CN205966754U - Arsenic slag contaminated sites soil electronic PRB prosthetic devices - Google Patents
Arsenic slag contaminated sites soil electronic PRB prosthetic devices Download PDFInfo
- Publication number
- CN205966754U CN205966754U CN201620877364.2U CN201620877364U CN205966754U CN 205966754 U CN205966754 U CN 205966754U CN 201620877364 U CN201620877364 U CN 201620877364U CN 205966754 U CN205966754 U CN 205966754U
- Authority
- CN
- China
- Prior art keywords
- chamber
- soil
- anode
- cathode
- prb
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- 239000002689 soil Substances 0.000 title claims abstract description 80
- 229910052785 arsenic Inorganic materials 0.000 title claims abstract description 41
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 title claims abstract description 41
- 239000002893 slag Substances 0.000 title claims abstract description 14
- 239000002253 acid Substances 0.000 claims abstract description 15
- 230000005684 electric field Effects 0.000 claims abstract description 5
- 239000003792 electrolyte Substances 0.000 claims description 13
- 230000002572 peristaltic effect Effects 0.000 claims description 12
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 5
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims description 5
- 229910052804 chromium Inorganic materials 0.000 claims description 5
- 239000011651 chromium Substances 0.000 claims description 5
- 239000010439 graphite Substances 0.000 claims description 5
- 229910002804 graphite Inorganic materials 0.000 claims description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 5
- 239000003513 alkali Substances 0.000 claims description 4
- 239000008367 deionised water Substances 0.000 claims description 3
- 229910021641 deionized water Inorganic materials 0.000 claims description 3
- 239000000203 mixture Substances 0.000 claims description 3
- 238000003756 stirring Methods 0.000 claims description 3
- 238000011049 filling Methods 0.000 claims description 2
- 239000002872 contrast media Substances 0.000 claims 2
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 abstract description 23
- 230000008439 repair process Effects 0.000 abstract description 17
- 238000010979 pH adjustment Methods 0.000 abstract description 12
- 230000000694 effects Effects 0.000 abstract description 3
- 239000000243 solution Substances 0.000 description 25
- 238000000034 method Methods 0.000 description 16
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 15
- 239000007788 liquid Substances 0.000 description 8
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical group OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 4
- 239000003153 chemical reaction reagent Substances 0.000 description 4
- 238000005516 engineering process Methods 0.000 description 4
- 230000008569 process Effects 0.000 description 4
- 230000008901 benefit Effects 0.000 description 3
- 238000011065 in-situ storage Methods 0.000 description 3
- 230000002378 acidificating effect Effects 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- 230000005520 electrodynamics Effects 0.000 description 2
- 239000008151 electrolyte solution Substances 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- 239000003344 environmental pollutant Substances 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 238000002386 leaching Methods 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 231100000719 pollutant Toxicity 0.000 description 2
- 238000007711 solidification Methods 0.000 description 2
- 230000008023 solidification Effects 0.000 description 2
- 230000006641 stabilisation Effects 0.000 description 2
- 238000011105 stabilization Methods 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 239000002699 waste material Substances 0.000 description 2
- DJHGAFSJWGLOIV-UHFFFAOYSA-K Arsenate3- Chemical compound [O-][As]([O-])([O-])=O DJHGAFSJWGLOIV-UHFFFAOYSA-K 0.000 description 1
- 238000003723 Smelting Methods 0.000 description 1
- 239000003929 acidic solution Substances 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 238000007605 air drying Methods 0.000 description 1
- 150000001450 anions Chemical group 0.000 description 1
- QZPSXPBJTPJTSZ-UHFFFAOYSA-N aqua regia Chemical compound Cl.O[N+]([O-])=O QZPSXPBJTPJTSZ-UHFFFAOYSA-N 0.000 description 1
- 229940000489 arsenate Drugs 0.000 description 1
- 238000001391 atomic fluorescence spectroscopy Methods 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 230000000536 complexating effect Effects 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000005868 electrolysis reaction Methods 0.000 description 1
- 238000009393 electroremediation Methods 0.000 description 1
- 238000005265 energy consumption Methods 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 230000002427 irreversible effect Effects 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 238000005065 mining Methods 0.000 description 1
