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    24 March 1996, Volume 17 Issue 3
    Articles
    The Effect of Acidity and Metal Ions of Subphase on the Characteristic of Monolayer of 2-Hexadecylcarbamoyl-8-hydroxyquinoline
    OUYANG Jian-Ming, TAI Zi-Hou, QIAN Xiang-ping, TANG Wen-Xia
    1996, 17(3):  335-340. 
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    Anew amphiphilic ligand,2-hexadecylcarbamoyl-8-hydroxyquinoline(HHQ) was synthesized.The characteristics of monolayer of HHQwas investigated on subphases with different acidities and with different metal ions.The difference of the characteristics of HHQmonolayer is dependent on the difference of radii,nuclear charges and the structures of valence shell of metal ions.The 20-laver LBfilms of HHQon each side of the substrate were prepared by spreading a solution of HHQin chloroform,and UV-Vis absorption spectra of the LBfilms were recorded.Transitional metal ions can form complexes with HHQon the air/water interface,but alkali and alkali earth metal ions cannot.
    Investigation of Ion-exchange Property of Na5YSi4O12
    CUI De-Liang, FU Ge-Yan, PANG Guang-Sheng, XU Xiu-Ting, FENG Shou-Hua, XU Ru-Ren
    1996, 17(3):  341-344. 
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    Ion-exchange properties of Na5YSi4O12 with K+ and Ag+ were investigated by solution electrochemical and solid state electrode methods, The crystal structure, density and ionic conductivity of ion-exchanged samples KNYSand AgNYSwere studied.Compared to other ion-exchange methods,mgher ion-exchange degree can be obtained by the two methods mentioned above,and the result of elementary analysis coincides well with that of density measurement.
    The Phase Transitions of Hetero Atoms Substituted Molecular Sieves Me-VPI-5(Me=Mg,Ti,Sn,Si)and Their Influence on Spectra structures of Eu(Ⅲ)Ion
    SUN Jia-Yao, DU Hai-Yan, PANG Wen-Qin, SHI Chun-Shan
    1996, 17(3):  345-349. 
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    The hetero atom substituted aluminophosphate molecular sieves Me-VPI-5(Me=Mg,Ti,Sn,Si)were synthesized hydrothermally.Rare earth ions originally doped into these microporous materials by aqueous solution ion exchange procedures.The phase transitions of the microporous materials are investigated by high-temperature and high-pressure experimental techniques,The influence of the phase transitions on the rare earth ions'spectral structures is discussed.With the increase of temperature,Eu(Ⅲ)Mg-VPI-5 is converted into Eu(Ⅲ)Mg-AlPO4-8,then into tridymite phase.The pressure has a notable influence on Eu(Ⅲ) ion's spectral structures.The spectral structures have changed regularly with the increase of pressure.
    The Preparation of Water-soluble Fine Particles Na2C2O4 in the Triton X-100/C10H21OH/H2O Lamellar Liquid Crystal
    SHEN Ming, GUO Rong, YAN Peng-Quan, ZHU Xia-Shi
    1996, 17(3):  350-354. 
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    Water-soluble fine particle Na2C2O4 was prepared by replacing component water with Na2C2O4 saturated aqueous solution in Triton X-100/C10H21OH/H2Olamellar liquid crystal.The preparation was based on the penetration of solvent in the lamellar liquid crystal and the limitation of the change of thickness of solvation layer in the lamellar liquid crystal.The size of water-soluble fine particle Na2C2O4 was about 6 nm.
    Synthesis and Characterization of Hydrotalcite-like[CdxMg6-xAl2(OH)16]2+)[S·2H2O]2-
    BAO Yu-Min, LI Lian-Sheng, MA Shu-Jie, XIONG De-Cheng, FU Ge-Yan, FENG Shou-Hua, XU Ru-Ren
    1996, 17(3):  355-358. 
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    Hydrotalcite-like [CdxMg6-xAl2(OH)16]2+[S·2H2O]2- was synthesized hydrothermally and characterized by means of XRD,FT-IR,DTA-TGetc.,The influence of pH,Cd2+ ionic concentration and sulphuration time on the synthesis was studied.The synthetic optimal conditions are pH=9~10,[Cd2+]/[Mg2+]=1:5~1:9 and sulphuration time 5 min.It is suggested that Mg2+ ions can be only partially substituted by Cd 2+ ions in the hydrotalcite-like.
    Studies on the Directional Reaction of Silver with Reducing Agent Hydrazine of Various Valences
    CHENG De-Ping, XIA Shi-Jun
    1996, 17(3):  359-361. 
