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Understanding changes in volatile compounds and fatty acids of Jincheng orange peel oil at different growth stages using GC-MS
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作者 XIE Jiao CAO Qi +2 位作者 WANG Wen-jun ZHANG Hong-yan DENG Bing 《Journal of Integrative Agriculture》 SCIE CAS CSCD 2023年第7期2282-2294,共13页
Jincheng orange(Citrus sinensis Osbeck)is widely grown in Chongqing,China,and is commonly consumed because of its characteristic aroma contributed by the presence of diverse volatile compounds.The changes in aroma dur... Jincheng orange(Citrus sinensis Osbeck)is widely grown in Chongqing,China,and is commonly consumed because of its characteristic aroma contributed by the presence of diverse volatile compounds.The changes in aroma during the development and maturation of fruit are indicators for ripening and harvest time.However,the influence of growth stages on the volatile compounds in Jincheng orange remains unclear.In addition,volatiles originate from fatty acids,most of which are the precursors of volatile substances.On this basis,gas chromatography-mass spectrometry(GC-MS)was performed to elaborate the changes in volatile constituents and fatty acids as precursors.This study tested proximately 60 volatiles and 8 fatty acids at 9 growth and development stages(AF1-AF9).Of those compounds,more than 92.00%of total volatiles and 87.50%of fatty acids were terpenoid and saturated fatty acids,respectively.As shown in the PCA plot,the AF5,AF6,and AF9 stages were confirmed as completely segregated and appeared different.In addition,most of the volatiles and fatty acids first increased at the beginning of the development stage,then decreased from the AF6 development stage,and finally increased at the AF9 maturity stage.Moreover,the highest contents of terpenoid,alcohols,aldehydes,ketones,and saturated fatty acids in Jincheng orange peel oil were d-limonene,linalool,octanal,cyclohexanone,and stearic acid during development stages,respectively.Our results found that the growth stages significantly affected the volatile constituents and precursors in Jincheng orange peel oil. 展开更多
关键词 Jincheng orange volatile compounds fatty acids growth stages
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Activated persulfate by DBD plasma and activated carbon for the degradation of acid orange Ⅱ 被引量:1
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作者 Weigang CHEN Haixia WU +2 位作者 Jiawei FAN Zhi FANG Shaohua LIN 《Plasma Science and Technology》 SCIE EI CAS CSCD 2020年第3期59-65,共7页
