in formation, cycle life, and charge retention, but has worse specific power and low temperature performance than some other compositions. The high-rate dischargeabilities at lower rates were found to be limited by surface reactions, not bulk diffusion.     

XR-C1, a new CHO cell mutant which is defective in DNA-PKcs, is impaired in both V(D)J coding and signal joint formation

DNA-dependent protein kinase (DNA-PK) plays an important role in DNA double-strand break (DSB) repair and V(D)J recombination. We have isolated a new X-ray-sensitive CHO cell line, XR-C1, which is impaired in DSB repair and which was assigned to complementation group 7, the group that is defective in the XRCC7 / SCID ( Prkdc ) gene encoding the catalytic subunit of DNA-PK (DNA-PKcs). Consistent with this complementation analysis, XR-C1 cells lackeddetectable DNA-PKcs protein, did not display DNA-PK catalytic activity and were complemented by the introduction of a single human chromosome 8 (providing the Prkdc gene). The impact of the XR-C1 mutation on V(D)J recombination was quite different from that found in most rodent cells defective in DNA-PKcs, which are preferentially blocked in coding joint formation, whereas XR-C1 cells were defective in forming both coding and signal joints. These results suggest that DNA-PKcs is required for both coding and signal joint formation during V(D)J recombination and that the XR-C1 mutant cell line may prove to be a useful tool in understanding this pathway.