CN106283012A - 一种循环水无磷环保预膜剂 - Google Patents

一种循环水无磷环保预膜剂 Download PDF

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CN106283012A
CN106283012A CN201610766008.8A CN201610766008A CN106283012A CN 106283012 A CN106283012 A CN 106283012A CN 201610766008 A CN201610766008 A CN 201610766008A CN 106283012 A CN106283012 A CN 106283012A
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environmentally friendly
prefilming agent
recirculated water
phosphateless environmentally
water
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陈维忠
李洪社
喻果
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Weihai Xiang Yu Environmental Protection Science And Technology Co Ltd
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Weihai Xiang Yu Environmental Protection Science And Technology Co Ltd
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    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C22/00Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals
    • C23C22/05Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions
    • C23C22/06Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions using aqueous acidic solutions with pH less than 6
    • C23C22/48Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions using aqueous acidic solutions with pH less than 6 not containing phosphates, hexavalent chromium compounds, fluorides or complex fluorides, molybdates, tungstates, vanadates or oxalates
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C22/00Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals
    • C23C22/05Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions
    • C23C22/06Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions using aqueous acidic solutions with pH less than 6
    • C23C22/48Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions using aqueous acidic solutions with pH less than 6 not containing phosphates, hexavalent chromium compounds, fluorides or complex fluorides, molybdates, tungstates, vanadates or oxalates
    • C23C22/50Treatment of iron or alloys based thereon

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  • Chemical & Material Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Preventing Corrosion Or Incrustation Of Metals (AREA)

Abstract

本发明的目的在于提供一种用于循环水无磷环保预膜剂,具有良好的成膜效果,能在管道及换热器表面预先形成致密保护膜,从而起到保护设备、延长设备使用寿命的目的。同时,该预膜剂组分简单、原料易得、成本低廉、无毒性,不会形成二次环境污染。另外,本循环水无磷环保预膜剂,成膜速度快,成膜致密均匀,能够有效的提高设备管道的耐腐蚀性。

Description

一种循环水无磷环保预膜剂
技术领域
本发明属于循环水专用药剂,特别涉及一种用于循环水的无磷环保预膜剂。
背景技术
预膜剂是在工业水处理的预处理过程中必不可少的重要环节之一,能在管道及换热器表面预先形成致密保护膜的成膜化学品。预膜剂可在循环水系统开车运行之前,在新系统设备金属表面,或在化学清洗后尤其是酸洗后处于活化状态的金属表面上,预先生成一层完整致密的耐腐蚀保护膜,这是提高循环水系统耐腐蚀性能的重要手段。
传统工业循环水采用无机磷锌化学品进行预膜,包括六偏磷酸钠与七水硫酸锌(15:4),以及三聚磷酸钠与七水硫酸锌(3:1),用量为400-800mg/L,预膜pH值为6.5-7.2,预膜时间为36-48小时,传统预膜剂运行条件苛刻,且不利于环境保护:(1)传统预膜剂加药浓度不适,极易形成磷酸钙垢;(2)预膜过程中消耗大量硫酸调节pH值,且pH值不易稳定;(3)预膜结束后的循环水中含有高浓度的磷,直接排污对环境造成破坏,废水处理成本较高。
本发明提供一种用于循环水的无磷环保预膜剂,预膜过程中监控条件范围大,成膜效果好,且预膜后的循环水中不含有磷,属于环境友好型药剂。
发明内容
本发明的目的在于提供一种用于循环水的无磷环保预膜剂,具有良好的成膜效果,能在管道及换热器表面预先形成致密保护膜,从而起到保护设备、延长设备使用寿命的目的。同时,该预膜剂组分简单、原料易得、成本低廉、无毒性,不会形成二次环境污染。
本发明所采用的技术方案如下:
所述循环水无磷环保预膜剂,由以下重量百分含量的原料制成:含有丙烯酸-2-丙烯酰胺-2-甲基丙磺酸共聚物15-30%,水解聚马来酸酐10-20%,葡萄糖酸钠5-15%,硫酸锌1-10%,浓硫酸1-3%,余量为去离子水。
优选地,由以下重量百分含量的原料制成:含有丙烯酸-2-丙烯酰胺-2-甲基丙磺酸共聚物18-25%,水解聚马来酸酐12-18%,葡萄糖酸钠8-12%,硫酸锌5-8%,浓硫酸1-2%,余量为去离子水。
所述的硫酸锌为七水硫酸锌。
一种用于循环水无磷环保预膜剂使用方法,该方法为在循环冷却水系统正常运行前或是运行过程中,直接将无磷环保预膜剂加入清洗后的循环水小系统中,加药量为250-450mg/L。
与传统含磷预膜药剂相比,本发明具有以下有益效果:
(1)所述无磷环保预膜剂不含磷,避免传统含量预膜药剂极易引起水体富营养化问题,属于环境友好型药剂;
(2) 所述无磷环保预膜剂对碳钢进行预膜时,成膜速度快,成膜致密均匀,能够有效的提高设备管道的耐腐蚀性;
(3)预膜过程中不需要加酸调节pH值,简化预膜流程,降低预膜费用;
(4)预膜后的循环水无需排放或是置换,可直接进行正常运行,节约大量水资源,节省预膜成本。
实施例一
按重量百分比选取原料
丙烯酸-2-丙烯酰胺-2-甲基丙磺酸共聚物 20%
水解聚马来酸酐 15%
葡萄糖酸钠 10%
硫酸锌 5%
浓硫酸 1%
其余为去离子水,其总重量满足100%。
将上述配好的无磷环保预膜剂直接加入实验用水进行旋转挂片实验,投加浓度为45Omg/L,试验温度45℃,试验时间48h,实验用水水质为:钙硬度(以CaCO3计)15Omg/L,总碱度(以CaCO3计)100mg/L,pH为6.5,实验结果见表1。
实施例二
按重量百分比选取原料
丙烯酸-2-丙烯酰胺-2-甲基丙磺酸共聚物 18%
水解聚马来酸酐 14%
葡萄糖酸钠 8%
硫酸锌 5%
浓硫酸 1%
其余为去离子水,其总重量满足100%。
将上述配好的无磷环保预膜剂直接加入实验用水进行旋转挂片实验,投加浓度为45Omg/L,试验温度45℃,试验时间48h,实验用水水质为:钙硬度(以CaCO3计)15Omg/L,总碱度(以CaCO3计)100mg/L,pH为6.5,实验结果见表1。
实施例三
按重量百分比选取原料
丙烯酸-2-丙烯酰胺-2-甲基丙磺酸共聚物 22%
水解聚马来酸酐 18%
葡萄糖酸钠 10%
硫酸锌 8%
浓硫酸 1.5%
其余为去离子水,其总重量满足100%。
将上述配好的无磷环保预膜剂直接加入实验用水进行旋转挂片实验,投加浓度为45Omg/L,试验温度45℃,试验时间48h,实验用水水质为:钙硬度(以CaCO3计)15Omg/L,总碱度(以CaCO3计)100mg/L,pH为6.5,实验结果见表1。
实施例1-3的实验结果
实施例 药剂投加量mg/L 饱和硫酸铜显色时间(s)
实施例1 450 81
实施例2 450 72
实施例3 450 76
根据HG/T3778-2005要求,膜对饱和硫酸铜溶液滴定反应色变时间差应≥105,根据表1中的实验结果可知,该无磷环保预膜剂预膜效果远远优于HG/T3778-2005要求。

