CN111410346B - A kind of waste drilling fluid combined treatment device and method - Google Patents
A kind of waste drilling fluid combined treatment device and method Download PDFInfo
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- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F9/00—Multistage treatment of water, waste water or sewage
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- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/001—Processes for the treatment of water whereby the filtration technique is of importance
- C02F1/002—Processes for the treatment of water whereby the filtration technique is of importance using small portable filters for producing potable water, e.g. personal travel or emergency equipment, survival kits, combat gear
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- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/30—Treatment of water, waste water, or sewage by irradiation
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- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/46—Treatment of water, waste water, or sewage by electrochemical methods
- C02F1/469—Treatment of water, waste water, or sewage by electrochemical methods by electrochemical separation, e.g. by electro-osmosis, electrodialysis, electrophoresis
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- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/52—Treatment of water, waste water, or sewage by flocculation or precipitation of suspended impurities
- C02F1/5236—Treatment of water, waste water, or sewage by flocculation or precipitation of suspended impurities using inorganic agents
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- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F1/00—Treatment of water, waste water, or sewage
- C02F1/52—Treatment of water, waste water, or sewage by flocculation or precipitation of suspended impurities
- C02F1/54—Treatment of water, waste water, or sewage by flocculation or precipitation of suspended impurities using organic material
- C02F1/56—Macromolecular compounds
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- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2101/00—Nature of the contaminant
- C02F2101/10—Inorganic compounds
- C02F2101/20—Heavy metals or heavy metal compounds
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- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2101/00—Nature of the contaminant
- C02F2101/30—Organic compounds
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- C—CHEMISTRY; METALLURGY
- C02—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F—TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
- C02F2101/00—Nature of the contaminant
- C02F2101/30—Organic compounds
- C02F2101/32—Hydrocarbons, e.g. oil
- C02F2101/322—Volatile compounds, e.g. benzene
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Abstract
Description
技术领域technical field
本发明属于钻井液处理技术领域,具体涉及一种废弃钻井液联合处理装置及方法。The invention belongs to the technical field of drilling fluid treatment, and in particular relates to a combined treatment device and method for waste drilling fluid.
背景技术Background technique
钻井液是钻探过程中,孔内使用的循环冲洗介质,钻井液主要功用是:①冷却钻头、清净孔底、带出岩屑。②润滑钻具。③停钻时悬浮岩屑,保护孔壁防止坍塌,平衡地层压力、压住高压油气水层。④输送岩心,为孔底动力机传递破碎孔底岩石需要的动力等。废弃钻井液主要由钻井泥浆、钻井污水、钻屑及压裂作业返排液等组成,总体上表现出高COD值、高pH值、含有大量的泥浆和压裂液中的有机成分、无机盐和钻井液添加剂等,污染物浓度高,处理难度较大。Drilling fluid is the circulating flushing medium used in the hole during the drilling process. The main functions of the drilling fluid are: 1. Cool the drill bit, clean the bottom of the hole, and bring out the cuttings. ② Lubricate the drill. ③ Suspend cuttings when drilling stops, protect the hole wall from collapse, balance the formation pressure, and suppress the high-pressure oil and gas water layer. ④Conveying the core, and transmitting the power required for breaking the rock at the bottom of the hole for the power machine at the bottom of the hole. The waste drilling fluid is mainly composed of drilling mud, drilling sewage, drilling cuttings and fracturing flowback fluid, etc. It generally shows high COD value, high pH value, and contains a large amount of organic components and inorganic salts in the mud and fracturing fluid. And drilling fluid additives, etc., the pollutant concentration is high, and the treatment is difficult.
现有技术中,对于废弃钻井液的处理一般都是采用离心分离的方式,将钻井液中的固相物进行分离,例如申请号201320657605.9的实用新型专利公开了一种废弃油基钻井液回收利用装置,主要由废弃油基钻井液储罐、清水储罐、阀门、加热搅拌罐、破乳剂储罐、三相旋流分离器、回收油储罐、污水回收池、废弃泥沙固化池与固化剂储罐组成,所述废弃油基钻井液储罐、清水储罐与破乳剂储罐通过管道连于加热搅拌罐的上端,管道上均设有阀门加热搅拌罐的底端连于三相旋流分离器的顶端,用于回收油的回收油储罐与三相旋流分离器中部相连,用于盛放污水的污水回收池与废弃泥沙固化池分别与三相旋流分离器的下端与底端向连,污水回收池的底端与固化剂储罐分别与废弃泥沙固化池相连。In the prior art, the treatment of waste drilling fluid generally adopts centrifugal separation to separate the solid phase in the drilling fluid. The device mainly consists of waste oil-based drilling fluid storage tanks, clean water storage tanks, valves, heating and stirring tanks, demulsifier storage tanks, three-phase cyclone separators, recovered oil storage tanks, sewage recovery tanks, waste sediment solidification tanks and solidification tanks. The waste oil-based drilling fluid storage tank, the clean water storage tank and the demulsifier storage tank are connected to the upper end of the heating and stirring tank through a pipeline, and the bottom end of the heating and stirring tank is equipped with a valve on the pipeline, which is connected to the three-phase rotary At the top of the flow separator, the recovered oil storage tank for recovering oil is connected to the middle of the three-phase cyclone separator, and the sewage recovery tank and waste sediment solidification tank for holding sewage are respectively connected with the lower end of the three-phase cyclone separator. Connected to the bottom end, the bottom end of the sewage recovery tank and the solidifying agent storage tank are respectively connected with the waste sediment solidification tank.
