TW200524B - - Google Patents

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TW200524B
TW200524B TW081103529A TW81103529A TW200524B TW 200524 B TW200524 B TW 200524B TW 081103529 A TW081103529 A TW 081103529A TW 81103529 A TW81103529 A TW 81103529A TW 200524 B TW200524 B TW 200524B
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TW
Taiwan
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paste
surfactant
powder
alkyl
acid
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TW081103529A
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Chinese (zh)
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Procter & Gamble
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    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D11/00Special methods for preparing compositions containing mixtures of detergents
    • C11D11/0082Special methods for preparing compositions containing mixtures of detergents one or more of the detergent ingredients being in a liquefied state, e.g. slurry, paste or melt, and the process resulting in solid detergent particles such as granules, powders or beads
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D11/00Special methods for preparing compositions containing mixtures of detergents
    • C11D11/04Special methods for preparing compositions containing mixtures of detergents by chemical means, e.g. by sulfonating in the presence of other compounding ingredients followed by neutralising
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D17/00Detergent materials or soaps characterised by their shape or physical properties
    • C11D17/06Powder; Flakes; Free-flowing mixtures; Sheets
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D17/00Detergent materials or soaps characterised by their shape or physical properties
    • C11D17/06Powder; Flakes; Free-flowing mixtures; Sheets
    • C11D17/065High-density particulate detergent compositions

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  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Detergent Compositions (AREA)

Description

^00524 ^00524 經濟部屮央楳準易员工消费合作社印製 A6 ____ B6_ 五、發明説明(1) 窈昍節圊 本發明係藺於製備包括稠合去污劑顆粒之姐合物的方法 〇 發明背备 粒吠去汚劑姐合物到目前為止原則上是藉曠霧乾燥製備 之。在唄霧乾燦製程中,去污劑组份,諸如界面活性劑及 肋洗劑,與多達35 — 50%的水混合,κ形成一淤漿。獲得 之淤漿垤加熱及哦霧乾埭,此為昂貴方法。然而良好的附 聚方法會是較便宜的方法。 噴霧乾埭需要去除30 — 40重量%的水。用於進行噴孩乾 烽的設備是昂貴的。所獲得之顆粒具有良好溶解度,但是 低鬆密度,所以包装體稹大。而且,藉噴S乾烯獲得之顆 粒的流動性質,受大表面不規則性的不利影響|因此粒化 品具有不良外観。藉噴霧乾堞法製備之粒狀去污劑堪有其 他已知的缺點。 有許多製造去污劑顆粒之前項技g的非哦S乾嫌方法。 它們一樣有缺點。大部分需求一個K上的混合器及一分開 成粒操作。其他則需要使用酸形式界面活性劑工作。一些 其他的則箱要高溫分解起始物筲。因為其黏性關係,在逭 些方法中都避免高活性界面活性劑糊。 1984年8月13日公佈之歐洲専利一 A-0 110 731 ,掲 示為了不用任何蒸發乾»形成固《 *箱由將界面活性劑溶 液在一淸深相中*與肋洗劑粉混合·製造去污劑粉之方法 。描述供碾酹用之固«條或瑰之製程·但是沒有教等《附 —3 — 本紙張尺度遑用中國《家#毕(CNS)〒4規格(210X297公釐) 81. 5. 20,000(H) (請先閲讀背面之注意事項再填寫本頁) 裝· 線_ 200524 B6 五、發明説明(2 ) 經濟部屮央櫺準局员工消費合作社印製 聚作用,由糊調理直接形成高活性粒。 1989年12月6日公佈之歐洲專利一A — 〇 345 090 ,掲 示微粒吠去污劑姐合物的製法,其包括將去污劑酸與中和 劑接觭,及藉由此去B劑酸與微粒吠中和劑或去污劑鹽與 載劑,在吸收帶接觸,提供微粒子。 1990年1月3日公佈之歐洲專利一A - 〇 349 201 ,揭 示將细碎分散之乾去污肋洗劑及高活性界面活性爾,放人 -均匀漿檷(dough )中,_後冷卻並且使用细分散成粒 •形成均勻自由流動粒狀粒子,製造縮合去污劑顆粒之方 法。 1990年10月3日公佈之歐洲專利-0 390 251 ,掲示粒 狀去污劑或姐合物之連續製造方法*其包括首先將去污劑 界面活性劑之微粒狀起始物霣及助洗劑,在高速混合器中 處理,其次在中等速度成粒器/稠化器中處理•第三則在 乾堍/冷卻装置中處理,在第二步或第一及第二步之間, 添加粉*以滅低遇大粒子的量。 A . Davidsohn及 B . M . Mi ldwidskv.在 Synthetic Dpt, ergpnt. s,John Wiley & Sons 1978 年第 6 版中,掲示 一般去污教授,包括製成之去污劑產品的製造。 高剪切及冷混合方法本霣上是巳知方法,但是它們需要 額外碾磨步》或一些其他作用。例如—些使用酸形式界面 活性劑與碳酸納混合之乾》中和技術。參閲1985年5月7 日發行之Brooks的美國専利菜第4,515.707 II ; 1983年9 月30日搮出之Kao 8E皂公司之日本專利持許公開申讅莱第 -4- (請先閲讀背面之注意事項再填寫本頁) 裝. ί, 轉_ 本紙Λ尺度遑用中《家«準(CNS)甲4規格(210x297公釐) 81. 5 . 20,000(Η) 五、發明説明(3 ) A 6 B6 經濟部屮央橾準局貝工消货合作社印製 183540/1983號;及1986年6月5日之Lion K.1C.的日本 申請案Sho. 6卜1 1 8500。典型都需求過量碳酸鹽(2 — 20克分子遇量),以確保界面活性劑酸之合理轉化。遇量 碳酸鹽不利地提高洗滌水之pH至很鹼範圍,其特別不宜於 一些低磷酸鹽配方。 界面活性劑酸的使用一般需要立刻使用或冷卻溫度貯存 ,因為高度反應性酸諸如:硫酸烷酯酸類除非冷卻*否則 會進行降解,它們於貯存期間,傾向進行水解•形成自由 態硫酸及酵。實務上稱此棰前項技藝方法需要界面活性劑 酸產生與需要額外資本投資之成粒作用的密切结合。 第二種途徑·在此範圍上热知者並且描述在專利文獻上 ,其為陰離子型界面活性劑酸與苛性溶液(例如:50%氫 氧化納)或苛性粉(例如:碳酸碳),在正要成粒步驗之 前或期間•在原位中和。在此情況下,注意需要確保酸之 完全中和,以避免於貯存/或洗滌期間,對刺餘界面·活性 劑基霣之不合宜作用。所得之粒子為可併人粒吠去污商ί之 高度滬厚的顆粒。 當此第二棰途徑使用比攪和及噴S乾烽更低溫度及&少 深度剪切條件時•它有許多的限制。一方面需要成粒步a 期間或正好成粒之前,進行化學反應(中和)’相當限制 可使用(溫度化學品等等)之加工條件範園。除離子型界 面活性_酸之很低pH·防止對這些酸性條件敏!® = 的併入。尤其•就那些呈酸形式之化學不安定或 定之除離子界面活性劑的情況·此方法需要碗 (請先閲讀背面之注意事項再填窝本頁) 裝- -訂- 線- _ — 5 — 本紙張尺度遑用中《家樣芈(CNS)甲4規格(210X297公*) ' 81. 5. 20.000(H) 200讲 A6 ____ B6 五、發明説明(4 ) 化單元與中和/成粒步琢之密切结合。此導致相當限制這 些方法之容易後勤學(logistics )及/或設計以及重要 的是增加整個方法之控制系统的複雑性及困雞性。 經濟部屮央檁準局貝工消贽合作社印製 本發明解決上述困難並且於粒狀去污劑之加工提供更具 彈性及可變通途徑。本發明是基於一附聚/成粒步驟,其 完全不與硫酸化/磺化方法结合。Μ獲得大大增加附聚物 之界面活性劑活性,本發明能夠增加期對能夠形成鬆脆顆 粒之粉的比例。此藉由糊之化學及/或物理構建,諸如添 加特殊化學構建劑及/或去除水分,溫度控制,即可達到 目的。本發明之基礎是將陰離子型界面活性劑導入其鹽, 最佳其納鹽之水合,高度濃縮溶液。這些高活性(低水分 )界面活性劑糊為高黏度糊,但是於界面活性劑安定之溫 度下,仍保持可泵送。此保證能夠將化學品自製造位置運 送及轉移至成粒位點並且於粒子形成之前,能夠促進遇當 貯存。軚那些情況而言,硫酸鹽化/磺化兩者緊接在成粒 步驟之前,其提供安装中間媛衝桶之可能性,簡化整個單 元的控制。就一些陰離子型界面活性劑或其混合物而言, 其中發生相眚鲇滯液體结晶相者,此工技需要可形成較低 鲇滯相(例如:潔淨相(neat phases ))或需要使用一 些黏度修飾蜊(例如:水溶增溶劑(hydro tropes ))。 本發明也描述進行糊調理的方法。已蛵發現添加化學構 速劑·溫度的控制及/或自糊去除水分·對物理性質是Μ 踺•例如:酤度熔貼及黏性,其依次決定由糊之混合/或 粒製得之去污粒的特性。頃發現逹到此糊調理之很有效的 81. 5. 20,000(H) (請先閲讀背面之注意事項再填寫本頁) 本紙張尺度遑用中國家樣毕(CNS)甲4規格(210x297公*) A 6 __B6 五、發明説明(5 ) 經濟部屮央橾準扃员工消费合作社印製 方式是使用擠壓機。 本發明之一重要目的是藉由與哦霧乾埭方法相反之附聚 方法,製造稠化•濃縮之去污劑顆粒。本發明之其他目的 從下面將可明顯的看出。 發明埔垂 本發明係闞於製造一稠化,濃縮去污劑顆粒產物的經濟 方法,及尤其包括很高活性縮合去污劑顆粒之姐合物,其 中前述方法包括高活性糊附聚步驟,聪同所得之糊的化學 處理。 本發明特別可應用於所有中和AS水合糊。其可證明可懕 用於各種不同的界面活性劑。 太發明之詳钿描沭 本發明係闞於製造自由流動之粒吠去污劑的方法,其包 括:將有效量之化學構建劑及至少有40%去污活性之有效 量的水合界面活性劑捆混合;由前述混合物,於20~90t 之糊溫度下•迅速地形成一均匀稠厚糊:將前述糊,於與 乾燥去污劑混合時成粒*其中前述界面活性劑糊是由至少 一陰離子型界面活性劑姐成,且若存在有任何其他界面活 性劑時,是S自包括陰離子型,非離子型’兩性離子型( zwitterionic),兩性(amphol_ytic)及隔離子型界面活 性劑及其混合物。在較佳方法中•前述化學構建劑是>乂連 嫌方法添加。 本發明是以製造高活性界面活性劑糊之方法為基礎•有 附聚/成粒步明,其與疏酸Μ化及磺化製程完全分開’且 (請先閱讀背面之注意事項再填寫本頁) 裝· 訂- 線. _-7-_ 本紙張尺度遑用中《家搮準(CNS)甲4規格(210x297公釐) 81. 5. 20.000(H)^ 00524 ^ 00524 Printed A6 ____ B6_ by the Employee Consumer Cooperative of Biyangyi, Ministry of Economic Affairs. V. Description of the invention (1) Zangjiejie The present invention is concerned with the preparation of sister compounds including condensed detergent particles. The compound of the invention Beibei Granule Detergent has been prepared in principle by drying in open fog so far. In the mist-drying process, detergent components, such as surfactants and rib cleaners, are mixed with up to 35-50% water, and κ forms a slurry. The obtained slurry is heated and the mist is dried, which is an expensive method. However, a good agglomeration method will be a cheaper method. Spray drying needs to remove 30-40% by weight of water. The equipment used for spray drying is expensive. The granules obtained have good solubility, but low bulk density, so the package is large. Moreover, the flow properties of the granules obtained by spraying S stemene are adversely affected by the irregularities of the large surface | therefore, the granulated products have a bad appearance. Granular detergents prepared by spray dry castellation have other known disadvantages. There are many non-standard methods for manufacturing detergent particles. They also have disadvantages. Most require a mixer on K and a separate granulation operation. Others require the use of acid form surfactants. Some others require pyrolysis of the starting material Shao. Because of its viscosity relationship, high-activity surfactant pastes are avoided in these methods. European A-1 110 731, published on August 13, 1984, is shown to dry without any evaporation »forming a solid" * The box is made by mixing the surfactant solution in a deep phase * mixed with rib lotion powder Method of detergent powder. Describe the process of solid «strips or rubs for rolling; but there is no teaching etc." Attached-3-This paper scale uses the Chinese "Home #Bi (CNS) 〒 4 specifications (210X297 mm) 81. 5. 20,000 ( H) (Please read the precautions on the back before filling in this page) 装 · 线 _ 200524 B6 V. Description of invention (2) The printing and aggregation function of the Employee Consumer Cooperative of the Central Bureau of Economic Development of the Ministry of Economic Affairs, directly forming high activity from paste conditioning grain. European Patent No. A-〇345 090, published on December 6, 1989, shows the preparation method of the micro-barrel detergent compound, which includes connecting the detergent acid with the neutralizer, and removing the B agent Acid and particulate bark neutralizer or detergent salt and carrier, in contact with the absorption belt, provide particulates. European Patent No. A-〇349 201, published on January 3, 1990, discloses that the finely divided dry decontamination rib lotion and the highly active interfacial active agent are placed in a uniform slurry, after cooling and Use finely dispersed granules to form uniform free-flowing granulated particles to produce condensed detergent particles. European Patent-0 390 251, published on October 3, 1990, shows a continuous manufacturing method of granular detergents or sister compounds. It includes first the particulate starter of the detergent surfactant and the builder The agent is processed in a high-speed mixer, followed by a medium-speed granulator / thickener • The third is processed in a dry grain / cooling device, added in the second step or between the first and second steps Powder * to reduce the amount of large particles encountered. A. Davidsohn and B. M. Mi ldwidskv. In Synthetic Dpt, ergpnt. S, John Wiley & Sons 1978, 6th edition, show the general decontamination professor, including the manufacture of manufactured detergent products. High-shear and cold mixing methods are well-known methods, but they require additional grinding steps or some other functions. For example, some use the acid form surfactant mixed with sodium carbonate to dry "neutralization technology. Please refer to Brooks' American No. 4,515.707 II issued on May 7, 1985; Kao 8E Soap Company's Japanese Patent Grant Public Publication No. -4- issued on September 30, 1983 (please read the back Please pay attention to this page and then fill in this page). Ί, turn _ This paper is used in the "Home" standard (CNS) A 4 specifications (210x297 mm) 81. 5. 20,000 (Η) V. Description of the invention (3) A 6 B6 The Ministry of Economic Affairs, Pyongyang Bureau of Industry and Commerce Co., Ltd. printed 183540/1983; and June 5, 1986 Lion K.1C. Japanese application Sho. 6 Bu 1 1 8500. Typically, excess carbonate (2-20 moles) is required to ensure a reasonable conversion of surfactant acid. The amount of carbonates unfavorably raises the pH of the wash water to a very alkaline range, which is particularly unsuitable for some low phosphate formulations. The use of surfactant acids generally requires immediate use or storage at cooling temperature, because highly reactive acids such as alkyl sulfate acids will degrade unless cooled *, and they tend to hydrolyze during storage and form free sulfuric acid and leaven during storage. It is practically stated that this prior art method requires a close combination of surfactant acid generation and granulation that requires additional capital investment. The second way is well known in this range and described in the patent literature, which is anionic surfactant acid and caustic solution (for example: 50% sodium hydroxide) or caustic powder (for example: carbon carbonate), in Just before or during granulation step test • Neutralize in situ. In this case, care should be taken to ensure the complete neutralization of the acid to avoid undesirable effects on the thorny interface and active agent base during storage and / or washing. The resulting particles are highly thick particles that can be combined with human particles and decontamination agents. When this second channel uses lower temperatures and & less deep shearing conditions than agitating and spraying, it has many limitations. On the one hand, it is necessary to perform a chemical reaction (neutralization) during the granulation step a or just before granulation, which is quite restrictive and can be used (temperature chemicals, etc.). In addition to ionic interface activity_acid of very low pH · prevent sensitive to these acidic conditions! ® = incorporation. Especially for the chemically unstable or deionized surfactants in acid form. This method requires a bowl (please read the precautions on the back before filling the nest page).--Order-Line-_ — 5 — The size of this paper is used in the "Home-like Chia (CNS) A 4 specifications (210X297 g *) '81. 5. 20.000 (H) 200 lectures A6 ____ B6 5. Description of the invention (4) Chemical unit and neutralization / granulation Step by step, close integration. This leads to the ease of logistics and / or design of these methods that are quite limited and it is important to increase the complexity and sleepiness of the control system of the entire method. Printed by the Beiyang Purification Bureau Beigong Xiaozhi Cooperative of the Ministry of Economic Affairs The present invention solves the above-mentioned difficulties and provides a more flexible and flexible approach to the processing of granular detergents. The present invention is based on an agglomeration / granulation step, which is not at all combined with the sulfation / sulfonation method. M obtains a surfactant which greatly increases the surfactant activity of the agglomerates, and the present invention can increase the ratio of the period to the powder capable of forming brittle particles. This can be achieved by chemical and / or physical construction of the paste, such as adding special chemical construction agents and / or removing moisture, and temperature control. The basis of the present invention is to introduce anionic surfactants into their salts, preferably the hydration of their sodium salts, and highly concentrated solutions. These high-activity (low-moisture) surfactant pastes are high-viscosity pastes, but they can still be pumped at a stable temperature of the surfactant. This guarantees that the chemicals can be transported and transferred from the manufacturing site to the granulation site and before the particles are formed, it can facilitate the storage of the dang. In those cases, sulfation / sulfonation are immediately before the granulation step, which provides the possibility of installing intermediate flushing barrels, simplifying the control of the entire unit. For some anionic surfactants or mixtures thereof, where the phase stagnate stagnate liquid crystal phase occurs, this process requires the formation of a lower stagnate phase (eg, clean phase (neat phases)) or the use of some viscosity Modified clams (for example: hydro tropes). The invention also describes a method of paste conditioning. It has been found that the addition of chemical rate-building agents, temperature control, and / or removal of water from the paste, the physical property is Μ 踺 • For example: fusion bonding and viscosity, which in turn determines the mixture of pastes / or granules. Characteristics of decontamination particles. It is found that this paste is very effective in conditioning 81. 5. 20,000 (H) (please read the precautions on the back before filling in this page). This paper uses the Chinese National Sample (CNS) A4 specification (210x297 *) A 6 __B6 V. Description of the invention (5) The printing method of the Employee Consumer Cooperative of the Central Committee of the Ministry of Economic Affairs is the use of an extruder. An important object of the present invention is to produce thickened and concentrated detergent particles by an agglomeration method contrary to the Ogushi-Dai method. Other objects of the present invention will be apparent from the following. Invention The invention is an economical method for manufacturing a thickened, concentrated detergent particle product, and in particular a sister compound that includes highly active condensed detergent particles, wherein the aforementioned method includes a high-activity paste agglomeration step, Chemical treatment of the paste obtained by Cong Tong. The invention is particularly applicable to all neutralizing AS hydrated pastes. It can be proved that it can be used for various surfactants. The invention is a method for manufacturing a free-flowing granular bark detergent, which includes: an effective amount of a chemical builder and an effective amount of a hydrated surfactant having at least 40% detersive activity Bundle mixing; from the aforementioned mixture, at a paste temperature of 20 ~ 90t • A uniform thick paste is quickly formed: the aforementioned paste is granulated when mixed with a dry detergent * wherein the aforementioned surfactant paste is composed of at least one Anionic surfactants are successful, and if there are any other surfactants, they include anionic, non-ionic, zwitterionic, amphoteric, and isolating surfactants and their mixture. In a preferred method, the aforementioned chemical constructing agent is added by the above method. The present invention is based on the method of making a high-activity surfactant paste. • It has agglomeration / granulation steps, which are completely separated from the acid-sulfurizing and sulfonating processes. Page) Binding · Binding-Thread. _-7-_ This paper is used in the "Chinese home standard (CNS) A 4 specifications (210x297 mm) 81. 5. 20.000 (H)

