首页 > 最新文献

Central European Journal of Chemistry最新文献

英文 中文
Synthesis, structure and capacitive properties of cobalt hydroxide films on stainless steel substrates 不锈钢基板上氢氧化钴薄膜的合成、结构和电容性能
Pub Date : 2014-05-15 DOI: 10.2478/s11532-014-0570-y
I. Barauskienė, E. Valatka
AbstractCobalt (hydro)oxide films on AISI 304 stainless steel and sintered metal fibre filter Bekipor ST 20AL3 were prepared using electrochemical deposition from neutral cobalt acetate solutions under galvanostatic conditions. Deposited films were structurally characterized using X-ray diffraction, Fourier transform infrared spectroscopy and scanning electron microscopy. All electrochemical measurements were performed in aqueous NaOH solution. Capacitive behavior of different films was evaluated using cyclic voltammetry data. The highest specific capacitance (965 F g−1) was reached when Bekipor ST 20AL3 mesh was used as a support for electroactive substance.
摘要以中性醋酸钴溶液为原料,在恒流条件下电化学沉积,在AISI 304不锈钢和烧结金属纤维过滤器Bekipor ST 20AL3上制备了钴(氢)氧化膜。利用x射线衍射、傅里叶变换红外光谱和扫描电镜对沉积膜进行了结构表征。所有电化学测量均在NaOH水溶液中进行。利用循环伏安法对不同薄膜的电容行为进行了评价。Bekipor ST 20AL3网片作为电活性物质载体时,比电容达到最高(965 F g−1)。
{"title":"Synthesis, structure and capacitive properties of cobalt hydroxide films on stainless steel substrates","authors":"I. Barauskienė, E. Valatka","doi":"10.2478/s11532-014-0570-y","DOIUrl":"https://doi.org/10.2478/s11532-014-0570-y","url":null,"abstract":"AbstractCobalt (hydro)oxide films on AISI 304 stainless steel and sintered metal fibre filter Bekipor ST 20AL3 were prepared using electrochemical deposition from neutral cobalt acetate solutions under galvanostatic conditions. Deposited films were structurally characterized using X-ray diffraction, Fourier transform infrared spectroscopy and scanning electron microscopy. All electrochemical measurements were performed in aqueous NaOH solution. Capacitive behavior of different films was evaluated using cyclic voltammetry data. The highest specific capacitance (965 F g−1) was reached when Bekipor ST 20AL3 mesh was used as a support for electroactive substance.\u0000","PeriodicalId":9888,"journal":{"name":"Central European Journal of Chemistry","volume":"114 1","pages":"1206-1211"},"PeriodicalIF":0.0,"publicationDate":"2014-05-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"88000824","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 6
Crystallographic and structural characterization of heterometallic platinum complexes Part VI. Heterohexanuclear complexes 异金属铂配合物的晶体学和结构表征。第六部分。杂六核配合物
Pub Date : 2014-05-15 DOI: 10.2478/s11532-014-0558-7
M. Melnik, P. Mikuš, C. Holloway
AbstractThis review classifies and analyzes heterohexanuclear platinum clusters into seven types of metal combinations:Pt5M, Pt4M2, Pt3M3, Pt2M4, PtM5, Pt2M3M′, and Pt2M2M2′. The crystals of these clusters generally belong to six crystal classes: monoclinic, triclinic, orthorhombic, tetragonal, trigonal and cubic. Among the wide range of stereochemistry adopted by these clusters, octahedral and capped square-pyramidal are the most common. Although platinum is classified as a soft metal atom, it bonds to a variety of soft, borderline and hard metals. Nineteen different heterometal ions are involved in hexanuclear platinum clusters. The shortest Pt-M bond distance in the case of M being a non-transition element is 2.395(4) Å for germanium and for M being a transition metal ion it is 2.402(2) Å for Cobalt. The shortest Pt-Pt bond distance observed in these clusters is 2.532 Å. Several relationships between the structural parameters are identified and discussed. Some clusters exist in two isomeric forms and some show crystallographically independent molecules within the same crystal. Such isomers and independent molecules are examples of distortion isomerism.
