WO1997013733A1 - Lignin-based concrete admixtures - Google Patents

Lignin-based concrete admixtures Download PDF

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Publication number
WO1997013733A1
WO1997013733A1 PCT/US1995/013836 US9513836W WO9713733A1 WO 1997013733 A1 WO1997013733 A1 WO 1997013733A1 US 9513836 W US9513836 W US 9513836W WO 9713733 A1 WO9713733 A1 WO 9713733A1
Authority
WO
WIPO (PCT)
Prior art keywords
lignin
admixture
concrete
air
cement
Prior art date
Application number
PCT/US1995/013836
Other languages
English (en)
French (fr)
Inventor
Theodore Bremner
Jiri Zhor
Gopal C. Goyal
Jairo H. Lora
Original Assignee
Alcell Technologies Inc.
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Alcell Technologies Inc. filed Critical Alcell Technologies Inc.
Priority to JP9515015A priority Critical patent/JPH11513358A/ja
Priority to PCT/US1995/013836 priority patent/WO1997013733A1/en
Priority to CA002231641A priority patent/CA2231641A1/en
Priority to CA002231630A priority patent/CA2231630A1/en
Priority to PCT/US1996/016232 priority patent/WO1997013732A2/en
Priority to EP96938620A priority patent/EP0855995A4/en
Priority to CN96198372.8A priority patent/CN1219921A/zh
Priority to JP9515194A priority patent/JPH11513653A/ja
Publication of WO1997013733A1 publication Critical patent/WO1997013733A1/en
Priority to NO981626A priority patent/NO981626L/no
Priority to NO981625A priority patent/NO981625L/no

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B24/00Use of organic materials as active ingredients for mortars, concrete or artificial stone, e.g. plasticisers
    • C04B24/16Sulfur-containing compounds
    • C04B24/18Lignin sulfonic acid or derivatives thereof, e.g. sulfite lye
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B28/00Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements
    • C04B28/02Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements containing hydraulic cements other than calcium sulfates