申请号为201610566660.5专利公开了一种油气田废弃水基钻井液固液分离方法,The patent application number 201610566660.5 discloses a solid-liquid separation method for waste water-based drilling fluid in oil and gas fields,
(1)新疆地区(1) Xinjiang region
一开阶段膨润土体系废弃水基钻井液,采用静置沉降法,使其中的悬浮固相物质自然沉降,形成污泥,再用过滤法,实现固液分离;In the first stage, the waste water-based drilling fluid of the bentonite system adopts the static settling method, so that the suspended solid phase substances in it are naturally settled to form sludge, and then the filtration method is used to realize the solid-liquid separation;
二开阶段聚合物体系废弃水基钻井液,1m3废弃水基钻井液投加絮凝剂PAC14~15kg,使固相物质凝聚,再用过滤法,滤出固相物质,实现固液分离;In the second stage, the polymer system waste water-based drilling fluid, 1m3 of waste water-based drilling fluid is added with flocculant PAC14~15kg, so that the solid phase material coagulates, and then the filtration method is used to filter out the solid phase material to achieve solid-liquid separation;
三开、四开阶段聚磺体系废弃水基钻井液,1m3废弃水基钻井液投加絮凝剂PAC 14~15kg,助凝剂PAM 0.45~0.6kg;使其中的固相物质凝聚,再用过滤法,滤出固相物质,实现固液分离;Three-stage and four-stage polysulfonic system waste water-based drilling fluid, 1m3 of waste water-based drilling fluid is added with flocculant PAC 14-15kg, and coagulant PAM 0.45-0.6kg; the solid phase material in it is coagulated, and then filtered method to filter out the solid phase material to achieve solid-liquid separation;
(2)川东地区(2) East Sichuan area
一开阶段膨润土体系废弃水基钻井液,采用静置沉降法,使其中的固相物质自然沉降,形成污泥,再用过滤法,实现固液分离;In the first stage, the waste water-based drilling fluid of the bentonite system adopts the static settling method, so that the solid phase material in it is naturally settled to form sludge, and then the filtration method is used to realize the solid-liquid separation;
二开阶段聚合物体系废弃水基钻井液,1m3废弃水基钻井液投加絮凝剂PAC18~20kg、助凝剂PAM0.05~0.06kg、稳定剂2~2.5kg,使其中的固相物质凝聚,再用过滤法,滤出固相物质,实现固液分离;In the second stage, the polymer system waste water-based drilling fluid, 1m3 of waste water-based drilling fluid is added with flocculant PAC18~20kg, coagulant aid PAM0.05~0.06kg, stabilizer 2~2.5kg, so that the solid phase material in it coagulates , and then use the filtration method to filter out the solid phase material to achieve solid-liquid separation;
三开阶段聚磺体系废弃水基钻井液,1m3废弃水基钻井液投加复配破胶剂30~35kg,絮凝剂PAC3~4kg,助凝剂PAM0.05~0.06kg,稳定剂2~2.5kg,使胶体离子破裂,其中的液相物释放,固相物质凝聚,再用过滤法,滤出固相物质,实现固液分离;Three-stage polysulfonic system waste water-based drilling fluid, 1m3 of waste water-based drilling fluid is added with 30~35kg of compound breaker, 3~4kg of flocculant PAC, 0.05~0.06kg of coagulant aid PAM, and 2~2.5kg of stabilizer kg, the colloidal ions are broken, the liquid phase is released, the solid phase is condensed, and then the solid phase is filtered out by filtration to achieve solid-liquid separation;
(3)川西地区(3) Western Sichuan area
一开阶段聚合物体系废弃水基钻井液,1m3废弃水基钻井液投加破胶剂10~11kg,絮凝剂PAC3~5kg、稳定剂4~6kg,使胶体离子破裂,其中的液相物质释放,固相物质凝聚,再用过滤法,滤出固相物质,实现固液分离;In the first stage of the polymer system waste water-based drilling fluid, 1m3 of waste water-based drilling fluid is added with 10-11kg of gel breaker, 3-5kg of flocculant PAC, and 4-6kg of stabilizer to break the colloidal ions and release the liquid phase substances. , the solid phase material is condensed, and then the filtration method is used to filter out the solid phase material to achieve solid-liquid separation;
二开及以后阶段聚磺体系废弃水基钻井液,1m3废弃钻井液投加破胶剂20kg、絮凝剂PAC3~4kg、稳定剂10~12kg,使胶体离子破裂,其中的液相物释放,固相物质凝聚,再用过滤法,滤出固相物质,实现固液分离。In the second stage and later stage, the waste water-based drilling fluid of the polysulfonic acid system, 1m3 of waste drilling fluid is added with 20kg breaker, 3~4kg flocculant PAC, and 10~12kg stabilizer to break the colloidal ions, and the liquid phase in it is released and solidified. The phase material is condensed, and then the solid phase material is filtered out by filtration to achieve solid-liquid separation.
所述絮凝剂PAC是聚合氯化铝,所述助凝剂PAM是聚丙烯酰胺,所述稳定剂是氧化钙,所述破胶剂是硫酸铝,所述复配破胶剂是硫酸铝和硫酸的混合物,其配比为硫酸铝30-35kg:2mol/L的硫酸0.02L。The flocculant PAC is polyaluminum chloride, the coagulation aid PAM is polyacrylamide, the stabilizer is calcium oxide, the gel breaker is aluminum sulfate, and the compound gel breaker is aluminum sulfate and The mixture of sulfuric acid, its proportion is 30-35kg of aluminum sulfate: 0.02L of sulfuric acid of 2mol/L.
所述助凝剂PAM是分子量≥600万的阳离子聚丙烯酰胺。The coagulation aid PAM is a cationic polyacrylamide with a molecular weight of ≥6 million.
又例如申请号为201810283692.3的发明专利公开了一种废弃钻井液固液分离处理方法及应用,包括超声波处理、废弃钻井液离心、固液相分离三个步骤,超声波处理是将废弃钻井液输送至超声波处理装置水槽中,将超声波处理震板等间距放入超声波处理装置水槽,对废弃钻井液进行超声波处理,超声波处理时间分别为15min~60min,超声波处理频率为18kHz~25kHz;废弃钻井液离心是将超声波处理后的废弃钻井液通入到离心机中,对超声波处理后的废弃钻井液进行离心,所述离心机离心时间为10min~60min,离心机离心转速为2000r/min~4000r/min;固液相分离是指对离心机离心后的废弃钻井液进行分离。Another example is the invention patent with the application number of 201810283692.3, which discloses a method and application for solid-liquid separation of waste drilling fluid, including three steps of ultrasonic treatment, waste drilling fluid centrifugation, and solid-liquid phase separation. In the water tank of the ultrasonic treatment device, put the ultrasonic treatment vibration plates into the water tank of the ultrasonic treatment device at equal intervals, and ultrasonically treat the waste drilling fluid. The ultrasonic treatment time is 15min~60min respectively, and the ultrasonic treatment frequency is 18kHz~25kHz; Passing the ultrasonically treated waste drilling fluid into a centrifuge, and centrifuging the ultrasonically treated waste drilling fluid, the centrifugal time of the centrifuge is 10min-60min, and the centrifugal speed of the centrifuge is 2000r/min-4000r/min; Solid-liquid phase separation refers to the separation of waste drilling fluid after centrifugation.
正如上述讲述的现有技术,对于废弃钻井液的处理方法主要是:采用化学处理方法以及离心方法进行固液分离。As described above in the prior art, the treatment methods for the waste drilling fluid are mainly: solid-liquid separation by chemical treatment and centrifugation.
