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双语推荐:醇解

采用醇解法对废弃冰箱聚氨酯(Waste Polyurethane Foam,WPUF)进行回收处理,获得了可循环利用的再生混合多元。考察了不同原料、反应时间、反应温度对醇解效果的影响。通过对醇解产物的羟值、粘度和红外谱图分析得到最佳醇解条件为:采用乙二醇解剂,氢氧化钠为催化剂,固液比为100%WPUF、催化剂用量为1%WPUF,实验温度为197.85℃、反应时间为1 h条件下获得的混合多元最佳。
In this study, glycolysis was chosen to treat the waste polyurethane foam (WPUF) from waste refrigerators and regenerated WPUF mixed polyols which could be recycled. The influence of raw material type, reaction time, and the temperature on the glycolysis effect was investigated. The determination of hydroxyl value, the viscosity, and the characterization of infrared spectroscopic analysis suggested the optimum condition are as follows:the ethylene glycol is used as the glycolysis agent, and the sodium hydroxide as the catalyst, the solid-to-liquid ratio is 100%WPUF , the dosage of catalyst is 1%WPUF , the reaction temperature is 197.85℃, and the reaction time is 1 h.

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β–谷甾是食品和医学领域广泛使用,且是植物界最普遍存在的甾。用TG–DTG/DTA方法研究了两种含量分别为40%和80%的β–谷甾过程及热动力学。TG和DTG分析结果表明,该物质的失重过程分两步完成。第一步为结晶水脱出,第二步为甾和挥发性物质蒸发。热过程中,加热速率对两种植物甾有显著作用。使用Popescu分别计算出40%和80%β–谷甾的热活化能分别为111和132 kJ/mol。对常用41种热动力学机理函数,确定了两种植物甾过程均为三维扩散的反Jander方程(g(α)=[(1+α)^1/3–1]^2。
β–sitosterol is widely used in food and medicine,and is ubiquitous in plantage. Thermal decomposition and kinetics of 40%β–sitosterol and 80%β–sitosterol were studied by TG–DTG/DTA. The TG–DTG curve showed the process of mass loss of the substance proceeded in two steps. The first stage could be attributed to the expulsion of water of crystallization. The second stage was corresponding to the devolatilization and decomposition of the molecular structure. Heating rate had a significant effect on the pyrolysis of the two phytosterols. The activation energy E of the second stage of degradation process obtained by Popescu method were 111(for 40%β–sitosterol)and 132 kJ/mol (for 80%β–sitosterol). According to Popescu mechanism functions,the possible kinetic model was estimated to be Reverse Jander Equation(g(α)=[(1+α)1/3–1]2.

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乙二、1,2-/1,3-丙二等小分子二元在精细和有机化工、生物医药等领域应用广泛.与石化路径相比,以可再生的生物质多元(丙三、山梨/木糖)为原料选择性催化氢制取上述小分子二元具有过程简单、绿色高效等显著优势,已成为生物质催化转化的研究热点.本文综述了典型生物质多元山梨/木糖和丙三选择性催化氢为乙二、1,2-/1,3-丙二等小分子二元,重点阐述了丙三选择性氢制1,2-丙二、1,3-丙二和山梨/木糖选择性氢制小分子二元的催化剂体系和反应机理,并对该领域的发展前景作了展望,提出开发高效稳定的催化剂体系和工艺是未来的研究重点.
Selectively catalytic hydrogenolysis of biomass derived polyols (sorbitol,xylitol and glycerol) to small molecular diols (glycol and 1,2-/1,3-propanediols) has attracted more and more attention due to the wide application of these small molecular diols in fine and organic chemical, biology and pharmaceutical industries. Compared to the multi-stepped transformation of fossil based ethylene and propylene feedstocks,selective hydrogenolysis of biomass derived polyols to small molecular diols shows higher efficiency,simpler processing and more friendly to environment. This review is focused on the catalyst and reaction mechanism of selective hydrogenolysis of glycerol to 1,2-/1,3-propanediols and selective hydrogenolysis of sorbitol and xylitol to small molecular diols. The perspective of efficient catalyst and process for producing small molecular diols by hydrogenolysis of biomass derived polyols is discussed.