In this study, the effect of activated peroxydisulfate(PDS) by dielectric barrier discharge(DBD) plasma and activated carbon(HGAC) on the removal of acid orange Ⅱ(AOⅡ) was investigated. The effects of applied voltag... In this study, the effect of activated peroxydisulfate(PDS) by dielectric barrier discharge(DBD) plasma and activated carbon(HGAC) on the removal of acid orange Ⅱ(AOⅡ) was investigated. The effects of applied voltage, PDS dosage, HGAC dosage, initial pH value, and inorganic anions on the removal rate of AOⅡ were discussed. The main free radicals degrading azo dyes during the experiment were also studied. Experimental results show that the removal rate of AOⅡ in DBD/HGAC/PDS synergistic system is much higher than that in the single system. With the applied voltage of 16 kV, HGAC dosage of 1 g l-1, PDS and AOⅡ molar ratio of 200:1, initial pH value of 5.4 and concentration of AOⅡ solution of 20 mg l-1, the removal rate of AOⅡ reached 97.6% in DBD/HGAC/PDS process after 28 min of reaction.Acidic and neutral conditions are beneficial for AOⅡ removal. Sulfate and hydroxyl radicals play an important role in the removal of AOⅡ. Inorganic anions are not conducive to the removal of AOⅡ. 展开更多
关键词 DBD plasma ACTIVATED carbon PERSULFATE SULFATE radical acid orange
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含铁柱撑膨润土光催化降解Orange Ⅱ 被引量:8
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作者 李益民 温丽华 +1 位作者 刘颖 李海洋 《功能材料》 EI CAS CSCD 北大核心 2005年第6期874-876,880,共4页
制备了两种含铁柱撑膨润土(FeAlBent和FeBent),用XRD、BET、TEM对它们进行了性能表征。以偶氮染料OrangeⅡ为目标降解物,考察了它们作为复相Fenton催化剂的光催化性能,以及溶液的pH、H2O2浓度、催化剂用量对OrangeⅡ降解的影响,并与相... 制备了两种含铁柱撑膨润土(FeAlBent和FeBent),用XRD、BET、TEM对它们进行了性能表征。以偶氮染料OrangeⅡ为目标降解物,考察了它们作为复相Fenton催化剂的光催化性能,以及溶液的pH、H2O2浓度、催化剂用量对OrangeⅡ降解的影响,并与相应的均相Fenton反应进行了比较。结果表明FeAlBent和FeBent具有很高的比表面积(分别为194.2和114.6m2/g),用FeAlBent或FeBent作光催化剂的复相光助Fenton反应的催化性能明显优于相应的均相光助Fenton反应。此外复合铁铝柱撑膨润土(FeAlBent)比单一的铁柱撑膨润土(FeBent)在反应过程中具有更低的铁离子溶出量,它们还具有分离简单、重复使用性好等特点。 展开更多
关键词 光催化降解 铝铁柱撑膨润土 光助Fenton orange
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Degradation of Acid Orange Ⅱ Using Negative Pulsed Discharge Plasma from a Nozzle-cylinder Electrode Coated with TiO2
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作者 SUN Ming WANG Shaoqi ZHANG Ying 《高电压技术》 EI CAS CSCD 北大核心 2013年第10期2514-2519,共6页
Many sub-products of pulsed discharge,such as ultraviolet light,strong electric fields,shock waves and active species,are effective in treating wastewater.To improve the efficiency of the discharge plasma technology i... Many sub-products of pulsed discharge,such as ultraviolet light,strong electric fields,shock waves and active species,are effective in treating wastewater.To improve the efficiency of the discharge plasma technology in removing pollutants,adding TiO2 photo-catalyst to pulsed discharges could help.A negative-pulsed-discharge system,which has nozzle discharge electrodes with or without TiO2 coating,is used to degrade azo dye Acid Orange Ⅱ,and the effects of several key conditions(maximum pulse voltage,pulse repetition frequency,initial mass concentration of Acid Orange Ⅱ initial solution pH,treatment duration,the phase of discharge,and the existence of TiO2) on the degradation are experimentally investigated.The degradation of