多元复合原油破乳剂的研究和应用

本文评价了几种破乳剂对克拉玛依原油的破乳效果。进行了单剂和复配剂的化学破乳及除油率的筛选。结果表明复配破乳剂在加药浓度、净化油含水和净化水含油、脱水速度等方面均优于单剂。表明复配破乳剂是高效原油破乳剂的研究方向之一。     

新型高效原油破乳剂PNT-05的研制与应用

针对中原油田采油六厂二区原油破乳脱水过程中存在的脱水速度慢,乳化中间层厚等问题,通过分子结构设计手段,在非离子型破乳剂基础上,经酯化,在破乳剂分子中引入阳离子基团,合成出季胺盐阳离子型破乳剂PNT－05,利用季胺盐阳离子型破乳剂与助剂复配的方法室内解决了中原油田二区原油破乳脱水过程中顾在的问题,与油田现场用破乳剂相比,新的破乳剂体系脱水速度快,脱水效率高,使乳化中间层变薄或消失,同时探讨了季胺盐阳离子型破乳剂PNT－05的作用机制。     

TA4812和AP442原油破乳剂的复配研究

为了解决陕北油田现用原油破乳剂脱水率低、污水含油和悬浮物多等问题,合成TA4812和AP442两种新破乳剂单剂,并与助剂ECH用不同比例复配,用陕北油田有代表性的河庄坪和子长原油进行脱水实验。结果表明,对河庄坪原油,在55℃,破乳剂总用量100 mg.L-1,脱水时间6 h,TA4812、AP442与ECH复配比例为4:1时,脱水率最高,分别达到96.7%和97.7%;对子长原油,在65℃,破乳剂总用量200 mg.L-1,脱水时间6 h,TA4812与ECH复配比例为4:1、AP442与ECH复配比例为2:3时,脱水率最高,达到98.3%。     

优秀原油破乳剂所具备的性能初探

原油破乳剂是国内外油田矿场所必需的化学药剂,可在针对性的破乳剂性能选择上一直缺乏系统的理论支持。由于原油组成的复杂性,加上影响形成乳化原油的因素众多,给原油破乳剂的研究工作带来许多困难。本文从原油乳状液的形成机理入手,分析了乳状液的稳定性原因、破乳机理、破乳剂分子结构性能、物化性能与破乳效果,提出了优秀的原油破乳剂所应具备的性能。     

微波用于破乳的研究

原油自井下开采出来要穿过窄隙,与水和气混在一起。油中含有沥青质、石油环烷酸;水中含有各种矿物质,都是天然的乳化剂。因此,大量原油将以乳状液的形式被开采出来,大多数为油包水型(W/O),开发到中后期还会出现油包水、水又包油(O/W/O)型。这种原油无法进一步加工,于是,原油脱水成为采油和集输中一个普遍关注的问题。原油脱水国外较多使用化学破乳法,我国各油田多使用电—化学破乳。电—化学脱水法对高含水原油的适应性差,还需增设预脱水工序。而纯化学脱水,试剂昂贵,生产费用较高。因而,近年来人们开始探索将超声技术、微波技术用于破乳。本文考察了微波破乳效果及其机制,并与常规法进行比较。     

海上含聚稠油深度脱水破乳剂研究

2018年渤海某聚驱稠油油田开始大幅提产,原油流程超负荷运行导致外输原油含水率升高至15%。通过分析原油系统各级分离器乳化液稳定性,确定了深度脱水破乳剂的开发方向。分别以乙二醇、丙二醇和丙三醇为起始剂合成EO-PO-EO型嵌段聚醚破乳剂。室内实验表明,破乳剂A2321能够大幅降低聚驱稠油中的含水率和乳化液含量,其脱水效果明显优于破乳剂AE8051、BP169和SP169。矿场试验结果表明,破乳剂A2321可将外输原油含水率从15%降低至8%,有效解决了电脱水器中乳化液的深度脱水问题。     

微波辐射破乳研究进展

综述了微波辐射破乳的有关研究进展。微波辐射是一种有效的破乳手段，与重力沉降、化学、加热等破乳方法相比，能显著地加速稠油体系，含天然表面活性物质、无机盐、固体粒子、三元复合驱剂等乳状液的破乳，提高破乳效果，并且能够提高破乳脱出水的透光率。无机盐与微波辐射两种破乳方式存在加和作用，在极少量的NaCl，MgCl2，caCl2，KCl存在时，用微波辐射120～150s，破乳率可达100％。微波辐射破乳作为一种很有吸引力的破乳方法已在实验室和油田现场取得成功。     

