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Electrosynthesis of hydroxylamine from earth-abundant small molecules
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作者 Wen-Bo Wei Qi-Long Zhu 《Chinese Journal of Structural Chemistry》 2025年第1期5-7,共3页
With the rapid evolution of contemporary society,there is an increasing demand for the production of bulk chemicals such as fertilizers,fuels,and pharmaceuticals.However,current synthetic approaches for these bulk che... With the rapid evolution of contemporary society,there is an increasing demand for the production of bulk chemicals such as fertilizers,fuels,and pharmaceuticals.However,current synthetic approaches for these bulk chemicals predominantly depend on conventional fossil fuel-based chemical refining processes.This dependence poses a substantial challenge to both environmental sustainability and energy resources[1].An example of this issue is the synthesis of hydroxylamine(NH2OH). 展开更多
关键词 earth abundant small molecules ELECTROSYNTHESIS synthesis hydroxylamine nh oh synthetic approaches energy resources hydroxylamine environmental sustainability bulk chemicals
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Effects of Hydroxylamine Sulfate and Sodium Nitrite on Microstructure and Friction Behavior of Zinc Phosphating Coating on High Carbon Steel 被引量:1
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作者 许育东 齐三 +5 位作者 王雷 石敏 丁宁 庞志成 汪泉 彭旭东 《Chinese Journal of Chemical Physics》 SCIE CAS CSCD 2015年第2期197-202,I0002,共7页
Hydroxylamine sulfate (HAS) and sodium nitrite are used as the accelerators for zinc phos- phate coating on high carbon steel. Phase evolution of phosphate coating was investigated by X-ray diffraction. It is found ... Hydroxylamine sulfate (HAS) and sodium nitrite are used as the accelerators for zinc phos- phate coating on high carbon steel. Phase evolution of phosphate coating was investigated by X-ray diffraction. It is found that the phosphating coatings are mainly composed of hopeite Zn3Fe(PO4)2.4H2O and phosphophyllite Zn2Fe(PO4)2.4H2O. The microstructural changes of the phosphate coating, as a function of phosphating time, were evaluated by scanning elec- tron microscopy. Four-ball friction experiments reveal that hydroxylamine sulfate instead of sodium nitrite can effectively reduce the friction coefficient of lubricated phosphating coat- ing. Therefore, it may be expected that HAS will be widely used as a fast and ECO-friendly accelerator in phosphate industry. 展开更多
关键词 hydroxylamine sulfate ACCELERATOR Phosphate coating FRICTION
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铵锌镉-盐酸羟胺转化法测试硝酸盐氮同位素方法研究及应用
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作者 陈培宇 杨海丽 尹希杰 《应用海洋学学报》 北大核心 2026年第1期107-113,共7页
研究氮的地球化学行为对于理解和预测生态系统的结构与功能具有重要意义。硝酸盐作为氮的重要形式之一,准确识别和追踪其来源及其转化过程,有助于深入认识区域氮循环动态。传统的硝酸盐氮(NO_(3)^(-)-N)同位素分析样品前处理方法,如铵... 研究氮的地球化学行为对于理解和预测生态系统的结构与功能具有重要意义。硝酸盐作为氮的重要形式之一,准确识别和追踪其来源及其转化过程,有助于深入认识区域氮循环动态。传统的硝酸盐氮(NO_(3)^(-)-N)同位素分析样品前处理方法,如铵蒸馏法、氨扩散法、离子交换法等存在样品需求量大、前处理要求高、适用性受限等问题。本研究利用锌镉将硝酸盐还原为亚硝酸盐,盐酸羟胺(NH_(2)OH·HCl)进一步还原为N_(2)O,并测试其氮同位素组成。通过对硝酸盐标准样品氮同位素进行测试,确定了该方法的实验条件、转化率、精密度和准确度等关键指标,并建立不同丰度氮同位素的校准曲线。实验结果表明,当NH_(2)OH与NO_(3)^(-)的比例达到4∶1以上,且反应温度在37~42℃时,硝酸盐转化率均超过90%。经过空白校正后不同浓度硝酸盐的氮同位素测定值标准偏差为0.21‰。5种丰度的硝酸盐氮同位素标样扣除空白后校准曲线的斜率为0.481,相关系数为0.999,显示出良好的相关性,表明转化过程中基本没有氮同位素分馏。通过对自来水、河水和海水中硝酸盐氮同位素测试结果显示,标准偏差分别为0.49‰、0.45‰和0.56‰(n=5)。该方法中利用盐酸羟胺替代剧毒且易爆的叠氮化钠试剂,具有更高的环境友好性,同时在方法的精密度和准确度方面表现优异,能够满足不同类型环境水样中硝酸盐氮同位素分析的测试要求。 展开更多