摘要本文将杂己核铂簇划分为Pt5M、Pt4M2、Pt3M3、Pt2M4、PtM5、Pt2M3M′和Pt2M2M2′七种金属组合。这些团簇的晶体一般属于六个晶类:单斜、三斜、正交、四方、三角和立方。在这些簇所采用的广泛的立体化学结构中,八面体和盖顶方锥体是最常见的。虽然铂被归类为软金属原子,但它能与各种软金属、边缘金属和硬金属结合。六核铂簇中有19种不同的异金属离子。当M为非过渡元素时,锗的最短Pt-M键距为2.395(4)Å,而当M为过渡金属离子时,钴的最短Pt-M键距为2.402(2)Å。在这些簇中观察到的最短Pt-Pt键距离为2.532 Å。确定并讨论了结构参数之间的几种关系。有些团簇以两种同分异构体形式存在,有些在同一晶体中显示出晶体学上独立的分子。这种异构体和独立分子是扭曲异构体的例子。
{"title":"Crystallographic and structural characterization of heterometallic platinum complexes Part VI. Heterohexanuclear complexes","authors":"M. Melnik, P. Mikuš, C. Holloway","doi":"10.2478/s11532-014-0558-7","DOIUrl":"https://doi.org/10.2478/s11532-014-0558-7","url":null,"abstract":"AbstractThis review classifies and analyzes heterohexanuclear platinum clusters into seven types of metal combinations:Pt5M, Pt4M2, Pt3M3, Pt2M4, PtM5, Pt2M3M′, and Pt2M2M2′. The crystals of these clusters generally belong to six crystal classes: monoclinic, triclinic, orthorhombic, tetragonal, trigonal and cubic. Among the wide range of stereochemistry adopted by these clusters, octahedral and capped square-pyramidal are the most common. Although platinum is classified as a soft metal atom, it bonds to a variety of soft, borderline and hard metals. Nineteen different heterometal ions are involved in hexanuclear platinum clusters. The shortest Pt-M bond distance in the case of M being a non-transition element is 2.395(4) Å for germanium and for M being a transition metal ion it is 2.402(2) Å for Cobalt. The shortest Pt-Pt bond distance observed in these clusters is 2.532 Å. Several relationships between the structural parameters are identified and discussed. Some clusters exist in two isomeric forms and some show crystallographically independent molecules within the same crystal. Such isomers and independent molecules are examples of distortion isomerism.\u0000","PeriodicalId":9888,"journal":{"name":"Central European Journal of Chemistry","volume":"3 1","pages":"1101-1126"},"PeriodicalIF":0.0,"publicationDate":"2014-05-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"80241732","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 3
Biodegradation of Benzo[a]Pyrene through the use of algae 利用藻类降解苯并[a]芘
Pub Date : 2014-05-15 DOI: 10.2478/s11532-014-0567-6
A. Takáčová, M. Smolinská, J. Ryba, T. Mackuľak, Jana Jokrllová, P. Hronec, G. Čík
AbstractIn this work for disposal of the biologically hard decomposed pollutant Benzo[a]Pyrene (BaP) photooxidation Chlorella kessleri was used. The simulation model system under the different experimental conditions (varying biomass and light intensity) was evaluated. For quantitative analysis of the decrease in BaP, GC/MS technique was used. The highest degradation efficiency was achieved in the case of biomass from the culture of live algae (29%) and light intensity at level of 13.5 W m−2. When the dry biomass was used, degradation under the same conditions was lower because of lack of enzymatic activity in the system.