- 238000012544 monitoring process Methods 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 238000003900 soil pollution Methods 0.000 description 1
- 239000002910 solid waste Substances 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 238000005728 strengthening Methods 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
Landscapes
- Processing Of Solid Wastes (AREA)
Abstract
一种砷渣场地污染土壤的电动修复装置,包括土样室、阳极室、阴极室、直流电源、电流表、滤网、pH调节系统、电极、溢流孔、酸液槽、碱液槽、收集槽、Fe0‑PRB;所述土样室中垂直电场方向设置Fe0‑PRB,在土样室左右两边相邻的为阳极室、阴极室;土样室与阳、阴极室相邻的内壁上贴有滤网,在阳极、阴极室中间分别设有电极,将两个电极采用电线连接,其中间设有直流电源、电流表;所述酸液槽与阴极室通过胶管连接,中间设有pH调节系统;所述碱液槽与阳极室通过胶管连接,中间设有pH调节系统;所述阴极室与阳极室的上端设有溢流孔,溢流孔通过导管连接到收集槽,该结构简单,可操作性强,除砷效果好。
An electric repair device for soil contaminated by arsenic slag site, including soil sample chamber, anode chamber, cathode chamber, DC power supply, ammeter, filter screen, pH adjustment system, electrode, overflow hole, acid solution tank, lye solution tank, collection Groove, Fe 0 ‑PRB; Fe 0 ‑PRB is set in the vertical electric field direction in the soil sample chamber, and the anode chamber and the cathode chamber are adjacent to the left and right sides of the soil sample chamber; the inner walls adjacent to the anode and cathode chambers of the soil sample chamber A filter screen is pasted on the top, and electrodes are respectively set in the middle of the anode and cathode chambers, and the two electrodes are connected by wires, with a DC power supply and an ammeter in the middle; the acid tank is connected to the cathode chamber through a rubber hose, and a pH Adjustment system; the lye tank is connected to the anode chamber through a rubber hose, and a pH adjustment system is provided in the middle; an overflow hole is provided at the upper end of the cathode chamber and the anode chamber, and the overflow hole is connected to the collection tank through a conduit. The structure is simple , strong operability and good arsenic removal effect.
Description
技术领域technical field
本实用新型属于环境技术土壤污染修复技术领域,尤其涉及一种砷渣场地污染土壤的电动修复装置。The utility model belongs to the technical field of soil pollution restoration of environmental technology, in particular to an electric restoration device for soil polluted by arsenic slag sites.
背景技术Background technique
砷渣是一种剧毒的固体废渣,主要来源是含砷矿产开采和冶炼过程中的排放,集中发生在新疆、内蒙古、湖南省、广东省等地。中国的砷矿产资源约占全球总量的70%,在含砷矿山活动区,每年砷渣产量约为50吨,大量未经无害处理、任意堆放的闲置含砷矿渣,导致砷进入附近土壤造成了大面积的土壤砷污染。土壤砷污染具有隐蔽性、长期性和不可逆性等特点,因此土壤一旦遭受砷污染,其治理难度大、且周期长。Arsenic slag is a highly toxic solid waste, the main source of which is the discharge from the mining and smelting of arsenic-containing minerals, concentrated in Xinjiang, Inner Mongolia, Hunan Province, Guangdong Province and other places. China's arsenic mineral resources account for about 70% of the world's total. In areas where arsenic-containing mines are active, the annual output of arsenic slag is about 50 tons. A large number of idle arsenic-containing slags that have not been harmlessly treated and piled up arbitrarily have caused arsenic to enter the nearby soil Large areas of soil arsenic pollution have been caused. Soil arsenic pollution has the characteristics of concealment, long-term and irreversible. Therefore, once the soil is polluted by arsenic, its treatment is difficult and the cycle is long.
目前,处理砷污染土壤的主要方法有客土法、淋洗法、固化/稳定法、植物修复法和电动修复法。客土法工程量较大,费时费力。淋洗法和固化/稳定化法并未将土壤中的砷彻底去除,易造成土壤的二次污染,并且不适于大规模场地修复。植物修复法一般耗时较长,可能需要几十年的时间。电动修复方法作为一种新兴的原位修复技术,具有操作简单、适用性强、周期短等特点,但是电动修复只是将污染物迁移到电极液中,需要二次处理。将电动修复技术与PRB联合使用,可以结合电动与PRB技术的优势,提高土壤中砷的去除效率,修复时间较短,且不扰动土层,适用于低渗透性的土壤,同时可回收砷,能够有效降低二次污染、减少后续处理工作量,并且提高经济效益。At present, the main methods for dealing with arsenic-contaminated soils include guest soil method, leaching method, solidification/stabilization method, phytoremediation method and electrokinetic remediation method. The engineering quantity of guest-soil method is large, time-consuming and labor-intensive. The leaching method and solidification/stabilization method did not completely remove the arsenic in the soil, which easily caused secondary pollution of the soil, and was not suitable for large-scale site restoration. Phytoremediation is generally time-consuming and may take decades. As an emerging in-situ repair technology, the electrokinetic repair method has the characteristics of simple operation, strong applicability, and short cycle. However, electrokinetic repair only migrates pollutants into the electrode solution and requires secondary treatment. The combined use of electrodynamic restoration technology and PRB can combine the advantages of electrodynamic and PRB technologies to improve the removal efficiency of arsenic in the soil, the restoration time is shorter, and the soil layer is not disturbed. It is suitable for low-permeability soils, and arsenic can be recovered at the same time. It can effectively reduce secondary pollution, reduce the workload of subsequent treatment, and improve economic benefits.