Definitions

  • Cement compositions are brought into a workable form by mixing the solid components with an amount of water which is greater than that required to hydrate the cement components therein.
  • the mixed mineral binder composition is poured into a form and allowed to harden at atmospheric temperature. During the hardening, some of the excess water remains, leaving cavities in the formed structural unit and, thus, reduces the mechanical strength of the resultant unit. It is well known that the compressive strength of the resultant structure generally bears an inverse relationship to the water-cement ratio of the starting mix. The need to use smaller quantities of water is limited by the required flow and workability properties of the fresh mixture.
  • Concrete admixtures refer to compounds and compositions added to concrete mixtures to alter their properties.
  • Water-reducing agents have been used as concrete admixtures. They are generally used to improve workability while decreasing water addition so that a stronger and more durable concrete is obtained.
  • Water- reducing agents are classified by their ability to reduce water content as superplasticizers or high-range water reducers and plasticizers or normal-range water reducers. Plasticizers and superplasticizers are made using chemicals with surface-active characteristics.
  • One of the traditional resources for the manufacture of water- reducing admixtures for concrete are the waste products from the pulp and paper industry, namely lignin and its derivatives. Traditionally, sulfite pulping has been the major source of lignosulfonates which after extended purification are used as normal range water-reducing and retarding admixtures for concrete.
  • Lignin-type water-reducing agents are well known for use in preparing concrete mixes. Such agents serve to reduce the amount of water that would ordinarily be required to make a pourable mix, without however disturbing most of the other beneficial properties of the mix. On various occasions, however, the use of such water-reducing agents may entrain air into the mix.
  • Entrained air tends to reduce compressive strength. As a general rule, with every one volume percent air in the concrete, 5% of strength is lost. Thus, 5% air means about 25% strength loss. However, air entrainment maybe desirable in certain applications such as the manufacture of concrete blocks.
  • Lignosulfonates are also known to slow down the curing of concrete thus causing what is known in the art as set retardation. Set retardation is particularly increased when the lignosulfonate contains impurities such as wood sugars.
  • Lignosulfonates are classified as anionic surfactants since the hydrophilic groups associated with the organic polymers are sulfonates. It has been reported that when absorbed onto cement particles, these surfactants impart a strong negative charge which lowers the surface tension of the surrounding water and greatly enhances the fluidity of the system.
  • Lignosulfonates also exhibit set retarding properties. Lignosulfonates, when used in an amount sufficient to furnish the desired water reduction in a mix, normally entrain more air than desired and retard the setting time of concrete far beyond the ranges for a high-range water-reducing admixture.
  • Lignosulfonate-based concrete admixtures are usually prepared from the waste liquor formed by the production of sulfite pulp. By neutralization, precipitation and fermentation of this liquor a range of lignosulfonates of varying purity, composition and molecular weight distribution is produced. A number of researchers have reported several attempts to enhance the lignosulfonates so that they would meet the requirements of a superplasticizer as a high range water-reducing admixture. To date no purely lignosulfonate based superplasticizer for concrete has been placed on the market .
  • U.S. Pat. No. 4,239,550 is disclosed a flowing agent for concrete and mortar based on lignin sulfonate and on ring-sulfonated or sulfomethylolated aromatic substances.
  • the flowing agent imparts to concrete or mortar high fluidity without leading to undesirably long setting times.
  • 4,460,720 is disclosed a superplasticizer cement admixture for portland cement based compositions formed from a low molecular weight alkali metal poly-acrylate in combination with an alkali metal or alkaline earth metal poly-naphthalene sulfonate- formaldehyde or an alkali metal lignosulfonate or an alkaline earth metal lignosulfonate or mixtures thereof.
  • a superplasticizer cement admixture for portland cement based compositions formed from a low molecular weight alkali metal poly-acrylate in combination with an alkali metal or alkaline earth metal poly-naphthalene sulfonate- formaldehyde or an alkali metal lignosulfonate or an alkaline earth metal lignosulfonate or mixtures thereof.
  • 4,623,682 is disclosed cement mixes having extended workability without substantial loss in rate of hardening when containing an admixture combination of a sulfonated naphtalene-formaldehyde condensate and fractionated sulfonated lignin such as ultra-filtered lignosulfonate.
  • a sulfonated naphtalene-formaldehyde condensate and fractionated sulfonated lignin such as ultra-filtered lignosulfonate.
  • U.S. Pat. No. 4,351,671 is disclosed an additive for lignin type water-reducing agent which reduces air entrainment in the concrete mix
  • U.S. Pat. No. 4,367,094 is disclosed an agent for preventing deterioration in the slump properties of mortar concrete, containing as a main ingredient a lignin sulfonate.
  • This organosolv lignin can be suitable as a raw material for the preparation of a superplasticizer water-reducing admixtures for concrete .
  • an environmentally friendly organosolv lignin- based superplasticizing and water-reducing admixture composition can impart a high degree of fluidity to cement compositions, can cause retention of the fluidity over extended time and can achieve these results at low dosages.
  • By manipulation of the conditions for the manufacture of the admixture it is possible to obtain products that do not have an adverse effect on set retardation.
  • the lignin-based admixtures of this invention are high in purity and free of sugar contamination.
  • the invention provides for a novel lignin-based admixture produced from derivatized organosolv lignin.
  • This lignin-based admixture uses a coproduct from an environmentally friendly process while fulfilling a need in the construction industry.
  • the novel lignin-based admixture is produced by derivatizing organosolv lignin by treating the lignin in a sulfomethylolation step.
  • the derivatized lignin can be formulated with an air detrainer and the resulting admixture when added to concrete mixes effectively functions as a superplasticizer and as a high- range water reducer.
  • the lignin which can be employed in this invention is a high purity lignin, particularly an organosolv lignin.
  • the lignin is separated as a by-product of the pulping and chemical delignification of plant biomass with organic solvents, for example ethanol.
  • Organosolv lignin is a nontoxic, free-flowing, powder. It is soluble in aqueous alkali and in selected organic solvents. It is generally characterized by its hydrophobicity, high purity, melt flow and a low level of carbohydrates and inorganic contaminants.
  • organosolv lignins such as regular ALCELL ® lignin or low molecular weight ALCELL ® lignin.
  • the regular ALCELL ® lignin can be characterized by a number average molecular weight of about 700 to 1500 g/mol and the low molecular weight ALCELL ® lignin can be characterized by a low average molecular weight in the range of less than 600 g/mol.
  • organosolv lignins Alternatively to organosolv lignins, it is believed that high purity lignins such as steam explosion or soda lignins can be suitable to accomplish the objectives of the invention.
  • the organosolv lignins of the invention can be derivatized using a sulfomethylolation procedure. Before carrying the sulfomethylolation procedures described below, the lignin is solubilized into an alkaline solution.