Acid Orange Ⅱ increases with maximum pulse voltage,pulse repetition frequency,and treatment duration,and it is larger when putting the discharge electrode on the solution surface than in air or inside the solution,i.e.the discharge in gas phase is more effective than that in gas-liquid phase or liquid phase.The degradation decreases as the initial mass concentration of the solution increases.It also relates to pH and is higher at acidic conditions than at neutral or alkaline conditions.Compared to treatments without TiO2,the ones using the nozzle discharge electrode with TiO2 coated increase the degradation of Acid Orange Ⅱ by 5 %.It is concluded that the proposed system with TiO2 added in can remove Acid Orange Ⅱ from wastewater effectively. 展开更多
关键词 脉冲放电等离子体 TIO2光催化剂 酸性橙 放电电极 降解 表面覆盖 喷嘴 二氧化钛涂层
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Formation of the Inclusion Complex of Orange Ⅱ with β-Cyclodextrin and Its Photostability 被引量:2
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作者 LuPing LiuBin +2 位作者 ZhangZhe WuFeng DengNan-sheng 《Wuhan University Journal of Natural Sciences》 CAS 2003年第04A期1147-1152,共6页
Inclusion complex of Orange II with β-Cyclodextrin (β-CD) and the anti-photolysis effect under UV-light were investigated. The molar ratio of inclusion complex of β-Cyclodextrin and Orange Ⅱ is 1∶1. The formation... Inclusion complex of Orange II with β-Cyclodextrin (β-CD) and the anti-photolysis effect under UV-light were investigated. The molar ratio of inclusion complex of β-Cyclodextrin and Orange Ⅱ is 1∶1. The formation constant K=1.236×10 3 L/mol was determined by the UV and Fluorescence spectra respectively, which was quite in accordance with the calculation with a modified Benesi-Hildbrand equation. The inclusion complex was characterized by the IR spectra and the molar ratio of inclusion complex is 1∶1 too. The formation constant K=1.266×10 3 L/mol was determined by 1 H NMR analysis and was nearly the same by UV and fluorescence spectra. The photocatalytic decolorization rate of Orange Ⅱ solutions containing β-CD and TiO_ 2 was smaller by 51.9% than that of the Orange Ⅱ solutions only containing TiO_ 2 , while in the case of direct photolysis of Orange Ⅱ solutions, β-CD can lower the photolysis rate by 48.1% under UV-light. This result indicates β-CD can inhibit the photolysis and photocatalytic decolorization of Orange Ⅱ under UV-light. The β-CD inclusion complex was found to be persistent to UV-light photolysis. 展开更多
关键词 Β-CYCLODEXTRIN orange inclusion complex PHOTOSTABILITY
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Photocatalytic Degradation of Organic Dye Methyl Orange with Phosphotungstic Acid 被引量:1
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作者 Weiping Wang Shuijin Yang 《Journal of Water Resource and Protection》 2010年第11期979-983,共5页
