JPH0788456B2 - Method for producing water-soluble polymer composition - Google Patents
Method for producing water-soluble polymer compositionInfo
- Publication number
- JPH0788456B2 JPH0788456B2 JP61171828A JP17182886A JPH0788456B2 JP H0788456 B2 JPH0788456 B2 JP H0788456B2 JP 61171828 A JP61171828 A JP 61171828A JP 17182886 A JP17182886 A JP 17182886A JP H0788456 B2 JPH0788456 B2 JP H0788456B2
- Authority
- JP
- Japan
- Prior art keywords
- polymer
- water
- weight
- surfactant
- polymer composition
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000000203 mixture Substances 0.000 title claims description 18
- 238000004519 manufacturing process Methods 0.000 title claims description 12
- 229920003169 water-soluble polymer Polymers 0.000 title claims description 11
- 229920000642 polymer Polymers 0.000 claims description 34
- 239000002245 particle Substances 0.000 claims description 23
- 239000004094 surface-active agent Substances 0.000 claims description 18
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 12
- 239000000017 hydrogel Substances 0.000 claims description 11
- 229920002401 polyacrylamide Polymers 0.000 claims description 11
- 239000000843 powder Substances 0.000 claims description 9
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims description 7
- 238000000034 method Methods 0.000 claims description 5
- 238000005469 granulation Methods 0.000 claims description 4
- 230000003179 granulation Effects 0.000 claims description 4
- 239000010419 fine particle Substances 0.000 claims description 3
- 238000001125 extrusion Methods 0.000 claims description 2
- 239000000463 material Substances 0.000 claims description 2
- 239000011248 coating agent Substances 0.000 claims 1
- 238000000576 coating method Methods 0.000 claims 1
- -1 amide sulfonic acids Chemical class 0.000 description 8
- 150000003839 salts Chemical class 0.000 description 6
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 5
- 239000007863 gel particle Substances 0.000 description 5
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 4
- 229940048053 acrylate Drugs 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 4
- 238000004090 dissolution Methods 0.000 description 4
- 238000011156 evaluation Methods 0.000 description 4
- 239000000178 monomer Substances 0.000 description 4
- 229920001223 polyethylene glycol Polymers 0.000 description 4
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 3
- 239000002202 Polyethylene glycol Substances 0.000 description 3
- 235000014113 dietary fatty acids Nutrition 0.000 description 3
- 239000000194 fatty acid Substances 0.000 description 3
- 229930195729 fatty acid Natural products 0.000 description 3
- 239000000499 gel Substances 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 238000003860 storage Methods 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical class CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 239000003999 initiator Substances 0.000 description 2
- 235000013372 meat Nutrition 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 229920002503 polyoxyethylene-polyoxypropylene Polymers 0.000 description 2
- 238000007711 solidification Methods 0.000 description 2
- 230000008023 solidification Effects 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 238000002834 transmittance Methods 0.000 description 2
- ZORQXIQZAOLNGE-UHFFFAOYSA-N 1,1-difluorocyclohexane Chemical compound FC1(F)CCCCC1 ZORQXIQZAOLNGE-UHFFFAOYSA-N 0.000 description 1
- PQUXFUBNSYCQAL-UHFFFAOYSA-N 1-(2,3-difluorophenyl)ethanone Chemical compound CC(=O)C1=CC=CC(F)=C1F PQUXFUBNSYCQAL-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- 229920000536 2-Acrylamido-2-methylpropane sulfonic acid Polymers 0.000 description 1
