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PEG-400

PEG-400的相关文献在2000年到2022年内共计79篇,主要集中在化学、化学工业、药学 等领域,其中期刊论文79篇、专利文献929篇;相关期刊55种,包括商丘师范学院学报、西北师范大学学报(自然科学版)、甘肃联合大学学报(自然科学版)等; PEG-400的相关文献由252位作者贡献,包括王喜存、权正军、张海军等。

PEG-400—发文量

期刊论文>

论文:79 占比:7.84%

专利文献>

论文:929 占比:92.16%

总计:1008篇

PEG-400—发文趋势图

PEG-400

-研究学者

  • 王喜存
  • 权正军
  • 张海军
  • 施磊
  • 杨亮庆
  • 胡怀生
  • 陈建村
  • 刘劲松
  • 叶鹤琳
  • 姜国华
  • 期刊论文
  • 专利文献

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    • 刘红
    • 摘要: 采用简单易行且对环境污染小的化学合成法将p型半导体CuO纳米材料沉积在n型半导体四针状氧化锌晶须(T-ZnOw)表面制备复合半导体催化剂样品,对样品进行XRD和SEM检测研究其晶体组成和微观形貌,观察不同反应时间状态下纳米CuO的形貌,推测其形成机理,同时通过紫外光照条件下样品对甲基橙(MO)溶液的降解来表征其光催化活性。研究发现,聚乙二醇(PEG, Mw=400)和T-ZnOw对纳米CuO的生成起着重要作用,T-ZnOw表面沉积纳米CuO可有效提高其光催化活性。
    • 罗丽霞; 朱彦荣
    • 摘要: 在微波加热无溶剂条件下,将噻吩、联苯甲酰、醋酸铵三组分采用"一锅法"反应,合成了 2-(2'-噻吩)-4,5-二苯基咪唑,考察了微波辐射功率、反应时间、催化剂种类与用量对产物产率的影响,优化了反应条件,并通过红外光谱、核磁共振谱和质谱对产物的结构进行了表征.该方法快捷、简便,为2-(2'-噻吩)-4,5-二苯基咪唑的合成提供了一种环境友好的方法.
    • 鲍芃丞; 毕莹; 田军; 宋歌; 张会京; 范小鹏; 孙春光
    • 摘要: 在传统UV-531合成方法的基础上,对UV-531合成工艺进行进一步研究,采用KI与PEG-400作为催化剂,极大提高反应速率,减少副产物生成,在此反应条件下,采用过滤去除盐等固体杂质,方便工业操作,最终UV-531收率可以达到95.8%,HPLC纯度99.7%.
    • 郭琳娜; 魏月; 赵影; 许国贺; 马晶军
    • 摘要: 以线性氨基酸L-丙氨酸为催化剂,PEG-400∶H2O(3∶2)为反应体系,室温下直接催化环己酮与不同R基取代的芳香醛进行不对称Aldol反应,产物具有良好的对映选择性(68% ee~96% ee).该方法操作简单,环境友好,催化剂易回收循环利用,利用过渡态理论结合烯胺机理对环己酮与4-溴苯甲醛反应中的过渡态分子构型(TS、SR-anti、TS-RS-anti)进行了理论研究,并在BL3YP/6-311G (2d,2p)理论水平下经IRC计算证明其构型的合理性.
    • 张红刚1; 曹景平1; 赵永1; 王桂云1; 王利平1
    • 摘要: 本实验以碳酸乙烯酯(EC)与聚乙二醇(PEG400)的共混物为液化剂,浓硫酸为催化剂,在反应温度160°C,反应时间90 min下,研究了EC与PEG400的质量比对液化产物的残渣含量、酸值、羟值的影响。实验结果表明:随着混合液化剂中EC含量的降低,液化产物残渣含量和羟值逐渐升高,酸值先降低后增加,在EC/PEG400 = 4:6 w:w时达到最低值7.23 mgKOH/g,在EC与PEG400共混体系中,液化剂可能是分阶段发生作用的,首先是EC发生作用,而后是PEG400,临界点为EC/PEG400 = 4:6 w/w。
    • Atnafu Guadie Assefa; Rongali Srinivasu; Pulipaka Shyamala; Gollapalli Nageswara Rao
    • 摘要: The acid-base equilibrium of 1,10-phenanthroline (1,10-phen) in the presence of polyethylene glycol 400 (PEG-400, non-ionic) and tetrabutylammonium bromide (TBAB, ionic) micellar media has been studied by Calvin-Wilson titration technique at different mole fractions (0.5% - 2.5%) of PEG-400 and TBAB micellar solutions at an ionic strength of 0.16 mol dm-3 NaCl and at a temperature of 298 K. The pH metric data were subjected to SCPHD program to obtain correction factor and Kw which were given as initial inputs for MINIQUAD75 program to refine protonation constants. HySS program was then used to generate the species distribution diagrams versus pH using the results obtained from the MINIQUAD75 program and SIM run data. The difference in values of protonation constants in aqueous medium (logβ1 = 4.93 & logβ2 = 6.22) and in the micellar media (PEG-400, logβ1 = 4.89 & logβ2 = 5.91 and TBAB, logβ1 = 4.84 & logβ2 = 5.73) is attributed to different intrinsic solvent characteristics of micelles. In case of ionic surfactants, the electrostatic micellar surface is an additional contributing factor.