目前的电动修复装置设计复杂,实用性不强,对污染物的去除效果不佳,产生的酸碱废液没有回收再利用,对环境造成二次污染。The current electric repair device is complex in design, not strong in practicability, and has poor removal effect on pollutants. The acid-base waste liquid generated is not recycled and reused, causing secondary pollution to the environment.
实用新型内容Utility model content
为解决上述技术问题,本实用新型提供了一种针对原位修复砷渣场地污染土壤的电动-PRB联合修复装置。该装置能够快速、经济、有效的、原位的修复砷场地污染土壤,能够回收酸碱废液实现循环再利用。In order to solve the above technical problems, the utility model provides an electric-PRB combined restoration device for in-situ restoration of soil contaminated by arsenic slag sites. The device can quickly, economically, effectively, and in-situ repair the arsenic site-contaminated soil, and can recover acid-base waste liquid for recycling.
本实用新型通过以下技术方案实现:The utility model is realized through the following technical solutions:
一种砷渣场地污染土壤的电动修复装置,包括土样室、阳极室、阴极室、直流电源、电流表、滤网、pH调节系统、电极、溢流孔、酸液槽、碱液槽、收集槽、Fe0-PRB;所述土样室中垂直电场方向设置Fe0-PRB,在土样室左右两边相邻的为阳极室、阴极室;土样室与阳、阴极室相邻的内壁上贴有滤网,在阳极、阴极室中间分别设有电极,将两个电极采用电线连接,其中间设有直流电源、电流表;所述酸液槽与阴极室通过胶管连接,中间设有pH调节系统;所述碱液槽与阳极室通过胶管连接,中间设有pH调节系统;所述阴极室与阳极室的上端设有溢流孔,溢流孔通过导管连接到收集槽。An electric repair device for soil contaminated by arsenic slag site, including soil sample chamber, anode chamber, cathode chamber, DC power supply, ammeter, filter screen, pH adjustment system, electrode, overflow hole, acid solution tank, lye solution tank, collection Groove, Fe 0 -PRB; Fe 0 -PRB is set in the vertical direction of the electric field in the soil sample chamber, and the anode chamber and cathode chamber are adjacent to the left and right sides of the soil sample chamber; the inner walls of the soil sample chamber adjacent to the anode and cathode chambers A filter screen is pasted on the top, and electrodes are respectively set in the middle of the anode and cathode chambers, and the two electrodes are connected by wires, with a DC power supply and an ammeter in the middle; the acid tank is connected to the cathode chamber through a rubber hose, and a pH Adjustment system; the lye tank is connected to the anode chamber through a rubber hose, and a pH adjustment system is arranged in the middle; an overflow hole is provided at the upper end of the cathode chamber and the anode chamber, and the overflow hole is connected to the collection tank through a conduit.
所述土样室1是用于装填供试土壤,其尺寸比例为长:宽:高=3:2:1。The soil sample chamber 1 is used for filling the soil to be tested, and its size ratio is length: width: height = 3:2:1.
所述供试土壤为将铬渣场地、铬污染土壤粉碎,过筛,上述土壤与酸性溶液混合,使土壤含水率为25%-45%,搅拌,均衡即可。The soil to be tested is crushed chromium slag site and chromium-contaminated soil, sieved, mixed with acidic solution to make the moisture content of the soil 25%-45%, stirred and balanced.
所述的铬渣场地、铬污染土壤优选砷渣堆放场地土壤,土壤呈弱酸性,pH值一般在5-7之间,其中土壤中砷的浓度较高,总砷浓度一般在100-100000mg/kg之间。The chromium slag site and the chromium-contaminated soil are preferably the soil of the arsenic slag stacking site, the soil is weakly acidic, the pH value is generally between 5-7, and the concentration of arsenic in the soil is relatively high, and the total arsenic concentration is generally 100-100000mg/ between kg.
所述Fe0-PRB厚度为1-5cm,优选3-5cm,最佳3cm。The thickness of the Fe 0 -PRB is 1-5 cm, preferably 3-5 cm, most preferably 3 cm.
所述阳极室、阴极室尺寸为长:宽:高=1:2:1。The dimensions of the anode chamber and the cathode chamber are length: width: height = 1:2:1.
所述滤网为400-650目,优选500目。The filter screen is 400-650 mesh, preferably 500 mesh.
所述直流电源的电压梯度为1-2V/cm。The voltage gradient of the DC power supply is 1-2V/cm.
所述电极采用棒状石墨电极,电极分别放在阴阳极室中心位置,插入阴阳极室底部。The electrodes are rod-shaped graphite electrodes, and the electrodes are respectively placed in the center of the cathode and anode chambers and inserted into the bottom of the cathode and anode chambers.
所述阳极室里加入电解液,阴极室里加入电解液及增强试剂。Electrolyte is added into the anode chamber, and electrolyte and strengthening reagent are added into the cathode chamber.