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研究戊唑与氟环唑的光特征,为其环境风险评估提供依据,采用室内模拟方法,比较了0 Lux(黑暗对照)、4000 Lux和8000 Lux光照处理的戊唑与氟环唑在水相中的光差异。结果表明:戊唑与氟环唑在水相中的光变化率0 Lux处理均小于3.1%,4000 Lux的光速率为0.013/h和0.029/h,8000 Lux的光速率为0.031/h和0.045/h。光动态特征符合一级动力学方程;戊唑与氟环唑在水相中的光半衰期4000 Lux处理为53.3 h和23.9 h,而8000 Lux处理为22.4 h和15.4 h。说明,光照强度对戊唑与氟环唑在水相中的光有重要影响,且戊唑难于氟环唑。
In order to study on photolysis characteristics of tebuconazole and epoxiconazole,so as to provide the basis for the environmental risk assessment,the indoor simulation method was employed to compare the photolysis differences of epoxiconazole and tebuconazole in the water treated with 0 Lux(dark control),4000 Lux and 8 000 Lux.Results:Photolysis rate of tebuconazole and epoxiconazole processed by 0 Lux in water were less than 3.1%.To 4000 Lux photolysis rate was 0.013/h-1 and 0.029/h-1 respectively,and to 8 000 Lux was 0.031/h-1 and 0.045/h-1 separately.The photolysis half-life of tebuconazole and epoxiconazole under 4000 Lux was 53.3 h and 23.9 h,but under 8000 Lux was 22.4 h and 1 5 .4 h.Light intensity had important influence on photolysis of tebuconazole and epoxiconazole in the water and tebuconazole was harder to be photolyzed.

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粉唑是重要的三唑类农药,广泛运用于农业生产及农产品的运输与储存。本文通过建立超高效液相色谱( UPLC-PDA)检测土壤中粉唑含量的方法。考察了粉唑在贵州,湖南,安徽土壤中的降行为。探讨了土壤中主要因素:有机质、微生物、含水率以及pH值对粉唑的影响。结果表明:土壤中有机质含量越高,微生物越多,含水率越高, pH越大,粉唑在土壤中的降速率越快。
Flutriafol is an important triazole pesticide, widely used in agricultural production, transportation and storage of crops. A method of determining flutriafol in soil was developed by ultra-performance liquid chromatography-photodiode array detection. The degradation of flutriafol in the soil of Guizhou, Hunan and Anhui province were studied, respectively. Effects of soil organic matter, soil microorganism, soil moisture and pH on degradation of flutriafol were also studied. The result showed that the higher organic matter, microorganism, pH, moisture content in soil, the faster speed of flutriafol degrade in the soil.

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目的研究云厚朴提物中厚朴酚、和厚朴酚在贮放、浓缩、干燥工序中的降规律。方法通过高效液相色谱法测定云厚朴提物中厚朴酚与和厚朴酚在不同贮放、浓缩、干燥条件下的含量变化,得出降规律。结果云厚朴提液在室内常温下贮放20天,和厚朴酚、厚朴酚含量基本不变;云厚朴提液在60℃浓缩和干燥,厚朴酚及和厚朴酚的降动力学符合零级反应,在100℃降较快。结论云厚朴提液在室温下贮放20天基本稳定,但是不能长时间在高温条件下浓缩、干燥,以免有效成分损失,在100℃干燥时降较快,制剂生产中应避免提液长时间高温干燥、浓缩。
Objective To study degradation law of magnolol and honokiol in the ethanol extraction of magnolia rostrata during storage , concentrating and drying .Methods To find the law of degradation , the contents of magnolol and honokiol were tested by high performance liquid chromatography under stor -age, concentrating and drying conditions .Results The content of magnolol and honokiol in the ethanolextraction remained almost the same within 20 days when kept indoors .The degradation reactions of magno-lol and honokiol were zero-order when concentrating at 60℃and drying .When drying at 100℃, the rate of degradation was faster .Conclusion Magnolol and honokiol in the ethanol extraction are almost stable within 20 days when kept indoors , but can not be dried and concentrated longer under higher temperature . The rate of degradation is faster when drying at 100℃.In order to ensure the preparation quality , higher temperature and longer time should be avoided during drying and conce

