JPH0554549B2 - - Google Patents
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- Publication number
- JPH0554549B2 JPH0554549B2 JP30444187A JP30444187A JPH0554549B2 JP H0554549 B2 JPH0554549 B2 JP H0554549B2 JP 30444187 A JP30444187 A JP 30444187A JP 30444187 A JP30444187 A JP 30444187A JP H0554549 B2 JPH0554549 B2 JP H0554549B2
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- 239000000839 emulsion Substances 0.000 claims description 71
- 229920005989 resin Polymers 0.000 claims description 31
- 239000011347 resin Substances 0.000 claims description 31
- 239000003822 epoxy resin Substances 0.000 claims description 22
- 229920000647 polyepoxide Polymers 0.000 claims description 22
- 239000007787 solid Substances 0.000 claims description 19
- 239000003795 chemical substances by application Substances 0.000 claims description 16
- 239000000203 mixture Substances 0.000 claims description 16
- 239000010426 asphalt Substances 0.000 claims description 13
- 238000000034 method Methods 0.000 claims description 13
- 239000002245 particle Substances 0.000 claims description 10
- 229920006243 acrylic copolymer Polymers 0.000 claims description 6
- 238000002156 mixing Methods 0.000 claims description 5
- 239000005038 ethylene vinyl acetate Substances 0.000 claims description 4
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 claims description 4
- 239000010410 layer Substances 0.000 description 24
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- 238000010276 construction Methods 0.000 description 7
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 5
- 239000004593 Epoxy Substances 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
- 239000004848 polyfunctional curative Substances 0.000 description 3
- 239000011241 protective layer Substances 0.000 description 3
- 239000004575 stone Substances 0.000 description 3
- 229920003002 synthetic resin Polymers 0.000 description 3
- 239000000057 synthetic resin Substances 0.000 description 3
- 238000004078 waterproofing Methods 0.000 description 3
- 229920002126 Acrylic acid copolymer Polymers 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 239000002518 antifoaming agent Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 238000010828 elution Methods 0.000 description 2
- 239000003995 emulsifying agent Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 230000001681 protective effect Effects 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 238000010998 test method Methods 0.000 description 2
- FKOKUHFZNIUSLW-UHFFFAOYSA-N 2-Hydroxypropyl stearate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(C)O FKOKUHFZNIUSLW-UHFFFAOYSA-N 0.000 description 1
- BHIZVZJETFVJMJ-UHFFFAOYSA-N 2-hydroxypropyl dodecanoate Chemical compound CCCCCCCCCCCC(=O)OCC(C)O BHIZVZJETFVJMJ-UHFFFAOYSA-N 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- 229930185605 Bisphenol Natural products 0.000 description 1
