新型配筋小跨高比洞口连梁的性能及设计方法

洞口连梁是钢筋混凝土抗震联肢剪力墙中保证延性及耗能性能的关键部件,但小跨高比洞口连梁因其特殊剪切受力机理,使它在不采取特殊配筋构造措施的前提下难以满足所需的延性要求。本文作者所在研究组通过对小跨高比洞口连梁的剪 弯受力机理的分析研究,提出了一种采用附加对角斜筋和菱形筋的新型配筋方案。经过共计20个接近足尺连梁试件低周反复加载试验证实,这种配筋方案的洞口连梁具有良好的延性及耗能性,且施工难度不大。本文在总结已完成试验结果的基础上,为此类新型配筋小跨高比连梁提出了一整套设计方法,供工程设计及修订国家标准参考。     

Bioactivity of wollastonite/aerogels composites obtained from a TEOS–MTES matrix

Organic–inorganic hybrid materials were synthesized by controlled hydrolysis of tetraethoxysilane (TEOS), methyltrimethoxysilane (MTES), synthetic wollastonite powders and polydimethylsiloxane (PDMS) in an ethanol solution. Aerogels were prepared from acid hydrolysis of TEOS and MTES with different volume ratio in ethanol, followed by addition of wollastonite powder and PDMS in order to obtain aerogels with 20 wt% of PDMS and 5 wt% of CaO of the total silica. Finally, when the wet gels were obtained, they were supercritically dried at 260 °C and 90 bar, in ethanol. In order to obtain its bioactivity, one method for surface activation is based on a wet chemical alkaline treatment. The particular interest of this study is that we introduce hybrid aerogels, in a 1 M solution of NaOH, for 30 s at room temperature. We evaluate the bioactivity of TEOS–MTES aerogel when immersed in a static volume of simulated body fluid (SBF). An apatite layer of spherical-shaped particles of uniform size smaller than 5 microns is observed to form on the surface of the aerogels after 25 days soaking in SBF.     

江西某铁尾矿综合回收铁试验研究

江西某铁矿主要为褐铁矿,该矿含泥含水大且可选性差,据此采用磁化焙烧等选矿方法进行了试验研究.获得了较为理想的试验指标.     

钢框架—支撑体系侧向刚度分析

从弹性位移限制、最小剪重比、重力二阶效应、结构的整体稳定四个方面就钢框架—支撑体系在多遇地震作用下合理确定其抗侧刚度进行分析探讨,以利于工程初步方案的设计。     

Preparation and luminescence of SrAl2O4: Eu2+,Dy3+ phosphors coated with maleic anhydride

In this paper, maleic anhydride is directly coated on the surface of SrAl₂O₄: Eu²⁺, Dy³⁺ (SAO‐ED) phosphors by an interfacial coordination chemistry method. Fourier transform infrared spectroscopy (FTIR), X‐ray photoelectron spectra (XPS), X‐ray diffraction (XRD), and scanning electron microscopy (SEM) methods are used to characterize the coating. The experimental result shows that a dense coating layer is consisting of maleic anhydride coordination with metal ions on the surface of the phosphors and the coating process does not destroy the crystal structure of the phosphors. It is also found that the introduction of maleic anhydride does not change the excitation and emission spectra of SAO‐ED phosphors, but decreases the luminous intensity, which is verified by the photoluminescence (PL) measurement. Afterglow delay curves show that the initial brightness of coated SAO‐ED phosphors decreases, but the afterglow decay rate of coated phosphors is slower than that of uncoated phosphors after they both are immersed into water for one month. This indicates that the coating layer protects the phosphors and the crystal structure of coated phosphors in water was not destroyed.     

Complex-radical copolymerization of <Emphasis Type="Italic">N-</Emphasis>vinyl pyrrolidone with isostructural analogs of maleic anhydride

Radical copolymerizations of N-vinyl-2-pyrrolidone (VP) with isostructural analogs of maleic anhydride (MA), such as citraconic anhydride (CA) and N-substituted maleimides [maleimide (MI), N-ethylmaleimide (EMI) and N-phenylmaleimide (PhMI)] were studied. Compositions of copolymers synthesized in a wide range of monomer feed ratios were determined by alkali titration (for anhydride copolymers), FTIR and ¹H NMR spectroscopy using 1495 and 630 cm^-1 (for VP-MI), 1289 and 1225 cm^-1 (for VP-EMI) and 1050 and 3067 cm^-1 (for VP-PhMI) analytical bands and integral areas of CH₂ (pyrrolidone ring) and CH (MI), CH₃ (EMI) and CH= (benzene ring in PhMI) groups, respectively. Electron-donor VP monomer was found to have substantially different reactivities in the radical copolymerization with MA, CA and N-substituted (H, C₂H₅ and phenyl) malemides as electron-acceptor comonomers. Effects of H-bonding and N→O=C coordination on the monomer reactivity ratios were evaluated. Tendency to alternation of the monomer pairs increases in the order of VP–MA > VP–CA > VP-MI > VP-PhMI > VP-EMI. Structure-thermal property-relationship for the synthesized copolymers was also studied.     

