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油气田含油污泥是石油钻井、运输、储存过程中产生的主要污染物。随着油气田开发的逐步深入,含油污泥所带来的生产和环境矛盾越来越突出。原有的含油污泥处理方式已经不适用新的环保要求。目前,物理化学处理方法初步实现了含油污泥减量化和原油资源回收,但其并不能从根本上去除含油污泥的石油污染物,甚至有可能造成二次污染。生物处理方法有低毒、环保、效率高等特点,具有较广泛的应用前景。本文介绍了含油污泥的来源、特征、处理标准和环境影响。将生物处理技术分为生物表面活性剂(BSF)洗油法和生物降解法,并从BSF的类型和特性、洗油机理、降解工艺、降解菌、对处理效果的影响因素以及BSF增强生物降解作用等方面进行了详细阐述。文章指出BSF洗油法主要应用于高含油污泥(含油率≥6%)的处理,含油率可降到2%以下;对于低含油污泥(含油率≤6%)采用微生物降解技术处理,可达到0.3%的生态标准。生物处理技术是最有前景的满足资源回收的环保型的含油污泥处理技术。 相似文献
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原油的开采和运输过程中会产生大量含油污泥,为了达到资源化,无害化的目标,需要对含油污泥进行处理来达到节约资源保护环境的目的。含油污泥等固体废弃物可以通过热解、填埋、焦化、固化、微生物处理等多种处理技术。含油污泥热解处理技术可以使含油污泥中的原油成分再次利用,不造成资源浪费,并且对含油污泥处理彻底。本文主要讲解热解含油污泥技术,通过改变反应温度、反应时间、升温速率、控制氮气流量和添加催化剂来对含油污泥资源化回收利用进行总结。 相似文献
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为研究含油废水处理产生的剩余污泥和气浮污泥的厌氧消化性能,试验采取序批式厌氧消化两种含油污泥的方法,对含油污泥的组成变化及产气性能进行测定,并将其结果与市政剩余污泥进行对比。试验结果显示,经过35天的厌氧消化,含油剩余污泥和含油气浮污泥的可挥发固体(VS)降解率分别为4.98%和3.74%,TCOD降解率分别为10%和3.4%,产气量分别为0.97 L/gVS和0.56 L/gVS。经过和市政剩余污泥对比后表明,含油气浮污泥厌氧消化性能差,不宜进行厌氧消化处理;含油剩余污泥厌氧消化性能相对强于含油气浮污泥,但弱于市政剩余污泥。 相似文献
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桩基工程施工废弃泥浆直接排放的污染风险较大,需要对其进行处理。因此,以某桩基工程施工废弃泥浆经过絮凝和脱水处理后的絮凝体为研究对象,开展了泥浆固化处理实验研究,以固结体的无侧限抗压强度为评价指标,主要考察了固化剂类型、固化剂掺量、泥浆絮凝体含水量、养护温度和养护时间等因素对固化处理效果的影响。结果表明:不同类型固化剂的加入均能提高固结体的无侧限抗压强度,其中新型复合固化剂GT-2的固化处理效果最好。当实验用泥浆絮凝体的含水量固定在40%时,目标桩基施工废弃泥浆固化处理的最佳实验参数为:选择固化剂类型为新型复合固化剂GT-2,固化剂的掺量为6%,养护温度为35℃,养护时间为28 d。在此实验条件下泥浆固结体的无侧限抗压强度值可以达到0.631 MPa,达到了良好的固化处理效果。现场应用结果表明,新型复合固化剂GT-2的加入能够对现场桩基施工废弃泥浆起到较好的固化效果,并且处理成本较低,具有良好的环境、经济和社会效益。 相似文献
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The effect of the solvent 1-methyl-2-pyrrolidinone (NMP) on the curing of polyimide resins synthesized from pyromellitic dianhydride (PMDA) and 4,4′-oxydianiline (ODA) has been investigated. Three polyimide precursors, i.e., the polyamic acid (PAA), with controlled amount of NMP were prepared. The study was aimed first to independently investigate the decomplexation process, which involved the evolution of hydrogen-bonded NMP from PAA, without interference from imidization. This was accomplished by TGA at varying heating rates using different solvent content in PAA. The observed one-stage decomplexation process suggested that the complex formation of NMP and PAA was not the same as the model compound studied by others. An average value of 150 kJ/mol for the activation energy of the decomplexation process was obtained. The study then sought to identify the effect of the decomplexation on the imidization kinetics by employing DSC at several drying temperatures and also varying heating rates. This allowed one to control the extent of plasticization that occurred to facilitate the imidization process. Our DSC data showed that over-drying PAA resulted in prolonged imidization due mainly to the lack of plasticization by decomplexed NMP. The estimated enthalpy of imidization and that of decomplexation were 114 KJ/mol and 53 kJ/mol NMP, respectively. Finally, the imidization kinetics was independently investigated using FTIR, without the interference from decomplexation process. The results indicated that there were four stages during the entire imidization process. Up to a temperature of 150°C, less than 20% of amide groups had reacted to give imide groups and the reaction was slow. Most of the imidization took place between 150 and 180°C with conversion as high as 90%. The imidization process was completed after the temperature was further raised to 250°C. Above 250°C, the reverse reaction became more significant (due probably to configurational and packing preference) and resulted in a lowering of final conversion back to 80%. © 1992 John Wiley & Sons, Inc. 相似文献
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Summary The curing reaction of diglycidyl ether of Bisphenol A(DGEBA) with triethylene tetramine(TETA) was studied by the differential scanning calorimetry(DSC). The reaction was affected as the vitrification occurred when the glass transition temperature(Tg) of the reaction mixture exceeded the curing temperature. In order to describe the curing reaction in the rubbery state as well as in the glassy state, the reaction kinetic equation containing the generalized WLF equation term was proposed and the parameters were determined from the DSC data.Nomenclature aT
time temperature shift factor, dimensionless
- AT