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    The reaction of hydrazine with silver or several silver complexes was studied.We found that a trace copper(Ⅱ)ion is an effective catalyst.In the presence of copper(Ⅱ) ion,the rate of reaction is accelerated,and the ratio of four-electron directional reaction of hydrazine is greatly increased.With the increase of the stability constants(β2)of several silver coordination compounds.The ratio of four-electron reaction of hydrazine is decreased.The ratio of four-electron reaction against 1gβ2 of several silver coordination compounds is linear in the absence of copper(Ⅱ)ion.In the presence of copper(Ⅱ) ion, the logarithm of the ratio of one-electron reaction of hydrazine is proportional to 1/1gβ2.
    Analysis of DNA Fragments and PCR Products from Oncogene Using Capillary Electrophoresis with Laser-Induced Fluorescence Detection
    REN Ji-Cun, DENG Xi-Yun, CAO Ya, YAO Kai-Tai
    1996, 17(3):  362-366. 
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    Capillary electrophoresis-laser induced fluorescence detection system is applied to detect DNAfragments and PCRproducts from oncogene using hydroxypropylmethylcellulose and no-cross-linked polyacrylamide as sieving media.The effects of sieving medium concentration,electrolyte concentration and intercalating agent concentration on separation of DNAfragments have been investigated in detail.The relationship between peak area and concentration of DNAfragments in pressure injection has been compared with that of electrokinetic injection.
    Theoretical Investigation o the New Type Two-Dimensional Packed-Capillary Column GC System──Effect of the Column Conditions on Retention Time and Peak Spreading
    ZHANG Wei-Bing, XU Guo-Wang, SHI Jing-Jiang, ZHANG Yu-Kui, LU Pei-Zhang
    1996, 17(3):  367-372. 
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    In this paper,the first moments of the peaks eluted from a two-dimensional packed-capillary column GCsystem were derivde by means of chromatographic dynamics.Based on this expression,the effect of the precolumn temperature, the precolumn pressure and the split ratio on the retention time and the peak spreading were discussed.The results showed that split stream was a bridge between the main column and the precolumn,the split ratio was an important factor affecting the retention time and the peak spreading.Because the retention period of the solute in precolumn was shorter,the effect of the change of the precolumn condition on retention time was smaller if the main column condition was fixed.The higher the temperature of precolumn and the more narrow the peak,and the pead profile could be improved in a regular scope by the change of the split ratio between the two column.In accordance with the relationship between the main column and precolumn,some special rules were observed in the two-dimensional packed-capillary column GCsystem.
    The PAS and Relaxation Process of Chlorophyll a
    SU Qing-De, WANG Qin, YANG Yue-Tao, ZHAO Gui-Wen
    1996, 17(3):  373-376. 
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    The photoacoustic(PA)spectrum in amplitude and phase of chlorophyll a(chl a)has been used to study the energy level and relaxation processes(see Fig.1).At the two main absorption bands S1 and S2 of chl.a, the phase angles are 6.5°and 0°,which indicate that the relaxation processes of excited states are different:the S1 band relaxation undergoes the lowest triplet state(T0) while the S2 band relaxation does not.According to the relaxation processes,a model and corresponding rate equations have been established (see Fig.2).The absorption spectrum of chl.a compared with the PAspectrum has also been reported(see Fig.3),and the fluorescence quantum yield (Q) has been deduced from the intensity ratio of absorption and PAsignal.The result Q=0.24 is obtained which is consistent with the original references,It is proved that the PAspectroscopy is a promising and convenient analytical technique in the energy levels and relaxation studies of biological substances.
    Determination of(Ⅵ),Cu(Ⅱ)in Aqueous Solution by Liquid-Core Optical Fiber Spectrophotometry
    WANG Ju-Fang, LIAO Yuan-Min, FENG Ming-Zhao, WANG Wei, LIN Jun-Xiu, HE Qu-She, WU Guan-Yan, PAN LI-Ying, ZHAO Yu-Shan, HE Tian
    1996, 17(3):  377-380. 
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    This paper presents the transmission characteristics and spectrum for liquid-core optical fiber filled with low refractive index liquids(n>1.346)and aqueous solutions.The methods are studied for the determination of Cr(Ⅵ),Cu(Ⅱ) in aqueous solutions of about 70% alcohol and 50% dioxane.With the 110 cm liquid-core optical fiber in length,the sensitivities(1/ng·mL-1)of Cr(Ⅵ), Cu(Ⅱ)are 0.052 and 0.017 respectively;the linear ranges are 0~25,0~24 ng/mLwith RSDbeing1.0%~4.8%.The Cr in the animal gum and national standard are determined with recoveries of 94%~102%.