Silicotungstic acid and phosphotungstic acid were prepared and characterized by Fourier Transform Infrared Spectroscopy (FTIR) and X-ray diffraction (XRD). The results showed that the prepared catalysts possess classi... Silicotungstic acid and phosphotungstic acid were prepared and characterized by Fourier Transform Infrared Spectroscopy (FTIR) and X-ray diffraction (XRD). The results showed that the prepared catalysts possess classical Keggin structure. The factors on the degradation of methyl orange, such as the kind of catalyst, the amount of catalyst, the original concentration of dye and illumination time were investigated under metal halide lamp. The degradation of methyl orange is up to 93.6% with phosphotungstic acid at the best reaction conditions at 8.89 g/L concentration of phosphotungstic acid, 5.56 mg/L concentration of methyl orange and 80 min illumination time. 展开更多
关键词 Phosphotungstic acid PHOTOCATALYTIC DEGRADATION METHYL orange
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Regeneration of Acid Orange 7 Exhausted Granular Activated Carbon Using Pulsed Discharge Plasmas 被引量:1
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作者 王慧娟 郭贺 +1 位作者 刘永杰 依成武 《Plasma Science and Technology》 SCIE EI CAS CSCD 2015年第10期881-886,共6页
In this paper, a pulsed discharge plasma (PDP) system with a multi-needle-to-plate electrodes geometry was set up to investigate the regeneration of acid orange 7 (AO7) exhausted granular activated carbon (GAC).... In this paper, a pulsed discharge plasma (PDP) system with a multi-needle-to-plate electrodes geometry was set up to investigate the regeneration of acid orange 7 (AO7) exhausted granular activated carbon (GAC). Regeneration of GAC was studied under different conditions of peak pulse discharge voltage and water pH, as well as the modification effect of GAC by the pulse discharge process, to figure out the regeneration efficiency and the change of the GAC structure by the PDP treatment. The obtained results showed that there was an appropriate peak pulse voltage and an optimal initial pH value of the solution for GAC regeneration. Analyses of scanning electron microscope (SEM), Boehm titration, Brunauer-Emmett-Teller (BET), Horvath-Kawazoe (HK), and X-ray Diffraction (XRD) showed that there were more mesopore and macropore in the regenerated GAC and the structure turned smoother with the increase of discharge voltage; the amount of acidic functional groups on the GAC surface increased while the amount of basic functional groups decreased after the regeneration process. From the result of the XRD analysis, there were no new substances produced on the GAC after PDP treatment. 展开更多
关键词 pulsed discharge plasma acid orange 7 granular activated carbon REGENERATION pore structure functional groups
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超高效液相色谱-串联质谱法测定禽用饲料中苏丹红、罗丹明B和酸性橙Ⅱ等6种染色剂含量
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作者 李宏 贺习文 +3 位作者 晁娟娟 李俊 武治勇 杨森 《中国饲料》 北大核心 2024年第3期118-124,共7页