- XHZPRMZZQOIPDS-UHFFFAOYSA-N 2-Methyl-2-[(1-oxo-2-propenyl)amino]-1-propanesulfonic acid Chemical compound OS(=O)(=O)CC(C)(C)NC(=O)C=C XHZPRMZZQOIPDS-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- MUHFRORXWCGZGE-KTKRTIGZSA-N 2-hydroxyethyl (z)-octadec-9-enoate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCCO MUHFRORXWCGZGE-KTKRTIGZSA-N 0.000 description 1
- FLCAEMBIQVZWIF-UHFFFAOYSA-N 6-(dimethylamino)-2-methylhex-2-enamide Chemical compound CN(C)CCCC=C(C)C(N)=O FLCAEMBIQVZWIF-UHFFFAOYSA-N 0.000 description 1
- XZIIFPSPUDAGJM-UHFFFAOYSA-N 6-chloro-2-n,2-n-diethylpyrimidine-2,4-diamine Chemical compound CCN(CC)C1=NC(N)=CC(Cl)=N1 XZIIFPSPUDAGJM-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 241000567769 Isurus oxyrinchus Species 0.000 description 1
- 241000604742 Machilus thunbergii Species 0.000 description 1
- 238000006683 Mannich reaction Methods 0.000 description 1
- 241000047703 Nonion Species 0.000 description 1
- 229920001214 Polysorbate 60 Polymers 0.000 description 1
- MZVQCMJNVPIDEA-UHFFFAOYSA-N [CH2]CN(CC)CC Chemical group [CH2]CN(CC)CC MZVQCMJNVPIDEA-UHFFFAOYSA-N 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 125000004103 aminoalkyl group Chemical group 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 239000000701 coagulant Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 238000010410 dusting Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000000244 polyoxyethylene sorbitan monooleate Substances 0.000 description 1
- 235000010482 polyoxyethylene sorbitan monooleate Nutrition 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229920000053 polysorbate 80 Polymers 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 239000012966 redox initiator Substances 0.000 description 1
- 239000010802 sludge Substances 0.000 description 1
- 229940047670 sodium acrylate Drugs 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 229940035044 sorbitan monolaurate Drugs 0.000 description 1
- 239000001593 sorbitan monooleate Substances 0.000 description 1
- 235000011069 sorbitan monooleate Nutrition 0.000 description 1
- 229940035049 sorbitan monooleate Drugs 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 238000004065 wastewater treatment Methods 0.000 description 1
Landscapes
- Separation Of Suspended Particles By Flocculating Agents (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Description
【発明の詳細な説明】 産業上の利用分野 本発明は、水溶性アクリルアミド系ポリマーを主成分と
する溶解性と取扱性の良好な水溶性高分子組成物の製造
方法に関する。TECHNICAL FIELD The present invention relates to a method for producing a water-soluble polymer composition containing a water-soluble acrylamide polymer as a main component and having good solubility and handleability.
従来の技術 アクリルアミド系重合体は廃水処理用凝集剤、抄紙用粘
剤、汚泥脱水用助剤、石油回収用薬剤等各種の分野で広
く使用されているが、一般に粉末の形で供給され、前記
分野で使用する際、これ等重合体粉末を水に溶解させて
水溶液の形で供される。BACKGROUND ART Acrylamide-based polymers are widely used in various fields such as coagulants for wastewater treatment, thickeners for papermaking, sludge dewatering aids, chemicals for oil recovery, etc. When used in the field, these polymer powders are dissolved in water and provided in the form of an aqueous solution.
発明が解決しようとする問題点 この溶解作業に際して、重合体粉末中には微粒子も含ま
れる為粉塵が立ち易く、環境上の問題としてしばしば指
摘されている。またいわゆる「まゝこ」が発生して長い
溶解時間を要するケースも多い。Problems to be Solved by the Invention At the time of this melting operation, since the polymer powder also contains fine particles, dust easily forms, which is often pointed out as an environmental problem. In addition, there are many cases in which so-called "maco" occurs and a long dissolution time is required.
このような粉体による上記欠点を避ける為、ポリマー純
分20重量%程度のゲル状品で供給されることもあるが、
この場合、溶解作業時に電動式肉挽機等の細断機により
細断しても、粉末品に比べ粒子を細くする事が困難な為
に長い溶解時間を要する。またポリマー純分10重量%以
下のペースト状品も一部に使用されているが、ゲル状
品、ペースト状品共通の問題点は固形分が低い事による
輸送コスト、保管コストの増大等非経済である。In order to avoid the above-mentioned drawbacks due to such powder, it may be supplied in the form of gel in which the polymer content is about 20% by weight.