脂肪醇对环氧乙烷环氧丙烷嵌段共聚物破乳效果的影响 Ⅱ.O/W型乳状液的破坏

环氧乙烷(EO)环氧丙烷(PO)的共聚物有较好的破乳效果,是目前较理想的破乳剂,已在油田得到应用。这类表面活性剂的特点是只要适当调节EO和PO的比例,就既可用作W/O型乳状液的破乳剂,也可用作O/W型乳状液的破乳剂,但关于后者的研究很少。前已报导加入脂肪醇可显著提高这类表面活性剂对W/O型乳状液的破乳效果。本文继续研究脂肪醇对这类表面活性剂破坏O/W型乳状液的影响。     

含聚稠油高效破乳剂研究与应用

2014年以来渤海某注聚稠油油田产出液聚合物浓度高、原油黏度大导致原油脱水困难,原破乳剂脱水效果无法满足要求。通过苯酚、多乙烯多胺与甲醛合成酚胺树脂起始剂,然后与环氧乙烷、环氧丙烷聚合得到多支化嵌段聚醚破乳剂108#。破乳剂108#具有使用浓度低、脱水速度快的特点,且最终脱水率接近90%。矿场试验结果表明,108#破乳剂加注量比原破乳剂减少48%,外输原油含水从15%-16%降低至9%,原油脱水效果明显改善。     

支状嵌段聚醚的界面聚集行为及对原油乳状液的破乳作用

合成了三种不同聚氧丙烯/聚氧乙烯(PPO/PEO)比例的含苯环支状嵌段聚醚, 通过界面张力、界面流变、表面压以及对原油乳状液的破乳脱水效果的测定, 考察了其界面聚集行为和破乳作用对PEO含量和分子量的依赖性, 并且对比研究了三种支状聚醚分子交联前后的破乳性能. 结果表明, PEO含量高且分子量大者,其单分子界面占据面积大, 在油/水界面达到吸附平衡的时间短, 其油/水界面扩张模量及扩张弹性均高于PEO含量较少者. 但是对原油乳状液的破乳脱水效果则是PEO含量居中的聚醚最好. 温度影响和交联与否的研究表明, 交联并不能提高分子量较大的聚醚对原油乳状液的破乳效果, 温度对聚醚分子交联前后的破乳效果有不同的影响规律. 本研究可为原油集输过程中化学品的选择与应用提供一定的依据.     

α-Amino acid derived enaminones and their application in the synthesis of N-protected methyl 5-substituted-4-hydroxypyrrole-3-carboxylates and other heterocycles

A new and simple synthesis of novel N-protected methyl 5-substituted-4-hydroxypyrrole-3-carboxylates, which exist in equilibrium with their 4-oxo tautomers, has been developed in two steps starting from N-protected α-amino acids. The key intermediates are enaminones, which can also be isolated, characterized, and used for the construction of other functionalized heterocycles, before they spontaneously decompose to pyrrole products. 4-Hydroxypyrroles are prone to partial aerial oxidation but can be efficiently alkylated or reduced to stable polysubstituted pyrrolidine derivatives.     

Specific intramolecular aromatic CH insertion of diazosulfonamides

The chemoselectivity in the intramolecular CH insertion of various diazosulfonamides has been experimentally studied. The results reveal that the aliphatic 1,4-, 1,5-, or 1,6-C(sp³)?H insertions of diazosulfonamides are not accessible, while the aromatic 1,5-C(sp²)?H insertion can be realized specifically by adjusting the diazo-adjacent group. In addition, the general chemoselectivities in the intramolecular CH insertions of diazosulfonyl compounds are summarized. Generally, diazosulfones undergo both aromatic 1,5-C(sp²)?H and aliphatic 1,5- and 1,6-C(sp³)?H insertions, while diazosulfonates undergo aliphatic 1,5- and 1,6-C(sp³)?H insertions. However, diazosulfonamides only undergo aromatic 1,5-C(sp²)?H insertion.     