所述电解液为KCl溶液,其浓度为0.05-0.15mol/L,优选浓度为0.1mol/L。The electrolyte is a KCl solution with a concentration of 0.05-0.15 mol/L, preferably 0.1 mol/L.
所述增强试剂为EDTA溶液,其浓度为0.001-0.1mol/L,优选浓度为0.005mol/L。The enhancing reagent is EDTA solution, its concentration is 0.001-0.1mol/L, preferably 0.005mol/L.
所述pH调节系统主要由pH电极、蠕动泵、软件控制系统组成;设定pH范围,当pH电极测得阳极室或阴极室pH超过设定的pH范围时,通过软件控制系统给蠕动泵指令,蠕动泵将配置的酸液或碱液崩入阴极室或阳极室,从而调节pH。优选pH5为5-7之间。The pH adjustment system is mainly composed of a pH electrode, a peristaltic pump, and a software control system; the pH range is set, and when the pH electrode measures the pH of the anode chamber or the cathode chamber beyond the set pH range, the peristaltic pump is instructed by the software control system , the peristaltic pump collapses the configured acid or lye into the cathode chamber or anode chamber to adjust the pH. The preferred pH5 is between 5-7.
有益效果Beneficial effect
本实用新型的装置中放入土壤,并在土壤样品室垂直电场方向加入Fe0-PRB,土壤样品室与相邻的阴阳极室之间使用滤布隔开,连接电力系统及pH平衡调节系统。电动/PRB联合修复过程中,使用直流电源,在土壤两端施加稳定电压,在外加电场作用下,土壤中五价砷和三价砷分别以含氧阴离子基团和阳离子基团的形式分别迁移到阳极室和阴极室电解液中,以及与PRB介质Fe0发生吸附作用而去除。由于EDTA具有络合性可以与砷酸盐反应形成溶解态的络合物,提高砷的可移动性,从而显著提高砷的去除率。修复过程中,实时监测阴阳极液pH值,并使用pH平衡调节系统,使用蠕动泵分别向阴、阳极液中滴加乙酸溶液与氢氧化钠溶液,调节阴阳极的电解液,使其pH在5~7之间,保持弱酸性,可以有效控制阴极电解产生的OH-向土壤中迁移从而使土壤pH变得更为碱性。通过本装置的使用对总砷的去除效果达到了40%,且主要以残渣态砷存在,残留砷的生物可利用性降低。Put soil into the device of the utility model, and add Fe 0 -PRB in the direction of the vertical electric field in the soil sample chamber, use filter cloth to separate the soil sample chamber from the adjacent anode and cathode chambers, and connect the power system and the pH balance adjustment system . In the electric/PRB joint restoration process, a DC power supply is used to apply a stable voltage across the soil. Under the action of an external electric field, pentavalent arsenic and trivalent arsenic in the soil migrate in the form of oxygen-containing anion groups and cationic groups, respectively. into the anode chamber and cathode chamber electrolyte, and remove it by adsorption with PRB medium Fe 0 . Due to the complexing property of EDTA, it can react with arsenate to form a dissolved complex, which improves the mobility of arsenic, thereby significantly improving the removal rate of arsenic. During the restoration process, the pH value of the cathode and anode liquids is monitored in real time, and the pH balance adjustment system is used to add acetic acid solution and sodium hydroxide solution to the cathode and anode liquids respectively by using a peristaltic pump to adjust the electrolytes of the cathode and anode so that the pH is at Between 5 and 7, maintain weak acidity, which can effectively control the migration of OH - produced by cathodic electrolysis into the soil and make the soil pH more alkaline. The removal effect of the total arsenic by the use of the device reaches 40%, and the arsenic mainly exists in the residual state, and the bioavailability of the residual arsenic is reduced.
本实用新型适用于砷浓度较高,总砷浓度一般在100-100000mg/kg之间的砷污染土壤。The utility model is suitable for the arsenic-polluted soil where the arsenic concentration is relatively high, and the total arsenic concentration is generally between 100-100000 mg/kg.
本实用新型的溢流孔及其溢流孔通过导管连接的收集槽,能够将大量的酸碱液回收再利用,二次污染风险降低,做到了高效环保。The overflow hole of the utility model and the collection tank connected by the overflow hole through the conduit can recycle and reuse a large amount of acid and alkali liquid, reduce the risk of secondary pollution, and achieve high efficiency and environmental protection.
附图说明:Description of drawings:
图1为本实用新型的电动-PRB修复装置的结构示意图。Fig. 1 is a schematic structural diagram of the electric-PRB repair device of the present invention.