关键词 铵锌镉 盐酸羟胺 氮同位素 硝酸盐 前处理方法
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Promoting effect of ethanol on the synthesis of N-(2-methylphenyl)-hydroxylamine from o-nitrotoluene in Zn/H_2O/CO_2 system 被引量:7
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作者 Shi Juan Liu Yan Hua Wang +1 位作者 Yuan Ping Hao Jing Yang Jiang 《Chinese Chemical Letters》 SCIE CAS CSCD 2011年第2期221-224,共4页
The promoting effect of ethanol on the synthesis of N-(2-methylphenyl)hydroxylamine from o-nitrotoluene in Zn/H2O/CO2 system was observed.By adding appropriate amount of ethanol,the selectivity of N-(2-methylphenyl... The promoting effect of ethanol on the synthesis of N-(2-methylphenyl)hydroxylamine from o-nitrotoluene in Zn/H2O/CO2 system was observed.By adding appropriate amount of ethanol,the selectivity of N-(2-methylphenyl)hydroxylamine increased from 71%to 90%when the reduction was carried out at 25℃under normal pressure of CO2. 展开更多
关键词 O-NITROTOLUENE N-(2-Methylphenyl)hydroxylamine Reduction ZN CO2/H2O
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Purification and Characterization of a Low-temperature Hydroxylamine Oxidase from Heterotrophic Nitrifier Acinetobacter sp.Y16 被引量:6
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作者 ZHANG Shu Mei LI Wei Guang +3 位作者 ZHANG Duo Ying HUANG Xiao Fei QIN Wen SHA Chang Qing 《Biomedical and Environmental Sciences》 SCIE CAS CSCD 2014年第7期515-522,共8页
Objective To purify a low-temperature hydroxylamine oxidase (HAO) from a heterotrophic nitrifying bacterium Acinetobacter sp. Y26 and investigate the enzyme property. Methods A HAO was purified by an anion-exchange ... Objective To purify a low-temperature hydroxylamine oxidase (HAO) from a heterotrophic nitrifying bacterium Acinetobacter sp. Y26 and investigate the enzyme property. Methods A HAO was purified by an anion-exchange and gel-filtration chromatography from strain Y16. The purity and molecular mass were determined by RP-HPLC and SDS-PAGE. The HAO activity was detected by monitoring the reduction of potassium ferricyanide using hydroxylamine as substrate and ferricyanide as electron acceptor. The partial amino acid sequence was determined by mass spectrometry. Results The low-temperature HAO with a molecular mass of 61 kDa was purified from strain Y26 by an anion-exchange and gel-filtration chromatography. The enzyme exhibited an ability to oxidize hydroxylamine in wide temperature range (4-40 ℃) in vitro using hydroxylamine as substrate and ferricyanide as electron acceptor. It was stable in the temperature range of 4 to 25 ℃ and pH range of 6.0 to 8.5 with less than 30% change in its activity. The optimal temperature and pH were 15 ℃ and 7.5, respectively. Three peptides were determined by mass spectrometry which were shown to be not identical to other reported HAOs. Conclusion This is the first study to purify a low-temperature HAO from a heterotrophic nitrifier Acinetobecter sp. It differs from other reported HAOs in molecular mass and enzyme properties. The findings of the present study have suggested that the strain Y26 passes through a hydroxylamine-oxidizing process catalyzed by a low-temperature HAO for ammonium removal. 展开更多
