中国通货膨胀与相对价格可变性——基于长期效应与短期效应的实证分析

在构建通货膨胀与RPV关系理论模型的基础上,运用面板数据固定效应估计量来检验中国通货膨胀对RPV影响的长期效应,并构建向量误差修正模型来分析中国通货膨胀对RPV影响的短期效应.研究得出,在不考虑确定性因素和外生变量的情况下,从全国来看,总体是短期效应大于长期效应;相反则是长期效应略大于短期效应.在上述两种情况下,各地区的长期效应与短期效应也明显不同.因此,国家应该多考虑不同地区通货膨胀对RPV影响的长期效应与短期效应大小,从而有效地治理通货膨胀和稳定物价水平.     

All-pole biquadratic filter realization with the minimum ripple due to parameter variations

In this work, the minimization of the ripple in the relative change of the transfer function amplitude due to parameter variations is studied for the signal-flow graph of the state equations realizing all-pole second-order transfer function. First the measure for the ripple is defined and then branch transmittances minimizing the measure are found. the results obtained in this study can be used in all-pole active filter realizations with the minimum ripple measure.     

Melt processing of ethylene–vinyl acetate/banana starch/Cloisite 20A organoclay nanocomposite films: structural,thermal and composting behavior

This work shows the preparation of ethylene vinyl acetate copolymer/banana starch/Cloisite 20A organoclay (EVA/starch/C20A) nanocomposites by melt processing. Wide angle X-ray diffraction (WAXD), field emission scanning electron microscopy (FE-SEM), differential scanning calorimetry and thermogravimetric analysis were used to characterize the obtained nanocomposites. Mechanical properties were also determined. In addition, the performance of the nanocomposite films under composting was preliminarily studied; it was conducted using the soil burial test method. Despite knowing that the starch is difficult to process by extrusion, nanocomposite films with high homogeneity were obtained. In this case, C20A organoclay acts as an effective surfactant to make the starch natural polymer compatible with the EVA synthetic polymer. The good compatibility between EVA, starch and C20A clay was also deduced by the formation of intercalated and intercalated-exfoliated structures determined by WAXD and FE-SEM. Physical evidence of the damage in EVA/starch/C20A nanocomposite films after the composting test was observed. It is worth noting that despite the absence of starch, the EVA/C20A nanocomposite film, used as a control, also showed surface damage. This behavior is related to the organic modifier linked to clay C20A, which contains molecules derived from fatty acids that can be used as a food source for microorganisms.

     

Formation of Triterpenoids throughout <Emphasis Type="Italic">Olea europaea</Emphasis> Fruit Ontogeny

Drupes were handpicked from olive (Olea europaea L.) trees, cv chemlali, at 13 distinct stages of fruit development, referred to as weeks after flowering (WAF), and analyzed for their free and esterified sterols and triterpenoids content. These two classes of compounds are synthesized via the acetate/mevalonate pathway and share common precursors up to oxidosqualene (OS). Cyclization of OS in either cycloartenol or beta-amyrin constitutes a branch point between primary (sterol pathway) and secondary (triterpenoid pathway) metabolisms. At the onset of fruit development, i.e., between 12 and 18 WAF, drupes were found to contain high amounts of alpha- and beta-amyrins as well as more-oxygenated compounds such as triterpenic diols (erythrodiol and uvaol) and acids (oleanolic, ursolic and maslinic acids). Concomitantly, sterol precursors were barely detectable. From 21 WAF, when the olive fruit reached its final size and began to turn from green to purple, alpha- and beta-amyrins were no longer present, while 4,4-dimethyl- and 4alpha-methylsterols started to be formed, indicating a redirection of the carbon flux from the triterpenoid pathway towards the sterol pathway. Between 21 and 30 WAF, sterol end products, mainly represented by sitosterol, progressively accumulated and triterpenic diols were replaced by triterpenic acids, essentially maslinic acid. Interestingly, the developing olive fruit was found to accumulate significant amounts of parkeol as an ester conjugate. Whatever the stage of development, triterpenoids represent the major triterpenic compounds of the olive fruit.     

Bioactive and Physicochemical Properties of Persimmon as Affected by Drying Methods

In this study, the effects of three different drying methods (freeze drying, oven drying, and vacuum oven drying) on bioactive (total phenolics, total flavonoids, condensed tannin and total hydrolyzable tannin contents, antiradical activity, and antidiabetic activity) and some physicochemical (dry matter, ash, water activity (a _w ), color, protein, hydroxymethylfurfural, glucose and fructose content) properties of persimmon fruit were investigated. Simplex lattice mixture design methodology was applied to determine the best solvent mixture for the extraction of phenolics from the samples. It was found that the mixture of acetone:water at the ratio of 50:50 % (v/v) was the best solvent mixture for the extraction. The persimmon powder sample obtained from freeze drying showed significantly (p <0.05) higher bioactivity values than oven- and vacuum-oven-dried samples. Antiradical activity changed significantly depending on the drying method employed and it was superior in freeze-dried samples than that of the other drying methods.     

