CN1569643A - 微量元素添加剂碱式氯化锌的制备方法 - Google Patents

微量元素添加剂碱式氯化锌的制备方法 Download PDF

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CN1569643A
CN1569643A CNA2004100231407A CN200410023140A CN1569643A CN 1569643 A CN1569643 A CN 1569643A CN A2004100231407 A CNA2004100231407 A CN A2004100231407A CN 200410023140 A CN200410023140 A CN 200410023140A CN 1569643 A CN1569643 A CN 1569643A
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zinc chloride
zinc
basic zinc
trace mineral
mineral supplement
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CN1328171C (zh
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黄逸强
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Changsha Xingjia Biological Engineering Co Ltd
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Abstract

一种微量元素添加剂碱式氯化锌的制备方法,其特征在于:氧化锌与氯化锌以摩尔比为4∶1,在温度75-95℃下,控制pH值6-8,常压条件下反应1.5-3小时,生成碱式氯化锌,然后离心分离、水洗、烘干、粉碎、包装成成品。本发明具有工艺简单、成本低、收率高、成品品质好、无杂质、环境污染少、优于饲料卫生标准等优点。

Description

微量元素添加剂碱式氯化锌的制备方法
技术领域:
本发明涉及一种微量元素添加剂碱式氯化锌的制备方法。
背景技术:
在当今的养殖中锌的应用是不可缺的,但一般都是用硫酸锌或氧化锌来作为锌元素添加剂,这两种锌元素存在的问题是吸收慢并且吸收率低,因此用量也大。而螯合锌(蛋氨酸锌等)虽然好则因价格过高难以推广应用。碱式氯化锌作为饲料应用,在解决养殖动物中要求锌吸收快、吸收率高、减少排泄物由于锌含量高对环境造成的污染并且价格不能过高等方面起到了积极的作用。以往碱式氯化锌的生产有用废锌生产的,也有用电镀版或线路版的蚀刻液中的锌来生产的,这些方法的缺点就是产品中含杂质较多,重金属含量过高处理很难,因此难以达到饲料卫生标准。
发明内容:
本发明所要解决的技术问题是,提供一种收率高、环境污染少、成本低、工艺简单、成品品质好、无杂质、卫生标准高的饲料添加剂微量元素碱式氯化锌的制备方法。
本发明的制备方法如下:
1、氧化锌与氯化锌以摩尔比为4∶1,在温度75-95℃下,控制PH值6-8,常压条件下反应1.5~3小时,生成碱式氯化锌;其反应如下:
2、离心分离、水洗;
3、烘干、粉碎、包装成成品。
以此种方法来制备碱式氯化锌可以提高碱式氯化锌的纯度,因为在此种方法中利用氯化锌的酸性和氧化锌的碱性来直接进行中和反应,并不需要加入另外的促进反应剂,所以在最后的反应物中没有其他的副产物。本发明还具有工艺简单、收率高、成品品质好、无杂质、优于饲料卫生标准等优点。
具体实施方式:
实施例1:
反应步骤如下:4摩尔氧化锌加1摩尔氯化锌在80℃±5℃的反应温度下,调节PH值为6.5~7.5,反应2~3小时,离心分离、水洗、烘干、粉碎、即可成成品。其中锌含量为60%。
实施例2:
反应步骤如下:4摩尔氧化锌与1摩尔氯化锌在80℃~95℃反应温度下,控制PH值为6-8左右,反应1.5~2小时,生成碱式氯化锌,其中锌含量为61%。
用本添加剂按氧化锌用量30-60%喂公猪,可促进生长、提高抗病能力;延长种猪繁殖使用寿命;
用本添加剂按氧化锌用量30-60%喂肥育猪可促进生长,改善料肉比,改善肉色,使猪皮肤红润,毛色光亮。
用本添加剂按氧化锌用量30-60%饲喂乳仔猪,可提高抗应激能力与免疫力,促进生长,预防乳仔猪下痢,显著提高饲料的经济价值;
用本添加剂按氧化锌用量30-60%喂肉禽可使生长速度提高,料肉比下降,增强羽毛光泽度,提高其应激能力,降低死亡率。
用本添加剂按氧化锌用量30-60%喂水产动物,可增强免疫力,降低发病率与死亡率,促进生产,减少疾病发生,减少水溶性损失提高饲料利用率。

Claims (1)

1、一种微量元素添加剂碱式氯化锌的制备方法,其特征在于:氧化锌与氯化锌以摩尔比为4∶1,在温度75~95℃下,控制PH值6~8,常压条件下反应1.5-3小时,生成碱式氯化锌,其反应如下:
                ;然后离心分离、水洗、烘干、粉碎、包装成成品。
CNB2004100231407A 2004-04-26 2004-04-26 微量元素添加剂碱式氯化锌的制备方法 Expired - Lifetime CN1328171C (zh)

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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2007137460A1 (fr) * 2006-05-25 2007-12-06 Yiqiang Huang Procédé de préparation de chlorure de zinc basique d'éléments traces
WO2014139193A1 (zh) * 2013-03-11 2014-09-18 深圳市危险废物处理站有限公司 一种碱式氯化锌的制备方法
WO2018105738A1 (ja) * 2016-12-09 2018-06-14 Jfeミネラル株式会社 亜鉛イオン徐放性に優れる塩化水酸化亜鉛およびその製造方法

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4264568A (en) * 1978-02-13 1981-04-28 Tosco Corporation Method for easily removing zinc from carbon black contaminated with zinc
CN86107833A (zh) * 1986-11-17 1988-07-20 吉林省化学纤维技术研究所 合成醋酸乙烯用氧化锌催化剂

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2007137460A1 (fr) * 2006-05-25 2007-12-06 Yiqiang Huang Procédé de préparation de chlorure de zinc basique d'éléments traces
CN100366539C (zh) * 2006-05-25 2008-02-06 黄逸强 一种微量元素添加剂碱式氯化锌的制备方法
WO2014139193A1 (zh) * 2013-03-11 2014-09-18 深圳市危险废物处理站有限公司 一种碱式氯化锌的制备方法
WO2018105738A1 (ja) * 2016-12-09 2018-06-14 Jfeミネラル株式会社 亜鉛イオン徐放性に優れる塩化水酸化亜鉛およびその製造方法
CN110035761A (zh) * 2016-12-09 2019-07-19 杰富意矿物股份有限公司 锌离子缓释性优异的氯化锌氢氧化物及其制造方法

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