但是由于废弃钻井液中的金属盐离子和微小固相很难通过离心的方式完成分离,从而导致金属盐离子和微小固相分离效果差。However, it is difficult to separate the metal salt ions and the micro solid phase in the waste drilling fluid by centrifugation, resulting in poor separation effect of the metal salt ions and the micro solid phase.
发明内容SUMMARY OF THE INVENTION
本发明为了解决现有废弃钻井液中金属盐离子和微小固相分离效果差的问题,而提供一种废弃钻井液联合处理装置及方法。In order to solve the problem of poor separation effect of metal salt ions and tiny solid phases in the existing waste drilling fluid, the present invention provides a waste drilling fluid joint treatment device and method.
为解决技术问题,本发明所采用的技术方案是:For solving the technical problem, the technical scheme adopted in the present invention is:
一种废弃钻井液联合处理装置,其特征在于,包括电吸附光催化联合处理装置,所述电吸附光催化联合装置包括电吸附箱,所述电吸附箱的左右两侧分别设置有电极板,所述电极板分别与外部的电源连通,所述电极板的两侧分别套设有夹板,所述电吸附箱的上端设置有紫外光灯管,所述紫外光灯管与外部的电源连通。A combined treatment device for waste drilling fluid is characterized in that it includes an electro-adsorption-photocatalysis combined treatment device, the electro-adsorption-photocatalysis combined device includes an electro-adsorption box, and electrode plates are respectively provided on the left and right sides of the electro-adsorption box, The electrode plates are respectively connected with an external power source, the two sides of the electrode plates are respectively sleeved with splints, and the upper end of the electro-adsorption box is provided with an ultraviolet light tube, which is communicated with the external power source.
进一步的,所述电吸附箱的外部设置有第一控制箱,所述第一控制箱内设置有第一电源,所述第一电源与电极板连通,所述第一控制箱上设置有用于控制第一电源的第一电源控制器;所述电吸附箱的外部还设置有第二控制箱,所述第二控制箱内设置有第二电源,所述第二电源与紫外光灯管连通,所述第二控制箱上设置有用于控制第二电源的第二电源控制器。Further, a first control box is arranged outside the electro-adsorption box, a first power supply is arranged in the first control box, the first power supply is communicated with the electrode plate, and a first control box is arranged on the first control box for A first power supply controller for controlling the first power supply; a second control box is also arranged outside the electro-adsorption box, and a second power supply is arranged in the second control box, and the second power supply is communicated with the ultraviolet light tube , the second control box is provided with a second power supply controller for controlling the second power supply.
进一步的,所述电吸附箱的两侧分别设置有排液管和进液管道,所述进液管道连通有第二循环泵。Further, two sides of the electro-adsorption box are respectively provided with a liquid discharge pipe and a liquid inlet pipe, and the liquid inlet pipe is connected with a second circulating pump.
进一步的,所述第二循环泵的进料端设置有过滤箱,所述过滤箱内设置有过滤网,所述第二循环泵的进料端连通在过滤网下端的过滤箱内,所述过滤网上端的过滤箱内经管道和第一循环泵与废弃钻井液连通。Further, the feed end of the second circulating pump is provided with a filter box, the filter box is provided with a filter screen, the feed end of the second circulation pump is connected to the filter box at the lower end of the filter screen, the The filter box at the upper end of the filter screen is communicated with the waste drilling fluid through a pipeline and a first circulating pump.
一种废弃钻井液联合处理方法,其特征在于,包括废弃钻井液联合处理装置,该废弃钻井液联合处理装置对废弃钻井液的处理包括如下步骤:A method for the joint treatment of waste drilling fluid, characterized in that it comprises a joint treatment device for waste drilling fluid, and the treatment of the waste drilling fluid by the joint treatment device for waste drilling fluid comprises the following steps:
(1)预处理;(1) Preprocessing;
(2)过滤;(2) filtering;
(3)电吸附和光催化处理。(3) Electrosorption and photocatalytic treatment.
进一步的,所述预处理包括先向废弃钻井液中加入聚合氯化铝,聚合氯化铝将废弃钻井液中的电荷和胶体脱稳形成细小絮体,并使用搅拌器进行搅拌;然后再加入聚丙烯酰胺再进行搅拌,搅拌后静置然后取上清液。Further, the pretreatment includes adding polyaluminum chloride to the waste drilling fluid first, and the polyaluminum chloride destabilizes the charge and colloid in the waste drilling fluid to form fine flocs, which are stirred with a stirrer; and then add The polyacrylamide was stirred again, and after stirring, it was left to stand and the supernatant was taken.
进一步的,所述聚合氯化铝的加入量为每L废弃钻井液中加入8-12g,所述聚丙烯酰胺的加入量为每L废弃钻井液中加入8-12g;废弃钻井液中加入聚合氯化铝后搅拌时间为25-40min,废弃钻井液中加入聚丙烯酰胺后搅拌时间为5-6.5h;加入聚丙烯酰胺搅拌后静置的时间为20-30h。Further, the polyaluminum chloride is added in an amount of 8-12g per L of waste drilling fluid, and the polyacrylamide is added in an amount of 8-12g per L of discarded drilling fluid; The stirring time after aluminum chloride is 25-40min, the stirring time after adding polyacrylamide to the waste drilling fluid is 5-6.5h; the stirring time after adding polyacrylamide is 20-30h.
进一步的,所述过滤为利用过滤箱中的过滤网的滤掉上清液中的块状物及杂质。Further, the filtration is to filter out lumps and impurities in the supernatant by using the filter screen in the filter box.
进一步的,所述电吸附和光催化处理包括:Further, the electrosorption and photocatalytic treatment includes:
(1)电吸附箱中的两个电极板之间电压为20-40v,两个电极板之间的间距为0.8-5cm;两个电极板施加电压的时间为25-60min;(1) The voltage between the two electrode plates in the electro-adsorption box is 20-40v, and the distance between the two electrode plates is 0.8-5cm; the time for applying the voltage to the two electrode plates is 25-60min;
(2)向进入到电吸附箱中的上清液中加入TIO2-石墨烯复合光催化剂,所述TIO2-石墨烯复合光催化剂的加入量为每L废弃钻井液中加入0.45-0.55mg,所述紫外光灯管发出的紫外光的波长为350-370nm,所述紫外光灯管的功率为10-20w。(2) adding TIO 2 -graphene composite photocatalyst to the supernatant liquid entering the electrosorption box, the addition amount of the TIO 2 -graphene composite photocatalyst is to add 0.45-0.55mg per L of waste drilling fluid , the wavelength of the ultraviolet light emitted by the ultraviolet light tube is 350-370nm, and the power of the ultraviolet light tube is 10-20w.
