含芳香基团的梳状聚合物型降凝剂与沥青质协同改善合成蜡油的流变性

采用流变学实验、 差示扫描量热(DSC)分析、 显微观察及沥青质沉淀实验研究了聚丙烯酸十八酯-马来酸酐(POM)、 聚丙烯酸十八酯-马来酸酐-苯胺(POMA)及聚丙烯酸十八酯-马来酸酐-萘胺(POMN)梳状聚合物对合成蜡油的流变性能的影响规律. 实验结果表明, 这3种梳状聚合物降凝剂均能在一定程度上改善不含沥青质合成蜡油(MO-1)的低温流变性, 其中POM对MO-1蜡油的流变性改善效果最佳. 添加500 mg/kg POM后, MO-1的凝点从29 ℃降至23 ℃, 屈服值从627.20 Pa降至83.35 Pa. 而POM, POMA和POMN可以显著改善含0.3%(质量分数)沥青质的合成蜡油(MO-2)的低温流变性, 且添加500 mg/kg POMA后MO-2蜡油的流变改善效果最佳: 凝点降至3 ℃, 屈服值降至1.27 Pa. 可见, 本文制备的梳状聚合物降凝剂均能与沥青质协同改善MO-2蜡油的流变性, 并且向POM中引入芳香基团能进一步促进沥青质与降凝剂分子的相互作用, 进而增强梳状聚合物降凝剂与沥青质的协同作用.     

聚丙烯酸十八酯原油管道添加剂的合成与表征综合性实验

介绍一个聚丙烯酸十八酯原油管道添加剂的合成与表征综合性实验。基于溶液自由基聚合反应合成聚丙烯酸十八酯,利用红外光谱仪分析聚合物的结构,通过流变测量和偏光显微镜观察考察聚丙烯酸十八酯对人工蜡油体系宏观流动性与微观析蜡特性的影响。该实验综合了油气储运专业学生在“油气储运用剂”课程中所学习的化学剂合成、结构表征与性能评价等基本内容,对于提高课程的教学效果具有重要意义。     

含蜡原油降凝剂与石蜡作用机理的研究进展与探讨

高分子降凝剂产品已广泛应用于原油的开采和输送工艺中,但是,对降凝剂降凝机理认识的不足制约了降凝剂的开发和应用.降凝剂与油品中石蜡的相互作用决定其降凝机理.本文综述了近年来人们在研究降凝剂与石蜡作用机理方面所使用的研究方法和所取得的进展,并深入探讨了降凝剂与石蜡的具体作用方式.对于含蜡原油,降凝剂主要通过与石蜡的共晶、吸附作用使蜡晶结构更紧凑,并促进小蜡晶聚集成较大尺寸的聚集体,从而大大降低蜡.油界面积,破坏蜡晶三维网络的形成,宏观上表现为原油凝点降低,低温流动性改善.     

降凝剂结构性质对原油化学改性的影响及流变学改进机理

概述了用于改善含蜡原油变性的高分子降凝剂的分子结构特点及其对原油化学改性效果的影响，并对其流变改进机理进行了探讨。     

倍半硅氧烷/改性乙烯-乙酸乙烯酯共聚物复配降凝剂对蜡油倾点的影响

乙烯-乙酸乙烯酯共聚物(EVA)是原油常用的降凝剂(PPDs),但其分子结构相对比较单一,对部分油品降凝效果不佳。 为了提高EVA的降凝效果,使用硬脂酰氯与羟基化的EVA直接反应的方法制备烷基长链接枝改性EVA,并与带有烷基长链的倍半硅氧烷(SS)纳米粒子进行复配。 研究了改性EVA和SS复配降凝剂对蜡油的降凝效果和降凝机理。 结果表明:复配降凝剂为蜡提供晶核,使蜡晶变小并降低蜡的沉淀量,导致蜡油中形成的蜡晶难以搭接在一起,形成了松散的结构,当复配质量比m(EVA-g)∶m(SS-L)=1∶2时,在蜡油中的质量分数为0.1%时,蜡油倾点降低了25 ℃。     

降凝剂对蜡油中蜡析出与溶解影响的物理化学研究

用DSC热分析仪研究了合成蜡油的加热与冷却过程,测定了蜡油在不同蜡浓度下,添加降凝剂前后的平衡蜡溶点和析蜡点以及溶解度和饱和度,并进行了热力学分析.结果表明,含蜡油的平衡蜡溶点高于平衡析蜡点,降凝剂使平衡蜡溶点进一步升高,析蜡点进一步降低,导致含蜡油凝点较大幅度降低.在实验浓度和温度范围内,该过程符合Van′tHoff方程,降凝剂使蜡的溶解焓和溶解熵增大,析出焓和析出熵减少.降凝剂提高了蜡晶析出的临界半径,增大了成核位垒,使蜡晶析出困难.     