In this case, it is difficult to make the particles finer than those of the powdered product, even if the product is shredded by a shredder such as an electric meat grinder during the melting work, and thus a long melting time is required. In addition, some paste products with a polymer content of 10 wt% or less are also used, but the common problems with gel products and paste products are non-economical factors such as increased transportation costs and storage costs due to low solid content. Is.
本発明の目的は高分子量で、且つ、水溶性の良好なアク
リルアミド系重合体を主成分とする水溶性高分子組成物
の製造方法を提供することにある。An object of the present invention is to provide a method for producing a water-soluble polymer composition having a high molecular weight and a good water-soluble acrylamide polymer as a main component.
問題点を解決するための手段 即ち、本発明はアクリルアミド系ポリマーの含水ゲル粒
子と界面活性剤とを含有してなり、この界面活性剤は前
記粒子のポリマー純分に対して500〜20000ppmであるこ
とを特徴とする水溶性高分子組成物及び(2)アクリル
アミド系ポリマーの含水ゲル粒子と、界面活性剤を含有
してなる水溶性高分子組成物を製造する方法において、
ポリマー純分20重量%以上のアクリルアミド系含水ゲル
粒子を粒径3〜10mmになるよう、切断細粒化し、これを
ポリマー純分85〜95重量%になる迄乾燥し、次いで、こ
の乾燥物を粉砕して粒径2mm以下の粉砕物とした後、こ
の粉砕物のポリマー純分に対し500〜20000ppmの界面活
性剤を添加しながら、ポリマー純分が50〜85重量%にな
るよう加湿造粒することを特徴とする水溶性高分子組成
物の製造方法である。Means for Solving the Problems That is, the present invention comprises hydrogel particles of an acrylamide polymer and a surfactant, and the surfactant is 500 to 20000 ppm with respect to the polymer content of the particles. A water-soluble polymer composition and (2) a method for producing a water-soluble polymer composition containing a hydrogel particle of an acrylamide polymer and a surfactant,
Acrylamide-containing hydrogel particles having a polymer content of 20% by weight or more are cut into fine particles so as to have a particle size of 3 to 10 mm and dried to a polymer content of 85 to 95% by weight. After pulverizing to a pulverized product with a particle size of 2 mm or less, add 500 to 20000 ppm of surfactant to the pulverized polymer content of this pulverized product, and moisturize granulation so that the polymer content is 50 to 85% by weight. And a method for producing a water-soluble polymer composition.
作用 以下、本発明の構成要件を作用と共に説明する。Action Hereinafter, the constituent features of the present invention will be described together with the action.
本発明組成物はアクリルアミド系ポリマーを主成分と
し、これに少量の界面活性剤を含有させたものである。
アクリルアミド系重合体を得るため重合させる単量体
は、アクリルアミドのみの場合と、これと共重合可能な
ものを用いる場合とがある。共重合可能な単量体として
は、メタアクリルアミド、(メタ)アクリル酸メチル、
(メタ)アクリル酸エチル等の(メタ)アクリル酸エス
テル類、アクリル酸及びその塩、メタアクリル酸及びそ
の塩、2−アクリルアミド−2−メチルプロパンスルフ
ォン酸等のアミドスルフォン酸及びその塩、ジメチルア
ミノエチル(メタ)アクリレート、ジエチルアミノエチ
ル(メタ)アクリレート等のアミノアルキルエステル類
及びその塩、ジメチルアミノプロピルメタアクリルアミ
ド等のアミノアルキルアミド類及びその塩等が挙げられ
る。The composition of the present invention comprises an acrylamide polymer as a main component and a small amount of a surfactant contained therein.
The monomer to be polymerized to obtain the acrylamide polymer may be acrylamide alone or may be a monomer copolymerizable with acrylamide. Examples of the copolymerizable monomer include methacrylamide, methyl (meth) acrylate,
(Meth) acrylic acid esters such as ethyl (meth) acrylate, acrylic acid and salts thereof, methacrylic acid and salts thereof, amide sulfonic acids such as 2-acrylamido-2-methylpropanesulfonic acid and salts thereof, dimethylamino Examples thereof include aminoalkyl esters such as ethyl (meth) acrylate and diethylaminoethyl (meth) acrylate and salts thereof, and aminoalkylamides such as dimethylaminopropylmethacrylamide and salts thereof.