    • 陆国太; 马玉洁; 姜迪; 杨刚; 邢卫红
    • 摘要: 以PEG-400为相转移催化剂,采用溶媒法制备羧甲基菊粉(CMI),通过单因素和正交试验考察了催化剂用量、NaOH用量及添加方式、碱化时间、氯乙酸用量、醚化时间对取代度的影响规律.结果表明,优化工艺条件为:1%菊粉质量的PEG-400、n(NaOH):n(菊粉):n(氯乙酸)=2.5:1:1.2(两步加碱法)、碱化时间0.7 h、醚化时间4 h.此条件下制得取代度达到1.2145的羧甲基菊粉.%With ethanol as the reactive media, the phase transfer catalytical method of PEG-400 was used to prepare carboxymethyl inulin(CMI).The synthesis technology of CMI was optimized with single factor and orthog-onal experiments.Effects of the amount of catalyst,the dosage and feeding ways of NaOH,alkalization time,the amount of chloroacetic acid and etherification time were investigated.The substitution degree of CMI was affected by the operating conditions.The best CMI with a substitution degree of 1.2145 was produced and the optimized conditions were as follows:PEG-400 accounted for the proportion of inulin quality 1%,n(NaOH):n(inulin):n(chloroacetic acid)=2.5:1:1.2(feeding NaOH by two steps), alkalization time 0.7 h,etherification time 4 h.
    • 王睿; 糜莉萍; 张恒; 王李波
    • 摘要: 以三聚氰胺为前驱体采用焙烧法制备二维纳米材料g-C3N4,用X射线衍射(XRD)对g-C3N4粉体样品进行物相分析,同时用扫描电子显微镜(SEM)分析g-C3N4表面形貌.采用四球摩擦磨损试验机考察g-C3N4作为聚乙二醇400 (PEG400)添加剂对钢-钢摩擦副摩擦磨损性能的影响,并采用扫描电子显微镜及X射线光电子能谱仪分析试验后钢球磨损表面形貌、元素分布及典型元素的化学状态.结果表明,所制备的g-C3N4具有二维层状纳米结构,作为添加剂在PEG400中具有良好的减摩抗磨性能.SEM和XPS分析表明,在摩擦学过程中g-C3N4沉积在摩擦副表面形成了润滑保护膜,从而提高了PEG400的摩擦学性能.%Two-dimensional nanomaterial,g-C3N4 was chemically synthesized using the melamine.The morphologies and crystalline structures of the g-C3N4 powder were characterized by scan electron microscopy (SEM) and X-ray diffraction (XRD).The tribological properties of the prepared g-C3N4 nanomaterial as an additive in PEG400 were evaluated with a four-ball tester.The morphology of steel ball worn surface,the distribution of elements and the chemical state of typical elements were analyzed by SEM and XPS.The results show that the prepared g-C3N4 has two dimensional layered nanostructure,it exhibits excellent friction reducing properties and good anti-wear ability in PEG400.SEM and XPS analysis indicate that physical adhesion film mainly composed of g-C3N4 and some adsorbed organic compounds is formed during the friction process.These contribute to the good friction reducing and anti-wear ability of g-C3N4 nanomaterial as PEG400 additive.
    • 雷英杰; 丁玫; 吴新世; 姚庆佳