柴油降凝剂的合成及性能研究

合成了新型聚合物型柴油降凝剂,并采用红外光谱对聚合物进行了表征。X射线衍射技术对不同降凝剂的结晶性能分析表明,聚合物的结晶性能差别很大,结晶度不同,蜡晶分散效果不同。同时发现,当两者结晶性能状态匹配时蜡晶分散效果变好,降凝性能最佳,并由柴油体系降凝性能证实。     

改性聚丙烯酸高级酯的合成及其降凝效果的考察

用酯化和热聚合同时进行的方法合成了聚丙烯酸高级醇酯（PAE），并对其进行改性，得到改性聚丙烯酸高级酯（MPAE），在实验室评价了MPAE对几种0#柴油的低温流动性能的改进效果。结果表明，该工艺路线产品的收率几乎达到100％，成本低。并且，改性后的聚丙烯酸高级酯在较宽的分子量范围内具有较好的降凝效果；相比之下，改性之前聚丙烯酯高级酯只在很窄的分子量范围内具有降凝效果。与其它柴油降凝剂相比，MPAE对柴油具有良好的感受性，一般能降低柴油冷滤点3℃－6℃，凝固点降幅在10℃－12℃左右，具备了工业化价值。     

含mPEG侧链的水溶性梳状聚合物的合成及其侧链受限结晶行为研究

采用大单体与小单体共聚的技术,通过自由基引发溶液聚合,合成了一系列水溶性梳状聚合物———聚丙烯酸接枝聚乙二醇单甲醚(PAA-g-mPEG).制备过程分两步进行,首先合成大单体聚乙二醇单甲醚丙烯酸酯,然后将大单体与丙烯酸单体共聚,合成了梳状聚合物.通过控制反应条件,获得了一系列主链和支链组成比不同的接枝共聚物.用傅立叶变换红外光谱(FT-IR)和核磁共振氢谱(1H-NMR)表征了共聚物的结构,并对其侧链的结晶行为进行了研究.采用差热扫描量热法(DSC)表征并分析了不同侧链长度的mPEG的热性能及其结晶情况.利用相差显微镜和原子力显微镜(AFM)观察薄膜的结晶形貌,表明梳状聚合物的侧链mPEG在受限条件下的薄膜结晶形貌为高度支化的晶体,初步分析了mPEG链长及其在共聚物中的重量百分含量对晶体形貌的影响.     

原油加剂降凝的研究

采用高温气相色谱分析了越南、阿曼和大庆原油中蜡的碳数及分布组成,采用偏光显微镜观察了不同蜡含量原油的蜡晶形态变化时,分析了蜡结晶过程中的结构、分布状态和生长规律与不同原油组成的关系,得出了蜡结晶过程与原油组成之间的变化规律。结合采用X射线衍射仪和DSC差示扫描量热仪对自制聚合物(MOA)的结晶度和热性能的分析测试,表明原油中蜡晶结构与聚合物的结晶度密切相关,结晶度变化时,蜡晶分散效果有所区别,两者匹配状态时分散效果最佳,体系的粘温特性研究也证明了这一点。同时,降凝剂使得系统的热性能——溶解焓和溶解熵均发生了改变,原油中石蜡的熔程变长,相变能变大。     

Dichroism of absorption and polarization of phosphorescence of molecules of the closed form of nitrobenzospirothiopyran

The spectral-polarization characteristics of absorption and phosphorescence of molecules of the initial form of nitro-substituted indolinospirobenzothiopyran were studied in oriented polyethylene films and in solutions with different polarity. An oscillator model of the electron transitions responsible for the formation of absorption and luminescence spectra was suggested. It was established that the principal differences in the spectral and photophysical properties of the compound studied and its oxygen-containing analog are associated with the fact that the electronegativity of the S atom is lower than that of the O atom. Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 6, pp. 1143–1146, June, 1997.     

非那雄胺合成工艺改进

非那雄胺能抑制5α-还原酶的活性,明显降低二氢睾酮水平,是一种治疗良性前列腺增生的有效药品。该合成工艺以甾烯酮酸为原料,将其与氯化亚砜反应,无须分离即与叔丁胺反应得17β-酰胺化合物,再氧化开环,环合,氢化,脱氢合成了非那雄胺。经元素分析、IR、1HNMR、13CNMR、MS分析表征了其结构。该法无须使用昂贵的2,2-二吡啶二硫化物和剧毒药品苯亚硒酸酐,且以乙酸铵代替氨气,降低了对设备的要求和腐蚀,更适用于工业生产。     

Synthesis of phenolic components of Grains of Paradise

Two vanilloids, (5E)-8-(4-hydroxy-3-methoxyphenyl)oct-5-en-4-one (1) and 4-[3-hydroxydecyl]-2-methoxyphenol (2), isolated from the dried seeds of Grains of Paradise (Aframomum melegueta), were synthesized; the latter compound was made as the S-enantiomer and the material derived from the seeds was found to be a 1:1.7 mixture of the R and S isomers. The synthetic route used should allow the preparation of analogs having extended alkyl chains and consequently different lipophilicity, and 3, a homolog of 2, was also prepared.     