該重合体は、アニオン、カチオン、ノニオンのいずれの
タイプであってもよく、ホモポリマーでも、コポリマー
であっても良い。The polymer may be any type of anion, cation and nonion, and may be a homopolymer or a copolymer.
アクリルアミド系重合体の重合方法は、一般的には通常
のフリーラジカル開始による重合であり、水溶液重合の
場合には15〜85重量%の上記単量体濃度の水溶液に通常
の過酸化物開始剤、レドックス開始剤及びアゾ系開始剤
の中から1種または2種以上を用い重合せしめる。尚、
アクリルアミド系重合体は、重合完了後、各種の変成、
例えばアルカリによる加水分解反応を行わせ、陰イオン
性カルボキシル基に変成させる方法、マンニッヒ反応
は、ホフマン分解反応により、カチオン性アミノ基を導
入させる方法等を行ったものでもよい。通常は、以上の
方法で得られた重合体を乾燥工程に於いて乾燥させる
と、含水率20〜95重量%の含水ゲル粒子が得られる。The acrylamide polymer is generally polymerized by free radical initiation, and in the case of aqueous solution polymerization, an ordinary peroxide initiator is added to an aqueous solution having the above monomer concentration of 15 to 85% by weight. Polymerization is carried out using one kind or two or more kinds among redox initiators and azo initiators. still,
Acrylamide-based polymers, after the completion of polymerization, various modifications,
For example, a method of carrying out a hydrolysis reaction with an alkali to convert it into an anionic carboxyl group, and a Mannich reaction may be carried out by a method of introducing a cationic amino group by a Hoffmann decomposition reaction. Usually, the polymer obtained by the above method is dried in the drying step to obtain hydrogel particles having a water content of 20 to 95% by weight.
本発明においては上記の如き含水ゲル粒子のうち、アク
リルアミド系ポリマー50〜85重量%、好ましくは60〜80
重量%及び水分50〜15重量%、好ましくは40〜20重量%
の粒径2mm以下の含水ゲル粒子を用いる。In the present invention, among the hydrogel particles as described above, the acrylamide polymer is 50 to 85% by weight, preferably 60 to 80%.
Wt% and moisture 50 to 15 wt%, preferably 40 to 20 wt%
The hydrous gel particles having a particle size of 2 mm or less are used.
この場合ポリマー純分が50重量%未満であると、水分が
多くなるので粉末粒子がケーキングを起こすと共に製品
輸送費が嵩むので好ましくない。一方ポリマー純分が85
重量%を超えると粉立ちが生じ、又、溶解時に「まゝ
こ」になり易い。尚粒径2mm以下とするのは溶解速度を
大にする為である。In this case, if the polymer pure content is less than 50% by weight, the water content is increased, so that the powder particles cause caking and the product transportation cost increases, which is not preferable. On the other hand, the polymer content is 85
If it exceeds 5% by weight, dusting occurs, and it tends to become "makko" when dissolved. The particle size of 2 mm or less is for increasing the dissolution rate.
本発明組成物は上記含水ゲル粒子に対し、ポリマー純分
当り、500〜20000ppmの界面活性剤を配合したものであ
るが、本発明組成物に含有する界面活性剤の具体例とし
ては、平均分子量400以上のポリエチレングリコール、
同じくポリプロピレングリコール、ポリオキシアルキル
エーテル、ポリオキシエチレンアルキルフェニルエーテ
ル、ポリオキシエチレン脂肪酸エステル、ポリオキシエ
チレンポリオキシプロピレンブロックポリマー、ポリオ
キシエチレンソルビタン脂肪酸エステル、ソルビタン脂
肪酸エステル等の非イオン型界面活性剤が挙げられる。
これらのうち、特にソルビタンモノオレート、平均分子
量1000以上のポリエチレングリコールが好ましい。界面
活性剤としてはさらにこれら以外の界面活性剤、無機
塩、油類等を含有させることができる。この界面活性剤
は、含水ゲル粒子の保存時のケーキングを防止する為に
有効であり、500ppm未満ではケーキング防止が不十分で
あり、このケーキングは溶解時の「まゝこ」の原因とも
なる。又、20000ppm超ではコスト高になると共に組成物
がベタベタし、流動性が悪化し取扱い性が悪くなる。The composition of the present invention, with respect to the water-containing gel particles, is one in which a surfactant of 500 to 20000 ppm is blended per polymer pure content, and as a specific example of the surfactant contained in the composition of the present invention, the average molecular weight is 400+ polyethylene glycols,
Similarly, nonionic surfactants such as polypropylene glycol, polyoxyalkyl ether, polyoxyethylene alkylphenyl ether, polyoxyethylene fatty acid ester, polyoxyethylene polyoxypropylene block polymer, polyoxyethylene sorbitan fatty acid ester, sorbitan fatty acid ester, etc. Can be mentioned.