本研究基于超高效液相色谱-串联质谱(UPLC-MS/MS)结合QuEChERS快速净化方法,旨在建立禽用饲料中苏丹红等6种化工染料的定量分析方法。样品用乙腈提取,C_(18)+PSA净化材料净化,净化液经Hypersil GOLD C_(18)反向色谱柱分离,在电喷雾离子... 本研究基于超高效液相色谱-串联质谱(UPLC-MS/MS)结合QuEChERS快速净化方法,旨在建立禽用饲料中苏丹红等6种化工染料的定量分析方法。样品用乙腈提取,C_(18)+PSA净化材料净化,净化液经Hypersil GOLD C_(18)反向色谱柱分离,在电喷雾离子源(ESI)正、负离子双扫描模式下多反应监测(MRM),以标准曲线外标法定量。结果表明:6种化合物线性关系良好;相关系数(R^(2))>0.999,4种苏丹红和酸性橙Ⅱ检出限(LOD)为0.5μg/kg,定量限(LOQ)为1.0μg/kg,罗丹明B LOD为0.05μg/kg,LOQ为0.1μg/kg。添加回收率为90%~110%,相对标准偏差<10%。本研究方法具有快速、灵敏等优势,可实现禽用饲料中6种化工染料的准确定量分析,为禽用饲料的质量安全提供技术参考。 展开更多
关键词 禽用饲料 苏丹红 罗丹明B 酸性橙 超高效液相色谱-串联质谱法 QuEChERS
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羟基磷灰石复合腐植酸及其对Mn(Ⅱ)的去除
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作者 裴晓港 张鹏 +2 位作者 董珊珊 葛姗姗 赵月龙 《无机盐工业》 CAS CSCD 北大核心 2024年第5期70-77,共8页
以硝酸钙和磷酸氢铵为原料,采用化学沉淀法成功合成羟基磷灰石(HAP),并将其与腐植酸(HA)复合,制备出复合吸附剂HAP-HA。通过傅里叶变换红外光谱(FT-IR)、比表面积及孔径分析、差热-热重分析(TGDSC)及扫描电镜(SEM)等方法对样品进行表征... 以硝酸钙和磷酸氢铵为原料,采用化学沉淀法成功合成羟基磷灰石(HAP),并将其与腐植酸(HA)复合,制备出复合吸附剂HAP-HA。通过傅里叶变换红外光谱(FT-IR)、比表面积及孔径分析、差热-热重分析(TGDSC)及扫描电镜(SEM)等方法对样品进行表征。结果表明:腐植酸成功负载到羟基磷灰石上;HAP-HA孔径主要分布在3~5 nm,比表面积较大,且具有较好的稳定性;HAP-HA表面粗糙不平、孔隙较多,这增大了比表面积,为重金属离子提供了大量的活性位点。以Mn(Ⅱ)为目标污染物,将Mn(Ⅱ)的去除率作为指标,通过吸附实验考察吸附剂HAP-HA对污染物的吸附性能。结果表明:在常温、pH为8.0、投加量为0.15 g、吸附时间为150 min的条件下,吸附剂HAP-HA对Mn(Ⅱ)的去除率最高,可稳定达到99.0%以上;该吸附过程符合Freundlich等温吸附模型。同时,对吸附后的吸附剂进行脱附及再生吸附实验,以NaOH溶液作为洗脱剂可取得较好的脱附效果,脱附效率可达78.1%,再生循环吸附6次后HAP-HA仍具有良好的吸附性能。 展开更多
关键词 羟基磷灰石 腐植酸 吸附剂 金属Mn()
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羟胺强化Cu(Ⅱ)活化过氧乙酸降解有机染料
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作者 欧杰丽 刘义青 +1 位作者 唐钰琦 付永胜 《中国环境科学》 EI CAS CSCD 北大核心 2024年第10期5547-5555,共9页
采用盐酸羟胺(HA)强化Cu(Ⅱ)活化过氧乙酸(PAA)降解亚甲基蓝(MB),考察了溶液初始pH值、反应物投加量及水环境中常见阴离子、天然有机物对HA/Cu(Ⅱ)/PAA体系去除MB效果的影响;通过鉴别体系中的主要活性物质,探究PAA在HA/Cu(Ⅱ)/PAA体系... 采用盐酸羟胺(HA)强化Cu(Ⅱ)活化过氧乙酸(PAA)降解亚甲基蓝(MB),考察了溶液初始pH值、反应物投加量及水环境中常见阴离子、天然有机物对HA/Cu(Ⅱ)/PAA体系去除MB效果的影响;通过鉴别体系中的主要活性物质,探究PAA在HA/Cu(Ⅱ)/PAA体系中的活化机理.结果表明:pH值为7.0条件下,当Cu(Ⅱ)和PAA投加量均为200μmol/L时,向Cu(Ⅱ)/PAA体系中加入400μmol/L的HA,经过30min的反应,MB的去除率可由14.7%增加到74.1%,降解速率由0.0047min^(-1)提高至0.2271min^(-1);HA的引入推动了Cu(Ⅱ)向Cu(Ⅰ)的转化,促进了PAA的催化分解,导致体系中生成更多的活性物种.基于自由基淬灭实验结果,羟基自由基(HO•)主导了MB的氧化降解.溶液pH值对MB降解影响较大,中性和弱碱性环境更有利于HA/Cu(Ⅱ)/PAA体系对MB的降解.共存Cl^(-)和HCO_(3)^(-)会抑制MB降解,而天然有机质对MB降解起一定促进作用. 展开更多
关键词 过氧乙酸 Cu() 盐酸羟胺 高级氧化 亚甲基蓝
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改性球状纤维素基复合材料的制备及对Pb(Ⅱ)的吸附探究
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作者 尚路得 潘远凤 《化工技术与开发》 CAS 2024年第9期1-7,共7页
本文以纯化后的蔗渣纤维素(SBC)和不溶性腐植酸(IHA)为基材,通过添加海泡石(SEP)来提升复合材料的热学性能,以碳酸钙为制孔剂,使用3-氨丙基三乙氧基硅烷(APTES)和戊二酸酐对复合微球进行改性,引入羧基基团,成功制备了一种新型吸附材料SI... 本文以纯化后的蔗渣纤维素(SBC)和不溶性腐植酸(IHA)为基材,通过添加海泡石(SEP)来提升复合材料的热学性能,以碳酸钙为制孔剂,使用3-氨丙基三乙氧基硅烷(APTES)和戊二酸酐对复合微球进行改性,引入羧基基团,成功制备了一种新型吸附材料SIS-COOH,并将其用于水体中Pb(Ⅱ)的去除。通过SEM、BET、FTIR、TGA等手段对SIS-COOH进行了表征,探究了其形貌和结构特性。采用静态吸附法,系统研究了影响SIS-COOH吸附性能的因素,包括溶液的pH值、SIS-COOH的投放量、Pb(Ⅱ)的初始浓度以及温度等。实验结果表明,在pH=5、SIS-COOH投放量为5g·L^(-1)、Pb(Ⅱ)的初始浓度为1500mg·L^(-1)的条件下,SIS-COOH的吸附容量达到最佳,且吸附过程在120min内即可达到平衡状态。再生实验证实,SIS-COOH具有出色的再生性能,经历5次循环实验后,其吸附容量仍维持在90%以上。 展开更多