摘要本研究采用小球藻光氧化法处理生物难分解污染物苯并[a]芘(BaP)。对不同实验条件下(不同生物量和光强)的模拟模型系统进行了评价。采用GC/MS技术定量分析BaP的减少情况。在光强度为13.5 W m−2的情况下,来自活藻培养的生物量(29%)的降解效率最高。当使用干生物质时,由于系统中缺乏酶活性,在相同条件下的降解率较低。
{"title":"Biodegradation of Benzo[a]Pyrene through the use of algae","authors":"A. Takáčová, M. Smolinská, J. Ryba, T. Mackuľak, Jana Jokrllová, P. Hronec, G. Čík","doi":"10.2478/s11532-014-0567-6","DOIUrl":"https://doi.org/10.2478/s11532-014-0567-6","url":null,"abstract":"AbstractIn this work for disposal of the biologically hard decomposed pollutant Benzo[a]Pyrene (BaP) photooxidation Chlorella kessleri was used. The simulation model system under the different experimental conditions (varying biomass and light intensity) was evaluated. For quantitative analysis of the decrease in BaP, GC/MS technique was used. The highest degradation efficiency was achieved in the case of biomass from the culture of live algae (29%) and light intensity at level of 13.5 W m−2. When the dry biomass was used, degradation under the same conditions was lower because of lack of enzymatic activity in the system.\u0000","PeriodicalId":9888,"journal":{"name":"Central European Journal of Chemistry","volume":"44 1","pages":"1133-1143"},"PeriodicalIF":0.0,"publicationDate":"2014-05-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"77229786","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 33
Determination of 210Po content of vietnamese tobacco samples 越南烟草样品中210Po含量的测定
Pub Date : 2014-05-15 DOI: 10.2478/s11532-014-0569-4
T. Kovács, M. Horváth, Z. Sas, B. D. Dung, Tran Khanh Minh
Smoking is one of the leading causes of preventable death. In recent years, numerous countries have initiated the prohibition of smoking in restaurants, workplaces and public spaces. The Vietnamese government intends to follow the precautions against public smoking as well. Over and above the number of some hazardous chemical components found in tobacco, 210Po isotope content could enhance the probability of the development of lung cancer. In this study 14 Vietnamese tobacco products (commercial cigarettes and pipe tobacco) 210Po activity concentration were determined using PIPS semiconductor alpha spectrometry. The results showed that the 210Po activity concentration of the investigated samples varied between 7.40 ± 1.09–128.64 ± 11.22 mBq g−1. The average 210Po content of commercial cigarettes was 15.5 mBq g−1, whilst the average of pipe tobacco was 20.4 mBq g−1. To estimate the risk of inhalation of 210Po isotopes originating as a result of smoking, dose estimations were carried out.
吸烟是可预防死亡的主要原因之一。近年来,许多国家已经开始禁止在餐馆、工作场所和公共场所吸烟。越南政府也打算遵循公共场所吸烟的预防措施。超过烟草中某些有害化学成分的含量,210Po同位素含量会增加肺癌发生的概率。采用PIPS半导体α光谱法测定了14种越南烟草制品(商品卷烟和烟斗卷烟)的210Po活性浓度。结果表明,所研究样品的210Po活性浓度在7.40±1.09 ~ 128.64±11.22 mBq g−1之间变化。商品卷烟的210Po平均含量为15.5 mBq g - 1,烟斗卷烟的210Po平均含量为20.4 mBq g - 1。为了估计吸入因吸烟而产生的210Po同位素的风险,进行了剂量估计。
{"title":"Determination of 210Po content of vietnamese tobacco samples","authors":"T. Kovács, M. Horváth, Z. Sas, B. D. Dung, Tran Khanh Minh","doi":"10.2478/s11532-014-0569-4","DOIUrl":"https://doi.org/10.2478/s11532-014-0569-4","url":null,"abstract":"Smoking is one of the leading causes of preventable death. In recent years, numerous countries have initiated the prohibition of smoking in restaurants, workplaces and public spaces. The Vietnamese government intends to follow the precautions against public smoking as well. Over and above the number of some hazardous chemical components found in tobacco, 210Po isotope content could enhance the probability of the development of lung cancer. In this study 14 Vietnamese tobacco products (commercial cigarettes and pipe tobacco) 210Po activity concentration were determined using PIPS semiconductor alpha spectrometry. The results showed that the 210Po activity concentration of the investigated samples varied between 7.40 ± 1.09–128.64 ± 11.22 mBq g−1. The average 210Po content of commercial cigarettes was 15.5 mBq g−1, whilst the average of pipe tobacco was 20.4 mBq g−1. To estimate the risk of inhalation of 210Po isotopes originating as a result of smoking, dose estimations were carried out.","PeriodicalId":9888,"journal":{"name":"Central European Journal of Chemistry","volume":"82 1","pages":"1127-1132"},"PeriodicalIF":0.0,"publicationDate":"2014-05-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"91244098","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 9
Syngas production by biogas reforming over the Co-based multicomponent catalysts 基于co基多组分催化剂的沼气重整制合成气
Pub Date : 2014-05-12 DOI: 10.2478/s11532-014-0571-x
S. Itkulova, G. D. Zakumbaeva, A. Mukazhanova, Y. Y. Nurmakanov
The new multicomponent Co-based catalysts with additives of group 8 metal and rare earth elements and supported on alumina have been tested in the dry and steam conversion of a model biogas. The processes were carried out in a flow quartz reactor under the following conditions: atmospheric pressure, a gas hourly space velocity of 1000 h−1 and temperatures of 300–800°C. The catalysts were characterised using electron microscopy, BET and X-ray analysis.The methane is almost completely converted in the dry reforming of biogas at T≤800°C. Synthesis gas with a ratio of H2/CO>1.0 is a main product of biogas reforming over the multicomponent catalysts studied. Adding steam in a feed composition increases both the methane conversion and the hydrogen yield at lower temperatures. Almost complete methane conversion occurs at T<750°C in the steam reforming of biogas. The catalysts are highly effective and exhibit stable activity throughout 100 h of continuous testing.