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- BCKXLBQYZLBQEK-KVVVOXFISA-M Sodium oleate Chemical compound [Na+].CCCCCCCC\C=C/CCCCCCCC([O-])=O BCKXLBQYZLBQEK-KVVVOXFISA-M 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- WGLPBDUCMAPZCE-UHFFFAOYSA-N Trioxochromium Chemical compound O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 229910000423 chromium oxide Inorganic materials 0.000 description 1
- 229920006026 co-polymeric resin Polymers 0.000 description 1
- 239000000701 coagulant Substances 0.000 description 1
- 230000015271 coagulation Effects 0.000 description 1
- 238000005345 coagulation Methods 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 238000012669 compression test Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 239000010779 crude oil Substances 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- XRPZVNIXPWZPCA-UHFFFAOYSA-N ethenyl acetate;styrene Chemical compound CC(=O)OC=C.C=CC1=CC=CC=C1 XRPZVNIXPWZPCA-UHFFFAOYSA-N 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 229960005150 glycerol Drugs 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 239000001023 inorganic pigment Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N iron oxide Inorganic materials [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 1
- 125000005395 methacrylic acid group Chemical group 0.000 description 1
- 239000004570 mortar (masonry) Substances 0.000 description 1
- NDLPOXTZKUMGOV-UHFFFAOYSA-N oxo(oxoferriooxy)iron hydrate Chemical compound O.O=[Fe]O[Fe]=O NDLPOXTZKUMGOV-UHFFFAOYSA-N 0.000 description 1
- 238000005192 partition Methods 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 229940096992 potassium oleate Drugs 0.000 description 1
- MLICVSDCCDDWMD-KVVVOXFISA-M potassium;(z)-octadec-9-enoate Chemical compound [K+].CCCCCCCC\C=C/CCCCCCCC([O-])=O MLICVSDCCDDWMD-KVVVOXFISA-M 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 229940026235 propylene glycol monolaurate Drugs 0.000 description 1
- 229940093625 propylene glycol monostearate Drugs 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000001256 steam distillation Methods 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 238000005292 vacuum distillation Methods 0.000 description 1
- 230000003313 weakening effect Effects 0.000 description 1
Landscapes
- Road Paving Structures (AREA)
Description
(産業上の利用分野)
本発明は建造物の陸屋根における防水層の保護
押え用として使用する砂利を固定するのに有効な
方法に関するものである。
(従来の技術)
従来、建造物の陸屋根おける防水層の直射日光
による老化防止や外力による損傷防止のため、防
水層の上面に保護押え層を設ける所謂押え防水工
法が用いられている。屋上を歩行等の利用に供す
る場合には、防水層の上にコンクリートの打設な
どを必要とするが、歩行等の用に供さない屋上に
は砂利押えによる工法が行われている。この方法
は防水層の上面へ砂利をふた並べ以上の厚さに敷
きならすもので、欧米では、かなり普及してお
り、コンクリート押え層を設けるのに比較して、
防水層の補修などに際し、押えの砂利を移動させ
るだけですむという簡便さがあるが、わが国では
欧米にくらべて自然条件が厳しく、単に砂利を敷
き並べるだけの工法では台風などによる砂利の吹
き飛びが懸念されるので、その対策として砂利の
粒径を25mm以上と大きくし、広い屋根面では約3
m平方毎に仕切りを設けるなどの処置をとり、ル
ーフドレン回りには砂利が寄らないように仕切る
必要があるので、これらを見込んだ場合には価格
のうえでも必ずしも有利ではなく簡便な工法とは
云い難い。
(発明が解決しようとする問題点)
そこで近年粒径25mm以下の砂利を敷き並べた上
からアスフアルトエマルシヨンまたは合成樹脂エ
マルシヨンを撒布する方法が多く採られるように
なつて来たが、この方法ではエマルシヨンの水分
が蒸発により乾燥固化するのに長時間を要し、途
中で降雨があつたりするとエマルシヨンが流出し
てしまい、砂利相互の固着力が弱められてしま
