Structures and Magnetic Properties of Europium-Transition Metal-Gallium Ternary Intermetallic Compounds with 1:3 Type

The crystal structures and magnetic properties of novel Eu TrGa3-r （T=Pd, It, Rh） in termetallic compounds are investigated by using powder x-ray diffraction and magnetic measurements. EuTrGa3-r crystallizes in orthorhombic structure with space group of Cmcm and Z = 4. There are four kinds of nonequivalent 4c crystal positions in EuTrGaa-r unit cell, which are occupied by 4Eu, 4GaⅠ, 4（GaⅡ, T） and 4GaⅢ, respectively. EuTrGa3-r ex- hibits the complex magnetic states in low-temperature regime, with the three-, two- and one-antiferromagnetic transitions occurring for T=Ir, T=Rh and T=Pd, respectively. It might be due to the Kondo effect： a localized antiferromagnetic interaction of the isolated impurity spins with the surrounding conduction electrons at low-temperature regime.

STUDIES ON THE PROPERTIES OF SCHIFF BASE TYPE ARYLMERCURY COMPOUNDS Ⅲ TRANSMETALLATION REACTION OF SCHIFF BASE TYPE ARYLMERCURY COMPOUNDS WITH METALLIC TIN

The transmetallation reaction of 4 Schiff base type arylmercury compounds with metallic tin has been carried out in refluxing xylene.It was found that the reaction proceeds in the same manner as that of chloro[2-(phenylazo)phenyl]mercury(Ⅱ) to give dichlorobisaryltin(Ⅳ).The ~1H NMR spectra of the products provide evidence for the presence of N→Sn intramolecular coordination.The formation of dichlorobisaryltin(Ⅳ)as a unique product probably arises from the N→Sn intramolecular coordination which results in the increasing of the stability of the molecule.

Enhanced Disinfection Effect of a Compound Disinfectant against Bovine Herpes Virus Type 1 at Low Temperature

A compound disinfectant, which consisted of didecyldimethylammonium chloride (DDAC), ortho-dichlorobenzene (1,2-dichlorobenzene, ODB), and chlorocresol (4-chloro-3-methylphenol, CC), and its component chemicals were individually tested for effectiveness against bovine herpes virus type 1 (BHV-1). DDAC, DDAC+ODB, DDAC+CC, and DDAC+ODB+CC showed effectiveness against BHV-1 at room temperature. However, ODB, CC, and ODB+CC showed no virucidal effects. The effects of all disinfectants tested were decreased at low temperature. DDAC showed disinfectant effects at a dilution of 1/800 and DDAC+ODB, DDAC+CC, and DDAC+ODB+CC at dilutions of 1/800 and 1/1600 at low temperature in the presence of 2% fetal bovine serum (FBS) but ODB, CC, and ODB+CC showed no virucidal effects. At low temperature and in the presence of 10% FBS, DDAC, DDAC+ODB, and DDAC+CC showed disinfectant effects at dilutions of 1/800, whereas ODB, CC, and ODB+CC showed no virucidal effects. DDAC+ ODB+CC was more effective (at 1/800 and 1/1600) than the other disinfectants under these conditions. In conclusion, a combination of three disinfectant components (DDAC+ODB+CC), enhanced the disinfectant effects at low temperature and in organic matter contamination.

FORMABILITY AND CRYSTAL TYPES OF RARE EARTH-SILICON CONTAINING TERNARY COMPOUNDS

By pattern recognition chemical bond parameter method, the formability of NaZn13 type and BaCd11 type ternary compounds in RE-M Si （RE=La-Lu, M is any metallic element） systems has been investigated. And the existence of unknown ternary compounds is predicted by the pattern recognition method.

A NEW TYPE OF CHAIN COMPOUND,STRUCTURE OF TA_4(TE_2)_4TE_4I

Ta_4(Te_2)_4Te_4I,Mr=2381.90,Monoclinic,C2/c,a=21.987(2),b=6.153(2),c= 19.936(3),β=122.42(14),V=2276.7 ~3,z=4,Dm=6.8(5)g/cm^3,Dc=6.95g/cm^3,λ(Mok)= 0.71073,μ=354.0cm^(-1),F(000)=3876,T=296(1)k,R=5.3%,Rw=6.8%,for 1118 unique observed reflections(1>3σ(Ⅰ)).The structure is composed of [Ta_4(Te_2)_4Te_4I]_∞~ chains,which are formed by the four-nuclear butterfly cluster units "Ta_4(Te_2)_4Te_4" with the Ⅰ atoms as the bridging atoms between different cluster units.

XPS Study of the Oxygen on A_2BO_4-type Compounds-A New Discovery of O_(1S) Peaks

By means of XPS, a new O1s peak which reflects the lattice oxygen on A_2BO_4-typecompounds is discovered, suggesting that the lattice oxygen might have two energy states on thistype of material.