进一步的,所述紫外光灯管的照射时间为50-70min。Further, the irradiation time of the ultraviolet light tube is 50-70 min.
与现有技术相比,本发明具有以下有益效果:Compared with the prior art, the present invention has the following beneficial effects:
本发明的废弃钻井液联合处理装置,对废弃钻井液通过电吸附和光催化进行联合处理,在处理过程中,两个电极板之间施加电压形成电场用于对废弃钻井液当中的金属盐离子和微小固相进行有效的吸附,吸附后的金属盐离子(Na+,Mg2+,Al3+,Ca2+,K+,Hg2+,Pb2+,Cu2+)和微小固相粘附在夹板上,当需要对夹板上的金属盐离子和微小孤星进行清除时,取下夹板清理干净或者重新套上夹板即可进行连续作业;同时在电吸附的时候,在废弃钻井液中加入TIO2-石墨烯复合光催化剂并通过紫外光灯管进行照射,在紫外光照射作用下,TiO2纳米粒子价带电子受激发而跃迁到导带,光生电子与空穴发生分离,电子流导入石墨烯片层结构中,石墨烯良好的导电性抑制了空穴与电子的复合几率,大大提高了TiO2半导体光催化的活性。另一方面,石墨烯表面积较大,表面有丰富的∏-∏共轭键,可以将含有苯环的有机物吸附到表面上,提供较多的光催化位,从而提高金属盐离子、微小固相以及有机物的吸附能力。经试验,本发明的金属盐离子吸附脱出率为60-70%,同时能够将废弃钻井液中的固相颗粒含量从70%降低至54.9-55.3%之间,从而极大的提高了对废弃钻井液中固相颗粒的吸附能力;同时还能够降低废弃钻井液中固相颗粒的粒径。The waste drilling fluid combined treatment device of the present invention performs combined treatment on the waste drilling fluid through electro-adsorption and photocatalysis. During the treatment process, a voltage is applied between the two electrode plates to form an electric field, which is used to treat the metal salt ions and the metal salt ions in the waste drilling fluid. The micro-solid phase performs effective adsorption, and the adsorbed metal salt ions (Na + , Mg 2+ , Al 3+ , Ca 2+ , K + , Hg 2+ , Pb 2+ , Cu 2+ ) and the micro-solid phase stick to It is attached to the splint. When the metal salt ions and tiny lone stars on the splint need to be removed, the splint can be removed to clean it up or put on the splint again for continuous operation. The TIO 2 -graphene composite photocatalyst is added and irradiated by an ultraviolet light tube. Under the action of ultraviolet light, the electrons in the valence band of TiO 2 nanoparticles are excited and transition to the conduction band, the photogenerated electrons and holes are separated, and the electron flow Introduced into the graphene sheet structure, the good electrical conductivity of graphene inhibits the recombination probability of holes and electrons, and greatly improves the photocatalytic activity of TiO2 semiconductors. On the other hand, graphene has a large surface area and abundant ∏-∏ conjugated bonds on the surface, which can adsorb organic substances containing benzene rings onto the surface, providing more photocatalytic sites, thereby increasing the concentration of metal salt ions, micro-solid phase and the adsorption capacity of organic matter. Tests show that the metal salt ion adsorption and removal rate of the present invention is 60-70%, and at the same time, the solid phase particle content in the waste drilling fluid can be reduced from 70% to 54.9-55.3%, thereby greatly improving the efficiency of waste drilling. The adsorption capacity of solid phase particles in drilling fluid; at the same time, it can also reduce the particle size of solid phase particles in waste drilling fluid.
附图说明Description of drawings
图1为本发明的废弃钻井液联合处理装置一实施例的结构示意图;1 is a schematic structural diagram of an embodiment of the waste drilling fluid combined treatment device of the present invention;
图2为图1的剖视图示意图;Fig. 2 is the schematic sectional view of Fig. 1;
图3为未经过本发明处理之前的固相颗粒的粒径分布表;该图表中左侧的曲线代表粒径点,右侧的曲线代表固相颗粒的累积含量;Fig. 3 is the particle size distribution table of the solid phase particles before being processed by the present invention; the curve on the left side of the graph represents the particle size point, and the curve on the right side represents the cumulative content of the solid phase particles;
图4为本发明处理之后的固相颗粒的粒径分布表;该图表中左侧的曲线代表粒径点,右侧的曲线代表固相颗粒的累积含量;Fig. 4 is the particle size distribution table of the solid phase particles after the treatment of the present invention; the curve on the left side of the graph represents the particle size point, and the curve on the right side represents the cumulative content of the solid phase particles;
图中标记:1、过滤箱,2、框体,3、过滤网,4、第一导流管,5、第一循环泵,6、第一机箱,7、进液管,8、第二导流管,9、第二循环泵,10、第二机箱,11、第三导流管,12、电吸附箱,13、活性炭纤维布,14、电极板,15、第一控制箱,16、第一电源控制器,17、第一导线,18、排液管,19、排液阀门,20、立柱,21、顶板,22、第二导线,23、第二控制箱,24、第二电源控制器25、紫外光灯管。Labels in the figure: 1, filter box, 2, frame, 3, filter screen, 4, first guide pipe, 5, first circulation pump, 6, first chassis, 7, liquid inlet pipe, 8, second Draft tube, 9, Second circulating pump, 10, Second chassis, 11, Third draft tube, 12, Electrosorption box, 13, Activated carbon fiber cloth, 14, Electrode plate, 15, First control box, 16 , the first power controller, 17, the first wire, 18, the drain pipe, 19, the drain valve, 20, the column, 21, the top plate, 22, the second wire, 23, the second control box, 24, the
具体实施方式Detailed ways
下面结合实施例对本发明作进一步的描述,所描述的实施例仅仅是本发明一部分实施例,并不是全部的实施例。基于本发明中的实施例,本领域的普通技术人员在没有做出创造性劳动前提下所获得的其他所用实施例,都属于本发明的保护范围。The present invention will be further described below with reference to the embodiments, and the described embodiments are only a part of the embodiments of the present invention, not all of the embodiments. Based on the embodiments of the present invention, other used embodiments obtained by persons of ordinary skill in the art without creative efforts shall fall within the protection scope of the present invention.