What Role Does Ozone Play in Preventing Dental Caries? An Evidence-Based Review

Ozone, which is also referred to as triatomic oxygen or trioxygen, is a naturally occurring inorganic molecule that consists of three oxygen atoms. Ozone has proven microbiological properties and, for this reason, it is extensively used in modern medical practices. Ozone is a powerful oxidant that demonstrates bactericide, virucide, and fungicide effects. The strong oxidation effect it produces results in the formation of highly reactive free radicals that have the capability to destroy microorganisms. Ozone has been proposed as a means of preventing caries, and existing research confirms that this form of therapy does have promising potential. However, very few clinical studies have examined the impact that ozone treatment can have on the management of caries lesions. This article presents a detailed literature review of existing peer-reviewed sources that have examined the role ozone plays in preventing and treating caries.     

Palladium-PEPPSI-NHC Complexes Bearing Imidazolidin-2-Ylidene Ligand: Efficient Precatalysts for the Direct C5-Arylation of N-Methylpyrrole-2-Carboxaldehyde

Catalysis Letters - The Pd-catalyzed direct arylation of pyrroles is an important research field for organic synthesis and catalysis chemistry. However, imidazolidin-2-ylidene based Pd-NHC...     

Thermal decomposition behavior of oligo(4‐hydroxyquinoline)

In this study, the kinetic parameters and reaction mechanism of decomposition process of oligo(4‐hydroxyquinoline) synthesized by oxidative polymerization were investigated by thermogravimetric analysis (TGA) at different heating rates. TGA‐derivative thermogravimetric analysis curves showed that the thermal decomposition occurred in two stages. The methods based on multiple heating rates such as Kissinger, Kim–Park, Tang, Flynn–Wall–Ozawa method (FWO), Friedman, and Kissinger–Akahira–Sunose (KAS) were used to calculate the kinetic parameters related to each decomposition stage of oligo(4‐hydroxyquinoline). The activation energies obtained by Kissinger, Kim–Park, Tang, KAS, FWO, and Friedman methods were found to be 153.80, 153.89, 153.06, 152.62, 151.25, and 157.14 kJ mol^?1 for the dehydration stage, 124.7, 124.71, 126.14, 123.75, 126.19, and 124.05 kJ mol^?1 for the thermal decomposition stage, respectively, in the conversion range studied. The decomposition mechanism and pre‐exponential factor of each decomposition stage were also determined using Coats–Redfern, van Krevelen, Horowitz–Metzger methods, and master plots. The analysis of the master plots and methods based on single heating rate showed that the mechanisms of dehydration and decomposition stage of oligo(4‐hydroxyquinoline) were best described by kinetic equations of A_n mechanism (nucleation and growth, n = 1) and D_n mechanism (dimensional diffusion, n = 6), respectively. POLYM. ENG. SCI., 54:992–1002, 2014. © 2013 Society of Plastics Engineers     

Microcellular polymeric foams based on 1‐vinyl‐2‐pyrrolidone and butyl‐acrylate with tuned thermal conductivity

Microcellular polymers have been produced by ScCO₂ foaming, based on 1‐vinyl‐2‐pyrrolidone (VP) and butyl‐acrylate (BA). Three different copolymers were prepared, varying the compositions of VP and BA, following a simple radical polymerization process using an UV initiator. The samples a good foaming behavior and also excellent flexibility and handle ability, with expansion ratios between 1.53 and 1.72, and cell sizes in the microcellular range (below 5 µm). However, it was observed that the gas distribution and, consequently, the cellular structure inside the polymer foams was highly dependent on the VP and BA proportions, leading to very different thermal conductivity values, even for similar volume gas fraction values. These results were related to the copolymer nanostructuration, which seems to have an influence in the final pore structure, thus opening the possibility of designing microcellular foams with similar macroscopic characteristics but different thermal conductivity values. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 45872.     

Synthesis and film properties of epoxy esters modified with amino resins from glycolysis products of postconsumer PET bottles

Glycolysis of waste polyethylene terephthalate (PET) flakes obtained from grinding postconsumer bottles was carried out at 225–250°C and molar ratios of PET/ethylene glycol were taken as 1/1, 1/1.5, 1/5, and 1/10. Reaction product was extracted by hot water for three times and water‐soluble crystallizable fraction and water‐insoluble fraction were obtained. These fractions were characterized by acid and hydroxyl value determinations, differential scanning calorimeter analysis, and ¹H‐NMR analysis. Glycolysis product was used for synthesis of PET‐based epoxy resin. This epoxy resin was used to prepare epoxy ester resins having 40% and 50% oil content. Epoxy ester resin having 40% oil content was modified with urea‐formaldehyde and melamine‐formaldehyde resins for synthesis of epoxy ester–amino resin. Physical and chemical film properties of epoxy ester and modified epoxy ester resins were investigated. All the epoxy ester and modified epoxy ester films were having excellent adhesion, water, and salt water resistance properties. Modification of PET‐based epoxy ester resins with amino resin has significantly improved hardness, impact resistance, and alkaline and acid resistance of resin films. As a result, PET oligomers obtained from glycolysis of postconsumer PET bottles are suitable for manufacturing of amino‐resin‐modified epoxy ester resins that have improved physical and chemical surface coating properties. POLYM. ENG. SCI., 55:2519–2525, 2015. © 2015 Society of Plastics Engineers