う。また砂利を敷き並べた上からエマルシヨンを
撒布する方法のため、撒布量が不正確になり易
く、部分的には必要以上のエマルシヨンを撒布す
ることになり不経済である。
さらに、砂利とエマルシヨンをあらかじめ均一
に混ぜたものを防水層の上面に敷き並べてから、
分解剤を撒布してエマルシヨンを急速に分解し、
凝固させる方法も行われているが、分解が砂利層
の上層からはじまるため分解剤が砂利層の下層全
体に行きわたらない場合が多く、均一な砂利押え
保護層を得ることができない。
このほかエマルシヨンの中に遅効性凝固剤をあ
らかじめ混ぜておき、砂利を敷き並べた上から撒
布する方法もあるが、この場合徐々にエマルシヨ
ンが増粘し砂利と砂利の間から下層に浸透しにく
くなり、とくに防水層と砂利の界面にほとんど浸
透しないことも多く見られる。
本発明の目的は、以上のような従来の砂利押え
工法の欠点をすべて解消し、砂利相互の固着力が
充分保持され、強風による砂利の吹き飛びが全く
ない安定した防水層保護押え砂利の固定方法を提
供するものである。
(問題点を解決するための手段)
本発明者らは上記の問題点を解決するため鋭意
研究を行ない、建造物の陸屋根における防水層の
保護押え用として使用する砂利を固定するのに有
効な方法を見出し本発明を完成した。
すなわち本発明は、(A)粒径5〜25mmの砂利、(B)
アスフアルト、アクリル系共重合樹脂、およびエ
チレン−酢酸ビニル系共重合樹脂のいずれか一種
のエマルシヨン、(C)エポキシ樹脂エマルシヨンお
よびその硬化剤、以上(A),(B),(C)を用いてそれぞ
れ固形分換算で(B)100重量部に対して(C)を5〜25
重量部の割合で個別にまたはあらかじめ両者を混
合し、(B),(C)の固形分換算合計量が(A)100重量部
に対し0.5〜3.5重量部の範囲で加えて均一に混合
した砂利組成物を使用直前に調製し、これを建造
物の屋上等に施した防水層の上面に層状に載置し
て乾燥硬化させることを特徴とするものである。
本発明に使用する砂利は、河川から採取される
玉砂利または安山岩などの原石を粗砕した砕石砂
利であるが、粒径が5乃至25mmの範囲のものが好
適に用いられる。粒径が25mm以上では従来の如く
砂利を固定しなくても実用上差支えなく、一方粒
径が5mm以下になると砂利全体の総表面積が大と
なりエマルシヨンの使用量を多くしなければなら
ないので不経済である。
本発明に用いるエマルシヨンは、アスフアル
ト、アクリル系共重合樹脂、およびエチレン−酢
酸ビニル共重合樹脂のうちのいずれか一種のエマ
ルシヨンとエポキシ樹脂エマルシヨンおよびエポ
キシ樹脂用硬化剤である。これらの樹脂エマルシ
ヨンは汎用されているものはほとんど問題なく用
いることができるが、特にアスフアルトエマルシ
ヨンでは通常原油中のビチユーメンを減圧蒸留お
よび/または水蒸気蒸溜して得られるストレート
アスフアルトのうちで針入度60乃至120の範囲の
ものをアニオン系乳化剤例えばオレイン酸カリウ
ム、オレイン酸ナトリウムなどの脂肪酸金属塩を
用いてエマルシヨン化したもの、またはノニオン
系乳化剤例えばグリセリン、プロピレングリコー
ルモノステアレート、プロピレングリコールモノ
ラウレートなどを用いてエマルシヨン化したもの
がよく知られており、これらが好適に使用され
る。アクリル系共重合樹脂エマルシヨンとしては
アクリル酸エステルと、メタクリル酸エステル、
酢酸ビニル、スチレン、アクリロニトリル、アク
リル酸などの共重合エマルシヨンがあげられる。
本発明にこれらの樹脂エマルシヨンが使われる
理由は、これらの樹脂の乾燥被膜が耐候性におい
て非常にすぐれていることおよび耐水性、砂利に
対する付着性において比較的よいことによるもの
である。
さらに本発明に用いられるエポキシ樹脂エマル
シヨンとしては通常のビスフエノールとエピクロ
ルヒドリンとを反応させて得られるエポキシ樹脂
を乳化させたものでよい。またエポキシ樹脂用硬
化剤としては常温硬化が可能である第1級および
第2級ポリアミン、ポリアミドの自己乳化タイプ
のものが使用できる。
本発明は、砂利とエマルシヨンの混合物を施工
後短時間でエマルシヨンを分解、硬化させて均一
な保護押え層を形成させるものであるが、アスフ
アルト、アクリル共重合樹脂およびエチレン−酢
酸ビニル共重合樹脂のいずれか一種のエマルシヨ
ンに対しエポキシ樹脂エマルシヨンおよびエポキ
シ樹脂用硬化剤を添加することにより、樹脂の乾
燥被膜の耐水性および砂利に対する付着性を飛躍
的に向上する。また短時間で硬化させることがで
きるので降雨などによりエマルシヨンが流出する
危険性も少なくなる。アスフアルトなどのエマル
シヨンに、エポキシ樹脂エマルシヨンおよびエポ
キシ樹脂用その硬化剤を添加して混合したものを
さらに砂利と混合して防水層の上に施工すると、
先ず、エポキシ硬化反応が開始される。それと同
時にエマルシヨンの分解が起り、エマルシヨン粒
子の融着そして造膜が進行する。またエマルシヨ
ンの水の蒸発も行なわれ、これらの作用により施
工後短時間で樹脂被膜が乾燥硬化し耐水性が発現
するのである。こゝでアスフアルトなどのエマル
シヨンに対し添加されるエポキシ樹脂エマルシヨ
ンおよびその硬化剤の量はそれぞれ固形分換算で
前者100重量部に対して後者を5乃至25重量部で
ある。5重量部以下では硬化が遅く樹脂の耐水性
が発現するまでに24時間以上かかる。一方25重量
部以上では硬化が早過ぎ通常の作業で可使時間が
とりにくくなり施工上問題がある。
また砂利との混合に使用するアスフアルトなど
のエマルシヨン、エポキシ樹脂エマルシヨンおよ
びその硬化剤の量は砂利100重量部に対し、固形
分換算で0.5乃至3.5重量部である。0.5重量部以下
の場合には樹脂の量が不足するので完全に砂利相
互を固着することができない。3.5重量部以上で
は樹脂量が多くなり過ぎ不経済である。
アクリル樹脂系またはエチレン−酢酸ビニル共
重合樹脂エマルシヨンを用いて砂利を固定する場
合にはこれらの樹脂エマルシヨンに、あらかじめ
着色剤を加えて調整された着色樹脂エマルシヨン
を用いて行なうことも可能である。この場合に用
いられる着色剤は耐候性のよい無機顔料が好適で
あり、例えばルチル型の酸化チタン、酸化第二
鉄、酸化クロムなどを用いる。
施工現場において、砂利と樹脂エマルシヨンを
混合するには、コンクリートモルタルの練り混ぜ
に使用される搬送式の小型ミキサーで簡単に行な
うことができる。
先ず所定量の砂利をミキサー内へ投入し、次い
でアスフアルトなどのエマルシヨン、エポキシ樹
脂エマルシヨンおよびその硬化剤を、個々に、も
しくはあらかじめ混ぜたものとして所要量添加し
て撹拌混合する。混合時間は数分乃至10分程度で
よく、砂利の表面が完全に樹脂エマルシヨンで覆
われれば充分である。こうして得られた砂利混合
物を防水層の上に一定の厚さに敷きならすのであ
