CN108504058B - 自增氧微生物降解填料及其制备方法 - Google Patents
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Abstract
本发明公开了一种自增氧微生物降解填料及其制备方法。本发明的产品挂膜速度快,生物附着性强,不易脱落,处理效率高,特别使用于BOD5含量较高的生活污水及工业废水处理,本发明的产品具有极强的亲水性和生物亲和性,且填料本身含载氧材料,可减小空气气泡与水面之间的表面张力,促进氧气溶解于污水中,有利于微生物生长,缩短挂膜时间,提高微生物处理效率。其氨氮去除率高于90%,COD的去除效率均超过80%,相比于现有填料可以更好的处理BOD5含量较高的污水。
Description
技术领域
本发明涉及高分子材料技术领域,具体是一种自增氧微生物降解填料及其制备方法。
背景技术
生化处理是现有污水处理技术中应用范围最广,性价比相对较高的一种处理方式,但是污水处理厂往往需要消耗巨大的投资及运行成本为生化反应提供氧气,受温度、压力和水气接触面积等多种因素的综合作用,水体中的溶解氧直接制约了污水生化处理所需的时间和处理量。现有的增加水体中溶解氧的方式主要是通过空气压缩机泵入大量的空气,增加水体中气泡的数量,达到增加水体中溶解氧的目的。在温度、压力、水体混合均匀程度相同的条件下,水体中溶解氧主要由水气接触界面上气泡与水面之间的表面张力所决定。直接或者间接的减小气泡与水面之间的表面张力,增加水气接触时间,可以大大的增加水体中的溶解氧。因此,一种可以携带氧气、能促使水体中溶解氧增加的微生物填料迫切需要开发。
发明内容
本发明的目的是,提供一种自增氧微生物降解填料及其制备方法,它既是生化处理单元中微生物的生长载体,填料表面材料又可以有载氧作用,这样不仅可以促使填料挂膜时间缩短,填料在水体中运动时可以携带氧气,促使水体中溶解氧含量大幅增加。
本发明是这样实现的:自增氧微生物降解填料及其制备方法,按质量份数计算,包括聚羟基烷酸酯35-45份、聚乳酸20-30份、轻质碳酸钙10-15份、天然生物质核桃砂5-20份、马来酸酐3-5份、硫酸亚铁0.3~0.6份、氯化镁0.2~0.4份、复合偶联剂0.5-1份、白油0.5-1份、聚乙烯醇1.8~4份、硬脂酸0.6~1.5、氯化钙0.6~1.5份、二棕榈酰磷脂酰胆碱5-10份为制备原料。
所述的天然生物质核桃砂粒径大于320目。
自增氧微生物降解填料包括填料骨架材料和功能性共混材料的制备方法,按上述质量份数取各组分,包括如下步骤:
1)取上述各组成溶于四氢呋喃和乙醇混合溶液中,固体组分与混合溶液的料液比为8-12:200,单位是g/ml,混合溶液由99.9%的四氢呋喃和无水乙醇按体积比为8:2的例组成,充分搅拌均匀;
2)将步骤1)中混匀的物料加入双螺杆挤出机中挤出造粒;
3)将步骤2)获得的颗粒再投入螺杆机挤出中,通过挤出模具挤压成型,得到填料成品;填料成品的外部为倒圆台形结构,填料成品的顶部呈漏斗形结构,在漏斗形结构的中部设有贯通填料成品的通孔;在漏斗形结构的内壁上设有羽片结构,羽片结构能增加填料成品的比表面积,使填料分布均匀、受力均匀。漏斗形结构的作用是为了控制填料重心,使其在水中处于直立状态,受力后便于定向移动。
与现有的技术相比,本发明具有如下优点:
1、本发明的产品挂膜速度快,生物附着性强,不易脱落,处理效率高,特别使用于BOD5含量较高的生活污水及工业废水处理,本发明的产品具有极强的亲水性和生物亲和性,且填料本身含载氧材料,可减小空气气泡与水面之间的表面张力,促进氧气溶解于污水中,有利于微生物生长,缩短挂膜时间,提高微生物处理效率。其氨氮去除率高于90%,COD的去除效率均超过80%,相比于现有填料可以更好的处理BOD5含量较高的污水。
2、本发明的产品由聚羟基烷酸酯、聚乳酸及轻质碳酸钙为主要材料,既可以为微生物生长提供缓释碳源,又保证了微生物填料的强度,为微生物生长提供附着基体;天然生物质核桃砂的多孔结构可以为生物物生长提供更多多的附着空间,缩短微生物的挂膜时间,硫酸亚铁和氯化镁不仅可以增强填料强度,在填料降解过程中被释放出来也可以为微生物代谢提供所需营养盐,促使微生物生长;马来酸酐、复合偶联剂、白油、聚乙烯醇、硬脂酸和氯化钙加固组成材料各部分之间粘合力,在填料组成材料内部形成强有力的结合,进一步增强填料自身强度;本发明将二棕榈酰磷脂酰胆碱作为功能性材料,使产品具有具备载氧功能,可以使气泡与水面表面张力减小使得水中溶解氧含量增加,可为微生物生长提供所需的氧气,微生物快速增长,使得污水处理效率提高。
3、本发明的产品设计独特结构,便于在污水处理过程中做往复运动,填料整体密度接近于水的密度,受填料本身重力、浮力和水流运动剪切力的综合作用,填料在生化处理单元处于运动状态,这不仅可以使污水混合均匀,也使水中氧气混合均匀,填料在其中起搅拌作用,从而降低污水处理能耗。