    • 摘要: To develop new 1,3,4-oxadiazole compounds with high biological activity,some derivatives modified with thioacetamide group(3a~3f)by means of the condensation reaction between the intermediate 5-aryl-l,3,4-oxadiazole-2-thione,which was pre-pared from 3,4,5-trimethoxy-benzoic acid hydrazide with carbon disulfide,with(substitued)2-chloro-N-4-tolylacetamide in alkaline media under ultrasound irradiation in the presence of PEG-400 had been reported,with a yielding of 80~88%respectively. Struc-tures of the corresponding products were elucidated by IR,1 HNMR spectra and elemental analysis. Preliminary bioassay results indi-cated that some of the target compounds had significant antifungal activity against Candida albicans and Aspergillus niger.%为寻找具有较高活性新型1,3,4-噁二唑类杂环化合物,利用3,4,5-三甲氧基苯甲酰肼和二硫化碳环合生成的5-芳基-1,3,4-噁二唑-2-硫酮为活性基团,超声波辐射聚乙二醇-400相转移催化条件下,与(取代)N-氯乙酰基苯胺反应制备得到硫代乙酰胺修饰的1,3,4-噁二唑衍生物(3a~3f),合成收率为80~88%,其结构经IR、1 HNMR和元素分析等测试技术加以确证;初步的活性测试结果表明,目标产物对白色念珠菌和黑曲霉等有较显著的抗菌活性.
    • 李仁; 张治国; 兰新媛; 蒲俊文
    • 摘要: The 50% PEG400 aqueous and a hybrid solution of PEG 400 ( 50%) and ε-caprolactone (ε-CL ) ( 50%) were separately used to investigate the dehydration and reinforcement of waterlogged scotch pine wood simulating the archaeological waterlogged wood.The dehydration process included catalyst pre-treatment, impregnation under room temperature and 50 °Chot dry aggregate .And the weight and dimensional changes of the different stages were analyzed , which was applied to evaluated the effects of process on the dimensional stability , weight gain percentage and reversibility of wood .And then the treated wood was characterized by FT-IR, TGA-DTA and SEM.The results showed that the PEG400 and the hybrid solution of PEG400 andε-CL both had good dehydration and reinforcement effect on waterlogged scotch pine wood with good reversibility .The weight gain percentage of the wood samples treated by the hybrid solution of PEG 400 and ε-CL increased obviously and the value of was 124.1%.After the dehydration and reinforcement , the shrinkages of tangential direction , radial direction and volume were 0.01%、0 and 0.01%,respectively, indicating of the dimensional stability .The ring opening polymerization (ROP) of CL was carried out inside the wood structures to form polycaprolactone ( PCL).The wood cell walls were coated and filled by PCL and PEG400, resulting in the increased thickness of the cell wall .However, the thermostability of wood filled with PLC and PEG 400 was turned to decrease .PLC would firstly degrade at 150 °Cto protect the cell wall of wood .%以人工速生材樟子松为原料,通过热水蒸煮法模拟饱水木材试件,选择50%PEG400水溶液和50%PEG400/50%ε-己内酯(ε-CL)复配溶液用于樟子松饱水木材试件的脱水定型研究.通过催化剂预浸渍、常温置换脱水和50°C热干燥聚合工艺,对比研究了PEG400和PEG400复配ε-CL对樟子松饱水试件的脱水定型效果,分析了各个阶段的质量和尺寸变化,探讨了脱水定型工艺对木材的尺寸稳定性、质量增加率、可逆性的影响;并对脱水定型后的木材试件进行红外光谱(FT-IR)、热重-差热联用(TGA-DTA)、扫描电子显微镜(SEM)分析表征.结果表明:PEG400及PEG400复配ε-CL溶液对樟子松饱水木材试件脱水定型效果良好,均表现出良好的可逆性,PEG400复配ε-CL脱水定型处理的木材试件质量增加明显,脱水定型试件干质量增加率为124.1%,干燥定型过程弦向、径向和体积收缩率分别为0.01%、0和0.01%,表现出良好的尺寸稳定性;FT-IR、TGA-DTA和SEM分析表明,ε-CL单体在木材内部发生开环聚合反应形成聚己内酯(PCL),PCL与PEG400包覆木材细胞壁,填充于木材内部结构中,加固木材细胞壁结构;PCL与PEG400的填充作用导致木材热稳定性降低,PCL于150°C最先发生降解,保护木材细胞壁成分.
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