STUDIES ON THE PROPERTIES OF SCHIFF BASE TYPE ARYLMERCURY COMPOUNDS.II ^(199)Hg NMR SPECTRA OF MERCURATED DERIVATIVES OF SUBSTITUTED BENZYLIDENEANILINES

^(199)Hg NHR spectra of 18 Schiff base type arylmercury compounds have been studied.It was further confirmed that in the molecule of XC_6H_4CH=NC_6H_3-2-HgC1-4-CH_3 there exists an intramolecular N→Hg coordination via a four-membered ring.For the series of XC_6H_4CH=NC_6H_3-2-HgCl-4-CH_3(X is a para-or mera-substituent),there is a good linear correlation between δ^(199)Hg and Hammett's o constants.The influence of substituents of C-pheny1 ring on the δ ^(199)Hg can be explained in terms of the intramolecular N→Hg coordination.

FA006 Type Compound Cotton Holding Machine

TheFA006TypeCompoundCottonHoldingMachinemadebytheZhengzhouTextileMachineryFactoryinHenanProvinceishighlyautomatic,andcanholdsmallamountsofcottonevenlyandwithoutdamage.Theoutputreached1000kg/h,withtheindexreachingtheworldleveloftheearly1990s.FA006 Typ...

Magnetic Field Induced Entropy Change for La-Fe Based NaZn_(13)-Typed Compounds

Magnetic field induced entropy change was investigated for La-Fe based NaZn13-type compounds with magnetic first-order phase transition. In view of magnetic refrigeration at room temperature, the developing of the materials and the understanding of the entropy change were., reviewed. For La-Fe-Si compounds, the entropy change about 29 J·kg^- 1·K^-1 was obtained at 190 K under the magnetic field of 5 T.While a large entropy change of about 15 J·kg^-1·K^-1 near room temperature under 5 T can be obtained by the substitution of Co for Fe in the compounds. It is found that the entropy change is mainly composed of that contributed from magnetic ordering and crystal lattice. The large entropy change consumed by lattice contribution is mainly due to the magnetic ordering one.

原人参二醇型皂苷活性代谢物Compound K药理活性的研究进展

人参皂苷Compound K〔20-O-β-D-葡萄糖基-20(S)-原人参二醇,CK〕是原人参二醇型人参皂苷在人体内主要吸收形式和药效实体。近年来,CK的药理活性研究又有了新进展:①CK可通过活化胱天蛋白酶8直接或通过线粒体途径间接地激活胱天蛋白酶3,诱导肿瘤细胞凋亡;下调基质金属蛋白酶9基因的表达,抑制肿瘤细胞的转移;②可通过下调多种炎症因子如白细胞介素-4(IL-4),IL-6,肿瘤坏死因子α等及环氧合酶2与一氧化氮合酶的表达而发挥抗炎、抗过敏和神经保护作用;③可阻断ATP敏感性K+离子通道,促进胰岛素分泌,增强组织胰岛素敏感性,抑制糖异生,促进糖酵解,对胰岛素依赖性糖尿病表现出良好的疗效;④可上调核苷切除修复相关蛋白基因的表达,减少紫外线引起的DNA损伤,防止皮肤老化等。本文重点对近几年有关CK的药理活性及其作用机制研究新进展进行综述。

Effect of background electrolytes on the adsorption of nitroaromatic compounds onto bentonite

To further elucidate interaction of nitroaromatic compounds with mineral surface, the sorption of m-dinitrobenzene （m-DNB） and nitrobenzene to original bentonite in aqueous solution containing different electrolytes （i.e., KCl, NH4Cl, CaCl2 and Tetramethylammonium bromide （TMAB）） was studied. The sorption of m-DNB was greatly enhanced with the presence of KCl and NH4Cl, while little influence was observed with CaCl2 and TMAB, following the order of KCl 〉 NH4Cl 〉〉 TMAB, CaCl2, or DI water. For nitrobenzene, sorption enhancement only occurred at high nitrobenzene concentrations in the presence of KCl, and the solute equilibrium concentration at inflexion point was lowered with increasing KCl concentration. These sorption enhancements were significantly promoted with the increase of electrolyte concentration. The salting-out effect is insufficient to account for the sorption enhancement by original bentonite with increasing KCI or NH4Cl concentration. X-ray diffraction patterns of bentonite suspensions indicated that the sorption enhancement of m-DNB was attributed to the intercalation of K^＋ or NH4^＋ into bentonite interlayer and then dehydration with m-DNB to form inner-sphere complexes, which caused previously expanded bentonite interlayers to collapse in aqueous suspension, thus further enhanced the interaction of phenyl with siloxane surface. In comparison, the sorption enhancement of NB is attributed to the formation of outer-sphere complexes with K^＋ at high solute-loadings （〉 20（0-400 mg/kg）. The sorption of m-DNB to initially modified TMA^＋-bentonite and K^＋-bentonite was almost the same as respective sorption to original bentonite in solution containing TMA^＋ and K^＋.