  • the amount of alkali used can vary depending on the type of lignin and the reaction conditions. For example, with ALCELL ® lignin or low molecular weight ALCELL ® lignin, from about 8% to about 20% caustic based on lignin solids can be used. The amount of water used was adjusted to obtain a solids content in the final admixture of from about 30% to about 45%.
  • the molecular weight of the lignin can be increased by cross-linking reactions. This can be accomplished by heating the lignin in alkaline solution for from about 1 to about 4 hours at from about 60°C to about 95°C.
  • An alternative cross ⁇ linking approach consists in taking lignin in alkaline solution and reacting it with an aldehyde. When for example formaldehyde is used, the reaction between the lignin and formaldehyde is a methylolation reaction.
  • the aldehyde can be added in a range of from about 0.3 to about 0.8 moles of aldehyde per lignin C-9 unit or of from about 5% to about 13% on a lignin weight basis.
  • the methylolation reaction can be carried out at from about 60°C to about 95°C for from about 1 to about 3 hours.
  • the lignin in alkaline solution can be sulfomethylolated in a number of ways.
  • the lignin can be reacted with a salt of hydroxymethane sulfonic acid such as for example its sodium salt.
  • the latter is also known as "adduct" and is available commercially. It is the addition product resulting from the reaction of formaldehyde with either sodium bisulfite or sodium sulfite.
  • the amount of adduct used for sulfomethylolation can be from about 8% to about 30% adduct solids based on a weight basis with the lignin and the sulfomethylolation reaction time is from about 2 to about 6 hours.
  • Sulfomethylolation is generally performed at from about 70°C to about 100°C.
  • the lignin can also be sulfomethylolated in a two-step process by initially reacting the lignin solution with excess of an aldehyde such as formaldehyde to methylolate the lignin thus introducing reactive aliphatic hydroxyl groups. This is done by following a similar procedure as described above to increase molecular weight but using higher levels of aldehyde such as for example of from about 10 to about 30% formaldehyde on lignin weight. This methylolation step is generally followed by reaction with from about 10 to about 25% sodium sulfite on a weight basis with lignin, at from about 120°C to about 160°C for from about 1 to about 4 hours.
  • an aldehyde such as formaldehyde
  • the lignin-based admixtures can be mixed with a concrete mix in a range of from about 0.2% to about 1% on a weight basis with the cement in the concrete.
  • the admixture causes a water reduction of from about 5% to bout 15% resulting in higher concrete strength and improved resistance to freeze and thaw.
  • An air detrainer such as tributyl phosphate, dibutyl phthalate, octyl alcohol, water-insoluble esters, carbonic and boric acids and silicones can be used.
  • Tributyl phosphate (TBP) can be added to the derivatized lignin in a range of from about 0.3% to about 5% weight basis based on lignin solids resulting in a reduction in the air content of from about 9% to about 32% to as low as from about 2% to about 3% while maintaining reasonably high slump values.
  • the adduct can be prepared by addition of about 60 grams of 50% formaldehyde to a solution of about 126 grams sodium sulfite in about 700 milliliters of water.
  • Example II Manufacture of Admixtures
  • a series of lignin-based admixtures were prepared by sulfomethylolation using as starting materials low molecular weight organosolv lignin, organosolv lignin and their methylolated counterparts. Initially, the lignins were dissolved in an aqueous solution of sodium hydroxide containing the alkali levels specified in Table 1. The amount of water used was adjusted to obtain a solids content in the final admixture of approximately 35% by weight. Those samples that were methylolated were treated with 0.5 moles of formaldehyde per lignin C-9 unit for 2 hours at 70°C. The sulfomethylolation was carried at a temperature of about 95°C and for 6 hours with adduct prepared as in Example I and using the levels described in Table 1.
  • the sulfomethylolated organosolv lignin-based admixtures were tested in cement slurries.
  • the mixes were prepared by mixing together the following ingredients:
  • Table 2 shows the initial set retardation on cement slurries. In general, the retardation decreases when the molecular weight and the level of adduct used decreases .
  • Table 3 shows the initial set retardation on cement slurries. In general, the retardation decreases when the molecular weight and the level of adduct used decreases .
  • Table 3 shows the fluidifying effect of the lignin admixtures on cement slurries as determined by decrease in torque resistance. In general, lower molecular weight and high levels of adduct resulted in a greater fluidifying effect.
  • Sulfomethylolated low molecular weight lignin is obtained with a ratio of 0.31 moles per C-9 unit using the procedure of Example II was evaluated as an admixture in concrete mixes.
  • the effect of tributyl phosphate as an air entrainer agent was also evaluated.
  • the proportions of the concrete mixes were as follows :
  • Table 4 shows the plasticizing effect of the low molecular weight sulfomethylolated organosolv lignin on concrete as shown by the high slump numbers relative to the case where no admixture is used. If an air detrainer is not used, a high air content can be observed which causes a decrease in concrete strength. Tributyl phosphate can be added to reduce the air content while maintaining a high slump and high strength. As can be seen, by adjusting the amount of detrainer agent added, a wide variety of air contents can be attained, including air contents for non- air entrained concrete (below 3.5%) and air contents for typical air entrained concrete of 4 to 8%. Table 4
  • sulfomethylolated low molecular weight organosolv lignin formulated with an air detrainer showed a higher plasticity over a commercial lignosulfonate such as for example PDA-25XL from Conchem.
  • a low molecular weight lignin- based admixture prepared as in Example II with a 0.31 moles of adduct per lignin C-9 unit was subjected to superplasticizing admixture qualification tests.
  • the admixture contained about 1.5% TBP as an air detrainer.
  • Two basic mix proportions were used, one for the non-air- entrained concrete and one for the air-entrained concrete. The following concrete mix proportions were used.
  • Reference mixes were prepared without the superplasticizer admixture.
  • Reference air entrained mix was prepared using 147 mL of air entraining agent per m 3 .
  • the mixing procedure was in accordance with CSA Standard CAN3-A266.6-M85.
  • Fresh concrete was tested for workability by measuring the slump in accordance with ASTM specification C-143-90a.
  • the time of setting was determined by measuring the penetration resistance on mortar extracted from the concrete mixture in accordance with ASTM specification C403-92.
  • the compressive strength of hardened concrete was measured in accordance with ASTM specification C-192-90a, ASTM specification C-39-86 and ASTM specification C-617-87.
  • Length change was measured in accordance with CAN/CSA-A23.2-3C and CAN/CSA-A23.2-14A.
  • Durability factor was calculated from relative dynamic modulus of elasticity changes in concrete prisms exposed to repeated cycles of freezing and thawing in accordance with ASTM specification C666-92.
  • Table 6 is a summary of the superplasticizing admixture qualification tests for the non air-entrained mix compositions.
  • Sulfomethylolated low molecular weight lignin with 35% solids content by weight was tested in concrete blocks production, both as a water reducer and as replacement for an air entrainer agent .
  • Each mix was prepared with 172 kg of cement and 1814 kg of fine aggregate. The amount of water per mix was adjusted to obtain the desired workability of concrete.
  • the admixture and quantities were as follows:
  • blocks were prepared from each concrete mix. All blocks were prepared and cured using standard procedure.
  • Control 8 100 Control 15 100 Mix 1 8 115 Mix 2 15 98 Mix 3 15 107 Mix 4 15 108 Mix 5 15 118