經濟部中央橾準局β工消费合作社印製 另外包括藉由將前述方法產生的糊之化學調理,獲得高活 性顆粒。糊之調理意思是將其物理特性修飾,以形成較高 活性附聚物,此附聚物於正常操作條件下,用別的方法是 不容易獲得的。本發明特別可應用於所有中和纟5水合糊。 其可證明可應用於各種不同的界面活性劑(例如:Coco, Tallovr··等等)。在本發明之一具體實施例中,將陰離子 型界面活性劑導入其鹽,較佳其納鹽之高度濺縮水溶液中 。這些高活性(且較佳低水分者)界面活性爾糊是高黏度 糊,但是於界面活性劑安定之溫度下,保持可泵送。本發 明之其他具體簧例中,陰離子型界面活性劑或混合物包括 至少一陰離子型界面活性劑,其中發生高度黏滯液雅结晶 相,其需要形成較低黏滯相或使用一些黏度修飾劑。在更 佳具體實例中,於此柚添加改變界面活性劑糊之物理構造 及/或物理特性之有機及/或無機化合物。頃發現此添加 對界面活性劑捆減少糊之黏度*增加其黏度且增加其软化 點。此容許於附聚過程期間,添加更多的糊’因此導致更 高的活性附聚物,即多於50%。此界面活性劑糊之處理方 法|可分批及連續•較佳連續進行。 在本發明之較佳具體«例中,使用擠壓機調理糊。此擠 «拥是多用途設備,其能夠將2或多棰糊混合及/或將此 化學構建蜊添加至此黏滞期並且與黏滯糊混合。而且能狗 於興空下去除水分•並且能抅控制糊之溫度。 如本文所定義者,捆之調理意思是:a)播加其表覼粘 度· b)埔加其有效瑢黏,c)埔加糊之"硬度"及d) (請先閱讀背面之注意事項再填寫本頁) 裝· 訂- 本紙張尺度边用中ΒΒ家樣準(CNS)甲4規格(210x297公*) 81. 5. 20.000(H)Printed by the β-Consumer Cooperative of the Central Bureau of Economic Affairs of the Ministry of Economic Affairs. Also includes chemical conditioning of the paste produced by the aforementioned method to obtain highly active particles. The conditioning of paste means that its physical properties are modified to form higher active agglomerates, which are not easily obtained by other methods under normal operating conditions. The present invention is particularly applicable to all hydrating pastes that are neutralized. It can be proved to be applicable to various surfactants (for example: Coco, Tallovr, etc.). In a specific embodiment of the present invention, an anionic surfactant is introduced into its salt, preferably a highly splashed aqueous solution of its sodium salt. These high-activity (and preferably low-moisture) surface-active pastes are high-viscosity pastes, but they remain pumpable at a temperature where the surfactant is stable. In other specific examples of the present invention, the anionic surfactant or mixture includes at least one anionic surfactant, in which a highly viscous liquid crystalline phase occurs, which requires the formation of a lower viscosity phase or the use of some viscosity modifier. In a more preferred embodiment, organic and / or inorganic compounds that change the physical structure and / or physical properties of the surfactant paste are added to the pomelo. It was found that this addition reduced the viscosity of the paste to the surfactant bundle * increased its viscosity and increased its softening point. This allows more paste to be added during the agglomeration process, thus resulting in higher active agglomerates, i.e. more than 50%. The processing method of this surfactant paste | can be batch and continuous • preferably continuously. In a preferred embodiment of the present invention, an extruder is used to condition the paste. This squeeze is a multi-purpose device that can mix 2 or more pastes and / or add this chemical building clam to this viscosity period and mix with the viscous paste. Moreover, it can remove water under Xingkong and control the temperature of the paste. As defined in this article, the conditioning of the bale means: a) the viscosity of the surface cascade · b) the effective viscosity of the poca-coa, c) the "hardness" and d) of the poca-paa (please read the back (Notes and then fill out this page) Binding · Order-This paper is used in the standard BB home sample standard (CNS) A 4 specifications (210x297 g *) 81. 5. 20.000 (H)

Kt 005 A6 B6 五、發明説明(7) 經濟部中央楳準局貝工消費合作社印製 減低形成之顆粒的黏性。捆之硬度及柔软度,可藉由根據 ASTM 217-IP50或ISO 2137之柔软度穿透計测量之。以此 方式澜得之糊硬度應少於2公分,較佳少於1公分。 此糊之調理可«由i)冷卻,ii)乾煉,诅)於高活性 去污劑期添加構建劑(通常是電解質)。本發明有用之糊 將由至少40重量%的陰離子型界面活性劑之鹽類,此糊當 於701C及25秒—切變速率测量時*其黏度至少10泊•秒。 化璺纔逋麵 黏滯化學構建劑,當添加至界面活性劑糊時•會等致修 改糊之化學及/或物理特性· Μ便形成很高活性之附聚物 。這些劑可呈固體,液體或溶液形式,依其特殊化學性霣 而定。在本發明有用之劑的實例包括50%氫氣化纳水溶液 ,50%氫氧化鉀水溶液,氱化納·隣酸鹽,矽酸鹽,矽石 ,澱粉,聚合物及共聚物•非離子型界面活性劑及脲。上 述劑依其可配位性•可分開使甩或彼此混合使用。 I 用於本發明之捆較佳是一或各種不同的除離子型界面活 性劑之《的水合糊*較佳是陰離子界面活性_之納鹽期。 在較佳具《*施例中,陰離子型界面活性劑較佳盡可能湄 縮(即*具最低可能水分含量•使其以液《方式流動者) *使得於其保持安定之溫度下•可泵送者。於成粒蒔使用 之各裡不同之纯粹或混合界面活性劑為巳知,因為本發明 «際使用在工業上並且等致併入粒狀去污蜊之遘當物理性 -9- (請先閱讀背面之注意事項再填窝本頁) 装- 線· 本紙張尺度遑用中«家樣準(CNS)甲4規格(210x297公釐) 81. 5. 20.000(H) 〇〇〇0^3 ^ A 6 B6 五、發明説明(8) 經濟部中央採準局貝工消贽合作社印製 質的粒子,陰離子型界面活性劑必須是捆的一部分’其濃 度高於10%,較佳10-95%,更佳20 — 95% ·最佳40 — 95¾ 者。 最好在界面活性劑水合糊中的水分是盡可能低,而维持 糊之流勡性時,因為低水分將會導致在製成之粒子中,界 面活性劑的濃度較高。較佳此糊包含5 — 40%的水分,更 佳5-30%水分,最佳5% — 20%水分。降低糊水分的相 當吸引人的操作棋式,進入附聚機之前有很高的黏度但是 沒有問題,是因為在線上安裝有其出口接至附聚楗之空氣 或真空快速乾堍機。 最好使用高活性界面活性劑糊,使於混合*成粒及乾埭 期間•在系统中的水分含量降至最低。較低水分含量容許 :⑴較高活性界面活性劑對助洗劑的比例•例如1 : 1 ; (2)在配方中其他液雅較高濃度,而不會引起糊團或顆粒黏 性;⑶較少冷卻,由於較高可容許之成粒溫度;及⑷較少 顆粒乾燥,以符合最終水分限度。 此界面活性劑糊之2個重要參數|其可影響混合及成粒 步软的是糊溫度及黏度。其中黏度是濃度及溫度的函數· 在此應用範圃内黏度是由約IO.OOOcps至10,000,000cps 。較佳,砷進人糸统的黏度是約20,000 —約100,OOOcps, 且更佳是約30.000 -約70,OOOcps 。本發明之糊的鲇度是 於70*0之通度下涮定。 此期可於最初溫度介於其软化點(一般在40 — 60t之溫 度範画)及其分解點(依梱之化學特性而定•例如:疏酸 (請先閱讀背面之注意事項再填寫本頁) 裝· 訂·Kt 005 A6 B6 V. Description of the invention (7) Printed by the Beigong Consumer Cooperative of the Central Bureau of Economics of the Ministry of Economic Affairs to reduce the viscosity of the particles formed. The hardness and softness of the bale can be measured by a softness penetration meter according to ASTM 217-IP50 or ISO 2137. In this way, the paste hardness should be less than 2 cm, preferably less than 1 cm. This paste can be conditioned by i) cooling, ii) refining, cursing) adding a build agent (usually an electrolyte) during the period of highly active detergent. A paste useful in the present invention will consist of at least 40% by weight of anionic surfactant salts. The paste has a viscosity of at least 10 poises when measured at 701C and a shear rate of 25 seconds. Huayin Caizhi A viscous chemical builder, when added to a surfactant paste, will wait for the chemical and / or physical properties of the paste to be modified. M will form highly active agglomerates. These agents can be in solid, liquid or solution form, depending on their special chemical properties. Examples of agents useful in the present invention include 50% aqueous sodium hydroxide solution, 50% aqueous potassium hydroxide solution, sodium phthalate, silicate, silica, starch, polymer and copolymer • Nonionic interface Active agent and urea. The above agents can be used separately or mixed with each other according to their coordination properties. I The bundle used in the present invention is preferably one or a variety of different deionizing surfactants, "Hydrated paste * is preferably anionic interface active salt period. In the preferred embodiment, the anionic surfactant is preferably as shrinkable as possible (that is, it has the lowest possible moisture content • it is allowed to flow in a liquid way) * to keep it at a stable temperature Pumper. The different pure or mixed surfactants used in granulation are well known, because the present invention is used in industry and is equivalent to the physical properties of granular decontamination -9- (please first Read the precautions on the back and fill in this page.)-Line · This paper is used in the standard «Home Sample Standard (CNS) A 4 specifications (210x297 mm) 81. 5. 20.000 (H) 〇〇〇0 ^ 3 ^ A 6 B6 V. Description of the invention (8) The printed particles of anionic surfactant must be part of the bundle of the printed particles of the Beigong Xiaozhi Cooperative of the Central Acquisition Bureau of the Ministry of Economic Affairs. Its concentration is higher than 10%, preferably 10- 95%, better 20-95% · best 40-95¾. It is best to keep the moisture in the surfactant hydrated paste as low as possible, while maintaining the fluidity of the paste, because low moisture will cause a higher concentration of surfactant in the particles produced. Preferably, the paste contains 5-40% moisture, more preferably 5-30% moisture, and most preferably 5% -20% moisture. A relatively attractive operation to reduce the moisture content of the paste. It has a high viscosity before entering the agglomeration machine but there is no problem because the outlet is connected to the air or vacuum rapid drying machine on the agglomeration. It is best to use a high-activity surfactant paste to minimize the moisture content in the system during mixing * granulation and drying. The lower moisture content allows: ⑴ higher ratio of active surfactant to builder • eg 1: 1; (2) higher concentration of other liquids in the formula without causing paste or particle stickiness; ⑶ Less cooling due to a higher allowable granulation temperature; and ⑷ Less granule drying to meet the final moisture limit. Two important parameters of this surfactant paste | which can affect the mixing and granulation step is the paste temperature and viscosity. The viscosity is a function of concentration and temperature. In this application range, the viscosity is from about 1,000 to 10,000,000 cps. Preferably, the viscosity of arsenic into the human system is about 20,000 to about 100,000 cps, and more preferably about 30.000 to about 70,000 cps. The catfish degree of the paste of the present invention is set at 70 * 0. In this period, the initial temperature can be between its softening point (usually within the temperature range of 40-60t) and its decomposition point (depending on the chemical characteristics of 梱) • For example: acid-repellent (please read the precautions on the back before filling in this Page) Pack · Order ·