Remove of Phenolic Compounds in Water by Low-Temperature Plasma: A Review of Current Research

Phenolic compounds have very strong toxicity, so it has been paid sharply attention to find an effective way of controlling the wastewater containing phenolic compounds. The work on this subject done by domestic and overseas scholars is studied in this paper, and the progress of researches on low-temperature plasma treatment is summarized through the electrical discharge types, mechanism, kinetics of phenolic compounds decomposition and combination of several methods with low-temperature plasma treatment. In addition, the crucial problem and the developing tendency on low-temperature plasma treatment for phenol-bearing wastewater are briefly discussed.

Evaluating the Environmental Health Effect of Bamboo-Derived Volatile Organic Compounds through Analysis the Metabolic Indices of the Disorder Animal Model

Objective To identify the bamboo VOCs (volatile organic compounds) effect on animal physiological indices, which associated with human health. Methods GC/MS was used to analyze the volatile organic compounds from Moso bamboo (Phyllostachys heterocyla cv. pubescens). The effect of VOCs on environmental health was evaluated by analyzing the metabolic indices of the type 2 diabetic mouse model. Results Spectra of VOC generated by GC/MS were blasted against an in-house MS library confirming the identification of 33 major components that were manually validated. The relative constituent compounds as a percentage of total VOCs determined were alcohols (34.63%), followed by ether (22.02%), aldehyde (15.84%), ketone (11.47%), ester (4.98%), terpenoid (4.38%), and acids (3.83%). Further experimentation established that the metabolic incidence of the disease can be improved if treated with vanillin, leaf alcohol,β-ionone and methyl salicylate. The effects of these VOCs on type 2 diabetes were evident in the blood lipid and blood glucose levels. Conclusion Our model suggests that VOCs can potentially control the metabolic indices in type 2 diabetes mice. This experiment data also provides the scientific basis for the comprehensive utilization of ornamental bamboos and some reference for other similar study of environmental plants.

The First Hybrid Wells-Dawson-type Polytungstate Monosupported by Cd-coordination Complex via Di-bridging O-atom

Polyoxometalates（POMs） with Cd-coordination complexes acting as supporting units are rarely reported. The linkage of the supporting units with inorganic building block（polyanion） is generally established on terminal O-atoms, but scarcely via bridging O-atoms. By introducing liquid small organic molecule（pyridine, C5NH5） as assistant ＂structure-directing agent＂, we obtained a novel organic-inorganic hybrid polytungstate,（Hpy）4[Cd（phen）2（P2W18O62）]·nH2O（1, n ≈ 3, py = pyridine, phen = 1,10-phenanthroline）, under hydrothermal conditions. The single-crystal X-ray diffraction analysis shows that 1 is the first compound containing an asymmetric heteropolyanion, [Cd（phen）2（P2W18O62）]4–, a Wells-Dawson-type polyanion monosupported by Cd-coordination complex via di-bridging O-atoms.

Preparation and Water-Gas Shift Catalytic Activities of the Perovskite Type Complex Oxide La_(1-x) Ce_xFeO_3

The perovskite type rare earth iron complex (REIC) oxide La 1-x Ce xFeO 3 is designed and prepared as water gas shift catalyst. Activity evaluation and heat resisting test show that the perovskite type compounds La 1-x Ce xFeO 3(·K) has a good thermal stability if x is less than or equal to 0.5 . But when x is greater than 0.5 , La 1-x Ce xFeO 3(·K) will turn out to be ceria and magnetite partially or completely at high temperature in the shift reaction atmosphere. In the case of x=0.5, the conversion of carbon monoxide is about 68% at 530 ℃. Potassium can greatly improve the low temperature activity, but slightly lower the high temperature activity, and has little impact on the thermal stability. La 0.5 Ce 0.5 FeO 3 (·K) is a promising chromium free high temperature shift catalyst.

Enhanced thermoelectric performance in p-type Mg3Sb2 via lithium doping

The Zintl compound Mg3Sb2 has been recently identified as promising thermoelectric material owing to its high thermoelectric performance and cost-effective,nontoxicity and environment friendly characteristics.However,the intrinsically p-type Mg3Sb2 shows low figure of merit（z T = 0.23 at 723 K） for its poor electrical conductivity.In this study,a series of Mg（3-x）LixSb2 bulk materials have been prepared by high-energy ball milling and spark plasma sintering（SPS） process.Electrical transport measurements on these materials revealed significant improvement on the power factor with respect to the undoped sample,which can be essentially attributed to the increased carrier concentration,leading to a maximum z T of0.59 at 723 K with the optimum doping level x = 0.01.Additionally,the engineering z T and energy conversion efficiency are calculated to be 0.235 and 4.89%,respectively.To our best knowledge,those are the highest values of all reported p-type Mg3Sb2-based compounds with single element doping.