    β-Cyclodextrin Induced Room Temperature Phosphorescence From 1-Bromonaphthalene in the Presence of Naphthalene and 1-Butanol
    DU Xin-Zhen, ZHANG Yong, HUANG Xian-Zhi, LI Yao-Qun, JIANG Yun-Bao, CHEN Guo-Zhen
    1996, 17(3):  381-382. 
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    Intense room temperature phosphorescence(RTP)from host-guest inclusion complex of β-cyclodextrin(β-CD)with 1-bromonaphthalene(1-BrN),stabilized by naphthalene (N)and 1-butanol(B), has been investigated, It has been confirmed that Nand Bare incorporated into the nonpolar cavity of β-CDas the second guest and the third one.The extra space inside the cavity is further filled by Nand B, and β-CDmore effectively shields 1-BrN from quenchers in aqueous solution.Bcompletely hinders the formation of Nexcimer.The greater rigidity of the complex was achieved.Consequently, much more intense fluorescence of RTPappears in comparison with the ternary β-CD:1-BrN:Bor β-CD:1-BrN:Ncomplex.The limit of detection is 7.38×10-8mol/Lfor 1-BrNand 1.36×10-6 mol/L for N.
    Effect of Structures of Modifiers on Electrochemistry of Di-μ-oxo Dimanganese 2,2'-bipyridine Complex
    WU Cong-Xiao, ZHENG Jun-Wei, LU Tian-Hong
    1996, 17(3):  383-385. 
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    The gold electrodes modified with 2-picolinic acid,nicotinic acid,iso-nicotinic or thiophene were prepared using membrane transfer method.The electrochemistry of di-μ-oxodimanganese 2,2'- bipyridine complex was studied in the acetic acid buffer solution at different modified gold electrodes.It was found that the modifiers which can promote the electrochemical reaction of the complex should be of at least two functional groups.One group can be bound to the electrode surface and the other can form electron transfer pathway between the modifier and the complex through salt bridge or hydrogen bond.In addition,the mechanism of the electrochemical reaction was discussed.
    Extraction Equilibria of Amino Acids with Di-(2-ethylhexyl)phosphoric Acid
    CAO Han-Jin, WANG De-Bao, LIU Pei-Yan, WU Zi-Sheng, YAN Zhong
    1996, 17(3):  386-388. 
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    The extraction equilibria of various amino acids with di-(2-ethylhexyl)phosphoric acid(P204) were studied in the lower pHrange.P204 reacts with the cations of amino acids according to the stoichiometric ratio determined by ionic valency.For monovalent cations, the reaction forming complex can be expressed as follows: A+ + 2(HL)2=AL(HL)3 + H+ The values of extraction equibibrium constant Kex of several amino acids were obtained.The effects of some parameters on the distribution ratio of amino acids were also studied.
    Multielements Analysis of Mare's Milk Wine by Inductively Coupled Plasma Atomic Emission Spectrometry
    GA Ri-Di, WU-Di
    1996, 17(3):  389-391. 
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    Adirect determination method for trace multielements in mare's milk wine with ICP-AESwas described.The Multielements determined included Fe,Zn,Mn,Cu,Cr,Mo,Ni,Co,Sn,Sr and Se.The 11 elements are necessary for humen health.Without any Chemical treatment on the mare's milk wine,the determination of multielements in it is easy,fast and sensitive.
    Synthesis of Diacetylenic Lipids and Studies on the Preparation and Stability of Polymerized Liposomes
    YU Kai, SUN Yan, ZHANG Bao-Shen, ZNOU Xiu-Zhong
    1996, 17(3):  392-395. 
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    The seven lipids with diacetylenic structure were synthesized,using lipids Ⅰ-Ⅶ polymerized liposomes were prepared,and their stabilitics under different environmental conditions(e.g.,alcohol,acid,alkaline,salt and buffer solutions)were investigated.The results indicated that the polymerized liposome prepared with pentacosa-10, 12-diyne-1-olphosphoryl ethanolamine exhibited an enhanced stabilities.
    Synthesis of Artificial Receptor of Organic Anion
    LU Guo-Yuan, HE Wei-Jiang, HU Hong-Wen
    1996, 17(3):  396-400. 
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    The optically active(2R,8R)-bis(hydroxymethyl)-1,5,9-triazabicyclo[4.4.0]dec-9-ene has been synthesized from D-asparaginate with a total yield of 25.4%.In the synthesis,the key intermediate is a thiourea derivative from reduction and coupling of the starting materials and the key reaction is it's methylation and double SNreaction to form bicyclic skeleton.Amino and hydroxy are protected by tosyl and silyl groups which can be cleaved under very mild conditions respectively.The target molecule is a useful intermediate in the construction of chiral and selective receptors of organic anions.