一 1 0 — 本紙張尺度遑用中《«家«準(CNS)甲4規格(210x297公釐) 81. 5. 20(〇〇〇W 五、發明説明(9) 經濟部中央櫺準局貝工消费合作社印製 烷酯糊高於75-85¾時,傾向降解)之間,導入混合器中 。高溫降低黏度,簡化糊之泵送,但是將導致較低活性附 聚物。可是在管線中水分降低步驟的使用(例如:快速乾 埭),需要使用較高溫度(高於1〇〇 tn 。在本發明中, 由於水分的消除,可維持高附聚物活性。 糊導入混合器可κ許多方式進行之,於進入混合拥之前 ,可由簡單傾倒至於管子末端,經小孔高壓泵送。而所有 這些方式都能製造具良好物理性質之附聚物,頃發現在本 發明之較佳具體實例中,糊之擠壓,導致在琨合器中較好 分佈,其改善預期大小之粒子的產量。於進入混合物之前 •使用高泵送壓力•等致增加最终附聚物的活性。薄由將 2種作用混合,及將糊娌過小至足夠容許預期流速之孔( 擠壓),但是保持系统中泵送懕力達最大可行性,將可達 到相當有利的结果。 离活袢界而沃袢麵細 此水合界面活性劑糊之活性至少30%且可高達約95% ; 較佳活性是:50 — 80%及65— 75%。糊之平衡主要是水· 但可包括加工肋劑諸如:非離子型界面活性劑。於較高活 性湄度時,為了糊之冷成粒作用,需少許或無助洗劑。所 得之漘縮界面活性劑顆粒,可添加至乾燥肋洗劑或粉劑或 以習用之附聚搡作使用之。此水合界面活性劑櫬包含一種 有拥界面活性劑,係選自包括除離子型.兩性離子型,兩 性及陽離子型界面活性劑,及其混合物。陰離子型界面活 性劑較佳、非離子型界面活性劑使用作為第二種界面活性 (請先閲讀背面之注意事項再填寫本頁) ---- —11 — 本紙張尺度逍用中《國家樣率(CNS)甲4規格(210x297公*) 81 5. 20,000(H) 五、發明説明(ίο) A6 B 61 1 0 — This paper is used in the «Home» Standard (CNS) Grade 4 Specification (210x297 mm) 81. 5. 20 (〇〇〇W V. Description of the invention (9) Central Bureau of Economic Development When the alkyl ester paste printed by the industrial and consumer cooperatives is higher than 75-85¾, it tends to degrade) and is introduced into the mixer. High temperatures reduce the viscosity and simplify the pumping of the paste, but will result in lower active agglomerates. However, the use of a moisture reduction step in the pipeline (for example: quick drying) requires the use of a higher temperature (above 100tn. In the present invention, due to the elimination of moisture, high agglomerate activity can be maintained. Paste introduction The mixer can be carried out in many ways. Before it enters the mixing hump, it can be simply dumped to the end of the tube and pumped through a small hole at high pressure. All of these methods can produce agglomerates with good physical properties. In a preferred embodiment, the extrusion of the paste leads to a better distribution in the kneader, which improves the production of particles of the expected size. Before entering the mixture • Use high pumping pressure • Equally increase the final agglomerate Activity. Thin by mixing the two actions, and making the pores too small to allow holes (squeeze) to allow the expected flow rate, but maintaining the pumping force in the system to the maximum feasibility will achieve quite favorable results. Bottom layer and fertile side are thin. The activity of this hydrated surfactant paste is at least 30% and can be as high as about 95%; the preferred activities are: 50-80% and 65-75%. The balance of the paste is mainly water but can be included Including processing rib agents such as non-ionic surfactants. At higher activity levels, a little or no builder is required for the cold granulation of the paste. The resulting condensed surfactant particles can be added to dry Rib lotion or powder or use conventional agglomerates. This hydrated surfactant contains a kind of surfactant, which is selected from deionized, zwitterionic, amphoteric and cationic surfactants. And their mixtures. Anionic surfactants are preferred, and nonionic surfactants are used as the second type of surfactant (please read the precautions on the back and then fill out this page) ---- —11 — This paper is for standard use In the "National Sample Rate (CNS) A 4 specifications (210x297 g *) 81 5. 20,000 (H) V. Description of invention (ίο) A6 B 6

經濟部屮央樣準局8工消费合作社印M 劑或加工肋劑並不包括在本文中作為'"活性〃界面活性劑 。本文有用之界面活性爾列於197 2年5月23日公佈之· Norris美國專利案3,664,961號;及1975年12月30日發佈 之1^1^111丨〇等人之美國專利茱第3,919,678號。有用之陽 離子型界面活性劑也包括那些在1980年9月16日公佈之 Cockrell的美國專利案第4,222,905號,及1980年12月 16日發佈之Murphy的美困專利案第4,239.659號中。可是 ,陽離子型界面活性劑與本文之鋁矽酸鹽材料,一般較少 可配位性,因此,既然在本發明之组合物中使用,較佳W 低濃度使用之。下面為在本姐合物中有用之界面活性麵的 代表性寊例。 較高脂肪酸之水可溶鹽類,即''肥皂〃為本文之姐合物 中有甩之陰雛子型界面活性劑。此包括嫌金颶肥皂諸如含 約8 —約2 4個碳原子,較佳約12 -約18個碳原子之較高碳 脂肪酸的纳、鉀、銨、及烷基銨鹽。肥皂可由脂質及油霣 直接皂化或藉自由態脂肪酸中和製造之。特別有用的是由 椰子油及動物脂衍生之脂肪酸混合物的納鹽及鉀鹽*即納 脂或鉀脂及椰子肥皂。 有用之陰離子型界面活性劑也包括水可溶鹽,較佳有機 碲酸反應產物之驗金颺,銨及烷基箝鹽,在其分子構造中 烷基包含約10—約20倨碳原子及《酸或硫酸賭基者(包括 在Λ烷基〃一詞中的是醯基的烷基部分)a合成界面活性 劑之此基的買例是烷基碗酸納及鉀,尤其那些由較高碳數 酵(Ce-Cie碳原子)班酸麵化獲得者•諸如由醣物脂或 -12- (請先閱讀背面之注意事項再填寫本頁) 裝- 訂< 線_ 本紙張尺度遑用中國國家#準(CNS) f 4規格(210 x 297公釐) 81. 5. 20.000(H)The printing agent M or the processing rib agent of the 8th Industrial Consumer Cooperative of the Central Bureau of Economic Development of the Ministry of Economic Affairs is not included in this article as a "" active" surfactant. Useful interface activities for this article are listed in 197 Norris US Patent No. 3,664,961 published on May 23, 197; and US Patent No. 3,919,678 issued on December 30, 1975 by 1 ^ 1 ^ 111 丨 〇 et al. . Useful positive ionic surfactants also include those in Cockrell U.S. Patent No. 4,222,905 issued September 16, 1980, and Murphy's U.S. Patent No. 4,239.659 issued December 16, 1980. However, cationic surfactants and the aluminosilicate materials herein are generally less coordinated. Therefore, since they are used in the composition of the present invention, they are preferably used at low concentrations. The following are representative examples of interface active surfaces useful in this compound. The water-soluble salts of higher fatty acids, namely "soap", is a yin type surfactant in the sister composition of this article. This includes gold-like soaps such as sodium, potassium, ammonium, and alkylammonium salts of higher carbon fatty acids containing from about 8 to about 24 carbon atoms, preferably from about 12 to about 18 carbon atoms. Soap can be made by direct saponification of lipids and oils or by neutralization of free fatty acids. Particularly useful are the sodium and potassium salts * of fatty acid mixtures derived from coconut oil and tallow, namely sodium or potassium fat and coconut soap. Useful anionic surfactants also include water-soluble salts, preferably gold-extracted organic reaction products of telluric acid, ammonium and alkyl clamp salts. In their molecular structure, the alkyl group contains about 10 to about 20 Å carbon atoms and "Acid or sulfuric acid bases (including the alkyl part of the acyl group in the term Λalkyl) a. Examples of the purchase of this group of synthetic surfactants are sodium alkyl acid and potassium, especially those High-Carbon Number Fermentation (Ce-Cie Carbon Atom) Benzoic Acid Surface Finishing Winners • Such as made of sugar lipids or -12- (please read the precautions on the back before filling out this page) Binding-Order &Line; This paper size Using Chinese National #quasi (CNS) f 4 specifications (210 x 297 mm) 81. 5. 20.000 (H)