るが、砂利の先端で防水層を損傷するおそれがあ
るので、防水層の上にはアスフアルトフエルト、
合成樹脂延伸クロス、合成樹脂フイルムなどを敷
き養生したうえその上に砂利混合物を敷きならす
のがよい。砂利混合物はコテで押えながら平滑に
一定の厚みに仕上げられる。
(実施例)
以下、実施例および比較例を開示して本発明の
構成および作用効果を更に明らにする。この場合
砂利100重量部に対し添加するエマルシヨンの総
量を固形分換算で2重量部とし、アクリル系共重
合樹脂などの各樹脂エマルシヨンに対するエポキ
シ樹脂エマルシヨンおよびその硬化剤の添加量を
いろいろ変えた場合の例を挙げ、さらにそれらの
性能評価を示す。
実施例 1
容量100の小型コンクリートミキサーに6号
砕石(粒径5〜13mm)100Kgを入れ撹拌しながら
モビニール709(ヘキスト合成(株)製アクリル酸エス
テル−アクリル酸共重合樹脂エマルシヨン、固形
分46%)にごく少量の消泡剤、防腐剤、防〓剤お
よび低温造膜助剤を加えたものとACRエポキシ
EM−1−60(エー・シー・アール(株)製エポキシ
樹脂エマルシヨン、固形分60%)およびACRハ
ードナーH−23−50W(エー・シー・アール(株)製
エポキシ樹脂用硬化剤、固形分50%)を所定量加
えたが、この量は樹脂エマルシヨンの総量として
固形分換算で2Kgであり、かつモビニール709の
固形分換算で100重量部に対しACRエポキシEM
−1−60およびACRハードナーH−23−50Wを
それぞれ固形分換算で、2.9重量部および2.1重量
部になる割合で加えた。実際に加えたエマルシヨ
ンの重量は次の通りであつた。
モビニール709 2×100/105÷0.46=4.140Kg
ACRエポキシEM−1−60
2×2.9/105÷0.6=0.092Kg
ACRハードナーH−23−50W
2×2.1/105÷0.5=0.080Kg
これらのエマルシヨンが加えられてから10分間
撹拌混合した。その結果、樹脂エマルシヨンが砂
利の表面を全面的に被覆した状態になり、均一な
砂利混合物が得られたので、この混合物をコンク
リートミキサーから取出して、約30mmの厚さに敷
き並べコテで押えながら平滑に仕上げ、約9時間
後に硬化させることができた。
実施例 2〜12
第1表に記載の組成のもので実施例1と同様に
して砂利を固着させた。
比較例 1〜12
第2表に記載の組成のごとくアクリル系共重合
樹脂エマルシヨンなどに対するエポキシ樹脂エマ
ルシヨンおよびその硬化剤を本発明の範囲外の量
で使用して実施例と同様に砂利を固着させた。
性能評価方法:
初期耐水性は施工後、降雨によりエマルシヨン
の流出の有無を判定するもので、砂利混合物を型
枠に入れ20℃で硬化させたものを1時間毎に一部
切り取り20℃の静水中に浸漬し、エマルシヨンの
溶出の有無を目視により測定するが、エマルシヨ
ンの溶出がなくなるまでの時間を測定した。6時
間以内で溶出のなくなるものを非常に良、6時間
以上12時間以内を良、12時間以上24時間以内を
やゝ不良、24時間以上経過後も溶出するものを不
良とした。
砂利相互の固着性は砂利混合物をコンクリート
ミキサーから流出して防水層上に一定の厚さにコ
テ押えしながら敷き並べるのに1時間程度の可使
時間が必要であるが、エポキシ樹脂およびその硬
化剤の量が多過ぎると1時間以内に硬化が進み結
果として砂利相互の固着性が悪くなる。試験方法
は20℃の室温で金属性型枠(40×40×10mm)に砂
利混合物を充填し7日間養生する。養生後脱型し
試料を鉄板(40×40×5mm)ではさんで圧縮試験
を行ない圧縮強度を求めるものである。(この場
合の圧縮速度は0.5mm/min、試験温度は20℃)
このように砂利相互の固着性は上記試験方法に
よる圧縮強度の数値の大小により良否を判定する
が圧縮強度が5Kg/cm2以上の場合を非常に良、3
Kg/cm2以上5Kg/cm2以下の場合を良、3Kg/cm2以
下の場合を不良とした。
使用樹脂の種類の表示:
B1…アクリル酸エステル−アクリル酸共重合
樹脂エマルシヨン (固形分46%)
B2…アクリル酸エステル−スチレン共重合樹
脂エマルシヨン (固形分56%)
B3…スチレン−酢酸ビニル共重合樹脂エマル
シヨン (固形分56%)
B4…アスフアルトエマルシヨン
(固形分50%)
C1…エポキシ樹脂エマルシヨン
(固形分60%)
C2…エポキシ樹脂用硬化剤 (固形分50%)
C1+C2…エポキシ樹脂およびその硬化剤
評価の表示:
◎…非常に良 〇…良 △…やや不良 ×…
不良
(Industrial Application Field) The present invention relates to an effective method for fixing gravel used as a protective holddown for a waterproof layer on a flat roof of a building. (Prior Art) Conventionally, in order to prevent the waterproofing layer of a flat roof of a building from aging due to direct sunlight and from being damaged by external forces, a so-called pressurized waterproofing method has been used in which a protective presser layer is provided on the upper surface of the waterproof layer. When a rooftop is used for walking, etc., it is necessary to pour concrete on top of the waterproof layer, but for rooftops that are not used for walking, etc., construction using gravel is used. This method involves laying gravel on top of the waterproof layer to a thickness that is at least as thick as a lid, and is quite popular in Europe and the United States.