Acid hydrolysis of carboxymethylcellulose of low degree of substitution

Cotton cellulose was swollen in a sodium hydroxide solution and carboxymethylated by a two-bath method for different periods of time for each process. The kinetics of acid hydrolysis and the crystallinity of the swollen and carboxymethylated samples were measured. The proportion of broken bonds, rate constants for hydrolysis, and permeability of cellulose to hydrolyzing agents were calculated. The susceptibility of glycosidic linkages to acid hydrolysis was improved by carboxymethylation more than by swelling in alkali. The increased accessibility of carboxymethylcellulose to acid was regarded as a consequence of increased intra-and intercrystalline swelling and of the glycosidic bonds' weakness caused by the electron-attracting carboxymethyl group on the C-6 position.     

Study of hydration of two cements of different strengths

Main hydration products of two cement pastes, i.e. CSH-gel, portlandite (P) (and specific surface S) were studied by static heating, and by SEM, TEM and XRD, as a function of cement strength (C-33 and C-43) hydration time (th) and subsequent hydration in water vapour.Total change in mass on hydration and air drying, M_o, increased with strength of cement paste and with hydration time. Content of water escaping at 110 to 220°C, defined as water bound with low energy, mainly interlayer and hydrate water, was independent on cement strength but its content increased with (th). Content of chemically bound (zeolitic) water in CSH-gel, escaping at 220-400°C, was slightly dependent on strength and increased with (th). It was possibly derived from the dehydroxylation of CSH-gel and AFm phase. Portlandite water, escaping at 400-500°C, was independent on cement strength and was higher on longer hydration. Large P crystals were formed in the weaker cement paste C-33. Smaller crystals were formed in C-43 but they increased with (th). Carbonate formated on contact with air (calcite, vaterite and aragonite), decomposed in cement at 600-700^oC. It was high in pastes C-33(1 month) and C-43(1 month), i.e. 5.7 and 3.3%, respectively; it was less than 1% after 6 hydration months (low sensitivity to carbonation) in agreement with the XRD study showing carbonates in the air dry paste (1month), and its absence on prolonged hydration (6 months) and on acetone treatment. Water vapour treatment of (6 months) pastes or wetting-drying increased this sensitivity.Nanosized P-crystals, detected by TEM, could contribute to the cement strength; carbonate was observed on the rims of gel clusters.This revised version was published online in November 2005 with corrections to the Cover Date.     

恶臭嗅辨实验室建设探讨

针对恶臭测试的环境影响问题,提出了解决的实例方案,并对方案的要点及优缺点进行讨论,此方案在实际操作中具有较好的效果。     

Estimation of Kinetic Parameters of Thermal Oxidation of Ilmenite

The aim of the presented work was the investigation of thermal oxidation of ilmenite in static air atmosphere. The investigations were carried out by use of a derivatograph (MOM, Hungary). The changes of crystallographic structure of investigated samples were identified by X-ray diffractometry on Philips PW-1710 diffractometer. In temperature above 500°C appears structure of hematite Fe₂O₃. On the basis of the thermogravimetric measurements, the contracting area and contracting volume models were found as the best fitting experimental data. This revised version was published online in August 2006 with corrections to the Cover Date.     

Mechanism of action of base-catalyzed oxygenation of phenol derivatives

Cyclopropyl derivative of 2,6-di-tert-butylphenol is synthesized as a probe to investigate the mechanism of base-catalyzed autooxidation of phenol derivatives. Our study indicates that one electron reduction of molecular oxygen from phenolate gives phenoxyl radical 3, a key intermediate of autooxidation. The coupling of phenoxyl radical and superoxide radical gives peroxylate anion 4 and produces the final epoxy alcohol adduct 6.     

氯氧化镁生成热的研究

用氧化镁氯化镁水溶液制备了8水合氯氧化镁[nMg(OH)2·MgCl2·8H2O], 并测定了其在盐酸中的溶解热, 实验结果表明, 氯氧化镁溶解热与n值呈线性关系, 根据溶解热求出5Mg(OH)2·MgCl2·8H2O和3Mg(OH)2·MgCl2·8H2O的生成热分别为-7727.1和5888.1kJ·mol^1^-。