(JK A 6 B6 五、發明説明(LI) 經濟部+央樣準局员工消費合作社印製 椰子油之甘油酯堪 烷基在直鍵或支鐽 :那些在美國專利 所描述之類型。特 中在烷基部分碳原 -Ci3 LAS 。 本文其他陰離子 尤其那些由動物脂 油脂肪酸單甘油酯 10單位瑁氧乙烷且 酚環氧乙烷鰱硫酸 10單位環氧乙烷且 $環氧乙烷醚硫酸 本文其他有用之 含約6 — 20個碳原 α —磺酸化脂肪酸 9個碳原子且在鐽 氧基一鏈烷一 1 一 20皤碾原子及含約 含約12 - 24僩碳原 1 一 3個碳原子且 一烷氧基鍵烷磺酸 者,但是此酸中和 較佳除離子型界 原製得的;及烷基 姐態上含約9 一約 案第2,220,099號 別有價值的是直鍵 子的平均數目約11 型界面活性劑是烷 及椰子油衍生之較 磺酸納及硫酸納; 其中烷基含約8 — 之納鹽或鉀鹽;及 其中烷基含約10 — 之納鹽或鉀鹽。 陰離子型界面活性 子而且在酯基中含 之酯的水可溶鹽類 烷部分含約9 一約 磺酸之水可溶鹽類 1 一 30莫耳環氧乙 子之烯磺酸之水可 在《烷部分含約8 酯。雖然此酸式》 可依细分敗混合步 面活性劑糊是其焼 苯磺酸納及鉀•'其中 15届碳原子者,例如 及第2,477,383號中 伏烷基苯磺酸酯,其 —13者*確寫為Cii 基甘油基醚磺酸納, 高碳酵之链類;椰子 每分子含約1 一約 約12儷碳原子之烷基 毎分子含約1 一約 約20個碳原子之烷基 劑包括在脂肪酸基中 約1 — 10個碳原子之 ;在皤基中含約2 — 23個碳原子之2 —醢 ;在烷基含約1 0 — 烷之烷基醚硫酸酯; 溶鹽類:及烷基含約 —約20個碳原子之冷 是典型被討論友使用 «的一部分豳行之。 基有10 — 16個碳原子 13- (請先閲讀背面之注意事項再填寫本頁) 裝- 訂· 線. 本紙張尺度遑用中《家«毕(MS)甲4規格(210 x 297公;St) 81. 5. 20.000(H) A6 ___B6 五、發明説明(12) 之直媒形或分支烷基苯磺酸酯之混合物及有10- 18®烷基 碳原子之硫酸烷酯。這些糊通常是由液體有機物質與三氧 化硫反應,Μ產生磺酸及硫酸,然後將酸中和,以產生該 酸之鹽製造之。此鹽在整個此文件中是Μ界面活性劑糊討 論之。納蘧較佳,由於氫氧化納對其他中和劑的最終效率 益處及成本•但不裔像其他可使用之劑諸如:氫氧化鉀。 水可溶非離子型界面活性_在本發明之組合物中•也可 使用作為第二種界面活性劑。事«上,較佳方法是使用陰 離子型/非離子型摻合物。特定較佳糊包括非離子型及陰 離子型界面活性爾之摻合物,其兩者之比例約0.01:1 — 約1 ·· 1 ,更佳約0.05: 1者。非離子型可使用高達等量 之第一種有櫬界面活性劑。此種非離子型物質包括由伸烷 氧基(親水特性者)與有櫬疏水化合物,其可為脂族或烷 基芳族特性者之縮合作用製造之。具任何特定疏水基之聚 伸烷氧基的長度,可容易地調整,Κ產生親水及疏水组份 間有預期平衡程度之水可溶化合物。 經濟部屮央橾準局貝工消费合作社印製 適宜之非離子型界面活性劑包括烷基酚之聚氣化乙烯缩 合物,例如:烷基含約6— 16儷碳原子,呈直a或分支構 型之烷基酚的縮合產物,每其耳烷基酚有約4 一 25其耳的 瓖氣乙烷者。 較佳非鐮子型是含8 — 22個碳原子•圼直_或分支構型 ,每與耳醉有4 一 25舆耳瓖氧乙烷之脂族酵的水可溶縮合 產物。特定較佳是烷基含約9 一 15個碳原子•毎莫耳酵有 4 一 25莫耳環氧乙烷之酵的埔合產物;及丙二酵與環氧乙 —1 4 一 81. 5. 20.000(H) (請先閱讀背面之注意事項再填寫本頁) 本紙張尺度遑用中《家樣毕(CNS)甲4規格(210x297公*) _B6 五、發明説明(13) 烷之縮合產物。 半極性非離子型界面活性劑包括含一烷基部分約10 — 1δ個碳原子及2涠部分選自包括烷基及羥烷基含1 一約3 個碳原子之水可溶胺氧化物;水可溶膦氧化物含一烷基部 分約10-18個碳原子及2個部分選自包括含約1 — 3個碳 原子之烷基及羥烷基者;及水可溶亞®其含約10— 18個碳 原子之一烷基部分及一部分選自包括約1 一 3個碳原子之 烷基及羥烷基部分者。 兩性界面活性劑包括脂族衍生物及雜瓖二级及三级胺之 脂族衍生物,其中脂族部分可為直鍵或分支鐽而且其中一 脂族取代基包含約8 — 18届碳原子且至少一脂族取代基包 含一陰離子型水增溶基。 兩性離子界面活性劑包括胞族四级銨辚·及擁化合物之 衍生物,其中脂族取代基其中之一包含約8 — 18個碳原子 者。 經濟部中央櫺準扃貝Η消費合作社印製 本文特定較佳界面活性劑包括烷基含約11— 14倨碳原子 之線狀烷基苯磺酸酯;動物脂烷基硫酸酯;椰子烷基甘油 基醚磺酸酯;烷基醚硫酸酯,其中烷基部分包含約14 -18個碳原子且其中羥乙基化平均程度約1 一 4 :烯或石蟠 磺酸酯含·約14 - 16涠碳原子者;氧化烷基二甲胺,其中烷 基含約U - 16個礦原子:烷基二甲銨基丙磺酸酯及烷基二 甲箝基羥丙磺酸_·其中烷基含約14 一 18個碳原子者;含 約12—18個碳原子之高碳数脂肪酸之肥皂;Ce-Cie酵與 約3 — 8葜耳環氣乙烷之埔合產物,及其混合物。 — 15 — 81. 5. 20,000(Η) (請先閲讀背面之注意事項再填寫本頁) 本紙張尺度遑用中«國家«华(CNS)甲4規格(210X297公*) 經濟部屮央櫺準局β工消贽合作杜印製 〇〇0〇^4 A 6 _B6 五、發明説明(14> 有用之陽離子界面活性劑包括RdsReRvfTX —型*其中 R4是10-20,較佳12— 18個碳原子,且RB,1^及!?7各為 h-Cy烷基*較佳甲基;X -是陰離子,例如:氯化物之水 可溶四级銨化合物。此種三甲銨化合物之實例包括C12 — C14烷基三甲基銨氯化物及椰子烷基三甲銨甲硫酸酯。 本文使用之特殊較佳界面活性劑包括:線型Cu - C13 烷基苯磺酸納;α—烯系磺酸酯;三乙酵銨Cu — C13烷 基苯磺酸酯;硫酸烷酯(動物脂•椰子•棕ffi *合成起源 者,例如:C45等等);烷基硫酸納;MES ;椰子烷基甘 油基醚磺酸納;動物脂酵與約4莫耳環氧乙烷之硫酸化縮 合產物之納鹽;椰子脂肪酵與約6奠耳環氧乙烷之縮合產 物;動物脂脂肪酵與約11莫耳環氧乙烷之縮合產物;含約 14一約15個碳原子之脂肪酵與約7奠耳環氧乙烷之縮合物 ;C12 — C13脂肪醇與約3莫耳環氧乙烷之縮合產物;3 —(N,N —二甲基一 N—椰子烷基銨基)一2 —羥丙烷 —1 一磺酸酯;3 — (N ,N —二甲基—N —椰子烷銨基 )一丙烷一1 一磺酸酯;6 — (N —十二烷基苄基一 N, N —二甲銨基)己酸酯;+二烷基二甲胺氧化物;椰子烷 基二甲胺氧化物;及椰子及動物脂脂肪酸之水可溶納及鉀 鹽。 如本文所使用之'"界面活性劑〃一詞•除非另外特別指 明•否則其蕙義涤指無非離子型界面活性劑。界面诖性劑 活性(排除非離子型)對乾》去污劑肋洗劑或粉劑之比例 範圍 0.005 — 19: 1 ,較佳 0.05— 10: 1 .更佳 0.1 : 1 ____~ 1 6 ~_ 本紙张尺度遑用中》國家楳毕(CHS)肀4規格(210x297公藿) 81. 5. 20.000(H) (請先閱讀背面之注意事項再填寫本頁) 裝- 訂 五、發明説明〇·5) A 6 B6 經濟部中央橾準局貝工消費合作社印製(JK A 6 B6 V. Description of Invention (LI) Ministry of Economic Affairs + Central Bureau of Standards and Practitioners Employee Consumer Cooperative Printed Coconut Oil's Glyceryl Ester Glyceryl Ester in a straight bond or branch: those described in US patents. Special In the alkyl part of the carbon-Ci3 LAS. Other anions in this article are especially those made from tallow oil fatty acid monoglyceride 10 units oxyethylene and phenol ethylene oxide silver carp sulfate 10 units ethylene oxide and ethylene oxide ether sulfate Other useful materials in this article contain about 6-20 carbon atoms alpha-sulfonated fatty acids with 9 carbon atoms and a milling atom in the oxy-alkane 1-20 ton, and about 12-24 carbon atoms 1-3 A carbon atom and an alkoxy bond alkane sulfonic acid, but this acid is preferably obtained by neutralization of the ion-exchange; and the alkyl group contains about 9 to about 1, No. 2,220,099. The average number of straight bonds is about 11. The surfactant is derived from alkane and coconut oil compared to sodium sulfonate and sodium sulfate; wherein the alkyl group contains about 8-sodium salt or potassium salt; and the alkyl group contains about 10- Sodium salt or potassium salt. Anionic interface activator and ester contained in ester group The soluble salt of the alkyl part contains about 9 to about 1 sulfonic acid water. The soluble salt 1 to 30 moles of ethylene oxide olefin sulfonic acid water can contain about 8 esters in the "alkane part. Although this acid formula" can be The subdivided mixed step surfactant paste is its sodium and potassium benzenesulfonate. • Among them, the 15th carbon atom, for example, and the No. 2,477,383 middle alkyl benzene sulfonate, whose -13 is written as Cii Sodium glyceryl ether sulfonate, a high-carbon yeast chain; coconuts contain about 1 to about 12 carbon atoms per molecule of alkyl group. Each molecule contains about 1 to about 20 carbon atoms. Approximately 1-10 carbon atoms in the base; 2-anhydride containing approximately 2-23 carbon atoms in the base; alkyl ether sulfate containing approximately 10-alkanes in the alkyl group; soluble salts: and alkyl The base contains about — about 20 carbon atoms is typically used by discussion friends «part of it. The base has 10 — 16 carbon atoms 13- (please read the precautions on the back before filling out this page) · Line. This paper uses the standard "Home" Bi (MS) A 4 specifications (210 x 297 g; St) 81. 5. 20.000 (H) A6 ___B6 V. The straight media or points of the invention description (12) A mixture of alkylbenzene sulfonates and alkyl sulfates with 10-18® alkyl carbon atoms. These pastes are usually composed of liquid organic substances that react with sulfur trioxide to produce sulfonic acid and sulfuric acid, and then neutralize the acid, It is made with a salt that produces the acid. This salt is discussed throughout this document as a M surfactant paste. Na is preferred because of the final efficiency benefits and costs of sodium hydroxide for other neutralizers. Other agents that can be used are such as: potassium hydroxide. Water-soluble non-ionic surfactant _ in the composition of the present invention can also be used as a second surfactant. In fact, the preferred method is to use anionic / nonionic blends. Particularly preferred pastes include blends of nonionic and anionic surfactants, the ratio of which is about 0.01: 1 to about 1.1, more preferably about 0.05: 1. The nonionic type can use up to the same amount of the first surfactant. Such non-ionic substances include those produced by the condensation of alkyleneoxy groups (hydrophilic properties) and hydrophobic compounds that can be aliphatic or alkylaromatic properties. The length of the polyalkyleneoxy group with any specific hydrophobic group can be easily adjusted. K produces water-soluble compounds with a desired degree of balance between the hydrophilic and hydrophobic components. The non-ionic surfactants printed by the Beigong Consumer Cooperative of the Ministry of Economic Affairs of the People ’s Republic of China. Suitable non-ionic surfactants include polyphenol condensates of alkyl phenols. The condensation product of the branched configuration of alkylphenols has about 4 to 25 oz of gaseous ethane per alkyl phenol. The preferred non-sickle type is a water-soluble condensation product of an aliphatic leaven containing 8 to 22 carbon atoms, straight or branched configuration, and 4 to 25 mg per ear of drunken ear. Particular preference is given to alkyl groups containing about 9 to 15 carbon atoms. • Each molar enzyme has 4 to 25 molar ethylene oxide fermentation products; and malonylase and ethylene oxide—1 4 to 81. 5 . 20.000 (H) (Please read the precautions on the back before filling in this page) This paper is used in the "Home Sample Bi (CNS) A 4 specifications (210x297 g *) _B6 V. Invention description (13) Condensation of alkanes product. Semi-polar nonionic surfactants include water-soluble amine oxides containing an alkyl group of about 10-1δ carbon atoms and 2 parts selected from alkyl and hydroxyalkyl groups containing 1 to about 3 carbon atoms; The water-soluble phosphine oxide contains an alkyl moiety of about 10-18 carbon atoms and 2 moieties selected from those including alkyl and hydroxyalkyl containing about 1-3 carbon atoms; An alkyl portion and a portion of about 10 to 18 carbon atoms are selected from alkyl and hydroxyalkyl portions including about 1 to 3 carbon atoms. Amphoteric surfactants include aliphatic derivatives and aliphatic derivatives of secondary and tertiary amines, wherein the aliphatic portion may be a straight bond or a branched branch and one of the aliphatic substituents contains about 8-18 carbon atoms And at least one aliphatic substituent contains an anionic water solubilizing group. Zwitterionic surfactants include derivatives of quaternary quaternary ammonium compounds of the family and derivatives, and one of the aliphatic substituents contains about 8 to 18 carbon atoms. Printed by the Ministry of Economic Affairs of the Central Ministry of Economic Cooperation and Consumer Cooperatives. Specific preferred surfactants include linear alkylbenzene sulfonates with alkyl groups containing about 11 to 14 carbon atoms; tallow alkyl sulfates; coconut alkyl groups Glyceryl ether sulfonate; alkyl ether sulfate, in which the alkyl portion contains about 14-18 carbon atoms and wherein the average degree of hydroxyethylation is about 1 to 4: alkene or sulfonate contains about 14- Those with 16 carbon atoms; alkyl dimethylamine oxides, where the alkyl group contains about U-16 mineral atoms: alkyl dimethyl ammonium propane sulfonate and alkyl dimethyl ammonium hydroxypropane sulfonate The base contains about 14 to 18 carbon atoms; soaps containing high carbon number fatty acids of about 12-18 carbon atoms; Ce-Cie leaven and about 3 to 8 round earrings gas ethane combined products, and mixtures. — 15 — 81. 5. 20,000 (Η) (please read the notes on the back before filling in this page) This paper uses the Chinese «National« China (CNS) A 4 specifications (210X297) *) Ministry of Economic Affairs Quasi-bureau β-work dissipation co-production duo printing 〇〇〇〇 ^ 4 A 6 _B6 V. Description of the invention (14> useful cationic surfactants include RdsReRvfTX-type * where R4 is 10-20, preferably 12-18 Carbon atoms, and RB, 1 ^ and! 7 are each h-Cy alkyl * preferably methyl; X-is an anion, for example: chloride water-soluble quaternary ammonium compound. Examples of such trimethylammonium compounds Including C12-C14 alkyl trimethyl ammonium chloride and coconut alkyl trimethyl ammonium methosulfate. The particularly preferred surfactants used in this article include: linear Cu-C13 sodium alkylbenzene sulfonate; alpha-olefin sulfonic acid Ester; Triethylammonium Cu—C13 alkylbenzene sulfonate; alkyl sulfate (tallow • coconut • brown ffi * synthetic origin, for example: C45, etc.); sodium alkyl sulfate; MES; coconut alkyl glycerin Sodium ether ether sulfonate; sodium salt of animal lipase and sulfated condensation product of about 4 moles of ethylene oxide; coconut lipase and about 6 moles of epoxy Condensation products of alkanes; Condensation products of tallow fat and about 11 moles of ethylene oxide; Condensates of lipase containing about 14 to about 15 carbon atoms and about 7 moles of ethylene oxide; C12-C13 fatty alcohols Condensation products with about 3 moles of ethylene oxide; 3- (N, N-dimethyl-N-coconut alkyl ammonium) -2-hydroxypropane-1 monosulfonate; 3- (N, N— Dimethyl-N-coconut alkylammonium) -propane-1 monosulfonate; 6- (N-dodecylbenzyl-N, N-dimethylammonium) hexanoate; + dialkyldi Methylamine oxide; Coconut alkyl dimethylamine oxide; and the water-soluble sodium and potassium salts of coconut and tallow fatty acids. As used herein, the term '" surface active agent 〃 unless otherwise specifically indicated otherwise Its meaning means that there is no non-ionic surfactant. The interfacial agent activity (excluding non-ionic) on dry "detergent detergent rib lotion or powder ratio range 0.005-19: 1, preferably 0.05-10: 1 .Better 0.1: 1 ____ ~ 1 6 ~ _ This paper is in use "National Standard (CHS) Yu 4 Specification (210x297 Commonweed) 81. 5. 20.000 (H) (please first Read the precautions on the back and then fill out this page) Binding-Order V. Description of invention 〇 · 5) A 6 B6 Printed by Beigong Consumer Cooperative, Central Central Bureau of Economic Affairs