在本发明的描述中,需要说明的是,术语“中心”、“上”、“下”、“左”、“右”、“竖直”、“水平”、“内”、“外”等指示的方位或位置关系为基于附图所示的方位或位置关系,仅是为了便于描述本发明和简化描述,而不是指示或暗示所指的装置或元件必须具有特定的方位、以特定的方位构造和操作,因此不能理解为对本发明的限制;术语“第一”、“第二”、“第三”仅用于描述目的,而不能理解为指示或暗示相对重要性;此外,除非另有明确的规定和限定,术语“安装”、“相连”、“连接”应做广义理解,例如,可以是固定连接,也可以是可拆卸连接,或一体地连接;可以是机械连接,也可以是电连接;可以是直接相连,也可以通过中间媒介间接相连,可以是两个元件内部的连通。对于本领域的普通技术人员而言,可以具体情况理解上述术语在本发明中的具体含义。In the description of the present invention, it should be noted that the terms "center", "upper", "lower", "left", "right", "vertical", "horizontal", "inner", "outer", etc. The indicated orientation or positional relationship is based on the orientation or positional relationship shown in the accompanying drawings, which is only for the convenience of describing the present invention and simplifying the description, rather than indicating or implying that the indicated device or element must have a specific orientation or a specific orientation. construction and operation, and therefore should not be construed as limiting the invention; the terms "first", "second", "third" are used for descriptive purposes only and should not be construed as indicating or implying relative importance; furthermore, unless otherwise Clearly stipulated and defined, the terms "installed", "connected" and "connected" should be understood in a broad sense, for example, it may be a fixed connection, a detachable connection, or an integral connection; it may be a mechanical connection or a Electrical connection; it can be directly connected, or indirectly connected through an intermediate medium, and it can be the internal connection of two components. For those of ordinary skill in the art, the specific meanings of the above terms in the present invention can be understood in specific situations.
结合附图,本发明的废弃钻井液联合处理装置,包括电吸附光催化联合处理装置,所述电吸附光催化联合装置包括电吸附箱12,所述电吸附箱12的左右两侧分别设置有电极板14,所述电极板14分别与外部的电源连通,所述电极板14的两侧分别套设有夹板13,所述电吸附箱12的上端设置有紫外光灯管25,所述紫外光灯管25与外部的电源连通。With reference to the accompanying drawings, the combined treatment device for waste drilling fluid of the present invention includes an electro-adsorption photocatalysis combined treatment device, and the electro-adsorption photocatalysis combined device includes an electro-
进一步的,所述电吸附箱12的外部设置有第一控制箱15,所述第一控制箱15内设置有第一电源,所述第一电源与电极板14连通,所述第一控制箱15上设置有用于控制第一电源的第一电源控制器16;所述电吸附箱12的外部还设置有第二控制箱23,所述第二控制箱23内设置有第二电源,所述第二电源与紫外光灯管25连通,所述第二控制箱23上设置有用于控制第二电源的第二电源控制器24。Further, a
其中第一控制箱15用于安装和固定第一电源、第一电源控制器16,第二控制箱23用于安装和固定第二电源和第二电源控制器24。其中第一电源控制器和第二电源控制器均属于现有技术产品,本领域的技术人员都能明白和理解,在此不再赘述。The
在一些实施例中,紫外光灯管25经第二导线22与第二电源控制器24连接,电极板14经过第一导线17与第一电源控制器16连接。In some embodiments, the
例如本发明的电源控制器采用采用的是天津荣兴凯盛电热材料有限公司生产的BJW-51型号及其相关的配套电源和电路。该型号的电源控制器的技术参数为:电压380v,BJW-51的控制器温度0-200℃。For example, the power supply controller of the present invention adopts the BJW-51 model produced by Tianjin Rongxing Kaisheng Electric Heating Material Co., Ltd. and its related supporting power supply and circuit. The technical parameters of this type of power controller are: voltage 380v, controller temperature of BJW-51 0-200℃.
在一些实施例中,所述电吸附箱12的两个相对的内壁对称固接有八个相同的夹板13,每两个所述夹板13为一组,四组所述夹板13分别夹持在两个电机板14的两侧,便于固定电机板14。其中电吸附箱12左右两内壁的电机板14根据电吸附箱12在竖直方向上的中轴线对称设置。In some embodiments, the two opposite inner walls of the electro-
在一些实施例中,夹板13采用活性炭纤维布制作而成,活性炭纤维布制作而成的夹板13不仅能够实现对电极片14的夹持,同时也便于电吸附箱12电吸附完成后,便于从活性炭纤维布上挂下吸附的固相和重金属。In some embodiments, the splint 13 is made of activated carbon fiber cloth, and the splint 13 made of activated carbon fiber cloth can not only realize the clamping of the
在一些实施例中,电吸附箱12的上部安装有立柱20、立柱20的上端安装有顶板21,紫外光灯管25安装在顶板21上,从而使得紫外光灯管25发出的紫外线能够对电吸附箱12内钻井液进行照射。In some embodiments, a
进一步的,所述电吸附箱12的两侧分别设置有排液管18和进液管道,所述进液管道连通有第二循环泵9。其中,排液管18上设置有排液阀门19,排液阀门19用于控制排液管18的开闭;电吸附箱的进液管道用于与第三导流管11连通,第三导流管11连通与第二循环泵9连通,即是说电吸附箱12的进液管道经过第三导流管11与第二循环泵9连通。Further, two sides of the electro-
在一些实施例中,电吸附箱12的进液管道也可以直接与第二循环泵9连通。In some embodiments, the liquid inlet pipeline of the electro-
进一步的,所述第二循环泵9的进料端设置有过滤箱1,所述过滤箱1内设置有过滤网3,所述第二循环泵9的进料端连通在过滤网3下端的过滤箱1内,所述过滤网3上端的过滤箱1内经管道和第一循环泵5与废弃钻井液连通。即是说,第二循环泵9的进料端用于与过滤网3下方的过滤箱连通,第二循环泵9的出料端用于与电吸附箱12连通。其中,过滤网3的目数的大小决定了滤网的孔径,作为本发明一种优选的方式,为了提高过滤网3的过滤效果,过滤网3的目数为400目(过滤网孔径为38微米左右),从而使得过滤网能够过滤出1-2微米的固相颗粒,以降低后续电吸附箱1的工作量。其中过滤网3便于过滤钻井液内的块状物、工业垃圾以及部分固相。Further, the feed end of the second circulating
在一些实施例中,第二循环泵9的进料端连通有第二导流管8,第二导流管8的一端与第二循环泵9的进料端连通,第二导流管8的另一端与过滤网3下方的过滤箱1连通。In some embodiments, the feed end of the
在一些实施例中,过滤箱1的上端安装有框体2,过滤网3安装在框体2内,通过框体用于对过滤网3进行固定。In some embodiments, a frame body 2 is installed on the upper end of the
在一些实施例中,过滤网3上端的过滤箱上安装有第一导流管4,第一导流管4用于与第一循环泵5连通,第一循环泵5的进料端连通有用于伸入到废弃钻井液中的进液管7。在一些实施例中,为了能够在野外对第一循环泵5和第二循环泵9进行保护,同时也便于安装和运输,第一循环泵5安装在第一机箱6内,第二循环泵9安装在第二机箱10内。In some embodiments, a first guide pipe 4 is installed on the filter box at the upper end of the filter screen 3, the first guide pipe 4 is used for communicating with the first circulating pump 5, and the feed end of the first circulating pump 5 is useful for communicating with In the
其中,第一循环泵5和第二循环泵9均属于现有技术产品,本领域的技术人员都能明白和理解,例如第一循环泵5和第二循环泵9均采用上海贝德泵业有限公司生产的ISG型号及其相关的配套电源和电路。Among them, the first circulating pump 5 and the second circulating
该ISG型号的循环泵型号说明如下:The description of the circulating pump model of this ISG model is as follows:
ISG50-160(I)A(B) 50----泵进出口直径为50mm,160----叶轮名义外径为160mm,I---流量分类,A---叶轮外径切割代号,ISG-----单级单吸管道离心泵。ISG50-160(I)A(B) 50----The diameter of the pump inlet and outlet is 50mm, 160----The nominal outer diameter of the impeller is 160mm, I---Flow classification, A---Impeller outer diameter cutting code , ISG-----single-stage single-suction pipeline centrifugal pump.