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Ceramic Engineering (AREA)
  • Materials Engineering (AREA)
  • Structural Engineering (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Inorganic Chemistry (AREA)
  • Curing Cements, Concrete, And Artificial Stone (AREA)
PCT/US1995/013836 1995-10-11 1995-10-11 Lignin-based concrete admixtures WO1997013733A1 (en)

Priority Applications (10)

Application Number Priority Date Filing Date Title
JP9515015A JPH11513358A (ja) 1995-10-11 1995-10-11 リグニンに基づくコンクリート添加剤
PCT/US1995/013836 WO1997013733A1 (en) 1995-10-11 1995-10-11 Lignin-based concrete admixtures
CA002231641A CA2231641A1 (en) 1995-10-11 1995-10-11 Lignin-based concrete admixtures
CA002231630A CA2231630A1 (en) 1995-10-11 1996-10-11 Sulfomethylolated lignin-based concrete admixtures
PCT/US1996/016232 WO1997013732A2 (en) 1995-10-11 1996-10-11 Sulfomethylolated lignin-based concrete admixtures
EP96938620A EP0855995A4 (en) 1995-10-11 1996-10-11 CONCRETE ADDITIVES BASED ON SULFOMETHYLOLATED LIGNIN
CN96198372.8A CN1219921A (zh) 1995-10-11 1996-10-11 磺甲基羟配聚化的木质素基的混凝土外加剂
JP9515194A JPH11513653A (ja) 1995-10-11 1996-10-11 スルホメチロール化リグニンに基づくコンクリート添加剤
NO981626A NO981626L (no) 1995-10-11 1998-04-08 Sulfometylolerte ligninbaserte betongblandinger
NO981625A NO981625L (no) 1995-10-11 1998-04-08 Lignin-baserte betongblandinger