其中,1-土样室、2-阳极室、3-阴极室、4-直流电源、5-电流表、6-滤网、7-pH调节系统、8-电极、9-溢流孔、10-酸液槽、11-碱液槽、12-收集槽、13-Fe0-PRBAmong them, 1-soil sample chamber, 2-anode chamber, 3-cathode chamber, 4-DC power supply, 5-ammeter, 6-filter, 7-pH adjustment system, 8-electrode, 9-overflow hole, 10- Acid tank, 11-alkali tank, 12-collection tank, 13-Fe 0 -PRB
具体实施方式detailed description
下面将结合本实用新型实施例中的附图,对本实用新型实施例中的技术方案进行清楚、完整的描述,显然,所描述的实施例仅是本实用新型一部分实施例,而不是全部的实施例。基于本实用新型中的实施例,本领域普通技术人员在没有做出创造性劳动前提下所获得的所有其他实施例,都属于本实用新型保护的范围。下面配合所附图对本发明的特征和优点作详细说明。The technical solutions in the embodiments of the present invention will be clearly and completely described below in conjunction with the accompanying drawings in the embodiments of the present invention. Obviously, the described embodiments are only a part of the embodiments of the present invention, not all of them. example. Based on the embodiments of the present utility model, all other embodiments obtained by persons of ordinary skill in the art without making creative efforts belong to the scope of protection of the present utility model. The features and advantages of the present invention will be described in detail below in conjunction with the accompanying drawings.
本实用新型的电动-PRB修复装置,如图1所示,包括:土样室1、阳极室2、阴极室3、直流电源4、电流表5、滤网6、pH调节系统7、电极8、溢流孔9、酸液槽10、碱液槽11、收集槽12、Fe0-PRB 13。The electric-PRB repair device of the present utility model, as shown in Figure 1, comprises: soil sample chamber 1, anode chamber 2, cathode chamber 3, DC power supply 4, ammeter 5, filter screen 6, pH adjustment system 7, electrode 8, Overflow hole 9, acid solution tank 10, lye solution tank 11, collection tank 12, Fe 0 -PRB 13.
其中,土样室1是用于装填供试土壤,其尺寸比例为长:宽:高=3:2:1。在土样室1中加入Fe0-PRB 13,厚度为5cm。在土样室1左右两边相邻的为阳极室2、阴极室3,阳极室2、阴极室3尺寸为长:宽:高=1:2:1。在土样室与阳、阴极室相邻的内壁上贴有滤网6,在阳极室2、阴极室3中间分别设有电极8,将两个电极8采用电线连接,中间设有直流电源4、电流表5。电极8采用棒状石墨电极,电极8分别放在阴阳极室中心位置并插入阴阳极室底部。Among them, the soil sample chamber 1 is used to fill the soil for testing, and its size ratio is length: width: height = 3:2:1. Add Fe 0 -PRB 13 to soil sample chamber 1 with a thickness of 5 cm. Adjacent to the left and right sides of the soil sample chamber 1 are the anode chamber 2 and the cathode chamber 3, and the dimensions of the anode chamber 2 and the cathode chamber 3 are length: width: height = 1:2:1. A filter screen 6 is pasted on the inner wall adjacent to the anode and cathode chambers of the soil sample chamber, electrodes 8 are respectively arranged in the middle of the anode chamber 2 and the cathode chamber 3, and the two electrodes 8 are connected by wires, and a DC power supply 4 is arranged in the middle , Ammeter 5. The electrodes 8 are rod-shaped graphite electrodes, and the electrodes 8 are respectively placed in the center of the cathode and anode chambers and inserted into the bottom of the cathode and anode chambers.
酸液槽10与阴极室3通过胶管连接,中间设有pH调节系统7,碱液槽11与阳极室2通过胶管连接,中间设有pH调节系统7;阴极室3与阳极室2的上端设有溢流孔9,溢流孔9通过导管连接到收集槽12。The acid solution tank 10 is connected with the cathode chamber 3 by rubber hose, and a pH adjustment system 7 is arranged in the middle, and the lye tank 11 is connected with the anode chamber 2 by a rubber hose, and the pH adjustment system 7 is arranged in the middle; There is an overflow hole 9 which is connected to a collection tank 12 by a conduit.
pH调节系统主要由pH电极、蠕动泵、软件控制系统组成(pH电极、蠕动泵、软件控制系统图1中没有标注);设定pH范围,当pH电极测得阳极室或阴极室pH超过设定的pH范围时,通过软件控制系统给蠕动泵指令,蠕动泵将配置的酸液或碱液崩入阴极室或阳极室,从而调节pH。The pH adjustment system is mainly composed of a pH electrode, a peristaltic pump, and a software control system (the pH electrode, peristaltic pump, and software control system are not marked in Figure 1); the pH range is set, and when the pH of the anode chamber or cathode chamber measured by the pH electrode exceeds the set value When the pH range is specified, the peristaltic pump is instructed by the software control system, and the peristaltic pump will collapse the configured acid or alkali into the cathode chamber or anode chamber to adjust the pH.