When repairing the waterproof layer, it is easy to just move the gravel, but the natural conditions in Japan are more severe than in Europe and the United States, and the method of simply laying gravel can cause the gravel to be blown away by typhoons. As a countermeasure, the particle size of the gravel should be increased to 25 mm or more, and on large roof surfaces, the particle size should be increased to about 3 mm.
It is necessary to take measures such as installing partitions every m square to prevent gravel from gathering around the roof drain, so if you take these into account, it is not necessarily advantageous in terms of price and is not a simple construction method. hard. (Problem to be solved by the invention) Therefore, in recent years, a method of spreading asphalt emulsion or synthetic resin emulsion over gravel with a particle size of 25 mm or less has been increasingly adopted. It takes a long time for the water in the emulsion to dry and solidify due to evaporation, and if it rains during the process, the emulsion washes away, weakening the mutual adhesion of the gravel. Furthermore, since the emulsion is spread over the gravel, the amount of application tends to be inaccurate, and in some areas more emulsion than necessary is applied, which is uneconomical. Furthermore, after spreading a uniform mixture of gravel and emulsion on top of the waterproof layer,
Spray a decomposer to rapidly decompose the emulsion,
Coagulation methods have also been used, but because the decomposition starts from the upper layer of the gravel layer, the decomposer often does not reach the entire lower layer of the gravel layer, making it impossible to obtain a uniform gravel retaining protective layer. Another method is to mix a slow-acting coagulant into the emulsion in advance and spread it over the gravel, but in this case the emulsion gradually thickens and is difficult to penetrate between the gravel and the gravel. In many cases, the water hardly penetrates into the interface between the waterproof layer and the gravel. The purpose of the present invention is to eliminate all the drawbacks of the conventional gravel pressing method as described above, and to provide a stable method of fixing gravel for protecting a waterproof layer, in which the adhesion of gravel to each other is sufficiently maintained, and the gravel is not blown away by strong winds. It provides: (Means for Solving the Problems) In order to solve the above problems, the present inventors have conducted intensive research and found a method that is effective for fixing gravel used as a protective layer for waterproofing layers on flat roofs of buildings. We found a method and completed the present invention. That is, the present invention uses (A) gravel with a particle size of 5 to 25 mm, (B)
An emulsion of any one of asphalt, an acrylic copolymer resin, and an ethylene-vinyl acetate copolymer resin, (C) an epoxy resin emulsion and its curing agent, using the above (A), (B), and (C). 5 to 25 parts of (C) per 100 parts by weight of (B) in terms of solid content.
