Polycyclic aromatic hydrocarbons as universal bases in peptide nucleic acid

Polycyclic aromatic hydrocarbons were found to be promising universal bases in PNA·DNA double helices. Several of the arenes paired promiscuously with any of the four canonical bases. However, the stabilities of the duplexes depended on the size and shape of the arene.     

内埋炸药下超高韧性水泥基复合材料的抗爆性能

为研究超高韧性水泥基复合材料(ultra-high toughness cementitious composites, UHTCC)在内埋炸药爆炸下的抗爆性能和损伤破坏规律,对不同炸药埋深下的UHTCC和高强混凝土(high-strength concrete, HSC)进行了内埋炸药抗爆实验。得到了两种材料靶体的破坏状态,并利用接触爆炸的实验结果计算出了两种材料的抗爆性能参数。结果表明,在相同条件下,UHTCC抗爆性能优于高强混凝土。为了进一步探究UHTCC的抗压强度、抗拉强度以及拉伸韧性对靶体在内埋炸药下抗爆性能的影响,首先,采用改进的K&C模型对炸药埋深为40 mm的超高韧性水泥基复合材料靶体进行数值模拟,模拟结果与实验结果基本吻合,并根据数值模拟的结果得到了爆炸冲击波沿靶体径向衰减速度大于轴向衰减速度这一规律,验证了数值模型的有效性;然后,通过调整改进K&C模型中与抗压强度、抗拉强度以及拉伸韧性相关的参数,数值预测了不同抗压强度、抗拉强度以及拉伸韧性下UHTCC靶体的破坏状态,发现增强UHTCC的韧性可以有效防止靶体发生整体性破坏,增大UHTCC的抗拉强度可以减小靶体迎爆面的开坑直径,增大UHTCC的抗压强度对减小开坑直径效果不明显。     

Investigation of structural and electronic properties of β- HgS: Molecular dynamics simulations

The pressure induced phase transition of β-HgS is studied using an ab initio molecular dynamics simulation. The structural phase transformation from the zinc-blende structure to the NaCl-type structure (space group $Fm\overline{3}m$) and from this structure to CsCl-type structure ($Pm\overline{3}m$) with the application of hydrostatic pressure is predicted. Additionally, the electronic properties of HgS and various physical properties such as the lattice constants, the bulk modulus and the pressure derivative of the bulk modulus are revealed. Furthermore, these phase transitions are obtained using the total energy and enthalpy calculations. According to these calculations these transformations are occurring at about 20?GPa and 28?GPa for $F\overline{4}3m$ →$Fm\overline{3}m$ and $Fm\overline{3}m$ →$Pm\overline{3}m$, respectively.     

High-intensity lasers and controlled fusion

The use of high-intensity lasers to cause ignition in inertial confinement fusion is presented, with emphasis on current experimental programs and physical concepts that are at the forefront of the field. In particular, we highlight the issues of fast electron transport through dense materials, an essential element of the Fast Ignitor concept.Received: 22 November 2002, Published online: 5 August 2003PACS: 52.20.Fs Electron collisions - 52.38.Kd Laser-plasma acceleration of electrons and ions     

Poly(aryl ether)s containing o‐terphenyl subunits. III. Random copoly(ether imide)s

The synthesis of a new diamine monomer, N‐n‐butyl 3,12‐diamino‐5,6,9,10‐tetrahydro[5]helicene‐7,8‐dicarboxylic imide (4), that contains a helically locked, U‐shaped 4′,4″‐o‐terphenyl moiety is described. The monomer was polymerized with 3,3′,4,4′‐oxydiphthalic dianhydride and 2,2‐bis[4‐(4‐aminophenoxy)phenyl]propane to form a series of copoly(ether imide)s (5a–e). The incorporation of 4 into the poly(ether imide)s varied the glass‐transition temperature of the copolymers of which it was a part. There was a tendency to form macrocyclic materials at higher molar percentages of 4 during polymerization. The fluorescence of all the copoly(ether imide)s gradually decreased as the content derived from monomer 4 increased in the polymer. © 2000 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 38: 758–763, 2000     

Measuring naphthenic acids concentrations in aqueous environmental samples by liquid chromatography

Naphthenic acids are found in wastewaters from petroleum refineries and oil sands extraction plants. Currently, the concentrations of these toxic carboxylic acids are determined by extracting them into methylene chloride and measuring the absorption of the carboxyl group by Fourier-transform infrared (FTIR) spectroscopy. An improved HPLC method, that is simpler and faster than the FTIR method, was used to detect the 2-nitrophenylhydrazides of the naphthenic acids at concentrations as low as 5 mg l(-1). Analyses of 58 oil sands water samples showed that the naphthenic acids concentrations determined by FTIR were on average 11% higher than those determined by HPLC.     

Post-Harvest Operations to Generate High-Quality Medicinal Cannabis Products: A Systemic Review

The traditional Cannabis plant as a medicinal crop has been explored for many thousands of years. The Cannabis industry is rapidly growing; therefore, optimising drying methods and producing high-quality medical products have been a hot topic in recent years. We systemically analysed the current literature and drew a critical summary of the drying methods implemented thus far to preserve the quality of bioactive compounds from medicinal Cannabis. Different drying techniques have been one of the focal points during the post-harvesting operations, as drying preserves these Cannabis products with increased shelf life. We followed or even highlighted the most popular methods used. Drying methods have advanced from traditional hot air and oven drying methods to microwave-assisted hot air drying or freeze-drying. In this review, traditional and modern drying technologies are reviewed. Each technology will have different pros and cons of its own. Moreover, this review outlines the quality of the Cannabis plant component harvested plays a major role in drying efficiency and preserving the chemical constituents. The emergence of medical Cannabis, and cannabinoid research requires optimal post-harvesting processes for different Cannabis strains. We proposed the most suitable method for drying medicinal Cannabis to produce consistent, reliable and potent medicinal Cannabis. In addition, drying temperature, rate of drying, mode and storage conditions after drying influenced the Cannabis component retention and quality.     

Diffusion of dextran within poly(methacrylic acid) hydrogels

We describe an investigation of fluorescence correlation spectroscopy into the diffusion of fluorescein‐tagged dextran (FDEX) in a poly(methacrylic acid) (PMAA) hydrogel. The temperature dependence of FDEX diffusion is shown to follow Zimm behavior in pure water, and the decrease in the diffusion coefficient when in the PMAA hydrogel has been modeled. The addition of acid and alkali (HCl and NaOH, respectively) not only control the swelling and collapse of the hydrogel but also reveal a strong pH dependence of the dextran diffusion coefficient, which shows a (nonmonatonic) increase with pH. The addition of NaCl and CaCl₂ salts similarly showed evidence of network swelling, most notably at low salt concentration, but also that the diffusion coefficient within the gel at these low concentrations is larger than that in the equivalent solution without the hydrogel, indicating that the combination of hydrogel and salt works to increase the diffusion coefficient above that in pure water. © 2012 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys, 2012