为了与该型号的循环泵相互对应,进液管7和排液管18的管径50mm,与此同时,第一导流管4、第二导流管8和第三导流管11的管径均为50mm。In order to correspond to the circulating pump of this model, the diameter of the
本发明提供的废弃钻井液联合处理方法,包括废弃钻井液联合处理装置,对于废弃钻井液联合处理装置的结构在前面已经进行描述,在此不再赘述。该废弃钻井液联合处理装置对废弃钻井液的处理包括如下步骤:The method for joint treatment of waste drilling fluid provided by the present invention includes a joint treatment device for waste drilling fluid. The structure of the joint treatment device for waste drilling fluid has been described above, and will not be repeated here. The treatment of the waste drilling fluid by the waste drilling fluid combined treatment device includes the following steps:
(1)预处理;(1) Preprocessing;
(2)过滤;(2) filtering;
(3)电吸附和光催化处理。(3) Electrosorption and photocatalytic treatment.
进一步的,所述预处理包括先向废弃钻井液中加入聚合氯化铝(PAC),聚合氯化铝将废弃钻井液中的电荷和胶体脱稳形成细小絮体,并使用搅拌器进行搅拌;然后再加入聚丙烯酰胺(PAM)再进行搅拌,搅拌后静置然后取上清液。Further, the pretreatment includes adding polyaluminum chloride (PAC) to the waste drilling fluid first, and the PAC destabilizes the charge and colloid in the waste drilling fluid to form fine flocs, and stirs with a stirrer; Then, polyacrylamide (PAM) was added and the mixture was stirred. After stirring, the mixture was allowed to stand and the supernatant was collected.
进一步的,所述聚合氯化铝的加入量为每L废弃钻井液中加入8-12g,所述聚丙烯酰胺的加入量为每L废弃钻井液中加入8-12g;废弃钻井液中加入聚合氯化铝后搅拌时间为25-40min,废弃钻井液中加入聚丙烯酰胺后搅拌时间为5-6.5h;加入聚丙烯酰胺搅拌后静置的时间为20-30h。Further, the polyaluminum chloride is added in an amount of 8-12g per L of waste drilling fluid, and the polyacrylamide is added in an amount of 8-12g per L of discarded drilling fluid; The stirring time after aluminum chloride is 25-40min, the stirring time after adding polyacrylamide to the waste drilling fluid is 5-6.5h; the stirring time after adding polyacrylamide is 20-30h.
进一步的,所述过滤为利用过滤箱中的过滤网滤掉预处理之后的上清液中的块状物及杂质。Further, the filtration is to use the filter screen in the filter box to filter out lumps and impurities in the pretreated supernatant.
进一步的,所述电吸附和光催化处理包括:Further, the electrosorption and photocatalytic treatment includes:
(1)电吸附箱中的两个电极板之间电压为20-40v,两个电极板之间的间距为0.8-5cm;两个电极板施加电压的时间为25-60min;(1) The voltage between the two electrode plates in the electro-adsorption box is 20-40v, and the distance between the two electrode plates is 0.8-5cm; the time for applying the voltage to the two electrode plates is 25-60min;
(2)向进入到电吸附箱中的上清液中加入TIO2-石墨烯复合光催化剂,所述TIO2-石墨烯复合光催化剂的加入量为每L废弃钻井液中加入0.45-0.55mg,所述紫外光灯管发出的紫外光的波长为350-370nm,所述紫外光灯管的功率为10-20w。(2) adding TIO 2 -graphene composite photocatalyst to the supernatant liquid entering the electrosorption box, the addition amount of the TIO 2 -graphene composite photocatalyst is to add 0.45-0.55mg per L of waste drilling fluid , the wavelength of the ultraviolet light emitted by the ultraviolet light tube is 350-370nm, and the power of the ultraviolet light tube is 10-20w.
在一些实施例中,所述TIO2-石墨烯复合光催化剂的加入量为每L废弃钻井液中加入0.5mg。In some embodiments, the TIO 2 -graphene composite photocatalyst is added in an amount of 0.5 mg per L of waste drilling fluid.
在一些实施例中,TIO2-石墨烯复合光催化剂的加入时间可以为步骤(1)中预处理之后得到的上清液中直接加入,也可以直接向先吸附向内进行加入。In some embodiments, the adding time of TIO 2 -graphene composite photocatalyst can be directly added to the supernatant obtained after pretreatment in step (1), or directly added to the first adsorption inward.
进一步的,所述步骤(3)电吸附和光催化处理包括:先进行光催化处理一段时间,然后光催化处理和电吸附同时处理一段时间。Further, the step (3) of the electrosorption and photocatalytic treatment includes: firstly performing the photocatalytic treatment for a period of time, and then performing the photocatalytic treatment and the electrosorption treatment simultaneously for a period of time.