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PCT/US1995/013836 WO1997013733A1 (en) 1995-10-11 1995-10-11 Lignin-based concrete admixtures

Publications (1)

Publication Number Publication Date
WO1997013733A1 true WO1997013733A1 (en) 1997-04-17

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Family Applications (2)

Application Number Title Priority Date Filing Date
PCT/US1995/013836 WO1997013733A1 (en) 1995-10-11 1995-10-11 Lignin-based concrete admixtures
PCT/US1996/016232 WO1997013732A2 (en) 1995-10-11 1996-10-11 Sulfomethylolated lignin-based concrete admixtures

Family Applications After (1)

Application Number Title Priority Date Filing Date
PCT/US1996/016232 WO1997013732A2 (en) 1995-10-11 1996-10-11 Sulfomethylolated lignin-based concrete admixtures

Country Status (6)

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EP (1) EP0855995A4 (no)
JP (2) JPH11513358A (no)
CN (1) CN1219921A (no)
CA (2) CA2231641A1 (no)
NO (2) NO981625L (no)
WO (2) WO1997013733A1 (no)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN118307227A (zh) * 2024-04-07 2024-07-09 东北电力大学 一种混凝土电杆用免蒸养活性掺合料混凝土材料及制备方法

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AU2749901A (en) * 1999-11-04 2001-05-30 Lignotech Usa, Inc. Low retarding, high fluidity producing lignin dispersant for concrete
DE10313937A1 (de) 2003-03-27 2004-10-14 Wacker Polymer Systems Gmbh & Co. Kg Dispergiermittel
CN100400458C (zh) * 2005-01-04 2008-07-09 华南理工大学 木质素系地铁盾构注浆外加剂及其制备方法
CN101575418B (zh) * 2009-06-19 2011-06-22 华南理工大学 一种高磺化度高分子量木质素基高效减水剂及其制备方法
PL3401410T3 (pl) 2010-06-26 2021-11-29 Virdia, Llc Sposoby wytwarzania mieszanek cukrów
IL206678A0 (en) 2010-06-28 2010-12-30 Hcl Cleantech Ltd A method for the production of fermentable sugars
WO2012000773A1 (de) 2010-06-29 2012-01-05 Construction Research & Technology Gmbh Halbstarre deckschicht
IL207329A0 (en) 2010-08-01 2010-12-30 Robert Jansen A method for refining a recycle extractant and for processing a lignocellulosic material and for the production of a carbohydrate composition
IL207945A0 (en) 2010-09-02 2010-12-30 Robert Jansen Method for the production of carbohydrates
PT106039A (pt) 2010-12-09 2012-10-26 Hcl Cleantech Ltd Processos e sistemas para o processamento de materiais lenhocelulósicos e composições relacionadas
US9512495B2 (en) 2011-04-07 2016-12-06 Virdia, Inc. Lignocellulose conversion processes and products
CN102627673A (zh) * 2012-03-23 2012-08-08 辽宁岩砂晶建材有限公司 木质素降解磺甲基化的方法
CN111333358A (zh) * 2020-05-08 2020-06-26 中建西部建设西南有限公司 一种混凝土防冻剂及其制备方法和应用

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Publication number Priority date Publication date Assignee Title
CN118307227A (zh) * 2024-04-07 2024-07-09 东北电力大学 一种混凝土电杆用免蒸养活性掺合料混凝土材料及制备方法

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CA2231630A1 (en) 1997-04-17
JPH11513358A (ja) 1999-11-16
WO1997013732A3 (en) 1997-05-15
EP0855995A4 (en) 2000-01-12
NO981626D0 (no) 1998-04-08
JPH11513653A (ja) 1999-11-24
NO981625L (no) 1998-06-05
NO981626L (no) 1998-06-05
CN1219921A (zh) 1999-06-16
CA2231641A1 (en) 1997-04-17
WO1997013732A2 (en) 1997-04-17
EP0855995A2 (en) 1998-08-05
NO981625D0 (no) 1998-04-08

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