Both were mixed individually or in advance in the proportion of parts by weight, and the total amount of (B) and (C) in terms of solid content was added in the range of 0.5 to 3.5 parts by weight per 100 parts by weight of (A) and mixed uniformly. This method is characterized in that a gravel composition is prepared immediately before use, placed in a layer on the upper surface of a waterproof layer applied to the roof of a building, etc., and dried and hardened. The gravel used in the present invention is crushed stone gravel obtained by coarsely crushing raw stones such as gravel or andesite collected from rivers, and those having a particle size in the range of 5 to 25 mm are preferably used. If the particle size is 25 mm or more, there is no practical problem even if the gravel is not fixed as in the conventional method, but if the particle size is 5 mm or less, the total surface area of the entire gravel becomes large and the amount of emulsion used becomes uneconomical. It is. The emulsion used in the present invention is an emulsion of any one of asphalt, an acrylic copolymer resin, and an ethylene-vinyl acetate copolymer resin, an epoxy resin emulsion, and a curing agent for the epoxy resin. General-purpose resin emulsions can be used without any problems, but asphalt emulsions in particular have a higher penetration than straight asphalt, which is usually obtained by vacuum distillation and/or steam distillation of bitumen in crude oil. 60 to 120, emulsified using anionic emulsifiers such as fatty acid metal salts such as potassium oleate and sodium oleate, or nonionic emulsifiers such as glycerin, propylene glycol monostearate, and propylene glycol monolaurate. Emulsions made using, for example, emulsions are well known, and these are preferably used. Acrylic copolymer resin emulsions include acrylic esters, methacrylic esters,
Examples include copolymer emulsions of vinyl acetate, styrene, acrylonitrile, acrylic acid, and the like. The reason why these resin emulsions are used in the present invention is that the dry coatings of these resins have excellent weather resistance and relatively good water resistance and adhesion to gravel. Furthermore, the epoxy resin emulsion used in the present invention may be one obtained by emulsifying an epoxy resin obtained by reacting ordinary bisphenol and epichlorohydrin. As the curing agent for epoxy resins, self-emulsifying types of primary and secondary polyamines and polyamides that can be cured at room temperature can be used. The present invention decomposes and hardens the emulsion in a short time after applying a mixture of gravel and emulsion to form a uniform protective layer. By adding an epoxy resin emulsion and an epoxy resin curing agent to any one type of emulsion, the water resistance and adhesion to gravel of the dried resin film can be dramatically improved. Furthermore, since the emulsion can be cured in a short time, there is less risk of the emulsion flowing out due to rain or the like. When an emulsion such as asphalt is mixed with an epoxy resin emulsion and its curing agent for epoxy resin, it is further mixed with gravel and applied on top of the waterproof layer.
First, the epoxy curing reaction is initiated. At the same time, decomposition of the emulsion occurs, and fusion of emulsion particles and film formation proceed. Water in the emulsion also evaporates, and due to these effects, the resin coating dries and hardens within a short time after application, resulting in water resistance. The amounts of the epoxy resin emulsion and its curing agent added to the asphalt emulsion are 5 to 25 parts by weight per 100 parts by weight of the former in terms of solid content. If it is less than 5 parts by weight, curing is slow and it takes more than 24 hours for the resin to develop water resistance. On the other hand, if it exceeds 25 parts by weight, the curing will be too rapid and it will be difficult to obtain a pot life during normal work, which will cause problems in construction. Further, the amount of emulsion such as asphalt, epoxy resin emulsion, and its curing agent used for mixing with gravel is 0.5 to 3.5 parts by weight in terms of solid content per 100 parts by weight of gravel. If the amount is less than 0.5 parts by weight, the amount of resin will be insufficient and the gravel will not be completely bonded to each other. If it exceeds 3.5 parts by weight, the amount of resin becomes too large and is uneconomical. When fixing gravel using an acrylic resin emulsion or an ethylene-vinyl acetate copolymer resin emulsion, it is also possible to use a colored resin emulsion prepared by adding a coloring agent to these resin emulsions in advance. The colorant used in this case is preferably an inorganic pigment with good weather resistance, such as rutile-type titanium oxide, ferric oxide, chromium oxide, or the like. At the construction site, gravel and resin emulsion can be easily mixed using a small conveyor-type mixer used for mixing concrete mortar. First, a predetermined amount of gravel is put into a mixer, and then the required amounts of an emulsion such as asphalt, an epoxy resin emulsion, and its curing agent are added individually or as a premixed mixture, and the mixture is stirred and mixed. The mixing time may be from several minutes to about 10 minutes, and it is sufficient that the surface of the gravel is completely covered with the resin emulsion. The gravel mixture obtained in this way is spread over the waterproof layer to a certain thickness, but since there is a risk of damaging the waterproof layer with the tips of the gravel, asphalt felt is placed on top of the waterproof layer.