关键词 hydroxylamine oxidase PURIFICATION Heterotrophic nitrifier Acinetobacter sp Y16
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New Di-(p-hydroxybenzyl) A Hydroxylamine from Gastrodia eleta Bl 被引量:6
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作者 Xiao Yan HAO Ning Hua TAN Jun ZHOU(Department of Medicinal Chemistry Guiyang Medical Guiyan Guizhou 530004 Laboratory of Phytochemistry Kuming Institute of Botany Chinese Aademy of Sciences.Heilongtan Kunming.Yunnan 650204) 《Chinese Chemical Letters》 SCIE CAS CSCD 1999年第6期467-468,共2页
It is the first reported that a new nitrogen-containing non-amino acid type organiccomponent 1 isolated from one of the well known traditional chinese herb medicines. Gastrodiaelela BI. Structure elucidation and unamb... It is the first reported that a new nitrogen-containing non-amino acid type organiccomponent 1 isolated from one of the well known traditional chinese herb medicines. Gastrodiaelela BI. Structure elucidation and unambiguous NMR assignments for the title compound werecarried out mainly Oil the basis of' 1D and 2D NMR experiments. 展开更多
关键词 Gastrodia eleta Bl di-(p-hydroxybenzzy ) hydroxylamine ID NMR 2D NMR
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Amplification effects of magnetic field on hydroxylamine-promoted ZVI/H_(2)O_(2) near-neutral Fenton like system 被引量:3
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作者 Wei Xiang Mingjie Huang +3 位作者 Xiaohui Wu Fugang Zhang Dan Li Tao Zhou 《Chinese Chemical Letters》 SCIE CAS CSCD 2022年第3期1275-1278,共4页
This study has demonstrated an interesting amplification effect of magnetic field (MF) on the hydroxylamine (HA)-promoted zero valent iron (ZVI)/H_(2)O_(2) Fenton-like system. Sulfamethoxazole (SMX) could be efficient... This study has demonstrated an interesting amplification effect of magnetic field (MF) on the hydroxylamine (HA)-promoted zero valent iron (ZVI)/H_(2)O_(2) Fenton-like system. Sulfamethoxazole (SMX) could be efficiently degraded at near neutral pH. Conditional parameters affecting the SMX degradation in the ZVI/H_(2)O_(2)/HA/MF system, e.g., pH and the dosages of ZVI, HA and H_(2)O_(2), were investigated. Unlike the acid-favorable ZVI/H_(2)O_(2) and ZVI/H_(2)O_(2)/HA systems, the MF-assisted system exhibited good performances even at pH up to 6.0 and highest degradation rate at pH of 5.0. ^(·)OH was still identified as the responsible oxidant. A mechanism involving the MF-enhanced heterogeneous-homogeneous iron cycle was proposed in the near-neutral ZVI/H_(2)O_(2)/HA system. Without MF, HA-induced reductive dissolution of the surface iron oxides occurred and thus leaded to homogeneous Fenton reactions. After the introduction of MF, the gradient magnetic field formed on the ZVI particles would induce the generation of concentration cells of Fe(II) and local corrosion of iron. Large amounts of aqueous and bounded Fe(II) catalyzed H_(2)O_(2) to efficiently produce ^(·)OH, while HA maintained the surface and bulk cycles of Fe(II)/Fe(III). The result of study is expected to provide a green, energy-free method in improving the effectiveness of ZVI-based Fenton-like technologies at weak-acidic circumstances. 展开更多