关键词 纤维素 腐植酸 海泡石 APTES Pb()离子吸附
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氮掺杂多孔污泥炭活化过二硫酸盐降解橙黄Ⅱ
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作者 李文奇 罗才贵 +1 位作者 熊瑜婷 罗仙平 《工业水处理》 CAS CSCD 北大核心 2024年第3期133-141,共9页
以市政污泥为碳源、碳酸氢钾为活化剂、尿素为氮源,制备了氮掺杂多孔污泥生物炭(NKBC),并采用N2吸附-脱附实验、SEM、XRD、XPS对其比表面积、表面特征进行了系列表征与分析,结果表明,NKBC具有较大的比表面积,由于N负载于NKBC孔道内,其... 以市政污泥为碳源、碳酸氢钾为活化剂、尿素为氮源,制备了氮掺杂多孔污泥生物炭(NKBC),并采用N2吸附-脱附实验、SEM、XRD、XPS对其比表面积、表面特征进行了系列表征与分析,结果表明,NKBC具有较大的比表面积,由于N负载于NKBC孔道内,其表面褶皱、缺陷较多,活化位点较多。将NKBC用于活化过二硫酸盐(PDS)降解橙黄Ⅱ,考察NKBC/PDS体系降解橙黄Ⅱ的性能,结果表明,在加入PDS 20 min后,NKBC/PDS体系对橙黄Ⅱ的降解率高达99.7%;该体系可在较宽pH范围(3~11)及常见阴离子存在条件下发挥作用。自由基猝灭实验和EPR光谱结果表明,NKBC/PDS体系降解橙黄Ⅱ的主要活性物种有·OH、SO_(4)^(·-)和^(1)O_(2),且以^(1)O_(2)为主。该研究所构建的NKBC/PDS体系可应用于染料废水的处理,实现“以废治废”的目标。 展开更多
关键词 氮掺杂 污泥生物炭 过二硫酸盐 橙黄
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基于4-羟基间苯二甲酸和含氮杂环配体的Zn(Ⅱ)配合物的合成、晶体结构与荧光性质研究
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作者 李波 王霏宇 +2 位作者 沈红 毛逢银 李勇辉 《人工晶体学报》 CAS 北大核心 2024年第4期692-700,共9页
在水热法条件下,4-羟基间苯二甲酸(H 2HPHA)和锌离子分别与1,2二(吡啶-4-基)乙烯(dpee)及4,4′-联吡啶(4,4′-bpy)反应得到了2个三维的配位聚合物[Zn(HPHA)(dpee)·(DMA)2]n(配合物1)和[Zn(HPHA)2(4,4′-bpy)2·DMA]n(配合物2)... 在水热法条件下,4-羟基间苯二甲酸(H 2HPHA)和锌离子分别与1,2二(吡啶-4-基)乙烯(dpee)及4,4′-联吡啶(4,4′-bpy)反应得到了2个三维的配位聚合物[Zn(HPHA)(dpee)·(DMA)2]n(配合物1)和[Zn(HPHA)2(4,4′-bpy)2·DMA]n(配合物2)。用X射线单晶衍射测定了配合物的晶体结构,结果显示:配合物1属于单斜晶系,C2空间群,每个不对称单元由一个锌离子,一个4-羟基间苯二甲酸配体及一个1,2-二(吡啶-4-基)乙烯组成;配合物2属于单斜晶系,P12/c1空间群,每个不对称单元由两个锌离子,两个4-羟基间苯二甲酸配体及两个4,4′-联吡啶配体组成。荧光光谱分析结果表明:配合物1的最强激发峰和发射峰在分别在251和397 nm,配合物2的最强激发峰和发射峰分别在415和513 nm。热重分析表明两个配合物在室温下稳定。 展开更多
关键词 锌配合物 4-羟基间苯二甲酸 1 2-二(吡啶-4-基)乙烯 4 4′-联吡啶 水热法 晶体结构 荧光光谱
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Synthesis of the Prospective Anticancer Molecule Perillic Acid from Orange Essential Oil by the Yeast <i>Yarrowia lipolytica</i>
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作者 Marcelo R. R. Tappin Felipe M. Knopp +5 位作者 Igor C. Cardoso Roberta T. Santos Bruna S. Drummond Antonio C. Siani Elba P. S. Bon Maria Antonieta Ferrara 《Green and Sustainable Chemistry》 2017年第2期172-184,共13页
The bioconversion of the hydrophobic and volatile limonene to perillic acid, a potential anticancer agent, by the yeast Yarrowia lipolytica was studied in two steps. Firstly, experimental design was used for process o... The bioconversion of the hydrophobic and volatile limonene to perillic acid, a potential anticancer agent, by the yeast Yarrowia lipolytica was studied in two steps. Firstly, experimental design was used for process optimization using high-purity limonene as substrate and secondly orange essential oil containing 89.1% limonene was used as substrate under the previously optimized conditions. Limonene concentration and pH were identified by fractional factorial design as significant factors and were optimized by central composite design. Under optimized process conditions (0.16% (v/v) limonene;pH 6.9), the 24 h biotransformation process resulted