It is best to spread a synthetic resin stretched cloth, synthetic resin film, etc. for curing, and then spread a gravel mixture on top of it. The gravel mixture is pressed down with a trowel and finished smooth to a uniform thickness. (Examples) Hereinafter, Examples and Comparative Examples will be disclosed to further clarify the structure and effects of the present invention. In this case, the total amount of emulsion added to 100 parts by weight of gravel is 2 parts by weight in terms of solid content, and the amounts of epoxy resin emulsion and its curing agent added to each resin emulsion such as acrylic copolymer resin are varied. Examples are given and their performance evaluations are also presented. Example 1 100 kg of No. 6 crushed stone (particle size 5 to 13 mm) was placed in a small concrete mixer with a capacity of 100, and while stirring, Movinyl 709 (acrylic ester-acrylic acid copolymer resin emulsion manufactured by Hoechst Synthesis Co., Ltd., solid content 46%) was added. ) with very small amounts of antifoaming agents, preservatives, anti-foaming agents, and low-temperature coating aids, and ACR epoxy.
EM-1-60 (epoxy resin emulsion manufactured by A.C.R. Co., Ltd., solid content 60%) and ACR Hardener H-23-50W (hardening agent for epoxy resin, manufactured by A.C.R. Co., Ltd., solid content) 50%) was added, but this amount was 2 kg in terms of solid content as the total amount of resin emulsion, and ACR epoxy EM was added to 100 parts by weight in terms of solid content of Movinyl 709.
-1-60 and ACR Hardener H-23-50W were added in proportions of 2.9 parts by weight and 2.1 parts by weight, respectively, in terms of solid content. The weight of the emulsion actually added was as follows. Movinyl 709 2×100/105÷0.46=4.140Kg ACR Epoxy EM-1-60 2×2.9/105÷0.6=0.092Kg ACR Hardener H-23-50W 2×2.1/105÷0.5=0.080Kg These emulsions Stir and mix for 10 minutes after addition. As a result, the resin emulsion completely covered the surface of the gravel and a uniform gravel mixture was obtained. This mixture was taken out of the concrete mixer, spread out to a thickness of about 30 mm, and pressed down with a trowel. It had a smooth finish and was able to be cured after about 9 hours. Examples 2 to 12 Gravel was fixed in the same manner as in Example 1 using the compositions shown in Table 1. Comparative Examples 1 to 12 Gravel was fixed in the same manner as in Examples by using an epoxy resin emulsion and its curing agent for acrylic copolymer resin emulsion etc. in an amount outside the range of the present invention as shown in Table 2. Ta. Performance evaluation method: Initial water resistance is determined by determining whether or not the emulsion has flowed out due to rainfall after construction.The gravel mixture was placed in a mold and cured at 20℃, and a portion of it was cut out every hour and kept at 20℃. The sample was immersed in water and the presence or absence of elution of the emulsion was visually determined, and the time until the elution of the emulsion stopped was measured. A sample that did not elute within 6 hours was rated as very good, a sample of 6 to 12 hours was graded as good, a sample of 12 to 24 hours was graded as poor, and a sample that continued to elute even after 24 hours was graded as poor. The mutual adhesion of gravel requires about an hour of pot life to pour the gravel mixture out of the concrete mixer and spread it on the waterproof layer while troweling it to a certain thickness. If the amount of the agent is too large, curing will proceed within one hour, resulting in poor adhesion between gravels. The test method is to fill a metal mold (40 x 40 x 10 mm) with gravel mixture at a room temperature of 20°C and cure it for 7 days. After curing, the sample is removed from the mold, sandwiched between iron plates (40 x 40 x 5 mm) and subjected to a compression test to determine the compressive strength. (In this case, the compression speed is 0.5 mm/min, and the test temperature is 20℃) In this way, the adhesion of gravel to each other is judged by the magnitude of the compressive strength value according to the above test method, but the compressive strength is 5 kg/cm 2 The above cases are very good, 3
A case of Kg/cm 2 or more and 5 Kg/cm 2 or less was considered good, and a case of 3 Kg/cm 2 or less was judged as poor. Indication of the type of resin used: B1...Acrylic acid ester-acrylic acid copolymer resin emulsion (solid content 46%) B2...Acrylic acid ester-styrene copolymer resin emulsion (solid content 56%) B3...Styrene-vinyl acetate copolymerization Resin emulsion (solid content 56%) B4…Asphalt emulsion
(Solid content 50%) C1…Epoxy resin emulsion
(Solid content 60%) C2...Curing agent for epoxy resin (Solid content 50%) C1+C2...Display of epoxy resin and its curing agent evaluation: ◎...Very good 〇...Good △...Slightly poor ×...