关键词 Fenton like Zero valent iron hydroxylamine Magnetic field
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Enhancement of Fenton oxidation for removing organic matter from hypersaline solution by accelerating ferric system with hydroxylamine hydrochloride and benzoquinone 被引量:12
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作者 Siwei Peng Weijun Zhang +3 位作者 Jie He Xiaofang Yang Dongsheng Wang Guisheng Zeng 《Journal of Environmental Sciences》 SCIE EI CAS CSCD 2016年第3期16-23,共8页
Fenton oxidation is generally inhibited in the presence of a high concentration of chloride ions.This study investigated the feasibility of using benzoquinone(BQ) and hydroxylamine hydrochloride(HA) as Fenton enha... Fenton oxidation is generally inhibited in the presence of a high concentration of chloride ions.This study investigated the feasibility of using benzoquinone(BQ) and hydroxylamine hydrochloride(HA) as Fenton enhancers for the removal of glycerin from saline water under ambient temperature by accelerating the ferric system.It was found that organics removal was not obviously affected by chloride ions of low concentration(less than 0.1 mol/L),while the mineralization rate was strongly inhibited in the presence of a large amount of chloride ions.In addition,ferric hydrolysis-precipitation was significantly alleviated in the presence of HA and BQ,and HA was more effective in reducing ferric ions into ferrous ions than HA,while the H_2O_2 decomposition rate was higher in the BQ-Fenton system.Electron spin resonance analysis revealed that OH production was reduced in high salinity conditions,while it was enhanced after the addition of HA and BQ(especially HA).This study provided a possible solution to control and alleviate the inhibitory effect of chloride ions on the Fenton process for organics removal. 展开更多
关键词 Saline solution Fenton oxidation Hydroxyl radicals Benzoquinone hydroxylamine hydrochloride
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Synthesis and kinetics of 2,5-dicyanofuran in the presence of hydroxylamine ionic liquid salts 被引量:2
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作者 Xuan Gao Zhihui Li +2 位作者 Dongsheng Zhang Xinqiang Zhao Yanji Wang 《Chinese Journal of Chemical Engineering》 SCIE EI CAS CSCD 2023年第1期310-316,共7页
2,5-Dicyanofuran(DCF)is an important biomass-derived platform compound primarily used to prepare bio-based adiponitrile,which is the key precursor for the synthesis of nylon 66 and 1,6-hexanediisocyanate(HDI).In this ... 2,5-Dicyanofuran(DCF)is an important biomass-derived platform compound primarily used to prepare bio-based adiponitrile,which is the key precursor for the synthesis of nylon 66 and 1,6-hexanediisocyanate(HDI).In this study,one-pot,green and safe synthesis of DCF from 2,5-diformylfuran(DFF)and hydroxylamine ionic liquid salts was proposed.Eco-friendly hydroxylamine ionic liquid salts were used as the nitrogen source.Ionic liquid exhibited three-fold function of cosolvent,catalysis and phase separation.The conversion of DFF and yield of DCF reached 100%under the following