    Syntheses of New Biferrocene Derivatives Containing a α,β-Unsaturated Carbonyl Bridge and Their Langmuir Monolayers
    ZHANG Cheng-Ru, YANG Kong-Zhang
    1996, 17(3):  401-404. 
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    Ferrocenyl-2-crotonyl chloride was prepared by three-step reactions from 3-ferrocenyl-2-crotonic ester.Four new biferrocene derivatives containing α,β-unsaturated carbonyl bridge have been synthesized by the reaction of 3-ferrocenyl-2-crotonyl chloride with itself or carbonyl ferrocene derivatives and characterized by 1HNMR, IRspectra and elemental analysis.These new compounds are able to form Langmuir monolayers on the surface of water.Surface pressure-area(π~A) isotherms of these compounds were obtained.
    Studies on Derivatives of Teucvidin from Teucrium quadrifarium
    CHEN Huan-Ming, XIE Ning, MIN Zhi-Da
    1996, 17(3):  405-408. 
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    Eight derivatives of teucvidin,a known nor-clerodane diterpenoid isolated from Teucrium quadrifarium(Labiatae)were prepared by catalytic hydrogenation,ester exchange and hydrolysis.Their structures were established by spectroscopic means.Preliminary bioassay indicated that teucvidin and its derivatives,especially Ⅱ and Ⅳ a showed significant antifeedant activities against larvae of Leucania separata (Walker).
    Studies on Racemization in Thioester Condensation
    WANG Hong, JI Hong, ZHANG Ruo-Heng, XU Xiao-Jie, TANG You-Qi
    1996, 17(3):  409-413. 
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    In order to study the racemization in thioester condensation,a model coupling reaction between Boc-Ala-Ala-SCH2CH2CO-GlyOBzl and GlyOBzl·TosOHwas monitored by RP-HPLC.To optimize reaction conditions,the effects of solvents,additives and bases were checked.From the results, we conclude that THFis recommendable as a solvent and when thioester:HOsu:NMMis 1:15:12(molar ratio),there is the least racemization(<2%).
    Studies on the Synthesis of S-Alkyl-O-polychlorophenyl Thiophosphoric(─nic) Acid Derivatives and Their Fungicidal Activities
    TANG Chu-Chi, JIN Gui-Yu, HUANG Guang-Yan, MA Fu-Peng, WU Gui-Ping, HE Zheng-Jie, LI Shu-Zheng, LI Bing-Wu, ZHANG Shu-Hua
    1996, 17(3):  414-418. 
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    The isomerization/chlorination of O,O-dialkyl thiophosphate(-onate)1 with phosphorus oxychloride gives S-alkyl thiophosphorochloride(-nochloride)2,then,the reaction of compounds 2 with polychlorophenol in the presence of triethylamine afford the title compounds 4.Compounds 4 have also been prepared by using the traditional method, thus,the reaction of S-alkyl thiophosphorodichloride 5 with polychorophenol, then with another nucleophile R' Hin the presence of triethylamine can also give the title compounds(4).The results of the tests in the fungicidal activity towards the twelve plant disease fungus show that the twenty-eight compounds 4 prepared possess a satisfactory or excellent fungicidal activity.
    Studies on Isolobal Displacement Reactions──The Molecular Structure or Chiral Cluster Complex[(η5-MeO2CC5H4)(CO)2MO][(η5-MeO2CC5H4)(CO)2W]Fe(CO)33-S)
    SONG Li-Cheng, HU Qing-Mei, SHEN Jin-Yu, WANG Ru-Ji, Mak Thomas C. W.
    1996, 17(3):  419-423. 
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    The molecular structure of[(η5-MeO2CC5H4)(CO)2MO][(η5-MeO2CC5H4)(CO)2W] Fe(CO)33-S), prepared through isolobal displacement reaction between η5-MeO2CC5H4)(CO)3MONa and [(η5-MeO2CC5H4)(CO)2W]Fe(CO)3Co(Co)33-S) has been determined by X-ray diffraction technique.The crystal belongs to triclinic space group P1 with α=0.87162(5) nm,b=0.76218(4) nm,c=1.87111(8)nm,α=94.164(4)°,β=97.979(2)°γ=99.108(2)°,Z=2,μ=5.9cm-1.The final agreement factor R=0.036 for 4180 observed reflectional points.There is a tetrahedral MoWFeScluster core in the molecule of this complex with Mo and Woccupying two apexes disorderly in the ratio of 1:1.