in the accumulation of 0.368 g·L-1 of perillic acid corresponding to a molar yield of 23.1%. A subsequent substrate addition under the same reaction conditions doubled perillic acid concentration to 0.793 g·L-1 and a molar yield of 24.2%. The use of orange essential oil under the optimized reaction conditions increased both perillic acid accumulation and yield to 0.872 g·L-1 and 29.7%, respectively. The robustness of Y. lipolytica allowed the efficient biotransformation of a crude by-product of the citrus industry into a valuable fine chemical. 展开更多
关键词 YARROWIA lipolytica Bioconversion Perillic acid LIMONENE orange Essential Oil
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高效液相色谱法测定肉制品中酸性橙Ⅱ的含量探究
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作者 刘晓楠 《现代食品》 2024年第8期163-165,共3页
通过高效液相色谱法对肉制品当中的酸性橙Ⅱ含量进行测量,流动相设定为甲醇-乙酸铵溶液,紫外波长调整为484 nm。检测结果表明,当浓度范围为0.5~10μg·mL^(-1)之间时,线性关系良好(r=0.9996),检出限和定量限分别为0.01 mg·kg^(... 通过高效液相色谱法对肉制品当中的酸性橙Ⅱ含量进行测量,流动相设定为甲醇-乙酸铵溶液,紫外波长调整为484 nm。检测结果表明,当浓度范围为0.5~10μg·mL^(-1)之间时,线性关系良好(r=0.9996),检出限和定量限分别为0.01 mg·kg^(-1)和0.05 mg·kg^(-1),加标回收率超过95%,标准差未超过5%,可对肉制品当中的酸性橙II含量进行快速的检测,且检测准确性较高,有较高应用价值。 展开更多
关键词 高效液相色谱 肉制品 酸性橙 萃取
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钙(Ⅱ)和铜(Ⅱ)吡嗪-2-甲酸配合物的合成、结构和性能研究
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作者 陈美娟 郭铭成 +1 位作者 谷长生 郝晓敏 《化学研究与应用》 CAS 北大核心 2024年第8期1851-1860,共10页
配体吡嗪-2-甲酸将其与CaCl_(2)和CuSO_(4)·5H_(2)O在水溶液中反应得到了两个新的单核钙和铜配合物。并通过X-射线单晶衍射、红外和元素分析表征了其晶体结构。配合物1为一个Ca(Ⅱ)离子与二个配体和四个配位水分子形成的单核结构,... 配体吡嗪-2-甲酸将其与CaCl_(2)和CuSO_(4)·5H_(2)O在水溶液中反应得到了两个新的单核钙和铜配合物。并通过X-射线单晶衍射、红外和元素分析表征了其晶体结构。配合物1为一个Ca(Ⅱ)离子与二个配体和四个配位水分子形成的单核结构,配合物2为一个Cu(Ⅱ)离子与一个配体和一个配位水分子形成的单核结构,单核结构之间通过O—H…H、N—H…H氢键作用组装成三维超分子网络结构。测试了配合物的紫外可见光和荧光吸收及配合物2非均相类Fenton试剂的催化性质。测试结果表明,两个配合物在不同溶剂中紫外可见吸收峰均在268 nm,配合物1固态荧光发射峰在414 nm和441 nm及配合物1和2在不同溶剂中荧光发射峰均为364 nm。含Cu(Ⅱ)的配合物2对甲基橙(MO)溶液可以达到81.76%的降解率,显示了良好的类Fenton催化性质,表明其是一种潜在的催化降解有机污染物材料。 展开更多
关键词 Ca()配合物 Cu()配合物 吡嗪羧酸 催化降解
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Adsorption of acid orange 7 from aqueous solutions by bottom ash
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作者 QU Yan-zhi SUN Wei-ling YE Zheng-fang YU Qing NI Jin-ren 《Journal of Environmental Science and Engineering》 2008年第10期1-13,共13页
Bottom ash. a power plant waste, was used to adsorb acid orange 7. The adsorption of acid orange 7 in aqueous solutions onto bottom ash was studied as functions of particle size. dosage, initial concentration and agit... Bottom ash. a power plant waste, was used to adsorb acid orange 7. The adsorption of acid orange 7 in aqueous solutions onto bottom ash was studied as functions of particle size. dosage, initial concentration and agitation time by batch experiments. Under conditions of bottom ash dosage of 1.5 g/50 ml and 5 g/50 ml for 〈0.074 mm and 0.074 mm-0.2 mm of bottom ash, respectively, it could achieve 99.1% and 87.6% dye removal efficiency. The adsorption isotherms for the