optimum reaction conditions:temperature of 120℃ for 70 min,volume ratio of paraxylene:[HSO_(3)-b-Py]HSO4 of 2:1,and molar ratio of DFF:(NH_(2)OH)_(2)[HSO_(3)-b-Py]HSO4 of 1:1.5.The reaction mechanism for the synthesis of DCF was proposed,and the kinetic model was established.The reaction order with respect to DFF and intermediate product 2,5-diformylfuran dioxime(DFFD)was 1.06 and 0.16,and the reaction activation energy was 64.07 kJ·mol^(-1) and 59.37 kJ·mol^(-1) respectively.After the reaction,the ionic liquid was easy to separate,recover and recycle. 展开更多
关键词 2 5-Dicyanofuran hydroxylamine ionic liquid salts Green synthesis KINETICS
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Chemiluminescence Sensor for the Determination of Hydroxylamine by Electrostatically Immobilizing Luminol and Periodate 被引量:1
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作者 ZHANG Si chun ZHOU Guo jun JU Huang xian 《Chemical Research in Chinese Universities》 SCIE CAS CSCD 2003年第2期155-159,共5页
A novel chemiluminescence(CL) sensor, which can be used for hydroxylamine determination in combination with flow injection analysis, was developed by electrostatically immobilizing luminol and periodate on anion exch... A novel chemiluminescence(CL) sensor, which can be used for hydroxylamine determination in combination with flow injection analysis, was developed by electrostatically immobilizing luminol and periodate on anion exchange resin respectively. Hydroxylamine was sensed by its enhancing effect on the weak CL reaction between luminol and periodate, which were eluted from the ion exchange column. The response of the sensor to hydroxylamine was linear in the concentration range of 8.0×10^(-8)-2.0×10^(-6)mol/L with a detection limit of 4.0×10^(-8)mol/L hydroxylamine(3σ).The relative standard deviation(RSD) was 2.0% for 9 repetitive determinations at a hydroxylamine concentration of 5.0×10^(-7) mol/L. The sensor could be reused for over 400 times with a good reproducibility and was used to determine hydroxylamine in wastewater. 展开更多
关键词 Chemical sensor CHEMILUMINESCENCE LUMINOL PERIODATE hydroxylamine
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Feasibility of low-intensity ultrasound treatment with hydroxylamine to accelerate the initiation of partial nitrification and allow operation under intermittent aeration
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作者 Jianxiong Jian Xiaojian Liao +7 位作者 Zhihua Mo Shoupeng Li Lei Li Shaojin Chen Zhenhua Huang Junhao Chen Wencan Dai Shuiyu Sun 《Journal of Environmental Sciences》 SCIE EI CAS CSCD 2024年第5期446-459,共14页
Partial nitrification is a key aspect of efficient nitrogen removal,although practically it suf-fers from long start-up cycles and unstable long-term operational performance.To address these drawbacks,this study inves... Partial nitrification is a key aspect of efficient nitrogen removal,although practically it suf-fers from long start-up cycles and unstable long-term operational performance.To address these drawbacks,this study investigated the effect of low intensity ultrasound treatment combined with hydroxylamine(NH2OH)on the performance of partial nitrification.Results showthat compared with the control group,low-intensity