Organochlorine pesticide residues in 4 types of vegetable oils

The present study had as objectives to identify and to quantify organochlorine pesticide residues (OCP) hexachlorobenzene (HCB), lindane, cis-chlordane, heptachlor, aldrin, dieldrin, endrin and o,p'-DDT in vegetable oils of corn, soybean, sunflower and mixtures of oils, sold in the city of Maracaibo, Venezuela. 30 samples of 4 types of vegetable oils of 10 commercial brands were analyzed. The extraction of OCP residues was done according to the Official Method of AOAC. A gas chromatograph with an electronic capture detector (GC-ECD) was used for identification and quantification of OCP residues and confirmation was done with a gas chromatograph coupled with a mass spectrometer (GC-MS). All the OCP residues investigated were detected in the analyzed samples. Aldrin (0.0088), lindane (0.0054) and o,p'-DDT (0.0035) were the OCP residues detected in higher concentrations (microg/g). The statistical analysis showed significant differences (P<0.05) for the concentration of OCP in the different types and commercial brands of vegetable oils. Lindane concentration in the corn oil (0.0125 microg/g), as well as cischlordane (0.0091 microg/g) and aldrín (0.0287 microg/g) in the soybean oil exceeded maximal residual limits (MRL) established by Food and Agriculture Organization of the United Nations/World Health Organization (FAO/WHO). In conclusion, it was detected a high incidence of OCP residues in vegetable oils analyzed.     

煤矸石/粉煤灰对赤泥钠化还原焙烧反应的影响机制

煤矸石或粉煤灰与赤泥协同钠化还原焙烧均可实现其所含铁、铝、硅等元素的形态转化,使其易于分离回收;但对于它们分别与赤泥协同钠化还原焙烧反应差异性及机制的研究目前尚未见报道。采用X射线衍射分析方法,分别考察了煤矸石-赤泥、粉煤灰-赤泥体系钠化还原焙烧过程中,气氛类型、钠助剂添加量、焙烧温度、焙烧时间对还原焙烧产物物相组成的影响规律,并对两个反应体系中铁磁化效果及铝硅活化效果的差异性进行分析。结果表明：在钠化还原焙烧过程中,煤矸石-赤泥、粉煤灰-赤泥体系均可同步实现含铁物相的磁化和铝硅物相的活化,且随着钠助剂添加量、焙烧温度、焙烧时间的变化,含铁物相和铝硅物相呈现规律性变化;在相同铁磁化和铝硅活化效果前提下,煤矸石-赤泥体系所需钠助剂添加量、焙烧温度和焙烧时间均略低于粉煤灰-赤泥体系,这主要与煤矸石、粉煤灰中所含还原性物质和铝硅矿物的赋存形态、含量及微观结构有关。研究将为煤矸石、粉煤灰等煤基固废与赤泥协同钠化还原焙烧回收有价元素的原料筛选提供理论指导。     

酯类化合物降低原油与二氧化碳体系最小混相压力实验

针对试验区近井地带达到混相驱、远井地带尚未达到混相驱的问题,通过注入油溶性表面活性剂(柠檬酸异丁酯或柠檬酸异戊酯)来降低原油与二氧化碳体系的最小混相压力,该表面活性剂既能够溶于原油中降低原油黏度,又能够溶解在超临界二氧化碳中降低原油与二氧化碳之间的界面张力,从而降低原油与二氧化碳之间的最小混相压力。采用长细管驱替实验的方法,测定了2种油溶性表面活性剂对试验区原油与二氧化碳体系的最小混相压力的影响。实验表明,注入的油溶性表面活性剂能够明显降低试验区原油与二氧化碳体系的最小混相压力,2种表面活性剂降低的最小混相压力值分别为7.2 MPa和6.6 MPa,并且随着表面活性剂注入段塞的增大,测得的原油与二氧化碳体系的最小混相压力逐渐降低,但是降低幅度越来越小,结合表面活性剂制备价格,得到最经济的表面活性剂注入段塞量为0.003 PV,并建议选择柠檬酸异丁酯作为试验区降低最小混相压力的化学试剂。