修复过程:Repair process:
(1)取自然风干的铬污染的土壤,剔除其中杂物,使用粉碎机粉碎后,过0.50mm粒径的标准筛,待用;(1) Get the naturally air-dried chromium-contaminated soil, remove foreign matter therein, use a pulverizer to pulverize, cross a standard sieve with a particle size of 0.50 mm, and set aside;
(2)将上述待用土壤与去离子水2:1混合,使其含水率25-45%,搅拌均匀后均衡一天;(2) Mix the above-mentioned soil to be used with deionized water at a ratio of 2:1 to make the water content 25-45%, stir well and balance for one day;
(3)取上述均衡后土壤于电动-PRB修复装置的土样室1中,土样室1两端加放500目滤网6,防止修复过程中土壤迁移至阳极室2、阴极室3,将阴、阳极室充满电解液,电解液采用0.1mol/L KCl溶液,向阴极室3中添加0.1mol/L KCl溶液,同时添加浓度为0.005mol/L增强试剂EDTA溶液。(3) Take the above-mentioned balanced soil in the soil sample chamber 1 of the electric-PRB repair device, and place a 500-mesh filter screen 6 at both ends of the soil sample chamber 1 to prevent the soil from migrating to the anode chamber 2 and cathode chamber 3 during the repair process. The cathode and anode chambers are filled with electrolyte, and the electrolyte is 0.1mol/L KCl solution, and 0.1mol/L KCl solution is added to the cathode chamber 3, and 0.005mol/L enhancement reagent EDTA solution is added at the same time.
(4)将石墨电极8插入阴阳极室中间位置,插放至底部,连接电源4与电流表5,修复开始后,调节电压梯度1-2V/cm,持续至修复结束。(4) Insert the graphite electrode 8 into the middle of the cathode and anode chamber, insert it to the bottom, connect the power supply 4 and the ammeter 5, and after the repair starts, adjust the voltage gradient to 1-2V/cm, and continue until the repair is completed.
(5)在修复过程中,实时监测阴阳极液pH值,并使用pH平衡调节系统7,使用蠕动泵向阴极3的电解液滴加酸液槽10中的乙酸溶液,向阳极2的电解液中滴加碱液槽11中的氢氧化钠溶液,以调节阴极电解液、阳极电解液各自的pH,使各电解液处于5-7,保持弱酸性。(5) During the repair process, real-time monitoring of the pH value of the anode and cathode solution, and use the pH balance adjustment system 7, use the peristaltic pump to drip the acetic acid solution in the acid solution tank 10 to the electrolyte solution of the cathode 3, and add the acetic acid solution to the electrolyte solution of the anode 2 Add dropwise the sodium hydroxide solution in the lye tank 11 to adjust the respective pH of the catholyte and the anolyte, so that each electrolyte is at 5-7 to keep weak acidity.
在电动修复过程中,要不断补充乙酸溶液与氢氧化钠溶液,所以阴阳极的电解液会由溢流孔9排出,收集储存由溢流孔9排出的阴阳极电解液到收集槽12中,与电动修复结束后的阴阳极液统一处理。实施例2During the electric restoration process, the acetic acid solution and the sodium hydroxide solution must be continuously replenished, so the cathode and anode electrolytes will be discharged from the overflow hole 9, and the cathode and anode electrolytes discharged from the overflow hole 9 will be collected and stored in the collection tank 12. Unified treatment with the anode and cathode solution after electric restoration. Example 2
使用实施例1的装置修复砷污染的土壤,包括如下步骤:Use the device of embodiment 1 to remediate arsenic-contaminated soil, comprising the following steps:
步骤(1)取自然风干后的砷污染的土壤,(其中,该土壤中总砷含量为土壤总砷含量447.5mg/kg,土壤As(III)含量67.9mg/kg,土壤As(V)含量379.6mg/kg,pH=6.8),剔除其中杂物,使用粉碎机粉碎后,过细度为0.50mm筛后,待用;Step (1) takes the arsenic-contaminated soil after natural air-drying, (wherein the total arsenic content in the soil is 447.5 mg/kg of the total arsenic content of the soil, 67.9 mg/kg of the As(III) content of the soil, and 67.9 mg/kg of the As(V) content of the soil 379.6mg/kg, pH=6.8), remove the sundries therein, pulverize with a pulverizer, sieve with a fineness of 0.50mm, and set aside;
步骤(2)将上述待用土壤5kg与2.5L的去离子水混合,使用不锈钢铲搅拌均匀,静置一天;Step (2) Mix 5 kg of the above-mentioned soil to be used with 2.5 L of deionized water, stir evenly with a stainless steel shovel, and let stand for one day;
步骤(3)取上述均衡后土壤4kg于电动/PRB联合修复装置的土样室,其中,土样室尺寸30cm×20cm×10cm,两端的阴、阳电极室尺寸10cm×20cm×10cm,土样室两端加放500目滤布,防止修复过程中土壤迁移至阴、阳极室,将阴、阳极室充满0.1mol/L的KCl溶液,同时向阴极室滴加0.005mol/L的增强试剂EDTA溶液;Step (3) Take 4 kg of the above-mentioned equalized soil in the soil sample chamber of the electric/PRB joint restoration device, wherein the soil sample chamber measures 30cm×20cm×10cm, and the negative and positive electrode chambers at both ends measure 10cm×20cm×10cm. Add 500-mesh filter cloths at both ends of the chamber to prevent the soil from migrating to the cathode and anode chambers during the restoration process. Fill the cathode and anode chambers with 0.1mol/L KCl solution, and at the same time add 0.005mol/L enhanced reagent EDTA to the cathode chamber solution;