以氧化铝为载体,添加8族金属和稀土元素的新型多组分co基催化剂在模型沼气的干式和汽式转化中进行了试验。该过程在石英流动反应器中进行,条件为常压,气体每小时空速为1000 h−1,温度为300-800℃。采用电子显微镜、BET和x射线分析对催化剂进行了表征。在T≤800℃的条件下,沼气在干式重整中几乎完全转化。多组分催化剂上沼气重整的主要产物是H2/CO>1.0的合成气。在进料组合物中加入蒸汽可在较低温度下提高甲烷转化率和氢气产量。沼气蒸汽重整在T<750℃时甲烷几乎完全转化。该催化剂在100小时的连续测试中表现出稳定的活性。
{"title":"Syngas production by biogas reforming over the Co-based multicomponent catalysts","authors":"S. Itkulova, G. D. Zakumbaeva, A. Mukazhanova, Y. Y. Nurmakanov","doi":"10.2478/s11532-014-0571-x","DOIUrl":"https://doi.org/10.2478/s11532-014-0571-x","url":null,"abstract":"The new multicomponent Co-based catalysts with additives of group 8 metal and rare earth elements and supported on alumina have been tested in the dry and steam conversion of a model biogas. The processes were carried out in a flow quartz reactor under the following conditions: atmospheric pressure, a gas hourly space velocity of 1000 h−1 and temperatures of 300–800°C. The catalysts were characterised using electron microscopy, BET and X-ray analysis.The methane is almost completely converted in the dry reforming of biogas at T≤800°C. Synthesis gas with a ratio of H2/CO>1.0 is a main product of biogas reforming over the multicomponent catalysts studied. Adding steam in a feed composition increases both the methane conversion and the hydrogen yield at lower temperatures. Almost complete methane conversion occurs at T<750°C in the steam reforming of biogas. The catalysts are highly effective and exhibit stable activity throughout 100 h of continuous testing.","PeriodicalId":9888,"journal":{"name":"Central European Journal of Chemistry","volume":"33 1","pages":"1255-1261"},"PeriodicalIF":0.0,"publicationDate":"2014-05-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"75561605","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 4
Chemical and technological characterization of medieval glass bracelets from South-East Bulgaria 保加利亚东南部中世纪玻璃手镯的化学和技术特征
Pub Date : 2014-05-06 DOI: 10.2478/s11532-014-0560-0
R. Georgieva, A. Detcheva, Y. Dimitriev
AbstractThe present paper deals with chemical and physicochemical characterization of seven glass fragments of medieval glass bracelets from South-East Bulgaria. Samples were investigated by Fourier-transform infrared spectroscopy (FT-IR), transmission electron microscopy (TEM) and differential thermal analysis (DTA). Gravimetric chemical analysis was used for silica assessment. Flame photometry was applied to determine sodium and potassium content while aluminium, calcium and magnesium were determined by flame atomic absorption spectrometry after dissolution using a mixture of acids. All investigated artefacts are soda-lime-silica glasses and when produced two different recipe norms were used. Important technological parameters of glass manufacturing were determined and discussed. This investigation throws light on the technological development and production of glass during medieval times.