附图说明
图1为本发明的结构示意图;
图2为附图1的俯视图。
具体实施方式
实施例1:自增氧微生物降解填料及其制备方法,按质量份数计算,包括聚羟基烷酸酯35份、聚乳酸30份、轻质碳酸钙10份、天然生物质核桃砂18份、马来酸酐3份、硫酸亚铁0.3份、氯化镁0.2份、复合偶联剂0.5份、白油0.5份、聚乙烯醇1.5份、硬脂酸0.5份、氯化钙0.5份及二棕榈酰磷脂酰胆碱6份为制备原料;天然生物质材料核桃砂需预先使用超细粉碎机进行粉碎,粉碎后目数大于320目。
自增氧微生物降解填料包括填料骨架材料和功能性共混材料的制备方法,按上述质量份数取各组分,包括如下步骤:
1)取上述各组成溶于四氢呋喃和乙醇混合溶液中,固体组分与混合溶液的料液比为8-12:200,单位是g/ml,混合溶液由99.9%的四氢呋喃和无水乙醇按体积比为8:2的例组成,充分搅拌均匀;
2)将步骤1)中混匀的物料加入双螺杆挤出机中挤出造粒;
3)将步骤2)获得的颗粒再投入螺杆机挤出中,通过挤出模具挤压成型,得到填料成品;填料成品的外部为倒圆台形结构,填料成品的顶部呈漏斗形结构,在漏斗形结构的中部设有贯通填料成品的通孔;在漏斗形结构的内壁上设有羽片结构。
实施例2:自增氧微生物降解填料及其制备方法,按质量份数计算,包括聚羟基烷酸酯45份、聚乳酸25份、轻质碳酸钙12份、天然生物质核桃砂12份、马来酸酐4份、硫酸亚铁0.5份、氯化镁0.3份、硫酸亚铁与氯化镁0.8份、复合偶联剂0.8份、白油0.8份、聚乙烯醇2.5份、硬脂酸1份、氯化钙1份及二棕榈酰磷脂酰胆碱8份为制备原料;天然生物质材料核桃砂需预先使用超细粉碎机进行粉碎,粉碎后目数大于320目。
制备方法同实施例1。
实施例3:自增氧微生物降解填料及其制备方法,按质量份数计算,包括聚羟基烷酸酯44份、聚乳酸30份、轻质碳酸钙8份、天然生物质核桃砂6份、马来酸酐5份、硫酸亚铁0.6份、氯化镁0.4份、复合偶联剂1.0份、白油1.0份、聚乙烯醇4份、硬脂酸1.25份、氯化钙1.25份及二棕榈酰磷脂酰胆碱10份为制备原料;天然生物质材料核桃砂需预先使用超细粉碎机进行粉碎,粉碎后目数大于320目。
制备方法同实施例1。
比较例1
采用与实施例1相同的制备方法,不同之处在于产品组成中不加入二棕榈酰磷脂酰胆碱,得到填料产品4#,密度为0.948g/cm3。
比较例2
采用与实施例1相同的制备方法,不同之处在于产品组成中不加入天然生物质材料核桃砂,得到填料产品5#密度为0.895g/cm3。
取等质量的实施例(1#、2#、3#)和比较例(4#、5#)共5件产品置于水中浸泡六小时,取出静置30min后测定含水率,所得5件产品含水率如表1所示;
表1所得产品含水率
产品编号 | 1# | 2# | 3# | 4# | 5# |
含水率(%) | 18.6 | 19.3 | 19.2 | 14.1 | 13.4 |
取等质量的实施例(1#、2#、3#)和比较例(4#、5#)产品置于5个平行移动床膜生物反应器中进行实验。其中污泥和废水均来自某工厂生活污水处理装置,悬浮填料填充率为35%,反应器中水质pH6.5~7.8,温度23~27.5℃,C/N/P=100:5:1,溶解氧浓度为2~3.5mg/L,COD浓度250mg/L,氨氮浓度为35mg/L,水力停留时间为4h,实验结果如表2所示;
表2不同填料进出水效果及去除率
由表2可见,本发明制备的自增氧微生物可降解填料挂膜时间显著缩短,COD和氨氮的去除率明显提高。
Claims (3)
1.一种自增氧微生物降解填料,其特征在于:按质量份数计算,包括聚羟基烷酸酯35-45份、聚乳酸20-30份、轻质碳酸钙10-15份、天然生物质核桃砂5-20份、马来酸酐3-5份、硫酸亚铁0.3~0.6份、氯化镁0.2~0.4份、复合偶联剂0.5-1份、白油0.5-1份、聚乙烯醇1.8~4份、硬脂酸0.6~1.5、氯化钙0.6~1.5份、二棕榈酰磷脂酰胆碱5-10份为制备原料。
2.根据权利要求1所述的一种自增氧微生物降解填料,其特征在于:所述的天然生物质核桃砂粒径大于320目。
3.一种如权利要求1所述的自增氧微生物降解填料的制备方法,其特征在于,按上述质量份数取各组分,包括如下步骤:
1)取上述各组成溶于四氢呋喃和乙醇混合溶液中,固体组分与混合溶液的料液比为8-12:200,单位是g/ml,混合溶液由99.9%的四氢呋喃和无水乙醇按体积比为8:2的例组成,充分搅拌均匀;
2)将步骤1)中混匀的物料加入双螺杆挤出机中挤出造粒;
3)将步骤2)获得的颗粒再投入螺杆机挤出中,通过挤出模具挤压成型,得到填料成品;填料成品的外部为倒圆台形结构,填料成品的顶部呈漏斗形结构,在漏斗形结构的中部设有贯通填料成品的通孔;在漏斗形结构的内壁上设有羽片结构。
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