defective
【表】【table】
【表】
(発明の効果)
本発明によれば、砂利に特定の樹脂エマルシヨ
ンをエポキシ樹脂およびその硬化剤と共にそれぞ
れ特定量、施工直前に機械的に混合することによ
り、砂利表面を完全に樹脂エマルシヨンで被覆せ
しめることができ、従つて施工後の砂利相互の固
着性が強固となり、かつ防水層との接着性もよく
極めて優れた押え効果が発揮される。また施工後
短時間で硬化が進み、降雨によるエマルシヨンの
流出のおそれは殆んどなくなり、耐水性、耐候性
も高い押え層を形成することができる。[Table] (Effects of the invention) According to the present invention, by mechanically mixing specific amounts of a specific resin emulsion with epoxy resin and its curing agent into gravel immediately before construction, the gravel surface can be completely coated with the resin emulsion. Therefore, the adhesion of the gravel to each other after construction is strong, and the adhesion to the waterproof layer is also good, providing an extremely excellent holding effect. Furthermore, curing progresses in a short time after application, there is almost no risk of the emulsion flowing out due to rain, and a presser layer with high water resistance and weather resistance can be formed.
Claims (1)
クリル系共重合樹脂、およびエチレン−酢酸ビニ
ル共重合樹脂のいずれか一種のエマルシヨン、(C)
エポキシ樹脂エマルシヨンおよびその硬化剤、以
上(A),(B),(C)を用いて、それぞれ固形分換算で(B)
100重量部に対して(C)を5〜25重量部の割合で個
別にまたはあらかじめ両者を混合し、(B),(C)の固
形分換算合計量が(A)100重量部に対し0.5〜3.5重
量部の範囲で加えて均一に混合して砂利組成物を
使用直前に調製し、これを建造物の屋上等に施し
た防水層の上面に層状に載置して乾燥硬化させる
ことを特徴とする屋上防水層保護押え砂利の固定
方法。1 (A) Gravel with a particle size of 5 to 25 mm, (B) An emulsion of any one of asphalt, acrylic copolymer resin, and ethylene-vinyl acetate copolymer resin, (C)
Using epoxy resin emulsion and its curing agent, (A), (B), and (C), each has (B) in terms of solid content.
(C) is added individually or mixed in advance at a ratio of 5 to 25 parts by weight per 100 parts by weight, and the total amount of (B) and (C) in terms of solid content is 0.5 parts by weight per 100 parts by weight of (A). A gravel composition is prepared immediately before use by adding and uniformly mixing 3.5 parts by weight, and this is placed in a layer on the top of a waterproof layer applied to the roof of a building, etc., and allowed to dry and harden. Features: Rooftop waterproof layer protection gravel fixing method.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP30444187A JPH01151641A (en) | 1987-12-07 | 1987-12-07 | Method of fixing roof waterproof layer protective hold-down gravel |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP30444187A JPH01151641A (en) | 1987-12-07 | 1987-12-07 | Method of fixing roof waterproof layer protective hold-down gravel |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH01151641A JPH01151641A (en) | 1989-06-14 |
JPH0554549B2 true JPH0554549B2 (en) | 1993-08-12 |
Family
ID=17933046
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP30444187A Granted JPH01151641A (en) | 1987-12-07 | 1987-12-07 | Method of fixing roof waterproof layer protective hold-down gravel |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH01151641A (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2623135B2 (en) * | 1989-02-27 | 1997-06-25 | 菊水化学工業株式会社 | Flat roof waterproofing method |
-
1987
- 1987-12-07 JP JP30444187A patent/JPH01151641A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPH01151641A (en) | 1989-06-14 |
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