Of these, sorbitan monooleate and polyethylene glycol having an average molecular weight of 1000 or more are particularly preferable. As the surfactant, a surfactant other than these, inorganic salts, oils and the like can be further contained. This surfactant is effective for preventing caking of the hydrogel particles during storage, and if it is less than 500 ppm, caking prevention is insufficient, and this caking also causes "maco" during dissolution. On the other hand, if it exceeds 20,000 ppm, the cost becomes high and the composition becomes sticky, resulting in poor fluidity and poor handleability.
このような水溶性高分子組成物の好ましい製造方法とし
ては、まず、アクリルアミド系ポリマーは通常の製造方
法においてポリマー純分20重量%以上粒径3〜10mmの含
水ゲル粒子として得られる。これを乾燥し、ポリマー純
分を85〜95重量%とし、且つ、所定の粒径にポリマーを
細粒化し、これを再び加湿してポリマー純分50〜85重量
%好ましくは60〜80重量%のゲル粒子とする。As a preferred method for producing such a water-soluble polymer composition, first, an acrylamide polymer is obtained as a hydrogel particle having a polymer content of 20% by weight or more and a particle diameter of 3 to 10 mm in a usual production method. This is dried to a polymer content of 85 to 95% by weight, and the polymer is finely divided into particles having a predetermined particle size, and this is re-wet to obtain a polymer content of 50 to 85% by weight, preferably 60 to 80% by weight. Gel particles.
このようにポリマー純分を一旦85〜95重量%まで乾燥し
た後、再びポリマー純分50〜85重量%に加湿するのは該
ポリマーは含水ゲル状に於て極めて細粒化し難い為であ
る。The reason why the polymer pure content is once dried to 85 to 95% by weight and then humidified to the polymer pure content of 50 to 85% by weight is because the polymer is extremely difficult to be finely granulated in the hydrogel state.
即ち、通常の製法においてポリマー純分が例えば20〜35
重量%の含水ゲル粒子は切断機、好ましくはカッターミ
ル、又はミートチョッパーを用いて粒径3〜10mmに切断
細粒化され、次いでポリマー純分85〜95重量%になる迄
乾燥される。この乾燥ゲル粒子は粉砕機によって容易に
2mm以下の粉体に粉砕される。That is, in the usual production method, the polymer content is, for example, 20 to 35.
The wt% hydrogel particles are chopped to a particle size of 3-10 mm using a cutter, preferably a cutter mill, or a meat chopper, and then dried to a polymer content of 85-95 wt%. This dry gel particle can be easily
It is crushed to a powder of 2 mm or less.
上記のようにして得られた粉砕物に所定の量(ポリマー
純分に対し500〜20000ppm含有するに必要な量)の界面
活性剤と水とを別々に、または水溶液として添加して捏
和すると、乾燥ゲル粒子は水分を吸ってゲル状となり、
0.1mm程度より細かい微粉はくっつき合い造粒され、全
体として2mm以下の粉立ちしない顆粒物となる。そして
その表面は界面活性剤によりほぼ被覆された状態とな
り、これを保存する時ケーキングが防止され、取扱いが
容易で、溶解性にすぐれたものが得られる。When a predetermined amount (amount necessary to contain 500 to 20000 ppm relative to the polymer content) of the pulverized product obtained as described above and a surfactant and water are added separately or as an aqueous solution and kneaded. , The dried gel particles absorb water to form a gel,
Fine powder finer than about 0.1 mm is stuck and granulated to form a granule of 2 mm or less that does not stand up. Then, the surface thereof is almost covered with the surfactant, and when it is stored, caking is prevented, handling is easy, and a highly soluble product is obtained.