ultrasound treatment(0.10W/mL,15 min)combined with NH2OH(5 mg/L)reduced the time required for partial nitrification initiation by 6 days,increasing the nitrite accumulation rate(NAR)and ammonia nitro-gen removal rate(NRR)by 20.4% and 6.7%,respectively,achieving 96.48% NRR.Mechanis-tic analysis showed that NH2OH enhanced ammonia oxidation,inhibited nitrite-oxidizing bacteria(NOB)activity and shortened the time required for partial nitrification initiation.Furthermore,ultrasonication combined with NH2OH dosing stimulated EPS(extracellular polymeric substances)secretion,increased carbonyl,hydroxyl and amine functional group abundances and enhanced mass transfer.In addition,16S rRNA gene sequencing results showed that ultrasonication-sensitive Nitrospira disappeared from the ultrasound+NH_(2)OH system,while Nitrosomonas gradually became the dominant group.Collectively,the results of this study provide valuable insight into the enhancement of partial nitrification start-up during the process of wastewater nitrogen removal. 展开更多
关键词 Partial nitrification Low-intensity ultrasound hydroxylamine Ammonia oxidizing bacteria Nitrite oxidizing bacteria
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Studies on the Reaction of Vinyl Triazole Derivatives with Hydroxylamine
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作者 Gui Yu JIN Guo Feng ZHAO +2 位作者 Zhong Fa LIU Jin REN Yu Chang LI (Institute of Elemento-Organic Chemistry, National Key Laboratory of Elemento-Organic Chemistry.Nankai University, Tianjin 30007) 《Chinese Chemical Letters》 SCIE CAS CSCD 1997年第6期467-470,共4页
In this paper the reaction of vinyl triazole derivatives with hydroxylamine hydrochloride under the action of sodium carbonate was studied. The result indicated that cyclization took place and new heterocyclic compoun... In this paper the reaction of vinyl triazole derivatives with hydroxylamine hydrochloride under the action of sodium carbonate was studied. The result indicated that cyclization took place and new heterocyclic compounds of 1,2-oxazocyclopentanes were obtained. 展开更多
关键词 PPM OH NH Studies on the Reaction of Vinyl Triazole Derivatives with hydroxylamine Ph IR
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Study on the Inert Coordination Compound in the System of“Molybdenum(Ⅵ)—TAE—Hydroxylamine”and its Analytical Application
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作者 Chen Huaxu Shao Guangdi Department of Chemistry,University of Science and Technology BeijingBai Linshan Department of Chemical Engineering,East China Institute of Metallurgy 《Rare Metals》 SCIE EI CAS CSCD 1989年第2期58-63,共6页
In the presence of ethyl alcohol or emulsifier OP,molybdenum(Ⅵ) forms 1∶1∶1'water soluble colored coordination com- pound with both of 2-(2-thiazolylazo)-5-diethylaminophenol (abbreviation TAE) and hydroxylamin... In the presence of ethyl alcohol or emulsifier OP,molybdenum(Ⅵ) forms 1∶1∶1'water soluble colored coordination com- pound with both of 2-(2-thiazolylazo)-5-diethylaminophenol (abbreviation TAE) and hydroxylamine.This deep blue coordination compound is inert characteristically and remains stable in 1.7 mol/L sulfuric acid,2.4 mol/L hydrochloric or ni- tric acid.It will not be decomposed by