摘要本文研究了保加利亚东南部出土的7块中世纪玻璃手镯碎片的化学和物理化学特征。采用傅里叶变换红外光谱(FT-IR)、透射电镜(TEM)和差热分析(DTA)对样品进行了表征。用重量化学分析法对二氧化硅进行了评价。用火焰光度法测定钠、钾的含量,用混合酸溶解后用火焰原子吸收法测定铝、钙、镁的含量。所有被调查的人工制品都是钠石灰硅玻璃,当生产时使用了两种不同的配方规范。确定并讨论了玻璃生产的重要工艺参数。这项调查揭示了中世纪玻璃的技术发展和生产。
{"title":"Chemical and technological characterization of medieval glass bracelets from South-East Bulgaria","authors":"R. Georgieva, A. Detcheva, Y. Dimitriev","doi":"10.2478/s11532-014-0560-0","DOIUrl":"https://doi.org/10.2478/s11532-014-0560-0","url":null,"abstract":"AbstractThe present paper deals with chemical and physicochemical characterization of seven glass fragments of medieval glass bracelets from South-East Bulgaria. Samples were investigated by Fourier-transform infrared spectroscopy (FT-IR), transmission electron microscopy (TEM) and differential thermal analysis (DTA). Gravimetric chemical analysis was used for silica assessment. Flame photometry was applied to determine sodium and potassium content while aluminium, calcium and magnesium were determined by flame atomic absorption spectrometry after dissolution using a mixture of acids. All investigated artefacts are soda-lime-silica glasses and when produced two different recipe norms were used. Important technological parameters of glass manufacturing were determined and discussed. This investigation throws light on the technological development and production of glass during medieval times.\u0000","PeriodicalId":9888,"journal":{"name":"Central European Journal of Chemistry","volume":"11 1","pages":"1169-1175"},"PeriodicalIF":0.0,"publicationDate":"2014-05-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"89776666","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Metals content of soil, leaves and wild fruit from Serbia 塞尔维亚土壤、树叶和野果的金属含量
Pub Date : 2014-05-06 DOI: 10.2478/s11532-014-0566-7
S. Randjelovic, D. Kostić, G. Stojanović, S. Mitić, M. Mitić, B. Arsić, A. Pavlović
AbstractThe concentrations of Zn, Mn, Fe, Pb, Ni, Cu and Cd in soil, leaves and edible wild fruit (Crataegus laevigata L., Cornus mas L. and Prunus spinosa L.) from southeast Serbia were determined by atomic absorption spectroscopy. Metal translocations from soil to fruit were calculated as well as their oral intake and health risk indices. Positive correlations were found among metal concentrations in soil, leaves and fruit.
摘要采用原子吸收光谱法测定了塞尔维亚东南部地区土壤、树叶和食用野果(山楂、山茱萸和樱)中Zn、Mn、Fe、Pb、Ni、Cu和Cd的含量。计算土壤金属向水果的迁移量、口腔摄入量和健康风险指数。土壤、叶片和果实中金属含量呈显著正相关。
{"title":"Metals content of soil, leaves and wild fruit from Serbia","authors":"S. Randjelovic, D. Kostić, G. Stojanović, S. Mitić, M. Mitić, B. Arsić, A. Pavlović","doi":"10.2478/s11532-014-0566-7","DOIUrl":"https://doi.org/10.2478/s11532-014-0566-7","url":null,"abstract":"AbstractThe concentrations of Zn, Mn, Fe, Pb, Ni, Cu and Cd in soil, leaves and edible wild fruit (Crataegus laevigata L., Cornus mas L. and Prunus spinosa L.) from southeast Serbia were determined by atomic absorption spectroscopy. Metal translocations from soil to fruit were calculated as well as their oral intake and health risk indices. Positive correlations were found among metal concentrations in soil, leaves and fruit.\u0000","PeriodicalId":9888,"journal":{"name":"Central European Journal of Chemistry","volume":"14 1","pages":"1144-1151"},"PeriodicalIF":0.0,"publicationDate":"2014-05-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"87524506","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 10
Aerobic oxidation of cumene catalysed by 4-alkyloxycarbonyl-N-hydroxyphthalimide 4-烷基氧羰基- n -羟基邻苯二胺催化异丙苯的好氧氧化
Pub Date : 2014-05-06 DOI: 10.2478/s11532-014-0565-8
Kornela Kasperczyk, Beata Orlińska, J. Zawadiak
Abstract4-Hexyloxycarbonyl-, 4-dodecyloxycarbonyl- and 4-hexadecyloxycarbonyl-N-hydroxyphthalimides were synthesised using trimellitic anhydride chloride as the starting material. The obtained lipophilic derivatives of N-hydroxyphthalimide were applied as catalysts of the cumene oxidation reaction with oxygen performed in polar acetonitrile, in non-polar tert-butylbenzene and in the absence of a solvent. The courses of reactions catalysed by N-hydroxyphthalimide and its derivatives were compared.