以上のようにして得られた本発明組成物について以下実
施例を挙げて説明する。The composition of the present invention obtained as described above will be described below with reference to Examples.
実施例 通常の製法で製造した粉状ポリマー(ポリマー90重量
%、水分10重量%、アクリルアミドとアクリル酸ソーダ
とのモル比が85:15、粒径2mm以下)各1000gを回転ドラ
ム型混合造粒機に仕込み、回転させながら界面活性剤を
溶解した添加水を手押し式スプレーでスプレーし、約30
分間攪拌混合した。その試験条件および製品の評価結果
を第1表及び第2表に示す。Example A powdery polymer produced by an ordinary production method (90% by weight of polymer, 10% by weight of water, molar ratio of acrylamide and sodium acrylate is 85:15, particle size is 2 mm or less) 1000 g of each is produced by rotary drum type mixing granulation. We put it in a machine and, while rotating it, spray the added water in which the surfactant was dissolved with a hand-push type sprayer, about 30
Stir and mix for minutes. The test conditions and the evaluation results of the products are shown in Tables 1 and 2.
又、湿式押し出し型造粒機を用いても同様な実験を行
い、回転ドラム型混合造粒機と同様な結果を得た。Also, the same experiment was conducted using a wet extrusion type granulator, and the same result as that of the rotary drum type mixing granulator was obtained.
第1表及び第2表の界面活性剤品名の記号は次のものを
表わし、又評価は次の方法によって行った。 The symbols of the surfactant product names in Tables 1 and 2 represent the following, and the evaluation was performed by the following method.
1)界面活性剤品名 A:ソルビタンモノラウレート(商品名レオドールSP・L1
0) B:ポリエチレングリコールモノオレエート(商品名エマ
ノーン4110) C:ポリオキシエチレン高級アルコールエーテル(商品名
エマルゲン707) D:ポリオキシエチレンソルビタンモノオレート(商品名
レオドールTW-0120) E:ポリオキシエチレンポリオキシプロピレンブロックポ
リマー(商品名エマルゲンPP-230) F:ポリエチレングリコール♯400 G: 〃 ♯6000 2)評価試験と評価基準 (1)粉立ちテスト サンプル100gを50cmの高さから落下させ、落下点より30
cmはなれた所に置いた5×5cmの水平ガラス板上の光透
過率を測定した。光透過率は分光々度計を使用し波長48
0nmにて測定した。1) Surfactant Product name A: Sorbitan monolaurate (Product name Leodol SP ・ L1
0) B: Polyethylene glycol monooleate (trade name Emanone 4110) C: Polyoxyethylene higher alcohol ether (trade name Emulgen 707) D: Polyoxyethylene sorbitan monooleate (trade name Leodol TW-0120) E: Polyoxyethylene Polyoxypropylene block polymer (Brand name Emulgen PP-230) F: Polyethylene glycol # 400 G: 〃 # 6000 2) Evaluation test and evaluation criteria (1) Powder standing test Drop 100 g of sample from a height of 50 cm, and drop point Than 30
The light transmittance was measured on a 5 × 5 cm horizontal glass plate placed at a distance of cm. The light transmittance is 48 wavelength using a spectrophotometer.
It was measured at 0 nm.
(2)溶解時のまゝこ発生 静止水1000ml中に1gのサンプルを一時に投下し、その後
400rpm×60分攪拌し未溶解分を150メッシュ金網で濾過
し評価。(2) Mako generation during dissolution 1g of sample was dropped at a time in 1000ml of still water, then
After stirring at 400 rpm for 60 minutes, the undissolved content was filtered through a 150 mesh wire net and evaluated.