步骤(4)将石墨电极插入阴阳极室中间位置,插放至底部,连接直流电源与电流表,维持直流电电压梯度为2V/cm,持续至修复结束;Step (4) Insert the graphite electrode into the middle of the cathode and anode chamber, insert it to the bottom, connect the DC power supply and the ammeter, and maintain the DC voltage gradient at 2V/cm until the repair is completed;
其中,在修复过程中,实时监测阴阳极液pH值,并使用pH平衡调节系统,使用蠕动泵分别向阴阳极液中滴加乙酸溶液与氢氧化钠溶液,调节阴阳极液pH在5-7之间,保持弱酸性。Among them, during the repair process, the pH value of the cathode and anode liquids is monitored in real time, and the pH balance adjustment system is used to use a peristaltic pump to add acetic acid solution and sodium hydroxide solution to the cathode and anode liquids respectively to adjust the pH of the cathode and anode liquids at 5-7. In between, keep slightly acidic.
步骤(5)将修复后的土壤样品经(1+1)王水水浴消解后,采用原子荧光光谱法测定总砷浓度。Step (5) After the repaired soil sample is digested in a (1+1) aqua regia water bath, the total arsenic concentration is determined by atomic fluorescence spectrometry.
结果:试验运行五天后,本发明方法对总砷的去除效果达到了40%,且主要以残渣态砷存在,残留砷的生物可利用性降低。较普通电动修复砷去除效率16%显著提升。同时,能耗由7.44kWh/g降低至6.43kWh/g。Results: After five days of test operation, the method of the present invention can remove 40% of the total arsenic, and the arsenic mainly exists in the residual state, and the bioavailability of the residual arsenic is reduced. The arsenic removal efficiency of ordinary electric restoration is significantly improved by 16%. At the same time, the energy consumption is reduced from 7.44kWh/g to 6.43kWh/g.
Claims (10)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201620877364.2U CN205966754U (en) | 2016-08-12 | 2016-08-12 | Arsenic slag contaminated sites soil electronic PRB prosthetic devices |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201620877364.2U CN205966754U (en) | 2016-08-12 | 2016-08-12 | Arsenic slag contaminated sites soil electronic PRB prosthetic devices |
Publications (1)
Publication Number | Publication Date |
---|---|
CN205966754U true CN205966754U (en) | 2017-02-22 |
Family
ID=59978157
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201620877364.2U Expired - Fee Related CN205966754U (en) | 2016-08-12 | 2016-08-12 | Arsenic slag contaminated sites soil electronic PRB prosthetic devices |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN205966754U (en) |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN108326030A (en) * | 2018-01-11 | 2018-07-27 | 上海理工大学 | The heavy metal-polluted soil prosthetic device of convertible array-type electrode |
CN108435787A (en) * | 2018-05-23 | 2018-08-24 | 江南大学 | A kind of device and method using electric field and reactive barrier repairing polluted soil |
CN108746194A (en) * | 2018-08-08 | 2018-11-06 | 重庆大学 | A kind of experimental rig and test method closing repairing polluted soil based on magnetic-Electricity Federation |
CN109317506A (en) * | 2018-09-05 | 2019-02-12 | 上海大学 | Electric device for repairing arsenic-contaminated soil and method for repairing arsenic-contaminated soil |
CN110102566A (en) * | 2019-03-19 | 2019-08-09 | 广东筑奥生态环境股份有限公司 | A kind of heavy metal adsorption method for the modified reparation of soil pollution |
CN110180886A (en) * | 2019-07-05 | 2019-08-30 | 河南科技大学 | A kind of device and method of in-situ immobilization fluoride pollution soil |
CN113275373A (en) * | 2021-04-27 | 2021-08-20 | 中交疏浚技术装备国家工程研究中心有限公司 | Portable potential acidic sulfate soil electrochemical oxidation repair test device and method |
CN114472495A (en) * | 2022-01-21 | 2022-05-13 | 西安建筑科技大学 | Device and method for combined electrodynamic remediation of polluted soil with chelating agent and osmotic reaction wall |
-
2016
- 2016-08-12 CN CN201620877364.2U patent/CN205966754U/en not_active Expired - Fee Related
Cited By (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN108326030A (en) * | 2018-01-11 | 2018-07-27 | 上海理工大学 | The heavy metal-polluted soil prosthetic device of convertible array-type electrode |
CN108326030B (en) * | 2018-01-11 | 2020-11-24 | 上海理工大学 | Soil heavy metal prosthetic devices of convertible array electrode |
CN108435787A (en) * | 2018-05-23 | 2018-08-24 | 江南大学 | A kind of device and method using electric field and reactive barrier repairing polluted soil |
CN108435787B (en) * | 2018-05-23 | 2020-07-07 | 江南大学 | Device and method for repairing polluted soil by using electric field and reaction barrier |