N-Heterocyclic carbene-palladacyclic complexes: synthesis,characterization and their applications in the C-N coupling and α-arylation of ketones using aryl chlorides

N-Heterocyclic carbene-palladacyclic complexes 3 were successfully achieved in a one-pot procedure under mild conditions. The structure of 3a was unambiguously confirmed by X-ray single crystal diffraction and it was an active catalyst in the Buchwald-Hartwig amination and α-arylation of ketones even at very low catalyst loadings (0.01?mol%).     

Iodine-mediated oxidative Pictet-Spengler reaction using terminal alkyne as the 2-oxoaldehyde surrogate for the synthesis of 1-aroyl-β-carbolines and fused-nitrogen heterocycles

An efficient iodine-mediated oxidative Pictet-Spengler reaction in dimethyl sulphoxide (DMSO) using terminal alkynes as the 2-oxoaldehyde surrogate for the synthesis of aryl (9H-pyrido[3,4-b]indol-1-yl)methanones is described. The scope of the protocol includes the total synthesis of Fascaplysin, Eudistomins Y₁ and Y₂. The methodology is extended for preparing pyrrolo[1,2-a]-quinoxaline and indolo[1,5-a]quinoxaline derivatives. The utility of 1-aroyl-β-carbolines was demonstrated by performing palladium-catalyzed β-carboline directed ortho-C(sp2)-H functionalization of the phenyl ring with thiomethyl (SMe) group using DMSO as source and for accessing 4-aryl-canthin-6-ones.     

Facile synthesis of bicyclic 1-arylpyrazol-5-ones

In this Letter, we described a facile method for constructing fused bicyclic 1-arylpyrazol-5-one ring system. We employed various methylene-containing carboxylic acids as the substrates and proved that the pyrazolone ring closure requires activated methylene group in intermediate II. Accordingly, a series of structurally diversified, fused bicyclic 1-arylpyrazol-5-ones was prepared in moderate to high yields using the requisite substrates.     

Synthesis of pyrrolo[1,2-a]pyrazines and pyrazino[1,2-a]indoles by Curtius reaction in Morita-Baylis-Hillman derivatives

Synthesis of substituted pyrrolo[1,2-a]pyrazines and pyrazino[1,2-a]indoles from the Morita-Baylis-Hillman derivatives of acrylates via saponification followed by Curtius reaction is described.     

正丁胺对激光染料荧光谱影响的研究

用正丁胺作为碳源,采用射频辉光放电制备碳膜,选用激光染料R6G和聚乙二醇混合液作为蒸气源,采用单源热蒸发,在蒸发室与染料同时沉积得到混合膜,用拉曼光谱和红外光谱分析了碳膜的结构和键合方式,分析表明:碳膜中存在胺基团和氢原子.混合膜的荧光谱测量结果表明,认为正丁胺对染料荧光谱的影响是因为胺基和氢原子的存在.     

Cu0-catalysed 1,3-dipolar cycloadditions of α-amino acid derived N,N-cyclic azomethine imines to ynones

A series of 20 CuAIAC reactions between eight 4-acylamino substituted pyrazolidine-3-one-1-azomethine imines and four terminal ynones were performed using Cu⁰ as catalyst. The corresponding fluorescent cycloadducts were obtained in very high yields upon simple workup. Thus, Cu-metal turned out to be a better catalyst than Cu^I in terms of yield and ease of isolation. Availability of azomethine imines, mild reaction conditions, and simple workup enable a “click” access to libraries of densely substituted 2,3-dihydro-1H,5H-pyrazolo[1,2-a]pyrazol-1-ones. Reactivity of differently substituted dipoles was evaluated experimentally and by quantum chemical methods (DFT).     

Synthesis and antioxidative/anti-inflammatory activity of novel fullerene–polyamine conjugates

(E)-4-(Fullerenopyrrolidin-1-yl)-3-methylbut-2-enoic acid and its corresponding succinimidyl ester, readily obtained through Prato-type modification of C₆₀, were used for the selective N-acylation of polyamines. The thus obtained conjugates were evaluated for their antioxidative and anti-inflammatory activity and their cytotoxicity was determined. Members of this family of compounds showed interesting anti-lipid peroxidation, anti-lipoxygenase and anti-inflammatory activity and comparable cytocompatibility to spermidine.