进一步的,所述步骤(3)中,电吸附箱中的两个电极板之间电压为30-36v,两个电极板之间的间距为1-2.5cm;两个电极板施加电压的时间为30-35min。在这个条件下,既能够保证电吸附效果最好,同时也能够使得光催化剂的活性达到最高值,从而提高金属盐离子和微小固相的吸附能力。Further, in the step (3), the voltage between the two electrode plates in the electro-adsorption box is 30-36v, and the distance between the two electrode plates is 1-2.5cm; the time for applying the voltage to the two electrode plates for 30-35min. Under this condition, it can not only ensure the best electrosorption effect, but also make the activity of the photocatalyst reach the highest value, thereby improving the adsorption capacity of metal salt ions and tiny solid phases.
进一步的,先进行光催化处理25-35min,然后光催化处理和电吸附再一起进行30-35min,先通过紫外光灯管处理25-35min之后,再同时进行光催化处理和电吸附,能够使得光催化剂和活性达到最好,从而提高金属盐离子和微小固相的吸附能力。Further, the photocatalytic treatment is carried out for 25-35min first, then the photocatalytic treatment and the electrosorption are carried out together for 30-35min, and then the photocatalytic treatment and the electrosorption are carried out at the same time after being treated by an ultraviolet lamp for 25-35min. The photocatalyst and activity are maximized, thereby improving the adsorption capacity of metal salt ions and tiny solid phases.
进一步的,所述紫外光灯管的照射时间为50-70min。Further, the irradiation time of the ultraviolet light tube is 50-70 min.
废弃钻井液在经过预处理后,取上清液样品50ml,利用固相含量测定仪进行室内试验,可以测出预处理后的上清液中的固相含量为70%。经过电吸附和光催化处理之后的试验数据表如下:After the waste drilling fluid is pretreated, take a 50ml sample of the supernatant, and use a solid phase content analyzer to conduct an indoor test. It can be measured that the solid phase content in the pretreated supernatant is 70%. The experimental data table after electrosorption and photocatalytic treatment is as follows:
通过上述表可以直观看出,本发明经过电吸附和光催化处理之后,能够大幅度降低钻井液中的固相含量,固相颗粒含量能够从原来的70%降低至54.9-55.3%之间。It can be seen intuitively from the above table that the present invention can greatly reduce the solid phase content in the drilling fluid after electrosorption and photocatalytic treatment, and the solid phase particle content can be reduced from the original 70% to 54.9-55.3%.
本发明的固相含量的主要是通过作差法计算得出对应条件下的固相颗粒吸附量(即微小固相和重金属盐离子),实验前利用固相含量测定仪测出固相含量的百分比,实验后,每次吸附量(包括固相颗粒和重金属盐离子)的多少表征在活性炭纤维布上,利用烘箱烘干,称量累加起来,可以计算出固相颗粒也就是杂质的去除量,进而计算出去除率。正因为如此,本发明的夹板采用活性炭纤维布的作用不仅能够起到夹持电极板的作用,同时由于活性炭纤维布的特性,能够尽可能的减少固相颗粒的粘附,从而提高测量的准确性。The solid phase content of the present invention is mainly calculated by the difference method to obtain the adsorption amount of the solid phase particles (that is, the tiny solid phase and heavy metal salt ions) under the corresponding conditions. Before the experiment, the solid phase content analyzer is used to measure the solid phase content. Percentage, after the experiment, the amount of each adsorption (including solid phase particles and heavy metal salt ions) is represented on the activated carbon fiber cloth, dried in an oven, weighed and accumulated, and the solid phase particles, that is, the removal of impurities, can be calculated. , and then calculate the removal rate. Because of this, the function of using the activated carbon fiber cloth for the splint of the present invention can not only play the role of clamping the electrode plate, but at the same time, due to the characteristics of the activated carbon fiber cloth, the adhesion of solid phase particles can be reduced as much as possible, thereby improving the accuracy of measurement. sex.
在本发明的装置处理之前,利用激光粒度仪对预处理后的废弃钻井液粒度分布进行测定,测定的粒径分布情况如附图3所示,该附图3中的图表中左侧的曲线代表粒径点,右侧的曲线代表固相颗粒的累积含量。Before being processed by the device of the present invention, the particle size distribution of the pretreated waste drilling fluid is measured by using a laser particle size analyzer. The measured particle size distribution is shown in FIG. 3 , and the curve on the left side of the graph in FIG. 3 represents the particle size point, and the curve on the right represents the cumulative content of solid phase particles.
经过本发明处理之后的粒径分布情况如附图4所示,该附图4中的图表中左侧的曲线代表粒径点,右侧的曲线代表固相颗粒的累积含量。The particle size distribution after the treatment of the present invention is shown in FIG. 4 . The curve on the left side of the graph in FIG. 4 represents the particle size point, and the curve on the right side represents the cumulative content of solid phase particles.
通过附图3和附图4的对比可以直观的看出,本发明能够降低废弃钻井液中的固相含量的粒径,从而便于后续加工对废弃钻井液进行循环使用,解决了现有中废弃钻井液中由于固相含量的粒径不达标而无法重新加工循环使用的难题。It can be seen intuitively from the comparison of Fig. 3 and Fig. 4 that the present invention can reduce the particle size of the solid phase content in the waste drilling fluid, thereby facilitating the recycling of the waste drilling fluid in subsequent processing, and solving the problem of waste drilling fluid in the existing The problem that the drilling fluid cannot be reprocessed and recycled because the particle size of the solid phase content is not up to standard.
