CHA无机凝胶体系的研究及应用

过去低渗油藏调剖，注入性和堵塞性很难统一，新研制的CHA无机凝胶体系是一种易注入、堵塞能力强的调剖剂，而且成胶时间在一定范围内可控。研究了配比、温度对CHA无机凝胶体系成胶时间的影响，成胶前的注入性，成胶后在高温高盐条件下的堵塞能力，得到了可应用于现场的CHA无机凝胶体系。该调剖剂在濮城油田沙三段和文卫结合部等高温、高盐低渗油藏应用后，取得了很好的效果。     

Novel one-step route for synthesizing sub-micrometer PSt hollow spheres via redox interfacial-initiated method in inversed emulsion

Interfacial-initiated polymerization of styrene (St) was carried out in inversed emulsion with cumene hydroperoxide (CHPO) and ferrous sulfate (FeSO₄)/disodium ethylenediaminetetraacetate (NaEDTA)/sodium formaldehyde sulfoxylate (SFS) as the redox initiation system. The water-soluble Fe²⁺-NaEDTA-SFS acted as the reducing component and the oil-soluble CHPO as the oxidant component of the redox initiation system. Therefore, the primary radicals were produced mainly at the oil/water interface to initiate the polymerization of St. Thus, sub-micrometer hollow polystyrene (PSt) spheres were obtained by one-stage polymerization, which was supported by the techniques of transmission electron microscopy (TEM) and field emission scanning electron microscopy (FESEM).     

Mid-Temperature Synthesis of CeO2-TiO2 Complex Compound and Its XRD Structure Study

TiO2 andCeO2 aresemiconductormaterials .TiO2hasthepropertiesofphoto catalysis[1] whileCeO2 hastheabilityofoxygenstorageandcanpromotethedispersionofprecionsmetalsonthesupporter[2 ] .CeO2 TiO2 com plexcompoundwasusedascatalystandspecialfunction almaterial[3～ 5] .ThetraditionalsynthesisofCeO2 TiO2complexcompoundisbyceramicmethodthatusesoxidesasrawmaterialsanditiscalcinedabove 130 0℃[6～ 8] .However ,thestructureandmicrostructureofthecomplexcompoundarenotsuitableforcatalystandfunctionalm…     

深部调剖驱油交联剂的研究

为提高非均质性严重的地层原油采出率 ,合成了用于聚合物驱油的 4种交联剂 ,并对聚合物种类、用量和其与交联剂组成的体系进行了评价。 4 0℃下铝交联剂凝胶粘度低 ,酚醛树脂交联剂低温下不成胶 ,而有机铬交联剂 (J2 )和有机复合胺 (J3)交联效果好。当选用HPAM/有机铬交联剂 /有机酸交联体系时 ,其中HPAM相对分子质量为 2 1× 10 7,可通过改变体系pH值调节成胶速度 ,pH值 6 5时 ,14 0 0mg/LHPAM和 4 0 0mg/LJ2组成的体系在 4 0℃、30d可形成粘度为12 0mPa·s以上的凝胶 ,且热稳定性好 ,成胶时间能满足现场施工需要。 14 0 0mg/LHPAM和10 0 0mg/LJ3交联剂组成的体系 ,成胶时间长 ,有利于油田深部调剖驱油     

香豆胶衍生物的化学结构及稳定性研究

将市售商品溶于水,用异丙醇沉析提纯,溶于0.1 mol/L NaNO3纯水溶液中,经0.5μm滤膜过滤后用水相凝胶渗透色谱法(GPC)测定,测得香豆胶(FG)、羟丙基香豆胶(HPFG)、阳离子香豆胶(CFG)的数均、重均相对分子质量Mn、Mw分别为:1.19×105、3.36×105,8.52×104、2.85×105,9.33×104、2.87×105。用甘露聚糖链在碱性条件下醚化时发生降解,解释两种改性FG的相对分子质量较FG低而多分散性(Mw/Mn)较FG高的测试结果。认为商品FG的1%水溶液黏度(1300 mPa.s)高于商品HPFG和CFG(分别为705和610 mPa.s)的原因是前者相对分子质量较高且残渣含量也较高(~10%,后二者为1%~2%)。HPFG的取代度为0.12,根据文献发表的13C-NMR数据确认HPFG分子链上羟丙基取代位置为C6。讨论了香豆胶(半乳甘露聚糖)的化学结构。热重分析法测定的热稳定性,HPFG高于CFG,CFG又高于FG。图6表3参13。     