bottom ash could be well described by both Freundlich and Langmuir isotherms. The calculated dye adsorption capacities of bottom ash for the particle size of 0.074 mm -0.2 mm and 〈0.074 mm were 2.78 mg/g and 10.21 mg/g, respectively. The results indicated that the dye uptake process fitted to the pseudo-first-order kinetic model better than the pseudo-second-order. The data were also fitted to intraparticle diffusion model by two adsorption stages, due to the difference in rate of mass transfer in the initial and final stages of adsorption. Significant variations were observed in the FTIR spectra and Stem photographs of bottom ash after adsorption. The column parameters were calculated by breakthrough curves at different flow rates and bed depths. 展开更多
关键词 ADSORPTION bottom ash acid orange 7 asotherm kinctics column operation
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铝镁混悬液(Ⅱ)在酸相关性疾病中的应用
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作者 张德新 张延祯 +1 位作者 熊哲锟 魏明通 《智慧健康》 2024年第8期80-83,共4页
目的探究铝镁混悬液(Ⅱ)在酸相关性疾病中的应用现状分析。方法选取2022年4月—2023年4月本院收治的酸相关性疾病患者202例临床资料开展回顾性分析。分析患者基本人口学特征、生命体征、既往史、主要临床症状及诊断、疗效结果分析、治... 目的探究铝镁混悬液(Ⅱ)在酸相关性疾病中的应用现状分析。方法选取2022年4月—2023年4月本院收治的酸相关性疾病患者202例临床资料开展回顾性分析。分析患者基本人口学特征、生命体征、既往史、主要临床症状及诊断、疗效结果分析、治疗期间不良反应发生情况,为优化诊疗方案寻求循证医学支持。结果抗酸药记录表1填写者202例,其中铝镁混悬液(Ⅱ)为抗酸药物使用最常见药物。使用铝镁混悬液(Ⅱ)治疗的130例患者中男性76例,女性54例;年龄阶段以23~55岁居多;收缩压平均值106~120mmHg居多;舒张压平均值66~80mmHg居多;体重平均值51~70kg居多;心率平均值76~90次/分居多;既往疾病史中发生率最高的为高血压;个人史中发生率最高为饮酒史;既往治疗用药最常见为奥美拉唑。常出现的几种症状发生率依次为反酸、烧心、腹痛、嗳气、黑便;而临床诊断统计中显示主要为慢性胃炎。铝镁混悬液(Ⅱ)治疗130例患者的总体疗效有效率为95.89%。药物不良反应者1例,具体为大便黏稠和胃肠道不适。结论铝镁混悬液(Ⅱ)在酸相关性疾病中临床应用较为普遍,使用群体较为广泛,临床治疗疗效较好,且安全性较好。 展开更多
关键词 酸相关性疾病 症状 治疗 铝镁混悬液() 应用现状
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钴/抗坏血酸/过氧化氢体系降解酸性橙Ⅱ
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作者 张柳 周雨芹 《山东化工》 CAS 2024年第16期264-267,共4页
应用钴/抗坏血酸/过氧化氢体系生成的羟基自由基降解酸性橙Ⅱ染料,考察不同降解条件(降解时间、降解温度、料液用量)对酸性橙Ⅱ的降解效果。结果表明单独组分降解对比实验效果均不明显;在混合体系中通过单因素实验得出在降解时间为30 mi... 应用钴/抗坏血酸/过氧化氢体系生成的羟基自由基降解酸性橙Ⅱ染料,考察不同降解条件(降解时间、降解温度、料液用量)对酸性橙Ⅱ的降解效果。结果表明单独组分降解对比实验效果均不明显;在混合体系中通过单因素实验得出在降解时间为30 min、抗坏血酸为0.075 mol、过氧化氢为0.063 mol、硝酸钴为0.18 mmol、降解温度为50℃时为最佳降解条件,降解率可达到91.25%。 展开更多
关键词 酸性橙 羟基自由基 抗坏血酸 过氧化氢
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柱前衍生化法测定复方氨基酸注射液(18AA-Ⅱ)中氨基酸的含量
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作者 尧爱珉 葛晓莹 申兰慧 《实验室检测》 2024年第4期1-6,共6页
目的建立复方氨基酸注射液(18AA-Ⅱ)的柱前衍生化含量分析方法。方法以邻苯二甲醛联合9-芴甲基氯甲酸酯(OPA-FMOC)进行在线衍生,采用Zorbax Eclipse-AAA柱,以40 mmol/L NaH_(2)PO_(4)溶液(pH7.8)为流动相A,乙腈-甲醇-水(45:45:10)为流动... 目的建立复方氨基酸注射液(18AA-Ⅱ)的柱前衍生化含量分析方法。方法以邻苯二甲醛联合9-芴甲基氯甲酸酯(OPA-FMOC)进行在线衍生,采用Zorbax Eclipse-AAA柱,以40 mmol/L NaH_(2)PO_(4)溶液(pH7.8)为流动相A,乙腈-甲醇-水(45:45:10)为流动相B,梯度洗脱,检测波长338、262 nm,柱温40℃。结果各氨基酸之间分离度良好,线性相关系数均不小于0.9994,平均回收率99%~103%,重复性RSD均小于2%。结论该法稳定、准确、高效,可为复方氨基酸注射液的含量测定和质量评估提供参考,并首次报道了OPA-FMOC衍生分析法中赖氨酸峰面积重复性不佳的优化方法。 展开更多
关键词 氨基酸 含量测定 柱前衍生 邻苯二甲醛 9-芴甲基氯甲酸酯 复方氨基酸注射液(18AA-)
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