一 5 : 1。甚至更佳是前述界面活性麵活性對助洗朗的比 例是0.15: 1—1 : 1 ;及0.2 : 1—0.5 : 1)。 檯壓維 在一連鑛基礎上,擄壓拥進行黏滯界面活性劑期之泵送 及混合之官能。一基本擠壓機是由一桶與一光滑内圓筒形 表面姐成。在此桶之内装有擠壓櫬揉旋。當嫘旋旋轉時, 引起瑚沿桶之長度移動,此為高活性糊之入口。 擠壓桷之詳佃設計使其可進行各種不同的功能。首先在 桶中有額外的入口,可容納其他組份,包括直接添加至此 桶中之化學構建黼。第二真空泵及鏡嫘旋軸之密封環•使 其可被抽真空,其使得水分含量降低。第三,加熱或冷卻 之工具*可安装在桶之壁上,供控制溫度。第四,擠懕櫬 螺旋之仔钿設計,促進糊本身與其他添加物兩者之混合。 較佳擠壓櫬是雙螺旋擠壓機。此類型擠壓機有2個螺旋 平行安装在相同桶中,其使得可以相同方向(共同旋轉) 或Μ相反方向(逆旋轉)旋轉。·共同旋轉之雙螺旋擠壓櫬 是本發明使用之最佳一種設備。 在本發明中擠壓櫬特別有用是因為藉由於桶中添加液氮 或固雎二氣化碳,可有效地將糊冷卻(此可能被認為令人 驚訝,因為為了克眼鲇滯剪切力•機械能输入的结果,通 常會導致摘《拥加热其内容物)•同時將增加黏滞(較冷 的)糊泵送出擠壓拥外並且進入混合拥/附聚拥發生或粒 作用。 在本發明中使用之通宜雙嫘旋搞壓機包括那些由:APV (請先閲讀背面之注意事項再填窝本頁) 裝< 訂· 線- 一 1 7 — 本紙張尺度遑用中••家«準(CNS)甲4規格(210x297公釐) 81. 5. 20,000(H) ^j00〇S4 A 6 B6 經濟部中央橾準局员工消費合作社印製 五、發明説明(L6) Baker (CP条列);Werner及Pfleiderer. (Continual 列);Wenger (TF糸列);Leistritz · (ZSE 系列); 及Buss (LR系列)提供者。 此擄®機容許藉由瀰度及溫度的減低•諝理糊。水分可 於真空,較佳在0«米汞柱(壓力表)及一 55«米汞柱( 壓力表)之間(大氣壓力Μ下0— 7,3仟巴)下去除之。 溫度可藉由於擠Κ捅中直接添加固體二氧化碳或液態氮 ,使其降低。較佳液態於高達糊之30重量%的量使用之。 粉狀涪 雖然本發明之方法的較佳具體實例包括依上述方法*经 糊中導入陰離子型界面活性蜊,但是可能有某些量是纆粉 吠流,例如:以裼色粉末之形式導入。在這些具體實例中 ,粉狀流之黏性及水分必須保持在低的程度*藉以防止增 加陰離子型界面活性劑之、、負荷"及,因此產生界面活性 劑之濃度太高的附聚物。較佳附聚方法之液髑流也可用於 導人其他界面活性劑及/或聚合物。此可藉由將界面活性 劑預混入一液體流施行之或變更為,藉由在附聚器中導入 各種不同的流。這兩棰方法之具賭實例,可產生不同性霣 之製成粒子(配藥,皤凝,溶解速率等等),尤其,若讓 混合之界面活性劑於粒子形成之前形成。那麽這些差異可 利用作為每一較佳方法之意圃應用的優點。 碓由使用目前描述之技術,也已娌覿察到,在最终配方 中,巳經可能併入之某些化學品(例如:非離子型•擰後 酸)的濃度比經任何其他巳知加工途徑更高*而對於此基 一 1 8 一 (請先閲讀背面之注意事項再填窝本頁) 裝. 訂· 線· 本紙張尺度逡《中諷家«準(CHS)甲4規格(210x297公釐) 81. 5. 20.000(H) 200524 A 6 B6 五、發明説明Ο·7) 經濟部中央橾準ijA工消費合作杜印製 霣之一些醐鍵性質,沒有有害的作用(结塊,κ實等等) 〇 油分齡珉会好成I»作用 如本文使用之"细分散混合及/或成粒作用"一詞,意 義是在一细分敗琨合器中,除非特別註明,否則指於絜片 尖端速度約5米/秒一約50米/秒之速度,將上述混合物 混合及/或成粒。混合及成粒遇程之结}停留時間,較佳在 0.1 — 10分之级次,更佳0.1 — 5 .最佳0.2 — 4分。更 佳混合及成粒尖端速度是約10— 45米/秒,及約15- 40米 /秒。 捆對粉之比例應加以選擇Κ便在此方法之所有階段都维 持肉眼可見,涸別粒子。這些粒子於較高溫度可膠粘,但 是必須實質上自由流動,使得混合成粒步驟可同時進行, 或陸績立刻進行,而不會引起混合器/成粒機堵塞。 任何裝置,工廠或構成單元適於界面活性劑加工者,都 可用於腌行根據本發明之方法。適宜之装置包括例如:降 膜磺化反應器,消化桶,酯化反懕器等等。為了混合/附 聚作用,若千混合器/附聚器中的任一種都可使用。在一 較佳具體«例中,連續施行本發明之方法。特別較佳的是 由日本Fukae Powtech Kogyo 公司製造之 FukaeR FS — G 系列之混合器;此装置本霣上係圼碗型容器之形式.經頂 端入口可進去•接近其基部,設有一》質上垂直袖之播拌 器,且有一切刀位於側壁上。此播拌器及切刀可彼此分開 ,並且於分關變化速度下搡作。此容器可装埔有冷卻套管 19- (請先閲讀背面之注意寧項再填寫本頁) 裝. 訂· 線- 本紙張尺度4用中釅家«毕(CNS)甲4規格(210 x297公*) 81. 5. 20.000(H) 經濟部中央橾準^s工消费合作社印製 〇〇0〇S^ A 6 ____B_6 五、發明説明〇_8) 或’若須要可装衡有低溫姐件。 在本發明之方法中纆發現通於使用之其他類型混合器包 括德困 Dierks & SShne 之 DiosnaR V e:{条列英國 TK Filder公司之Pharna Matrix* ex 。其他混合器相信應於 用在本發明之方法中的是日本的Fuji Sangyo公司之 PujiR VG — Cex系列;及義大利的 Zanchetta & Co srl 之 RotoR ex〇One 5: 1. Even more preferably, the ratio of the aforementioned surface-active surfactant to builders is 0.15: 1-1: 1; and 0.2: 1-0.5: 1). The platform pressure maintains the function of pumping and mixing viscous surfactants on the basis of a continuous mine. A basic extruder consists of a barrel and a smooth inner cylindrical surface. Inside this bucket is equipped with squeeze and knead. When the spin rotates, it causes the coral to move along the length of the barrel, which is the entrance of the highly active paste. The exquisite design of the extrusion base allows it to perform various functions. First of all, there are additional entrances in the barrel, which can accommodate other components, including the chemically constructed striated ribs added directly to the barrel. The sealing ring of the second vacuum pump and the mirror shaft of the rotating mirror • enables it to be evacuated, which reduces the moisture content. Third, heating or cooling tools * can be installed on the wall of the barrel for temperature control. Fourth, squeeze and squeeze the design of the spiral child to promote the mixing of the paste itself and other additives. The preferred extruder is a double screw extruder. This type of extruder has 2 spirals installed in parallel in the same barrel, which makes it possible to rotate in the same direction (co-rotation) or in the opposite direction (reverse rotation). · The co-rotating double spiral extruder is the best equipment used in the present invention. Extrusion is particularly useful in the present invention because by adding liquid nitrogen or solid-liquid carbon dioxide to the barrel, the paste can be effectively cooled (this may be considered surprising because of the stagnation of shear force • The result of mechanical energy input, which usually leads to excerpts heating the contents) • Simultaneously pumping increased viscosity (colder) paste out of the squeeze envelope and into mixed / agglomerated envelope occurrence or granulation. The Tongyi Shuangrong rotary presses used in the present invention include those made of: APV (please read the precautions on the back before filling the nest page). Installation &Order; Line-1 1 7-This paper size is not in use •• Home «Precision (CNS) A 4 specifications (210x297 mm) 81. 5. 20,000 (H) ^ j00〇S4 A 6 B6 Printed by the Central Consumer ’s Bureau of the Ministry of Economic Affairs Employee Consumer Cooperative V. Invention Instructions (L6) Baker (Article CP); Werner and Pfleiderer. (Continual column); Wenger (TF Shito column); Leistritz (ZSE series); and Buss (LR series) providers. This 掳 ® machine allows confusing by reducing the density and temperature. Moisture can be removed in a vacuum, preferably between 0 «mHg (pressure gauge) and a 55« mHg (pressure gauge) (0-7,3 thousand bar at atmospheric pressure M). The temperature can be reduced by adding solid carbon dioxide or liquid nitrogen directly during extrusion. The liquid is preferably used in an amount of up to 30% by weight of the paste. Powdered fuze Although preferred specific examples of the method of the present invention include the introduction of anionic interface active clam into the paste according to the above method *, there may be a certain amount of powdery bark flow, for example, in the form of a powdery powder. In these specific examples, the viscosity and moisture of the powder stream must be kept low * to prevent the increase of anionic surfactant, load, and therefore, agglomerates with too high surfactant concentration . The liquid agglomeration method of the preferred agglomeration method can also be used to introduce other surfactants and / or polymers. This can be implemented or pre-mixed by premixing the surfactant into a liquid stream, by introducing various streams in the agglomerator. These two examples of gambling methods can produce particles of different sexes (dispensing, coagulation, dissolution rate, etc.), especially if the mixed surfactant is allowed to form before the particles are formed. Then these differences can take advantage of the application of each preferred method. By using the techniques described so far, it has also been observed that in the final formulation, the concentration of certain chemicals that may be incorporated (for example: non-ionic • after-acid) is higher than that of any other known processing The way is higher * and for this base one 18 one (please read the precautions on the back before filling the nest page). Binding · Thread · The paper standard "Chinese sati« quasi (CHS) A 4 specifications (210x297 Mm) 81. 5. 20.000 (H) 200524 A 6 B6 V. Description of invention Ο · 7) Some of the bond properties of the central government ’s Ministry of Economic Affairs, ijA, industrial and consumer cooperation, Du Yin, and no harmful effects (agglomeration, κ 实, etc.) 〇The oil ageing Min will be good as I ». The term" fine dispersion and / or granulation "as used in this article means that it is in a subdivision mixer, unless otherwise specified. Otherwise, it refers to mixing and / or granulating the above mixture at a speed of about 5 meters / second to about 50 meters / second at the tip of the tablet. The end of the mixing and granulation process is preferably in the order of 0.1-10 points, more preferably 0.1-5. The best 0.2-4 points. Better mixing and granulation tip speeds are about 10-45 meters / second, and about 15-40 meters / second. The ratio of the bale to the powder should be selected Κ so that it remains visible to the naked eye at all stages of the method, eliminating particles. These particles can be glued at higher temperatures, but must be substantially free-flowing, so that the mixing and granulation steps can be performed at the same time, or Lu Ji can be carried out immediately, without causing blockage of the mixer / granulator. Any device, plant, or component that is suitable for surfactant processing can be used for curing the method according to the present invention. Suitable devices include, for example, falling film sulfonation reactors, digestion tanks, esterification reactors and the like. For mixing / agglomeration, any of the Thousand Mixer / Agglomerator can be used. In a preferred embodiment, the method of the present invention is continuously performed. Particularly preferred is the FukaeR FS-G series mixer manufactured by Japan Fukae Powtech Kogyo; this device is in the form of a bowl-shaped container. It can be accessed through the top entrance • close to its base, with a high quality The vertical sleeve of the mixer, and all the knives are located on the side wall. The seed mixer and cutter can be separated from each other, and work under the speed of the sub-gate change. This container can be filled with a cooling sleeve 19- (please read the note on the back side and fill in this page first). Order · Thread-This paper size 4 is used in the Zhongzhijia «Bi (CNS) A 4 specifications (210 x297 Public *) 81. 5. 20.000 (H) Printed by the Central Ministry of Economic Affairs ^ s Industrial and Consumer Cooperatives 〇〇〇〇S ^ A 6 ____B_6 V. Description of invention 〇_8) or 'If necessary, you can weigh and have a low temperature sister Pieces. In the method of the present invention, other types of mixers commonly used include DiosnaR V e: {Article Pharna Matrix * ex of TK Filder, UK). Other mixers believed to be used in the method of the present invention are the PujiR VG-Cex series from Fuji Sangyo of Japan; and the RotoR ex of Zanchetta & Co srl of Italy.

其他較佳之通宜設備可包括由德國Gustau Eirich Hardheim 製造之 EirichR ,RV系列;由德國 Paderborn 之 Lodige Machinenbau GmbH 製造,供分批混合之LodigeR ,FM系列,供連續混合/附聚之Baud Ο系列;德画 Mannkein之 Drais Werke GmbH製造之 DraisR Τ160糸列; 及由英國Bershire的Winkworth Machinery公司製造之 WinkworthR RT25 系列。Other preferred Tongyi equipment may include EirichR, RV series manufactured by Gustau Eirich Hardheim, Germany; LodigeR, FM series manufactured by Lodige Machinenbau GmbH, Paderborn, Germany, for batch mixing; Baud Ο series for continuous mixing / agglomeration; German painting DraisR Τ160 series made by Drais Werke GmbH of Mannkein; and WinkworthR RT25 series made by Winkworth Machinery in Bershire, England.