摘要以氯偏苯三酸酐为原料合成了4-己基氧羰基-、4-十二烷基氧羰基-和4-十六烷基氧羰基- n -羟基邻苯酞酰亚胺。得到的n-羟基邻苯亚胺亲脂衍生物作为催化剂,在极性乙腈、非极性叔丁基苯和无溶剂条件下进行了异丙烯的氧氧化反应。比较了n -羟基邻苯二胺及其衍生物催化反应的过程。
{"title":"Aerobic oxidation of cumene catalysed by 4-alkyloxycarbonyl-N-hydroxyphthalimide","authors":"Kornela Kasperczyk, Beata Orlińska, J. Zawadiak","doi":"10.2478/s11532-014-0565-8","DOIUrl":"https://doi.org/10.2478/s11532-014-0565-8","url":null,"abstract":"Abstract4-Hexyloxycarbonyl-, 4-dodecyloxycarbonyl- and 4-hexadecyloxycarbonyl-N-hydroxyphthalimides were synthesised using trimellitic anhydride chloride as the starting material. The obtained lipophilic derivatives of N-hydroxyphthalimide were applied as catalysts of the cumene oxidation reaction with oxygen performed in polar acetonitrile, in non-polar tert-butylbenzene and in the absence of a solvent. The courses of reactions catalysed by N-hydroxyphthalimide and its derivatives were compared.\u0000","PeriodicalId":9888,"journal":{"name":"Central European Journal of Chemistry","volume":"51 1","pages":"1176-1182"},"PeriodicalIF":0.0,"publicationDate":"2014-05-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"78294765","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 39
Occurrence of 2-phenylphenol in food paper packages 食品纸包装中2-苯基酚的含量
Pub Date : 2014-05-06 DOI: 10.2478/s11532-014-0563-x
L. Votavová, K. Hanušová, Lukáš Vápenka, J. Dobiáš, F. Kvasnička
AbstractTwenty three paper based packaging materials commercially used for food packaging in the Czech Republic were analysed with regard to 2-phenylphenol (OPP) content using HPLC technique with fluorimetric detection. The HPLC method was modified with the aim to increase its sensitivity. OPP was detected in quantities ranging from 10 mg kg−1 to 527 mg kg−1 in twenty tested samples. The level of OPP in packaging materials was in close correlation to the content of recycled pulp in used paper material. The migration of OPP from two packaging materials comprised of paperboard coated with low density polyethylene (LDPE) into food simulants was determined at 40°C for 10 days. The levels of migration into 3% acetic acid, 10% ethanol and olive oil were below the limit of detection of used analytical procedure. In the case of 95% ethanol, 13% and 21% of OPP present in tested samples were transferred into simulant. The found occurrence of OPP in paper packages does not pose any significant safety risk for food consumer, but OPP could be considered as wide spread contaminant in paper materials.