CN108746194A (en) * | 2018-08-08 | 2018-11-06 | 重庆大学 | A kind of experimental rig and test method closing repairing polluted soil based on magnetic-Electricity Federation |
CN108746194B (en) * | 2018-08-08 | 2020-08-04 | 重庆大学 | Test device and test method for repairing polluted soil based on magnetic-electric combination |
CN109317506A (en) * | 2018-09-05 | 2019-02-12 | 上海大学 | Electric device for repairing arsenic-contaminated soil and method for repairing arsenic-contaminated soil |
CN110102566A (en) * | 2019-03-19 | 2019-08-09 | 广东筑奥生态环境股份有限公司 | A kind of heavy metal adsorption method for the modified reparation of soil pollution |
CN110180886A (en) * | 2019-07-05 | 2019-08-30 | 河南科技大学 | A kind of device and method of in-situ immobilization fluoride pollution soil |
CN110180886B (en) * | 2019-07-05 | 2021-03-02 | 河南科技大学 | Device and method for in situ remediation of fluorine-contaminated soil |
CN113275373A (en) * | 2021-04-27 | 2021-08-20 | 中交疏浚技术装备国家工程研究中心有限公司 | Portable potential acidic sulfate soil electrochemical oxidation repair test device and method |
CN114472495A (en) * | 2022-01-21 | 2022-05-13 | 西安建筑科技大学 | Device and method for combined electrodynamic remediation of polluted soil with chelating agent and osmotic reaction wall |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN205966754U (en) | Arsenic slag contaminated sites soil electronic PRB prosthetic devices | |
CN105057339B (en) | A kind of restorative procedure in situ for removing chromium in chromium slag contaminated soil of site | |
CN106111693A (en) | A kind of method of in-situ immobilization arsenic slag contaminated soil of site | |
CN101786099B (en) | Electrodynamic method for removing fluorine contaminant in soil | |
CN101265007B (en) | Method for removing heavy metal in urban sludge by employing electric repairing technique | |
CN102513348A (en) | Electric complex-strengthening repairing method and device of heavy metal-organic co-contaminated soil | |
CN104858225B (en) | A kind of electronic combined remediation method of the elution of heavy-metal contaminated soil | |
CN210059318U (en) | Device for strengthening electric-complexing remediation of heavy metal contaminated soil by utilizing ionic membrane | |
CN108213070A (en) | A kind of original position is electronic-device and method of electrochemistry collaboration repairing polluted soil and underground water | |
Song et al. | Migration and decomplexation of metal-chelate complexes causing metal accumulation phenomenon after chelate-enhanced electrokinetic remediation | |
CN202499915U (en) | Acid etching waste liquid copper recovery system | |
CN106623386B (en) | Electric restoration vertical device for heavy metal contaminated soil | |
CN205869062U (en) | Soil heavy metal electrokinetic remediation experimental system | |
CN106904799B (en) | Electric repair strengthening device and method for removing heavy metals in sludge by using same | |
CN104492796A (en) | Electrokinetic remediation method of heavy metal contaminated soil | |
CN107282623A (en) | A kind of ionic membrane of organic polluted soil strengthens electronic oxidation restorative procedure | |
CN103194597A (en) | In-situ leaching method of electric field strengthened fine grain tailings | |
Yang et al. | Enhanced Electrokinetic Remediation of Heavy-Metals Contaminated Soil in presence tetrasodium N, N-bis (carboxymethyl) glutamic acid (GLDA) as chelator | |
CN109317506A (en) | Electric device for repairing arsenic-contaminated soil and method for repairing arsenic-contaminated soil | |
CN206316141U (en) | A kind of processing unit of electro reclamation heavy-metal contaminated soil | |
CN1331619C (en) | Cathode acidifying electric power repairing process for heavy metal contaminated soil | |
CN109610438A (en) | Device and method for strengthening soft soil foundation by electrochemical salt injection | |
CN108570694B (en) | A kind of electrochemical treatment method of arsenic-containing solid waste | |
CN105728456B (en) | A method of improving contaminated soil Electroremediation efficiency | |
CN109926444A (en) | A kind of chemical leaching method for heavy metal pollution of soil |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C14 | Grant of patent or utility model | ||
GR01 | Patent grant | ||
CF01 | Termination of patent right due to non-payment of annual fee | ||
CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20170222 |