Claims (4)

1.一种循环水无磷环保预膜剂,其特征在于重量百分含量的原料制成:含有丙烯酸-2-丙烯酰胺-2-甲基丙磺酸共聚物15-30%,水解聚马来酸酐10-20%,葡萄糖酸钠5-15%,硫酸锌1-10%,浓硫酸1-3%,余量为去离子水。
2.根据权利要求1所述循环水无磷环保预膜剂,其特征在于重量百分含量的原料制成:含有丙烯酸-2-丙烯酰胺-2-甲基丙磺酸共聚物18-25%,水解聚马来酸酐12-18%,葡萄糖酸钠8-12%,硫酸锌5-8%,浓硫酸1-2%,余量为去离子水。
3.根据权利要求1所述循环水无磷环保预膜剂,其特征在于:所述的硫酸锌为七水硫酸锌。
4.一种权利要求1-3任一所述用于循环水无磷环保预膜剂的使用方法,其特征在于:在循环冷却水系统正常运行前或是运行过程中,直接将无磷环保预膜剂加入清洗后的循环水小系统中,加药量为250-450mg/L。
CN201610766008.8A 2016-08-31 2016-08-31 一种循环水无磷环保预膜剂 Pending CN106283012A (zh)

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Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110143675A (zh) * 2018-12-11 2019-08-20 德蓝水技术股份有限公司 工业循环冷却水系统用无磷预膜剂及其制备方法
CN112626510A (zh) * 2020-12-14 2021-04-09 陕西省石油化工研究设计院 一种高效环保预膜剂
CN114086167A (zh) * 2021-11-11 2022-02-25 新疆水处理工程技术研究中心有限公司 一种无磷预膜剂及其制备方法
CN114318318A (zh) * 2021-04-15 2022-04-12 江苏特昊新材料有限公司 一种冷轧钢表面用聚电解质成膜液及其制备方法与应用

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110143675A (zh) * 2018-12-11 2019-08-20 德蓝水技术股份有限公司 工业循环冷却水系统用无磷预膜剂及其制备方法
CN110143675B (zh) * 2018-12-11 2021-11-19 德蓝水技术股份有限公司 工业循环冷却水系统用无磷预膜剂及其制备方法
CN112626510A (zh) * 2020-12-14 2021-04-09 陕西省石油化工研究设计院 一种高效环保预膜剂
CN114318318A (zh) * 2021-04-15 2022-04-12 江苏特昊新材料有限公司 一种冷轧钢表面用聚电解质成膜液及其制备方法与应用
CN114086167A (zh) * 2021-11-11 2022-02-25 新疆水处理工程技术研究中心有限公司 一种无磷预膜剂及其制备方法

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Application publication date: 20170104