masking agents even on boiled,while in that case,almost all the colored coordination com- pounds formed by other metal ions will be decomposed completely.This inert character of the coordination compound of molybdenum(Ⅵ) and its utilization in improving the analytical selectivity have been discussed.In the coexistence of various for- eign ions,especially in the presence of a great quantity of tungsten,which always interferes with the determination of molybdenum,the direct determination of molybdenum in the aqueous solution by applying this system has shown an acceptable sensitivity and reproducibility.From the results of determination in some synthetic and standard samples,it seems feasible to use this system in the determination of molybdenum in nonferrous alloys. 展开更多
关键词 and its Analytical Application Molybdenum hydroxylamine Study on the Inert Coordination Compound in the System of TAE
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Gaseous products of aqueous N,N-dimethyl hydroxylamine degraded by radiation
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作者 WANG Jinhua LI Chun +5 位作者 WU Minghong XU Gang BAO Borong ZHENG Weifang HE Hui ZHANG Shengdong 《Nuclear Science and Techniques》 SCIE CAS CSCD 2010年第4期233-236,共4页
In this work,the 0.1-0.5 mol·L-1 N,N-dimethylhydroxylamine(DMHA) were irradiated to 5-25 kGy,and gaseous products of mainly hydrogen,methane,ethane and n-butane were measured by gas chromatography.The results sho... In this work,the 0.1-0.5 mol·L-1 N,N-dimethylhydroxylamine(DMHA) were irradiated to 5-25 kGy,and gaseous products of mainly hydrogen,methane,ethane and n-butane were measured by gas chromatography.The results show that the volume fraction of hydrogen and methane increases with the concentration of DMHA and dose,and the latter does not change markedly at high doses. 展开更多
关键词 二甲基 气态产物 辐射降解 羟胺 气相色谱法 丁烷气体 体积分数
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Qualitative and quantitative analysis of hydrogen and carbon monoxide produced by radiation degradation of N, N-dimethyl hydroxylamine
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作者 WANGJinhua BAOBorong +4 位作者 WUMinghong SUNXilian ZHANGXianye HUJingxin YEGuoan 《辐射研究与辐射工艺学报》 CAS CSCD 北大核心 2005年第2期110-110,共1页
关键词 辐射衰退 一氧化碳 气相色谱 二甲基羟胺
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Cl^(-)对HA/PMS体系降解废水中有机物的影响机制 被引量:2
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作者 董紫君 韩苗苗 +1 位作者 李微 姜成春 《中国给水排水》 北大核心 2025年第3期89-96,共8页
沿海地区广泛存在的Cl-会在自由基作用下生成氯活性物质,进而影响废水中难降解有机物的去除效果。为探究Cl^(-)对羟胺(HA)活化过硫酸盐(过一硫酸盐,PMS)高级氧化技术去除废水中难降解有机物的影响及产物生成规律,以苯酚为目标污染物,从... 沿海地区广泛存在的Cl-会在自由基作用下生成氯活性物质,进而影响废水中难降解有机物的去除效果。为探究Cl^(-)对羟胺(HA)活化过硫酸盐(过一硫酸盐,PMS)高级氧化技术去除废水中难降解有机物的影响及产物生成规律,以苯酚为目标污染物,从初始pH、Cl^(-)浓度、活性组分的鉴定以及反应过程中的毒性变化等角度展开研究。结果表明,pH为4时苯酚的降解速率最快,硝基酚和亚硝基酚分别在pH为6和4时产量最高,分别为4.96和13.84μmol/L,产率分别为24.84%和69.19%。低浓度Cl^(-)会对苯酚的降解产生轻微抑制作用,高浓度的Cl^(-)则会产生促进作用,硝基酚与亚硝基酚的生成量随Cl^(-)浓度的增加而升高。Cl^(-)存在时,HA/PMS体系中存在羟基自由基(·OH)、硫酸根自由基(SO_(4)^(·-))、氯活性物质(RCS)及氮活性物质(RNS),这些活性组分的存在对污染物的降解及其硝基与亚硝基产物的生成具有重要作用。费氏弧菌发光试验结果显示,体系中生成的物质整体具有较高的毒性,随着氧化过程的进行,HA/PMS体系会进一步降解废水中高毒性的产物。 展开更多
关键词 氯离子 羟胺 过硫酸盐 苯酚 高级氧化
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羟胺强化水合氧化铁/H_(2)O_(2)体系氧化降解污染物机理与效能