    Studies on the Synthetic Peptied Antigens of Schistosoma Mansoni
    XU Jia-Xi, CAI Meng-Shen, SHI You-En
    1996, 17(3):  424-426. 
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    Six antigenic peptides of the 26KDa Glutathione S-transferase of schistosoma mansoni have been predicted according to its hydrophilicity, flexibility,accessibility,chargedistribution and β-turn in the secondary structure by the determination of its primary structure with the aid of computer and synthesized by using solid phase method.Two of them showed a good antigenicity by Dot-ELISAmethod with anti-schistosoma japonicum-immunoglobulin polyclonal antihody,anti-Sj-IgG PcAb and one of them also showed a good antigenicity with the anti-schistosoma surface membrane monoclonal antibody,A6McAb.
    Studies on the Total Synthesis of (±)-Demethyl Salvicanol
    WANG Xue-Chao, PAN Xin-Fu, CUI Yu-Xin, CHEN Yao-Zu
    1996, 17(3):  427-428. 
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    Demethyl salvicanol,9(10→20)-abeo-8,11,13-triene-10β,11,12-triol,has been synthesized for the first time by using the intramolecular zinc-promoted coupling reaction of benzyl bromide with ketone and the alkylation of iodide 1-(2-iodoethvl)-3,4-dimethoxy-5-isopropylbenzene with ketone 5,5-dimethyl-2-cyclohexen-l-one as the key steps.
    Synthesis of 5'-O-(N,N-Bis(2-chloroethyl) phosphoramide)-2',3',-O-isopropylidenenucleosides
    CHEN Ru-Yu, CHI Guo-Chen, CHEN Xiao-Ru
    1996, 17(3):  429-431. 
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    Anumber of new title compounds were synthesized.The structures of all the products had been confirmed by elementary analysis,1H NMRand IR.The results of preliminary biological tests indicated that the title compounds had the inhibition effect against HL-60 cell lines and BCap cell lines.
    Vibrational Spectroscopic Studies on the Acid Salts of Myristic Acid and Palmitic Acid
    BIAN Jiang, WENG Shi-Fu, ZHANG Xu, WU Jin-Guang, XU Guang-Xian
    1996, 17(3):  432-435. 
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    Fatty acids and their alkali soaps were well known as the biosurfactants in living system,however,little work had been published on the fatty acid-soap complexes,which were suggested here to have some unusual structures and properties.The acid sodium salts and acid potassium salts in molar ratio of 1:1 of both myristic acid and palmitic acid were investigated by FTIRand FT-Raman spectroscopies.The spectral results showed that very strong hydrogen bonds existed in these long-chain acid salts.In this paper,the possible structures of acid soaps were discussed according to spectroscopic data.
    Ab Initio Studies on Geometries and Electronic Properties of the Nereistoxin and Evisect
    WANG Yi-Bo, SHI Hong-Yun
    1996, 17(3):  436-439. 
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    Ab initio calculations have been carried out at the Hartree-Fock/6-31G*level to determine the geometries of the nereistoxin(C5H11NS2)and evisect(C5H11NS3).Two stable conformations of chair and boat forms of the evisect have been found in the global optimizations.At the second Moller-Plesset perturbation theory,MP2/6-31G* level, the chair form is 27.06 kJ/mol which is more stable than the boat form.The molecular electrostatic potentials obtained from MP2/6-31G* wave-functions.The relationship between biological activity and electrostatic potentials have been discussed.The atomic charges from Mulliken population analysis is faulty in the nereistoxin and evisect.Brenneman's CHELPGmethod was used in the calculations.
    Electronic Structure and Chemical Bond of (C5H5)2Ti(CO)20
    JIANG Xiao-Qin, WANG Yue, SHEN Er-Zhong, SUN Jia-Zhong
    1996, 17(3):  440-442. 
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    Ab initio method(STO-3G basis set)has been used to obtain the optimized structure for(C5H5)2Ti(CO)2.Ab initio(STO-3Gand STO-3-21Gbasis sets)calculations were carried out on the optimized structure to examine the electronic structure and chemical bond of(C5H5)2Ti(CO)2.The calculated results tally with the experimental ones,The theoretical study results show that the HOMO has the characteristic of back-donation to carbonyl orbital and the Ti-CO bonding is strongly dominated by back-bonding interaction.
    Effect of CeO2 on Oxidation of CO over Pd/Al2O3 Catalyst
    ZHOU Ren-Xian, XU Xiao-Ling, ZHENG Xiao-Ming
    1996, 17(3):  443-446. 