temperature dependent frequency factor, /sec
- ATg
temperature dependent frequency factor at Tg, /sec
- ATo
temperature dependent frequency factor at Tg, /sec
- A
empirical parameter in temperature dependent frequency factor, dimensionless
- B
empirical parameter in temperature dependent frequency factor, K
- C1
empirical parameter in the generalized WLF equation, dimensionless
- C2
empirical parameter in the generalized WLF equation, K
- D
correction parameter in temperature dependent frequency factor, K
- E
activation energy, cal/mole
- Ex/Em
ratio of lattice energies for crosslinked and uncrosslinked polymer, dimensionless
- Fx/Fm
ratio of segmental mobilities for crosslinked and uncrosslinked polymer, dimensionless
- Ht
cumulative heat generated up to time t, cal/g
- HRXN
heat of reaction under complete conversion, cal/g
- n
reaction order, dimensionless
- S r
scan rate of the DSC experiment, °C/sec
- t
time, second
- T
temperature, K
- Tg
glass transition temperature of the partially cured reaction mixture, K
- Tgo
glass transition temperature of uncured reactant, 253 K
- X
conversion, dimensionless 相似文献
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Nanocomposites of poly(vinyl alcohol) (PVA) with Mg‐Al layered double hydroxides (LDHs) were prepared with different compositions, viz., 2, 4, 6, and 8 wt %, of LDH, by solution‐intercalation method. The effect of LDH contents on thermal, physicomechanical, and morphological property of PVA films were investigated. Differential scanning calorimetric analysis reveals that LDH layers promote a new crystalline phase for PVA. The tensile analysis of PVA/LDH nanocomposites indicates reduction in tensile strength and modulus with change in LDH concentration and moisture. The microstructure analysis by optical microscopy and scanning electron microscopy demonstrates exfoliation and dispersion of LDHs in the PVA matrix in a disorderly fashion. The primary focus of the present investigation is to explore the potential of LDHs as nanofiller in a polyhydroxy polymer without surface modification. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010 相似文献
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考察了硫化体系中硫磺、促进剂M,促进剂TMTD,活性剂硬脂酸用量对再生胶制品拉伸强度以及断裂伸长率的影响.结果表明:适当提高硫化温度能减少硫磺的用量;在硫化温度为140℃,硫化时间为5min的条件下,当硫磺,促进剂M,促进剂TMTD和硬脂酸用量分别为1.5份,0.5份,0.5份,1.5份以及再生胶为100份时,再生胶硫... 相似文献
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The effect of some alcohols, acetylacetonates of transition metals, and manganese stearate and naphthenate on the curing reaction of a diglycidyl ether of ether of bisphenol-A with p-phenylenediamine is studied. Maximum catalytic activity is shown by the manganese compounds and triethanolamine. 相似文献
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The synergistic effect of dicyandiamide (Dicy) and phenolic substances was studied, with resorcinol as a model compound. It was found that when Dicy and resorcinol are used jointly, the curing temperature of epoxy resin can be significantly lowered. FTIR and DSC data were used to illustrate the mechanism of the synergism. The addition of the phenolic hydroxyl group to epoxide was facilitated by Dicy, which favors the formation of phenoxy anions. The reaction of Dicy with epoxide was facilitated by resorcinol, which can exert “electrophilic assistance” for the addition of the amino group to epoxide. The presence of resorcinol also favors the addition of the hydroxyl group to the cyano group. The thermal and mechanical properties of the epoxy resins cured with Dicy/resorcinol or Dicy/phloroglucinol were studied. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 89: 1869–1874, 2003 相似文献
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Summary Poly(phenylene sulfide) (PPS) was cured in the melt and solid states under air and/or nitrogen environments. Crystallization behavior of such cured materials as a function of cure time at 320°C and 255°C was studied via differential scanning calorimetry. It was found, on general, that while short-time curing leads to an increase in crystallization rate, prolonged curing leads to a decrease in both crystallinity and crystallization rate. In contrast to the enhanced crystallization rate caused by curing in nitrogen at the melt state, no significant change of crystallization rate is observed while curing is done in the solid state (in nitrogen). 相似文献