Littleford混合機,JIFM-130-D-12型,有内切碎片及 C u ί s ί n a「t F ο 〇 d 加工機,It D C X - P 1 u s 型,有 7 . 7 5 时( 19.7公分)刀片者,為2種適宜混合機之實例。任何其他 混合機有细分敗混合/成粒能力並且停留時間在〇·1 — 10分》级次者,都可使用。在旋轉軸上有幾個絜片之"絮 輪式"絮輪混合拥較佳。本發明可Μ分批次或連鑛.方式S 施0 播作通麻 較佳裸作溫度也應盡可能低•因為這將會導致在製成之 顆粒中較高的界面活性劑濺度。較佳於附聚期間的溫度少 一 2 0 — — 本紙張尺度遑用中《國家樣毕(CHS) 規格(210x297公*) 81. 5. 20.000(H) (請先閲讀背面之注意事項再填窝本頁) 装- 線· A 6 __B_6 五、發明説明(19) 於100亡,以10— 901C更佳,最佳是介於20— 80¾之間。 在本發明中有用之較低操作溫度,可薄由在此技藝上已知 之各棰不同的方法達到目的,諸如氮冷卻,設備之冷卻水 套層,添加固體二氣化碳等;較佳方法是固體二氧化碳, 最佳方法是液氮冷卻。 在本發明較佳具體實例中伴隨有高度吸引人之附件,以 進一步增加最終顆粒中界面活性_之瀟度,係於一含除離 子型界面活性劑及/或其他界面活性劑之液體流•附加導 致增加糊之黏度及/或熔點及/或滅低糊之黏性的其他要 素。在本發明之方法的較佳具體實例中,當糊泵送至附聚 器中時,可在管線中進行造些要素的添加。這些要素的實 例可為各種不同的粉末,將於本文更詳细地描述。 黑铢附驵合物 經濟部中央橾準^1¾工消费合作社印製 (請先閲讀背面之注意事項再填窝本頁) 本發明製造供用於去污劑姐合物之高密度顆粒。供併入 粒狀去污劑之最终附聚物的較佳姐合物,具有高界面活性 劑瀠度。藉由增加界面活性劑的湄度,由本發明製得之顆 粒/附聚物,更適於各種不同的配方。這些含顆粒狀附聚 物之高界面活性劑,需要較少完成技術,以達到最終附聚 物•因此,免除大量在全部去污劑製造過程(唄孩乾煉, 去粉等等)之其他加工步驟中可使用之加工肋劑(嫵機粉 等等)。 根據本發明製得之顆粒大,低臞粉且自由流動•較佳具 有約0.4 —約1.2克/ «升的鬆密度,更佳是約0.6 _約 0.8克/毫升。本發明之頼粒的重最平均粒子大小約200 一 2 1 — 本紙張尺度逍用令«家搮準(CNS)甲4規格(210x297公釐) 81. 5. 20,000(H) 2005: A 6 B6 五、發明説明(20) 經濟部+央標準局貝工消贫合作社印生Littleford mixer, model JIFM-130-D-12, with in-cut chips and C u ί s ί na "t F ο 〇d processor, It DCX-P 1 us model, 7. 7 5 hours (19.7 cm ) The blade is an example of 2 suitable mixers. Any other mixer has subdivision mixing / granulation ability and the residence time is in the range of 0.1-10 points. It can be used on the rotating shaft. Several "float wheels" of "float wheel" are preferred. The present invention can be divided into batches or continuous mines. Method S Application 0 Broadcasting of hemp is preferred. The temperature of bare work should also be as low as possible. This will result in a higher surfactant splash in the particles made. It is better to reduce the temperature during the agglomeration by one to 20. — This paper scale is not used in the “National Sample (CHS) Specification (210x297 *) 81. 5. 20.000 (H) (please read the precautions on the back before filling in the nest page) 装-线 · A 6 __B_6 5. Description of the invention (19) died at 100, preferably 10-901C, the best It is preferably between 20 and 80¾. The lower operating temperature useful in the present invention can be achieved by different methods known in the art, such as Cooling, the cooling water jacket of the equipment, the addition of solid carbon dioxide, etc .; the preferred method is solid carbon dioxide, the best method is liquid nitrogen cooling. In the preferred embodiment of the present invention is accompanied by a highly attractive accessory, to further Increasing the interfacial activity in the final granules is a liquid flow containing deionized surfactants and / or other surfactants. The addition leads to an increase in the viscosity and / or melting point of the paste and / or to eliminate the viscosity of the paste Other factors of the nature. In a preferred embodiment of the method of the present invention, when the paste is pumped into the agglomerator, some elements can be added in the pipeline. Examples of these elements can be various powders, It will be described in more detail in this article. Printed by the Black Baht Attachment Ministry of Economy Central Central Standards ^ 1¾ Industrial and Consumer Cooperatives (please read the precautions on the back before filling the nest) This invention is made for use in detergent High-density particles of the compound. The preferred sister compound for the final agglomerate to be incorporated into the granular detergent has a high surfactant level. It is produced by the present invention by increasing the degree of surfactant Particles / attached Agglomerates are more suitable for various formulations. These high surfactants containing granular agglomerates require less finishing technology to reach the final agglomerates. Therefore, a large amount of detergent is eliminated in the entire detergent manufacturing process (chant) It can be used in other processing steps (such as dry powder, powder removal, etc.) processing ribs (powder powder, etc.). The particles prepared according to the present invention are large, low in powder and free flowing. Preferably, it is about 0.4- The bulk density of about 1.2 g / «liter, more preferably about 0.6 _ about 0.8 g / ml. The weight of the grain of the present invention is the most average particle size of about 200 a 2 1 — the paper size is easy to use CNS) A4 specifications (210x297 mm) 81. 5. 20,000 (H) 2005: A 6 B6 V. Description of invention (20) Printed by the Ministry of Economic Affairs + Central Standards Bureau Beigong Poverty Alleviation Cooperative

-約1000微米。如此形成之較佳顆粒的粒子大小範園是 200 - 1000微米。如此形成之較佳頼粒的粒子大小範圍是 200 — 2000微米。更佳成粒溫度範圃約10C —約60¾,最 佳約 20*C -約 50t:。 乾悝 本發明之自由流動顆粒的預期水分含量•藉由在習用之 粉末乾嫌設備諸如流化床乾燥器中乾嫌,可調整至適於意 圖應用之程度。若使用热空氣流化床乾燁器*必須小心理 用*以避免顆粒之热敏感姐份分解。大規棋儲存之前*也 宜具有冷卻步驟。此步驟也可在用冷卻空氣搡作之習用流 化床中進行。附聚物之乾煉/冷卻,也可在通於粉末乾埭 諸如旋轉乾堍器等之任何其他設備中進行。 就去污劑應用而言,附聚物之最終水分必須維持低於附 聚物可以大量貯存及埋送的程度。正確水分含量,依附聚 物的姐成而定,但典型是達到自由態水(即在附聚物中水 不形成任何结晶性形式)的1 一 8%之程度,最典型是在 2 - 4 % ° 去污叻浼黼》粉劊 任何可配位之去污肋洗劑或助洗劑或粉劑之姐合•都可 用於本發明之方法及姐合物中。 本文之去污劑姐合物中可包含某些具下式之结晶性鋁砂 酸期離子交換物霣 Naz 〔 (Al〇2)z· (SiQa)y〕 · XHaO (請先閲讀背面之注意事項再填窝本頁) 裝· 訂- f -線· 木紙張尺度遑用中家樣準(CHS)甲4規格(210x297公釐) 81. 5. 20,000(H) -22- ;〇〇δ^ A 6 B6 五、發明説明(2+) 式中z及y至少約6 ,z尉y之克分子比例是約_ 約0.4且ζ是約10—約264 。本文有用之無定形水合組矽 酸鼸物質具有下列S驗式 Μζ(ζΑ1〇2· ySi〇2) 式中Μ是納,鉀,銨或經取代銨,z是約0.5 —的2且7 是1 ,前述物霣之鎂離子交換容量*每克無水猶矽酸籩至 少約50¾克當1的碳酸鈣硬度。水化納沸石A之粒子大小 較佳是約1 — 10微米。 經濟部屮央櫺準局貝工消费合作社印製 本文之鋁矽酸《離子交換助洗劑物質是圼水化形式,若 结晶性則含約10 -約28重最%的水,若呈無定形甚至含潛 在更高量的水。高度較佳之结晶性鋁矽酸邇離子交換物質 ,在其結晶基質中包含約18% —約22%的水。此结晶性鋁 矽酸锂離子交換物質進一步特色是粒子大小直徑的0.1微 米至約10微米。無定形物質通常較小,例如低至少於約 0.01微米。較佳離子交換物筲之粒子大小直徑約0.2微米 -約4微米。本文*粒子大小直徑〃代表一既定艟子交換 物笛依習用分析技術例如:利用掃瞄雷子顧微鏡之顧微鏑 測定,所測定之霪量比平均粒子大小直徑。本文之結晶性 鋁矽酸鹽離子交換物霣通常進一步具有之特色是其 交換容最· Μ無水為基準計算*每可鋁矽酸醱至少的2()() «克當最的碳酸钙水硬度,其一般範園是約300 23 81. 5. 20.000(H) (請先閲嘥背面之注意事項再蜞窝本頁) 本紙張尺度边用中 B家樣準(CNS)甲4規格(210x297公;Jt) 、〇0沾 A 6 B6 五、發明説明(22) 經濟部中央橾準局貝工消t合作社印製-About 1000 microns. The preferred size of the particles thus formed is 200-1000 microns. The particle size range of the better granules thus formed is 200-2000 microns. The better granulation temperature range is about 10C to about 60¾, and the best is about 20 * C to about 50t :. Dryness The expected moisture content of the free-flowing particles of the present invention can be adjusted to a degree suitable for the intended application by drying in conventional powder drying equipment such as fluidized bed dryers. If you use a hot air fluidized bed dryer * you must use it with a small mind * to avoid decomposition of the heat sensitive parts of the particles. It is also advisable to have a cooling step before storing large-scale chess. This step can also be carried out in a conventional fluidized bed with cooling air. Drying / cooling of agglomerates can also be carried out in any other equipment such as rotary dryers, etc., which are used for powder drying. For detergent applications, the final moisture content of the agglomerates must be kept below the level where the agglomerates can be stored and buried in large quantities. The correct moisture content depends on the agglomeration of the agglomerate, but it is typically 1 to 8% of the free state water (that is, water does not form any crystalline form in the agglomerate), and the most typical is 2 to 4 % ° Decontamination Lattices "powders can be used in any of the coordinated decontamination rib lotions or builders or powders can be used in the method and composition of the present invention. The detergent compound in this article may contain some crystalline aluminic acid phase ion exchangers Naz 〔(Al〇2) z · (SiQa) y〕 with the following formula: XHaO (please read the notes on the back first Matters refill on this page) Binding · Order-f-line · Wooden paper size used in the home sample standard (CHS) A 4 specifications (210x297 mm) 81. 5. 20,000 (H) -22-; 〇〇δ ^ A 6 B6 V. Description of the invention (2+) where z and y are at least about 6, the molar ratio of z y is about _ about 0.4 and ζ is about 10 to about 264. The amorphous hydrated group silicate material useful herein has the following formula Mζ (ζΑ10〇 · ySi〇2) where M is sodium, potassium, ammonium or substituted ammonium, z is about 0.5-2 and 7 is 1. Magnesium ion exchange capacity of the aforementioned substances * At least about 50¾ grams of calcium carbonate hardness per gram of anhydrous silicate. The particle size of sodium hydrated zeolite A is preferably about 1-10 microns. The aluminosilicate "Ion Exchange Builder Substance is a hydrated form, if crystalline, it contains about 10 to about 28% by weight of the most water, if there is no The setting even contains potentially higher amounts of water. The highly preferred crystalline aluminosilicate ion exchange material contains about 18% to about 22% water in its crystalline matrix. This crystalline lithium aluminum silicate ion exchange substance is further characterized by a particle size diameter of 0.1 micrometer to about 10 micrometers. Amorphous materials are usually small, for example, less than about 0.01 microns. Preferably, the particle size of the ion exchanger is about 0.2 microns to about 4 microns in diameter. In this paper, the particle size diameter 〃 represents a given scorpion exchange flute according to conventional analysis techniques, such as: the measurement of Gu Weidymium using the scanning Leizi Gu Weijing, and the measured amount of scant is larger than the average particle size diameter. The crystalline aluminosilicate ion exchangers in this article are usually further characterized by their most exchangeable capacity. Calculated on the basis of anhydrous * * At least 2 () () of each aluminosilicate; Hardness, its general range is about 300 23 81. 5. 20.000 (H) (please read the notes on the back of the page before spitting this page) This paper is used in the B home sample standard (CNS) A 4 specifications ( 210x297; Jt), 〇0 dip A 6 B6 V. Description of the invention (22) Printed by Beigongxiaot Cooperative, Central Bureau of Economic Affairs, Ministry of Economic Affairs