STRUCTURE OF MOLECULAR COMPOUND CRYSTAL A_2B(A =1, 6, 7, 8,-TETRA-PHENYL (3, 4-BENZO)BICYCLO[4, 2, 0]OCTA-7-ENE, B=CIS, CIS-1,2,3,4,-TETRAPHENYLBUTADIENE)

C100H78, (A: C36H28, B: C28H22) Mr = 1279. 74, monoclinic, P21/a, a=17. 282(3), b=10. 669(4), c= 19, 927(3) A , β =102. 99(1)°,V = 3580. 1(2) A3, Z=2, μ(MoKα) = 0. 623cm-1, F(000) = 1356, Dc=1. 187g/cm3, room temperature. The final R=0. 084, Rw = 0. 086 for 1255 independent observed reflections (I≥3σ(I)). Owing to the existence of 1,6,7, 8-Tetraphenyl (3,4-benzo)-bicyclo[4, 2, 0]octa-7-ene(A) , cis, cts-1, 2, 3, 4-Tetraphenylbutadiene (B) in A2B can take the different conformation from the one in the pure B crystal. The reason of the formation of this molecular compound crystal is put forward.

Magnetic properties and magnetocaloric effect in Nd_xLa_(1-x)Fe_(11.5)Al_(1.5) compounds

Effects of Nd-doping on the magnetic properties and magnetocaloric effects （MCEs） of NdxLa1-xFe11.5Al1.5 have been investigated. Substitution of Nd leads to a weakening of the antiferromagnetic （AFM） coupling and an enhancement of the ferromagnetic （FM） coupling. This in turn results in a complex magnetic behaviour for Nd0.2La0.8Fe11.5Al1.5 characterized by the occurrence of two phase transitions at ～188 K （PM AFM） and ～159 K （AFM-FM）. As a result, a table-like MCE （9 J/kg.K） is found in a wide temperature range （160-185 K） for a field change of 0-5T around the transition temperature, as evidenced by both the magnetic and calorimetric measurements. Based on the analysis of low-temperature heat capacity, it is found that the AFM-FM phase transition modifies the electron density significantly, and the major contribution to the entropy change comes from the electronic entropy change.

川东北宣汉地区海相“新型杂卤石钾盐矿”的发现、突破与前景

全球探明钾盐资源主体为古代海相可溶性固体钾盐矿床(氯化钾、光卤石),仅少量来自现代盐湖卤水钾矿。与国外不同的是,目前我国探明钾盐资源主体为现代陆相盐湖钾矿,古代海相可溶性固体钾盐找矿40余年,未获突破。四川盆地是我国主要大型海相成钾盆地之一,前人在中—下三叠统发现大量与硬石膏和白云石共伴生或互层的杂卤石,但绝大部分埋深超过2000 m,目前尚难以开发利用。2017年以来,笔者通过对四川盆地东北部宣汉盐盆普光地区卤水探井(恒成2、3井)岩芯复查,发现杂卤石主要与石盐共伴生,大量破碎的杂卤石碎屑颗粒分布于石盐基质中,KCl含量达边界工业品位以上,不同于钾石盐和光卤石,亦不同于前人发现的与硬石膏和白云石共伴生或互层的杂卤石(石膏型杂卤石),将之命名为“新型杂卤石钾盐矿”。小试和中试结果表明,该“新型杂卤石钾盐矿”可以采用对接井注水溶采,是能够得到规模化开发利用的“活矿”,是一种全新的硫酸盐+氯化物复合型海相可溶性固体钾盐矿床新类型。通过成钾条件、成矿规律综合研究,笔者提出了新型杂卤石钾盐矿“双控复合成矿”理论新认识、建立了“三高、两低、一大”综合测井识别新模型,创新理论技术指导设计部署“钾锂兼探”基准井——川宣地1井,探获厚29.46 m、氯化钾(KCl)平均含量12.03%(最高20.5%)的“新型杂卤石钾盐矿”厚层高品位工业矿层。与此同时,采用岩芯样品实测数据和测井解释数据拟合的方法,建立矿石K含量和密度参数的测井定量预测模型,结合“气钾兼探”,利用33口钻井数据,依据古代固体盐类勘查规范(2020),运用“几何法”,初步估算“新型杂卤石钾盐矿”氯化钾(KCl)资源规模:推断资源量2.45亿t(超大型)、潜在资源4.65亿t,合计7.1亿t,奠定了川东北达州市宣汉地区形成中国首个亿吨级海相钾盐基地的资源基础,取得了我国海相可溶性固体钾盐找矿的重大突破。