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利用酸化的乙二作溶剂对松木屑进行醇解,探讨了温度和时间对醇解转化率的影响。利用热重分析、红外光谱分析、扫描电镜及X射线衍射考察了醇解残渣的性质。分别利用傅里叶变换红外光谱及色质联用分析了正己烷不溶物和可溶物中组分的分布及特征。结果表明,松木屑转化率在90 min、160℃达到最大值95.3%。松木屑中纤维素无定形区的组分和木质素发生了离,醇解残渣的表面结构被破坏;正己烷不溶物是含有羟基、甲氧基及醚键等含氧官能团的化合物;正己烷可溶物主要由苯二甲酸酯、硬脂酸甲酯、2-甲基己酸丙酯、2-甲基丙酸、聚乙二及未反应的乙二组成。乙二与松木屑离的羧酸发生酯化反应,对液相产物具有稳定作用,促进了松木屑的醇解反应;醇解过程中乙二自缩聚生成聚乙二,增大了乙二的消耗。
The alcoholysis of pine sawdust with acidified ethylene glycol ( EG) as solvent was investigated;the influence of reaction temperature and time on the conversion of pine sawdust was examined.The alcoholysis residual was characterized by thermogravime try ( TG ) , Fourier transform infrared spectroscopy ( FT-IR ) , sac nning electron microscope ( SE M) and X-ray diffraction (X RD) , whereas the compso ition na dp roperties of h exan e insoluble com ponents ( HIS ) and hexane soluble ones ( HS ) were determined by FT-IR and gas chromatography-mass spectrometry ( GC-MS) .The results showed that the conversion of pinesa wdust reaches a maximum of 95.3% at 160 ℃ after reaction for 90 min.By the alcoholysis, the amorphous components of cellulose and lignin were decomposed and the surface structure of alcoholysis residual is destructed.The hexane insoluble components are composed of compounds with oxygen-bearing functional groups such as hydroxyl, methoxyl and ether, whereas the he

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简要介绍了苄基型催化氢的方法、催化剂和催化反应的机理.内容包括了用分子氢催化氢反应,取代基团、溶剂及卤代芳烃等因素对直接催化氢反应的影响;用非分子氢的催化转移氢反应,非分子氢氢源给氢能力的强弱;有机电化学在方面的应用等.
The methods, catalysts and reaction mechanism of the hydrogenolysis of benzyl-type alcohols are reviewed. The contents consist of hydrogenolysis with H2, the effect of substitutents, solvents, aryl halides on the reaction; the catalytic transfer hydrogenolysis with hydrogen donors, hydrogen-donating abilites of various formate salts; and the application of the organic electrochemistry at hydrogenolysis of benzyl-type alcohols.

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旨在筛选出分离纯化虎杖中白藜芦的最佳大孔吸附树脂以及工艺条件。静态吸附与吸、动态吸附与吸相结合的方法,以树脂的最大吸附量、吸率为考察指标,确定最佳的纯化工艺。H103树脂对白藜芦有较好的吸附与吸效果,其最佳的工艺条件为粗提液中白藜芦的质量浓度为0.72mg/mL、上样流速2BV/h,吸附饱和后先用4BV的蒸馏水进行洗涤,然后用8BV、75%的乙溶液以1.5BV/h的流速进行洗脱,白藜芦的含量可由纯化前的12.8%提升至53.5%。应用H103树脂对虎杖中的白藜芦进行纯化,其工艺稳定可行,具有吸附快、吸容易、吸液安全低毒且回收容易的特点,具有较高的应用价值。
Various macroporous resins with different properties were employed to purify the resveratrol from the roots of Polygonum cuspidatum. Static and dynamic adsorption and desorption experiments were conducted, meanwhile, the adsorption and desorption rates of resveratrol were concerned to test out the prominent macroporous resin and optimal processing parameters. H103 was subsequently selected as the best macroporous resin. The optimal processing parameters were obtained as follows: the crude extract containing resveratrol of 0.72 mg/mL was loaded at a flow rate of 2 BV/h, the H103 column was washed with 4 BV of distilled water for removing the impurities, and elution with 8 BV of 75% ethanol was at a flow rate of 1.5 BV/h. As a result, the content of purified resveratrol was increased from 12.8%to 53.5%. The method with H103 as the optimal macroporous resin undergoing with the modified purification process is a simple, safe and inexpensive technology, and has a promising potential of puri

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以丁二酸、丁二为原料,通过对不同端基的聚丁二酸丁二酯(PBS)进行合成和降,研究了羟基封端、羧基封端和等摩尔比的PBS在堆肥土土壤悬浮液中的降情况。通过检测降过程中失重率的变化及降前后薄膜表面形貌的变化,得出不同端基结构PBS的降性能。
Poly(butylene succinate) with different end-groups were synthesized by succinic acid (SA) and bu-tanediol ( BD) and were degraded with composting soil suspension.The polymers were observed by weight-loss rati-o and surface morphology.The results showed the degradation of PBS with different end-groups.

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