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    Surface reaction properties of CO,the desorption properties of surface oxygen over Pd catalysts and their carriers were investigated by means of TPSR-MSand TPD-MS.The oxidation activity of COon these catalysts was also examined at different concentrations of oxygen.It was found that the desorbed amount of CO2 and the order of peak temperature were in good agreement with their activities.The amount of CO2 in desorbed product on oxidized alumina-supported Pd was more than that on reduced alumina-supported Pd, the disproportionation reaction of COon H2-reduced Pd/Al2O3 would form carbon and CO2. The results of O2-TPDand CO-TPSRshowed that the addition of CeO2 would promote the desorption of surface oxygen and the surface reaction of COon Pd/Al2O3.
    Temperature Programmed Desorption of Basic Probes on Solid Superacids
    HUA Wei-Ming, CHEN Jian-Min, LIAO Chang-Xi, GAO Zi
    1996, 17(3):  447-450. 
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    Temperature programmed desorption of pyridine, benzene and toluene from various solid superacids was studied by using both TCDand FIDdetectors.The desorbed gases were collected at liquid N2 temperature and analyzed with a mass-spectrometer.It was found that all these compounds are oxidized on the solid superacids,and CO2 and SO2 are found to desorb above 400~500℃ instead of the probes.The peak temperatures and areas on the temperature programmed desorption profiles of the probes from the solid superacids are not correlated with their acid strengths and n-butane isomerization activities.Tlie results verify that pyridine, benzene and toluene cannot be used as the basic probes for the characterization of solid superacids.
    Terbium(Ⅲ) Luminescence Probes:Determination of Energy Transfer Distance Between Metal Ion and Tryptophan in Proteins and Postulation of Their Binding Sites
    YANG Jing-He, ZHAO Wei-Dong, TONG Chang-Lun, JIE Nian-Qin, ZHANG Gui-Ling, GAO Zu-Quan
    1996, 17(3):  451-455. 
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    The luminescence properties of the complex of Tb(Ⅲ)with bovine pancreatic deoxyribonuclease(BPD),bacillus subtilis α-amylase(BSα-A) were studied by using the fluorescence method.It was found that BPD, BSα-Acan coordinated with Tb(Ⅲ)at pH=7~8 and 5~6 respectively, and then emits a strong characteristic fluorescence of Tb(Ⅲ).The complex ratios for Tb (Ⅲ) and BPD, BSα-Awere 2:1 and 4:1 respectively.In this paper,Forster theory was used to determine the energy transfer distance between BPD,BSα-Aenergy-donor and Tb (Ⅲ) energy-acceptor.The values of the critical distance for 50% energy transfer,R0,of 0.336 nm and 0.390 nm were obtained.The donor-acceptor energy transfer distances,R,estimated from the measured efficiency were 1.39 nm,1.48 nm respectively.It is inferred that the binding sites between Tb (Ⅲ) and BPD, BSα-Awere Trp-178, Trp-188 and Trp-321,respectively.
    The Measurements of Quenching Rate Constants of Electronically Excited State CH (C2Σ+) Radical
    RAN Qin, CHEN Cong-Xiang, ZHANG Qun, YU Shu-Qin, LI Yue-Han, MA Xing-Xiao
    1996, 17(3):  456-459. 
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    The rate constants for quenching of CH (C2Σ+,v'=0) by O2,N2,n-C5H12,n-C6H14 and n-C7H16 molecules were measured at room temperature.CH (C2Σ+) was produced by 266 nm laser photolysis of CHBr3 and the total fluorescence intensity of CH(C→X) at (314.8±1) nm was then monitored using a fast digital storage oscilloscope coupled with a microcomputer.The rate constants (k) for the total removal of CH (C)are compared with those of CH (X,A,B) states,and show to be k (X)>k(B) and k(C)for alkane quenchers,and the tendency of quenching rate constants for CH(C) is similar to those for CH(X,A,B)showing the increase with increasing the number of C-Hbonds in alkane molecules.The results indicate that the quenching of CH (A,B,C)is probably the entrance-channel controlled process and the chemical reaction might play an important role in collisional quenching of CH (A,B,C).
    The Microcalorimetric Studies on the Inhibition Kinetics of Enzyme-catalyzed Reaction──Fluoride Ion Inhibiting Laccase-catalyzed Oxidation Reaction of o-Phenylenediamine
    XIONG Ya, WU Ding-Quan, ZHOU Guang-Ming, DU Yu-Min, QU Song-Sheng
    1996, 17(3):  460-463. 