摘要采用高效液相色谱-荧光法对捷克23种市售食品包装用纸中的2-苯基酚(OPP)含量进行了分析。对HPLC法进行了改进,以提高其灵敏度。在20个测试样品中检测到OPP的量从10 mg kg - 1到527 mg kg - 1不等。包装材料中OPP的含量与废纸中再生纸浆的含量密切相关。在40°C条件下,测定了两种包装材料(由涂有低密度聚乙烯(LDPE)的纸板组成)向食品模拟剂中的OPP迁移。对3%醋酸、10%乙醇和橄榄油的迁移量均低于常用分析方法的检出限。在95%乙醇的情况下,测试样品中存在的13%和21%的OPP被转移到模拟物中。纸包装中发现的OPP不会对食品消费者构成重大的安全风险,但OPP可以被认为是纸制品中广泛存在的污染物。
{"title":"Occurrence of 2-phenylphenol in food paper packages","authors":"L. Votavová, K. Hanušová, Lukáš Vápenka, J. Dobiáš, F. Kvasnička","doi":"10.2478/s11532-014-0563-x","DOIUrl":"https://doi.org/10.2478/s11532-014-0563-x","url":null,"abstract":"AbstractTwenty three paper based packaging materials commercially used for food packaging in the Czech Republic were analysed with regard to 2-phenylphenol (OPP) content using HPLC technique with fluorimetric detection. The HPLC method was modified with the aim to increase its sensitivity. OPP was detected in quantities ranging from 10 mg kg−1 to 527 mg kg−1 in twenty tested samples. The level of OPP in packaging materials was in close correlation to the content of recycled pulp in used paper material. The migration of OPP from two packaging materials comprised of paperboard coated with low density polyethylene (LDPE) into food simulants was determined at 40°C for 10 days. The levels of migration into 3% acetic acid, 10% ethanol and olive oil were below the limit of detection of used analytical procedure. In the case of 95% ethanol, 13% and 21% of OPP present in tested samples were transferred into simulant. The found occurrence of OPP in paper packages does not pose any significant safety risk for food consumer, but OPP could be considered as wide spread contaminant in paper materials.\u0000","PeriodicalId":9888,"journal":{"name":"Central European Journal of Chemistry","volume":"61 1","pages":"1162-1168"},"PeriodicalIF":0.0,"publicationDate":"2014-05-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"77469867","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 9
DNA molecules site-specific immobilization and their applications DNA分子定点固定及其应用
Pub Date : 2014-05-06 DOI: 10.2478/s11532-014-0557-8
Xiaoning Zhang, Hongmei Hu
AbstractIn addition to its role as a carrier of genetic information, DNA has been recognized as a construction material for the assembly of different objects and structural arrangements with nanoscale features. As a result of DNA’s self-recognition properties (based on the specific base-pairing of G-C and T-A), monolayer films of nucleic acids on solid supports have attracted an escalating attentions. Recently, numerous novel materials based on two-dimensional (2D) and three-dimensional (3D) DNA structures have been reported, which extends their utility to a large number of appliations. This review paper intends to be a new and comprehensive overview of recent strategies to site-specifically immobilized DNA on various materials, including carbonaceous substances, gold, and silica substrate, emphasizing the applications of site-specific DNA nanostructure-based devices for diagnostic, bioanalytical, food safety and environmental monitoring. Additionally, an up-to-date perspective is proposed at the end of this review.
DNA除了作为遗传信息的载体外,还被认为是具有纳米级特征的不同物体组装和结构排列的构建材料。由于DNA的自我识别特性(基于G-C和T-A的特定碱基配对),固体载体上的核酸单层膜越来越受到人们的关注。近年来,许多基于二维(2D)和三维(3D) DNA结构的新型材料被报道出来,这使它们的用途得到了广泛的应用。本文综述了近年来在碳质物质、金、二氧化硅等不同材料上特异位点固定化DNA的研究进展,重点介绍了特异位点DNA纳米结构装置在诊断、生物分析、食品安全和环境监测等方面的应用。此外,在本综述的最后提出了一个最新的观点。
{"title":"DNA molecules site-specific immobilization and their applications","authors":"Xiaoning Zhang, Hongmei Hu","doi":"10.2478/s11532-014-0557-8","DOIUrl":"https://doi.org/10.2478/s11532-014-0557-8","url":null,"abstract":"AbstractIn addition to its role as a carrier of genetic information, DNA has been recognized as a construction material for the assembly of different objects and structural arrangements with nanoscale features. As a result of DNA’s self-recognition properties (based on the specific base-pairing of G-C and T-A), monolayer films of nucleic acids on solid supports have attracted an escalating attentions. Recently, numerous novel materials based on two-dimensional (2D) and three-dimensional (3D) DNA structures have been reported, which extends their utility to a large number of appliations. This review paper intends to be a new and comprehensive overview of recent strategies to site-specifically immobilized DNA on various materials, including carbonaceous substances, gold, and silica substrate, emphasizing the applications of site-specific DNA nanostructure-based devices for diagnostic, bioanalytical, food safety and environmental monitoring. Additionally, an up-to-date perspective is proposed at the end of this review.\u0000","PeriodicalId":9888,"journal":{"name":"Central European Journal of Chemistry","volume":"139-140 1","pages":"977-993"},"PeriodicalIF":0.0,"publicationDate":"2014-05-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"79149321","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 8
期刊
Central European Journal of Chemistry
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1