(3)ケーキング サンプル200gをポリ袋に充填、密封し、100g/cm2の加重
を1週間加え、一度粒状化したものが加重により団結化
する状態を観察。(3) 200 g of caking sample was filled in a plastic bag and sealed, and a weight of 100 g / cm 2 was added for one week, and the state of once granulated and united by weight was observed.
◎…全く固結せず ○…わずかにブロック状になっているが、かるく触れた
だけで崩壊する。◎… No solidification at all ○… Slightly blocky, but it collapses when touched lightly.
△…固結が見られ押しつぶすことで崩壊する。Δ: Solidification is seen and the material collapses when crushed.
×…完全なブロックで解きほぐすのは困難。×: It is difficult to unravel with a complete block.
(4)溶解性 400rpmで攪拌している1000mlの水にサンプル1gを加え、
90分溶解後150メッシュ金網にて濾過、不溶解分を観
察。(4) Solubility Add 1g of sample to 1000ml water stirred at 400rpm,
After dissolving for 90 minutes, filter with a 150 mesh wire net and observe the insoluble matter.
発明の効果 以上詳述したごとく、本発明組成物は表面が界面活性剤
で被覆されているので、荷重下長期保存してもケーキン
グが生じないこと、使用時には粉立ちが全くなく取扱い
易いこと、水に溶解時まゝこになりにくいことなど発明
の効果は顕著である。また、従来技術では得られなかっ
た高分子量で、且つ水溶性の良好なアクリルアミド系重
合体を主成分とする水溶性高分子組成物が、本発明によ
れば非常に簡単で、しかも安価に得られる。Effects of the Invention As described in detail above, since the surface of the composition of the present invention is coated with a surfactant, caking does not occur even after long-term storage under load, and it is easy to handle without powdering at the time of use. The effects of the invention are remarkable, such as the fact that when dissolved in water, it does not easily become a cocoon. Further, according to the present invention, a water-soluble polymer composition having a high molecular weight and a water-soluble good acrylamide polymer as a main component, which has not been obtained in the prior art, can be obtained very easily and inexpensively. To be
───────────────────────────────────────────────────── フロントページの続き (72)発明者 坪井 彦忠 神奈川県横浜市港南区野庭町2636−23 (56)参考文献 特開 昭53−81555(JP,A) 特開 昭49−3950(JP,A) 特開 昭52−121658(JP,A) 特開 昭51−47937(JP,A) 特開 昭54−103450(JP,A) 特開 昭55−131055(JP,A) 特開 昭56−88463(JP,A) 特開 昭57−73039(JP,A) 特開 昭57−49643(JP,A) 特開 昭57−90035(JP,A) ─────────────────────────────────────────────────── ─── Continuation of the front page (72) Inventor Hikada Tsuboi 2636-23 Noba-cho, Konan-ku, Yokohama-shi, Kanagawa Prefecture (56) References JP-A-53-81555 (JP, A) JP-A-49-3950 (JP) , A) JP 52-121658 (JP, A) JP 51-47937 (JP, A) JP 54-103450 (JP, A) JP 55-131055 (JP, A) JP 56-88463 (JP, A) JP-A-57-73039 (JP, A) JP-A-57-49643 (JP, A) JP-A-57-90035 (JP, A)
Claims (2)
と、界面活性剤とを含有してなる水溶性高分子組成物を
製造する方法において、ポリマー純分20重量%以上のア
クリルアミド系含水ゲル粒子を粒径3〜10mmになるよう
に切断細粒化し、これをポリマー純分を85〜95重量%に
なる迄乾燥し、次いでこの乾燥物を粉砕して粒径2mm以
下の粉砕物とした後、この粉砕物のポリマー純分に対し
て500〜20000ppmの界面活性剤を水と共に添加しなが
ら、ポリマー純分が50〜85重量%となるよう加湿造粒す
る事を特徴とする水溶性高分子組成物の製造方法。1. A method for producing a water-soluble polymer composition comprising acrylamide polymer hydrogel particles and a surfactant, wherein the acrylamide hydrogel particles having a polymer content of 20% by weight or more are granulated. The product was cut into fine particles with a diameter of 3 to 10 mm, dried to a polymer content of 85 to 95% by weight, and then the dried product was crushed to obtain a crushed product having a particle size of 2 mm or less. A water-soluble polymer composition characterized by being humidified and granulated so that the polymer content is 50 to 85 wt% while adding a surfactant of 500 to 20000 ppm to the polymer content of the pulverized material together with water. Manufacturing method.