综上,本发明的废弃钻井液联合处理装置,对废弃钻井液通过电吸附和光催化进行联合处理,在处理过程中,两个电极板之间施加电压形成电场用于对废弃钻井液当中的金属盐离子和微小固相进行有效的吸附,吸附后的金属盐离子(Na+,Mg2+,Al3+,Ca2+,K+,Hg2 +,Pb2+,Cu2+)和微小固相粘附在夹板上,当需要对夹板上的金属盐离子和微小孤星进行清除时,取下夹板清理干净或者重新套上夹板即可进行连续作业;同时在电吸附的时候,在废弃钻井液中加入TIO2-石墨烯复合光催化剂并通过紫外光灯管进行照射,在紫外光照射作用下,TiO2纳米粒子价带电子受激发而跃迁到导带,光生电子与空穴发生分离,电子流导入石墨烯片层结构中,石墨烯良好的导电性抑制了空穴与电子的复合几率,大大提高了TiO2半导体光催化的活性。另一方面,石墨烯表面积较大,表面有丰富的∏-∏共轭键,可以将含有苯环的有机物吸附到表面上,提供较多的光催化位,从而提高金属盐离子、微小固相以及有机物的吸附能力,经试验,本发明的金属盐离子吸附脱出率为60-70%,相比于现有技术,能够提高金属盐离子吸附脱出率,解决了现有技术中由于金属盐离子由于含量过高而使得废弃钻井液不能回收循环利用的问题,同时能够将废弃钻井液中的固相含量从70%降低至54.9-55.3%之间,从而极大的提高了对废弃钻井液中固相颗粒含量的吸附能力;同时还能够降低废弃钻井液中固相颗粒的粒径。To sum up, the waste drilling fluid joint treatment device of the present invention performs combined treatment of waste drilling fluid through electro-adsorption and photocatalysis. During the treatment process, a voltage is applied between two electrode plates to form an electric field, which is used to treat the metals in the waste drilling fluid. The salt ions and the micro solid phase are effectively adsorbed, and the adsorbed metal salt ions (Na + , Mg 2+ , Al 3+ , Ca 2+ , K + , Hg 2 + , Pb 2+ , Cu 2+ ) and micro The solid phase adheres to the splint. When it is necessary to remove the metal salt ions and tiny lone stars on the splint, the splint can be removed to clean it up or put on the splint again for continuous operation. The TIO 2 -graphene composite photocatalyst is added to the drilling fluid and irradiated by an ultraviolet light tube. Under the action of ultraviolet light, the electrons in the valence band of TiO 2 nanoparticles are excited and transition to the conduction band, and the photogenerated electrons and holes are separated. , the electron flow is introduced into the graphene sheet structure, and the good electrical conductivity of graphene inhibits the recombination probability of holes and electrons, which greatly improves the photocatalytic activity of TiO 2 semiconductors. On the other hand, graphene has a large surface area and abundant ∏-∏ conjugated bonds on the surface, which can adsorb organic substances containing benzene rings onto the surface, providing more photocatalytic sites, thereby increasing the concentration of metal salt ions, micro-solid phase And the adsorption capacity of organic matter, after testing, the metal salt ion adsorption and removal rate of the present invention is 60-70%. Due to the high content, the waste drilling fluid cannot be recycled and reused. At the same time, the solid phase content in the waste drilling fluid can be reduced from 70% to 54.9-55.3%, which greatly improves the efficiency of the waste drilling fluid. The adsorption capacity of solid phase particle content; at the same time, it can also reduce the particle size of solid phase particles in the waste drilling fluid.
以上,仅为本发明较佳实施例,并非对本发明任何形式上和实质上的限制,应当指出,对于本技术领域的普通技术人员,在不脱离本发明方法的前提下,还将可以做出若干改进和补充,这些改进和补充也应视为本发明的保护范围。凡熟悉本专业的技术人员,在不脱离本发明的精神和范围的情况下,当可利用以上所揭示的技术内容而做出的些许更动、修饰与演变的等同变化,均为本发明的等效实施例;同时,凡依据本发明的实质技术对上述实施例所作的任何等同变化的更动、修饰与演变,均仍属于本发明的技术方案的范围内。The above are only preferred embodiments of the present invention, and are not intended to limit the present invention in any form or substance. It should be pointed out that those of ordinary skill in the art can make Several improvements and supplements should also be regarded as the protection scope of the present invention. All those skilled in the art, without departing from the spirit and scope of the present invention, can utilize the above-disclosed technical content to make some changes, modifications and equivalent changes of evolution, all belong to the present invention. Equivalent embodiments; at the same time, any modification, modification and evolution of any equivalent changes made to the above embodiments according to the essential technology of the present invention still fall within the scope of the technical solutions of the present invention.
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Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN2784393Y (en) * | 2004-12-27 | 2006-05-31 | 中国科学院广州地球化学研究所 | Apparatus for treating waste water in oil production |
| CN102757143A (en) * | 2012-08-14 | 2012-10-31 | 成都凯迈科技有限公司 | Well drilling wastewater flocculation precipitation treatment device and wastewater treating method |
| CN104829019A (en) * | 2015-04-28 | 2015-08-12 | 上海大学 | Photo-electric organic wastewater co-processing method based on graphene material and device thereof |
| CN205838748U (en) * | 2016-07-20 | 2016-12-28 | 成都恩承科技股份有限公司 | A kind of oil gas field waste horizontal stand processing system |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8347960B2 (en) * | 2010-01-25 | 2013-01-08 | Water Tectonics, Inc. | Method for using electrocoagulation in hydraulic fracturing |
| AU2014334657B2 (en) * | 2013-10-15 | 2017-06-29 | Halliburton Energy Services, Inc. | Methods of separating impurities from industrial minerals using electrocoagulation |
| US11046595B2 (en) * | 2014-05-23 | 2021-06-29 | Hydrus Technology Pty. Ltd. | Electrochemical treatment methods |
| CN110591670B (en) * | 2019-09-20 | 2021-11-09 | 西南石油大学 | Environment-friendly filtrate reducer for water-based drilling fluid, preparation method of filtrate reducer and drilling fluid |
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Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN2784393Y (en) * | 2004-12-27 | 2006-05-31 | 中国科学院广州地球化学研究所 | Apparatus for treating waste water in oil production |
| CN102757143A (en) * | 2012-08-14 | 2012-10-31 | 成都凯迈科技有限公司 | Well drilling wastewater flocculation precipitation treatment device and wastewater treating method |
| CN104829019A (en) * | 2015-04-28 | 2015-08-12 | 上海大学 | Photo-electric organic wastewater co-processing method based on graphene material and device thereof |
| CN205838748U (en) * | 2016-07-20 | 2016-12-28 | 成都恩承科技股份有限公司 | A kind of oil gas field waste horizontal stand processing system |
Non-Patent Citations (3)
| Title |
|---|
| "Functional characterization on colloidal suspensions containing xanthan gum (XGD) and polyanionic cellulose (PAC) used in drilling fluids for a shale formation";Villada, Y et al.;《 APPLIED CLAY SCIENCE 》;20171201;第149卷;第59-66页 * |
| "PAC-PAM复合混凝处理钻井液废水研究";邓磊等;《广州化工》;20170630;第45卷(第11期);第89-90页第1.3节以及第2-3节 * |
| "混凝沉降-微电解-催化氧化法处理钻井废水";赵立志等;《油气田环境保护》;20011230(第4期);第17-20页 * |
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