/克至約352藿克當量/克。|S矽酸鹽離子交換物質本文 進一步特激為其鈣離子交換速率,以鈣離子硬度為基準, 至少約2粒Ca — /加侖/分/克/加侖鋁矽酸鹽(無水為 基準),且一般是介於約2粒/加侖/分/克/加侖一約 6粒/加侖/分/克/加侖。助洗劑目的之最通鋁矽酸鹽 顯示鈣離子交換速率至少约4粒/加侖/分/克/加侖。 無定形鋁矽酸鼸離子交換物質普通Mg “交換至少約50¾ 克當悬CaC03 /克(12毫克Mg —/克)旦Mg —交換速宰至 少約1粒/加侖/分/克/加侖。當《铜(Cu)辐射( 1.54A單位)檢驗時,無定形物質未顯示可觀察之繞射圏 案。 在本發明之實務上有用之鋁矽酸鹽離子交換物質是商場 上可取得。在本發明中有用之i呂矽酸鹽,可呈结晶性或無 定形構造並且可為天然發生之鋁矽酸鹽或合成上衍生者。 製造鋁矽酸期離子交換物質之方法,被討論在1976年10月 12日發行之Krumnel等人之美画專利案第3,985,669號, 併於本文供參考。在本文有用之較佳合成结晶性IS矽酸鹽 離子交換物質是於Zeolite A · Zeolite B,及Zeolite X名下可取得。在特別較佳具雅《例中•此结晶性鋁矽酸 鹽離子交換物S具下列化學式 Haia 〔 (A10z)i2(Si〇2)i2〕 · XH2O (請先閲讀背面之注意事項再場窝本頁) 裝· 訂_ 線· 一 2 4 — 本紙張尺度逍用中BB家樣竿(CNS)甲4規格(210x297公*) 81. 5. 20,000(H) A 6 B6 五、發明説明(23) 式中X約20—約30,尤其約27,且粒子大小一般少於約5 微米。 本發明之粒狀去污劑可包含中性或鹺式鹽,其在溶液中 之pH為7或更大,並且可為有機或無機特性者。助洗劑醴 對本文之去污劑顆粒協肋提供預期密度及脹量。而鹽類中 的一些是梅性•它們中的許多在洗灌溶液中,也當作去污 肋洗麵物霣的作用。 中性水可溶邇類之實例包括鐮金羼,銨或經取代銨氯化 物,氟化物及硫酸鹽。上述鹽類以醮金屬,尤其納鹽較佳 。硫酸納為在去污鋼顆粒中典型被使用者且為特定較佳鹽 。檫檬酸及一般任何其他有櫬或無櫬酸,只要其化學上與 其餘附聚物姐合物可配伍者,都可併入本發明之粒狀去污 劑中。 其他有用之水可溶鹽包括普通已知為去污劑助洗劑物霣 之化合物。肋洗劑一般選自各種不同的水可溶*驗金鼸* 銨或經取代銨磷酸鹽,多磷酸鹽·膦酸鹽,多膦酸鹽,碳 酸鹽·矽酸鹽,硼_蘧•及多羥基磺酸鹽。較佳上述之馥 類是Ml金《鹽,尤其納鹽。 經濟部中央橾準而貝工消贽合作社印製 無機《酸鹽肋洗劑之特殊«例是聚合度約6 — 21之三多 磷酸納焦磷酸,聚合偏磷酸及原磷酸納及鉀。多磷酸嫌助 洗劑之*例是乙二膦酸之納及鉀》,乙烷1 一羥基一 1 , 1 一二瞩酸之納鼸及押鹽•乙烷1 · 1 ,2 —三膦酸之納 及钾薷*其他磷肋洗劑化合物掲示在美國專利案 3.159,581 ; 3,213,030 :3,422.021 :3.422.137 ; 一 2 5 — 81. 5. 20,000(H) (請先閲讀背面之注意事項再填窝本頁) 本紙張尺度遑用中面國家樣準(CNS)甲4規格(210x297公釐) 〇〇0〇^^ A6 ________B_6 五、發明説明(2磉 3,400,176及3,400 , 148中,併於本文供參考。 非磷,無櫬助洗劑之實例是碳酸納及鉀,碳酸氫納及鉀 •碳酸氫三納及鉀,四硼酸納及鉀十水合物及Si〇2對驗金 覼氧化物之克分子比例約0.5 —約4.0 ,較佳約1.〇 一約 2.4之矽酸鹽。由本發明之方法製得之组合物不需過黴加 工用之碳酸鹽,且較佳不含超過2%如1980年4月1日公 佈之Clarke等人之美醑専利案第4,196,093號中揭示之细 碎碳酸鈣,且較佳不含後者。 如上面提及之粉末,通常被用於去污劑的諸如沸石,碳 酸鹽•矽石,矽酸鹽,檸樺酸鹽•磷酸魍,遇硼酸鼸等’ 及加工酸諸如澱粉,都可用於本發明之較佳具賴實例中。 聚会物 經濟部屮央檁準^s工消费合作社印製 (請先閲讀背面之注意事項再填窝本頁) 各棰不同的有櫬聚合物也有用,其中一些也可作為肋洗 劑,Μ改菩去污力。被包括之此種聚合物中,可被提及者 有羧櫬低碳烷基纖維素納,低碳烷基链維素納及羥基-低 碳烷基纖维素納·諸如羧甲基纖维素納,甲基纖维素納及 羥丙基纖維素納,聚乙烯酵(其通常也包括一些聚醋酸乙 烯酯),聚丙烯醣胺,聚丙烯酸酯及各棰不同的共聚物, 諸如那些禺來酸及丙烯酸之共聚物。此棰聚合物之分子量 有宽赞化,但是大部分都在2,000 — 100,000之範圍以内 。 聚合多碳酸》肋洗劑敘述在1967年3月7日公佈之 Diehl的美囲専利3.308.067 。此種物質包括脂族'後酸諸 如馬來酸,衣康酸(itaconic acid ) ·中康酸( mesaconic acid),富馬酸,烏頭酸(aconitic acid ) 一 2 6 — 本紙張尺度逍用中《Β家樣毕(CNS)甲4規格(210x297公度) 81. 5. 20.000(H) A 6--—-— ----------B 6 五、發明説明¢5) 經濟部中央橾準扁貝工消費合作社印製 ’擰康酸(citraconic acid )及甲二丙二酸之均聚物及 共聚物的水可溶鹽。 附加物I 在去汚劑姐合物中普通使用之其他姐份都可包括在本發 明之组合物中。這些包括流動助劑,色料斑,漂白劑及漂 白活化劑。肥皂水增壓劑(Auds boosters )或泡沫抑制 劑(suds Auppressors),防绣劑及防腐蝕劑,土壤懸浮 劑,土壤釋出劑,染枓,填充麵,光亮劑,殺菌劑,pH調 整劑*非肋洗劑_性源,水溶肋長劑•酵素•酵素安定劑 ,螯合劑及番料。 本發明之去污劑顆粒在一袋形全自動洗滌(through — the — wash)產物特別有用。像過硼酸納四水合物及一水 合物物霣,可包括作為本發明之粒狀去B劑姐合物的一部 分。在此技藝揭示之袋形全自動洗滌產物,例如:那些揭 示在1988年4月26日公佈之Ho「tel等人的美國專利案 4,740,326中一般指定者。另外有用之袋具有其壁至少其 中之一是由细孔聚合瞑構成者。在本文所使用之"LAS 〃 及"AS"—詞其意義分別為、、+二烷基笨磺酸钠"及 ''硫 酸烷酯w 。“MES"意義是甲酯磺酸納。像、、C4S "—詞 除非另外特別指明·否則其意義是C i 4及C t s烷基。T AS 意親是動物脂烷基疏酸酯。 由下列非限制性《例•將會更了解本發明。在乾'嫌前的 百分比•除非特別指明,否則係Μ乾里為基準。緊接的表 有額外加工揭示內容。 一 2 7 - 本紙張尺度通用中《Β家楳毕(CNS)T4規格(210X297公*) 81. 5_ 20,000(H) (請先閲讀背面之注意事項再填寫本頁) 裝- 訂 線· 五、發明説明(26) A 6B6 經濟部中央楳準而A工消費合作社印製 富瓶例1 此實施例描述一中間工廠規模之高剪切混合器, Ei「ich RV02中,以分批模式之方法。混合器首先用將被 使用之粉末混合物填充,在此特定情況中Zeol Ue A對细 碎碳酸鹽或Zeolite A對细碎檸樺酸鹽的比例是2 : 1 。 界面活性劑是有78%去B活性之C4S AS之水合糊*水分含 量13%。在此實施例中,於開始成粒之前,將50%氫氧化 納溶液(0.6公斤)添加至在混合器(Ei「ich RV02 )中 之糊(3公斤)。於混合時,糊固化並且藉混合器,於 2500rpm磨碎。此製程停止後,添加粉(1.050公斤)。 搡作混合器,直至發生粒化。然後停止此製程並且在流化 床上使附聚物乾煉並且通過篩網分级。製得之附聚物其去 污活性60%,密度600克/ L。它們顯示出優異的物理性 質。 g确钏2 此實腌例類似實豳例1 。粉狀混合物又是Zeolite A對 细碎碳酸鹽之比例2 : 1的混合物。界面活性劑是具78% 去污活性且水分含量13%之C4BAS的水合糊。在此實施例 中,粉(1.05公斤)及糊(3公斤)兩者均於開始成粒之 前添加至混合器(E i「i c h R V 0 2 ) °於混合器也添加某些 最(2公斤)的乾冰,Μ使溫度降至一151CK下。混合器 再以1600 (2500) rpra之速度起動。首先•於達到低溫時 ,混合物圼细粉末形式。揲作混合器直至溫度提升至發生 粒化的那點(121C)。然後停止此製程,附聚物在流化床 (請先閱讀背面之注意事項再填窝本頁) •.裝- — 28 — 本紙張尺度逍用中《國家«华(CNS)甲4規格(210x297公;《:) 81. 5. 20.000(H) 經濟#中央標準局员工消費合作社印製 2〇0辦 A6 _____B_6 五、發明説明¢27) 上乾堞並且通遇篩網分级。製得之附聚物具有60%去污活 性,其密度625克/升。它們顯示出優異物理性霣。 奮倫俐3 此賁施例描述在實驗室規棋之高剪切混合器(食品加工 器)中,圼分批横式之方法。混合器首先用將被使用之粉 末混合物填充,在此特定情況中· Zeolite A對细碎碳酸 納之比例是2 : 1 。界面活性劑是去污活性72%,水分含 量24%之C 45 AS的水合糊。在此實施例中,矽石粉(40克 >於開始成粒之前,添加至混合器中的糊(400克)。停 止此製程並且將粉末(105克)添加至糊(335克)。搡 作混合器直至發生粒化。再停止此製程並且讓附聚物在流 化床上乾堍並且經篩網分级。製得之附聚物其去污活性 55-60%,密度650克/升。它們顯示出優異的物理性霣 〇 啻瓶锎4· 此實施例描述以連績横式,在一中間工廠雙蝸桿擠歷櫬 ,Werner and Pfleiderer C58 在 6 部分中有一桶,在其 中調理糊之方法,此捆檐出摘壓機後,在一實驗室規棋高 剪切混合器中立刻成粒。界面活性劑是具有78%去污活性 艮水分含鱖18%之垛型烷基苯磺酸納(NaL AS )糊。此糊 於溫度70t;且流速150公斤/小時下導入摘懕機。該糊在 «驗室規棋之高剪切混合器中,沸石A對细碎碳酸Η粉末 M2: 1重最比,於退出濟壓櫬時附聚。此糊添加至粉末 床,直至獲得附聚物之平均粒子大小介於400及800微米 __- 29 -_ 本紙»又度遑用中_國家樣卒(CNS)甲4規格(210X297公*) 81. 5 . 20,000(H) (請先閱讀背面之注意事項再填寫本頁) 裝· 訂· 經濟部屮央標準局貝工消费合作社印製 __Β6 五、發明説明(28) 之間。然後附聚物在流化床上乾埭並且分析其LAS含量( 本文以活性描述)。 此糊於100及120ΓΡΠΙ間操作,簡單地經擠魘櫬泵送。糊 退出擠壓機時,仍然維持在70¾ *所得之附聚物的活性是 32¾ ° g撫例5 使用與實施例4描述之相同設備及重量比例製造附聚物 。在此實豳例中|於鞯由在桶之前2部分用含15C自來水 冷卻旋管及在桶之後四部分用-20 υ乙二醇冷卻*經擠壓 機泵送。糊於穩定狀態情況下之出口溫度是30=,所得之 附聚物的活性是45%。 鬣施例_·6_ 使用與實胞例4所描述之相同設備及重曇比例製造附聚 物。在此實施例中,將馬來酸與丙烯酸之共聚物的固賭粉 末,於擠壓機之入口處,添加至糊。無任何冷卻,糊退出 擠壓櫬的溫度是681C,所得之附聚物的活性是38%。當於 擠壓桶加上冷卻,以和S拖例5所描述相同之方式冷卻’ 糊出口溫度是30 t,所得之附聚物的活性是54%。 使用與《施例4所描述之相同設備及垂悬比例製造附聚 物。可是在此ff施例中,NaUS被含60里最%烷基硫酸納 .C" 一 Cie碳鐽茛並且含25%水之界面活性劑糊取代° 入口溫度再次維持在70t。 此糊簡單地經擠臛櫬泵送並且於溫度7〇亡退出擠餒機° —3 0 — 本紙張尺度逍用中《«家«毕(CNS)甲4規格(210x297公釐〉 81. 5. 20,000(H) (請先閱讀背面之注意事項再填寫本頁) 装- 線- A 6 B 6 2〇0從 五、發明説明(29) 所得附聚物之活性是36%。 g淪例8 附聚物使用與實施例7所描述之相同設備及重量比例, 也使用該實施例之硫酸烷酯糊製造之。可是在此實施例中 ,在其中一桶中經一真空汽門藉由使用能夠傳送70毫巴真 空度之真空泵胞加真空。同時纆擠壓機内之內旋管,使用 乙二醇,於一20t:在桶之所有部分加以冷卻。糊退出擠壓 機有72%的活性,水分含量22%,溫度25¾。用此糊製得 之附聚物有60%的硫酸烷酯活性。 窖施例9 使用與實施例7所描述之相同設備及重量比例*也使用 該實施例之硫酸烷酯糊製造附聚物。在此寅施例中,糊藉 由使-2〇υ乙二醇通經冷卻旋管並且另外將液態氮以15公 斤/小時之速率注入桶之第四部分使冷卻。此糊擠出摘壓 橢之溫度151,所得之附聚物有65%的硫酸烷酯活性。 (請先閱讀背面之注意事項再填寫本頁) 經濟部中央櫺準曷员丁:消費合作社印製 3 1 — 81. 5. 20.000(H) 本紙張尺度逍用中國國家樣準(CNS)甲4規格(210x297公婕)/ G to about 352 huo equivalents / g. | S silicate ion exchange material This article further specializes in its calcium ion exchange rate, based on calcium ion hardness, at least about 2 grains of Ca — / gallon / min / g / gallon aluminosilicate (anhydrous basis), It is generally between about 2 capsules / gallon / minute / gram / gallon and about 6 capsules / gallon / minute / gram / gallon. The most common aluminosilicate for builder purposes shows a calcium ion exchange rate of at least about 4 tablets / gallon / minute / gram / gallon. Amorphous Aluminosilicate Ion Exchange Material Common Mg "exchange at least about 50¾ grams when suspended CaC03 / g (12 mg Mg-/ g) denier Mg-exchange at least about 1 capsule / gallon / minute / gram / gallon. When "In the examination of copper (Cu) radiation (1.54A units), the amorphous material did not show an observable diffraction case. The aluminosilicate ion exchange material useful in the practice of the present invention is available on the market. Ilusilicates useful in the invention can be crystalline or amorphous in structure and can be naturally-occurring aluminosilicates or synthetically derived. The method of manufacturing aluminosilicate ion exchange materials was discussed in 1976 Patent No. 3,985,669 of Krumnel et al.'S beautiful painting issued on October 12, and is hereby incorporated by reference. The preferred synthetic crystalline IS silicate ion exchange materials useful in this article are Zeolite A · Zeolite B, and Zeolite X It is available under the name. In the particularly preferred case "The Case • This crystalline aluminosilicate ion exchanger S has the following chemical formula Haia [(A10z) i2 (Si〇2) i2] · XH2O (please read the back Matters needing attention on this page) Pack · Order _ Line · One 2 4 — The BB home sample rod (CNS) A4 specification (210x297 g *) for this paper standard for ease of use 81. 5. 20,000 (H) A 6 B6 V. Description of the invention (23) where X is about 20 to about 30 , Especially about 27, and the particle size is generally less than about 5 microns. The granular detergent of the present invention may contain a neutral or swan salt whose pH in the solution is 7 or greater, and may be organic or inorganic Characteristic. The detergent builder provides the expected density and swelling of the detergent particles in this article. Some of the salts are plum. Many of them are also used as detergent ribs in the irrigation and irrigation solution. The role of noodles. Examples of neutral water-soluble compounds include Sickle King, ammonium or substituted ammonium chlorides, fluorides and sulfates. The above-mentioned salts are made of metal, especially sodium salts. Sodium sulfate is It is typically used by users in decontaminated steel particles and is a specific preferred salt. Citric acid and generally any other citric acid or citric acid, as long as it is chemically compatible with the remaining agglomerate compounds, can be combined It is included in the granular detergent of the present invention. Other useful water-soluble salts include compounds commonly known as detergent builders. The rib lotion is generally selected from a variety of different water-soluble * ammonium bromide * ammonium or substituted ammonium phosphates, polyphosphates, phosphonates, polyphosphonates, carbonates, silicates, boron 蘧 and Polyhydroxysulfonate. The above-mentioned compound is preferably Ml gold "salt, especially salt. The Central Ministry of Economic Affairs and the Beigong Xiaozhi Cooperative Society printed inorganic" special examples of acid salt rib lotion "is the degree of polymerization 6-21 tripolyphosphate, sodium pyrophosphate, polymeric metaphosphoric acid, sodium and potassium orthophosphate. Examples of polyphosphoric acid builders are sodium and potassium ethanediphosphonate, ethane 1 monohydroxy 1 1, 1 One or two sodium naphthalene and salt salts of acetic acid • Ethane 1 · 1, 2, 2-triphosphonic acid sodium and potassium arsenic * Other phosphorus rib lotion compounds are shown in US Patent 3.159,581; 3,213,030: 3,422.021: 3.422.137 ; 1 2 5 — 81. 5. 20,000 (H) (Please read the precautions on the back before filling in this page) This paper uses the National Standards (CNS) Grade 4 specifications (210x297 mm) of the paper. 〇〇 0〇 ^^ A6 ________B_6 V. Description of the invention (2, 3, 400, 176 and 3, 400, 148, and for reference herein. Examples of non-phosphorus, non-condensing builders are sodium and potassium carbonate, sodium bicarbonate and potassium • bi sodium and potassium bicarbonate, sodium and potassium tetraborate decahydrate, and the molar ratio of Si〇2 to gold oxide oxide The ratio is about 0.5 to about 4.0, preferably about 1.0 to about 2.4 silicate. The composition prepared by the method of the present invention does not require carbonates for mildew processing, and preferably does not contain more than 2% finely divided as disclosed in Clarke et al.'S Mirabi Case No. 4,196,093 published on April 1, 1980. Calcium carbonate, and preferably does not contain the latter. As mentioned above, powders such as zeolites, carbonates, silicas, silicates, citrates, citrates, phosphates, borates, etc. and processing acids such as starch can be used for detergents. The preferred embodiment of the present invention depends on the example. Printed by the Ministry of Economy, Ministry of Economics, Biyang Purin ^ s Industrial and Consumer Cooperative (please read the precautions on the back before filling the nest page). Different polymers are also useful, some of which can also be used as rib lotion, Μ Change Bodhisattva decontamination. Among such polymers that can be included, there may be mentioned carboxylated low-carbon alkyl cellulose sodium, low-carbon alkyl chain vitamins and hydroxy-low-carbon alkyl cellulose nano such as carboxymethyl cellulose Vesna, methylcellulose and hydroxypropylcellulose, polyvinyl yeast (which usually also includes some polyvinyl acetate), polyacrylamide, polyacrylate and different copolymers, such as Copolymers of acrylic acid and acrylic acid. The molecular weight of this polymer is broadly praised, but most of them are in the range of 2,000-100,000. "Polycarbonate" rib lotion describes Diehl's beauty of 3.308.067 published on March 7, 1967. Such substances include aliphatic 'post-acids such as maleic acid, itaconic acid, itaconic acid, mesaconic acid, fumaric acid, and aconitic acid. One 2 6 — This paper is used for free "B Family Samples (CNS) A 4 specifications (210x297 degrees) 81. 5. 20.000 (H) A 6 ------- ---------- B 6 V. Description of Invention ¢ 5) The Ministry of Economic Affairs, Central Hokkaido Industry Cooperative Consumer Cooperative printed the water-soluble salts of homopolymers and copolymers of citraconic acid and malonic acid. Supplement I Other ingredients commonly used in detergent compositions can be included in the composition of the present invention. These include flow aids, stains, bleach and bleach activators. Soap water boosters (Auds boosters) or foam inhibitors (suds Auppressors), anti-embroidering agents and anti-corrosion agents, soil suspending agents, soil release agents, dyes, filling surfaces, brighteners, fungicides, pH adjusters * Non-rib lotion_sexual source, water-soluble rib growth agent • enzyme • enzyme stabilizer, chelating agent and ingredients. The detergent particles of the present invention are particularly useful in a bag-shaped fully-through-the-wash product. Like sodium perborate tetrahydrate and monohydrate, may be included as part of the granular B-removing agent of the present invention. The bag-shaped full-automatic washing products disclosed in this technique are, for example, those specified in the US Patent No. 4,740,326 published in Ho'tel et al. On April 26, 1988. Another useful bag has at least one of its walls The first is composed of fine-pore polymerized kets. The terms "LAS" and "AS" as used in this article mean ", + dialkyl sodium sulfonate" and "alkyl sulfate w", respectively. "MES" means sodium methylsulfonate. Like,, C4S "-words Unless otherwise specified, otherwise the meaning is C i 4 and C t s alkyl. T AS meaning is tallow fatty acid alkyl ester. The following non-limiting examples will better understand the present invention. Percentage before doing it. Unless otherwise specified, it is based on Mengli. The following table has additional processing reveals. 1 2 7-The standard of this paper is "B Jia Yu Bi (CNS) T4 specification (210X297 public *) 81. 5_ 20,000 (H) (please read the precautions on the back before filling in this page) Packing-Threading · 5 2. Description of the invention (26) A 6B6 The Central Ministry of Economic Affairs and A Industrial Consumer Cooperative printed a rich bottle Example 1 This example describes an intermediate factory-scale high-shear mixer, Ei "ich RV02, in batch mode Method. The mixer is first filled with the powder mixture to be used, in this particular case the ratio of Zeol Ue A to finely divided carbonate or Zeolite A to finely divided citrate is 2: 1. The surfactant is 78% removed B active C4S AS hydrated paste * 13% moisture content. In this example, before starting to granulate, add 50% sodium hydroxide solution (0.6 kg) to the mixer (Ei "ich RV02) Paste (3 kg). During mixing, the paste solidifies and grinds at 2500 rpm with a mixer. After this process is stopped, add powder (1.050 kg). Use as a mixer until granulation occurs. Then stop this process The agglomerates were dried in a fluidized bed and classified through a screen. The polymer has a decontamination activity of 60% and a density of 600 g / L. They show excellent physical properties. G. Kuai 2 This example is similar to Example 1. The powdery mixture is the ratio of Zeolite A to finely divided carbonate. 2: Mixture of 1. Surfactant is a hydrated paste of C4BAS with 78% detersive activity and a moisture content of 13%. In this example, both powder (1.05 kg) and paste (3 kg) start to form Add the pellets to the mixer (E i "ich RV 0 2) ° before the mixer also add some of the most (2 kg) of dry ice, Μ lower the temperature to 151CK. The mixer is then 1600 (2500) rpra Speed start. Firstly, when the temperature is low, the mixture is in the form of fine powder. Use as a mixer until the temperature rises to the point where granulation occurs (121C). Then stop the process, the agglomerates are in the fluidized bed (please read first Note on the back and fill in this page) •.-28-This paper is used in the "National« China (CNS) A 4 specifications (210x297 ;;: :) 81. 5. 20.000 (H) Economy # Printed by Office for Consumer Cooperative of Central Bureau of Standards, Office 200, A6 _____B_6 V. Description of invention ¢ 27) Shangganjing It also meets the sieve classification. The agglomerates obtained have 60% decontamination activity, and their density is 625 g / l. They show excellent physical properties. Fenlunli 3 This example is described in the laboratory. In a high-shear mixer (food processor), a horizontal batch method. The mixer is first filled with the powder mixture to be used. In this particular case, the ratio of Zeolite A to finely divided sodium carbonate is 2: 1 . The surfactant is a hydrated paste of C 45 AS with a decontamination activity of 72% and a water content of 24%. In this example, silica powder (40 g) was added to the paste (400 g) in the mixer before starting granulation. The process was stopped and the powder (105 g) was added to the paste (335 g). It is used as a mixer until granulation occurs. The process is stopped and the agglomerates are dried on the fluidized bed and classified through a screen. The decontamination activity of the agglomerates obtained is 55-60%, and the density is 650 g / L. They show excellent physical properties. Cylinder CF4. This example describes a continuous performance, a double worm squeeze in an intermediate factory, Werner and Pfleiderer C58 has a bucket in part 6, where the paste is conditioned The method is that after the bundling is removed from the press, it is immediately granulated in a laboratory high-shear mixer. The surfactant is a 78% decontamination activity, a moisturizing alkyl benzene containing 18% mandarin. Sodium sulfonate (NaL AS) paste. The paste is introduced into the picking machine at a temperature of 70t; and the flow rate is 150 kg / hour. The paste is in a high shear mixer of «Laboratory regulations, zeolite A vs. finely divided H carbonate powder M2: 1 is the most important, and agglomerates when it is out of pressure. This paste is added to the powder bed until it is obtained The average particle size of the polymer is between 400 and 800 microns __- 29 -_ This paper is used again _ National Sample (CNS) A 4 specifications (210X297 g *) 81. 5. 20,000 (H) (please Read the precautions on the back first and then fill out this page) Binding · Order · Printed by the Beigong Consumer Cooperative of the Central Standards Bureau of the Ministry of Economic Affairs __Β6 5. Description of the invention (28). Then the agglomerates dry on the fluidized bed And analyze its LAS content (this article describes the activity). This paste is operated between 100 and 120ΓΡΠΙ, and is simply pumped through the squeeze. When the paste exits the extruder, it remains at 70¾ * The activity of the resulting agglomerate is 32¾ ° g Example 5 The same equipment and weight ratio as described in Example 4 were used to produce agglomerates. In this example, Yu Qianyou used 2 parts before the barrel to cool the coil with 15C tap water and four after the barrel. Partially cooled with -20 υ ethylene glycol * pumped through the extruder. The outlet temperature of the paste in a steady state is 30 =, and the activity of the resulting agglomerate is 45%. Cell 4 produces the agglomerate with the same equipment and proportion as described in Example 4. In this example, maleic acid and propylene The solid powder of the copolymer is added to the paste at the entrance of the extruder. Without any cooling, the temperature of the paste exiting the extrusion is 681C, and the activity of the resulting agglomerate is 38%. When it is in the extrusion barrel With cooling, it is cooled in the same manner as described in Example 5 Example 5. The paste outlet temperature is 30 t, and the activity of the resulting agglomerate is 54%. Use the same equipment and suspension ratio as described in Example 4. Manufacture of agglomerates. However, in this ff example, NaUS was replaced by a surfactant paste containing 60% of the most sodium alkyl sulfate. C " one Cie carbon ranunculus and 25% water ° The inlet temperature was again maintained at 70t . This paste is simply pumped through the squeeze and exits the squeeze machine at a temperature of 70 °-3 0-This paper standard is used in the "« Home «Bi (CNS) A 4 specifications (210x297 mm> 81.5 . 20,000 (H) (Please read the precautions on the back before filling in this page) 装-线-A 6 B 6 2〇0 From V. Description of invention (29) The activity of the agglomerates obtained is 36%. 8 The agglomerates were manufactured using the same equipment and weight ratio as described in Example 7 and also using the alkyl sulfate paste of this example. However, in this example, a vacuum valve was used Use a vacuum pump that can deliver a vacuum of 70 mbar to apply vacuum. At the same time, the inner spiral tube in the extruder uses ethylene glycol and cools in all parts of the barrel at one 20t. 72% of the paste exits the extruder Activity, water content 22%, temperature 25¾. The agglomerates prepared with this paste have 60% alkyl sulfate activity. Cellar Example 9 The same equipment and weight ratio as described in Example 7 were used. Example of alkyl sulfate paste to produce agglomerates. In this example, the paste is made by passing -2〇υ ethylene glycol through cooling In addition, liquid nitrogen is injected into the fourth part of the barrel at a rate of 15 kg / hour for cooling. The paste is extruded at a temperature of 151, and the resulting agglomerate has 65% alkyl sulfate activity. (Please read first Note on the back and then fill out this page) Central Government Department of Economic Affairs: Printed by Consumer Cooperatives 3 1 — 81. 5. 20.000 (H) This paper scale is free of China National Standards (CNS) Grade 4 (210x297 Gongjie)