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    Thermokinetic equation is proposed as Ω0-1=A[S0]-1 + B,which is available for all kinds of reversible inhibitions of single-substrate enzyme-catalyzed reactions.According to the relations between A/B, Band Kmm,the type of the reversible inhibition can be judged as competitive, non-competitive and uncompetitive inhibitions.The thermokinetic formula which can be used to calculated the apparent Michelis constant Km,app,inhibition constant Kand so on are given.The theory proposed has been applied to the kinetic determination of laccase-catalyzed oxidation reaction of o-phenylenediamine inhibited by fluoride ion.The experimental result shows that this reaction belongs to non-competitive inhibition,Km.app=9.712×10-2mol·L-1,Kt=2.090×10-2mol·L-1.
    The Change of Alcohol Amount on the Interface and Its Effect on the Structure of P507(K)/Alcohol/n-Heptane/Water Microemulsion
    SHEN Xing-Hai, GAO Hong-Cheng
    1996, 17(3):  464-466. 
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    The maximum solubilization of water (Smax) at various total amounts of alcohol(Vn) in P507(K)/alcohol (n-propanol,isopropanol,n-butanol,2-butanol,n-pentanol,2-pentanol,n-hexanol,3-hexanol,sec-octyl alcohol)/n-heptane/water microemulsions was investigated.Different trends of the change of Smax against Va were found.In the n-pentanol,2-hutanol,2-pentanol,3-hexanol and sec-octyl alcohol containing systems, Smax firstly increases and then becomes very low rapidly.This phenomenon was interpreted in terms of the formation of molecular solutions.It was also found that Smax firstly increases with Va and then remains unchanged in the n-propanol-containing system, while Smax increases rapidly at first and then increases gradually in the isopropanol-containing system.It was suggested that Rw, radius of water pool, is unchanged when Smax remains the same value in the former syxtem.In the latter system,Rw was also supposed to be unchnged when Smax begins to increase gradually,however,the detergentless microemulsion forms at the same time.In the n-hexanol-containing system,there exists a peak in the Smax vs.Va curve.It shows that there is a maximum value of I,molar ratio of alcohol to surfactant on the interface,in the system.
    Approximate Analytic Expressions for Interaction of Plane-Parallel Double Layers at Moderate Potential
    WANG Hao-Ping, JIN Jun
    1996, 17(3):  467-469. 
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    According to the suggestion of Sader et al.,who replaced the reduced surface potential Y=eψ/KTby the effective reduced surface potential Y(h)=4ekh/2·tanh-1[ekh/2·tanh (Y/4)](where ψis the surface potential of particles,k is Boltzmann's constant,Tis absolute temperature,h is the distance of closet approach between the particles,e is the proton charge,k is the Debye screening parameter),we return to the double layer interaction at moderate potential under the constant surface potential,and using improved Derjaguin method we derive formulae for the interaction energy between the two parallel plates,valid up to the moderate to high potential regime.Agreement with the exact numerical values of the interaction of idential or dissimilar plates is considerably improved for the moderate surface potential.
    Studies on Novel Acrylic Acid Crosslinked Chitosan Pervaporation Membrane(Ⅰ)──Membrane Structure and Crosslinking Mechanism
    ZHONG Wei, GE Chang-Jie, CHEN Xin, LI Wen-Jun
    1996, 17(3):  470-473. 
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    A novel acrylic acid crosslinked chitosan membrane was prepared through a homogeneous solution reaction and its crosslinking structure was investigated through swelling ratio test, tensile measurement,IRspectra and pervaporation separation of ethanol/water mixtures using four kinds of sample membranes such as uncrosslinked chitosan membrane(sample A), chitosan membrane crosslinked by acrylic acid with and without inhibitor and methyl acrylic acid(sample B,Cand D,respectively).The crosslinking is proved to be via the addition reaction of the amino group of chtotsan to the double bond of acrylic acid and the neutral reaction between the amino group and the carboxyl group of acrylic acid.
    Studies on Gaseous Phase Polymerization of Ethylene with Highly Active Catalyst(Ⅱ)──The Effect of Modifiers,Prepolylnerization of Catalyst and Various Polymerization Conditions on Gaseous Phase Polymerization of Ethylene
    WANG Hai-Hua, LIAO Rony-Hui, WU Qing, LU Ze-Jian, CHEN Xue-Xin
    1996, 17(3):  474-479. 