キサー型粉体ミキサー、流動造粒コーティング機、湿式
押出し型造粒機、粉体捏和機を用いて行なう特許請求の
範囲第(1)項記載の水溶性高分子組成物の製造方法。2. The method according to claim 1, wherein the humidification granulation is carried out by using a rotary drum type granulator, a ribbon mixer type powder mixer, a fluidized granulation coating machine, a wet extrusion type granulator, and a powder kneader. A method for producing the water-soluble polymer composition according to the item (1).
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP61171828A JPH0788456B2 (en) | 1986-07-23 | 1986-07-23 | Method for producing water-soluble polymer composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP61171828A JPH0788456B2 (en) | 1986-07-23 | 1986-07-23 | Method for producing water-soluble polymer composition |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6330554A JPS6330554A (en) | 1988-02-09 |
| JPH0788456B2 true JPH0788456B2 (en) | 1995-09-27 |
Family
ID=15930495
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP61171828A Expired - Lifetime JPH0788456B2 (en) | 1986-07-23 | 1986-07-23 | Method for producing water-soluble polymer composition |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0788456B2 (en) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IT1252950B (en) * | 1991-09-30 | 1995-07-06 | Gisulfo Baccini | SHEET LOCKING PROCEDURE FOR GREEN-TAPE CIRCUITS |
| DE69328378T2 (en) * | 1993-03-29 | 2000-12-07 | The Dow Chemical Co., Midland | Absorbent polymer with low dust formation tendencies |
| CA2852606C (en) * | 2011-10-19 | 2021-11-02 | Ashland Licensing And Intellectual Property Llc | Composition comprising a non-ionic surfactant and an ionic polymer |
| CN104017543B (en) * | 2014-05-23 | 2016-03-23 | 上海轶臣自动化科技有限公司 | Coal Transportation System environment-friendly type compound dustfall agent |
| ES2992902T3 (en) * | 2017-07-31 | 2024-12-19 | Ecolab Usa Inc | Process for fast dissolution of powder comprising low molecular weight acrylamide-based polymer |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1383367A (en) * | 1972-03-14 | 1974-02-12 | American Cyanamid Co | Polymers |
| US3849361A (en) * | 1974-10-24 | 1974-11-19 | Dow Chemical Co | Method of preparing water-dispersable polymer compositions |
| CA1066445A (en) * | 1975-02-18 | 1979-11-13 | Karl L. Krumel | Low-dusting, free-flowing acrylamide polymer composition |
| JPS5910694B2 (en) * | 1976-12-17 | 1984-03-10 | 三菱レイヨン株式会社 | Method for preventing adhesion of acrylamide polymer hydrogel |
| US4176107A (en) * | 1978-01-20 | 1979-11-27 | Buckman Laboratories, Inc. | Water-soluble dispersions of high molecular water-soluble polymers containing a surfactant and a water-soluble organic carrier which is a hydroxy compound containing repeating alkylene oxide units |
| JPS5941661B2 (en) * | 1979-04-02 | 1984-10-08 | 三菱化学株式会社 | Water-soluble polymer composition |
| JPS5688463A (en) * | 1979-12-21 | 1981-07-17 | Kurita Seizosho:Kk | Low-dust powdery high-molecular compound composition |
| JPS5749643A (en) * | 1980-09-08 | 1982-03-23 | Dai Ichi Kogyo Seiyaku Co Ltd | Preparation of water-soluble acrylamide high polymeric composition |
| JPS5773039A (en) * | 1980-10-23 | 1982-05-07 | Mitsubishi Chem Ind Ltd | Production of water-soluble granular polymer |
| JPS5790035A (en) * | 1980-11-26 | 1982-06-04 | Mitsubishi Chem Ind Ltd | Preparation of water-soluble granular polymer |
-
1986
- 1986-07-23 JP JP61171828A patent/JPH0788456B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6330554A (en) | 1988-02-09 |
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