Claims (1)

六、申請專利範園 B7 C7 D7 公舌本 2 一種製造濃縮粒狀去污劑姐合物之方法,其特徵包括 下列步揉: (i)以過1驗中和陰離子型界面活性劑酸得到 高活性(至少40重量%陰離子型界面活性劑)《8*當 於70TC及25秒剪切速率下測定時》前述糊之黏度至 少 10巴•秒(Pa.s), (Π )調理前述糊; (m t在有效去污劑粉的存在下*於高剪切混合器/ 成粒櫬中形成高活性去污劑顆粒。 ‘ 根據申請專利範園第1項之方法,其所進行步驟(ii )包括泵送•及/或降低水份*及/或冷卻及/或於 前述高活性糊添加化學構建劑·其特徵為使用擠壓櫬 (請先閱讀背面之注意事項再填寫本页) .裝· 經濟邡中央操準局印装 3. 根據申請專利範画第2 4〇·〇_8〇υ之溫度間及 空度(低於大氣壓力) 4. 根據申請専利範圃第2 內之一或多個输入口, 然後再於搞懕機內混合 a 根據申誚専利範圃第3 内之一或多儸输入口, 然後再於擠壓機内混合 a 根據申請専利範圃第2 微為擠壓楗之混合部分 項之方法, 於 0 - 7.3 下,進入擠 項之方法* 容許添加粉 之0 項之方法, 容許添加粉 之。 至5項中任 的桶係藉任 其特徵為該糊是於 仟巴(kPa )之真 壓桷之入口。 其特微為在搞壓捅 末及/或額外糊· 其特微為在搞懕捅 末及/或額外糊* 一項之方法•其特 何逋宜工具冷卻, _打· •線· ——I —— f 4(210X297 公廣) 2〇〇冰告本 g 一 .........................._ 六、申請專利範® 此冷卻工具包括於擠壓膛内直接添加高達糊的30重量 %之固態二氧化碳或液態氮。 7. 根據申請專利範圃第2至5項中任一項之方法•其特 戡為擠懕機是雙蝸桿擠壓機。 a 根據申誧專利範圃第1項之方法,其特徽為此化學構 建劑是呈粉狀形式。 (請先閑讀背面之注意事項再填荈本页) •装· •訂· •線· 經濟部中央標準局印裝 甲 4(210X297 公;¥)6. Patent application Fanyuan B7 C7 D7 Gong Tongben 2 A method for manufacturing a concentrated granular detergent compound, which features the following steps: (i) obtained by neutralizing the anionic surfactant acid through 1 test High activity (at least 40% by weight anionic surfactant) "8 * when measured at 70 TC and a shear rate of 25 seconds" The viscosity of the aforementioned paste is at least 10 bar • sec (Pa.s), (Π) conditioning the aforementioned paste ; (Mt in the presence of effective detergent powder * in the high-shear mixer / granulation to form highly active detergent particles. 'According to the method of patent patent application No. 1, the steps (ii ) Includes pumping and / or water reduction * and / or cooling and / or adding a chemical builder to the aforementioned high-activity paste.It is characterized by the use of extrusion (please read the precautions on the back before filling this page). Printed and printed by the Central Government Bureau of Economic Affairs 3. According to the patent application drawing No. 2 4〇 · 〇_8〇υ temperature and air space (lower than atmospheric pressure) 4. According to the application of the No. 2 One or more input ports, and then mix them in the machine a One or more of the input port, and then mix in the extruder a. According to the application method of the second part of the application of the fan, the mixing part of the extrusion, under 0-7.3, enter the method of squeezing * Allow addition The method of item 0 of the powder allows the addition of powder. The barrel of any one of item 5 is borrowed as the characteristic of the paste is the entrance to the true pressure of thousands of kPa (kPa). And / or extra paste. Its special feature is a method of stabbing at the end and / or extra paste *. • What is the special tool for tool cooling, _hit · • thread · ——I —— f 4 (210X297 male (Guangzhou) 2〇〇 冰 告 本 g I .......................... VI. Patent application Fan® This cooling tool is included in the extrusion Directly add up to 30% by weight of solid carbon dioxide or liquid nitrogen to the paste. 7. According to the method of any one of items 2 to 5 of the patent application. The special purpose is that the compressor is a double worm extruder. a According to the method of item 1 of the application for patent application, its special emblem is in the form of powder. (Please read the precautions on the back before filling this page) · Line · Printed Armor of the Central Bureau of Standards of the Ministry of Economic Affairs 4 (210X297; ¥)
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