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    In addition to the effects of type of alcobol,molar ratio on C2H5OH/Ti, and amount Of n-butyl ether in highly active catalyst of TiCl4/MgCl2/ZnCl2/SiCl4/alcohol/Al(i-Bu )3 on polymerization and morphology of the product,and the regularity of gaseous phase polymerization of ethylene and prepolymerization of catalyst have been studied.SEMand image analysis studies on morphology and particle size distribution of the catalyst and products of prepolymerization and polymerization showed that all the particle shapes were nearly spherical, and the particle ellipticity and dispersity of the catalyst were comparable to those of PEprepared with prepolymerized catalyst.
    Study of Poly (vinyl chloride)-Poly(ethylene oxide) Interaction Parameter by Inverse Gas Chromatography
    DU Qiang-Guo, YANG Xue-Jie
    1996, 17(3):  480-484. 
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    Polyvinyl chloride (PVC),polyethylene oxide(PEO) and their 50/50 blend were studied at 120℃ by inverse gas chromatography(IGC).The retention behavior was characterized for 36 probes.The IGC-derived PVC-PEOinteraction parameter X23,which ranged from-01 to 0.6,showed an apparent dependence on the nature of the probe.Specific retention volumes Vg23 of the blend were found to be equal to the weight-average Vg values of the two polymers for most probes.It is suggested that there existed phase separation in the blend.For phase separation system an approximate equation X23=(X12-X13)2/2 was given in this paper.This equation was verified by IGCresults of poly(vinyl chloride)-poly(ethylene oxide) blends.The probe dependence of X23 was well explained with this equation.
    Research on Monomer Structures and Reactivity of Poly(aryl ether ketone)s
    KE Yang-Chuan, FENG Ji-Kang, ZHENG Yu-Bin, WU Zhong-Wen, JI Xiang-Ling
    1996, 17(3):  485-489. 
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    Monomers of poly(aryl ether ketone)s famiy, such as,4,4'-hydroquinone(PD),4,4'-biphenol(S3)and 4,4'-difluorine benzophenone have been researched by ab initio RHFmethod.Results obtained show that these monomers have different torques in their aromatic rings.S3 has a dihedral angle of 51.8°,its reactivity is a bit stronger than that of PD, but it introduced more active branching points.Thus, polymer DPEEKfrom S3 has more serious chain branching and is more difficult in crystallizing than PEEKfrom PD.And also, it is found that there is a kind of red negative ion in DPEEK solution of concentrated H2SO4.
    Studies on Functional Redox Fiber──Preparation of Fibers Containing Hydroxy-alkylamine Groups and Their Redox Adsorption Reaction Towards Au3+
    TANG Shun-Qing, LU Yun, ZENG Han-Min
    1996, 17(3):  490-494. 
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    Three kinds of functional fibers Ⅰ,Ⅱ and Ⅲ are prepared by amination of reactive chloromethylated fiber with diethanolamine, ethanolamine and triethanolamine, and their nitrogen contained amount is 2.26,2.71 and 1.86 mmol/g,respectively.The results of adsorption experiments indicate that maximum adsorption amount of the fibers towards Au3+ is 550,620 and 409 mg/g, respectively,and they can reduce partly Au (Ⅲ) adsorbed into Au(0).By elemental analysis, IR, NMRand ESCA,it is proved that carbon atoms bonding with hydroxyl groups near nitrogen atoms are oxidized into carbonyl ones during redox reaction of fibers conatining hydroxy-alkylamine groups with Au (Ⅲ),but nitrogen atoms are not done.
    New Thermal Stable Silicone Containing Bismaleimide Derived from Diels-Alder Reaction──Synthesis and Characterization
    HAO Jain-Jun, JIANG Lu-Xia, CAI Xing-Xian
    1996, 17(3):  495-497. 
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    New bismaleimides (SIBMI) derived from Diels-Alder reaction of bis(4-maleimidophenyl) dimethyl silane[or bis(4-maleimidophenyl)diphenyl silane] and bis(2-furylmethoxy) dimethyl silane [or bis (2-furyl methoxy)diphenyl silane] were synthesized.Prepared products were then aromatized and silicone and imide containing bismaleimides (SIBMI) were obtained.The products were characterized by IR,1H NMRas well as elemental analysis,and the results were in accordance with the molecular structure.
    Banded Spherulites of Poly (ethylene oxide) and the Concentric Cracks Within a Single Spherulite
    DING Jian-Dong, ZHU Jun-Xiang, YANG Yu-Liang
    1996, 17(3):  498-499. 
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    Banded spherulites in bulk crystallization of poly (ethylene oxide)(PEO) are observed with polarizing optical microscopy.The interesting phenomenon is that the concentric bands can still be observed without polars and are assumed to results from the step-growing or spiral-growing of spherulites rather than from the lamellae twisting.The concentric cracks are also observed within every single spherulite together with the bands,which might be meaningful for research and application.