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作者 王凯 余华东 +3 位作者 王子钰 张志勤 吴礼光 李旭春 《水处理技术》 北大核心 2025年第7期85-89,104,共6页
芬顿工艺是工业废水预氧化与深度处理的重要方法,但是大量生成的芬顿污泥严重制约了其广泛使用。针对含铁芬顿污泥减量与资源化利用的技术挑战,本研究提出了羟胺(HA)强化的方法,以实现含铁污泥在多相芬顿氧化污染物中的资源化利用。以... 芬顿工艺是工业废水预氧化与深度处理的重要方法,但是大量生成的芬顿污泥严重制约了其广泛使用。针对含铁芬顿污泥减量与资源化利用的技术挑战,本研究提出了羟胺(HA)强化的方法,以实现含铁污泥在多相芬顿氧化污染物中的资源化利用。以新生态水合氧化铁(Fhy)为研究对象,研究了HA强化Fhy/H_(2)O_(2)氧化降解典型有机污染物的效能,考察了Fhy投加量、H_(2)O_(2)投加量、HA浓度、pH、温度等影响因素的作用规律,并揭示了其反应机理。结果表明,Fhy、HA和H_(2)O_(2)能显著促进污染物降解动力学;最佳pH为2.5~3;升高温度促进反应,且表观活化能约为50.1 kJ/mol;该方法可以利用实际芬顿污泥高效降解工业废水中的污染物。自由基淬灭实验、竞争反应动力学等表明,HA还原Fhy并释放部分Fe(II),通过均相芬顿与异相芬顿反应生成·OH及表面吸附态·OHads,从而高效氧化降解污染物。本研究结果为芬顿污泥的减量与资源化利用提供了方法参考。 展开更多
关键词 水合氧化铁 羟胺 高级氧化 污泥资源化
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电点火方式下HAN基推进剂点火及燃烧性能分析
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作者 金宝志 田国庆 +2 位作者 李国岫 李洪萌 鲍世国 《火箭推进》 北大核心 2025年第4期74-83,共10页
硝酸羟胺(hydroxylamine nitrate,HAN)基液体推进剂相比目前常用的肼类液体推进剂具有低毒性、高比冲等特点,在空天领域未来发展得到了广泛关注。目前HAN基液体推进剂常用点火方式是催化点火,催化点火依赖催化剂,需要长时间的预热,不能... 硝酸羟胺(hydroxylamine nitrate,HAN)基液体推进剂相比目前常用的肼类液体推进剂具有低毒性、高比冲等特点,在空天领域未来发展得到了广泛关注。目前HAN基液体推进剂常用点火方式是催化点火,催化点火依赖催化剂,需要长时间的预热,不能实现发动机的冷启动。电点火方法具有点火延迟低、响应快等优点,可以实现发动机的冷启动,有效弥补催化点火的不足。推进剂在喷入燃烧室前处于流动状态,为设计基于电点火方法的空间发动机,有必要先研究流动状态下HAN基液体推进剂电点火及燃烧性能。针对HAN基液体推进剂流动状态下电点火影响机制和燃烧性能开展研究。设计了HAN基液体推进剂流动状态下电点火实验系统。开展了不同初始电压、推进剂流速、推进剂种类下电点火研究。结果表明:推进剂在切断初始电压后能实现推进剂自维持燃烧。优化推进剂后燃烧更加剧烈,推进剂自分解主导了分解过程。推进剂的自分解是一个HNO_(3)作为中间体与另一个HNO_(3)反应,这加速了推进剂的分解速度。研究结论为电点火方式下HAN基液体推进剂空间发动机结构设计提供重要参考。 展开更多
关键词 硝酸羟胺基液体推进剂 电点火 自分解 燃烧性能
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HAN基电控凝胶推进剂的流变及点火燃烧特性
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作者 李春天 王之栋 +6 位作者 李濂 王志文 张千翼 刘海庆 方普懿行 沈瑞琪 张伟 《兵工学报》 北大核心 2025年第7期170-179,共10页
凝胶推进剂具有燃烧可控、易贮存和安全性好等优点,在空间微推进技术中具有良好的应用前景。为了有效改善凝胶推进剂管道运输效率和研究凝胶推进剂的点火和燃烧性能的影响因素,分别采用旋转流变仪和自主搭建的电化学燃烧诊断系统对硝酸... 凝胶推进剂具有燃烧可控、易贮存和安全性好等优点,在空间微推进技术中具有良好的应用前景。为了有效改善凝胶推进剂管道运输效率和研究凝胶推进剂的点火和燃烧性能的影响因素,分别采用旋转流变仪和自主搭建的电化学燃烧诊断系统对硝酸羟胺(Hydroxylamine Nitrate,HAN)基电控凝胶推进剂的流变特性、点火和燃烧特性进行了实验研究。结果表明:增加剪切力和提高环境温度,推进剂黏度显著降低;当凝胶推进剂受到的剪切作用较大时,其损耗模量会超过储能模量占据主导地位,推进剂开始由固体转变为流体;撤掉剪切力后,凝胶推进剂的黏度迅速升高,凸显固体特性;在本实验所采用的电极材料中,适合HAN基电控凝胶推进剂点火的电极材料为Mo电极,常温25℃下,当电压为250 V时其点火延迟低至0.3 s,体积燃速达到0.21 mL/s;另一方面,温度对凝胶推进剂的点火延迟有显著影响,在175 V电压下,随着温度的升高,其点火延迟时间从5.3 s降低至1.5 s,但是对凝胶推进剂的体积燃速无明显影响。结合热电偶测温技术,测得HAN基电控凝胶推进剂的稳定燃烧的火焰温度分布在1200~1400 K之间。 展开更多
关键词 电控凝胶推进剂 硝酸羟胺 流变特性 电点火 燃烧特性
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盐酸羟胺强化芬顿体系在近中性条件下去除2,4-DCP的性能及机理研究
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作者 廖兵 祝鑫宇 +3 位作者 黄倩倩 胥雯 寇梦瑶 郭娜 《化工学报》 北大核心 2025年第8期4273-4283,共11页
针对传统芬顿体系中低pH和低活性铁含量等问题,通过向Fenton体系加入碳酸氢盐,与H_(2)O_(2)反应生成HCO_(4)^(-),再经盐酸羟胺(HAH)还原提升活性铁含量,可实现近中性条件下对2,4-二氯苯酚(2,4-DCP)的高效降解。结果表明,HAH强化HCO_(3)^... 针对传统芬顿体系中低pH和低活性铁含量等问题,通过向Fenton体系加入碳酸氢盐,与H_(2)O_(2)反应生成HCO_(4)^(-),再经盐酸羟胺(HAH)还原提升活性铁含量,可实现近中性条件下对2,4-二氯苯酚(2,4-DCP)的高效降解。结果表明,HAH强化HCO_(3)^(-)改良Fenton体系在pH约为6.46的条件下,Fe^(2+)、NaHCO_(3)、H_(2)O_(2)与HAH的浓度分别为4、10、10和0.5 mmol·L^(-1)时,反应60 min后,2,4-DCP可被完全降解。高浓度的NO_(3)^(-)、Cl^(-)和共存有机质会对2,4-DCP的降解产生抑制作用。反应体系中HAH的引入促进了Fe^(2+)和Fe3+的循环,提高体系的催化能力,降低Fe^(2+)的用量。通过自由基淬灭实验和EPR检测验证了在反应过程中主要参与的自由基是HO·,^(1)O_(2)和O_(2)^(·-)的贡献很小。且毒性评估结果显示,在降解过程中产生的大多有机中间体的毒性相较于2,4-DCP明显降低。 展开更多
关键词 芬顿 碳酸氢盐 过氧化氢 盐酸羟胺 碳氢化合物 活化作用
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