溶胶-凝胶生物玻璃多孔材料显微结构和生物活性的扫描电镜及红外光谱分析

本文利用溶胶．凝胶法制备了CaO-P2O5-SiO，系统生物活性玻璃，并以其为原料制备了用于骨修复及骨组织工程支架的块状生物活性材料。利用体外实验方法(invitro)结合x射线衍射(XRD)、扫描电子显微镜(SEM)和傅立叶变换红外光谱分析(FTIR)技术对不同烧结工艺制备的材料结构、晶相和生物活性的影响进行了分析研究。研究表明，经800℃和1100℃烧结5min的两种材料均有硅磷酸钙Ca5(PO4)2SjO4微晶相析出。烧结温度越高，析出微晶相的体积比例越大，材料的生物活性则越低。在模拟生理溶液中碳酸羟基磷灰石(HCA)只在烧结体中的玻璃颗粒表面形成，而在其硅磷酸钙Ca5(PO4)2SiO4微晶相表面未发现HCA形成。     

Monitoring Proteolysis During Cheddar Cheese Ripening Using Two-Dimensional Gel Electrophoresis

A 2-D gel electrophoretic method, consisting of isoelectric focusing and alkaline urea-PAGE was used to monitor proteolysis during ripening (180d, 5°C and 8°C) of full- and reduced-fat Cheddar cheese. The method enabled quantifying changes in levels of peptides in cheese with good spot-resolution. Results can complement those from other analyses, especially those for determining low MW peptides. Notable effects were found for cheese composition and ripening temperature on gel pattern and on relative levels of selected proteolysis products. In both cheese varieties, most peptides reached a maximum during the first 3 ripening months and gradually disappeared as ripening advanced.     

CoFe2O4超细微粒催化剂的制备,性能与表征

用溶胶－凝胶法制备了钴铁复合氧化物超细微粒催化剂，用ＴＧ－ＤＴＡ、ＴＥＭ、ＸＲＤ等手段考察了加入聚乙二醇２００对其粉体特性及催化性能的影响，结果表明，添加金属量３％的聚乙二醇２００，可显著改善粒子团聚，得到平均粒径为３０ｎｍ、分散均匀的超细粒子，在３５０℃下焙烧２ｈ，可得到前驱体分解完全，非完整晶态的ＣｏＦｅ２Ｏ４，其对对甲酚催化氧化制取对羟基苯甲醛的性能较好。     

Inter- and intra-molecular ionic interactions of polyampholyte: Carboxymethyl-2-diethylaminoethylcellulose

Carboxymethyl-2-diethylaminoethylcellulose (CM-DEAE cellulose) was prepared by etherification of carboxymethylcellulose with diethylaminoethyl chloride in a NaOH solution. The behaviour of CM-DEAE cellulose in aqueous solution was studied by viscosity and GPC measurements. The degree of substitution (DS) and existing states of DEAE substituents were examined by the use of proton NMR, and those of the CM substituents were observed with FT-IR. The results reveal that the reduced viscosity and apparent molecular size of CM-DEAE cellulose vary with the concentration of sodium chloride and changes in pH and DS. These phenomena can be explained in terms of inter- and intra-molecular ionic interactions.     

高温延缓型有机硼OB-200交联压裂液的性能与应用

报道了实验考察高温延缓型有机硼交联剂OB 200在5g/L羟丙基瓜尔胶水基压裂液中的各项性能及其影响因素的结果,简述了在7口井上应用该压裂液的情况。OB 200/HPG压裂液在pH=11.5、温度5～35(40)℃时交联时间长达4.7～5.6min;不加破胶剂的压裂液在温度115～135℃时,8h内可完全破胶液化,讨论了OB 200体系的自动破胶机制;在135℃、170s-1条件下剪切2h,压裂液粘度>120mPa·s;高速(500s-1)剪切后,在低速下(80s-1)粘度可恢复到初始值的94.5%(95℃下)或70.0%(135℃下);在95～135℃滤失小,滤失系数为6.93×10-4～9.81×10-4m/(min)1/2;残渣含量低,135℃下破胶20h后为319mg/L,而对比硼酸盐压裂液(90℃)和有机钛压裂液(135℃)分别为364和457mg/L;在人造岩心上测得渗透率伤害率在5.74%～9.66%,平均7.32%,而对比有机钛压裂液为24.07%～29.98%,平均27.09%。在中原油田桥口和户部寨地区7口井2706～3769m井段用该压裂液压裂,施工成功率100%,获得了油、气增产效果。图5表4参3。